Chromosome Counts of Some Wetland Cyperaceous Species from the Mekong Delta, Vietnam

Total Page:16

File Type:pdf, Size:1020Kb

Chromosome Counts of Some Wetland Cyperaceous Species from the Mekong Delta, Vietnam © 2010 The Japan Mendel Society Cytologia 75(4): 335–339, 2010 Chromosome Counts of Some Wetland Cyperaceous Species from the Mekong Delta, Vietnam Hiroshi Uchiyama1*, Hideyuki Matoba1, Tomoko Aizawa1, Hiroaki Sumida2 and Do Minh Nhut3 1 Department of Applied Biological Science, College of Bioresource Sciences, Nihon University, 1866 Kameino, Fujisawa, Kanagawa 252–0880, Japan 2 Department of Chemistry and Life Science, College of Bioresource Sciences, Nihon University, 1866 Kameino, Fujisawa, Kanagawa 252–0880, Japan 3 Kien Giang Agriculture Extension Center, 1224 Nguyen Trung Truc, Rach Gia, Kien Giang, Vietnam Received March 15, 2010; accepted July 15, 2010 Summary Chromosome numbers were counted in root tip cells of 6 cyperaceous species growing in wetlands in the Mekong Delta, Vietnam. The results were as follows: Cyperus haspan, 2nϭ26; Eleocharis dulcis, 2nϭca. 212; Eleocharis spiralis, 2nϭ42; Fimbristylis ferruginea, 2nϭ20; Fimbristylis polytrichoides, 2nϭ10; Lepironia articulata, 2nϭ34. They were reported here for the first time using plant materials from Vietnam. Furthermore, the results of 2 species, Eleocharis spiralis and Lepironia articulata, were the first to be reported for these species. In addition, the dimorphism of Eleocharis dulcis shoots representing emerged and submerged culms was recorded. Key words Aquatic plants, Chromosome number, Cyperaceae, Diffuse centromere, Mapanioideae, Vietnam. The Cyperaceae is a large cosmopolitan family comprising 104 genera and over 5,000 species (Goetghebeur 1998) and shows intriguing cytological characteristics such as diffuse centromeres, post-reductinal meiosis and agmatoploidy (Greilhuber 1995, Hipp et al. 2009). According to the inventory by Roalson (2008), chromosome numbers have been counted in only approximately 16% of the species in the family, and there is a particular lack of chromosome counts in tropical genera. Indeed, there seems to be few chromosomal reports on cyperaceous species from Southeast Asia in genaral. The Mekong Delta, most of which lies in southern Vietnam, is a flat wide plain that floods annually during the rainy season. A large part of the delta wetlands is utilized for agriculture, mainly rice cropping, and fishery. However, acid sulfate soils (ASSs) and/or saline soils are causing problems for agricultural production in many areas. Under the research title, “Development of new bioremediation systems for the destroyed environment”, launched as part of the 21st Century Center of Excellence (COE) Program (Sasaki 2008), we previously performed research activities aimed at understanding the characteristic features of wild plants and other organisms, especially those growing in ASS fields. During this research, we revealed the chromosome numbers of some aquatic and wetland plants growing in ASS fields from central Thailand (Matoba and Uchiyama 2009). In this paper, we report the chromosome numbers of 6 cyperaceous species collected from ASS and saline soil fields in the Mekong Delta, Vietnam. Materials and methods Materials for the present study are listed in Table 1. Plant specimens were collected in wetland * Corresponding author, e-mail: [email protected] 336 H. Uchiyama et al. Cytologia 75(4) areas such as backswamps of mangroves and