Savannas of French Guiana
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Bulletin Biological Assessment Boletín RAP Evaluación Biológica
Rapid Assessment Program Programa de Evaluación Rápida Evaluación Biológica Rápida de Chawi Grande, Comunidad Huaylipaya, Zongo, La Paz, Bolivia RAP Bulletin A Rapid Biological Assessment of of Biological Chawi Grande, Comunidad Huaylipaya, Assessment Zongo, La Paz, Bolivia Boletín RAP de Evaluación Editores/Editors Biológica Claudia F. Cortez F., Trond H. Larsen, Eduardo Forno y Juan Carlos Ledezma 70 Conservación Internacional Museo Nacional de Historia Natural Gobierno Autónomo Municipal de La Paz Rapid Assessment Program Programa de Evaluación Rápida Evaluación Biológica Rápida de Chawi Grande, Comunidad Huaylipaya, Zongo, La Paz, Bolivia RAP Bulletin A Rapid Biological Assessment of of Biological Chawi Grande, Comunidad Huaylipaya, Assessment Zongo, La Paz, Bolivia Boletín RAP de Evaluación Editores/Editors Biológica Claudia F. Cortez F., Trond H. Larsen, Eduardo Forno y Juan Carlos Ledezma 70 Conservación Internacional Museo Nacional de Historia Natural Gobierno Autónomo Municipal de La Paz The RAP Bulletin of Biological Assessment is published by: Conservation International 2011 Crystal Drive, Suite 500 Arlington, VA USA 22202 Tel: +1 703-341-2400 www.conservation.org Cover Photos: Trond H. Larsen (Chironius scurrulus). Editors: Claudia F. Cortez F., Trond H. Larsen, Eduardo Forno y Juan Carlos Ledezma Design: Jaime Fernando Mercado Murillo Map: Juan Carlos Ledezma y Veronica Castillo ISBN 978-1-948495-00-4 ©2018 Conservation International All rights reserved. Conservation International is a private, non-proft organization exempt from federal income tax under section 501c(3) of the Internal Revenue Code. The designations of geographical entities in this publication, and the presentation of the material, do not imply the expression of any opinion whatsoever on the part of Conservation International or its supporting organizations concerning the legal status of any country, territory, or area, or of its authorities, or concerning the delimitation of its frontiers or boundaries. -
Diversification of Myco-Heterotrophic Angiosperms: Evidence From
BMC Evolutionary Biology BioMed Central Research article Open Access Diversification of myco-heterotrophic angiosperms: Evidence from Burmanniaceae Vincent Merckx*1, Lars W Chatrou2, Benny Lemaire1, Moses N Sainge3, Suzy Huysmans1 and Erik F Smets1,4 Address: 1Laboratory of Plant Systematics, K.U. Leuven, Kasteelpark Arenberg 31, P.O. Box 2437, BE-3001 Leuven, Belgium, 2National Herbarium of the Netherlands, Wageningen University Branch, Generaal Foulkesweg 37, NL-6703 BL Wageningen, The Netherlands, 3Centre for Tropical Forest Sciences (CTFS), University of Buea, Department of Plant & Animal Sciences, P.O. Box 63, Buea, Cameroon and 4National Herbarium of the Netherlands, Leiden University Branch, P.O. Box 9514, NL-2300 RA, Leiden, The Netherlands Email: Vincent Merckx* - [email protected]; Lars W Chatrou - [email protected]; Benny Lemaire - [email protected]; Moses N Sainge - [email protected]; Suzy Huysmans - [email protected]; Erik F Smets - [email protected] * Corresponding author Published: 23 June 2008 Received: 25 February 2008 Accepted: 23 June 2008 BMC Evolutionary Biology 2008, 8:178 doi:10.1186/1471-2148-8-178 This article is available from: http://www.biomedcentral.com/1471-2148/8/178 © 2008 Merckx et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Abstract Background: Myco-heterotrophy evolved independently several times during angiosperm evolution. Although many species of myco-heterotrophic plants are highly endemic and long- distance dispersal seems unlikely, some genera are widely dispersed and have pantropical distributions, often with large disjunctions. -
Atlantic Forest Southeast Reserves
