ARTIGO O Gênero Aeschynomene L. (Leguminosae, Faboideae, Dalbergieae) Na Planície De Inundação Do Alto Rio Paraná, Brasil1

Total Page:16

File Type:pdf, Size:1020Kb

ARTIGO O Gênero Aeschynomene L. (Leguminosae, Faboideae, Dalbergieae) Na Planície De Inundação Do Alto Rio Paraná, Brasil1 e B d io o c t i ê u t n i c t i s Revista Brasileira de Biociências a n s I Brazilian Journal of Biosciences U FRGS ISSN 1980-4849 (on-line) / 1679-2343 (print) ARTIGO O gênero Aeschynomene L. (Leguminosae, Faboideae, Dalbergieae) na planície de inundação do alto rio Paraná, Brasil1 Maria Conceição de Souza2*, Laíla Fadul Vianna3 e Kazue Kawakita4 e Silvia Teresinha Sfoggia Miotto5 Recebido: 28 de outubro de 2011 Recebido após revisão: 09 de março de 2012 Aceito: 02 de abril de 2012 Disponível on-line em http://www.ufrgs.br/seerbio/ojs/index.php/rbb/article/view/2082 RESUMO: (O gênero Aeschynomene L. (Leguminosae, Faboideae, Dalbergieae) na planície de inundação do alto rio Paraná, Brasil). Inventários da flora na planície de inundação do alto rio Paraná têm demonstrado que a família Leguminosae, em especial a subfamília Faboideae, apresenta uma das mais elevadas riquezas florísticas. Este estudo apresenta o levantamento do gênero Aeschynomene L., para a referida planície, localizada nos estados de Mato Grosso do Sul e Paraná (22°38’–22°57’ S e 53°05’–53°36’ W), no bioma Mata Atlântica. O material botânico foi obtido por coletas e exame do acervo do Herbário da Universidade Estadual de Maringá (HUEM). Foram reconhecidas oito espécies: Aeschynomene americana L., A. brasiliana DC., A. denticulata Rudd, A. falcata (Poir.) DC., A. fluminensis Vell., A. histrix Poir, A. montevidensis Vogel e A. sensitiva Sw., distribuídas nas seções Aeschynomene e Ochopodium. Palavras-chave: Fabaceae, levantamento florístico, vegetação ripária, estado do Paraná, estado de Mato Grosso do Sul. ABSTRACT: (The genus Aeschynomene (Leguminosae, Faboideae, Dalbergieae) in the Upper Paraná River floodplain, Brazil). Floristic inventories in the Upper Paraná River floodplain shows the family Leguminosae, Faboideae in particular, with one of the highest richness floristic. This study presents a survey of the genusAeschynomene L., to this floodplain in the states of Mato Grosso do Sul and Paraná (22°38’–22°57’ S and 53°05’–53°36’ W), in the Mata Atlântica Biome. The plant material was obtained by collection and examination of the Herbarium of the Universidade Estadual de Maringá (HUEM). They were recognized eight species: Aeschynomene americana L., A. brasiliana DC., A. denticulata Rudd, A. falcata (Poir.) DC., A. fluminensis Vell., A. histrix Poir, A. montevidensis Vogel and A. sensitiva Sw., and distributed in the sections Aeschy- nomene and Ochopodium. Key words: floristic inventory, riparian vegetation, Paraná state, Mato Grosso do Sul state. INTRODUÇÃO Pleuronerviae Rudd e Scopariae Rudd). A secção Aes- O gênero Aeschynomene L., circunscrito na família chynomene, segundo Rudd (1955), está representada Leguminosae, subfamíla Faboideae, tribo Dalbergieae por espécies predominantemente hidrófitas e, para a (Klitgaard & Lavin 2005), foi descrito por Linnaeus em bacia do Rio Paraná, são citadas diversas espécies anfí- 1753. Em 1859, Bentham reuniu, na Flora Brasilien- bias, da série Sensitivae. sis de Martius, 24 espécies, oito das quais novas para Para a Flora do Cone Sul (Fortunato et al. 2008) fo- a Ciência. Em 1938, Vogel apud Rudd (1955) propôs a ram listadas 24 espécies, sendo quatro endêmicas e uma divisão do gênero em duas secções: Eu-aeschynomene introduzida. Para o Brasil, além da Flora Brasiliensis L. e Ochopodium Vogel. Em 1955, Rudd realizou uma (Bentham 1859), foi realizado um levantamento mais revisão do gênero, renomeou a secção Eu-aeschynome- recente por Fernandes (1996), que listou 52 espécies e ne como Aeschynomene e estimou cerca de 350 espé- adicionou mais uma série (Sclerosae A. Fernandes) na cies, distribuídas nos