Uva-DARE (Digital Academic Repository)
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Pakaraimaea Dipterocarpacea
The Ectomycorrhizal Fungal Community in a Neotropical Forest Dominated by the Endemic Dipterocarp Pakaraimaea dipterocarpacea Matthew E. Smith1*, Terry W. Henkel2, Jessie K. Uehling2, Alexander K. Fremier3, H. David Clarke4, Rytas Vilgalys5 1 Department of Plant Pathology, University of Florida, Gainesville, Florida, United States of America, 2 Department of Biological Sciences, Humboldt State University, Arcata, California, United States of America, 3 Department of Fish and Wildlife Resources, University of Idaho, Moscow, Idaho, United States of America, 4 Department of Biology, University of North Carolina Asheville, Asheville, North Carolina, United States of America, 5 Department of Biology, Duke University, Durham, North Carolina, United States of America Abstract Ectomycorrhizal (ECM) plants and fungi can be diverse and abundant in certain tropical ecosystems. For example, the primarily paleotropical ECM plant family Dipterocarpaceae is one of the most speciose and ecologically important tree families in Southeast Asia. Pakaraimaea dipterocarpacea is one of two species of dipterocarp known from the Neotropics, and is also the only known member of the monotypic Dipterocarpaceae subfamily Pakaraimoideae. This Guiana Shield endemic is only known from the sandstone highlands of Guyana and Venezuela. Despite its unique phylogenetic position and unusual geographical distribution, the ECM fungal associations of P. dipterocarpacea are understudied throughout the tree’s range. In December 2010 we sampled ECM fungi on roots of P. dipterocarpacea and the co-occurring ECM tree Dicymbe jenmanii (Fabaceae subfamily Caesalpinioideae) in the Upper Mazaruni River Basin of Guyana. Based on ITS rDNA sequencing we documented 52 ECM species from 11 independent fungal lineages. Due to the phylogenetic distance between the two host tree species, we hypothesized that P. -
Download Download
Acta Brasiliensis 5(1): 25-34, 2021 Artigo Original http://revistas.ufcg.edu.br/ActaBra http://dx.doi.org/10.22571/2526-4338449 New records of Annonaceae in the Northeast Brazil Márcio Lucas Bazantea i , Marccus Alvesb i a Universidade Federal de Pernambuco, Recife, 50670-901, Pernambuco, Brasil. * [email protected] b Programa de Pós-graduação em Biologia Vegetal, Universidade Federal de Pernambuco, Recife, 50670-901, Pernambuco, Brasil. Received: August 2, 2020 / Accepted: November 8, 2020 / Published online: January 27, 2021 Abstract This study reports nine new records of Annonaceae for the states of Alagoas, Ceará, Paraíba and Pernambuco, in Northeastern Brazil: Duguetia lanceolata A.St.-Hil., D. ruboides Maas & He, D. sooretamae Maas, Guatteria tomentosa Rusby, Hornschuchia bryotrophe Nees, Pseudoxandra lucida R.E.Fr., Trigynaea duckei (R.E.Fr.) R.E.Fr.., Unonopsis guatterioides (A.DC.) R.E.Fr., and Xylopia ochrantha Mart. Descriptions, taxonomical and distributional comments, photos of diagnostic characters, geographic distribution maps and two identification keys, one of the genera of Annonaceae occurring in the Atlantic Forest and Caatinga and another for the new Duguetia records, are provided. Keywords: Atlantic forest, Caatinga, Pseudoxandra, Trigynaea, Unonopsis. Novos registros de Annonaceae no Nordeste do Brasil Resumo Este estudo reporta nove novos registros de Annonaceae para os estados de Alagoas, Ceará, Paraíba e Pernambuco, nordeste do Brasil: Duguetia lanceolata A. St. -Hil., D. ruboides Maas & He, D. sooretamae Maas, Guatteria tomentosa Rusby, Hornschuchia bryotrophe Nees, Pseudoxandra lucida R.E.Fr., Trigynaea duckei (R.E.Fr.) R.E.Fr., Unonopsis guatterioides (A.DC.) R.E.Fr., e Xylopia ochrantha Mart. -
Phylogeny of the Tropical Tree Family Dipterocarpaceae Based on Nucleotide Sequences of the Chloroplast Rbcl Gene1
