XVII International Botanical Congress – Abstracts
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(Ochnaceae) from the Brazilian Atlantic Forest
Phytotaxa 167 (1): 119–126 ISSN 1179-3155 (print edition) www.mapress.com/phytotaxa/ PHYTOTAXA Copyright © 2014 Magnolia Press Article ISSN 1179-3163 (online edition) http://dx.doi.org/10.11646/phytotaxa.167.1.8 A new cauliflorous white-flowered species of Ouratea (Ochnaceae) from the Brazilian Atlantic Forest CLAUDIO NICOLETTI DE FRAGA1,3 & MARIANA MACHADO SAAVEDRA2 1Instituto de Pesquisas Jardim Botânico do Rio de Janeiro, Rua Pacheco Leão, 915, 22.460-030, Jardim Botânico, Rio de Janeiro, Brazil. 2Instituto de Pesquisas Jardim Botânico do Rio de Janeiro, Escola Nacional de Botânica Tropical, Rua Pacheco Leão, 2040, 22.460- 030, Jardim Botânico, Rio de Janeiro, Brazil. 3Author for correspondence, email: [email protected] Abstract The new species Ouratea cauliflora is described, illustrated, and comments on its ecology, geographical distribution, and conservation status are provided. This species is morphologically similar to O. verticillata, but can be easily distinguished by its white flowers and the inflorescences cauliflorous or emerging from short and patent branches on the stem. The new species is endemic to a single locality in the central region of Espírito Santo, in the Brazilian Atlantic Forest, and according to the criteria of the IUCN Red List of endangered plant species, it is regarded as “vulnerable”. Key words: Brazil, endemism, Espírito Santo, new species, taxonomy Introduction The pantropical plant family Ochnaceae represents one of the well-supported subclades of the large order Malpighiales retrieved so far in molecular phylogenetic studies, which agrees with floral morphology, anatomy and histology (Matthews et al. 2012). The center of diversity of the family in the Neotropics is in the Amazon Basin, with some genera exclusive to this phytogeographic domain, and with a few with extra-Amazonian distributions, being restricted to the Andean Forests or to the Brazilian Cerrado and Atlantic Forest (Fiaschi et al. -
REVISION of the ANGIOSPERM FAMILY QUIINACEAE (MALPIGHIALES) Taxonomy and Systematics Julio V
RA 1.1 REVISION OF THE ANGIOSPERM FAMILY QUIINACEAE (MALPIGHIALES) Taxonomy and Systematics Julio V. Schneider & Georg Zizka Senckenberg Research Institute Frankfurt and Goethe-University Frankfurt Motivation and Results • Result 1 Taxonomy (4 genera, 46 species), data on distribution and ecology Document and analyze biodiversity. • Result 2 Phylogeny, character evolution and historical biogeography Peculiar leaf venation and occurence of diverse sex distribution make the evolution • Result 3 Peculiar leaf venation a singular development in angiosperms of the family of general botanical interest. Contribution to SGN Program Portfolio The monograph contributes to all key questions B of RA 1.1., also relates to RAs 1.2, 1.3, 2.2 and Infrastructure. Monographs are essentially based on scientific collections and are a major tool to develop collections, to communicate their data and to „put them in value“. A C Monographs are a key task of scientific collections. The revision of Quiinaceae is one example of these fundamental scientific products of Senckenberg, of which a recent variety from plant, fungus and animal kingdoms is presented in front of the poster. 2 Dated phylogeny of Quiinaceae and analysis 1 Fruits of Quiinaceae. A: Quiina amazonica, B: of biogeographic history. Lacunaria crenata and C: Froesia diffusa. Box A: distribution of the genera and the area of the Lake Pebas wetlands in the Miocene. 3 Leaf venation in Quiinaceae. A: Froesia, B: Box B: areas used for ancestral area Lacunaria, C: Quiina, D: Touroulia. Note reconstruction (Schneider & Zizka 2017). extremely dense, parallel tertiary veins in A,B and D – unique in angiosperms. Outlook Monographs of taxonomic groups are the base of biodiversity research and conservation. -
