White Waterlily Nymphaea Odorata Ssp. Odorata Ait
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Plant + Product Availability
12/2/2020 2020 A = Available AL = limited availability B = bud/bloom potted plants can not be shipped via UPS, FedEx or USPS all shipping is FOB origin and billed at actual cost Lotus Seeds & Pods Nelumbo lutea, American Lotus (native, yellow), for sprouting 12 seeds, gift wrapped $21.00 A 50 seeds $75.00 A 125 seeds $156.25 A 250 seeds $250.00 A 500 seeds $375.00 A 1000 seeds $600.00 A Nelumbo, mixed cultivars, parents unknown*, for sprouting 12 seeds, gift wrapped $23.00 A 50 seeds $80.00 A Nelumbo, mixed, pod parent known, labeled*, for sprouting 12 seeds, gift wrapped $25.00 A 50 seeds $87.50 A * FYI, there is no such thing as blue lotus; or turquoise, purple, black or orange, etc. Nelumbo seed pods, dried, each (generally w/o seeds) mini <2" $0.50 A small 2-3" $1.00 A medium 3-4" $1.50 A large 4-5" $2.00 A extra large 5"+ $3.00 A Book The Lotus Know It and Grow It $10.00 A by Kelly Billing and Paula Biles Gifts textiles, lotus color it takes approx 9200 stems to make one lotus scarf 100% lotus scarf 7" x 66" $103.00 A natural (no color) lotus thread is delicately extracted from the stem 100% lotus scarf 7" x 66" $103.00 A red sappan wood and woven by only a 100% lotus scarf 7" x 66" $167.00 blue indigo small number of skilled 100% lotus scarf 10" x 66" $149.00 natural (no color) craftspeople in Myanmar, Cambodia and Vietnam. -
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 -
In Planta Expression of Exocellulase Enzymes for Bio-Ethanol Production
In planta expression of exocellulase enzymes for Bio-ethanol production A thesis submitted in fulfilment of the requirements for the degree of Doctor of Philosophy Parsu Ram Budathoki Degree of Bachelor of Science, University of North Bengal, India Master of Science in Biotechnology, Bangalore University, India School of Science College of Science, Engineering and Health RMIT University March 2018 Declaration I certify that except where due acknowledgement has been made, the work is that of the author alone; the work has not been submitted previously, in whole or in part, to qualify for any other academic award; the content of the thesis is the result of work which has been carried out since the official commencement date of the approved research program; any editorial work, paid or unpaid, carried out by a third party is acknowledged; and, ethics procedures and guidelines have been followed. Parsu Ram Budathoki Date: 13/03/2018 i ACKNOWLEDGEMENTS I wish to thank my senior supervisor, Professor Trevor Stevenson for his help and advice during the period of research. I also thank my secondary supervisor Dr Gregory Nugent for his guidance and assistance. I thank Professor David Stalker for many useful discussions. I am indebted to Mrs. Kim Stevenson for her assistance and guidance in my laboratory work. I also thank Dr. Chung Hong Chen (former CSIRO Scientist) for providing me with plasmids and helping me in the cloning vectors. I acknowledge Dr. Chaitali Dekiwadia for assistance in sample preparation and imaging of TEM work at RMIT Microscopy and Microanalysis Facility. The research described in this thesis was carried on while I held a research scholarship from the ARC Linkage grant in partnership with Biomass Conversion Technologies, was funded from Chevron Technology Ventures in USA is gratefully acknowledged. -
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. -
Potamogeton Hillii Morong Hill's Pondweed
Potamogeton hillii Morong Hill’sHill’s pondweed pondweed, Page 1 State Distribution Best Survey Period Jan Feb Mar Apr May Jun Jul Aug Sept Oct Nov Dec Status: State threatened 1980’s. The type locality for this species, in Manistee County, has been destroyed. Global and state rank: G3/S2 Recognition: The stem of this pondweed is slender Other common names: pondweed and much branched, reaching up to 1 m in length. The alternate leaves are all submersed, and very narrow Family: Potamogetonaceae (pondweed family) (0.6-2.5 mm), ranging from 2-6 cm in length. The leaves are characterized by having three parallel veins Synonyms: Potamogeton porteri Fern. and a short bristle tip. The stipules are relatively coarse and fibrous (shredding when old) and are free Taxonomy: An extensive molecular analysis of the from each other and the leaf stalk bases. Short Potamogetonaceae, which