Response of Water Hyacinth Manure on Growth Attributes and Yield of Celosia Argentea L (Lagos Spinach)
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Pollen Ultrastructure of the Pontederiaceae Michael G
This article was downloaded by: [72.199.208.79] On: 25 May 2012, At: 23:08 Publisher: Taylor & Francis Informa Ltd Registered in England and Wales Registered Number: 1072954 Registered office: Mortimer House, 37-41 Mortimer Street, London W1T 3JH, UK Grana Publication details, including instructions for authors and subscription information: http://www.tandfonline.com/loi/sgra20 Pollen ultrastructure of the Pontederiaceae Michael G. Simpson a a Department of Biology, San Diego State University, San Diego, California, 92182, USA Available online: 05 Nov 2009 To cite this article: Michael G. Simpson (1987): Pollen ultrastructure of the Pontederiaceae, Grana, 26:2, 113-126 To link to this article: http://dx.doi.org/10.1080/00173138709429941 PLEASE SCROLL DOWN FOR ARTICLE Full terms and conditions of use: http://www.tandfonline.com/page/terms-and-conditions This article may be used for research, teaching, and private study purposes. Any substantial or systematic reproduction, redistribution, reselling, loan, sub-licensing, systematic supply, or distribution in any form to anyone is expressly forbidden. The publisher does not give any warranty express or implied or make any representation that the contents will be complete or accurate or up to date. The accuracy of any instructions, formulae, and drug doses should be independently verified with primary sources. The publisher shall not be liable for any loss, actions, claims, proceedings, demand, or costs or damages whatsoever or howsoever caused arising directly or indirectly in connection with or arising out of the use of this material. Grana 26: 113-126, 1987 Pollen ultrastructure of the Pontederiaceae Evidence for exine homology with the Haemodoraceae MICHAEL G. -
Eichhornia Azurea A
Aquatic Plant Anchored water hyacinth; Rooted water hyacinth I. Current Status and Distribution Eichhornia azurea a. Range Global/Continental Wisconsin Native Range South America, Central America, and Mexico1,2,3 Not recorded in Wisconsin6 Figure 1: U.S and Canada Distribution Map4 Several populations also reported from Southern Indiana5 Abundance/Range Widespread: Undocumented Not applicable Locally Abundant: Undocumented Not applicable Sparse: Puerto Rico, Southern Indiana3,4,5; India, Iran2; Florida3,7; Japan3 Not applicable Range Expansion Date Introduced: 1980s(3) Not applicable Rate of Spread: Undocumented Not applicable Density Risk of Monoculture: Can produce biomass up to 900 g/m2 (3) Undocumented Facilitated By: Nutrient enriched waters3 Undocumented b. Habitat Rivers, lakes, ponds, marshes, canals, reservoirs2,8 Tolerance Chart of tolerances: Increasingly dark color indicates increasingly optimal range Preferences Sandy, acidic, clay or alkaline soils9; larger leaves produced in lotic and high nutrient environments3,10; larger plants produced in deep-water habitats11 c. Regulation Noxious/Regulated4: Federal Noxious Weed List; AL, AZ, CA, FL, MA, NC, OR, SC, TZ, VT Minnesota Regulations: Not regulated Michigan Regulations: Not regulated Washington Regulations: Not regulated Page 1 of 5 Wisconsin Department of Natural Resources – Aquatic Invasive Species Literature Review II. Establishment Potential and Life History Traits a. Life History Perennial aquatic plant with submerged and emersed leaves2; usually rooted in mud but occasionally free-floating8 Fecundity High Reproduction Importance of Seeds: Can reproduce by seed2,3,8 Vegetative: Can reproduce by whole plants and stem fragments2,3,8 Hybridization Undocumented Overwintering Winter Tolerance: Undocumented Phenology: Flowers from June to October3,7,8 b. -
Diversityand Classification of Flowering Plants