Kenneth J. Wurdack 2,4 and Charles C. Davis
American Journal of Botany 96(8): 1551–1570. 2009. M ALPIGHIALES PHYLOGENETICS: GAINING GROUND ON ONE OF THE MOST RECALCITRANT CLADES IN THE ANGIOSPERM TREE OF LIFE 1 Kenneth J. Wurdack 2,4 and Charles C. Davis3,4 2 Department of Botany, Smithsonian Institution, P.O. Box 37012 NMNH MRC-166, Washington, District of Columbia 20013-7012 USA; and 3 Department of Organismic and Evolutionary Biology, Harvard University Herbaria, 22 Divinity Avenue, Cambridge, Massachusetts 02138 USA The eudicot order Malpighiales contains ~16 000 species and is the most poorly resolved large rosid clade. To clarify phyloge- netic relationships in the order, we used maximum likelihood, Bayesian, and parsimony analyses of DNA sequence data from 13 gene regions, totaling 15 604 bp, and representing all three genomic compartments (i.e., plastid: atpB , matK , ndhF, and rbcL ; mitochondrial: ccmB , cob , matR , nad1B-C , nad6, and rps3; and nuclear: 18S rDNA, PHYC, and newly developed low-copy EMB2765 ). Our sampling of 190 taxa includes representatives from all families of Malpighiales. These data provide greatly in- creased support for the recent additions of Aneulophus , Bhesa , Centroplacus , Ploiarium , and Raffl esiaceae to Malpighiales; sister relations of Phyllanthaceae + Picrodendraceae, monophyly of Hypericaceae, and polyphyly of Clusiaceae. Oxalidales + Huaceae, followed by Celastrales are successive sisters to Malpighiales. Parasitic Raffl esiaceae, which produce the world’ s largest fl owers, are confi rmed as embedded within a paraphyletic Euphorbiaceae. Novel fi ndings show a well-supported placement of Ctenolopho- naceae with Erythroxylaceae + Rhizophoraceae, sister-group relationships of Bhesa + Centroplacus , and the exclusion of Medu- sandra from Malpighiales. New taxonomic circumscriptions include the addition of Bhesa to Centroplacaceae, Medusandra to Peridiscaceae (Saxifragales), Calophyllaceae applied to Clusiaceae subfamily Kielmeyeroideae, Peraceae applied to Euphorbi- aceae subfamily Peroideae, and Huaceae included in Oxalidales. -
LETTER Doi:10.1038/Nature12872
LETTER doi:10.1038/nature12872 Three keys to the radiation of angiosperms into freezing environments Amy E. Zanne1,2, David C. Tank3,4, William K. Cornwell5,6, Jonathan M. Eastman3,4, Stephen A. Smith7, Richard G. FitzJohn8,9, Daniel J. McGlinn10, Brian C. O’Meara11, Angela T. Moles6, Peter B. Reich12,13, Dana L. Royer14, Douglas E. Soltis15,16,17, Peter F. Stevens18, Mark Westoby9, Ian J. Wright9, Lonnie Aarssen19, Robert I. Bertin20, Andre Calaminus15, Rafae¨l Govaerts21, Frank Hemmings6, Michelle R. Leishman9, Jacek Oleksyn12,22, Pamela S. Soltis16,17, Nathan G. Swenson23, Laura Warman6,24 & Jeremy M. Beaulieu25 Early flowering plants are thought to have been woody species to greater heights: as path lengths increase so too does resistance5. restricted to warm habitats1–3. This lineage has since radiated into Among extant strategies, the most efficient method of water delivery almost every climate, with manifold growth forms4. As angiosperms is through large-diameter water-conducting conduits (that is, vessels spread and climate changed, they evolved mechanisms to cope with and tracheids) within xylem5. episodic freezing. To explore the evolution of traits underpinning Early in angiosperm evolution they probably evolved larger conduits the ability to persist in freezing conditions, we assembled a large for water transport, especially compared with their gymnosperm cousins14. species-level database of growth habit (woody or herbaceous; 49,064 Although efficient in delivering water, these larger cells would have species), as well as leaf phenology (evergreen or deciduous), diameter impeded angiosperm colonization of regions characterized by episodic of hydraulic conduits (that is, xylem vessels and tracheids) and climate freezing14,15, as the propensity for freezing-induced embolisms (air bub- occupancies (exposure to freezing). -
