Las Palmeras En El Marco De La Investigacion Para El
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Anatomia Foliar De Allagoptera Nees (Arecaceae) Como Subsídio À
Universidade de Brasília Instituto de Ciências Biológicas Departamento de Botânica Programa de Pós Graduação em Botânica Dissertação de Mestrado Anatomia foliar de Allagoptera Nees (Arecaceae) como subsídio à taxonomia André Silva Pinedo Orientadora: Profª Drª Sueli Maria Gomes Brasília, março de 2015 i Universidade de Brasília Instituto de Ciências Biológicas Departamento de Botânica Programa de Pós Graduação em Botânica Dissertação de Mestrado Anatomia foliar de Allagoptera Nees (Arecaceae) como subsídio à taxonomia Dissertação apresentada ao Programa de Pós- Graduação em Botânica da Universidade de Brasília como um dos requisitos para obtenção do título de Mestre em Botânica. André Silva Pinedo Orientadora: Profª Drª Sueli Maria Gomes Brasília, março de 2015 ii Universidade de Brasília Instituto de Ciências Biológicas Departamento de Botânica Programa de Pós Graduação em Botânica Banca examinadora: iii Agradecimentos Primeiramente a Deus, sou eternamente grato pela minha vida, pela oportunidade proporcionada e pela capacitação de estar realizando este curso de pós-graduação, que tem sido uma grande experiência de amadurecimento para mim; À minha orientadora, Profª. Drª. Sueli Maria Gomes, pela sua paciência ao me ensinar e constantes críticas construtivas que fez ao longo do período em que trabalhamos juntos, que fizeram desse mestrado uma grande oportunidade para o meu crescimento profissional; À Profª. Drª. Renata Corrêa Martins, por sua parceria nesse projeto, auxiliando na coleta e identificação das espécies, além de ser uma profissional extremamente prestativa; À Profª. Drª. Cássia Munhoz, minha orientadora em estágio de Iniciação Científica na graduação, motivando-me a trabalhar com plantas; Ao Prof. Dr. Eduardo Gomes Gonçalves, por ter me incentivado a trabalhar com o grupo das palmeiras; À Profª. -
Index to Volume 60
PALM S Index to Vol. 60 Vol. 60(4) 2016 Index to Volume 60 A new species of Attalea from the Bolivian Attalea crassispatha 97, 113 lowlands 161 Attalea eichleri 111 A university palmetum 93 Attalea exigua 112 Acoelorrhaphe 97 Attalea huebneri 61, 69, 73, 74, 76, 114, Acoelorrhaphe wrightii 25–28, 97 117–119, 123 Acrocomia crispa 97, 113 Attalea insignis 76, 123 Adonidia dransfieldii 15 Attalea macrocarpa 122, 123 Adonidia merrillii 15, 97 Attalea maripa 59, 72, 74, 76 Aiphanes horrida 67, 70, 74, 113 Attalea moorei 58, 59, 62–64, 66–70, 72–74, Aiphanes minima 113 76, 117–121, 123 Aiphanes weberbaueri 72 Attalea osmantha 123 Andriamanantena, A.Z., as co-author 169 Attalea pacensis 162–165, 167 Ali, O.M.M.: The argun palm, Medemia Attalea peruviana 62, 64, 65, 77, 112, 122, argun , in the eastern Nubian Desert of 123 Sudan 145 Attalea phalerata 63, 68, 69, 73–76, 114, Allagoptera 111 117–120, 123, 162, 163, 165, 167 Areca 18 Attalea plowmanii 58, 62–64, 76, 110, 117, Areca catechu 3, 19 123 Arenga 17 Attalea polysticha 64, 65, 76, 112, 116 Arenga caudata 43 Attalea princeps 59, 71, 73, 76, 77, 118, 123, Arenga hookeriana 43 161, 162, 165, 167 Arenga pinnata 97 Attalea racemosa 62, 76 Arenga undulatifolia 97 Attalea rostrata 123 Aspects and causes of earlier and current Attalea salazarii 58, 61, 62 spread of Trachycarpus fortunei in the Attalea septuagenata 76 forests of southern Ticino and northern Attalea speciosa 76 Lago Maggiore (Switzerland, Italy) 125 Attalea tessmannii 59, 62, 64, 76, 113, 121, Astrocaryum 39, 113, 114 122 Astrocaryum carnosum 70 Attalea weberbaueri 59, 66, 67, 72, 73, 77, Astrocaryum faranae 70, 72 111, 112, 114, 119, 121, 123 Astrocaryum gratum 76 Attalea : Insights into the diversity and Astrocaryum huicungo 69 phylogeny of an intriguing genus 109 Astrocaryum perangustatum 72 Bactris 39 Astrocaryum ulei 74 Bactris gasipaes 39 Attalea 9, 11, 12, 18, 21, 39, 57–59, 63, 64, Bactris hirta 74 66, 69, 72, 74, 76, 77, 109–116, 121, Baker, W.J., W.L. -
Journal of the International Palm Society Vol. 58(4) Dec. 2014 the INTERNATIONAL PALM SOCIETY, INC
Palms Journal of the International Palm Society Vol. 58(4) Dec. 2014 THE INTERNATIONAL PALM SOCIETY, INC. The International Palm Society Palms (formerly PRINCIPES) Journal of The International Palm Society Founder: Dent Smith The International Palm Society is a nonprofit corporation An illustrated, peer-reviewed quarterly devoted to engaged in the study of palms. The society is inter- information about palms and published in March, national in scope with worldwide membership, and the June, September and December by The International formation of regional or local chapters affiliated with the Palm Society Inc., 9300 Sandstone St., Austin, TX international society is encouraged. Please address all 78737-1135 USA. inquiries regarding membership or information about Editors: John Dransfield, Herbarium, Royal Botanic the society to The International Palm Society Inc., 9300 Gardens, Kew, Richmond, Surrey, TW9 3AE, United Sandstone St., Austin, TX 78737-1135 USA, or by e-mail Kingdom, e-mail [email protected], tel. 44-20- to [email protected], fax 512-607-6468. 8332-5225, Fax 44-20-8332-5278. OFFICERS: Scott Zona, Dept. of Biological Sciences (OE 167), Florida International University, 11200 SW 8 Street, President: Leland Lai, 21480 Colina Drive, Topanga, Miami, Florida 33199 USA, e-mail [email protected], tel. California 90290 USA, e-mail [email protected], 1-305-348-1247, Fax 1-305-348-1986. tel. 1-310-383-2607. Associate Editor: Natalie Uhl, 228 Plant Science, Vice-Presidents: Jeff Brusseau, 1030 Heather Drive, Cornell University, Ithaca, New York 14853 USA, e- Vista, California 92084 USA, e-mail mail [email protected], tel. 1-607-257-0885. -
Species Delimitation and Hybrid Identification of Acrocomia Aculeata
Species delimitation and hybrid identification of Acrocomia aculeata and A. totai by genetic population approach Brenda D´ıaz1, Maria Zucchi2, Alessandro Alves-Pereira1, Joaquim Azevedo-Filho2, Mariana Sanit´a2, and Carlos Colombo2 1State University of Campinas 2Instituto Agronomico October 9, 2020 Abstract To the Neotropical genus Acrocomia (Arecaceae) is attributed eight species with a wide distribution in America. A. aculeata and A. totai are the most important species because of their high economic potential for oil production. However, there is no consensus in their classification as different taxons and their distinctiveness is particularly challenging due to morphological similarities with large plasticity of the traits. In addition, there is doubt about the occurrence of interspecific hybrids between both species. In this study, we applied a genetic population approach to assessing the genetic boundaries, diversity and to identify interspecific hybrids of A. aculeata and A. totai. Thirteen loci of simple sequence repeat (SSR) were employed to analyze twelve populations