paddy fields in Kien Giang Province, southern Vietnam, then cultivated in a greenhouse of the College of Bioresource Sciences, Nihon University, Japan. Voucher specimens were deposited in the herbarium of Nihon University, the College Museum of Bioresource Sciences, Fujisawa, Japan. Taxonomic treatment followed Simpson and Koyama (1998). Root tips were cut into 2–3 mm sections then pretreated with 2 mM 8-hydroxyquinoline at 20°C for 3 h before being fixed in ethanol–acetic acid (3 : 1) at 4°C for 24 h. Fixed root tips were washed 3 times in distilled water, then 10 to 30 samples were placed in a microcentrifuge tube containing 500 ml of enzyme solution (4% Cellulase Onozuka-RS (Yakult Honsha) and 2% Pectolyase Y-23 (Kikkoman), pH 4.2) and incubated at 37°C for 1 h. After washing 3 times with distilled water, some of the washed root tips were placed on a glass slide onto which 10–20 ml of fixative was dropped; the root tips were immediately spread apart. Air-dried slides were then Table 1. Chromosome numbers of the Cyperaceae species investigated in this study Species and Present Previous report Locality count (Voucher) (2n) n 2n Reference Cyperus haspan L. Hon Dat, paddy field 26 8 India (Sarkar et al. 1978) (Uchiyama 07056-58) 16 India (Sanyal 1972) 13 India (Rath and Patnaik 1978) 26 India (Nijalingappa et al. 1978, Tejavathi and Nijalingappa 1990) Thailand (Matoba and Uchiyama 2009) 30 Nigeria (Baquar 1978) 16 32 Japan: (Tanaka 1942) 18 India (Mehra and Sachdeva 1975) Eleocharis dulcis (Burm. f.) Trin. ex Hensch. Hon Dat, paddy field ca.212 38 India (Rath & Patnaik 1978) (Uchiyama 05087-88) c.172 Australia (Briggs 1970)* Kien Luong, paddy field ca.212 c.196 Japan (Yano et al. 2004) (Uchiyama 06102-103) Ͼ100 India (Rath and Patnaik 1974) c.212 Thailand (Matoba and Uchiyama 2009) c.108 India (Patnaik and Guru 1968; cited in Rath and Patnaik 1974) Eleocharis spiralis (Rottb.) Roem. & Schlt Kien Luong, backswamp 42 (Uchiyama 07079) Fimbristylis ferruginea (L.) Vahl Kien Luong, backswamp 20 5 India (Mehra and Sachdeva 1976, Rath and Patnaik (Uchiyama 07062-64) 1978, Bir et al. 1986) 10 India (Sanyal and Sharma 1972, Nijalingappa 1975) 10 India (Bir et al. 1992) 20 India (Sarker et al. 1978) Australia (Briggs 2002) 32 India (Subramanian 1988) Fimbristylis polytrichoides (Retz.) R. Br. Kien Luong, backswamp 10 5 India (Bir et al. 1992) (Uchiyama 07059-61) 10 India (Nijalingappa and Tejavathi 1984) 20 India (Sanyal and Sharma 1972) Lepironia articulata (Retz.) Domin Kien Luong, paddy field 34 (Uchiyama 05032-33) *: as E. equiseina. 2010 Chromosome numbers of some Vietnamese Cyperaceae 337 mounted in Vectashield mounting medium (Vector Lab.) containing 500 ng/ml 4Ј, 6-diamidino-2- phenylinodole (DAPI). At least 10 metaphase plates in the cytoplasm were observed and fluorescent photomicrographs were taken with an Olympus microscope BX60 using an Olympus DP50 CCD camera. Results and discussion Chromosome numbers counted in this study and those reported previously are listed in Table 1. Localities of the materials used for previous chromosomal observations are also shown. Photomicrographs of somatic chromosomes investigated in this study are shown in Fig. 1A–F. The chromosome number of Cyperus haspan L. was counted as 2nϭ26 (Fig. 1A), which is in agreement with reports from India and Thailand. The following chromosome numbers have also been reported for this species: nϭ8, 2nϭ16 and nϭ18 from India, 2nϭ30 from Nigeria, and nϭ16 and 2nϭ32 