Aquatic Weed Identification & Management
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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. -
A Key to Common Vermont Aquatic Plant Species
A Key to Common Vermont Aquatic Plant Species Lakes and Ponds Management and Protection Program Table of Contents Page 3 Introduction ........................................................................................................................................................................................................................ 4 How To Use This Guide ....................................................................................................................................................................................................... 5 Field Notes .......................................................................................................................................................................................................................... 6 Plant Key ............................................................................................................................................................................................................................. 7 Submersed Plants ...................................................................................................................................................................................... 8-20 Pipewort Eriocaulon aquaticum ...................................................................................................................................................................... 9 Wild Celery Vallisneria americana .................................................................................................................................................................. -
Floristic Account of Submersed Aquatic Angiosperms of Dera Ismail Khan District, Northwestern Pakistan
Penfound WT. 1940. The biology of Dianthera americana L. Am. Midl. Nat. Touchette BW, Frank A. 2009. Xylem potential- and water content-break- 24:242-247. points in two wetland forbs: indicators of drought resistance in emergent Qui D, Wu Z, Liu B, Deng J, Fu G, He F. 2001. The restoration of aquatic mac- hydrophytes. Aquat. Biol. 6:67-75. rophytes for improving water quality in a hypertrophic shallow lake in Touchette BW, Iannacone LR, Turner G, Frank A. 2007. Drought tolerance Hubei Province, China. Ecol. Eng. 18:147-156. versus drought avoidance: A comparison of plant-water relations in her- Schaff SD, Pezeshki SR, Shields FD. 2003. Effects of soil conditions on sur- baceous wetland plants subjected to water withdrawal and repletion. Wet- vival and growth of black willow cuttings. Environ. Manage. 31:748-763. lands. 27:656-667. Strakosh TR, Eitzmann JL, Gido KB, Guy CS. 2005. The response of water wil- low Justicia americana to different water inundation and desiccation regimes. N. Am. J. Fish. Manage. 25:1476-1485. J. Aquat. Plant Manage. 49: 125-128 Floristic account of submersed aquatic angiosperms of Dera Ismail Khan District, northwestern Pakistan SARFARAZ KHAN MARWAT, MIR AJAB KHAN, MUSHTAQ AHMAD AND MUHAMMAD ZAFAR* INTRODUCTION and root (Lancar and Krake 2002). The aquatic plants are of various types, some emergent and rooted on the bottom and Pakistan is a developing country of South Asia covering an others submerged. Still others are free-floating, and some area of 87.98 million ha (217 million ac), located 23-37°N 61- are rooted on the bank of the impoundments, adopting 76°E, with diverse geological and climatic environments. -
Summary Report of Nonindigenous Aquatic Species in U.S. Fish and Wildlife Service Region 5
Summary Report of Nonindigenous Aquatic Species in U.S. Fish and Wildlife Service Region 5 Summary Report of Nonindigenous Aquatic Species in U.S. Fish and Wildlife Service Region 5 Prepared by: Amy J. Benson, Colette C. Jacono, Pam L. Fuller, Elizabeth R. McKercher, U.S. Geological Survey 7920 NW 71st Street Gainesville, Florida 32653 and Myriah M. Richerson Johnson Controls World Services, Inc. 7315 North Atlantic Avenue Cape Canaveral, FL 32920 Prepared for: U.S. Fish and Wildlife Service 4401 North Fairfax Drive Arlington, VA 22203 29 February 2004 Table of Contents Introduction ……………………………………………………………………………... ...1 Aquatic Macrophytes ………………………………………………………………….. ... 2 Submersed Plants ………...………………………………………………........... 7 Emergent Plants ………………………………………………………….......... 13 Floating Plants ………………………………………………………………..... 24 Fishes ...…………….…………………………………………………………………..... 29 Invertebrates…………………………………………………………………………...... 56 Mollusks …………………………………………………………………………. 57 Bivalves …………….………………………………………………........ 57 Gastropods ……………………………………………………………... 63 Nudibranchs ………………………………………………………......... 68 Crustaceans …………………………………………………………………..... 69 Amphipods …………………………………………………………….... 69 Cladocerans …………………………………………………………..... 70 Copepods ……………………………………………………………….. 71 Crabs …………………………………………………………………...... 72 Crayfish ………………………………………………………………….. 73 Isopods ………………………………………………………………...... 75 Shrimp ………………………………………………………………….... 75 Amphibians and Reptiles …………………………………………………………….. 76 Amphibians ……………………………………………………………….......... 81 Toads and Frogs -