Nuclear and Plastid DNA Sequence-Based Molecular Phylogeography of Salvadora
bioRxiv preprint doi: https://doi.org/10.1101/050518; this version posted April 27, 2016. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Nuclear and Plastid DNA Sequence-based Molecular Phylogeography of Salvadora oleoides (Salvadoraceae) in Punjab, India Felix Bast1 and Navreet Kaur2 Centre for Plant Sciences, Central University of Punjab, Bathinda, Punjab, 151001, India 1Corresponding author; Telephone: +91 98721 52694; Email: [email protected] Email: [email protected] 1 bioRxiv preprint doi: https://doi.org/10.1101/050518; this version posted April 27, 2016. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Abstract Salvadora oleiodes is a tropical tree species belonging to the little-known family Salvadoraceae and distributed in the arid regions of Africa and Asia. Aims of our study were to trace the microevolutionary legacy of this tree species with the help of sequence-based multi-local phylogeography and to find the comparative placement of family Salvadoraceae within angiosperm clade malvids. A total 20 geographical isolates were collected from different regions of North India, covering a major part of its species range within the Indian Subcontinent. Sequence data from nuclear-encoded Internal Transcribed Spacer region (ITS1-5.8S-ITS2) and plastid-encoded trnL-F spacer region, were generated for this species for the first time in the world. -
The Genus Touroulia Aubl. (Quiinaceae)
Willdenowia 29 – 1999 227 GEORG ZIZKA & JULIO V. SCHNEIDER The genus Touroulia Aubl. (Quiinaceae) Abstract Zizka, G. & Schneider, J. V.: The genus Touroulia Aubl. (Quiinaceae). – Willdenowia 29: 227-234. 1999. – ISSN 0511-9618. Morphology, distribution, and leaf venation of the two species of Touroulia Aubl. (T. amazonica, T. guianensis) are described, and a key to the species is provided. Introduction The neotropical genus Touroulia (Quiinaceae) comprises two species, T. amazonica and T. guianensis. T. guianensis, described in 1775 by F. Aublet, is widespread in northern South America and comparatively well documented in herbarium collections. Touroulia amazonica was described in 1950 by J. M. Pires and even today only a few collec- tions of this species exist. Within the family Quiinaceae, the genus Touroulia is easily distin- guished from the other genera (Froesia, Lacunaria, Quiina) by the combination of the following characters: leaves pinnate, flowers androdioecious, gynoecium syncarpous and seeds villous. The leaf and stem anatomy provide additional characters (Gottwald & Parameswaran 1967, Roth 1973). Delimitation of the genus The very characteristic and unique leaf venation of Touroulia guianensis and various other Quiinaceae has been investigated and described by Hallier (1912), Foster (1950a, 1950b, 1951) and Roth (1996). T. amazonica has principally the same craspedodromous leaf venation as T. guianensis with numerous densely spaced and ± parallel running tertiary veins. Size and branch- ing pattern of the tertiary veins (of the leaflets) are similar in these species too and differ from those observed in the other genera of Quiinaceae. This fact supports a closer relationship of the two species. A noteworthy difference between them is that in T. -