WHC Nomination Documentation File Name: 893.pdf UNESCO Region: LATIN AMERICA AND THE CARIBBEANS __________________________________________________________________________________________________ SITE NAME: Atlantic Forest Southeast Reserves DATE OF INSCRIPTION: 4th December 1999 STATE PARTY: BRAZIL CRITERIA: N(ii)(iii)(iv) DECISION OF THE WORLD HERITAGE COMMITTEE: Excerpt from the Report of the 23rd Session of the World Heritage Committee IUCN informed the Committee that the evaluation of this property has been undertaken based on the revised nomination submitted by the State Party in April 1999. The Atlantic Forest Southeast Reserves contain the best and largest remaining examples of Atlantic forest in the Southeast region of Brazil. The 25 protected areas that make up the site display the biological richness and evolutionary history of the few remaining areas of Atlantic forest of Southeast Brazil. The area is also exceptionally diverse with high numbers of rare and endemic species. With its "mountains to the sea" attitudinal gradient, its estuary, wild rivers, karst and numerous waterfalls, the site also has exceptional scenic values. The Committee decided to inscribe the site under natural criteria (ii), (iii) and (iv). It also recommended that the State Party should be encouraged to restore natural conditions in the Serra do Mar State Park, which potentially could be incorporated in the site. The Delegate of Morocco noted the values of the site but highlighted the challenges of the management of serial sites. The Delegate of Australia noted that management in serial sites is complex but can be done with careful strategic planning and an appropriate legal framework. BRIEF DESCRIPTIONS The Atlantic Forest Southeast Reserves in the states of Parana and Sao Paolo, contain some of the best and largest examples of Atlantic forest in Brazil. -
A Monograph of the Burmanniaceae
A monograph of the Burmanniaceae BY F.P. Jonker (Published December 5th 1938) CONTENTS. Page I. Introduction 1 II. General Part 4 History of the Family 4 Place of the Family in the System of Monocotyledons 4 Subdivision of the 7 Family . Geographical Distribution 10 Habitat and Plant-Community 12 Use 14 III. Critical Part 15 Tribus I, Burmannieae 17 Subtribus 1, Euburmannieae 17 1. Campylosiphon Benth 17 2. Hexapterella Urb 17 3. Burmannia L 18 Taxonomy 18 Sect. 1, Foliosa Jonk 20 Sect. 2, Euburmannia Malme 21 Geography 25 Subtribus 2, Apterieae 26 4. Cymbocarpa Miers 26 5. Gymnosiphon B1 27 Limits of the Genus 27 Taxonomy 30 Sect. I, Eugymnosiphon Urb 30 Sect. II, Ptychomeria (Benth.) Urb 31 Subsect, 1, Inappendiculati Jonk 32 Subsect. 2, Appendiculati Jonk 32 PAGE 6. Apteria Nutt 35 Taxonomy 35 Geography 36 7. Marthella Urb 36 8. Dictyostega Miers 38 Taxonomy 38 Geography 38 9. Miersiella Urb 40 Tribus II, Thismieae 41 Subtribus 1, Euthismieae 41 10. Afrothismia Schltr 41 11. Triscyphus Taub 42 12. Glaziocharis Taub 42 13. Thismia Griff 42 14. Geomitra Becc 46 15. Scaphiophora Schltr 46 Subtribus 2, Oxygyneae 47 16. Oxygyne Schltr 47 IV. Taxonomical Part. 49 Burmanniaceae 51 Key to the tribes 52 Tribus I, Burmannieae Miers 52 Subtribus 1, Euburmannieae Benth. et Hook 53 1. Campylosiphon Benth 53 2. Hexapterella Urb 55 3. Burmannia L 57 Sect. I, Foliosa Jonk 58 Sect. II, Euburmannia Malme 67 Subtribus 2, Apterieae Miers 164 4. Cymbocarpa Miers 165 5. Gymnosiphon B1 168 Sect. I, Eugymnosiphon Urb 169 Sect. II, Ptychomeria (Benth.) Urb 177 Subsect. -
Subterranean Structures and Mycotrophy of the Achlorophyllous Dictyostega Orobanchoides (Burmanniaceae)
Rev. Biol. Trop., 49(1): 239-247, 2001 www.ucr.ac.cr www.ots.ac.cr www.ots.duke.edu Subterranean structures and mycotrophy of the achlorophyllous Dictyostega orobanchoides (Burmanniaceae) Stephan Imhof Morphologie und Systematik der Höheren Pflanzen, Fachbereich Biologie, Philipps-Universität, 35032 Marburg, Ger- many. Tel.: 06421-2825185. Fax: 06421-2822057. E-Mail: [email protected] Received 5-IV-2000. Corrected 17-VIII-2000. Accepted 19-IX-2000. Abstract: Plants of Dictyostega orobanchoides arise from about 1 mm thick rhizomes, which are densely cove- red by sessile, imbricate, peltate scale leaves. The resulting interfoliar spaces are inhabited by fungal hyphae up to 6 µm thick, often developing vesicle-like bladders. The fungus also colonizes the tissue of the scale leaves, inter- as well as intracellularly, forming vesicles but no arbuscules, and it even penetrates the vascular bundles of the leaves. The rhizome itself does not become infected. The 200 µm thick roots emerge from the rhizome and have a 2-layered cortex and voluminous rhizodermis, which both are delicate and often disrupted or mis- sing. In contrast, the strongly reinforced, tertiary endodermis and the central cylinder are durable and have a con- siderable tensile strength. Although the roots grow through the hyphal masses in the interfoliar spaces when emerging from the rhizome, they only become infected from the rhizosphere. A collar of rhizomogenous tissue hinders the interfoliar hyphae from direct contact to the roots. Only within the rhizodermis, the mycorrhizal fun- gus builds coils of heteromorphic hyphae, arbuscule-like structures, and vesicles. Hence, the mycorrhiza in D. -