American Journal of Botany 86(8): 1182±1190. 1999. PHYLOGENY OF THE TROPICAL TREE FAMILY DIPTEROCARPACEAE BASED ON NUCLEOTIDE SEQUENCES OF THE CHLOROPLAST RBCL GENE1 S. DAYANANDAN,2,6 PETER S. ASHTON,3 SCOTT M. WILLIAMS,4 AND RICHARD B. PRIMACK2 2Biology Department, Boston University, Boston, Massachusetts 02215; 3Harvard University Herbaria, 22 Divinity Avenue, Cambridge, Massachusetts 02138; and 4Division of Biomedical Sciences, Meharry Medical College, 1005 D. B. Todd, Jr. Boulevard, Nashville, Tennessee 37208 The Dipterocarpaceae, well-known trees of the Asian rain forests, have been variously assigned to Malvales and Theales. The family, if the Monotoideae of Africa (30 species) and South America and the Pakaraimoideae of South America (one species) are included, comprises over 500 species. Despite the high diversity and ecological dominance of the Dipterocar- paceae, phylogenetic relationships within the family as well as between dipterocarps and other angiosperm families remain poorly de®ned. We conducted parsimony analyses on rbcL sequences from 35 species to reconstruct the phylogeny of the Dipterocarpaceae. The consensus tree resulting from these analyses shows that the members of Dipterocarpaceae, including Monotes and Pakaraimaea, form a monophyletic group closely related to the family Sarcolaenaceae and are allied to Malvales. The present generic and higher taxon circumscriptions of Dipterocarpaceae are mostly in agreement with this molecular phylogeny with the exception of the genus Hopea, which forms a clade with Shorea sections Anthoshorea and Doona. Phylogenetic placement of Dipterocarpus and Dryobalanops remains unresolved. Further studies involving repre- sentative taxa from Cistaceae, Elaeocarpaceae, Hopea, Shorea, Dipterocarpus, and Dryobalanops will be necessary for a comprehensive understanding of the phylogeny and generic limits of the Dipterocarpaceae. -
GENOME EVOLUTION in MONOCOTS a Dissertation
GENOME EVOLUTION IN MONOCOTS A Dissertation Presented to The Faculty of the Graduate School At the University of Missouri In Partial Fulfillment Of the Requirements for the Degree Doctor of Philosophy By Kate L. Hertweck Dr. J. Chris Pires, Dissertation Advisor JULY 2011 The undersigned, appointed by the dean of the Graduate School, have examined the dissertation entitled GENOME EVOLUTION IN MONOCOTS Presented by Kate L. Hertweck A candidate for the degree of Doctor of Philosophy And hereby certify that, in their opinion, it is worthy of acceptance. Dr. J. Chris Pires Dr. Lori Eggert Dr. Candace Galen Dr. Rose‐Marie Muzika ACKNOWLEDGEMENTS I am indebted to many people for their assistance during the course of my graduate education. I would not have derived such a keen understanding of the learning process without the tutelage of Dr. Sandi Abell. Members of the Pires lab provided prolific support in improving lab techniques, computational analysis, greenhouse maintenance, and writing support. Team Monocot, including Dr. Mike Kinney, Dr. Roxi Steele, and Erica Wheeler were particularly helpful, but other lab members working on Brassicaceae (Dr. Zhiyong Xiong, Dr. Maqsood Rehman, Pat Edger, Tatiana Arias, Dustin Mayfield) all provided vital support as well. I am also grateful for the support of a high school student, Cady Anderson, and an undergraduate, Tori Docktor, for their assistance in laboratory procedures. Many people, scientist and otherwise, helped with field collections: Dr. Travis Columbus, Hester Bell, Doug and Judy McGoon, Julie Ketner, Katy Klymus, and William Alexander. Many thanks to Barb Sonderman for taking care of my greenhouse collection of many odd plants brought back from the field. -
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. -
Phylogeny and Historical Biogeography of Lauraceae