from Japan. The plants used in this study did not have creeping rhizomes as found in Thai materials (Matoba and Uchiyama 2009). In Eleocharis dulcis (Burm. f.) Trin. ex Hensch., approximately 200 chromosomes have been observed from India, Thailand and Japan; nϭ38 and 2nϭc.172 have also been reported from India and Australia, respectively. Although in the present study we were unable to fix the chromosome number due to the small size of the chromosomes (Ͻ1 mm), approximately 212 were counted in many cell plates observed (Fig. 1B). Interestingly, plants collected from 2 localities, both of which dry up during the dry season, had dimorphic shoots; one robust emerged culm, which is normally described in this species, and another tender submerged culm (Fig. 2). The submerged culm has been reported in this taxon from India (Joseph and Sivarajan 1984) but is rare, and to the best of our knowledge is recorded here for only the second time. The somatic chromosome number of Eleocharis spiralis (Rottb.) Roem. & Schult. was counted as 2nϭ42 (Fig. 1C), and is reported here for the first time for this species. This chromosome number is smaller than that of the species in the subgenus Limnochloa reported previously; E. acutangula (ϭfistulosa) (2nϭ54), E. ochrostachys (2nϭ74), E. sphacelata (2nϭ94–100, c.140, c.157, 176– Fig. 1. Fluorescent photomicrographs (color-reversed images) of the somatic chromosomes of 6 Cyperaceae species (A–F) investigated in this study. A, Cyperus haspan, 2nϭ26. B, Eleocharis dulcis, 2nϭca. 212. C, Eleocharis spiralis, 2nϭ42. D, Fimbristylis ferruginea, 2nϭ20. E, Fimbristylis polytrichoides, 2nϭ10. F, Lepironia articulata, 2nϭ34. Scale bar indicates 10 mm. 338 H. Uchiyama et al. Cytologia 75(4) 184, c.188) and E. dulcis (Briggs 1970, Rath and Patnaik 1978, Yano et al. 2004). Intraspecific polyploidy with xϭ5 has been investigated in the genus Fimbristylis. Chromosome numbers of F. ferruginea (L.) Vahl and F. polytrichoides (Retz.) R. Br. used in this study were tetraploid with 2nϭ20 (Fig. 1D) and diploid with 2nϭ10 (Fig. 1E), respectively. In both species, diploids and tetraploids have been reported from India. In F. ferruginea, tetraploids (2nϭ20) and hetero- ploids (2nϭ32) have also been reported from Australia and India, respectively. The somatic chromosome number of Lepironia articulata (Retz.) Domin (Fig. 1F) was counted as 2nϭ34, and is reported here for the first time. Furthermore, this is the first report for the species in the subfamily Mapanioideae (Goetghebeur 1998, Roalson 2008), which has been considered primitive in the family Cyperaceae. Diffuse centromeres are one of the distinct chromosomal features in the family Fig. 2. Photograph of the dimorphic shoots of Cyperaceae, and are considered as a Eleocharis dulcis growing in a rice field in Hon synapomorphy for the Cyperaceae-Juncaceae Dat, Kien Giang Province. lineage (Greilhuber 1995). Although a localized centromere has occasionally been described in some genera including Cyperus haspan, Fimbristylis ferruginea and F. polytrichoides (Sanyal 1972, Sanyal and Sharma 1972, Nijalingappa 1975, Bir et al. 1986, Subramanian 1988, Tejavathi and Nijalingappa 1990), obvious primary constrictions were hardly observed in these species used in this investigation (Fig. 1). Acknowledgements This work was supported by a Grant-in-Aid for the 21st COE Program from the Ministry of Education, Culture, Sports, Science, and Technology, Japan. References Baquar, S. R. 1978.