Najas Minor (Hydrocharitaceae) in North America: a Reappraisal
Aquatic Botany 126 (2015) 60–72 Contents lists available at ScienceDirect Aquatic Botany journal homepage: www.elsevier.com/locate/aquabot Najas minor (Hydrocharitaceae) in North America: A reappraisal a,∗ a,1 a,2 a,3 Donald H. Les , Elena L. Peredo , Nicholas P. Tippery , Lori K. Benoit , a a b,4 b c Hamid Razifard , Ursula M. King , Hye Ryun Na , Hong-Keun Choi , Lei Chen , a,5 d Robynn K. Shannon , Sallie P. Sheldon a Department of Ecology and Evolutionary Biology, University of Connecticut, Storrs, CT 06269-3043, USA b Department of Biological Sciences, Ajou University, Suwon 443-749, Republic of Korea c South China Botanical Garden, Chinese Academy of Sciences, Guangzhou 510650, China d Department of Biology, Middlebury College, Middlebury, VT 05753-6151, USA a r t i c l e i n f o a b s t r a c t Article history: Genetic studies of nonindigenous populations can help to determine their geographical origin, whether Received 19 March 2015 single or multiple introductions have occurred, and provide evidence of hybridization. We broadly sur- Received in revised form 16 June 2015 veyed Najas minor populations at several nuclear and chloroplast loci. Sequence data were obtained from Accepted 23 June 2015 nonindigenous N. minor populations in North America and portions of its native range in Europe (Italy) Available online 29 June 2015 and Asia (China, Korea). North American populations were mapped to evaluate the observed patterns of genetic variation geographically. We detected multiple genotypes of N. minor in collections originating Key words: from within Eurasia and North America. -
The Herbivorous Insect Fauna of a Submersed Weed, Hydrilla Verticillata (Alismatales: Hydrocharitaceae)
SESSION 5 Weeds of Aquatic Systems and Wetlands Proceedings of the X International Symposium on Biological Control of Weeds 307 4-14 July 1999, Montana State University, Bozeman, Montana, USA Neal R. Spencer [ed.]. pp. 307-313 (2000) The Herbivorous Insect Fauna of a Submersed Weed, Hydrilla verticillata (Alismatales: Hydrocharitaceae) C. A. BENNETT1 and G. R. BUCKINGHAM2 1 Department of Entomology and Nematology, University of Florida, and 2 USDA-ARS 1,2 Florida Biological Control Laboratory, P.O. Box 147100, Gainesville, Florida 32614-7100, USA Abstract Although relatively few insects have been reported to feed on submersed aquatic plants, field surveys on Hydrilla verticillata (L. F.) Royle for biological control agents have demonstrated that insect herbivores should be expected when surveying submersed aquatic plants in the native ranges. Beetles, or Coleoptera, especially the weevils (Curculionidae), are important herbivores. Weevils attack submersed plant species both when water is present and when water is absent during dry periods which leave the plants exposed. Pupal success appears to be the major determinant of weevil life cycle strategies. Donaciine leaf beetles (Chrysomelidae) attack the roots or crowns of submersed species, but their feeding and damage is difficult to determine. Leaf-mining Hydrellia flies (Diptera: Ephydridae) are diverse and common on submersed species. Other flies, the midges (Chironomidae), are also common on submersed species, but many utilize the plants only for shelter. However, midge larvae ate the apical meristems on the tips of hydrilla stems. Aquatic caterpillars (Lepidoptera: Pyralidae) are the herbivores most eas- ily observed on submersed species because of their large size and conspicuous damage, but their host ranges might be too broad for use as biological control agents. -
Maryland Aquatic Nuisance Species Management Plan