180 CHAPTER 6 EVOLUTION OF FLOWERING PLANTS F REFERENCES FOR FURTHER STUDY Andrews, H. N. 1961. Studies in Paleobotany. Wiley, New York. APG ifi. 2009. An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG III. Botanical Journal of the Linnean Society 161: 105—121. Crane, P. R., E. M. Friis, and K. Pedersen. 1995. The origin and early diversification of angiosperms. Nature 374: 27. 7 Crepet, W. L. 1998. The abominable mystery. Science 282: 1653—1654. Cronquist, A. 1981. An integrated system of classification of flowering plants. Columbia University Press, New York. Davies, T. J., T. G. Barraclough, M. W. Chase, P. 5. Soltis, D. E. Soltis, and V. Savolainen. 2004. Darwin’s abominable mystery: Insights from AND CLASSIFICATION a supertree of DIVERSITY the angiosperms. Proceedings of the National Academy of Sciences of the United States of America 101: 1904—1909. Doyle, J. A. 2006. Seed ferns and the origin of angiosperms. Journal of the Torrey Botanical Society 133: 169—209. Doyle, J. A. 2008. Integrating molecular phylogenetic and paleobotanical evidence on origin of the flower. International Journal of Plant FLOWERING PLANTS: Sciences 169: 816—843. OF Eames, A. J. 1961. Morphology of the angiosperms. McGraw Hill, New York. Friedman, W. and E., J. H. Williams. 2004. Developmental evolution of the sexual process in ancient flowering plant lineages. The Plant Cell NYMPHAEALE S, 16, S119—S 132, Supplement. AMBORELLALE S, Friedman, W. E., and K. C. Ryerson. 2009. Reconstructing the ancestral female gametophyte of angiosperms: insights from Amborella and other ancient lineages of flowering plants. -
2 ANGIOSPERM PHYLOGENY GROUP (APG) SYSTEM History Of
ANGIOSPERM PHYLOGENY GROUP (APG) SYSTEM The Angiosperm Phylogeny Group, or APG, refers to an informal international group of systematic botanists who came together to try to establish a consensus view of the taxonomy of flowering plants (angiosperms) that would reflect new knowledge about their relationships based upon phylogenetic studies. As of 2010, three incremental versions of a classification system have resulted from this collaboration (published in 1998, 2003 and 2009). An important motivation for the group was what they viewed as deficiencies in prior angiosperm classifications, which were not based on monophyletic groups (i.e. groups consisting of all the descendants of a common ancestor). APG publications are increasingly influential, with a number of major herbaria changing the arrangement of their collections to match the latest APG system. Angiosperm classification and the APG Until detailed genetic evidence became available, the classification of flowering plants (also known as angiosperms, Angiospermae, Anthophyta or Magnoliophyta) was based on their morphology (particularly that of the flower) and their biochemistry (what kinds of chemical compound they contained or produced). Classification systems were typically produced by an individual botanist or by a small group. The result was a large number of such systems (see List of systems of plant taxonomy). Different systems and their updates tended to be favoured in different countries; e.g. the Engler system in continental Europe; the Bentham & Hooker system in Britain (particularly influential because it was used by Kew); the Takhtajan system in the former Soviet Union and countries within its sphere of influence; and the Cronquist system in the United States. -
Monochoria Angustifolia (G. X. Wang) Boonkerd & Tungmunnithum, The
Songklanakarin J. Sci. Technol. 42 (4), 747-752, Jul. - Aug. 2020 Original Article Monochoria angustifolia (G. X. Wang) Boonkerd & Tungmunnithum, the new species of the genus Monochoria from Thailand Duangjai Tungmunnithum1, 2*, Norio Tanaka2, and Thaweesakdi Boonkerd3 1 Department of Pharmaceutical Botany, Faculty of Pharmacy, Mahidol University, Ratchathewi, Bangkok, 10400 Thailand 2 Department of Botany, Tsukuba Botanical Garden, National Museum of Nature and Science, Amakubo, Tsukuba, 305-0005 Japan 3 Department of Botany, Faculty of Science, Chulalongkorn University, Pathum Wan, Bangkok, 10330 Thailand Received: 8 May 2018; Revised: 15 February 2019; Accepted: 5 April 2019 Abstract Monochoria C. Presl is a genus member of the aquatic plant family Pontederiaceae which exhibits high morphological variations. The populations of Monochoria vaginalis exhibit extreme variations in their morphology. Previous morphological and phenetic studies suggested that M. vaginalis s.l. in Thailand contained cryptic species. In this recent study, the molecular data from DNA sequencing and phylogenetic analysis of 50 living plants from 10 populations of M. vaginalis with 3 outgroups using 5 regions from both cpDNA and nuclear DNA were intensely investigated. The results showed a similar trend as in previous studies that M. vaginalis populations should be separated into 2 species. The new species, M. angustifolia (G. X. Wang) Boonkerd & Tungmunnithum, is also described in this work. Keywords: Monochoria, new species, molecular data, Pontederiaceae, Thailand 1. Introduction M. vaginalis (Burm.f.) C.Presl is an aquatic flowering plant in the Pontederiaceae family occurring in According to the World Checklist of Selected Plant standing water bodies of tropical and subtropical regions Families (http://wcsp.science.kew.org/home.do), the genus (Chayamarit, 2005; Solms, 1883; Tungmunnithum, Boonkerd, Monochoria consists of 7 species worldwide: M. -