Recommended publications
  • Minimum Dietary Diversity for Women a Guide to Measurement
    FANTA III FOOD AND NUTRITION TECHNICAL A SSISTANCE Minimum Dietary Diversity for Women A Guide to Measurement Minimum Dietary Diversity for Women A Guide to Measurement Published by the Food and Agriculture Organization of the United Nations and USAID’s Food and Nutrition Technical Assistance III Project (FANTA), managed by FHI 360 Rome, 2016 Recommended citation: FAO and FHI 360. 2016. Minimum Dietary Diversity for Women: A Guide for Measurement. Rome: FAO. 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), or of FANTA/FHI 360 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 specific companies or products of manufacturers, whether or not these have been patented, does not imply that these have been endorsed or recommended by FAO, or FHI 360 in preference to others of a similar nature that are not mentioned. Additional funding for this publication was made possible by the generous support of the American people through the support of the Office of Health, Infectious Diseases, and Nutrition, Bureau for Global Health, U.S. Agency for International Development (USAID), under terms of Cooperative Agreement AID-OAA-A-12-00005 through the Food and Nutrition Technical Assistance III Project (FANTA), managed by FHI 360. The views expressed in this information product are those of the author(s) and do not necessarily reflect the views or policies of FAO, FHI 360, UC Davis, USAID or the U.S.
    [Show full text]
  • Sedges in Our Wetlands Typha Latifolia Schoeneplectus (Scirpus) Acutus • Native, Common, Sedge Family, up to 10’ Tall and S
    TULE (COMMON and CALIFORNIA) CATTAIL, COMMON/BROAD-LEAVED BULLRUSH (COMMON and SOUTHERN) Sedges in Our Wetlands Typha latifolia Schoeneplectus (Scirpus) acutus • Native, common, sedge family, up to 10’ tall and S. californicus • Wetland Obligate in fresh water up to 0.8 m • Native, common, sedge family, up to10’ tall “Sedges have edges. Rushes are round. depth • Wetland Obligate, in standing freshwater Grasses have knees that bend to the ground. ” • Intrudes into marshes when salinity decreases marshes, can tolerate slight salinity Description: The Cyperaceae are a family of graminoid (grass-like), monocot- • Can block channels, but lays down in high flow • Rhizomatous, dense monotypic colony yledonous flowering plants known as sedges. The family is large, with some 5,500 • Used as a bioremediator to absorb pollutants known species described in about 90 genera, the largest being the "true sedges" ge- • Terminal panicle inflorescence nus Carex with over 2,000 species. The stems of Cyperaceae are often triangular • Can be weaved into baskets, mats, seats, and • California Tule – bright green triangular stems (found in and mostly solid, whereas those of grasses are never triangular and are usually hol- binding for tule canoes ECWRF ponds) low except at the nodes. Sedges differ from grasses in many features, most obvious- Ethnobotany: All parts of the cattail are edible ly in their sheaths and the arrangement of the leaves on the stem. The leaves are ar- • Common Tule – grey green round stem (found in Shollen- when gathered at the appropriate stage of growth. ranged such that they spiral around the stem in 3-ranks and have a basal portion that berger Park channel) The young shoots are cut from the rhizomes sheaths the stem.
    [Show full text]
  • 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.
    [Show full text]
  • C6 Noncarice Sedge
    CYPERACEAE etal Got Sedge? Part Two revised 24 May 2015. Draft from Designs On Nature; Up Your C 25 SEDGES, FOINS COUPANTS, LAÎCHES, ROUCHES, ROUCHETTES, & some mostly wet things in the sedge family. Because Bill Gates has been shown to eat footnotes (burp!, & enjoy it), footnotes are (italicized in the body of the text) for their protection. Someone who can spell caespitose only won way has know imagination. Much of the following is taken verbatim from other works, & often not credited. There is often not a way to paraphrase or rewrite habitat or descriptive information without changing the meaning. I am responsible for any mistakes in quoting or otherwise. This is a learning tool, & a continuation of an idea of my friend & former employer, Jock Ingels, LaFayette Home Nursery, who hoped to present more available information about a plant in one easily accessible place, instead of scattered though numerous sources. This is a work in perpetual progress, a personal learning tool, full uv misstakes, & written as a personal means instead of a public end. Redundant, repetitive, superfluous, & contradictory information is present. It is being consolidated. CYPERACEAE Sauergrasgewächse SEDGES, aka BIESIES, SEGGEN Formally described in 1789 by De Jussieu. The family name is derived from the genus name Cyperus, from the Greek kupeiros, meaning sedge. Many species are grass-like, being tufted, with long, thin, narrow leaves, jointed stems, & branched inflorescence of small flowers, & are horticulturally lumped with grasses as graminoids. Archer (2005) suggests the term graminoid be used for true grasses, & cyperoid be used for sedges. (If physical anthropologists have hominoids & hominids, why don’t we have graminoids & graminids?) There are approximately 104 genera, 4 subfamilies, 14 tribes, & about 5000 species worldwide, with 27 genera & 843 species in North America (Ball et al 2002).
