Clayton, J.S. 2001. Border Control for Potential Aquatic Weeds. Stage 2. Weed Risk Assessment
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Aquatic Plants of Saratoga Lake
Saratoga Lake Aquatic Plant Survey – 2009 Prepared By Lawrence Eichler Research Scientist and Charles Boylen Associate Director Darrin Fresh Water Institute 5060 Lakeshore Drive Bolton Landing, NY 12814 (518) 644-3541 (voice) (518) 644-3640 (fax) [email protected] December 1, 2009 DFWI Technical Report 2009-6 TABLE OF CONTENTS Background . 1 Introduction . 1 Survey Site . 1 Methods . 3 Species List and Herbarium Specimens . 3 Point Intercept Survey . 3 Results and Discussion Saratoga Lake Survey Results . 5 Maximum Depth of Colonization . 6 Species Richness and Distribution . 7 Summary . 14 References . 19 Acknowledgements . 20 Appendix A. Saratoga Lake aquatic plant distribution maps . A-1 List of Tables Page Table 1 Aquatic plant species present in Saratoga Lake in 2009 ….………... 5 Table 2 Saratoga Lake point intercept percent frequency of occurrence …… 8 Table 3 Saratoga Lake point intercept percent frequency of occurrence in 2009 9 Table 4 Species richness for the point intercept surveys …………………… 13 List of Figures Page Figure 1 Distribution of point intercept survey points for Saratoga Lake ..…… 4 Figure 2 Depth distribution of Saratoga Lake sampling points ..……………… 7 Figure 3 Distribution of Eurasian watermilfoil in Saratoga Lake in 2009 10 Figure 4 Frequency of occurrence summaries for sampling points of all water depth 11 Figure 5 Frequency of occurrence summaries for sampling points of <6m water depth ………………………………………………………………….. 12 Figure 6 Species richness for native species in the point intercept survey ……. 13 Figure 7 A comparison of the distribution of Eurasian watermilfoil (Myriophyllum spicatum) growth in Saratoga Lake in 2004, 2007, 2008 and 2009…. 16 iii Report on Aquatic Vegetation of Saratoga Lake, New York Background Quantitative aquatic plant surveys were undertaken in 2009 for Saratoga Lake, New York as part of a cooperative effort between Aquatic Control Technologies (ACT) and the Darrin Fresh Water Institute, and supported by the Saratoga Lake Protection and Improvement District (SLPID). -
The Vascular Plants of Massachusetts
The Vascular Plants of Massachusetts: The Vascular Plants of Massachusetts: A County Checklist • First Revision Melissa Dow Cullina, Bryan Connolly, Bruce Sorrie and Paul Somers Somers Bruce Sorrie and Paul Connolly, Bryan Cullina, Melissa Dow Revision • First A County Checklist Plants of Massachusetts: Vascular The A County Checklist First Revision Melissa Dow Cullina, Bryan Connolly, Bruce Sorrie and Paul Somers Massachusetts Natural Heritage & Endangered Species Program Massachusetts Division of Fisheries and Wildlife Natural Heritage & Endangered Species Program The Natural Heritage & Endangered Species Program (NHESP), part of the Massachusetts Division of Fisheries and Wildlife, is one of the programs forming the Natural Heritage network. NHESP is responsible for the conservation and protection of hundreds of species that are not hunted, fished, trapped, or commercially harvested in the state. The Program's highest priority is protecting the 176 species of vertebrate and invertebrate animals and 259 species of native plants that are officially listed as Endangered, Threatened or of Special Concern in Massachusetts. Endangered species conservation in Massachusetts depends on you! A major source of funding for the protection of rare and endangered species comes from voluntary donations on state income tax forms. Contributions go to the Natural Heritage & Endangered Species Fund, which provides a portion of the operating budget for the Natural Heritage & Endangered Species Program. NHESP protects rare species through biological inventory, -
Phytochemical Screening of Tubers and Leaf Extracts of Sagittaria Sagittifolial.:Newsa (Arrowhead)
