Echinodorus Uruguayensis Arechav
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Ethnobotany and Popular Culture in the Use of Plants in Settlements on the Southern Edge of Southern Pantanal Mato Grosso
193 Original Article ETHNOBOTANY AND POPULAR CULTURE IN THE USE OF PLANTS IN SETTLEMENTS ON THE SOUTHERN EDGE OF SOUTHERN PANTANAL MATO GROSSO ETNOBÔTANICA E A CULTURA POPULAR NO USO DE PLANTAS EM ASSENTAMENTOS NA BORDA SUL DO PANTANAL SUL-MATO-GROSSENSE Jorge de Souza PINTO 1,2 ; Ademir Kleber Morbeck de OLIVEIRA 3; Valtecir FERNANDES 2; Rosemary MATIAS 3 1. Federal University of Mato Grosso do Sul, Campus do Pantanal, Campo Grande, MS, Brazil; 2. Postgraduate Program in Environment and Regional Development, University Anhanguera-Uniderp, Campo Grande, MS, Brazil; 3. University Anhanguera- Uniderp, Campo Grande, MS, Brazil. [email protected] ABSTRACT: Popular culture and its relationship with plants has been the subject of scientific studies and brought significant contributions to science. In this assessment, developed in two settlements in Corumbá and Ladário, Mato Grosso do Sul, was evaluated the use of plants for medicinal purposes. A structured questionnaire was administered to 10 raizeiros , residents of the area, asking which plants were used by them, their methods of preparation and therapeutic indications. Fifty-five plants from 28 families were catalogued among plants native to the region and of exotic and/or external origin, only 40% were native. The predominant form of use is tea (41 citations), followed by infusion (16 citations). The most used parts are the leaves, with 43 citations, followed by flowers (6 citations). There is a predominance of the type of problem for which the plant is used, with 12 citations for problems in the respiratory system, followed by eight for kidney and liver problems and seven for the stomach. -
Reproductive Phasirna Loci and DICER-LIKE5, but Not Microrna
bioRxiv preprint doi: https://doi.org/10.1101/2020.04.25.061721; this version posted April 27, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Reproductive phasiRNA loci and DICER‐LIKE5, but not microRNA loci, diversified in monocotyledonous plants Parth Patel2§, Sandra M. Mathioni1§, Reza Hammond2, Alex E. Harkess1, Atul Kakrana2, Siwaret Arikit3, Ayush Dusia2, and Blake C. Meyers1,2,4* 1Donald Danforth Plant Science Center, Saint Louis, Missouri 63132 2Center for Bioinformatics and Computational Biology, Delaware Biotechnology Institute, University of Delaware, Newark, Delaware 19716 3Department of Agronomy, Kamphaeng Saen and Rice Science Center, Kasetsart University, Nakhon Pathom 73140, Thailand 4Division of Plant Sciences, University of Missouri, Columbia, Missouri 65211 §These authors contributed equally to this work. *Corresponding author: [email protected] bioRxiv preprint doi: https://doi.org/10.1101/2020.04.25.061721; this version posted April 27, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. 1 Abstract (200 words) 2 In monocots other than maize and rice, the repertoire and diversity of microRNAs (miRNAs) and 3 the populations of phased, secondary, small interfering RNAs (phasiRNAs) are poorly 4 characterized. To remedy this, we sequenced small RNAs from vegetative and dissected 5 inflorescence tissue in 28 phylogenetically diverse monocots and from several early‐diverging 6 angiosperm lineages, as well as publicly available data from 10 additional monocot species. -
Low Risk Aquarium and Pond Plants
Plant Identification Guide Low-risk aquarium and pond plants Planting these in your pond or aquarium is environmentally-friendly. Glossostigma elatinoides, image © Sonia Frimmel. One of the biggest threats to New Zealand’s waterbodies is the establishment and proliferation of weeds. The majority of New Zealand’s current aquatic weeds started out as aquarium and pond plants. To reduce the occurrence of new weeds becoming established in waterbodies this guide has been prepared to encourage the use of aquarium and pond plants that pose minimal risk to waterbodies. Guide prepared by Dr John Clayton, Paula Reeves, Paul Champion and Tracey Edwards, National Centre of Aquatic Biodiversity and Biosecurity, NIWA with funding from the Department of Conservation. The guides will be updated on a regular basis and will be available on the NIWA website: www.niwa.co.nz/ncabb/tools. Key to plant life-forms Sprawling marginal plants. Grow across the ground and out over water. Pond plants Short turf-like plants. Grow in shallow water on the edges of ponds and foreground of aquariums. Includes very small plants (up to 2-3 cm in height). Most species can grow both submerged (usually more erect) and emergent. Pond and aquarium plants Tall emergent plants. Can grow in water depths up to 2 m deep depending on the species. Usually tall reed-like plants but sometimes with broad leaves. Ideal for deeper ponds. Pond plants Free floating plants. These plants grow on the water surface and are not anchored to banks or bottom substrates. Pond and aquarium plants Floating-leaved plants. Water lily-type plants. -
Aquatic Plant Propagation 8X5 Final Back-Up2a
Aquatic Plant Propagation Rooted floating leaved and Copyright ã 2003 marginal/emergent plants Use and reproduction of this information is not authorized for any purpose without prior written permission of the copyright holder. All information contained in this publication which is not original material has been included under fair use provisions, not being used for any commercial uses and contributors have been given full biographical credit. Compiled for the Colorado Water Garden Society by Rebecca Nash and Cyndie Thomas using the following sources: Nash, Helen, and Steve Stroupe, Aquatic Plants and Their Cultivation, New York: Sterling Publishing Company, Inc. 1998 Hartmann, Hudson T. and Dale E.Kester, Plant Propagation Principles and Practices, New Jersey: Prentice-Hall, Inc. 1983 Slocum, Perry D. and Peter Robinson, with Frances Perry, Water Gardening Water Lilies and Lotuses, Portland: Timberline Press 1996 Cover drawing an adaptation from illustrations presented by IFAS Center for Aquatic Plants, University of Florida, Gainsville. Colorado Water Garden Society 8 Aquatic Plant Propagation Planting Methods Tropical Water Lilies Propagation is the making of more plants to keep a plant variety going. Propagation Mexicana/upright type rhizomes should be prepared for and Upright type is also done to improve the health of a plant. Dividing and repotting a plant planting in the same way as other rhizomes. Placement of stimulates growth. Most aquatic plants need dividing every two years, some more Mexicana Hardy the plant in the new pot will be centered, with the growing tip above the soil level. often. Water Lilies. Planting Methods for small growing “eyes” Common Types of Propagation Small growing “eyes” should be potted in 4” pots in the same manner as larger rhizomes and grown to flowering size. -
Echinodorus Tenellus (Martius) Buchenau Dwarf Burhead
New England Plant Conservation Program Echinodorus tenellus (Martius) Buchenau Dwarf burhead Conservation and Research Plan for New England Prepared by: Donald J. Padgett, Ph.D. Department of Biological Sciences Bridgewater State College Bridgewater, Massachusetts 02325 For: New England Wild Flower Society 180 Hemenway Road Framingham, MA 01701 508/877-7630 e-mail: [email protected] • website: www.newfs.org Approved, Regional Advisory Council, May 2003 1 SUMMARY The dwarf burhead, Echinodorus tenellus (Mart.) Buch. (Alismataceae) is a small, aquatic herb of freshwater ponds. It occurs in shallow water or on sandy or muddy pond shores that experience seasonal drawdown, where it is most evident in the fall months. Overall, the species is widely distributed, but is rare (or only historical or extirpated) in almost every United States state in its range. This species has been documented from only four stations in New England, the northern limits of its range, with occurrences in Connecticut and Massachusetts. Connecticut possesses New England’s only extant population. The species is ranked globally as G3 (rare or uncommon), regionally by Flora Conservanda as Division 1 (globally rare) and at the regional State levels as endangered (Connecticut) or historic/presumed extirpated (Massachusetts). Threats to this species include alterations to the natural water level fluctuations, sedimentation, invasive species and their control, and off-road vehicle traffic. The conservation objectives for dwarf burhead are to maintain, protect, and study the species at its current site, while attempting to relocate historic occurrences. Habitat management, regular surveys, and reproductive biology research will be utilized to meet the overall conservation objectives. -
