Control of Potamogeton Crispus and Myriophyllum Spicatum in Crystal Lake, Middletown, CT
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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). -
Chemical Profile of the North American Native Myriophyllum
Chemical profile of the North American native Myriophyllum sibiricum compared to the invasive M. spicatum Michelle D. Marko a,b,*, Elisabeth M. Gross c, Raymond M. Newman a, Florence K. Gleason b a University of Minnesota, Department of Fisheries, Wildlife and Conservation Biology, 1980 Folwell Avenue, St. Paul, MN 55108, USA b University of Minnesota, Department of Plant Biology, 1445 Gortner Avenue, St. Paul, MN 55108, USA c Limnological Institute, University of Konstanz, PO Box M659, 78457 Konstanz, Germany Received 7 September 2006; received in revised form 10 August 2007; accepted 27 August 2007 Available online 2 September 2007 Abstract Myriophyllum spicatum L. is a nonindigenous invasive plant in North America that can displace the closely related native Myriophyllum sibiricum Komarov. We analyzed the chemical composition (including: C, N, P, polyphenols, lignin, nonpolar extractables, and sugars) of M. spicatum and M. sibiricum and determined how the chemistry of the two species varied by plant part with growing environment (lake versus tank), irradiance (full sun versus 50% shading), and season (July through September). M. spicatum had higher concentrations of carbon, polyphenols and lignin (C: 47%; polyphenols: 5.5%; lignin: 18%) than M. sibiricum (C: 42%; polyphenols: 3.7%; lignin: 9%) while M. sibiricum had a higher concentration of ash under all conditions (12% versus 8% for M. spicatum). Apical meristems of both species had the highest concentration of carbon, polyphenols, and tellimagrandin II, followed by leaves and stems. Tellimagrandin II was present in apical meristems of both M. spicatum (24.6 mg gÀ1 dm) and M. sibiricum (11.1 mg gÀ1 dm). -
Natural Communities of Michigan: Classification and Description
Natural Communities of Michigan: Classification and Description Prepared by: Michael A. Kost, Dennis A. Albert, Joshua G. Cohen, Bradford S. Slaughter, Rebecca K. Schillo, Christopher R. Weber, and Kim A. Chapman Michigan Natural Features Inventory P.O. Box 13036 Lansing, MI 48901-3036 For: Michigan Department of Natural Resources Wildlife Division and Forest, Mineral and Fire Management Division September 30, 2007 Report Number 2007-21 Version 1.2 Last Updated: July 9, 2010 Suggested Citation: Kost, M.A., D.A. Albert, J.G. Cohen, B.S. Slaughter, R.K. Schillo, C.R. Weber, and K.A. Chapman. 2007. Natural Communities of Michigan: Classification and Description. Michigan Natural Features Inventory, Report Number 2007-21, Lansing, MI. 314 pp. Copyright 2007 Michigan State University Board of Trustees. Michigan State University Extension programs and materials are open to all without regard to race, color, national origin, gender, religion, age, disability, political beliefs, sexual orientation, marital status or family status. Cover photos: Top left, Dry Sand Prairie at Indian Lake, Newaygo County (M. Kost); top right, Limestone Bedrock Lakeshore, Summer Island, Delta County (J. Cohen); lower left, Muskeg, Luce County (J. Cohen); and lower right, Mesic Northern Forest as a matrix natural community, Porcupine Mountains Wilderness State Park, Ontonagon County (M. Kost). Acknowledgements We thank the Michigan Department of Natural Resources Wildlife Division and Forest, Mineral, and Fire Management Division for funding this effort to classify and describe the natural communities of Michigan. This work relied heavily on data collected by many present and former Michigan Natural Features Inventory (MNFI) field scientists and collaborators, including members of the Michigan Natural Areas Council. -
(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. -
Fecundity of a Native Herbivore on Its Native and Exotic Host Plants and Relationship to Plant Chemistry