PHYLOGENY Andre'S. Chanderbali,2'3Henk van der AND HISTORICAL Werff,3 and Susanne S. Renner3 BIOGEOGRAPHY OF LAURACEAE: EVIDENCE FROM THE CHLOROPLAST AND NUCLEAR GENOMES1 ABSTRACT Phylogenetic relationships among 122 species of Lauraceae representing 44 of the 55 currentlyrecognized genera are inferredfrom sequence variation in the chloroplast and nuclear genomes. The trnL-trnF,trnT-trnL, psbA-trnH, and rpll6 regions of cpDNA, and the 5' end of 26S rDNA resolved major lineages, while the ITS/5.8S region of rDNA resolved a large terminal lade. The phylogenetic estimate is used to assess morphology-based views of relationships and, with a temporal dimension added, to reconstructthe biogeographic historyof the family.Results suggest Lauraceae radiated when trans-Tethyeanmigration was relatively easy, and basal lineages are established on either Gondwanan or Laurasian terrains by the Late Cretaceous. Most genera with Gondwanan histories place in Cryptocaryeae, but a small group of South American genera, the Chlorocardium-Mezilauruls lade, represent a separate Gondwanan lineage. Caryodaphnopsis and Neocinnamomum may be the only extant representatives of the ancient Lauraceae flora docu- mented in Mid- to Late Cretaceous Laurasian strata. Remaining genera place in a terminal Perseeae-Laureae lade that radiated in Early Eocene Laurasia. Therein, non-cupulate genera associate as the Persea group, and cupuliferous genera sort to Laureae of most classifications or Cinnamomeae sensu Kostermans. Laureae are Laurasian relicts in Asia. The Persea group -
Recommendation of Native Species for the Reforestation of Degraded Land Using Live Staking in Antioquia and Caldas’ Departments (Colombia)
UNIVERSITÀ DEGLI STUDI DI PADOVA Department of Land, Environment Agriculture and Forestry Second Cycle Degree (MSc) in Forest Science Recommendation of native species for the reforestation of degraded land using live staking in Antioquia and Caldas’ Departments (Colombia) Supervisor Prof. Lorenzo Marini Co-supervisor Prof. Jaime Polanía Vorenberg Submitted by Alicia Pardo Moy Student N. 1218558 2019/2020 Summary Although Colombia is one of the countries with the greatest biodiversity in the world, it has many degraded areas due to agricultural and mining practices that have been carried out in recent decades. The high Andean forests are especially vulnerable to this type of soil erosion. The corporate purpose of ‘Reforestadora El Guásimo S.A.S.’ is to use wood from its plantations, but it also follows the parameters of the Forest Stewardship Council (FSC). For this reason, it carries out reforestation activities and programs and, very particularly, it is interested in carrying out ecological restoration processes in some critical sites. The study area is located between 2000 and 2750 masl and is considered a low Andean humid forest (bmh-MB). The average annual precipitation rate is 2057 mm and the average temperature is around 11 ºC. The soil has a sandy loam texture with low pH, which limits the amount of nutrients it can absorb. FAO (2014) suggests that around 10 genera are enough for a proper restoration. After a bibliographic revision, the genera chosen were Alchornea, Billia, Ficus, Inga, Meriania, Miconia, Ocotea, Protium, Prunus, Psidium, Symplocos, Tibouchina, and Weinmannia. Two inventories from 2013 and 2019, helped to determine different biodiversity indexes to check the survival of different species and to suggest the adequate characteristics of the individuals for a successful vegetative stakes reforestation. -
Tropical Forests
1740 TROPICAL FORESTS / Bombacaceae in turn cause wild swings in the ecology and these Birks JS and Barnes RD (1990) Provenance Variation in swings themselves can sometimes prove to be beyond Pinus caribaea, P. oocarpa and P. patula ssp. tecunuma- control through management. In the exotic environ- nii. Tropical Forestry Papers no. 21. Oxford, UK: Oxford ments, it is impossible to predict or even conceive of Forestry Institute. the events that may occur and to know their Critchfield WB and Little EL (1966) Geographic Distribu- consequences. Introduction of diversity in the forest tion of the Pines of the