trópicos e em locais relativamente secção Ochopodium. Na lista da Flora do Brasil (Lima mais quentes das zonas temperadas sendo que, para o & Oliveira 2010) foram citadas 49 espécies e 24 va- continente americano, foram listadas 160 espécies. Esta riedades. Para o estado da Bahia, Lewis (1987) listou autora (l.c.) apresentou, ainda, cinco séries, com 29 es- 22 espécies; para Minas Gerais destaca-se o estudo de pécies no total, para a secção Aeschynomene (Ameri- Brandão (1992), com 19 espécies; para o Rio Grande do canae Rudd, Fluminensis Rudd, Montevidensis Rudd, Sul, o de Oliveira (2002), com nove e, para Mato Gros- Sensitivae Rudd e Indicae Rudd) e três séries, com 45 so do Sul, o de Lima et al. (2006), com 19 espécies. espécies, para a secção Ochopodium (Viscidulae Rudd, Espécies de Aeschynomene são citadas como fixa- 1. Apoio PELD/CNPq-sítio 6. 2. Bolsista de Pós-doutorado da Fundação Araucária. Universidade Estadual de Maringá/CCB/DBI/Nupélia/Laboratório de Mata Ci- liar. Av. Colombo, 5790. CEP 87020-900, Maringá, PR, Brasil. 3. Bolsista PIBIC/CNPq. Graduação em Ciências Biológicas/UEM - Nupélia/Laboratório de Mata Ciliar. Av. Colombo, 5790. CEP 87020-900, Maringá, PR, Brasil. 4. Universidade Estadual de Maringá/Nupélia/Laboratório de Mata Ciliar. Av. Colombo, 5790. CEP 87020-900, Maringá, PR, Brasil. 5. Bolsista de Produtividade em Pesquisa CNPq. Professora Associada do Departamento de Botânica, Instituto de Biociências, Univer- sidade Federal do Rio Grande do Sul (UFRGS). Av. Bento Gonçalves 9500, CEP 91570-000, Porto Alegre, RS, Brasil. R. bras. Bioci., Porto Alegre, v. 10, n. 2, p. 198-210, abr./jun. 2012 Aeschynomene no alto rio Paraná 199 doras de nitrogênio, apícolas, tóxicas para suínos, or- nas cheias e vazantes e alterado, assim, o regime de sa- namentais, forrageiras e para a fabricação de bóias de zonalidade (Agostinho et al. 2004, 2008). flutuação (Rudd 1955, Timm & Riet-Correa 1997, Pott Estudos sobre a vegetação ripária da PIARP têm sido et al. 2000, Ulibarri et al. 2002, Alves 2008). desenvolvidos sob diferentes aspectos como, por exem- O rio Paraná possui, em território brasileiro, 2.940 plo, taxonômicos (Romagnolo et al. 1994, Souza & km de extensão e nasce da junção dos rios Paranaíba e Souza 1998, Romagnolo & Souza 2004, 2006, Ferrucci Grande, na divisa entre os estados de Mato Grosso do & Souza 2008, Cabral et al. 2007), florísticos (Souza Sul, Minas Gerais e São Paulo. É o principal rio da Ba- & Monteiro 2005, Souza et al. 2009), fitossociológicos cia do rio da Prata e, também, um dos maiores do mun- (Campos et al. 2000, Romagnolo & Souza 2000) e su- do em descarga e área de drenagem, drenando desde os cessional (Kita & Souza 2003). Andes até a Serra do Mar, na Costa Atlântica. Esses estudos têm demonstrado que a família Legu- No seu alto curso, de uma planície com mais de 400 minosae reúne a maior riqueza florística, com 54 gêne- km de extensão resta um trecho restrito a 230 km, for- ros e 104 espécies que representam 13,4% do total de mado por uma rede de drenagem com canais secundá- espécies levantadas e, dentre suas subfamílias, Faboi- rios e afluentes, entre a Usina Hidrelétrica de Porto Pri- deae se destaca, com 59 espécies (Souza et al. 2009). mavera e o Reservatório de Itaipu, que está protegido O estudo do gênero Aeschynomene na PIARP está por três unidades de conservação, a Área de Proteção vinculado ao levantamento da família Leguminosae e Ambiental das Ilhas e Várzeas do Rio Paraná, o Parque da flora de maneira geral, que desde 1999 recebe apoio do CNPq, como parte dos estudos do Projeto Ecológico Nacional de Ilha Grande e o Parque Estadual do Rio Ivi- de Longa Duração (PELD/CNPq-sítio 6). nhema (Agostinho et al. 2008). Variações topográficas determinam ambientes com diferentes graus de umida- de, sendo que a margem esquerda, com relevo ondulado MATERIAL E MÉTODOS e barrancos com cerca de 15 m de altura, constitui área A área de estudo compreende a planície