BMC Evolutionary Biology Biomed Central
BMC Evolutionary Biology BioMed Central Research article Open Access Diversification of myco-heterotrophic angiosperms: Evidence from Burmanniaceae Vincent Merckx*1, Lars W Chatrou2, Benny Lemaire1, Moses N Sainge3, Suzy Huysmans1 and Erik F Smets1,4 Address: 1Laboratory of Plant Systematics, K.U. Leuven, Kasteelpark Arenberg 31, P.O. Box 2437, BE-3001 Leuven, Belgium, 2National Herbarium of the Netherlands, Wageningen University Branch, Generaal Foulkesweg 37, NL-6703 BL Wageningen, The Netherlands, 3Centre for Tropical Forest Sciences (CTFS), University of Buea, Department of Plant & Animal Sciences, P.O. Box 63, Buea, Cameroon and 4National Herbarium of the Netherlands, Leiden University Branch, P.O. Box 9514, NL-2300 RA, Leiden, The Netherlands Email: Vincent Merckx* - [email protected]; Lars W Chatrou - [email protected]; Benny Lemaire - [email protected]; Moses N Sainge - [email protected]; Suzy Huysmans - [email protected]; Erik F Smets - [email protected] * Corresponding author Published: 23 June 2008 Received: 25 February 2008 Accepted: 23 June 2008 BMC Evolutionary Biology 2008, 8:178 doi:10.1186/1471-2148-8-178 This article is available from: http://www.biomedcentral.com/1471-2148/8/178 © 2008 Merckx et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Abstract Background: Myco-heterotrophy evolved independently several times during angiosperm evolution. Although many species of myco-heterotrophic plants are highly endemic and long- distance dispersal seems unlikely, some genera are widely dispersed and have pantropical distributions, often with large disjunctions. -
Phylogeny and Evolution of Burmanniaceae (Dioscoreales) Based on Nuclear and Mitochondrial Data1
American Journal of Botany 93(11): 1684–1698. 2006. PHYLOGENY AND EVOLUTION OF BURMANNIACEAE (DIOSCOREALES) BASED ON NUCLEAR AND MITOCHONDRIAL DATA1 VINCENT MERCKX,2,5 PETER SCHOLS,2 HILTJE MAAS-VAN DE KAMER,3 PAUL MAAS,3 SUZY HUYSMANS,2 AND ERIK SMETS2,4 2Laboratory of Plant Systematics, K.U. Leuven, Kasteelpark Arenberg 31, BE-3001 Leuven, Belgium; 3National Herbarium of the Netherlands, Utrecht University Branch, Heidelberglaan 2, NL-3584 CS Utrecht, the Netherlands; and 4National Herbarium of the Netherlands, Leiden University Branch, P.O. Box 9514, NL-2300 RA Leiden, the Netherlands The mycoheterotrophic Burmanniaceae are one of the three families currently recognized in the order Dioscoreales. Phylogenetic inference using nucleotide sequences of the nuclear 18S rDNA region and the mitochondrial nad1 b-c intron revealed two well-supported, major lineages within the family, corresponding to the two tribes recognized in the family: Burmannieae and Thismieae. All data supported a strong relationship between Thismieae and Tacca (Dioscoreaceae) making both Burmanniaceae and Dioscoreaceae polyphyletic. The three largest Burmanniaceae genera, Burmannia, Gymnosiphon, and Thismia, are paraphyletic. The splitting of Burmanniaceae into Burmannieae and Thismieae indicates two independent origins of mycoheterotrophy and correlated loss of chlorophyll in Dioscoreales. In the genus Burmannia, in which many species still contain chlorophyll, the achlorophyllous species are nested in between the autotrophic species, suggesting many independent changes from autotrophy to heterotrophy or vice versa. A Bayesian relative rates test on the 18S rDNA data showed considerable variation in substitution rates among Burmanniaceae. The substitution rates in all Thismieae and many Burmannieae are significantly faster than in Dioscoreaceae, but there seems to be no correlation between rate increases and the loss of photosynthesis. -
Smithsonian Plant Collections, the Guianas 1991–1993 and 1995–2000, Bruce Hoffman
