Cayuga Lake Macrophyte ID Guide Who We Are and What We Do
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(BCF), Translocation Factor (TF) and Metal Enrichment Factor (MEF) Abilities of Aquatic Macrophyte Species Exposed to Metal Contaminated Wastewater
ISSN(Online): 2319-8753 ISSN (Print): 2347-6710 International Journal of Innovative Research in Science, Engineering and Technology (A High Impact Factor, Monthly, Peer Reviewed Journal) Visit: www.ijirset.com Vol. 8, Issue 1, January 2019 Evaluation of Bioaccumulation Factor (BAF), Bioconcentration Factor (BCF), Translocation Factor (TF) and Metal Enrichment Factor (MEF) Abilities of Aquatic Macrophyte Species Exposed to Metal Contaminated Wastewater S. S. Shingadgaon1, B.L. Chavan2 Research Scholar, Department of Environmental Science, School of Earth Sciences, Solapur University, Solapur, MS, India1 Former Professor and Head, Department of Environmental Science, Solapur University Solapur and presently working at Department of Environmental Science, Dr.Babasaheb Ambedkar Marathwada University, Aurangabad, MS, India 2 ABSTRACT: Wastewaters receiving aquatic bodies are quiet complex in terms of pollutants, the transport and interactions with heavy metals. This complexity is primarily due to high variability of pollutants, contaminants and related parameters. The macrophytes are plausible bio-indicators of the pollution load and level of metals within the aquatic systems than the wastewater or sediment analyses. The potential ability of aquatic macrophytes in natural water bodies receiving municipal sewage from Solapur city was assessed. Data from the studies on macrophytes exposed to a mixed test bath of metals and examined to know their potentialities to accumulate heavy metals for judging their suitability for phytoremediation technology -
An Updated Checklist of Aquatic Plants of Myanmar and Thailand
Biodiversity Data Journal 2: e1019 doi: 10.3897/BDJ.2.e1019 Taxonomic paper An updated checklist of aquatic plants of Myanmar and Thailand Yu Ito†, Anders S. Barfod‡ † University of Canterbury, Christchurch, New Zealand ‡ Aarhus University, Aarhus, Denmark Corresponding author: Yu Ito ([email protected]) Academic editor: Quentin Groom Received: 04 Nov 2013 | Accepted: 29 Dec 2013 | Published: 06 Jan 2014 Citation: Ito Y, Barfod A (2014) An updated checklist of aquatic plants of Myanmar and Thailand. Biodiversity Data Journal 2: e1019. doi: 10.3897/BDJ.2.e1019 Abstract The flora of Tropical Asia is among the richest in the world, yet the actual diversity is estimated to be much higher than previously reported. Myanmar and Thailand are adjacent countries that together occupy more than the half the area of continental Tropical Asia. This geographic area is diverse ecologically, ranging from cool-temperate to tropical climates, and includes from coast, rainforests and high mountain elevations. An updated checklist of aquatic plants, which includes 78 species in 44 genera from 24 families, are presented based on floristic works. This number includes seven species, that have never been listed in the previous floras and checklists. The species (excluding non-indigenous taxa) were categorized by five geographic groups with the exception of to reflect the rich diversity of the countries' floras. Keywords Aquatic plants, flora, Myanmar, Thailand © Ito Y, Barfod A. This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. -
(Potamogeton Crispus) in the Sacramento–San Joaquin Delta, California
J. Aquat. Plant Manage. 59: 1–6 Molecular confirmation of hybridization with invasive curly-leaf pondweed (Potamogeton crispus) in the Sacramento–San Joaquin Delta, California AJAY R. JONES AND RYAN A. THUM* ABSTRACT populations of hydrilla (Hydrilla verticillata) is influenced by DNA substitutions in the phytoene desaturase gene (Michel Weed managers recognize that hybridization can influ- et al. 2004), which can be detected by genetic screening ence invasiveness in target weeds. As such, the identification (Benoit and Les 2013). Similarly, different genotypes of of hybridization in target weeds has become of fundamental Eurasian (Myriophyllum spicatum) and hybrid watermilfoil (M. interest. Curly-leaf pondweed (Potamogeton crispus)isa spicatum 3 M. sibiricum) vary in their growth and response to heavily managed invasive aquatic weed in the United States. several herbicides (e.g., Glomski and Netherland 2009, The genus is known for extensive interspecific hybridiza- Berger et al. 2012, Thum et al, 2012, LaRue et al. 2013, tion, but the extent to which invasive P. crispus in the United Taylor et al. 2017, Netherland and Willey 2018), and distinct States hybridizes is unknown. In October 2018, an aquatic phenotypes of fanwort (Cabomba caroliniana) differ in their vegetation survey in the California Sacramento–San Joaquin response to several herbicides (Bultemeier et al. 2009). river delta identified plants that were suspected as P. crispus Hybridization between invasive species and their native hybrids. These plants closely resembled P. crispus but relatives is one source of genetic variation that can differed in several ways, including having smaller, finer influence invasiveness (Ellstrand and Schierenbeck 2000). leaves and lacking the presence of true turions. -
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 -
1.3 Impact of Invasive Aquatic Plants on Waterfowl