de inunda- mais seca enquanto que a margem direita, com baixios, ção do alto rio Paraná (PIARP), localizada no noroeste constitui propriamente a planície. do estado do Paraná e sudeste de Mato Grosso do Sul, Os pulsos de inundação são considerados como a 22°38’ - 22°57’ S e 53°05’ - 53°36’ W (Fig. 1). O clima principal função de força que regula a estrutura das co- da região é do tipo Cfa, segundo classificação de Koe- munidades e o funcionamento desse ecossistema. Os ppen; a precipitação anual é de 1400 a 1600 mm, sendo represamentos a montante da Planície de Inundação do o trimestre mais chuvoso, de dezembro a fevereiro e o Alto Rio Paraná (PIARP), principalmente o de Porto mais seco, de junho a agosto; a temperatura média anual Primavera (UHE Engenheiro Sérgio Motta), funcionan- é de 24 oC, o trimestre mais frio é de junho a agosto e do desde 1998, no entanto, têm provocado atenuações o mais quente, de dezembro a fevereiro, enquanto que, Figura 1. Localização da área de estudo. Planície de inundação do alto rio Paraná (PIARP), estados do Paraná e Mato Grosso do Sul. Crédito: Nupélia/UEM. R. bras. Bioci., Porto Alegre, v. 10, n. 2, p. 198-210, abr./jun. 2012 200 Miotto et al. a média anual de umidade relativa do ar é de 65 a 70% RESULTADOS E DISCUSSÃO (IAPAR 2008). Foram reconhecidas oito espécies de Aeschynomene A cobertura vegetal está inserida no bioma Mata circunscritas nas duas secções e em seis séries. A sec- Atlântica e na Região Fitoecológica da Floresta Esta- ção Aeschynomene está representada pelas espécies cional Semidecidual, com formações ripárias que vão Aeschynomene americana L. (série Americanae Rudd), desde as florestas até campos, secos ou inundáveis, sob A. denticulata Rudd (série Indicae), A. fluminensisVell. diferentes graus de perturbação antrópica e de regenera- (série Fluminensis), A. montevidensis Vogel (série Mon- ção (Souza et al. 2009). tevidensis) e A. sensitiva Sw. (série Sensitivae). Estas Coletas de material botânico e documentações espécies, com exceção de A. americana, ocorrem em fotográficas foram realizadas durante sete expedições à área, nos anos de 2008 a 2011, com duração média de áreas alagadas ou frequentemente alagáveis dos estados quatro dias cada uma e abrangendo todos os tipos de de Mato Grosso do Sul e Paraná.
Recommended publications
  • ISTA List of Stabilized Plant Names 7Th Edition
    ISTA List of Stabilized Plant Names th 7 Edition ISTA Nomenclature Committee Chair: Dr. M. Schori Published by All rights reserved. No part of this publication may be The Internation Seed Testing Association (ISTA) reproduced, stored in any retrieval system or transmitted Zürichstr. 50, CH-8303 Bassersdorf, Switzerland in any form or by any means, electronic, mechanical, photocopying, recording or otherwise, without prior ©2020 International Seed Testing Association (ISTA) permission in writing from ISTA. ISBN 978-3-906549-77-4 ISTA List of Stabilized Plant Names 1st Edition 1966 ISTA Nomenclature Committee Chair: Prof P. A. Linehan 2nd Edition 1983 ISTA Nomenclature Committee Chair: Dr. H. Pirson 3rd Edition 1988 ISTA Nomenclature Committee Chair: Dr. W. A. Brandenburg 4th Edition 2001 ISTA Nomenclature Committee Chair: Dr. J. H. Wiersema 5th Edition 2007 ISTA Nomenclature Committee Chair: Dr. J. H. Wiersema 6th Edition 2013 ISTA Nomenclature Committee Chair: Dr. J. H. Wiersema 7th Edition 2019 ISTA Nomenclature Committee Chair: Dr. M. Schori 2 7th Edition ISTA List of Stabilized Plant Names Content Preface .......................................................................................................................................................... 4 Acknowledgements ....................................................................................................................................... 6 Symbols and Abbreviations ..........................................................................................................................