INTRODUCTION Echinodorus Is a Genus That Belongs to Alismataceae
Naturalia (eISSN:2177 -0727) Rio Claro, v.3 3, p. 8-19 , 20 10 Year season on epicuticular waxes in leaves of Echinodorus grandiflorus (Cham. & Schltdl.) Micheli (Alismataceae) Walderez Moreira Joaquim 2, Elizabeth Orika Ono 3, Maria Luiza Faria Salatino4, João Domingos Rodrigues 3 2 Universidade do Vale do Paraíba - UNIVAP, 11244-000, São José dos Campos, SP, Brazil. 3 Instituto de Biociências, UNESP - Univ Estadual Paulista, Departamento de Botânica, , C.P. 510, 18618-000, Botucatu, SP, Brazil. E-mail: [email protected] 4 Universidade de São Paulo – USP, Departamento de Botânica, Instituto de Biociências, C.P. 11461, 05422-970, São Paulo, SP, Brazil. ABSTRACT The paper aimed to study the influence of different seasons of the year on epicuticular waxes in Echinodorus grandiflorus plants and to analyze the profile of n- alkanes in epicuticular waxes. The experiment used adventitious plantlets from the flower stem and approximately 10-cm-tall adventitious plantlets with an average of 4 to 5 leaves, planted in 10-liter pots containing a 40% soil, 40% rice hulls, and 20% vermicompost mixture. E. grandiflorus presented an intermediary profile between terrestrial and aquatic plants, with a main homologue C27 (heptacosane), followed by C25 (pentacosane) and C29 (nonacosane). The studies presented here provide information about ecological aspects and chemical and mechanical defenses of Echinodorus grandiflorus. Key words: phenology, n-alkanes, aquatic plants RESUMO Este trabalho objetivou estudar a influência das estações do ano sobre o conteúdo de ceras epicuticulares e a análise dos perfis dos n-alcanos da cera em folhas de Echinodorus grandiflorus . No experimento foram utilizadas mudas adventícias com aproximadamente 10 cm de altura e 4 a 5 folhas, que foram plantadas em vasos de 10 L, tendo como substrato a mistura de 40% de terra, 40% de palha de arroz e 20% de húmus de minhoca. -
Flora of New Zealand Seed Plants
FLORA OF NEW ZEALAND SEED PLANTS ALISMATACEAE K.A. FORD & P.D. CHAMPION Fascicle 7 – DECEMBER 2020 © Landcare Research New Zealand Limited 2020. Unless indicated otherwise for specific items, this copyright work is licensed under the Creative Commons Attribution 4.0 International licence Attribution if redistributing to the public without adaptation: "Source: Manaaki Whenua – Landcare Research" Attribution if making an adaptation or derivative work: "Sourced from Manaaki Whenua – Landcare Research" See Image Information for copyright and licence details for images. CATALOGUING IN PUBLICATION Ford, Kerry A. (Kerry Alison) Flora of New Zealand : seed plants. Fascicle 7, Alismataceae / K.A. Ford and P.D. Champion. -- Lincoln, N.Z. : Manaaki Whenua Press, 2020. 1 online resource ISBN 978-0- 947525-67-5 (pdf) ISBN 978-0-478-34762-3 (set) 1.Alismataceae -- New Zealand – Identification. I. Champion, P.D. II. Title. III. Manaaki Whenua – Landcare Research New Zealand Ltd. UDC 582.536 (931) DC 584.720993 DOI: 10.7931/jwc3-zg41 This work should be cited as: Ford K.A. & Champion P.D. 2020: Alismataceae. In: Wilton, A.D. (ed.) Flora of New Zealand — Seed Plants. Fascicle 7. Manaaki Whenua Press, Lincoln. http://dx.doi.org/10.7931/jwc3-zg41 Date submitted: 12 Jun 2019; Date accepted: 4 Jun 2020; Date published: 2 January 2021 Cover image: Alisma lanceolatum. Flower showing acute petal apices. Contents Introduction..............................................................................................................................................1 -
Guidelines for the USDA-APHIS- PPQ Weed Risk Assessment Process