Caracterización Y Tipificación Forestal De Ecosistemas En El Municipio De Inírida Y El Corregimiento De Cacahual (Departamento De Guainía)
Caracterización y tipificación forestal de ecosistemas en el municipio de Inírida y el corregimiento de Cacahual (Departamento de Guainía) Una Zonificación Forestal para la Ordenación de los Recursos MINISTERIO DE AMBIENTE, VIVIENDA Y DESARROLLO TERRITORIAL República de Colombia LUZ MARINA MANTILLA CÁRDENAS Directora General ROSARIO PIÑERES VERGARA Subdirectora Administrativa y Financiera CESAR HUMBERTO MELÉNDEZ SÁENZ Director General MARYI HASBLEIDY VARÓN IZQUIERDO Subdirectora de Recursos Naturales CARDENAS LÓPEZ, Dairon; BARRETO SILVA, Juan Sebastián; ARIAS GARCÍA, Juan Carlos; MURCIA GARCÍA, Uriel Gonzalo; SALAZAR CARDONA, Carlos Ariel; MEN- DEZ QUEVEDO, Orlando Caracterización y tipificación forestal de ecosistemas en el municipio de Inírida y el co- rregimiento de Cacahual (departamento del Guainía): una zonificación forestal para la ordenación de los recursos. Dairon Cárdenas López; Juan Sebastián Barreto Silva; Uriel Gonzalo Murcia García; Carlos Ariel Salazar Cardona; Orlando Méndez Quevedo. Bogotá, Colombia: Instituto Amazónico de Investigaciones Científicas –Sinchi-. Corporación para el Desarrollo Sostenible del Norte y el Oriente Amazónico, CDA, 2007 1. ORDENAMIENTO DEL TERRITORIO 2. ZONIFICACIÓN FORESTAL 3. USO DEL SUELO 4. RECURSOS FORESTALES 5. ECOSISTEMAS 6. GUAINÍA (COLOMBIA) ISBN: © Instituto Amazónico de Investigaciones Científicas – Sinchi © Corporación para el Desarrollo Sostenible del Norte y el Oriente Amazónico, CDA Ministerio de Ambiente, Vivienda y Desarrollo Territorial Primera edición: Octubre de 2007 Diseño: -
LETTER Doi:10.1038/Nature12872
LETTER doi:10.1038/nature12872 Three keys to the radiation of angiosperms into freezing environments Amy E. Zanne1,2, David C. Tank3,4, William K. Cornwell5,6, Jonathan M. Eastman3,4, Stephen A. Smith7, Richard G. FitzJohn8,9, Daniel J. McGlinn10, Brian C. O’Meara11, Angela T. Moles6, Peter B. Reich12,13, Dana L. Royer14, Douglas E. Soltis15,16,17, Peter F. Stevens18, Mark Westoby9, Ian J. Wright9, Lonnie Aarssen19, Robert I. Bertin20, Andre Calaminus15, Rafae¨l Govaerts21, Frank Hemmings6, Michelle R. Leishman9, Jacek Oleksyn12,22, Pamela S. Soltis16,17, Nathan G. Swenson23, Laura Warman6,24 & Jeremy M. Beaulieu25 Early flowering plants are thought to have been woody species to greater heights: as path lengths increase so too does resistance5. restricted to warm habitats1–3. This lineage has since radiated into Among extant strategies, the most efficient method of water delivery almost every climate, with manifold growth forms4. As angiosperms is through large-diameter water-conducting conduits (that is, vessels spread and climate changed, they evolved mechanisms to cope with and tracheids) within xylem5. episodic freezing. To explore the evolution of traits underpinning Early in angiosperm evolution they probably evolved larger conduits the ability to persist in freezing conditions, we assembled a large for water transport, especially compared with their gymnosperm cousins14. species-level database of growth habit (woody or herbaceous; 49,064 Although efficient in delivering water, these larger cells would have species), as well as leaf phenology (evergreen or deciduous), diameter impeded angiosperm colonization of regions characterized by episodic of hydraulic conduits (that is, xylem vessels and tracheids) and climate freezing14,15, as the propensity for freezing-induced embolisms (air bub- occupancies (exposure to freezing). -