largely corroborates the (5‑15 cm), curved fruiting stalks (peduncles) are separation of broad-leaved versus narrow-leaved terminated by globose flower/fruit clusters that pondweed species, is provided by Lindqvist et al. arise from leaf axils or stem tips. The tiny (2-4 mm) (2006). fruits have ridges along the backside. Other narrow- leaved species that lack floating leaves have either Range: This aquatic plant is rare throughout much of narrower leaves ( less than 0.5 mm in width, such as its range, which extends from Vermont to Michigan, and P. confervoides and P. bicupulatus), stipules that are south to Pennsylvania. Centers of distribution appear attached near their bases (P. foliosus, P. pusillus), to be in western New England and the north central longer peduncles (1.5-4 mm) (P. -
Diversity of Nymphaea L. Species (Water Lilies) in Sri Lanka D
Sciscitator. 2014/ Vol 01 DIVERSITY OF NYMPHAEA L. SPECIES (WATER LILIES) IN SRI LANKA D. P. G. Shashika Kumudumali Guruge Board of Study in Plant Sciences Water lilies are aquatic herbs with perennial rhizomes or rootstocks anchored in the mud. In Sri Lanka, they are represented by the genus Nymphaea L. It has two species, N. nouchali Burm. F. and N. pubescens Willd (Dassanayake and Clayton, 1996). Water-lilies have been popular as an ornamental aquatic plant in Sri Lanka from ancient times as they produce striking flowers throughout the year. In addition to these native water-lilies, few ornamental species are also been introduced in the past into the water bodies. Nymphaea nouchali (Synonym- N. stellata) N. nouchali has three colour variations, white, pink and violet blue. They are commonly known as “Manel”. According to the field observations pink flowered Nymphaea is not wide spread like others. Blue and white Nymphaea are widely spread mainly in dry zone, Anuradhapura, Polonnaruwa, and also in Jaffna, Ampara, Chilaw and Kurunegala. Among these, pale blue flower Nymphaea or “Nil Manel” is considered as the National flower of Sri Lanka. Figure 01. (A)- Pale blue flowered N. nouchali, (B)- upper surface of the leaf, (C)- Stamens having tongue shaped appendages, (D) Rose flowered N. nouchali , (E) White flowered N. nouchali Some morphological characters of N. nouchali (Sri Lankan National flower) are given below and illustrated in fig. 01; A- flower, B- leaf, and C- stamens. Flower : Diameter 20- 30cm. Petals : 8-30in number, Pale blue colour, linear shape , 3-6cm in length 0.7- 1.5cm width . -
Nuphar Lutea
1186 Notizen Oxygen Supply of Roots by Gas Transport to aerate their roots in wet soil and during periods in Alder-Trees of early spring floodings. Wolfgang Große und Peter Schröder Botanisches Institut der Universität zu Köln, Gyrhof- Materials and Methods straße 15, D-5000 Köln 41, Bundesrepublik Deutschland Studies were conducted on six- to twelve-month- Z. Naturforsch. 39 c, 1186 -1188 (1984); old alder-trees (Alnus glutinosa (L.) Gaertner) cul received August 3/September 6, 1984 tivated in the tree-nursery and transfered to a green Ainus glutinosa, Gas Transport, Oxygen Supply, house during the winter. Root Aeration, Thermo-Osmosis of Gases For the assays the young trees were inserted in an It is generally accepted that oxygen diffuses according to experimental glass chamber (Fig. 1) which is sepa the gradient of its partial pressure from the surface of the rated into two compartments by a sealing com plants into the heterotrophic tissues through the inter cellular spaces. The present experiments show evidence of pound (Carlofon, Cologne, W. Germany) and a an additional manifold higher oxygen supply due to a gas water trap. transport in leaved as well as leafless trees of Alnus glutinosa (L.) Gaertner. This gas transport is directed from The experiments were carried out either when the the stems to the roots. It is driven by a thermo-osmotic plants were equilibrated to room temperature or pressurisation within the air space system of the stems, when the plants obtained a specific temperature resulting from temperature gradients up to 3.6 K between the stem and the ambient air following the absorption of gradient between the inside of the stems and the light energy by the brownish pigments of the bark. -
Rare Plants of Louisiana