International Journal of Scientific and Research Publications, Volume 7, Issue 9, September 2017 431 ISSN 2250-3153 Phytochemical Screening of Tubers and Leaf extracts of Sagittaria sagittifoliaL.:Newsa (Arrowhead) Anita Rao and V. N. Pandey Experimental Botany and Nutraceutical Laboratory, Department of Botany,DDU Gorakhpur University, Gorakhpur - 273009, (U.P.) India [email protected]* Abstract:The present investigation deals with the preliminary phytochemical estimation of bio-functional partsi.e.Leaves and Tubers. Aquatic starchy tuberous plant Sagittariasagittifolia L. belonging to family Alismataceae, commonly known as Arrowhead. The biofunctional parts were extracted with five different organic solvents viz. Ethanol, Methanol, Acetone, Petroleum Ether, Chloroform and Distilled Water for their primary and secondary phytochemicals and their active constituents like Tannin, Saponins, Flavonoids, Phenols, Steroids, Glycosides, Protein, Amino-acids, Starch, Reducing sugars and Alkaloids. The results show the 31.1±0.08 extract of leaf and 35.7±0.15extract of tuber shows higher extractive value. The presence ofmaximum phytochemicals viz. glycosides, steroids, tannins, saponins, terpenoids, flavonoids, carbohydrates, alkaloids, and phenols in ethanol while minimum presence in acetone followed by aqueous.Thesephytochemicalsare useful in medicinal and therapeutic system as well as in traditional and modern medicinal system. Key Words: Sagittariasagittifolia. Phytochemicals, Extractive value, Therapeutics. Introduction Edible aquatic plants constitute an additional source of food and vegetable. They have high medicinal properties. Sagittaria sagittifolia L., a beautiful fresh water ethno-nutraceutical plant growing on the side bank of watershed, river, ponds, nullas and muddy substrata. The plant belongs to family Alismataceae native of Asia and Europe, commonly known as Arrowhead and Newsa an indigenous plant of North Eastern Terai Region of U.P. -
27April12acquatic Plants
International Plant Protection Convention Protecting the world’s plant resources from pests 01 2012 ENG Aquatic plants their uses and risks Implementation Review and Support System Support and Review Implementation A review of the global status of aquatic plants Aquatic plants their uses and risks A review of the global status of aquatic plants Ryan M. Wersal, Ph.D. & John D. Madsen, Ph.D. i The designations employed and the presentation of material in this information product do not imply the expression of any opinion whatsoever on the part of the Food and Agriculture Organization of the United Nations (FAO) concerning the legal or development status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. The mention of speciic companies or products of manufacturers, whether or not these have been patented, does not imply that these have been endorsed or recommended by FAO in preference to others of a similar nature that are not mentioned.All rights reserved. FAO encourages reproduction and dissemination of material in this information product. Non-commercial uses will be authorized free of charge, upon request. Reproduction for resale or other commercial purposes, including educational purposes, may incur fees. Applications for permission to reproduce or disseminate FAO copyright materials, and all queries concerning rights and licences, should be addressed by e-mail to [email protected] or to the Chief, Publishing Policy and Support Branch, Ofice of Knowledge Exchange, -
Hydrocotyle Sibthorpioides and H. Batrachium (Araliaceae) New for New York State
Atha, D. 2017. Hydrocotyle sibthorpioides and H. batrachium (Araliaceae) new for New York State. Phytoneuron 2017-56: 1– 6. Published 21 August 2017. ISSN 2153 733X HYDROCOTYLE SIBTHORPIOIDES AND H. BATRACHIUM (ARALIACEAE) NEW FOR NEW YORK STATE DANIEL ATHA Center for Conservation Strategy New York Botanical Garden Bronx, New York 10458 [email protected] ABSTRACT Spontaneous populations of Hydrocotyle sibthorpioides (lawn marsh pennywort) and H. batrachium (Araliaceae) are documented for New York state for the first time. Hydrocotyle batrachium is also new to North America. Hydrocotyle sibthorpioides was first found in 2013 in Queens county; H. batrachium was first