World. Washington, DC: USDA Miscellaneous Publications. through mixed ages, mixed species, rotation of Duffield JW (1952) Relationships and species hybridization species, silvicultural treatment, and genetic variation in the genus Pinus. Zeitschrift fu¨r Forstgenetik und may make ecology and management more complex Forstpflanzenzuchtung 1: 93–100. but it will render the crop ecosystem much more Farjon A and Styles BT (1997) Pinus (Pinaceae). Flora stable, robust, and self-perpetuating and provide Neotropica Monograph no. 75. New York: New York buffers against disasters. The forester must treat crop Botanical Garden. protection as part of silvicultural planning. Ivory MH (1980) Ectomycorrhizal fungi of lowland tropical pines in natural forests and exotic plantations. See also: Pathology: Diseases affecting Exotic Planta- In: Mikola P (ed.) Tropical Mycorrhiza Research, tion Species; Diseases of Forest Trees. Temperate and pp. 110–117. Oxford, UK: Oxford University Press. Mediterranean Forests: Northern Coniferous Forests; Ivory MH (1987) Diseases and Disorders of Pines in the Southern Coniferous Forests. Temperate Ecosystems: Tropics. Overseas Research Publication no. -
Isolation and Identification of Cyclic Polyketides From
ISOLATION AND IDENTIFICATION OF CYCLIC POLYKETIDES FROM ENDIANDRA KINGIANA GAMBLE (LAURACEAE), AS BCL-XL/BAK AND MCL-1/BID DUAL INHIBITORS, AND APPROACHES TOWARD THE SYNTHESIS OF KINGIANINS Mohamad Nurul Azmi Mohamad Taib, Yvan Six, Marc Litaudon, Khalijah Awang To cite this version: Mohamad Nurul Azmi Mohamad Taib, Yvan Six, Marc Litaudon, Khalijah Awang. ISOLATION AND IDENTIFICATION OF CYCLIC POLYKETIDES FROM ENDIANDRA KINGIANA GAMBLE (LAURACEAE), AS BCL-XL/BAK AND MCL-1/BID DUAL INHIBITORS, AND APPROACHES TOWARD THE SYNTHESIS OF KINGIANINS . Chemical Sciences. Ecole Doctorale Polytechnique; Laboratoires de Synthase Organique (LSO), 2015. English. tel-01260359 HAL Id: tel-01260359 https://pastel.archives-ouvertes.fr/tel-01260359 Submitted on 22 Jan 2016 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. ISOLATION AND IDENTIFICATION OF CYCLIC POLYKETIDES FROM ENDIANDRA KINGIANA GAMBLE (LAURACEAE), AS BCL-XL/BAK AND MCL-1/BID DUAL INHIBITORS, AND APPROACHES TOWARD THE SYNTHESIS OF KINGIANINS MOHAMAD NURUL AZMI BIN MOHAMAD TAIB FACULTY OF SCIENCE UNIVERSITY -
Vegetation and Floristics of Kwiambal
351 Vegetation and floristics of Kwiambal National Park and surrounds, Ashford, New South Wales John T. Hunter, Jennifer Kingston and Peter Croft John T. Hunter1, Jennifer Kingston2 and Peter Croft2 (175 Kendall Rd, Invergowrie, NSW 2350, 2Glen Innes District National Parks and Wildlife Service, Glen Innes, NSW 2370) 1999. Vegetation and floristics of Kwiambal National Park and surrounds, Ashford, New South Wales. Cunninghamia 6(2): 351–378 The vegetation of Kwiambal National Park and surrounds, 30 km north-west of Ashford (29°07'S, 150°58'E) in the Inverell Shire on the North Western Slopes, is described. Eight plant communities are defined based on flexible UPGMA analysis of relative abundance scores of vascular plant taxa. These communities are mapped based on ground truthing, air photo interpretation and geological substrate. All communities are of woodland structure and most are dominated by Callitris glaucophylla, Eucalyptus melanophloia and Eucalyptus dealbata. Communities are: 1) Mixed Stand Woodland (Dry Rainforest), 2) Granite Woodland, 3) Metasediment Woodland, 4) Riverine, 5) Metabasalt Woodland, 6) Granite Open Woodland, 7) Limestone Woodland, and 8) Alluvial Woodland. Many of the taxa (407 species were recorded) show phytogeographic affinities with western south-east Queensland flora. This is also true of the communities defined. Five ROTAP listed species have been found in the Park: Acacia williamsiana, Astrotricha roddii, Euphorbia sarcostemmoides, Olearia gravis and Thesium australe, three of these are listed on the NSW Threatened Species Conservation Act (1995). Another ten taxa are considered to be at their geographic limit or disjunct in their distribution. 17% are exotic in origin. Introduction Kwiambal National Park is approximately 130 km north-west of Glen Innes and 30 km north-west of Ashford (29°07'S, 150°58'E) in the Shire of Inverell on the North Western Slopes of NSW (Fig. -