The Chemistry of Brazilian Quiinaceae. 1. Constituents of Touroulia Guianensis and Lacunaria Jenmani
The Chemistry of Brazilian Quiinaceae. 1. Constituents of Touroulia guianensis and Lacunaria jenmani Otto R. Gottlieb ( 1), Mauro T. Magalhães (2), Geovane G. de Oliveira (3) e Arold<' Trainotti (3) The small family Ouiinaceae includes 4 The analysis of trunk wood of Touroulia genera (Froesia, Lacunaria, Quiina and Tou guianensis Aubl. revealed the presence of roulia) with 37 central and south american 2,6-dimethoxy-p-benzoquinone [Corrêa et ai., species. Although generally included in the 1970], friedelan-3oc-o l and friedelin [Drake & Campbe li, 1936], s itosterol and ~-sitostenone subclass Dilleniidae, arder Theales [Cronquist, [Lavie & Kaye, 1963]. and syringaresinol 1968]. and considered derived from t he [Weinges, 1961] . Friedelin, sitosterol and Ochnaceae or the Theaceae, the family has syringaresinol were also isolated from the even been placed in the subclass Rosidae, trunk wood of Lacunaria jenmani Ducke. arder Linales, and considered derived from the While, thus, both genera appear to be Linaceae [Hegnauer, 1968]. Jt was hoped that close chemical relatives, the analysis fails to chemical data, lacking at present time, mzy indicate affinities of the family, since the help to clarify the presently uncertain system isolated constituents are of widespread atic position. occurrence in the plant kingdom. ( 1 l - Instituto de Oufmlca, Universidade de São Paulo, São Paulo. ( 2 l - Centro de Tecnologia Agrícola e Alimentar, EMBRAPA, Rio de Janeiro. ( 3 l - lnsttiuto de Ciências Exatas, Universidade Federal de Minas Gerais, Belo Horizonte. ACTA AMAZONICA 7(2) - 291 lJTERAXURE CITED oxidative degradation o f friedelin. .J. Amer. Chem. Soe., 58 : 1681-1684 CORRÊA, D . DE B.; FONSECA E SILVA, L .G.; GorrLIEB, o R . -
Phylogeny of the Eudicots : a Nearly Complete Familial Analysis Based On
KEW BULLETIN 55: 257 - 309 (2000) Phylogeny of the eudicots: a nearly complete familial analysis based on rbcL gene sequences 1 V. SAVOLAINENI.2, M. F. FAyl, D. c. ALBACHI.\ A. BACKLUND4, M. VAN DER BANK ,\ K. M. CAMERON1i, S. A. ]e)H;-.;so:--.;7, M. D. LLWOI, j.c. PINTAUDI.R, M. POWELL', M. C. SHEAHAN 1, D. E. SOLTlS~I, P. S. SOLTIS'I, P. WESTONI(), W. M. WHITTEN 11, K.J. WCRDACKI2 & M. W. CHASEl Summary, A phylogenetic analysis of 589 plastid rbcl. gene sequences representing nearly all eudicot families (a total of 308 families; seven photosynthetic and four parasitic families are missing) was performed, and bootstrap re-sampling was used to assess support for clades. Based on these data, the ordinal classification of eudicots is revised following the previous classification of angiosperms by the Angiosperm Phylogeny Group (APG) , Putative additional orders are discussed (e.g. Dilleniales, Escalloniales, VitaiRs) , and several additional families are assigned to orders for future updates of the APG classification. The use of rbcl. alone in such a large matrix was found to be practical in discovering and providing bootstrap support for most orders, Combination of these data with other matrices for the rest of the angiosperms should provide the framework for a complete phylogeny to be used in macro evolutionary studies, !:--':TRODL'CTlON The angiosperms are the first division of organisms to have been re-classified largely on the basis of molecular data analysed phylogenetically (APG 1998). Several large scale molecular phylogenies have been produced for the angiosperms, based on both plastid rbcL (Chase et al. -
Flora Del Escudo Guayanés En Inírida (Guainía, Colombia)