1.3 Impact of Invasive Aquatic Plants on Waterfowl Ryan M. Wersal: Minnesota State University Mankato, Mankato MN; [email protected] Kurt D. Getsinger: US Army ERDC, Vicksburg MS; [email protected] Introduction Studies that evaluate the relationship between waterfowl and aquatic plants (native or nonnative) usually focus on the food habits and feeding ecology of waterfowl. Therefore, the purpose of this section is to describe the dynamics of waterfowl feeding in relation to aquatic plants. The habitats used by waterfowl for breeding, wintering and foraging are diverse and change based on the annual life cycle of waterfowl and seasonal conditions of the habitat. For example, waterfowl require large amounts of protein during migration, nesting and molting, and they fulfill this requirement by consuming aquatic invertebrates. As noted in Sections 1.1 and 1.2, a strong relationship exists between high numbers of aquatic invertebrates and diverse aquatic plant communities, so diverse plant communities also play an important role in waterfowl health by hosting the invertebrates needed to subsidize waterfowl migration, nesting and molting. After all, waterfowl native to the US have evolved alongside diverse plant communities that are likewise native to the US and utilize these plants and associated invertebrates to meet their energy needs. Metabolic energy demands of waterfowl are high during the winter months, so waterfowl need foods that are high in carbohydrates such as plant seeds, tubers and rhizomes during winter. Many waterfowl will sometimes abandon aquatic plant foraging while on their wintering grounds and feed instead on high-energy agricultural crops such as wheat, corn, rice and soybeans. -
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. -
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. -
Potamogeton Crispus L
Weed Risk Assessment for Michigan Department Potamogeton crispus L. of Agriculture and (Potamogetonaceae) – Curly leaf Rural Development pondweed May 10, 2016 Version 1 Top left: growth form (Leslie J. Mehrhoff, University of Connecticut, Bugwood.org), bottom left: P. crispus infestation (Chris Evans, University of Illinois, Bugwood.org), right: foliage close up with view of air bladders (Chris Evans, University of Illinois, Bugwood.org). Agency Contact : Cecilia Weibert Pesticide and Plant Pest Management Division Michigan Department of Agriculture and Rural Development P.O. Box 30017 Lansing, Michigan 48909 Telephone: 1-800-292-3939 Weed Risk Assessment for Potamogeton crispus Introduction The Michigan Department of Agriculture and Rural Development (MDARD) regulates aquatic species through a Prohibited and Restricted species list, under the authority of Michigan’s Natural Resources and Environmental Protection Act (NREPA), Act 451 of 1994, Part 413 (MCL 324.41301-41305). Prohibited species are defined as species which “(i) are not native or are genetically engineered, (ii) are not naturalized in this state or, if naturalized, are not widely distributed, and further, fulfill at least one of two requirements: (A) The organism has the potential to harm human health or to severely harm natural, agricultural, or silvicultural resources and (B) Effective management or control techniques for the organism are not available.” Restricted species are defined as species which “(i) are not native, and (ii) are naturalized in this state, and one or more of the following apply: (A) The organism has the potential to harm human health or to harm natural, agricultural, or silvicultural resources. (B) Effective management or control techniques for the organism are available.” Per a recently signed amendment to NREPA (MCL 324.41302), MDARD will be conducting reviews of all species on the lists to ensure that the lists are as accurate as possible. -
Curlyleaf Pondweed (Potamogeton Crispus L.) Angela Poovey FISH
Curlyleaf pondweed (Potamogeton crispus L.) Angela Poovey FISH 423 Fall 2008 1. Diagnostic information Basic identification key Class Liliopsida – Monocotyledons Curlyleaf pondweed (Potamogeton Subclass Alismatidae crispus L.) is a rooted submersed macrophyte that grows in freshwater lakes, ponds, rivers, and Order Najadales streams. It may be found in slightly brackish Family Potamogetonaceae – waters (Catling and Dobson 1985). It grows Pondweed family entirely underwater except for the flower stalk Genus Potamogeton – pondweed which rises above the water (WA-DOE 2001). Species crispus – curlyleaf Although most pondweeds exhibit plasticity, in pondweed which the appearance of the same species may vary depending on growing conditions, curlyleaf Common names pondweed is easily identified. It has olive-green curlyleaf pondweed, curly-leaved pondweed, to reddish-brown leaves (Figure 1). Leaves are curly pondweed, crisp pondweed, or curly attached to narrow slightly flattened stems in an muckweed alternate pattern. They are oblong (3-8 cm long, Figure 1. A stand of mature curlyleaf pondweed plants (left) and a plant stem (upper right). Note reddish-brown tinge with red midvein. Leaves have wavy edges and fine serrations (lower right). 5-12 mm wide) with margins that are distinctly Life-history and basic ecology wavy and finely serrated creating an overall leaf texture that is “crispy” (Borman et al. 1997). The cool water adaptations of curlyleaf Stems are branched and somewhat flattened; pondweed set it apart from other aquatic plants. they grow up to 90 cm (WA-DOE 2001). It survives as an entire plant under the ice Curlyleaf pondweed may be confused with (Wehrmeister and Stuckey 1992) while most Richardson’s pondweed (P.