representing a wide distribution of species, from Minas Gerais, Brazil to Formosa, Argentina. Based on the Bayesian analysis (STRUCTURE and NewHybrids) and Discriminant Analysis of Principal Components (DAPC), our study supports the recognition of A. aculeata and A. totai as two species and the estimates of genetic parameters revealed more genetic diversity in A. totai (HE=0.551) than in A. aculeata (HE=0.466). We obtained evidence of hybridization between the species and that admixed individuals were assigned as F2 hybrids. In conclusion, this study showed the usefulness of microsatellite markers to elucidate the genetic boundaries of A. aculeata and A. totai, supporting their classification as different species and increase our knowledge about genetic diversity at the level of populations and species. -
Red Ring Disease of Coconut Palms Is Caused by the Red Ring Nematode (Bursaphelenchus Cocophilus), Though This Nematode May Also Be Known As the Coconut Palm Nematode
1 Red ring disease of coconut palms is caused by the red ring nematode (Bursaphelenchus cocophilus), though this nematode may also be known as the coconut palm nematode. This disease was first described on coconut palms in 1905 in Trinidad and the association between the disease and the nematode was reported in 1919. The vector of the nematode is the South American palm weevil (Rhynchophorus palmarum), both adults and larvae. The nematode parasitizes the weevil which then transmits the nematode as it moves from tree to tree. Though the weevil may visit many different tree species, the nematode only infects members of the Palmae family. The nematode and South American palm weevil have not yet been observed in Florida. 2 Information Sources: Brammer, A.S. and Crow, W.T. 2001. Red Ring Nematode, Bursaphelenchus cocophilus (Cobb) Baujard (Nematoda: Secernentea: Tylenchida: Aphelenchina: Aphelenchoidea: Bursaphelechina) formerly Rhadinaphelenchus cocophilus. University of Florida, IFAS Extension. EENY236. Accessed 11-27-13 http://edis.ifas.ufl.edu/in392 Griffith, R. 1987. “Red Ring Disease of Coconut Palm”. The American Pathological Society Plant Disease, Volume 71, February, 193-196. accessed 12/5/2013- http://www.apsnet.org/publications/plantdisease/ba ckissues/Documents/1987Articles/PlantDisease71n02_193.PDF Griffith, R., R. M. Giblin-Davis, P. K. Koshy, and V. K. Sosamma. 2005. Nematode parasites of coconut and other palms. M. Luc, R. A. Sikora, and J. Bridges (eds.) In Plant Parasitic Nematodes in Subtropical and Tropical Agriculture. C.A.B. International, Oxon, UK. Pp. 493-527. 2 The host trees susceptible to the red ring nematode are usually found in the family Palmae. -
Palmas Nativas De Colombia, Ecuador, Perú Y Bolivia Palmas Nativas De Colombia, Ecuador, Perú Y Bolivia (M) T
Palmas nativas de Colombia, Ecuador, Perú y Bolivia Palmas nativas de Colombia, Ecuador, Perú y Bolivia Especies nativas Especies endémicas Zonas biogeográficas Categorías de uso terrenario ve rú rú xico Colombia Ecuador Pe Bolivia Colombia Ecuador Pe Bolivia y Orinoquia Amazonía Region caribeña S y SE de Amazonía Periferia Pacífica Costa Andes Alimentación animal Alimentación humana Ambiental Combustible Construcción Cultural Medicinal y Tó Utensilios y herramientas usos Otros Alt. (m) NOMBRE CIENTÍFICO Número total de especies 250 143 149 88 49 13 24 7 165 31 27 122 137 65 159 69 36 177 135 83 2 147 84 Mín. Máx. 1 Acrocomia aculeata Lodd. ex Mart. 0 1300 2 Acrocomia totai Mart. 200 450 3 Aiphanes acaulis Galeano & R. Bernal 90 700 4 Aiphanes bicornis Cerón & R. Bernal 200 760 5 Aiphanes buenaventurae R. Bernal & Borchs. 