2003 Vol. 6, Issue 1
Department of Systematic Biology - Botany & the U.S. National Herbarium The Plant Press New Series - Vol. 6 - No. 1 January-March 2003 Botany Profile Botanist Untangles Caribbean Vines By Robert DeFilipps ost people are surprised to the Serjania and Talisia being studied by Virgin Islands), to be published this year learn that the largely tropical Acevedo, exhibit a peculiar syndrome by Sheridan Press, Hanover, Pennsylva- dicot family Sapindaceae, wherein populations of the plants produce nia. The 387 species of vines treated here Msource of the edible fruit-bearing trees a male-flowered phase, followed by a are illustrated by Bobbi Angell, one of yielding akee (Blighia), rambutan female phase, and then by another male the most skilled botanical illustrators. (Nephelium) and leechee nuts (Litchi), phase. This little-explored phenomenon While a research fellow at the New also contains a large number of saponin- has been termed sequentially monoe- York Botanical Garden from 1983-1989, laden, toxic vines. The New World cious and (duo) dichogamy, and is Acevedo pursued graduate studies, with representatives of these vines are a believed by Acevedo to be a natural way Scott Mori (NY) as major professor, and special focus of research by curator to promote gene exchange among popula- received his Ph.D. from the City Univer- Pedro Acevedo-Rodríguez. tions. Altogether a fascinating array of sity of New York in May 1989, writing a Indeed, a mere look at some of the inquiries are presented by the neotropical dissertation on Serjania Sect. Platy- species epithets in the vine genus vines, but an even larger research subject, coccus. -
Plano De Manejo Do Parque Nacional Do Viruâ
PLANO DE MANEJO DO PARQUE NACIONAL DO VIRU Boa Vista - RR Abril - 2014 PRESIDENTE DA REPÚBLICA Dilma Rousseff MINISTÉRIO DO MEIO AMBIENTE Izabella Teixeira - Ministra INSTITUTO CHICO MENDES DE CONSERVAÇÃO DA BIODIVERSIDADE - ICMBio Roberto Ricardo Vizentin - Presidente DIRETORIA DE CRIAÇÃO E MANEJO DE UNIDADES DE CONSERVAÇÃO - DIMAN Giovanna Palazzi - Diretora COORDENAÇÃO DE ELABORAÇÃO E REVISÃO DE PLANOS DE MANEJO Alexandre Lantelme Kirovsky CHEFE DO PARQUE NACIONAL DO VIRUÁ Antonio Lisboa ICMBIO 2014 PARQUE NACIONAL DO VIRU PLANO DE MANEJO CRÉDITOS TÉCNICOS E INSTITUCIONAIS INSTITUTO CHICO MENDES DE CONSERVAÇÃO DA BIODIVERSIDADE - ICMBio Diretoria de Criação e Manejo de Unidades de Conservação - DIMAN Giovanna Palazzi - Diretora EQUIPE TÉCNICA DO PLANO DE MANEJO DO PARQUE NACIONAL DO VIRUÁ Coordenaço Antonio Lisboa - Chefe do PN Viruá/ ICMBio - Msc. Geógrafo Beatriz de Aquino Ribeiro Lisboa - PN Viruá/ ICMBio - Bióloga Superviso Lílian Hangae - DIREP/ ICMBio - Geógrafa Luciana Costa Mota - Bióloga E uipe de Planejamento Antonio Lisboa - PN Viruá/ ICMBio - Msc. Geógrafo Beatriz de Aquino Ribeiro Lisboa - PN Viruá/ ICMBio - Bióloga Hudson Coimbra Felix - PN Viruá/ ICMBio - Gestor ambiental Renata Bocorny de Azevedo - PN Viruá/ ICMBio - Msc. Bióloga Thiago Orsi Laranjeiras - PN Viruá/ ICMBio - Msc. Biólogo Lílian Hangae - Supervisora - COMAN/ ICMBio - Geógrafa Ernesto Viveiros de Castro - CGEUP/ ICMBio - Msc. Biólogo Carlos Ernesto G. R. Schaefer - Consultor - PhD. Eng. Agrônomo Bruno Araújo Furtado de Mendonça - Colaborador/UFV - Dsc. Eng. Florestal Consultores e Colaboradores em reas Tem'ticas Hidrologia, Clima Carlos Ernesto G. R. Schaefer - PhD. Engenheiro Agrônomo (Consultor); Bruno Araújo Furtado de Mendonça - Dsc. Eng. Florestal (Colaborador UFV). Geologia, Geomorfologia Carlos Ernesto G. R. Schaefer - PhD. Engenheiro Agrônomo (Consultor); Bruno Araújo Furtado de Mendonça - Dsc.