Alexander, Hoffman Alexander, Smithsonian Institution Scholarly Press , Kelloff, and Funk smithsonian contributions to botany • number 101 Smithsonian Institution Scholarly Press Smithson ian Contributions to Botany Smithsonian Plant Collections, the Guianas • Number 101 1991–1993 and 1995–2000, Bruce Hoffman Sara N. Alexander, Bruce Hoffman, 2014 Carol L. Kelloff, and V. A. Funk SERIES PUBLICATIONS OF THE SMITHSONIAN INSTITUTION REQUIREMENTS FOR SMITHSONIAN SERIES PUBLICATION Emphasis upon publication as a means of “diffusing knowledge” was ALL MANUSCRIPTS ARE REVIEWED FOR ADHER- ART must not be embedded in the main text. expressed by the first Secretary of the Smithsonian. In his formal plan ENCE TO THE SISP MANUSCRIPT PREPARATION AND for the Institution, Joseph Henry outlined a program that included STYLE GUIDE FOR AUTHORS (available on the “Submis- Figures must be original and submitted as individual TIFF or EPS files. Resolution for art files must be at least 300 dpi the following statement: “It is proposed to publish a series of reports, sions” page at www.scholarlypress.si.edu). Manuscripts not for grayscale and color images and at least 1200 dpi for line giving an account of the new discoveries in science, and of the changes in compliance will be returned to the author. Manuscripts in- art. Electronic images should measure no more than 100% made from year to year in all branches of knowledge.” This theme of tended for publication in the Contributions Series are evalu- ated by a content review board and undergo substantive peer and no less than 75% of final size when published. JPG files basic research has been adhered to through the years by thousands of review. -
A Sketch of the Vegetation and Flora of the Kappel Savanna Near Tafelberg, Suriname
A sketch of the vegetation and flora of the Kappel Savanna near Tafelberg, Suriname. I BY K.U. Kramer AND J. van Donselaar (Botanical Museum and Herbarium, Utrecht) (Communicated by Prof. J. Lanjouw at the meeting of September 28, 1968) Introduction In February and early March, 1961, the senior author spent three weeks on a small savanna in the approximate centre of Suriname, South of Tafelberg, (map 1). He was accompanied by Mr. W. H. A. Hekking. The and the time was spent in exploring the flora of the savanna adjacent forest. As a detailed study of the vegetation of the savannas of northern in Suriname was then in progress, several extensive papers being prepa- ration (Heyligers, 1963; Van Donselaar, 1965; Van Donselaar-Ten it of Bokkel Huinink, 1966), was felt that a more thorough inventory the the When the vegetation and flora of savanna might be rewarding. a general impression of the plant-cover of the area had been obtained, eight representative sample-plots were selected, their vegetation was analyzed and described after the method of the French-Swiss school of in phytosociology, and pits were dug the soil down to bedrock, samples being taken in every distinctive-looking layer. This work was carried out jointly by the senior author and W. H. A. Hekking; part of the floristic exploration was also done by or with Dr. R. M. Tryon, Harvard Herbarium, Mass. The results here It felt that in Cambridge, are presented. was order to integrate them with those obtained elsewhere in Suriname, the col- laboration of a specialist familiar with the Suriname savannas in general was required. -
Cover Page the Handle Holds
Cover Page The handle http://hdl.handle.net/1887/35731 holds various files of this Leiden University dissertation Author: Mennes, Constantijn Title: Antiquities of the rainforest : evolution of mycoheterotrophic angiosperms growing on Glomeromycota Issue Date: 2015-10-06 Chapter 5 Did mycoheterotrophic plant lineages with similar ancestral distribution ranges originate simultaneously? Collecting Thismia rodwayi and T. hillii in Australia and New Zealand. Photos: C.B. Mennes/ V.S.F.T. Merckx. Did mycoheterotrophic plant lineages with similar ancestral distribution ranges originate simultaneously? Constantijn B. Mennes1, Erik F. Smets1,2, Paul J.M. Maas1, Hiltje Maas-van de Kamer1, Vincent S.F.T. Merckx1 1Naturalis Biodiversity Center, Leiden University, PO Box 9517, Leiden, the Netherlands. 