found in 2016 in Westchester county. Both species are native to eastern Asia and show potential to be aggressive invaders in southeastern New York, particularly in wetlands. A key to the species of Hydrocotyle in New York State is provided. Prior to this report four species of Hydrocotyle were known from New York state, all of them native and all but one state-listed rarities: H. umbellata – Rare; H. verticillata var. verticillata – Endangered; and H. ranunculoides – Endangered (Young 2010). Among the native New York species, only H. americana occurs in abundance in the state. It is the only species historically reported for New York City and has not been documented for New York City since 1901. The present report documents two additional species for the New York flora, both native to Asia and naturalized in southeastern New York. Fertile herbarium specimens and DNA samples were obtained for all cited specimens and are available for analysis. Hydrocotyle sibthorpioides Lam. Spontaneous populations of Hydrocotyle sibthorpioides in New York were first detected and identified in Queens County by Nick Wagerik in the summer of 2013. -
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. -
Title Flowering Phenology and Anthophilous Insect Community at a Threatened Natural Lowland Marsh at Nakaikemi in Tsuruga, Japan
Flowering phenology and anthophilous insect community at a Title threatened natural lowland marsh at Nakaikemi in Tsuruga, Japan Author(s) KATO, Makoto; MIURA, Reiichi Contributions from the Biological Laboratory, Kyoto Citation University (1996), 29(1): 1 Issue Date 1996-03-31 URL http://hdl.handle.net/2433/156114 Right Type Departmental Bulletin Paper Textversion publisher Kyoto University Contr. biol. Lab. Kyoto Univ., Vol. 29, pp. 1-48, Pl. 1 Issued 31 March 1996 Flowering phenology and anthophilous insect community at a threatened natural lowland marsh at Nakaikemi in Tsuruga, Japan Makoto KATo and Reiichi MiuRA ABSTRACT Nakaikemi marsh, located in Fukui Prefecture, is one of only a few natural lowland marshlands left in westem Japan, and harbors many endangered marsh plants and animals. Flowering phenology and anthophilous insect communities on 64 plant species of 35 families were studied in the marsh in 1994-95. A total of 936 individuals of 215 species in eight orders of Insecta were collected on flowers from mid April to mid October, The anthophilous insect community was characterized by dominance of Diptera (58 9e of individuals) and relative paucity of Hymenoptera (26 9o), Hemiptera (6 9e), Lepidoptera (5 9e), and Coleoptera (5 9o), Syrphidae was the most abundant family and probably the most important pollination agents. Bee community was characterized by dominance of an aboveground nesting bee genus, Hylaeus (Colletidae), the most abundant species of which was a minute, rare little-recorded species. Cluster analysis on fiower-visiting insect spectra grouped 64 plant species into seven clusters, which were respectively characterized by dominance of small or large bees (18 spp.), syrphid fiies (13 spp.), Calyptrate and other flies (11 spp.), wasps and middle-sized bees (8 spp.), Lepidoptera (2 spp.), Coleoptera (1 sp.) and a mixture of these various insects (11 spp.). -
An Assessment of Exotic Species in the Tonle Sap Biosphere Reserve
AN ASSESSMENT OF EXOTIC SPECIES IN THE TONLE SAP BIOSPHERE RESERVE AND ASSOCIATED THREATS TO BIODIVERSITY A RESOURCE DOCUMENT FOR THE MANAGEMENT OF INVASIVE ALIEN SPECIES December 2006 Robert van Zalinge (compiler) This publication is a technical output of the UNDP/GEF-funded Tonle Sap Conservation Project Executive Summary Introduction This report is mainly a literature review. It attempts to put together all the available information from recent biological surveys, and environmental and resource use studies in the Tonle Sap Biosphere Reserve (TSBR) in order to assess the status of exotic species and report any information on their abundance, distribution and impact. For those exotic species found in the TSBR, it is examined whether they can be termed as being an