Aquatic Invasions (2017) Volume 12, Issue 3: 355–369 DOI: https://doi.org/10.3391/ai.2017.12.3.09 Open Access © 2017 The Author(s). Journal compilation © 2017 REABIC Special Issue: Invasive Species in Inland Waters Research Article Fecundity of a native herbivore on its native and exotic host plants and relationship to plant chemistry Michelle D. Marko1,2,* and Raymond M. Newman1 1Department of Fisheries, Wildlife and Conservation Biology, University of Minnesota, St. Paul, MN, 55108, USA 2Biology Department, Concordia College, Moorhead, MN 56562, USA *Corresponding author E-mail: [email protected] Received: 2 November 2016 / Accepted: 28 August 2017 / Published online: 20 September 2017 Handling editor: Liesbeth Bakker Editor’s note: This study was first presented at the special session on aquatic invasive species at the 33rd Congress of the International Society of Limnology (SIL) (31 July – 5 August 2016, Torino, Italy) (http://limnology.org/meetings/past-sil-congress/). This special session has provided a venue for the exchange of information on ecological impacts of non-native species in inland waters. Abstract The host range expansion of the specialist milfoil weevil, Euhrychiopsis lecontei, from the native Myriophyllum sibiricum (northern watermilfoil) to invasive M. spicatum (Eurasian watermilfoil) is one of the few examples of a native insect herbivore preferring, growing and surviving better on a nonindigenous host plant than it does on its native host plant. The milfoil weevil’s preference for the nonindigenous plant can be induced during juvenile development or through exposure to Eurasian watermilfoil as an adult. We evaluated how the fecundity of the milfoil weevil was affected over time by juvenile and adult exposure to the native, invasive and invasive × native hybrid milfoils and whether fecundity was correlated with host plant quality. -
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. -
Whorled Water-Milfoil, Myriophyllum Verticillatum
Natural Heritage Whorled Water-milfoil & Endangered Species Myriophyllum verticillatum L. Program www.mass.gov/nhesp State Status: Endangered Federal Status: None Massachusetts Division of Fisheries & Wildlife DESCRIPTION: The Whorled Water-milfoil (Myriophyllum verticillatum) is an aquatic herb of the Haloragaceae family. The plant grows submersed in water, except for the terminal inflorescence, which emerges above the surface. Small, sessile flowers are oppositely arranged along the uppermost portion of the spike. The stems are elongate and narrow, often branched, and bear whorled leaves that are pinnately dissected into fine segments. AIDS TO IDENTIFICATION: Distinguishing the various species of water-milfoils is difficult, especially in the vegetative condition, and a technical manual and an expert should always be consulted. This is one of a few water-milfoils that produce turions, which are small, bulb-like propagules that allow the plant to spread vegetatively. In this species, the turions are club-shaped (wider at the tips than at the base). Another diagnostic character is the presence of consistently deeply lobed floral bracts that greatly exceed (are more than twice as long as) the length of the female flowers. The combination of these characters, plus the presence of whorled leaves, serves to distinguish this species from the other water-milfoils in Massachusetts. Crow, Garrett, and C. Barre Hellquist. 2000. Aquatic and Wetland Plants. Volume 1. University of Wisconsin Press, Madison, Wisconsin. SIMILAR SPECIES: Common water-milfoils could easily be confused with the Whorled Water-milfoil. For example, the native Lowly Water-milfoil (Myriophyllum humile) differs in having leaves that are strictly alternate, rather than whorled as in the Whorled Water-milfoil. -
Proceedings of the Indiana Academy of Science 1 23
Proceedings of the Indiana Academy of Science 1 23 (1998) Volume 107 p. 123-139 AQUATIC PLANT SPECIES DIVERSITY AND FLORISTIC QUALITY ASSESSMENT OF SAUGANY LAKE, INDIANA Mitchell S. Alix and Robin W. Scribailo Biology and Chemistry Section Purdue University North Central Westville, Indiana 46391 ABSTRACT: Floristic surveys of Saugany Lake were conducted during the growing seasons of 1996 through 1998 to determine the distribution and abun- dance of submerged, emergent, and free-floating aquatic plant species. Forty- nine species in 33 genera were identified from 24 families. The localities for each identified species were mapped. Each species was assigned an overall relative abundance rank based on a mean score which incorporated the total area covered by the species and its total number of occurrences. Plant fami- lies exhibiting the greatest diversity were the Potamogetonaceae (nine species), Cyperaceae (six species), and Lemnaceae (four species). Among the species collected, four