0 255 6 Aiphanes chiribogensis Borchs. & Balslev 300 2000 7 Aiphanes concinna H.E. Moore 1900 3000 8 Aiphanes deltoidea Burret 100 1650 9 Aiphanes duquei Burret 1900 2600 10 Aiphanes eggersii Burret 0 700 11 Aiphanes erinacea (H. Karst.) H. Wendl. 700 2100 12 Aiphanes gelatinosa H.E. Moore 1200 1200 13 Aiphanes graminifolia Galeano & R. Bernal 1700 1700 14 Aiphanes grandis Borchs. & Balslev 1100 2700 15 Aiphanes hirsuta Burret 100 2200 16 Aiphanes horrida (Jacq.) Burret 180 2000 17 Aiphanes killipii (Burret) Burret 800 1500 18 Aiphanes leiostachys Burret 850 1100 19 Aiphanes lindeniana H. Wendl. 1700 2200 20 Aiphanes linearis Burret 1800 2600 21 Aiphanes macroloba Burret 100 1400 271 272 Especies nativas Especies endémicas Zonas biogeográficas Categorías de uso terrenario ve rú rú xico Pe Bolivia Colombia Ecuador Pe Bolivia S y SE de Amazonía Periferia Pacífica Costa Andes Alimentación animal Alimentación humana Ambiental Combustible Construcción Cultural Medicinal y Tó Utensilios y herramientas usos Otros Colombia Ecuador y Orinoquia Amazonía Region caribeña Alt. -
Monocotyledons and Gymnosperms of Puerto Rico and the Virgin Islands
SMITHSONIAN INSTITUTION Contributions from the United States National Herbarium Volume 52: 1-415 Monocotyledons and Gymnosperms of Puerto Rico and the Virgin Islands Editors Pedro Acevedo-Rodríguez and Mark T. Strong Department of Botany National Museum of Natural History Washington, DC 2005 ABSTRACT Acevedo-Rodríguez, Pedro and Mark T. Strong. Monocots and Gymnosperms of Puerto Rico and the Virgin Islands. Contributions from the United States National Herbarium, volume 52: 415 pages (including 65 figures). The present treatment constitutes an updated revision for the monocotyledon and gymnosperm flora (excluding Orchidaceae and Poaceae) for the biogeographical region of Puerto Rico (including all islets and islands) and the Virgin Islands. With this contribution, we fill the last major gap in the flora of this region, since the dicotyledons have been previously revised. This volume recognizes 33 families, 118 genera, and 349 species of Monocots (excluding the Orchidaceae and Poaceae) and three families, three genera, and six species of gymnosperms. The Poaceae with an estimated 89 genera and 265 species, will be published in a separate volume at a later date. When Ackerman’s (1995) treatment of orchids (65 genera and 145 species) and the Poaceae are added to our account of monocots, the new total rises to 35 families, 272 genera and 759 species. The differences in number from Britton’s and Wilson’s (1926) treatment is attributed to changes in families, generic and species concepts, recent introductions, naturalization of introduced species and cultivars, exclusion of cultivated plants, misdeterminations, and discoveries of new taxa or new distributional records during the last seven decades. -
Sfps Fall 2011 Sale Plant List
