Lianas Neotropicales, Parte 7
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Redalyc.Géneros De Lamiaceae De México, Diversidad Y Endemismo
Revista Mexicana de Biodiversidad ISSN: 1870-3453 [email protected] Universidad Nacional Autónoma de México México Martínez-Gordillo, Martha; Fragoso-Martínez, Itzi; García-Peña, María del Rosario; Montiel, Oscar Géneros de Lamiaceae de México, diversidad y endemismo Revista Mexicana de Biodiversidad, vol. 84, núm. 1, marzo, 2013, pp. 30-86 Universidad Nacional Autónoma de México Distrito Federal, México Disponible en: http://www.redalyc.org/articulo.oa?id=42526150034 Cómo citar el artículo Número completo Sistema de Información Científica Más información del artículo Red de Revistas Científicas de América Latina, el Caribe, España y Portugal Página de la revista en redalyc.org Proyecto académico sin fines de lucro, desarrollado bajo la iniciativa de acceso abierto Revista Mexicana de Biodiversidad 84: 30-86, 2013 DOI: 10.7550/rmb.30158 Géneros de Lamiaceae de México, diversidad y endemismo Genera of Lamiaceae from Mexico, diversity and endemism Martha Martínez-Gordillo1, Itzi Fragoso-Martínez1, María del Rosario García-Peña2 y Oscar Montiel1 1Herbario de la Facultad de Ciencias, Facultad de Ciencias, Universidad Nacional Autónoma de México. partado postal 70-399, 04510 México, D.F., México. 2Herbario Nacional de México, Instituto de Biología, Universidad Nacional Autónoma de México. Apartado postal 70-367, 04510 México, D.F., México. [email protected] Resumen. La familia Lamiaceae es muy diversa en México y se distribuye con preferencia en las zonas templadas, aunque es posible encontrar géneros como Hyptis y Asterohyptis, que habitan en zonas secas y calientes; es una de las familias más diversas en el país, de la cual no se tenían datos actualizados sobre su diversidad y endemismo. -
A Compilation and Analysis of Food Plants Utilization of Sri Lankan Butterfly Larvae (Papilionoidea)
MAJOR ARTICLE TAPROBANICA, ISSN 1800–427X. August, 2014. Vol. 06, No. 02: pp. 110–131, pls. 12, 13. © Research Center for Climate Change, University of Indonesia, Depok, Indonesia & Taprobanica Private Limited, Homagama, Sri Lanka http://www.sljol.info/index.php/tapro A COMPILATION AND ANALYSIS OF FOOD PLANTS UTILIZATION OF SRI LANKAN BUTTERFLY LARVAE (PAPILIONOIDEA) Section Editors: Jeffrey Miller & James L. Reveal Submitted: 08 Dec. 2013, Accepted: 15 Mar. 2014 H. D. Jayasinghe1,2, S. S. Rajapaksha1, C. de Alwis1 1Butterfly Conservation Society of Sri Lanka, 762/A, Yatihena, Malwana, Sri Lanka 2 E-mail: [email protected] Abstract Larval food plants (LFPs) of Sri Lankan butterflies are poorly documented in the historical literature and there is a great need to identify LFPs in conservation perspectives. Therefore, the current study was designed and carried out during the past decade. A list of LFPs for 207 butterfly species (Super family Papilionoidea) of Sri Lanka is presented based on local studies and includes 785 plant-butterfly combinations and 480 plant species. Many of these combinations are reported for the first time in Sri Lanka. The impact of introducing new plants on the dynamics of abundance and distribution of butterflies, the possibility of butterflies being pests on crops, and observations of LFPs of rare butterfly species, are discussed. This information is crucial for the conservation management of the butterfly fauna in Sri Lanka. Key words: conservation, crops, larval food plants (LFPs), pests, plant-butterfly combination. Introduction Butterflies go through complete metamorphosis 1949). As all herbivorous insects show some and have two stages of food consumtion. -