United States Guidelines for the USDA-APHIS- Department of PPQ Weed Risk Assessment Agriculture Process Animal and Plant Health Inspection Service Plant Protection and Quarantine February 11, 2019 Version 2.3 Agency Contact: Plant Epidemiology and Risk Analysis Laboratory Center for Plant Health Science and Technology Plant Protection and Quarantine Animal and Plant Health Inspection Service United States Department of Agriculture 1730 Varsity Drive, Suite 300 Raleigh, NC 27606 Table of Contents Table of Contents .......................................................................................................................... 1 List of Tables ................................................................................................................................. 3 List of Figures ................................................................................................................................ 4 Section 1: Introduction to the PPQ Weed Risk Assessment ..................................................... 5 Risk analysis framework ............................................................................................................. 5 Usage and meaning of the term “invasive” ................................................................................. 7 Section 2: Overview and Interpretation of the PPQ Weed Risk Assessment (WRA) ............ 8 The predictive model ................................................................................................................... 9 Secondary screening -
Evolution Along the Crassulacean Acid Metabolism Continuum
Review CSIRO PUBLISHING www.publish.csiro.au/journals/fpb Functional Plant Biology, 2010, 37, 995–1010 Evolution along the crassulacean acid metabolism continuum Katia SilveraA, Kurt M. Neubig B, W. Mark Whitten B, Norris H. Williams B, Klaus Winter C and John C. Cushman A,D ADepartment of Biochemistry and Molecular Biology, MS200, University of Nevada, Reno, NV 89557-0200, USA. BFlorida Museum of Natural History, University of Florida, Gainesville, FL 32611-7800, USA. CSmithsonian Tropical Research Institute, PO Box 0843-03092, Balboa, Ancón, Republic of Panama. DCorresponding author. Email: [email protected] This paper is part of an ongoing series: ‘The Evolution of Plant Functions’. Abstract. Crassulacean acid metabolism (CAM) is a specialised mode of photosynthesis that improves atmospheric CO2 assimilation in water-limited terrestrial and epiphytic habitats and in CO2-limited aquatic environments. In contrast with C3 and C4 plants, CAM plants take up CO2 from the atmosphere partially or predominantly at night. CAM is taxonomically widespread among vascular plants andis present inmanysucculent species that occupy semiarid regions, as well as intropical epiphytes and in some aquatic macrophytes. This water-conserving photosynthetic pathway has evolved multiple times and is found in close to 6% of vascular plant species from at least 35 families. Although many aspects of CAM molecular biology, biochemistry and ecophysiology are well understood, relatively little is known about the evolutionary origins of CAM. This review focuses on five main topics: (1) the permutations and plasticity of CAM, (2) the requirements for CAM evolution, (3) the drivers of CAM evolution, (4) the prevalence and taxonomic distribution of CAM among vascular plants with emphasis on the Orchidaceae and (5) the molecular underpinnings of CAM evolution including circadian clock regulation of gene expression. -
Threats to Australia's Grazing Industries by Garden
final report Project Code: NBP.357 Prepared by: Jenny Barker, Rod Randall,Tony Grice Co-operative Research Centre for Australian Weed Management Date published: May 2006 ISBN: 1 74036 781 2 PUBLISHED BY Meat and Livestock Australia Limited Locked Bag 991 NORTH SYDNEY NSW 2059 Weeds of the future? Threats to Australia’s grazing industries by garden plants Meat & Livestock Australia acknowledges the matching funds provided by the Australian Government to support the research and development detailed in this publication. This publication is published by Meat & Livestock Australia Limited ABN 39 081 678 364 (MLA). Care is taken to ensure the accuracy of the information contained in this publication. However MLA cannot accept responsibility for the accuracy or completeness of the information or opinions contained in the publication. You should make your own enquiries before making decisions concerning your interests. Reproduction in whole or in part of this publication is prohibited without prior written consent of MLA. Weeds of the future? Threats to Australia’s grazing industries by garden plants Abstract This report identifies 281 introduced garden plants and 800 lower priority species that present a significant risk to Australia’s grazing industries should they naturalise. Of the 281 species: • Nearly all have been recorded overseas as agricultural or environmental weeds (or both); • More than one tenth (11%) have been recorded as noxious weeds overseas; • At least one third (33%) are toxic and may harm or even kill livestock; • Almost all have been commercially available in Australia in the last 20 years; • Over two thirds (70%) were still available from Australian nurseries in 2004; • Over two thirds (72%) are not currently recognised as weeds under either State or Commonwealth legislation. -