    [Show full text]
  • Int. J. Biosci. 2017
    Int. J. Biosci. 2017 International Journal of Biosciences | IJB | ISSN: 2220-6655 (Print), 2222-5234 (Online) http://www.innspub.net Vol. 11, No. 4, p. 144-149, 2017 RESEARCH PAPER OPEN ACCESS Ability of local species plant in surface flow constructed wetland to reduce biochemical oxygen demand (BOD) and chemical oxygen demand (COD) in sasirangan wastewater Nopi Stiyati Prihatini*1, Jumar2, Rima Sari Arisnawati1, Raudhyna Zata Nadhillah1, Romadhini Putri Wulandari1, Dwi Apriliani Fazriati1, Soemarno3 1Department of Environmental Engineering, Lambung Mangkurat University, Indonesia 2Department of Agrotechnology, Lambung Mangkurat University, Indonesia 3Department of Soil Sciences, University of Brawijaya, Malang, Indonesia Key words: BOD, COD, Constructed wetlands (CW), Sasirangan http://dx.doi.org/10.12692/ijb/11.4.144-149 Article published on October 21, 2017 Abstract Sasirangan wastewater has characteristics of high pH as well as high level of biochemical oxygen demand(BOD)and chemical oxygen demand(COD). Sasirangan industries produce large amount of wastewater, which then is directly discarded around the environment without treatment processes. The effect afterward is the oxygen supply in the water diminishes and eventually triggers the activity of anoxic-anaerobic microorganisms that produces odors. Constructed wetlands are able to become the alternative to waste treatment technology at the economical household scale industries. This study was conducted to determine the ability of the removal of BOD and COD in the sasirangan effluent with constructed wetlands (CW) surface flow system using the batch method. Plants used in CW is Hydrilla verticillata, purun tikus (Eleocharis dulcis) and lotus (Nelumbo nucifera). CW was running for 0, 3, 6, 9 and 12 days.
    [Show full text]
  • Cyperaceae of Puerto Rico. Arturo Gonzalez-Mas Louisiana State University and Agricultural & Mechanical College
    Louisiana State University LSU Digital Commons LSU Historical Dissertations and Theses Graduate School 1964 Cyperaceae of Puerto Rico. Arturo Gonzalez-mas Louisiana State University and Agricultural & Mechanical College Follow this and additional works at: https://digitalcommons.lsu.edu/gradschool_disstheses Recommended Citation Gonzalez-mas, Arturo, "Cyperaceae of Puerto Rico." (1964). LSU Historical Dissertations and Theses. 912. https://digitalcommons.lsu.edu/gradschool_disstheses/912 This Dissertation is brought to you for free and open access by the Graduate School at LSU Digital Commons. It has been accepted for inclusion in LSU Historical Dissertations and Theses by an authorized administrator of LSU Digital Commons. For more information, please contact [email protected]. This dissertation has been 64—8802 microfilmed exactly as received GONZALEZ—MAS, Arturo, 1923- CYPERACEAE OF PUERTO RICO. Louisiana State University, Ph.D., 1964 B o ta n y University Microfilms, Inc., Ann Arbor, Michigan CYPERACEAE OF PUERTO RICO A Dissertation I' Submitted to the Graduate Faculty of the Louisiana State University and Agricultural and Mechanical College in partial fulfillment of the requirements for the degree of Doctor of Philosophy in The Department of Botany and Plant Pathology by Arturo Gonzalez-Mas B.S., University of Puerto Rico, 1945 M.S., North Carolina State College, 1952 January, 1964 PLEASE NOTE: Not original copy. Small and unreadable print on some maps. Filmed as received. UNIVERSITY MICROFILMS, INC. ACKNOWLEDGMENT The author wishes to express his sincere gratitude to Dr. Clair A. Brown for his interest, guidance, and encouragement during the course of this investigation and for his helpful criticism in the preparation of the manuscript and illustrations.