    [Show full text]
  • Fruits and Seeds of Genera in the Subfamily Faboideae (Fabaceae)
    Fruits and Seeds of United States Department of Genera in the Subfamily Agriculture Agricultural Faboideae (Fabaceae) Research Service Technical Bulletin Number 1890 Volume I December 2003 United States Department of Agriculture Fruits and Seeds of Agricultural Research Genera in the Subfamily Service Technical Bulletin Faboideae (Fabaceae) Number 1890 Volume I Joseph H. Kirkbride, Jr., Charles R. Gunn, and Anna L. Weitzman Fruits of A, Centrolobium paraense E.L.R. Tulasne. B, Laburnum anagyroides F.K. Medikus. C, Adesmia boronoides J.D. Hooker. D, Hippocrepis comosa, C. Linnaeus. E, Campylotropis macrocarpa (A.A. von Bunge) A. Rehder. F, Mucuna urens (C. Linnaeus) F.K. Medikus. G, Phaseolus polystachios (C. Linnaeus) N.L. Britton, E.E. Stern, & F. Poggenburg. H, Medicago orbicularis (C. Linnaeus) B. Bartalini. I, Riedeliella graciliflora H.A.T. Harms. J, Medicago arabica (C. Linnaeus) W. Hudson. Kirkbride is a research botanist, U.S. Department of Agriculture, Agricultural Research Service, Systematic Botany and Mycology Laboratory, BARC West Room 304, Building 011A, Beltsville, MD, 20705-2350 (email = [email protected]). Gunn is a botanist (retired) from Brevard, NC (email = [email protected]). Weitzman is a botanist with the Smithsonian Institution, Department of Botany, Washington, DC. Abstract Kirkbride, Joseph H., Jr., Charles R. Gunn, and Anna L radicle junction, Crotalarieae, cuticle, Cytiseae, Weitzman. 2003. Fruits and seeds of genera in the subfamily Dalbergieae, Daleeae, dehiscence, DELTA, Desmodieae, Faboideae (Fabaceae). U. S. Department of Agriculture, Dipteryxeae, distribution, embryo, embryonic axis, en- Technical Bulletin No. 1890, 1,212 pp. docarp, endosperm, epicarp, epicotyl, Euchresteae, Fabeae, fracture line, follicle, funiculus, Galegeae, Genisteae, Technical identification of fruits and seeds of the economi- gynophore, halo, Hedysareae, hilar groove, hilar groove cally important legume plant family (Fabaceae or lips, hilum, Hypocalypteae, hypocotyl, indehiscent, Leguminosae) is often required of U.S.
    [Show full text]
  • Bradyrhizobium/Aeschynomene Symbiosis
    Bacterial RuBisCO Is Required for Efficient Bradyrhizobium/Aeschynomene Symbiosis Benjamin Gourion1*¤, Nathanae¨l Delmotte2, Katia Bonaldi1, Nico Nouwen1, Julia A. Vorholt2, Eric Giraud1 1 Laboratoire des Symbioses Tropicales et Me´diterrane´ennes, Institut de Recherche pour le De´veloppement/SupAgro/Institut National de la Recherche Agronomique/ Universite´ Montpellier 2/Centre de Coope´ration Internationale en Recherche Agronomique pour le De´veloppement, Montpellier, France, 2 Institute of Microbiology, Eidgeno¨ssische Technische Hochschule Zurich, Zurich, Switzerland Abstract Rhizobia and legume plants establish symbiotic associations resulting in the formation of organs specialized in nitrogen fixation. In such organs, termed nodules, bacteria differentiate into bacteroids which convert atmospheric nitrogen and supply the plant with organic nitrogen. As a counterpart, bacteroids receive carbon substrates from the plant. This rather simple model of metabolite exchange underlies symbiosis but does not describe the complexity of bacteroids’ central metabolism. A previous study using the tropical symbiotic model Aeschynomene indica/photosynthetic Bradyrhizobium sp. ORS278 suggested a role of the bacterial Calvin cycle during the symbiotic process. Herein we investigated the role of two RuBisCO gene clusters of Bradyrhizobium sp. ORS278 during symbiosis. Using gene reporter fusion strains, we showed that cbbL1 but not the paralogous cbbL2 is expressed during symbiosis. Congruently, CbbL1 was detected in bacteroids by proteome analysis. The importance of CbbL1 for symbiotic nitrogen fixation was proven by a reverse genetic approach. Interestingly, despite its symbiotic nitrogen fixation defect, the cbbL1 mutant was not affected in nitrogen fixation activity under free living state. This study demonstrates a critical role for bacterial RuBisCO during a rhizobia/legume symbiotic interaction.