Rare Plants of Louisiana Agalinis filicaulis - purple false-foxglove Figwort Family (Scrophulariaceae) Rarity Rank: S2/G3G4 Range: AL, FL, LA, MS Recognition: Photo by John Hays • Short annual, 10 to 50 cm tall, with stems finely wiry, spindly • Stems simple to few-branched • Leaves opposite, scale-like, about 1mm long, barely perceptible to the unaided eye • Flowers few in number, mostly born singly or in pairs from the highest node of a branchlet • Pedicels filiform, 5 to 10 mm long, subtending bracts minute • Calyx 2 mm long, lobes short-deltoid, with broad shallow sinuses between lobes • Corolla lavender-pink, without lines or spots within, 10 to 13 mm long, exterior glabrous • Capsule globe-like, nearly half exerted from calyx Flowering Time: September to November Light Requirement: Full sun to partial shade Wetland Indicator Status: FAC – similar likelihood of occurring in both wetlands and non-wetlands Habitat: Wet longleaf pine flatwoods savannahs and hillside seepage bogs. Threats: • Conversion of habitat to pine plantations (bedding, dense tree spacing, etc.) • Residential and commercial development • Fire exclusion, allowing invasion of habitat by woody species • Hydrologic alteration directly (e.g. ditching) and indirectly (fire suppression allowing higher tree density and more large-diameter trees) Beneficial Management Practices: • Thinning (during very dry periods), targeting off-site species such as loblolly and slash pines for removal • Prescribed burning, establishing a regime consisting of mostly growing season (May-June) burns Rare Plants of Louisiana LA River Basins: Pearl, Pontchartrain, Mermentau, Calcasieu, Sabine Side view of flower. Photo by John Hays References: Godfrey, R. K. and J. W. Wooten. -
Native Or Invasive? Native and Invasive Aquatic Plants of the Eastern Lake Ontario Region
Aquatic Invasive Species Resource Education Series 2011 Native or Invasive? Native and Invasive Aquatic Plants of the Eastern Lake Ontario Region Invasive aquatic plants can interfere with recreation and diminish wildlife and fish habitat. Knowing some of the common plants that are native to our waters may help you spot invasive plants before they grow out of control. Read on for a sampling of our native aquatic plants, as well as some invasives to recognize. Right: Wetland at Black Pond Wildlife Management Area, Jefferson County, NY. Photo: Greg Chapman, New York Sea Grant Native and invasive plants with leaves that float upon the surface of the water White water lily Water chestnut Nymphaea odorata Trapa natans Native plant Invasive plant Flowers: Large, white, Triangular toothed leaves many-petaled in floating “rosettes” Round “lily pad” leaves, Seeds (nutlets) with four 6-8 inches across sharp prongs Forms dense mats Photo: Greg Chapman, New York Sea Grant Photo: Greg Chapman, New York Sea Grant Yellow pond lily European frogbit Nuphar lutea Hydrocharis morsus-ranae Native plant Invasive plant Yellow, bulbous flowers Small round leaves, less rise above the water than 2 inches across Shield-shaped leaves, up Flowers: Small, white, to 16 inches long three-petaled Forms dense mats Photo: Greg Chapman, New York Sea Grant Photo: Greg Chapman, New York Sea Grant Native and Invasive Aquatic Plants of the Eastern Lake Ontario Region Native and invasive plants that grow mostly beneath the water’s surface Coon’s tail Eurasian watermilfoil Ceratophyllum demersum Myriophyllum spicatum Native plant Invasive plant Branched, bristle-like Feather-like leaves leaves 3-6 leaves arranged in Provides cover for fish whorls around stem Eaten by some waterfowl Forms dense mats that interfere with boating Drawing: USDA-NRCS PLANTS Database / Britton, N.L., and A. -
The Utility of Nymphaeaceae Sclereids in Paleoenvironmental Research Robby R
The Utility of Nymphaeaceae Sclereids in Paleoenvironmental Research Robby R. Marrotte Department of Geography, McGill University; Montréal (Québec) Canada 2011 Supervisor: Gail L. Chmura Reader: Elisabeth Levac As entomophilous plants, water lilies (Nymphaea) and spatterdocks (Nuphar) have low pollen production, thus can be under represented in the sediment record. These macrophytes produce distinctly shaped sclerenchyma tissue referred to as stone-cells, trichosclereids, astrosclereid or simply sclereids. This study examines the utility of using sclereids from common species from the Nymphaeaceae Family as an alternative proxy to their pollen. Histological studies of fresh tissues of Nymphaea odorata and Nuphar lutea revealed that each has distinct sclereids and that there has been confusion in the application