Maryland Aquatic Nuisance Species Management Plan November 2016 Approved by the Aquatic Nuisance Species Task Force 1 This Aquatic Nuisance Species Management Plan was prepared by the Maryland Department of Natural Resources Invasive Species Matrix Team in partnership with Maryland agencies and organizations invested in invasive species management, and with input from the general public. Suggested citation : MDDNR (Maryland Department of Natural Resources). 2016. Maryland Aquatic Nuisance Species Management Plan. Annapolis. 77 pp + Appendices. 2 3 ACKNOWLEDGMENTS This Aquatic Nuisance Species Management Plan began development with the Maryland Department of Natural Resources' Invasive Species Matrix Team and a subcommittee formed by Jonathan McKnight, Joe Love, Mark Lewandowski, Jay Killian, Kerrie Kyde, Nancy Butowski, and Susan Rivers. It was greatly improved by the efforts of reviewers from State and Federal agencies, Don MacLean, the Aquatic Nuisance Species Task Force, and the general public. The Mid-Atlantic Panel on Aquatic Invasive Species importantly helped to inform the development of this Plan. 4 MARYLAND AQUATIC NUISANCE SPECIES MANAGEMENT PLAN EXECUTIVE SUMMARY An aquatic nuisance species (ANS) is a non-native species whose introduction does or is likely to cause economic or environmental harm or harm to human health. While many aquatic species may be introduced to a water body, very few become established, and fewer are regarded as ANS. In the Chesapeake Bay watershed, there are 120 introduced and established aquatic species -
Bay Grass Identification Key
Bay Grass Identification Key Select the Bookmark tab to the left or scroll down to see the individual SAV. There is a Dichotomous Key at the end of this document. Maryland DepartmentofNatural Resources Bladderwort Utricularia spp. Native to the Chesapeake Bay Family - Lentibulariaceae Distribution - Several species of bladderwort occur in the Chesapeake Bay region, prima- rily in the quiet freshwater of ponds and ditches. Bladderworts can also be found on moist soils associated with wetlands. Recognition - Bladderworts are small herbs that are found floating in shallow water or growing on very moist soils. The stems are generally horizontal and submerged. Leaves are alter- nate, linear or dissected often appearing opposite or whorled. The branches are often much dissected, appear rootlike and have bladders with bristles around the openings. Bladderworts are considered carnivorous because minute animals can be trapped and digested in the bladders that occur on the underwater leaves. Bladderwort Maryland DepartmentofNatural Resources Common Waterweed Elodea canadensis Native to Chesapeake Bay Family - Hydrocharitaceae Distribution - Common waterweed is primarily a freshwater species, and occasionally grows in brackish upper reaches in many of the Bay’s tributaries. It prefers loamy soil, slow-moving water with high nitrogen and phosphorous concentrations. Recognition - The leaves of common waterweed can vary greatly in width, size and bunching. In general, the leaves are linear to oval with minutely toothed margins and blunt tips. Leaves have no leaf stalks, and occur in whorls of 3 at stem nodes, becoming more crowded toward the stem tips. Common waterweed has slender, branching stems and a weak, thread-like root system. -
European Naiad: an Invasive Aquatic Plant Najas Minor
European Naiad: An Invasive Aquatic Plant Najas minor Description • Najas minor is an annual, rooted, submerged exotic aquatic plant originally from Europe. • Leaves are lime green, very slender and 1 ¾ inches long with 6-15 deep conspicuous teeth along the margin. Leaves are usually opposite each other with a wide base that tapers to a sharp tip. • The brittle, re-curved leaves branch profusely at the apex, giving N. minor a bushy appearance. • Small 1.5 – 3.0 mm fruits develop in the leaf axils. Fruits are slightly curved and have white ladder- like longitudinal rows. European Naiad Habitat European Naiad is a hardy species that is established in the alkaline waters of western Massachusetts. • N. minor has greater tolerance for turbidity and eutrophic conditions than other native Najas species, often driving them out of an area. • N. minor prefers slow moving waters including lakes and ponds but occasionally exists in rivers. Commonwealth of Massachusetts ~ Department of Conservation and Recreation ~ Office of Water Resources ~ Lakes and Ponds Program 1 Distribution Map Najas minor Reproduction European Naiad reproduces by both vegetative methods and from seed production. • Vegetatively, N. minor reproduces by stem fragmentation. Fragments often attach to boats, gear, wildlife or may drift to new locations and form pioneer colonies. • N. minor reproduces primarily from seeds. Small fruits develop in the leaf axils, and during late summer, the leaves become brittle and fragment. Impacts and Threats Posed by European Naiad European Naiad grows and reproduces rapidly, and often displaces native species, reduces biodiversity, hampers recreational uses, and reduces real estate and aesthetic values. -
Native Vascular Flora of the City of Alexandria, Virginia