SFPS FALL 2011 SALE PLANT LIST PLANTS VENDOR # Palms Acanthophoenix rubra 35 Acoelorrhaphe wrightii 26, 67 Acrocomia aculeata 50, 67 Actinokentia divaricata 35, 57, 66, 68, 72 Actinorhytis calapparia 72 Adonidia merrillii 31, 57, 66, 89 Adonidia merrillii var. "Golden Form" 35 Aiphanes aculeata = Aiphanes horrida - Aiphanes caryotifolia = Aiphanes horrida - Aiphanes erosa = Aiphanes minima - Aiphanes horrida 35, 68, 72 Aiphanes minima 68 Aiphanes vincentiana = Aiphanes minima - Allagoptera arenaria 57, 66, 67, 68, 72 Allagoptera campestris 67 Allagoptera leucocalyx 57 Alloschmidia glabrata = Basselinia glabrata - Alsmithia longipes = Heterospathe longipes - Archontophoenix cunninghamiana var. 'Illawara' 68 Archontophoenix maxima 67, 72 Archontophoenix myolensis 50, 66, 67, 68 Archontophoenix purpurea 57, 66, 72 Archontophoenix tuckeri 66, 68 Areca aliceae = Areca triandra - Areca camarinensis 57, 68 Areca catechu 57, 67, 72 Areca catechu var. 'Dwarf' 35, 50 Areca hutchinsoniana 68 Areca ipot 67 Areca latiloba = Areca montana - Areca macrocalyx var. 'Red Form' 35, 57, 68 Areca macrocarpa 68 Areca montana 57 Areca triandra 68, 72 Areca vestiaria 25, 35, 57, 67, 68 Areca vestiaria var. 'Orange Form' 25, 57, 67, 72 Areca vestiaria var. 'Maroon Leaf' 35, 57, 67 Areca vestiaria var. 'Red Leaf' 57, 67, 72 Areca sp. 'Yellow Crownshaft' 25 Arenga ambong = Arenga undulatifolia - Arenga brevipes 57 Arenga caudata 66 Arenga engleri 31, 66, 68, 72 Arenga hookeriana 35, 57, 66, 72 Arenga microcarpa 26, 66 Arenga obtusifolia 57, 66 PLANTS VENDOR # Arenga pinnata 50, 57, 66, 67, 68 Arenga porphyrocarpa 66 Arenga tremula 26, 57, 66, 68, 72 Arenga undulatifolia 35, 57, 66, 67 Arenga westerhoutii 68 Asterogyne martiana 57, 68, 72 Astrocaryum acaule 72 Astrocaryum alatum 35, 50, 57, 67 Astrocaryum mexicanum 72 Astrocaryum murumuru 72 Attalea butyracea 57, 67, 72 Attalea cohune 35 Attalea phalerata 50, 91 Attalea rostrata 68 Attalea speciosa 50, 66 Bactris bidentula 72 Bactris gasipaes 67 Bactris gasipaes var. -
Plants and Gall Hosts of the Tirimbina Biological Reserve
DOI 10.15517/RBT.V67I2SUPL.37233 Artículo Plants and gall hosts of the Tirimbina Biological Reserve, Sarapiqui, Costa Rica: Combining field sampling with herbarium records Plantas y hospederos de agallas de la Reserva Biológica Tirimbina, Sarapiquí, Costa Rica: combinando muestras del campo con registros del herbario Juan Manuel Ley-López1 José González2 Paul E. Hanson3* 1 Departamento Académico, Reserva Biológica Tirimbina. Sarapiquí, Heredia, Costa Rica; [email protected] 2 Independent consultant, Costa Rica; [email protected] 3 Escuela de Biología, Universidad de Costa Rica; San Pedro, 11501-2060 San José, Costa Rica; [email protected] * Correspondence Received 03-X-2018 Corrected 10-I-2018 Accepted 24-I-2019 Abstract There has been an increasing number of inventories of gall-inducing arthropods in the Neotropics. Nonetheless, very few inventories have been carried out in areas where the flora is well documented, and records of galls from herbaria and sites outside the study area have seldom been utilized. In this study we provide a checklist of the native vascular plants of a 345 ha forest reserve in the Caribbean lowlands of Costa Rica and document which of these plants were found to harbor galls. The gall surveys were carried out between November 2013 and December 2016. We also cross-checked our plant list with the previous gall records from elsewhere in the country and searched for galls on herbarium specimens of dicots reported from the reserve. In total, we recorded 143 families and 1174 plant species, of which 401 were hosts of galls. Plant hosts of galls were found in the following non-mutually exclusive categories: 209 in our field sampling, 257 from previous records, and 158 in herbarium specimens. -
Acrocomia Crispa Fruits Lipid Extract Prevents LPS-Induced Acute Lung Injury in Mice