Apiales, Aquifoliales, Boraginales, , Brassicales, Canellales
Kingdom: Plantae Phylum: Tracheophyta Class: Magnoliopsida Order: Apiales, Aquifoliales, Boraginales, , Brassicales, Canellales, Caryophyllales, Celastrales, Ericales, Fabales, Garryales, Gentianales, Lamiales, Laurales, Magnoliales, Malpighiales, Malvales, Myrtales, Oxalidales, Picramniales, Piperales, Proteales, Rosales, Santalales, Sapindales, Solanales Family: Achariaceae, Anacardiaceae, Annonaceae, Apocynaceae, Aquifoliaceae, Araliaceae, Bignoniaceae, Bixaceae, Boraginaceae, Burseraceae, Calophyllaceae, Canellaceae, Cannabaceae, Capparaceae, Cardiopteridaceae, Caricaceae, Caryocaraceae, Celastraceae, Chrysobalanaceae, Clusiaceae, Combretaceae, Dichapetalaceae, Ebenaceae, Elaeocarpaceae, Emmotaceae, Erythroxylaceae, Euphorbiaceae, Fabaceae, Goupiaceae, Hernandiaceae, Humiriaceae, Hypericaceae, Icacinaceae, Ixonanthaceae, Lacistemataceae, Lamiaceae, Lauraceae, Lecythidaceae, Lepidobotryaceae, Linaceae, Loganiaceae, Lythraceae, Malpighiaceae, Malvaceae, Melastomataceae, Meliaceae, Monimiaceae, Moraceae, Myristicaceae, Myrtaceae, Nyctaginaceae, Ochnaceae, Olacaceae, Oleaceae, Opiliaceae, Pentaphylacaceae, Phyllanthaceae, Picramniaceae, Piperaceae, Polygonaceae, Primulaceae, Proteaceae, Putranjivaceae, Rhabdodendraceae, Rhamnaceae, Rhizophoraceae, Rosaceae, Rubiaceae, Rutaceae, Sabiaceae, Salicaceae, Sapindaceae, Sapotaceae, Simaroubaceae, Siparunaceae, Solanaceae, Stemonuraceae, Styracaceae, Symplocaceae, Ulmaceae, Urticaceae, Verbenaceae, Violaceae, Vochysiaceae Genus: Abarema, Acioa, Acosmium, Agonandra, Aiouea, Albizia, Alchornea, -
Outline of Angiosperm Phylogeny
Outline of angiosperm phylogeny: orders, families, and representative genera with emphasis on Oregon native plants Priscilla Spears December 2013 The following listing gives an introduction to the phylogenetic classification of the flowering plants that has emerged in recent decades, and which is based on nucleic acid sequences as well as morphological and developmental data. This listing emphasizes temperate families of the Northern Hemisphere and is meant as an overview with examples of Oregon native plants. It includes many exotic genera that are grown in Oregon as ornamentals plus other plants of interest worldwide. The genera that are Oregon natives are printed in a blue font. Genera that are exotics are shown in black, however genera in blue may also contain non-native species. Names separated by a slash are alternatives or else the nomenclature is in flux. When several genera have the same common name, the names are separated by commas. The order of the family names is from the linear listing of families in the APG III report. For further information, see the references on the last page. Basal Angiosperms (ANITA grade) Amborellales Amborellaceae, sole family, the earliest branch of flowering plants, a shrub native to New Caledonia – Amborella Nymphaeales Hydatellaceae – aquatics from Australasia, previously classified as a grass Cabombaceae (water shield – Brasenia, fanwort – Cabomba) Nymphaeaceae (water lilies – Nymphaea; pond lilies – Nuphar) Austrobaileyales Schisandraceae (wild sarsaparilla, star vine – Schisandra; Japanese -
Pharmacognosy