    [Show full text]
  • Rbcl and Legume Phylogeny, with Particular Reference to Phaseoleae, Millettieae, and Allies Tadashi Kajita; Hiroyoshi Ohashi; Yoichi Tateishi; C
    rbcL and Legume Phylogeny, with Particular Reference to Phaseoleae, Millettieae, and Allies Tadashi Kajita; Hiroyoshi Ohashi; Yoichi Tateishi; C. Donovan Bailey; Jeff J. Doyle Systematic Botany, Vol. 26, No. 3. (Jul. - Sep., 2001), pp. 515-536. Stable URL: http://links.jstor.org/sici?sici=0363-6445%28200107%2F09%2926%3A3%3C515%3ARALPWP%3E2.0.CO%3B2-C Systematic Botany is currently published by American Society of Plant Taxonomists. Your use of the JSTOR archive indicates your acceptance of JSTOR's Terms and Conditions of Use, available at http://www.jstor.org/about/terms.html. JSTOR's Terms and Conditions of Use provides, in part, that unless you have obtained prior permission, you may not download an entire issue of a journal or multiple copies of articles, and you may use content in the JSTOR archive only for your personal, non-commercial use. Please contact the publisher regarding any further use of this work. Publisher contact information may be obtained at http://www.jstor.org/journals/aspt.html. Each copy of any part of a JSTOR transmission must contain the same copyright notice that appears on the screen or printed page of such transmission. The JSTOR Archive is a trusted digital repository providing for long-term preservation and access to leading academic journals and scholarly literature from around the world. The Archive is supported by libraries, scholarly societies, publishers, and foundations. It is an initiative of JSTOR, a not-for-profit organization with a mission to help the scholarly community take advantage of advances in technology. For more information regarding JSTOR, please contact [email protected].
    [Show full text]
  • Minutes of the Meeting of the S-9 Technical Committee On
    MINUTES OF THE MEETING OF THE S-9 TECHNICAL COMMITTEE ON THE INTRODUCTION, MULTIPLICATION, AND EVALUATION OF NEW PLANTS FOR AGRICULTURAL AND INDUSTRIAL USES AND THE PRESERVATION OF VALUABLE GERMPLASM University of Arkansas Fruit Substation Clarksville, Arkansas July 22-23,1986 Submitted by C. E. Watson Jr., Secretary S-9 Technical Committee 1985-86 AGENDA S-9 Technical Committee University of Arkansas Clarksville, Arkansas July 22 and 23, 1986 1. Call to Order, 8:00, July 22, 1986. 2. Introduction of Attendees. 3. Official Welcome - Dr. Dayton Steelman, Associate Director Arkansas Experiment Station and Acting S-9 Administrative Advisor. 4. Approval of Minutes, 1985 Meeting. 5. Additions to and Approval of Agenda, 1986 Meeting. 6. Appointment of Committees: A. Nominations B. Time and place of next meeting C. Resolutions 7. Introduction and Remarks from the Administrative Advisor. 8. State Progress Reports and Research Plans. 9. Discussion on Revision of the S-9 Project. 10. Other Agency Reports and Research Plans. 11. National Program Staff Reports. 12. Plant Exploration Proposals. 13. Committee Reports and Acceptance: A. Nominations B. Time and place of next meeting C. Resolutions 14. Unfinished or New Business. 15. Adjournment, Noon, July 23, 1986. 16. Tour, July 22, 1986. 1. CALL TO ORDER The meeting of the S-9 Technical Committee was called to order by Chairman Jeff Pederson at 8:00 AM, July 22. 2. INTRODUCTION OF ATTENDEES Name Address Phone * David L. Coffey Dept. of Plant & Soil Sciences 615-974-8829 Univ. of Tennessee 355 Ellington Plant Sci. Bldg. Knoxville, TN 37996 H. W. Everett USDA-SCS Fort Worth Federal Center P 0 Box 6567 Fort Worth, TX 76115 * Bill Fike Crop Science Dept.
    [Show full text]
  • Pannicle Jointvetch Aeaeschynomene Paniculata
    Invasive plant risk assessment Biosecurity Queensland Agriculture Fisheries and Department of Pannicle jointvetch AeAeschynomene paniculata Steve Csurhes First published 2009 Updated 2016 © State of Queensland, 2016. The Queensland Government supports and encourages the dissemination and exchange of its information. The copyright in this publication is licensed under a Creative Commons Attribution 3.0 Australia (CC BY) licence. You must keep intact the copyright notice and attribute the State of Queensland as the source of the publication. Note: Some content in this publication may have different licence terms as indicated. For more information on this licence visit http://creativecommons.org/licenses/ by/3.0/au/deed.en" http://creativecommons.org/licenses/by/3.0/au/deed.en Front cover: Aeschynomene paniculata Photo: Kendrick Cox Invasive plant risk assessment: Pannicle jointvetch Aeschynomene paniculata 2 Contents Summary 4 Introduction 5 Identity and taxonomy 5 Description 5 Origin and worldwide distribution 7 Distribution in Australia 7 History of introduction 7 Ecology and preferred habitat 8 Reproduction and dispersal 8 History as a weed elsewhere 8 Current impact in Queensland 8 Potential impact in Queensland 9 Uses 9 Control 10 Pests and diseases 10 References 11 Invasive plant risk assessment: Pannicle jointvetch Aeschynomene paniculata 3 Summary Aeschynomene paniculata (pannicle jointvetch) is a perennial legume native to tropical America. It was first planted in Queensland in the 1980s and 1990s, at c. 17 sites, to evaluate its potential use as a pasture legume. However, these trials concluded that it was of little value as cattle feed. A. paniculata is currently invading grassy understoreys within open tropical woodlands, near where it was planted in North Queensland.