invasive alien species (IAS). IAS are exotic species that pose a threat to native ecosystems, economies and/or human health. It is widely believed that IAS are the second most significant threat to biodiversity worldwide, following habitat destruction. In recognition of the threat posed by IAS the Convention on Biological Diversity puts forward the following strategy to all parties in Article 8h: “each contracting party shall as far as possible and as appropriate: prevent the introduction of, control, or eradicate those alien species which threaten ecosystems, habitats or species”. The National Assembly of Cambodia ratified the Convention on Biological Diversity in 1995. After reviewing the status of exotic species in the Tonle Sap from the literature, as well as the results from a survey based on questionnaires distributed among local communities, the main issues are discussed, possible strategies to combat the spread of alien species that are potentially invasive are examined, and recommendations are made to facilitate the implementation of a strategy towards reducing the impact of these species on the TSBR ecosystem. -
Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- BIBLIOGRAPHY
Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- BIBLIOGRAPHY BIBLIOGRAPHY Ackerfield, J., and J. Wen. 2002. A morphometric analysis of Hedera L. (the ivy genus, Araliaceae) and its taxonomic implications. Adansonia 24: 197-212. Adams, P. 1961. Observations on the Sagittaria subulata complex. Rhodora 63: 247-265. Adams, R.M. II, and W.J. Dress. 1982. Nodding Lilium species of eastern North America (Liliaceae). Baileya 21: 165-188. Adams, R.P. 1986. Geographic variation in Juniperus silicicola and J. virginiana of the Southeastern United States: multivariant analyses of morphology and terpenoids. Taxon 35: 31-75. ------. 1995. Revisionary study of Caribbean species of Juniperus (Cupressaceae). Phytologia 78: 134-150. ------, and T. Demeke. 1993. Systematic relationships in Juniperus based on random amplified polymorphic DNAs (RAPDs). Taxon 42: 553-571. Adams, W.P. 1957. A revision of the genus Ascyrum (Hypericaceae). Rhodora 59: 73-95. ------. 1962. Studies in the Guttiferae. I. A synopsis of Hypericum section Myriandra. Contr. Gray Herbarium Harv. 182: 1-51. ------, and N.K.B. Robson. 1961. A re-evaluation of the generic status of Ascyrum and Crookea (Guttiferae). Rhodora 63: 10-16. Adams, W.P. 1973. Clusiaceae of the southeastern United States. J. Elisha Mitchell Sci. Soc. 89: 62-71. Adler, L. 1999. Polygonum perfoliatum (mile-a-minute weed). Chinquapin 7: 4. Aedo, C., J.J. Aldasoro, and C. Navarro. 1998. Taxonomic revision of Geranium sections Batrachioidea and Divaricata (Geraniaceae). Ann. Missouri Bot. Gard. 85: 594-630. Affolter, J.M. 1985. A monograph of the genus Lilaeopsis (Umbelliferae). Systematic Bot. Monographs 6. Ahles, H.E., and A.E. -
Aquarium Plants
Aquarium Plants 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. Shipment of aquatic plants is prohibited in Puerto Rico. Shipment of Cabomba is restricted in CA, CT, MA, ME, VT, and WA. In all other cases, the USDA does not require any special permits to receive aquatic plants. However, in order to continue to protect our environment, you must house your aquatic plants in an aquarium. Under no circum- stances should you release your plants into the wild. Primary Hazard Considerations Always wash your hands thoroughly before and after you handle your aquatic plants, or anything it has touched. Availability Aquatic plants are generally available year round, and can be found in freshwater lakes and ponds. They are collected, so shortages may occur. The aquatic plants come packaged in plastic bags. Once received, open package and, using tap water, gently rinse away any debris or broken-off pieces. Some plants come in jars; remove lid and place in tank. Your plants do not need to be acclimated. Aquarium Needs Habitat: • Water from the tap in most cases contains chlorine, which can be detrimental to the health of your plants and aquatic animals. De-chlorinate your water by using a commercial chemical designed to do so, such as Ammonia/Chlorine Detoxifier, or by leaving your water out in an open container for 24–48 hours. Tropical plants need temperatures ranging from 66–77°F. For an aquarium to function well, a Filtration System 21 W 3535 is needed. -