    [Show full text]
  • Eleocharis Dulcis) and GIANT MOLESTA (Salvinia Molesta) EXTRACT
    Sys Rev Pharm 2020;11(12):916-924 A multifaceted review journal in the field of pharmacy PHYTOCHEMICAL COMPOUNDS AND ANTIOXIDANT ACTIVITY OF WATER CHESTNUT (Eleocharis dulcis) AND GIANT MOLESTA (Salvinia molesta) EXTRACT BAEHAKI, Ace1*; TAMPUBOLON1, Nindi Herawati, LESTARi; Shanti Dwita1 1Sriwijaya University, Faculty of Agriculture, Department of Fisheries Product Technology. Indonesia. * Corresponding author e-mail: acebaehaki_thi@unsri,ac,id ABSTRACT The purpose of this research was to observe of phytochemical The results of antioxidant activity with the water chesnut and giant content and antioxidant activity of chinese water chesnut molesta extracts had very weak IC50 values in n-hexan solvents (Eleocharis dulcis) and giant molesta (Salvinia molesta) extracts valued at 1977.22 ppm and 3211.2 ppm. Water chesnut of extract with three solvents of different levels of polarity. This study used had the highest ABTS value in ethyl acetate solvents at a an experimental laboratory method and data analysis was carried concentration of 1000 ppm at 85.253% and in giant molesta out descriptively. Some of the steps carried out include the stages extract at a concentration of 1000 ppm using ethanol solvent had of sampling, sample extraction, calculation of extract extracts, the highest value of 76.665%. Ethanol extract in water chesnut quantitative phytochemical analysis (flavonoid content, phenol extract and giant molesta had the highest reducing ability power content, phenolic content, and tannin content), and test of with a mean absorbance of 0.477 and 0.520. The best solvent for antioxidant activity (DPPH, ABTS and Reducing ability. The extracting water chesnut and giant molesta were ethanol.
    [Show full text]
  • Water Caltrop: a Potential Crop of Water Bodies
    Water caltrop: A potential crop of water bodies RASHTRIYA KRISHI Volume 11 Issue 2 December, 2016 7-11 e ISSN–2321–7987 | Article |Visit us : www.researchjournal.co.in| Water caltrop: A potential crop of water bodies Hiralal Jana Department of Agricultural Extension, College of Agriculture, Bidhan Chandra Krishi Viswavidyalaya, Agricultural Farm, BURDWAN (W.B.) INDIA (Email : [email protected]) Another name of water caltrop is water chestnut. generic name Trapa is derived from the Latin words of Water chestnut (Trapa natans) is one of the most “thistle” and “calcitrappa” (a four-pointed weapon as the important minor fruit crops grown in India. It is an aquatic seeds have four points), calcitrappa is another common nut crop grown mainly in the tropical and sub-tropical name for the water caltrop. The Chinese name is língjiao, region, as submersed plant community. It also thrives in líng meaning “caltrop” and jiao meaning “horn”. This is the soft nutrient rich waters in lakes, ponds and streams often rendered as ling nut by English-speakers. In India, with a neutral to slightly alkaline pH. The plant is well the plant has different regional names, such as singhada, adapted to life at the water’s edge and prospers even pani-phal in Hindi, or shingoda in Gujarati. This fruit’s when stranded along muddy shores. Bengali name is Paniphal, Singda or Singara. Two most common Indian names are Paniphal and Singhara. The plant’s name in Japanese is hishi, a word meaning “diamond- or lozenge-shaped”. The most common type in India is Trapa bispinosa and the common type in China is Trapa bicornis.