    [Show full text]
  • Wingleaf Primrose-Willow (Ludwigia Decurrens) Ecological Risk Screening Summary
    Wingleaf Primrose-willow (Ludwigia decurrens) Ecological Risk Screening Summary U.S. Fish and Wildlife Service, May 2021 Revised, June 2021 Web Version, 7/21/2021 Organism Type: Plant Overall Risk Assessment Category: High Photo: Clarence A. Rechenthin, USDA NRCS East Texas PMC. Public domain. Available: https://plants.sc.egov.usda.gov/ImageLibrary/original/lude4_002_php.jpg (June 2021). 1 Native Range and Status in the United States Native Range From Ramamoorthy and Zardini (1987): “[…] from southeastern United States where it is widely distributed from southern Missouri, southern Ohio, and northern Virginia (one collection from southern Wisconsin), south to the 1 Gulf of Mexico and from central Texas and central Oklahoma, east to the Atlantic coast, reappearing in southern Mexico (Chiapas, Tabasco, and Veracruz) and extending south to northeastern Argentina, and east from central Minas Gerais in Brazil west to western Ecuador. Abundant in all countries of Central America except Belize; rare in the West Indies; common in Surinam, Guyana, Venezuela, Colombia, and Ecuador; scattered in Peru and Brazil; more common in Paraguay and northeastern Argentina.” From POWO (2021): “Native to: Alabama, Argentina Northeast, Argentina Northwest, Bolivia, Brazil North, Brazil Northeast, Brazil South, Brazil Southeast, Brazil West-Central, Colombia, Costa Rica, Cuba, Ecuador, French Guiana, Guatemala, Guyana, Honduras, Illinois, Kentucky, Mexico Southeast, Mexico Southwest, Nicaragua, Panamá, Paraguay, Peru, South Carolina, Suriname, Tennessee, Trinidad- Tobago, Uruguay, Venezuela, Windward Is. [a “Botanical Country” including the Lesser Antillean islands of Dominica, Martinique, St. Lucia, St. Vincent and the Grenadines, Barbados, and Grenada]” From Acevedo-Rodríguez and Strong (2012): “Native to […] Lesser Antilles (St. Vincent) […]” According to USDA, NRCS (2021), this species is native to the following U.S.
    [Show full text]
  • Aeschynomene Villosa Scientific Name  Aeschynomene Villosa Poir
    Tropical Forages Aeschynomene villosa Scientific name Aeschynomene villosa Poir. Subordinate taxa: Inflorescences 3‒10 (‒15) Annual or weakly perennial, prostrate to flowered (CPI 93616) decumbent, herb to sub-shrub Aeschynomene villosa Poir. var. longifolia (Micheli) Rudd Aeschynomene villosa Poir. var. mexicana (Hemsl. & Rose) Rudd Aeschynomene villosa Poir. var. villosa Note: The genus, Aeschynomene, is separated into two sections: Aeschynomene and Ochopodium. The former Leaves about 2‒7 cm long, 20‒50 foliolate (CPI 37198) Pods villous-hispid, commonly 4‒6 encompasses predominantly species from humid seeded. Plant susceptible to powdery environments, such as A. americana, A. indica and A. mildew villosa, while the latter includes a number of dryland species, such as A. brasilianas, A. falcata and A. histrix. Synonyms Aeschynomene villosa: Aeschynomene javanica Miq. var. longifolia: Basionym: Aeschynomene americana Stem nodules var. longifolia Micheli var. mexicana: Basionym: Climacorachis mexicana Hemsl. & Rose Seeds Family/tribe Family: Fabaceae (alt. Leguminosae) subfamily: Faboideae tribe: Dalbergieae. Morphological description Annual or weakly perennial herb to sub-shrub with stems to about 1 m long, prostrate to weakly erect, glabrous to Seed crop of cv. Kretschmer Seed production for cultivar mixture, hispid. Leaves pinnate, about 2‒7 cm long, 20‒50- "Villomix" foliolate; leaflets 3‒15 mm long, 1‒4 mm wide. Inflorescences 3‒10 (‒15-flowered in var. longifolia), with hispid peduncles and pedicels; flowers usually yellow, 3‒9 mm long; calyx 2‒4 mm long, hispid; standard commonly 5‒7 mm long. Pods 3‒7 (commonly 4‒6) seeded, the articles 2.5‒3.0 (‒4) mm in diameter, villous-hispid, the tuberculate bases of the hairs often dark, in contrast with the otherwise straw-coloured or light brown fruits, usually dehiscing along the lower arcuate suture but sometimes along the transverse suture (cf.