Grandidentata in the Field at Ambient and Twice Ambient CO2 in Open
grandidentata in the field at ambient and twice ambient CO2 in open productivity(1-4) This observation has led to the suggestion that, by bottom root boxes filled with organic matter poor native soil. Nitrogen taking up CO2, the terrestrial biosphere might mitigate the potential was added to all root boxes at a rate equivalent to net N mineralization greenhouse warming associated with anthropogenic CO2 emissions(5). in local dry oak forests. Nitrogen added during August was enriched Whiting and Chanton(6) have found, however, that for wetlands of with N-25 to trace the flux of N within the plant-soil system. Above- and varying productivity around the world, higher net primary production is belowground growth, CO2 assimilation, and leaf N content were associated with higher emissions of methane-another important measured non- destructively over 142 d. After final destructive harvest, greenhouse gas. Here we present measurements of methane emissions roots, stems, and leaves were analyzed for total N and N-15. There was from a marsh that has been exposed to twice the present ambient no CO2 treatment effect on leaf area, root length, or net assimilation concentration of atmospheric CO2. We find that over a one-week period, prior to the completion of N addition. Following the N addition, leaf N the CO2-enriched sites had significantly higher emissions of methane content increased in both CO2 treatments, but net assimilation showed than the control sites. Our results suggest that future increases in a sustained increase only in elevated CO2 grown plants. Root relative atmospheric CO2 concentration may lead to significant increases in extension rate was greater at elevated CO2, both before and after the N methane emissions from wetlands. -
October 2020 Mpeda Newsletter 1 Cpf (India) Private Limited Cpf 3 Best Approach for Aquaculture
OCTOBER 2020 MPEDA NEWSLETTER 1 CPF (INDIA) PRIVATE LIMITED CPF 3 BEST APPROACH FOR AQUACULTURE PREMIUM FISH FEED PREMIUM SHRIMP FEED PREMIUM MINERAL PREMIUM PROBIOTIC PRODUCTS PRODUCTS Connect with Us: 2 OCTOBER 2020 MPEDA NEWSLETTER OCTOBER 2020 MPEDA NEWSLETTER 3 On the Platter MPEDA VOL. VIII / NO. 7 / OCTOBER 2020 Newsletter EDITORIAL BOARD K. S. Srinivas IAS DR. M. K. Ram Mohan Chairman JOINT DIRECTOR (QUALITY CONTROL) Mr. P. Anil Kumar Dear friends, JOINT DIRECTOR (MARKETING) Mr. K. V. Premdev The unlock process declared by the Government of India is slowly DEPUTY DIRECTOR (MPEDA MANGALORE) easing out the trade hurdles to a certain extent, though the markets are yet to warm up as expected. The year on year, the deficit in export EDITOR trade has reduced to 18%, as we analyze the export figures during DR. T. R. Gibinkumar DEPUTY DIRECTOR (MARKET PROMOTION April to October 2020. Though markets like USA and China have & STATISTICS) shown improvement, EU and Japan still remain at low key with fresh outbreaks of Covid-19. ASST. EDITOR Mrs. K. M. Divya Mohanan Meanwhile, it is reported that the Chinese Authorities are clearing SENIOR CLERK the consignments only after checking for Covid-19 nucleic material in the outer packs, and that delays the cargo clearance at the Chinese ports. This has also reportedly affected the payments from China to our exporters. The shortage of containers adds to the worries of the exporters to ship out seafood cargo from India to different destinations anticipating New Year demand. The General Administration and Customs China (GACC) has demanded a virtual inspection of two seafood processing units in India during the month and accordingly, two units were presented for virtual inspection by the end of the month to GACC on their preparedness on food safety, especially in tackling the Covid-19 contamination through seafood cargo.