Native Vascular Flora City of Alexandria, Virginia Photo by Gary P. Fleming December 2015 Native Vascular Flora of the City of Alexandria, Virginia December 2015 By Roderick H. Simmons City of Alexandria Department of Recreation, Parks, and Cultural Activities, Natural Resources Division 2900-A Business Center Drive Alexandria, Virginia 22314 [email protected] Suggested citation: Simmons, R.H. 2015. Native vascular flora of the City of Alexandria, Virginia. City of Alexandria Department of Recreation, Parks, and Cultural Activities, Alexandria, Virginia. 104 pp. Table of Contents Abstract ............................................................................................................................................ 2 Introduction ...................................................................................................................................... 2 Climate ..................................................................................................................................... 2 Geology and Soils .................................................................................................................... 3 History of Botanical Studies in Alexandria .............................................................................. 5 Methods ............................................................................................................................................ 7 Results and Discussion .................................................................................................................... -
Recent History of Submersed Aquatic Plants in Cayuga Lake
Recent History of Submersed Aquatic Plants in Cayuga Lake 1928 To 2017 Northwest Cayuga Lake 80 (+1 SE) 70 Acentria recorded 60 in lake - 1991 50 40 30 % Milfoil 20 10 0 87 88 89 90 91 92 93 94 95 96 97 98 99 Year Cayuga Lake Watershed Network’s Fall Community Conference November 4, 2017 Bob Johnson Albert Vogel’s Cornell Masters Thesis 1973 “Changes in the Submerged Aquatic Flora at the South End of Cayuga Lake between 1929 and Early aquatic plant history1970 from” Al’s Thesis (40 years) Myriophyllum exalbescens (a native species) ID’ed in his Thesis in 1970 is correct for earlier research before Al, however in 1970 his milfoil was the non- native invasive M. spicatum (Eurasian watermilfoil) Past records concentrated on the area south of line from Wheatons on the West shore, through the pile cluster to Willow Point on the East shore Muenscher 1928, Leister 1929, Eurasian watermilfoil Hewitt 1944 and Vogel 1973 Al Vogel conducted his study in 1970 and contrasted his findings with the researchers from 1928 to 1944 who were studying submerged aquatic plants as a food source for ducks. Vogel’s purpose of his study was to determine the changes over the last 40 years. His hypothesis was that abundant growth occurred over a larger area with fewer species and water milfoil as the dominant plant. That all happened, however the watermilfoil identification was not correct. A lot of confusion in the 1960’s as to ID of milfoils. Al Vogel finished his data collection and went back home to CA in 1971 to write his thesis. -
Naiads Najas Spp
Maryland DepartmentofNatural Resources Naiads Najas spp. Native to Chesapeake Bay except for N. minor; non-invasive Najas minor Family - Najadaceae Distribution - Four naiad species occur in Chesapeake Bay. The first two are more common than the latter two. · Najas guadalupensis (southern naiad or bushy pondweed) · Najas minor (no common name) · Najas flexilis (northern naiad) · Najas gracillima (slender naiad). Najas guadalupensis Naiads are native except for N. minor which was introduced from Europe. Naiads grow in small freshwater streams, and freshwater portions of Bay tributaries. Bushy pondweed tolerates slightly brackish water. Naiads prefer sandy substrates and tolerate relatively low light. Recognition - Naiads vary in size from inch-high tufts on sandy bottoms to highly branched plants two or three feet high on silty bottoms. In general the naiads have slender, branching stems with narrow leaves that broaden at the base and are opposite or in whorls. Naiads have small, fibrous roots without rhizomes or tubers. The four species in Chesapeake Bay resemble one another, however, their leaves provide distinguishing characteristics. Najas spp. Bushy pondweed and northern naiad have wider leaves than the other two species. Bushy pondweed leaves are flat and straight, whereas leaves of northern naiad curve out from the stem at maturity. Slender naiad and N. minor have slender leaves with a truncated (abruptly-ending) basal sheath. N. minor is distinguished from slender naiad by stiff, recurved leaves and lengthwise ribs on its seed coat. Slender naiad has minute leaf-margin teeth that are difficult to see, whereas leaf-margin teeth of N. minor are visible to the naked eye.