    [Show full text]
  • Host Choice in Rotylenchulus Species
    Available online at www.ijpab.com Rathore Int. J. Pure App. Biosci. 6 (5): 346-354 (2018) ISSN: 2320 – 7051 DOI: http://dx.doi.org/10.18782/2320-7051.6878 ISSN: 2320 – 7051 Int. J. Pure App. Biosci. 6 (5): 346-354 (2018) Research Article Host Choice in Rotylenchulus Species Y. S. Rathore* Principal Scientist (Retd.), Indian Institute of Pulses Research, Kanpur-208 024 (U.P.) India *Corresponding Author E-mail: [email protected] Received: 12.09.2018 | Revised: 9.10.2018 | Accepted: 16.10.2018 ABSTRACT The reniformis nematodes of the genus Rotylenchulus (Haplolaimidae: Nematoda) are sedentary semi-endoparasites of numerous crops. There are ten species out of which R. reniformis and R. parvus are important, and three species (R. amanictus, R. clavicadatus, R. leptus) are monophagous: two on monocots and one on Rosids. In general, Rotylenchulus species are capable of feeding from very primitive Magnoliids to plants of advanced category. Preference was distinctly observed towards the plants in Rosids (42.779%) followed by monocots (23.949%) and Asterids (21.755%). The SAI values were also higher for these groups of plants. The study on lineages further revealed intimate affinity to febids (25.594%), followed by commelinids (18.647%), malvids (16.088%), lamiids (11.883%), and campanulids (9.141%). Poales contribution within commelinids was 65.353%. Maximum affinity of Rotylenchulus species was observed by their association with plants from families Poaceae (7), followed by Fabaceae (6), Malvaceae (6), Asteraceae (4), Oleaceae (4), Soanaceae (4) and so on. Key words: Agiosperms, Gymnosperms, APG IV system, Reniform nemtodes, Monocots, Rosids, Asterids INTRODUCTION number of crops, whereas the other eight Plant parasitic nematodes pose a great species are of limited importance.
    [Show full text]
  • Tropical Aquatic Plants: Morphoanatomical Adaptations - Edna Scremin-Dias
    TROPICAL BIOLOGY AND CONSERVATION MANAGEMENT – Vol. I - Tropical Aquatic Plants: Morphoanatomical Adaptations - Edna Scremin-Dias TROPICAL AQUATIC PLANTS: MORPHOANATOMICAL ADAPTATIONS Edna Scremin-Dias Botany Laboratory, Biology Department, Federal University of Mato Grosso do Sul, Brazil Keywords: Wetland plants, aquatic macrophytes, life forms, submerged plants, emergent plants, amphibian plants, aquatic plant anatomy, aquatic plant morphology, Pantanal. Contents 1. Introduction and definition 2. Origin, distribution and diversity of aquatic plants 3. Life forms of aquatic plants 3.1. Submerged Plants 3.2 Floating Plants 3.3 Emergent Plants 3.4 Amphibian Plants 4. Morphological and anatomical adaptations 5. Organs structure – Morphology and anatomy 5.1. Submerged Leaves: Structure and Adaptations 5.2. Floating Leaves: Structure and Adaptations 5.3. Emergent Leaves: Structure and Adaptations 5.4. Aeriferous Chambers: Characteristics and Function 5.5. Stem: Morphology and Anatomy 5.6. Root: Morphology and Anatomy 6. Economic importance 7. Importance to preserve wetland and wetlands plants Glossary Bibliography Biographical Sketch Summary UNESCO – EOLSS Tropical ecosystems have a high diversity of environments, many of them with high seasonal influence. Tropical regions are richer in quantity and diversity of wetlands. Aquatic plants SAMPLEare widely distributed in theseCHAPTERS areas, represented by rivers, lakes, swamps, coastal lagoons, and others. These environments also occur in non tropical regions, but aquatic plant species diversity is lower than tropical regions. Colonization of bodies of water and wetland areas by aquatic plants was only possible due to the acquisition of certain evolutionary characteristics that enable them to live and reproduce in water. Aquatic plants have several habits, known as life forms that vary from emergent, floating-leaves, submerged free, submerged fixed, amphibian and epiphyte.