Field Release of Megamelus Scutellaris, Berg (Hemiptera: Delphacidae), for Biological Control of Water Hyacinth Eichhornia Crassipes Mart
United States Department of Agriculture Field Release of Marketing and Regulatory Megamelus scutellaris, Programs Animal and Berg (Hemiptera: Plant Health Inspection Service Delphacidae), for Biological Control of Water Hyacinth Eichhornia crassipes Mart. (Solms) (Pontederiales: Pontederiaceae) in the Continental United States Environmental Assessment, January 2010 Field Release of Megamelus scutellaris, Berg (Hemiptera: Delphacidae), for Biological Control of Water Hyacinth Eichhornia crassipes Mart. (Solms) (Pontederiales: Pontederiaceae) in the Continental United States Environmental Assessment, January 2010 Agency Contact: Shirley Wager-Page, Branch Chief Pest Permitting Plant Protection and Quarantine Animal and Plant Health Inspection Service U.S. Department of Agriculture 4700 River Road, Unit 133 Riverdale, MD 20737–1236 The U.S. Department of Agriculture (USDA) prohibits discrimination in all its programs and activities on the basis of race, color, national origin, sex, religion, age, disability, political beliefs, sexual orientation, and marital or family status. (Not all prohibited bases apply to all programs.) Persons with disabilities who require alternative means for communication of program information (Braille, large print, audiotape, etc.) should contact USDA’s TARGET Center at (202) 720–2600 (voice and TDD). To file a complaint of discrimination, write USDA, Director, Office of Civil Rights, Room 326–W, Whitten Building, 1400 Independence Avenue, SW, Washington, DC 20250–9410 or call (202) 720–5964 (voice and TDD). USDA is an equal opportunity provider and employer. Mention of companies or commercial products in this report does not imply recommendation or endorsement by the U.S. Department of Agriculture (USDA) over others not mentioned. USDA neither guarantees or warrants the standard of any product mentioned. -
Angiosperm Phylogeny Group (APG) System
Angiosperm Phylogeny Group (APG) system The Angiosperm Phylogeny Group, or APG, refers to an informal international group of systematic botanists who came together to try to establish a consensus view of the taxonomy of flowering plants (angiosperms) that would reflect new knowledge about their relationships based upon phylogenetic studies. As of 2010, three incremental versions of a classification system have resulted from this collaboration (published in 1998, 2003 and 2009). An important motivation for the group was what they viewed as deficiencies in prior angiosperm classifications, which were not based on monophyletic groups (i.e. groups consisting of all the descendants of a common ancestor). APG publications are increasingly influential, with a number of major herbaria changing the arrangement of their collections to match the latest APG system. Angiosperm classification and the APG Until detailed genetic evidence became available, the classification of flowering plants (also known as angiosperms, Angiospermae , Anthophyta or Magnoliophyta ) was based on their morphology (particularly that of the flower) and their biochemistry (what kinds of chemical compound they contained or produced). Classification systems were typically produced by an individual botanist or by a small group. The result was a large number of such systems (see List of systems of plant taxonomy). Different systems and their updates tended to be favoured in different countries; e.g. the Engler system in continental Europe; the Bentham & Hooker system in Britain (particularly influential because it was used by Kew); the Takhtajan system in the former Soviet Union and countries within its sphere of influence; and the Cronquist system in the United States. -
Macroinvertebrates of Eichhornia Crassipes (Pontederiaceae) Roots in the Alluvial Floodplain of Large Tropical Rivers (Argentina)