2Section Ecology, Evolution and Biodiversity Conservation, KU Leuven, Kasteelpark Arenberg 31, PO Box 2437, BE-3001 Leuven, Belgium. Antiquities of the rainforest 5.1. Abstract Mycoheterotrophy is a strategy in which plants obtain carbon from their mycorrhizal symbionts. This remarkable lifestyle is probably an adaptation to life in dark rainforest understories and has evolved many times independently in flowering plants. Many unrelated mycoheterotrophic species often grow together and have similar distribution ranges. Based on these observations we hypothesize that non- related lineages of mycoheterotrophic plants with similar ancestral distribution ranges originated contemporaneously. We addressed this hypothesis by constructing time-calibrated phylogenies for all lineages of arbuscular mycorrhizal (AM) mycoheterotrophic plants in a standardized way. In addition, we estimated the ancestral distribution range of the most recent common ancestor of each lineage. We subsequently used this information to compare the age and biogeographic origins of the groups. -
Antagonistic Plants Preferentially Target Arbuscular Mycorrhizal Fungi That Are Highly 4 Connected to Mutualistic Plants
bioRxiv preprint doi: https://doi.org/10.1101/867259; this version posted July 5, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 1 FULL PAPER 2 3 Antagonistic plants preferentially target arbuscular mycorrhizal fungi that are highly 4 connected to mutualistic plants 5 6 Sofia IF Gomes1, Miguel A Fortuna2, Jordi BasCompte2, VinCent SFT MerCkx3,4* 7 8 9 1 Institute of Biology, Leiden University, Leiden, the Netherlands 10 2 Department of Evolutionary Biology and Environmental Studies, University of ZuriCh, 11 Switzerland. 12 4 Naturalis Biodiversity Center, Leiden, the Netherlands 13 3 Department of Evolutionary and Population Biology, Institute for Biodiversity and ECosystem 14 DynamiCs, University of Amsterdam, Amsterdam, the Netherlands 15 16 * Corresponding author: [email protected] 1 bioRxiv preprint doi: https://doi.org/10.1101/867259; this version posted July 5, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 17 Summary 18 19 • How antagonists – myCoheterotrophiC plants that obtain Carbon and soil nutrients from 20 fungi – are integrated in the usually mutualistiC arbusCular myCorrhizal networks is 21 unknown. Here, we Compare mutualistiC and antagonistiC plant assoCiations with 22 arbusCular myCorrhizal fungi and use network analysis to investigate fungal assoCiation 23 preferences in the tripartite network. 24 • We sequenced root tips from mutualistiC and antagonistiC plants in a tropiCal forest to 25 assemble the Combined tripartite network between mutualistiC plants, myCorrhizal fungi, 26 and antagonistiC plants. -
Lista Anotada De Las Plantas Vasculares Registradas En La Región De Madidi
Ecología en Bolivia, Vol. 40(3): 70-169, Diciembre de 2005. P.M. Jørgensen et al. Lista anotada de las plantas vasculares registradas en la región de Madidi P.M. Jørgensen1, M.J. Macía2, A. Fuentes1,3, S.G. Beck3, M. Kessler4, N. Paniagua1,3, R. Seidel1,3, C. Maldonado1,3, A. Araujo-Murakami1,3, L. Cayola1,3, T. Consiglio1, T.J. Killeen1, W.H. Cabrera1,3, F. Bascopé1,3, D. De la Quintana1,3, T. Miranda1,3, F. Canqui1,3 & V. Cardona-Peña1,3 1Missouri Botanical Garden, P.O. Box 299, St. Louis, Missouri 63166-0299, USA; [email protected] 2Real Jardín Botánico (CSIC), Plaza de Murillo 2, E-28014 Madrid, España. [email protected] 3Herbario Nacional de Bolivia, Instituto de Ecología, Universidad Mayor de San Andrés, Casilla 10077, La Paz, Bolivia. 4Herbarium, Universität Göttingen, Untere Karspüle 2, D-37073 Göttingen, Germany Resumen Se presenta la primera lista anotada de la región de Madidi que incluye tres áreas protegidas: Parque Nacional Madidi (18.854 km2), Reserva de la Biosfera y Territorio Indígena Pilón Lajas (4.027 km2), Área Natural de Manejo Integrado Apolobamba (4.765 km2), y una gran área alrededor de estas áreas (83.434 km2). La lista anotada se elaboró en base a las 23.515 colecciones botánicas con coordenadas geográficas. El número total de especies fue de 3.981, en 1.360 géneros y 211 familias. Debido al escaso número de colecciones en las áreas, el inventario es todavía desigual ya que el número de especies encontrado en Madidi fue 2.741, en Apolobamba 570 y en Pilón-Lajas solamente 231.