are state-listed, and three are non-native. The floristic quality index (I) of the lake was 44, and the mean coefficient of conservatism (Q was 6.6. These values indicate that the lake represents a natural community with high species richness. In addition to the floristic quality index and mean coef- ficient of conservatism, the attached checklist provides baseline data for future monitoring of the aquatic plant species of Saugany Lake. KEYWORDS: Aquatic macrophytes, floristic quality assessment, Indiana flora, Saugany Lake, species diversity. INTRODUCTION Comprehensive floristic investigations of ponds, lakes, and streams in Indi- ana are rare despite concerns over eutrophication and the large number of aquat- ic vascular plant species listed as endangered, threatened, or rare in the State. -
WETLAND PLANTS – Full Species List (English) RECORDING FORM
WETLAND PLANTS – full species list (English) RECORDING FORM Surveyor Name(s) Pond name Date e.g. John Smith (if known) Square: 4 fig grid reference Pond: 8 fig grid ref e.g. SP1243 (see your map) e.g. SP 1235 4325 (see your map) METHOD: wetland plants (full species list) survey Survey a single Focal Pond in each 1km square Aim: To assess pond quality and conservation value using plants, by recording all wetland plant species present within the pond’s outer boundary. How: Identify the outer boundary of the pond. This is the ‘line’ marking the pond’s highest yearly water levels (usually in early spring). It will probably not be the current water level of the pond, but should be evident from the extent of wetland vegetation (for example a ring of rushes growing at the pond’s outer edge), or other clues such as water-line marks on tree trunks or stones. Within the outer boundary, search all the dry and shallow areas of the pond that are accessible. Survey deeper areas with a net or grapnel hook. Record wetland plants found by crossing through the names on this sheet. You don’t need to record terrestrial species. For each species record its approximate abundance as a percentage of the pond’s surface area. Where few plants are present, record as ‘<1%’. If you are not completely confident in your species identification put’?’ by the species name. If you are really unsure put ‘??’. After your survey please enter the results online: www.freshwaterhabitats.org.uk/projects/waternet/ Aquatic plants (submerged-leaved species) Stonewort, Bristly (Chara hispida) Bistort, Amphibious (Persicaria amphibia) Arrowhead (Sagittaria sagittifolia) Stonewort, Clustered (Tolypella glomerata) Crystalwort, Channelled (Riccia canaliculata) Arrowhead, Canadian (Sagittaria rigida) Stonewort, Common (Chara vulgaris) Crystalwort, Lizard (Riccia bifurca) Arrowhead, Narrow-leaved (Sagittaria subulata) Stonewort, Convergent (Chara connivens) Duckweed , non-native sp. -
NJ Native Plants - USDA
NJ Native Plants - USDA Scientific Name Common Name N/I Family Category National Wetland Indicator Status Thermopsis villosa Aaron's rod N Fabaceae Dicot Rubus depavitus Aberdeen dewberry N Rosaceae Dicot Artemisia absinthium absinthium I Asteraceae Dicot Aplectrum hyemale Adam and Eve N Orchidaceae Monocot FAC-, FACW Yucca filamentosa Adam's needle N Agavaceae Monocot Gentianella quinquefolia agueweed N Gentianaceae Dicot FAC, FACW- Rhamnus alnifolia alderleaf buckthorn N Rhamnaceae Dicot FACU, OBL Medicago sativa alfalfa I Fabaceae Dicot Ranunculus cymbalaria alkali buttercup N Ranunculaceae Dicot OBL Rubus allegheniensis Allegheny blackberry N Rosaceae Dicot UPL, FACW Hieracium paniculatum Allegheny hawkweed N Asteraceae Dicot Mimulus ringens Allegheny monkeyflower N Scrophulariaceae Dicot OBL Ranunculus allegheniensis Allegheny Mountain buttercup N Ranunculaceae Dicot FACU, FAC Prunus alleghaniensis Allegheny plum N Rosaceae Dicot UPL, NI Amelanchier laevis Allegheny serviceberry N Rosaceae Dicot Hylotelephium telephioides Allegheny stonecrop N Crassulaceae Dicot Adlumia fungosa allegheny vine N Fumariaceae Dicot Centaurea transalpina alpine knapweed N Asteraceae Dicot Potamogeton alpinus alpine pondweed N Potamogetonaceae Monocot OBL Viola labradorica alpine violet N Violaceae Dicot FAC Trifolium hybridum alsike clover I Fabaceae Dicot FACU-, FAC Cornus alternifolia alternateleaf dogwood N Cornaceae Dicot Strophostyles helvola amberique-bean N Fabaceae Dicot Puccinellia americana American alkaligrass N Poaceae Monocot Heuchera americana