    [Show full text]
  • Evaluation of Sacred Lotus (Nelumbo Nucifera Gaertn.) As an Alternative Crop for Phyto-Remediation by Warner Steve Orozco Oband
    Evaluation of Sacred Lotus (Nelumbo nucifera Gaertn.) as an Alternative Crop for Phyto-remediation by Warner Steve Orozco Obando A dissertation submitted to the Graduate Faculty of Auburn University in partial fulfillment of the requirements for the Degree of Doctor of Philosophy Auburn, Alabama May 6, 2012 Keywords: Aquaponics, Heavy Metals, Constructed Wetlands, CWs Copyright 2012 by Warner Orozco Obando Approved by Kenneth M. Tilt, Chair, Professor of Horticulture Floyd M. Woods, Co-chair, Associate Professor of Horticulture Fenny Dane, Professor of Horticulture J. Raymond Kessler, Professor of Horticulture Jeff L. Sibley, Professor of Horticulture Wheeler G. Foshee III, Associate Professor of Horticulture Abstract Lotus, Nelumbo nucifera, offers a wide diversity of uses as ornamental, edible and medicinal plant. An opportunity for growing lotus as a crop in Alabama also has the potential for phyto-remediation. Lotus was evaluated for remediation of trace elements focusing on manganese (Mn), organic compounds targeting s-metolachlor and filtering aquaculture waste water. Lotus was evaluated for filtering trace elements by establishing a base line for tissue composition and evaluating lotus capacity to grow in solutions with high levels of Mn (0, 5, 10, 15, or 50 mg/L). Increasing Mn concentrations in solution induced a linear increase in lotus Mn leaf concentrations. Hyper-accumulation of Al and Fe was detected in the rhizomes, while Na hyper-accumulated in the petioles, all without visible signs of toxicity. Mn treatments applied to lotus affected chlorophyll content. For example, chlorophyll a content increased linearly over time while chlorophyll b decreased. Radical scavenging activity (DPPH) did not change over time but correlated with total phenols content, showing a linear decrease after 6 weeks of treatment.
    [Show full text]
  • Fountain Grass - '" Turn Off the Spigot! 'V As If We Haven't Learned a Lesson from the Invasive Ability to Escape Cultivation in Florida
    :Fforitfa EPPC FLORIDA EXOTIC PEST PLANT COUNCIL ''An organization concerned with Florida's Environmental Future" Volume 6 Number 2 Spring 1996 Fountain grass - '" _ Turn off the spigot! 'V As if we haven't learned a lesson from the invasive ability to escape cultivation in Florida. Its preference for natal grass, Pennisetum purpureum, along comes foun­ dry sites could spell trouble for pineland and scrub habi­ tain grass, Pennisetum selaceum. 1bis African species is tats. widely cultivated as an ornamental in southern and cen­ tral Florida and has become popular with landscape The Asian grass Burma reed, Neyraudia reytllludiall/J, architects. It is also frequently offered through mail-or­ aggressively invades dry sites, especially the globally der gardening catalogs. imperiled pine rockland habitat in Dade County. Now that effective management techniques have been devel­ While the tall, exceptionally invasive natal grass oped to control this rampant grass, it is especially im­ colonizes low-lying, wetland areas and canal banks, portant that fountain grass be regulated before it too fountain grass seems to prefer dry sites and is included becomes an environmental and budgetary nightmare. on lists of potential plants for xeriscaping. On Key Largo in Monroe County, fountain Identification grass has recently been discovered as an escapee in three separate locali­ "This species war­ Fountain grass can be recog­ ties by Keith Bradley. Voucher speci­ nized by its clustering habit, narrow mens have been deposited in the rants being regulated elongate leaves to about one meter herbarium at Fairchild Tropical Gar­ because it is already a tall, and nodding plumose inflores­ den in Miami.
