Potamogeton Crispus L
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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. -
(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 -
(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 -
Morpho-Chronological Variations and Primary Production in Posidonia
Morpho-chronological variations and primary production in Posidonia sea grass from Western Australia Gérard Pergent, Christine Pergent-Martini, Catherine Fernandez, Pasqualini Vanina, Diana Walker To cite this version: Gérard Pergent, Christine Pergent-Martini, Catherine Fernandez, Pasqualini Vanina, Diana Walker. Morpho-chronological variations and primary production in Posidonia sea grass from Western Aus- tralia. Journal of the Marine Biological Association of the United Kingdom, Cambridge University Press, 2004, 84 (5), pp.895-899. 10.1017/S0025315404010161h. hal-01768985 HAL Id: hal-01768985 https://hal.archives-ouvertes.fr/hal-01768985 Submitted on 17 Apr 2018 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. J. Mar. Biol. Ass. U.K. (2004), 84, 895^899 Printed in the United Kingdom Morpho-chronological variations and primary production in Posidonia sea grass from Western Australia P Ge¤rard Pergent* , Christine Pergent-Martini*, Catherine Fernandez*, O Vanina Pasqualini* and Diana Walker O *Equipe Ecosyste' mes Littoraux, Faculty of Sciences, -
Redalyc.Mortality Rate Estimation for Eelgrass Zostera Marina
Revista de Biología Tropical ISSN: 0034-7744 [email protected] Universidad de Costa Rica Costa Rica Flores Uzeta, Olga; Solana Arellano, Elena; Echavarría Heras, Héctor Mortality rate estimation for eelgrass Zostera marina (Potamogetonaceae) using projections from Leslie matrices Revista de Biología Tropical, vol. 56, núm. 3, septiembre, 2008, pp. 1015-1022 Universidad de Costa Rica San Pedro de Montes de Oca, Costa Rica Available in: http://www.redalyc.org/articulo.oa?id=44918834004 How to cite Complete issue Scientific Information System More information about this article Network of Scientific Journals from Latin America, the Caribbean, Spain and Portugal Journal's homepage in redalyc.org Non-profit academic project, developed under the open access initiative Mortality rate estimation for eelgrass Zostera marina (Potamogetonaceae) using projections from Leslie matrices Olga Flores Uzeta, Elena Solana Arellano & Héctor Echavarría Heras Departamento de Ecología Marina, Centro de Investigación Científica y Educación Superior de Ensenada, Ensenada, Baja California México, P.O. Box 430222, San Diego, CA. 92143-0222, USA.Fax: (646) 175 05 00; oflores@cicese. mx; [email protected]; [email protected] Received 28-VIII-2006. Corrected 30-VI-2008. Accepted 31-VII-2008. Abstract: The main goal of this study is to provide estimations of mean mortality rate of vegetative shoots of the seagrass Zostera marina in a meadow near Ensenada Baja California, using a technique that minimizes destruc- tive sampling. Using cohorts and Leslie matrices, three life tables were constructed, each representing a season within the period of monthly sampling (April 1999 to April 2000). Ages for the cohorts were established in terms of Plastochrone Interval (PI). -