Flora del Escudo Guayanés en Inírida (Guainía, colombia) MINISTERIO DE AMBIENTE, VIVIENDA Y DESARROLLO TERRITORIAL República de Colombia CARDENAS LÓPEZ, Dairon (Editor) Flora del Escudo Guayanés en Inírida (Guainía, Colombia). Dairon Cárdenas López (Ed.).Bogotá, Colombia: Instituto Amazónico de Investigaciones Cien- tíficas –Sinchi-, 2007 1. FLORA 2. TAXONOMÍA 3. VEGETACIÓN 4. FITOGEOGRAFÍA 5. GUAYANA 6. INÍRIDA, GUAINÍA. ISBN: 978-958-8317-35-9 © Instituto Amazónico de Investigaciones Científicas – Sinchi Ministerio de Ambiente, Vivienda y Desarrollo Territorial Cartografía: Sonia Mireya Sua Fotografía: Olga Chols Agudelo, Zaleth Cordero-P., Dairon Cárdenas López, Nelson R. Salinas, Juliana Cárdenas Toro, Juan Carlos Arias Primera edición: diciembre de 2007 Diseño y diagramación: Julián R. Hernández Impresión: Impresol Ediciones Ltda.., PBX 250 82 44 Coordinación de la producción editorial: Diana Patricia Mora Rodríguez Reservados todos los Derechos El contenido de esta publicación es propiedad del Instituto Amazónico de Investi- gaciones Científicas -Sinchi- Prohibida su reproducción con fines comerciales. Disponible en: Instituto Sinchi Calle 20 No. 5-44 Tel.: 4442060 www.sinchi.org.co Impreso en Colombia Printed in Colombia Luz Marina Mantilla Cárdenas Directora General Rosario Piñeres Vergara Subdirectora Administrativa y Financiera Dairon Cárdenas López Director curador Herbario Amazónico Colombiano COAH Presentación El nororiente de la Amazonia colombiana, en particular el De- partamento del Guainía, constituye una zona de especial interés puesto que en ella se encuentran ecosistemas característicos del Es- cudo Guayanés, que solo se encuentran en esta zona del país y que presentan marcadas diferencias con otros; esta región que geológi- camente se encuentra entre las más antiguas del mundo y que pre- senta particularidades como los afloramientos rocosos, los bosques y sabanas sobre arenas blancas . -
Three Keys to the Radiation of Angiosperms Into Freezing Environments
LETTER doi:10.1038/nature12872 Three keys to the radiation of angiosperms into freezing environments Amy E. Zanne1,2, David C. Tank3,4, William K. Cornwell5,6, Jonathan M. Eastman3,4, Stephen A. Smith7, Richard G. FitzJohn8,9, Daniel J. McGlinn10, Brian C. O’Meara11, Angela T. Moles6, Peter B. Reich12,13, Dana L. Royer14, Douglas E. Soltis15,16,17, Peter F. Stevens18, Mark Westoby9, Ian J. Wright9, Lonnie Aarssen19, Robert I. Bertin20, Andre Calaminus15, Rafae¨l Govaerts21, Frank Hemmings6, Michelle R. Leishman9, Jacek Oleksyn12,22, Pamela S. Soltis16,17, Nathan G. Swenson23, Laura Warman6,24 & Jeremy M. Beaulieu25 Early flowering plants are thought to have been woody species to greater heights: as path lengths increase so too does resistance5. restricted to warm habitats1–3. This lineage has since radiated into Among extant strategies, the most efficient method of water delivery almost every climate, with manifold growth forms4. As angiosperms is through large-diameter water-conducting conduits (that is, vessels spread and climate changed, they evolved mechanisms to cope with and tracheids) within xylem5. episodic freezing. To explore the evolution of traits underpinning Early in angiosperm evolution they probably evolved larger conduits the ability to persist in freezing conditions, we assembled a large for water transport, especially compared with their gymnosperm cousins14. species-level database of growth habit (woody or herbaceous; 49,064 Although efficient in delivering water, these larger cells would have species), as well as leaf phenology (evergreen or deciduous), diameter impeded angiosperm colonization of regions characterized by episodic of hydraulic conduits (that is, xylem vessels and tracheids) and climate freezing14,15, as the propensity for freezing-induced embolisms (air bub- occupancies (exposure to freezing).