    [Show full text]
  • Patterns of Chromosomal Variation in Mexican Species of Aeschynomene (Fabaceae, Papilionoideae) and Their Evolutionary and Taxonomic Implications
    COMPARATIVE A peer-reviewed open-access journal CompCytogen 14(1): 157–182 (2020)Cytogenetics of Aeschynomene from Mexico 157 doi: 10.3897/CompCytogen.v14i1.47264 RESEARCH ARTICLE Cytogenetics http://compcytogen.pensoft.net International Journal of Plant & Animal Cytogenetics, Karyosystematics, and Molecular Systematics Patterns of chromosomal variation in Mexican species of Aeschynomene (Fabaceae, Papilionoideae) and their evolutionary and taxonomic implications Fernando Tapia-Pastrana1, Alfonso Delgado-Salinas2, Javier Caballero3 1 Facultad de Estudios Superiores Zaragoza, Universidad Nacional Autónoma de México, Laboratorio de Ge- necología, Batalla 5 de Mayo s/n esquina Fuerte de Loreto, Col. Ejército de Oriente, Iztapalapa, C.P. 09230, Ciudad de México, Mexico 2 Instituto de Biología, Departamento de Botánica, Universidad Nacional Autóno- ma de México, Apartado Postal 70-233, 04510, Cd. de México, Mexico 3 Jardín Botánico, Instituto de Bio- logía, Universidad Nacional Autónoma de México, Circuito Campos Deportivos, Ciudad Universitaria, Coyo- acán 04510, Cd. de México, Mexico Corresponding author: Fernando Tapia-Pastrana ([email protected]) Academic editor: A. Belyayev | Received 12 October 2019 | Accepted 5 February 2020 | Published 11 March 2020 http://zoobank.org/A12AECF8-C825-4955-9EEA-A0BC933D16D8 Citation: Tapia-Pastrana F, Delgado-Salinas A, Caballero J (2020) Patterns of chromosomal variation in Mexican species of Aeschynomene (Fabaceae, Papilionoideae) and their evolutionary and taxonomic implications. Comparative Cytogenetics
    [Show full text]
  • First Cytogenetic Register of an Allopolyploid Lineage of the Genus Aeschynomene Citation: F
    Firenze University Press Caryologia www.fupress.com/caryologia International Journal of Cytology, Cytosystematics and Cytogenetics First cytogenetic register of an allopolyploid lineage of the genus Aeschynomene Citation: F. Tapia-Pastrana, A. Delga- do-Salinas (2020) First cytogenetic register (Leguminosae, Papilionoideae) native to Mexico of an allopolyploid lineage of the genus Aeschynomene (Leguminosae, Papil- ionoideae) native to Mexico. Caryolo- gia 73(4): 17-26. doi: 10.13128/caryolo- Fernando Tapia-Pastrana1,*, Alfonso Delgado-Salinas2 gia-949 1 Facultad de Estudios Superiores Zaragoza, Universidad Nacional Autónoma de México, Received: May 24, 2020 Laboratorio de Genecología, Batalla 5 de Mayo s/n esquina Fuerte de Loreto, Col. Ejér- cito de Oriente, Iztapalapa, C.P. 09230, Ciudad de México, Mexico Accepted: November 10, 2020 2 Instituto de Biología, Departamento de Botánica, Universidad Nacional Autónoma de Published: May 19, 2021 México, Apartado Postal 70-233, 04510, Cd. de México, Mexico *Corresponding author. E-mail: [email protected] Copyright: © 2020 F. Tapia-Pastrana, A. Delgado-Salinas. This is an open access, peer-reviewed article pub- Abstract. A conventional cytogenetics analysis revealed for first time an allopolyploid lished by Firenze University Press lineage of the genus Aeschynomene in Mexico. The hybrid condition is confirmed after (http://www.fupress.com/caryologia) all the prometaphase and metaphase nuclei of the hybrids exhibited only one pair of and distributed under the terms of the SAT-chromosomes, confirming the existence of nucleolar dominance and amphiplasty. Creative Commons Attribution License, The karyotype formula for this lineage was 2n = 4x = 40 = 34 m + 6 sm with a total which permits unrestricted use, distri- diploid chromosome length (TDCL) = 28µm and an average chromosome size (AC) = bution, and reproduction in any medi- 1.40 µm.
    [Show full text]