of terminological used to designate their morphology. Some paleoecological reports have referred to Nymphaeaceae sclereids as trichosclereids, but our histological studies show that the cells are more appropriately classified as polyramous, astrosclereids, librosclereids and rhizosclereids. We also determined if palynological processing affects sclereid morphology or the efficiency of their retrieval. Tissues from both species were treated using HCL, KOH, acetolysis and HF and found that only the sclereids from N. lutea survived chemical treatments in a detectable form. Our study shows that sclereids from N. lutea can be a useful indicator of its presence while the chance of observing sclereids from N. odorata in pollen preparations is very low, severely limiting the utility of the latter as a paleoecological indicator. Another limitation to using sclereids as a proxy is that they originate from plant tissues, which require extended acetolysis treatments for; if they aren’t released from this matrix they stay hidden inside the tissue. -
The Birds of the Dar Es Salaam Area, Tanzania
Le Gerfaut, 77 : 205–258 (1987) BIRDS OF THE DAR ES SALAAM AREA, TANZANIA W.G. Harvey and KM. Howell INTRODUCTION Although the birds of other areas in Tanzania have been studied in detail, those of the coast near Dar es Salaam have received relatively little recent attention. Ruggles-Brise (1927) published a popular account of some species from Dar es Salaam, and Fuggles-Couchman (1939,1951, 1953, 1954, 1962) included the area in a series of papers of a wider scope. More recently there have been a few other stu dies dealing with particular localities (Gardiner and Gardiner 1971), habitats (Stuart and van der Willigen 1979; Howell 1981), or with individual species or groups (Harvey 1971–1975; Howell 1973, 1977). Britton (1978, 1981) has docu mented specimens collected in the area previous to 1967 by Anderson and others. The purpose of this paper is to draw together data from published reports, unpu blished records, museum specimens and our own observations on the frequency, habitat, distribution and breeding of the birds of the Dar es Salaam area, here defi ned as the portion of the mainland within a 64-km radius of Dar es Salaam, inclu ding the small islands just offshore (Fig. 1). It includes Dar es Salaam District and portions of two others, Kisarawe and Bagamoyo. Zanzibar has been omitted because its unusual avifauna has been reviewed (Pakenham 1979). Most of the mainland areas are readily accessible from Dar es Salaam by road and the small islands may be reached by boat. The geography of the area is described in Sutton (1970). -
Management Plan for the Western Painted Turtle (Chrysemys Picta Bellii)
Management Plan for The Western Painted Turtle (Chrysemys picta bellii ) in the Alouette River Watershed April 2012 Prepared for: BC Hydro’s Bridge Coastal Fish and Wildlife Restoration Program 6911 Southpoint Drive (E14) Burnaby, BC V3N 4X8 And Kym Welstead Ministry of Forests, Lands and Natural Resource Operations 10470 152 nd Street Surrey, BC V3R 0W8 BCRP Report No. 11.ALU.W.01 Prepared by: Aimee M. Mitchell, M.Sc., RPBio . 103-1516 E. 1 st Avenue Vancouver, BC V5N 1A5 i Abstract In 2011, funding was approved for the Bridge Coastal Restoration program project titled “Identify, conserve and restore populations of priority species at risk and their associated habitats within the Alouette River Watershed.” One of goals of this project, in cooperation with Western Painted Turtle Recovery program, is to identify sites occupied by Western Painted Turtles ( Chrysemys picta bellii ), and assess the available habitat, including potential threats, as well as opportunities for restoration. To properly assess these features, a detailed plan was developed to facilitate efficient surveys of any and all potential habitat within the Alouette Watershed, incorporating the North and the South Alouette drainages. ii Contents Abstract ......................................................................................................................................................... ii Background/Rationale .................................................................................................................................. 1 Status ...........................................................................................................................................................