Illustrated Flora of East Texas Illustrated Flora of East Texas
ILLUSTRATED FLORA OF EAST TEXAS ILLUSTRATED FLORA OF EAST TEXAS IS PUBLISHED WITH THE SUPPORT OF: MAJOR BENEFACTORS: DAVID GIBSON AND WILL CRENSHAW DISCOVERY FUND U.S. FISH AND WILDLIFE FOUNDATION (NATIONAL PARK SERVICE, USDA FOREST SERVICE) TEXAS PARKS AND WILDLIFE DEPARTMENT SCOTT AND STUART GENTLING BENEFACTORS: NEW DOROTHEA L. LEONHARDT FOUNDATION (ANDREA C. HARKINS) TEMPLE-INLAND FOUNDATION SUMMERLEE FOUNDATION AMON G. CARTER FOUNDATION ROBERT J. O’KENNON PEG & BEN KEITH DORA & GORDON SYLVESTER DAVID & SUE NIVENS NATIVE PLANT SOCIETY OF TEXAS DAVID & MARGARET BAMBERGER GORDON MAY & KAREN WILLIAMSON JACOB & TERESE HERSHEY FOUNDATION INSTITUTIONAL SUPPORT: AUSTIN COLLEGE BOTANICAL RESEARCH INSTITUTE OF TEXAS SID RICHARDSON CAREER DEVELOPMENT FUND OF AUSTIN COLLEGE II OTHER CONTRIBUTORS: ALLDREDGE, LINDA & JACK HOLLEMAN, W.B. PETRUS, ELAINE J. BATTERBAE, SUSAN ROBERTS HOLT, JEAN & DUNCAN PRITCHETT, MARY H. BECK, NELL HUBER, MARY MAUD PRICE, DIANE BECKELMAN, SARA HUDSON, JIM & YONIE PRUESS, WARREN W. BENDER, LYNNE HULTMARK, GORDON & SARAH ROACH, ELIZABETH M. & ALLEN BIBB, NATHAN & BETTIE HUSTON, MELIA ROEBUCK, RICK & VICKI BOSWORTH, TONY JACOBS, BONNIE & LOUIS ROGNLIE, GLORIA & ERIC BOTTONE, LAURA BURKS JAMES, ROI & DEANNA ROUSH, LUCY BROWN, LARRY E. JEFFORDS, RUSSELL M. ROWE, BRIAN BRUSER, III, MR. & MRS. HENRY JOHN, SUE & PHIL ROZELL, JIMMY BURT, HELEN W. JONES, MARY LOU SANDLIN, MIKE CAMPBELL, KATHERINE & CHARLES KAHLE, GAIL SANDLIN, MR. & MRS. WILLIAM CARR, WILLIAM R. KARGES, JOANN SATTERWHITE, BEN CLARY, KAREN KEITH, ELIZABETH & ERIC SCHOENFELD, CARL COCHRAN, JOYCE LANEY, ELEANOR W. SCHULTZE, BETTY DAHLBERG, WALTER G. LAUGHLIN, DR. JAMES E. SCHULZE, PETER & HELEN DALLAS CHAPTER-NPSOT LECHE, BEVERLY SENNHAUSER, KELLY S. DAMEWOOD, LOGAN & ELEANOR LEWIS, PATRICIA SERLING, STEVEN DAMUTH, STEVEN LIGGIO, JOE SHANNON, LEILA HOUSEMAN DAVIS, ELLEN D. -
Evaluation of Total Phenolic, Flavonoid and Antioxidant Activity of Sagittaria Sagittifolia L
Anita Rao et al. Int. Res. J. Pharm. 2019, 10 (5) INTERNATIONAL RESEARCH JOURNAL OF PHARMACY www.irjponline.com ISSN 2230 – 8407 Research Article EVALUATION OF TOTAL PHENOLIC, FLAVONOID AND ANTIOXIDANT ACTIVITY OF SAGITTARIA SAGITTIFOLIA L. Anita Rao *, Vageshwari and V. N. Pandey Experimental Botany and Nutraceutical LaBoratory, Department of Botany, DDU Gorakhpur University, Gorakhpur - 273009, (U.P.) India *Corresponding Author Email: [email protected] Article Received on: 11/02/19 Approved for puBlication: 25/03/19 DOI: 10.7897/2230-8407.1005168 ABSTRACT The present investigation is a study of the Leaves of Sagittaria sagittifolia L. with respect to potential as antioxidant in relation to their total content of Phenolic and Flavonoids compounds in five different organic solvents. The amounts of total phenols were analyzed with the Folin- Ciocalteu Reagent. Gallic acid was used as a standard compound and the total phenols were expressed as mg/g gallic acid equivalent. The antioxidant activity of extracts were expressed as percentage of DPPH radical inhibition and IC50 values in percentage ranged from 18.86± 0.23 % to 86.65 ± 0.43 % Maximum phenolic content was found in the methanolic extract (36.4± 0.30) where as maximum flavonoids are detected in ethanolic extract (16.60± 0.01). The high contents of phenolic and flavonoids compounds indicated that these compounds contriBute to the antioxidant activity. KEY WORDS: Phenolic, Flavonoid, Antioxidant, Sagittaria sagittifolia L. INTRODUCTION Our present investigation is a study of the Leaves of Sagittaria sagittifolia L. with respect to potential as antioxidant in relation Sagittaria sagittifolia L. (Faimily Alismataceae) commonly to their total content of Phenolic and Flavonoids compounds.