ISSN Printed: 0034-7744 ISSN digital: 2215-2075 Macroinvertebrates of Eichhornia crassipes (Pontederiaceae) roots in the alluvial floodplain of large tropical rivers (Argentina) Alicia S. G. Poi1, Juan J. Neiff1, Sylvina L. Casco1,2 & Luciana I. Gallardo1,2 1. Centro de Ecología Aplicada del Litoral- CECOAL (CCT Nordeste - CONICET- UNNE), Ruta 5 km 2.5, (3400) Corrientes, Argentina; [email protected]; [email protected] 2. Facultad de Ciencias Exactas y Naturales y Agrimensura-FACENA, Universidad Nacional del Nordeste-UNNE, (3400) Corrientes, Argentina; [email protected]; [email protected] Received 30-IX-2019. Corrected 07-VIII-2020. Accepted 31-VIII-2020. ABSTRACT. Introduction: Eichhornia crassipes is a dominant aquatic plant of neotropical-river floodplains and is invasive in warm waters of different continents. Plants provide food and habitat for fish, especially Prochilodus lineatus and Gymnotus omarorum, which are relevant to subsistence fishing by local indigenous communities. Objective: In this study we describe the main traits of E. crassipes floating meadows, and analyze the abundance and composition of macroinvertebrate assemblages associated with their roots in two floodplain wetlands of the Paraná River (within the Ramsar site Wetlands Chaco) and of the Pilcomayo River (within the Pilcomayo River National Park). Methods: During spring and summer, the macroinvertebrates were collected in monospecific stands of E. crassipes with a net of 962 cm2 area and 500 µm mesh size. Leaf density, the biomass of leaves and roots, the length of leaves and roots, and the water quality were measured simultaneously. Results: Temperature, oxygen concentration, and nutrient content were significantly higher and electrical conductivity was lower in the Pilcomayo than in the Paraná floodplain. -
Breeding System of Tristylous Eichhornia Azurea (Pontederiaceae) in the Southern Pantanal, Brazil
Plant Syst Evol DOI 10.1007/s00606-009-0170-z ORIGINAL ARTICLE Breeding system of tristylous Eichhornia azurea (Pontederiaceae) in the southern Pantanal, Brazil Nicolay Leme da Cunha Æ Erich Fischer Received: 11 April 2008 / Accepted: 17 February 2009 Ó Springer-Verlag 2009 Abstract The breeding system of Eichhornia azurea Introduction (Pontederiaceae) has been described as being both self- and heteromorphic incompatible based on crossing experiments Heterostyly is regarded as the most complex floral poly- performed on plants grown in an experimental garden. We morphism because it provides both mechanical and genetic studied the breeding system of tristylous E. azurea popu- barriers to prevent autogamy (Vuilleumier 1967; Ganders lation under natural conditions in the Pantanal wetlands, 1979; Barrett and Husband 1990). Heterostylous species Brazil. Controlled pollinations were conducted using 35 can exhibit either two (distyly) or three (tristyly) floral individuals of each floral morph. Legitimate pollinations morphs that differ reciprocally according to the stigmas produced more fruits than self- and illegitimate pollina- and anthers heights. Ancillary polymorphism of pollen and tions, except for the mid-styled morph which was highly stigmas are generally associated with heterostyly and such self- and heteromorphic compatible. The number of seeds differences are expected to be involved in self- and intra- per fruit was higher under legitimate pollinations than in morph incompatibility (Barrett and Cruzan 1994). the other treatments, but self- and illegitimate pollinations Tristyly is conspicuous in the Pontederiaceae, occur- produced more fruits and seeds in the Pantanal than for ring in three of eight Eichhornia and four of five individuals of E. azurea in other populations. -
Pontederia Cordata1
Fact Sheet FPS-490 October, 1999 Pontederia cordata1 Edward F. Gilman2 Introduction This native, eastern America aquatic plant is well adapted to Florida habitat (Fig. 1). It can be found in the wild from Nova Scotia through the entire state of Florida in shallow wetland areas around the edges of ponds and lakes. It grows in water no more than about 12 inches deep. Foliage emerges each spring from below the water surface and stands several feet above the water surface. Beautiful purple-blue flower spikes follow several weeks latter and are held slightly above the foliage. General Information Scientific name: Pontederia cordata Pronunciation: pon-tee-DEER-ree-uh kor-DAY-tuh Common name(s): Pickerel-Weed Family: Pontederiaceae Plant type: aquatic plant USDA hardiness zones: 3B through 10 (Fig. 2) Planting month for zone 7: year round Planting month for zone 8: year round Figure 1. Pickerel-Weed. Planting month for zone 9: year round Planting month for zone 10: year round Spread: depends upon supporting structure Origin: native to Florida Plant habit: upright Uses: water garden; attracts butterflies Plant density: open Availablity: somewhat available, may have to go out of the Growth rate: fast region to find the plant Texture: coarse Description Height: 3 to 5 feet 1.This document is Fact Sheet FPS-490, one of a series of the Environmental Horticulture Department, Florida Cooperative Extension Service, Institute of Food and Agricultural Sciences, University of Florida. Publication date: October, 1999 Please visit the EDIS Web site at http://edis.ifas.ufl.edu. 2. Edward F. Gilman, professor, Environmental Horticulture Department, Cooperative Extension Service, Institute of Food and Agricultural Sciences, University of Florida, Gainesville, 32611. -
Flora of the Guianas Project
Leiden, October 2012 The Flora of the Guianas is a co-operative programme of: Botanischer Garten und Botanisches Museum Berlin-Dahlem, Berlin; Institut de Recherche pour le Développement, IRD, Centre de Cayenne, Cayenne; Department of Biology, University of Guyana, Georgetown; Herbarium, Royal Botanic Gardens, Kew; New York Botanical Garden, New York; Nationaal Herbarium Suriname, Paramaribo; Muséum National d’Histoire Naturelle, Paris; Nationaal Herbarium Nederland, Utrecht University branch, Utrecht, and Department of Botany, Smithsonian Institution, Washington, D.C. For further information see the website: http://www.nationaalherbarium.nl/FoGWebsite/index.html Published on June 2014 Flora of the Guianas Newsletter no 18. Nationaal Herbarium Nederland, Naturalis Biodiversity Center, Einsteiweg 2, 2333 CC, Leiden, The Netherlands 2 CONTENTS In Memorian M.F.Prévost, J. Florschutz 1. MEETING PROGRAM ...................................................................................................... 6 2. MINUTES OF THE ADVISORY BOARD MEETING .............................................................. 7 2.1. Opening and report on previous meeting in Washigton .............................................. 7 2.2. Board personnel changes ............................................................................................ 7 2.3. Memorandum of Understanding ................................................................................. 7 2.4. Report by the executive editor ................................................................................... -
First Record of Monochoria Hastata: a New Alien Weed of Rice in Pakistan
INTERNATIONAL JOURNAL OF AGRICULTURE & BIOLOGY ISSN Print: 1560–8530; ISSN Online: 1814–9596 17–0368/2018/20–1–165–168 DOI: 10.17957/IJAB/15.0470 http://www.fspublishers.org Full Length Article First Record of Monochoria hastata: A new Alien Weed of Rice in Pakistan Mubarak Ali, Asad Shabbir* and Iram Mujahid Ecology and Evolution Lab, Department of Botany, University of the Punjab, Lahore 54590 Pakistan *For correspondence: [email protected] Abstract Monochoria hastata (L.) Solms. of family Pontederiaceae is the first time reported as a new species in the alien weed flora of Pakistan. M. hastata has been found in flooded rice fields, ponds and swampy places in the District Narowal of the Province Punjab, Pakistan. It has been also reported as a weed of rice fields in many countries of South and Southeast Asia and is an aggressive weed that reproduces both sexually (seed) and vegetatively (stolons). The comprehensive morphometric description, preliminary distribution, importance and resemblance with closely related plants species, M. Vagenalis (Burm.f.) C. Presl ex Kunthare presented. At present, this exotic weed is not widespread in Pakistan hence, it is may be possible to eradicate it before it is widely established and difficult to control. © 2018 Friends Science Publishers Keywords: Leaf pondweed; Exotic species; Naturalized plant; Flooded rice weed; Monochoria hastata Introduction toothache, asthma, cough, cold, fever, but also for stomach and liver disorders, haemorrhage, hepatitis, The family Pontederiaceae consists of widespread annual anemia, scurvy and diabetes (Ileperuma et al., 2015). or perennial aquatic herbs which are floating or rooted in Phytoremediation potential of M.