BOLETÍN LATINOAMERICANO Y DEL CARIBE DE PLANTAS MEDICINALES Y AROMÁTICAS 18 (1): 16 - 26 (2019) © / ISSN 0717 7917 / www.blacpma.usach.cl Artículo Original | Original Article Acrocomia crispa fruits lipid extract prevents LPS-induced acute lung injury in mice [Extracto lipídico de los frutos de Acrocomia crispa previene el daño pulmonar agudo inducido por LPS en ratones] Licet Mena, Roxana Sierra, Maikel Valle, Vivian Molina, Sandra Rodriguez, Nelson Merino, Zullyt Zamora, Victor González & Jose Alberto Medina Pharmacology Department, Centre of Natural Products, National Centre for Scientific Research, Havana City, Cuba Contactos | Contacts: Vivian MOLINA - E-mail address: [email protected] Abstract: The aim of this study was to evaluate the effects of single oral doses of D-005 (a lipid extract obtained from the fruit oil of Acrocomia crispa) on LPS-induced acute lung injury (ALI) in mice. D-005 batch composition was: lauric (35.8%), oleic (28.4%), myristic (14.2%), palmitic (8.9%), stearic (3.3%), capric (1.9%), caprylic (1.2%), and palmitoleic (0.05%) acids, for a total content of fatty acids of 93.7%. D-005 (200 mg/kg) significantly reduced lung edema (LE) (≈ 28% inhibition) and Lung Weight/Body Weight ratio (LW/BW) (75.8% inhibition). D-005 (25, 50, 100 and 200 mg/kg) produced a significant reduction of Histological score (59.9, 56.1, 53.5 and 73.3% inhibition, respectively). Dexamethasone, as the reference drug, was effective in this experimental model. In conclusion, pretreatment with single oral doses of D-005 significantly prevented the LPS-induced ALI in mice. -
Early Inflorescence and Floral Development in Cocos Nucifera L. (Arecaceae: Arecoideae) ⁎ P.I.P
Available online at www.sciencedirect.com South African Journal of Botany 76 (2010) 482–492 www.elsevier.com/locate/sajb Early inflorescence and floral development in Cocos nucifera L. (Arecaceae: Arecoideae) ⁎ P.I.P. Perera a,d, , V. Hocher b, L.K. Weerakoon a, D.M.D. Yakandawala c,d, S.C. Fernando a, J.-L. Verdeil e a Coconut Research Institute, Tissue Culture Division, 61150 Lunuwila, Sri Lanka b Institute for Research and Development (IRD), UMR 1098 BEPC, IRD, BP 64501-911 Avenue Agropolis, 34394 Montpellier Cedex 1, France c Department of Botany, University of Peradeniya, Sri Lanka d Postgraduate Institute of Science, University of Peradeniya, Sri Lanka e CIRAD, TA40/02 Avenue Agropolis, 34398 Montpellier Cedex 5, France Received 9 September 2009; received in revised form 17 March 2010; accepted 18 March 2010 Abstract Palms are generally characterized by a large structure with a massive crown that creates difficulties in anatomical studies. The flowering behaviour of palm species may be a useful indicator of phylogenetic relationships and therefore evolutionary events. This paper presents a detailed histological study of reproductive development in coconut (Cocos nucifera L.), from initiation up to maturation of staminate and pistillate flowers. Reproductive development in coconut consists of a sequence of individual events that span more than two years. Floral morphogenesis is the longest event, taking about one year, while sex determination is a rapid process that occurs within one month. The inflorescence consists of different ultimate floral structural components. Pistillate flowers are borne in floral triads that are flanked by two functional staminate flowers. -
Literaturverzeichnis
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