    [Show full text]
  • Directions for Management of Perennial Sedges in Lowland Rice Jonne Rodenburg – Africa Rice Center
    Directions for Management of Perennial Sedges in Lowland Rice Jonne Rodenburg – Africa Rice Center Some of the most frequently encountered perennial sedges of rice in rain‐fed and irrigated lowlands include: Bolboschoenus maritimus, Cyperus distans, Cyperus esculentus, Cyperus exaltatus, Cyperus haspan, Cyperus rotundus, Eleocharis acutangula, Eleocharis dulcis, Eleocharis mutata, Fimbristylis dichotoma, Fimbristylis ferruginea, Fuirena stricta, Fuirena umbellata, Kyllinga erecta, Kyllinga pumila, Mariscus longibracteatus, Pycreus lanceolatus, Rhynchospora corymbosa, Scleria depressa, Scleria verrucosa and Scleria vogelii. Perennial weeds can live for more than two years and use vegetative structures such as rhizomes or bulbs for their survival and propagation. Rhizomatous weeds develop underground stems that propagate and produce new plants. Examples of rhizotomous sedges are: Cyperus distans, Cyperus esculentus and Cyperus rotundus (both having rhizomes ending in tubers). Besides vegetative reproduction and survival strategies, perennial weeds also propagate through the production of seeds. Any management practice, in order to provide effective control of perennial weeds, should focus on prevention of seed production (like with annual weeds) and removal or killing of the vegetative underground structures. This can be done mechanically by deep tillage in the off‐season, trying to bring all stem, root and other propagation structures to the soil surface to be collected and removed (and burned) or killed by exposure to the sun (drying out) or by using herbicides. Another cultural method that proved successful to control perennial sedges is the use of a crop rotation with a dryland crop such as maize, groundnut, mungbean or combinations of these (Lacsina and Datta, 1975, Datta and Jereza, 1976). It is mainly the disruption of the favourable wet conditions that helps to reduce the perennial sedges.
    [Show full text]
  • Floristic and Phytosociology of Weeds in Pastures in Maranhão State, Northeast Brazil1
    Revista Ciência Agronômica, v. 47, n. 2, p. 414-420, abr-jun, 2016 Centro de Ciências Agrárias - Universidade Federal do Ceará, Fortaleza, CE Nota Científica www.ccarevista.ufc.br ISSN 1806-6690 Floristic and phytosociology of weeds in pastures in Maranhão State, Northeast Brazil1 Florística e fitossociologia de plantas invasoras em pastagens no Estado do Maranhão Jaílson Penha Costa2 and Mário Luiz Ribeiro Mesquita3* ABSTRACT - Knowledge of weed floristic composition and phytosociology are key factors for improving weed management in pastures. Information on weed species that occur in pastures in Northeast Brazil, particularly in Maranhão State is very limited. It is, therefore, important, to search for information to help farmers to control weeds in livestock farming. This paper describes the weed flora diversity and community structure parameters, including density, frequency, abundance and importance value for each weed species found in five pastures of same age and management in Maranhão State, Northeast Brazil. The weed survey was carried out using a wooden frame (80 cm x 30 cm) placed randomly on the soil surface 30 times in each pasture (n = 150). Weeds were pulled out, separated by species and counted. The weed flora was represented by 996 individuals, from nine families, 15 genera and 19 species. Weed density within pastures was of 44.3 plants m-2. The weed flora was dominated by species of the Cyperaceae and Poaceae families. The most important weed species based on Importance Value were Eragrostis ciliaris (IV = 32.97), Cyperus rotundus (IV = 31,95), Cyperus luzulae (IV = 27,50), Cyperus sphacelatus (IV = 27,42), Pycreus lanceolatus (IV = 27,33) Cyperus haspan (IV = 25,72) and Eleusine indica (IV = 23,49).
    [Show full text]