Pharmacognosy Third stage Dr. Enass Najem 2nd semester Lec:8 ERGOT, ERGOT ALKALOIDS, AND LSD When the parasitic fungus Claviceps purpurea lives on rye and other cereal crops, a poisonous alkaloid and called ergot is produced. Ergot was the subject of great fear previously, because people who ate rye products infected with this, fungus experienced a strange and debilitating, and frequently lethal, disease. Ergot contains alkaloids that contract the blood vessels of arms and legs, preventing circulation of the blood, and gangrene results. Thus, people suffering from ergot poisoning lost their hands and legs without bleeding (ergotism), after they became darkened. Although it was well known that ergot was very dangerous, midwives in Europe were also using it for promotion of the contraction of the womb post-parturition. Subsequently, studies of the active principle(s) of ergot responsible for the contractions were initiated. The first alkaloid isolated in crystalline form was ergotinine , but it did not possess the uterocontracting activity. Ergotoxine was the first biologically active alkaloid isolated, and was shown to be a mixture of ergocristine, ergocornine, and related alkaloids. Ergotamine was isolated later in a pure form. The common skeleton of these ergot alkaloids is known as lysergic acid, and ergotamine comprises a structure based on lysergic acid coupled with a peptide moiety. The universal skeleton of the ergot alkaloids is known as the ergoline nucleus. It was shown by using cultivated Claviceps that the ergoline skeleton was derived biosynthetically from tryptophan and a C5 unit of mevalonic acid origin. 1 Pharmacognosy Simple lysergic acid amides, such as ergine and lysergic acid hydroxyethylamide, are obtained from the ergot that lives on wild grass. -
Lições Das Interações Planta – Beija-Flor
UNIVERSIDADE ESTADUAL DE CAMPINAS INSTITUTO DE BIOLOGIA JÉFERSON BUGONI REDES PLANTA-POLINIZADOR NOS TRÓPICOS: LIÇÕES DAS INTERAÇÕES PLANTA – BEIJA-FLOR PLANT-POLLINATOR NETWORKS IN THE TROPICS: LESSONS FROM HUMMINGBIRD-PLANT INTERACTIONS CAMPINAS 2017 JÉFERSON BUGONI REDES PLANTA-POLINIZADOR NOS TRÓPICOS: LIÇÕES DAS INTERAÇÕES PLANTA – BEIJA-FLOR PLANT-POLLINATOR NETWORKS IN THE TROPICS: LESSONS FROM HUMMINGBIRD-PLANT INTERACTIONS Tese apresentada ao Instituto de Biologia da Universidade Estadual de Campinas como parte dos requisitos exigidos para a obtenção do Título de Doutor em Ecologia. Thesis presented to the Institute of Biology of the University of Campinas in partial fulfillment of the requirements for the degree of Doctor in Ecology. ESTE ARQUIVO DIGITAL CORRESPONDE À VERSÃO FINAL DA TESE DEFENDIDA PELO ALUNO JÉFERSON BUGONI E ORIENTADA PELA DRA. MARLIES SAZIMA. Orientadora: MARLIES SAZIMA Co-Orientador: BO DALSGAARD CAMPINAS 2017 Campinas, 17 de fevereiro de 2017. COMISSÃO EXAMINADORA Profa. Dra. Marlies Sazima Prof. Dr. Felipe Wanderley Amorim Prof. Dr. Thomas Michael Lewinsohn Profa. Dra. Marina Wolowski Torres Prof. Dr. Vinícius Lourenço Garcia de Brito Os membros da Comissão Examinadora acima assinaram a Ata de Defesa, que se encontra no processo de vida acadêmica do aluno. DEDICATÓRIA À minha família por me ensinar o amor à natureza e a natureza do amor. Ao povo brasileiro por financiar meus estudos desde sempre, fomentando assim meus sonhos. EPÍGRAFE “Understanding patterns in terms of the processes that produce them is the essence of science […]” Levin, S.A. (1992). The problem of pattern and scale in ecology. Ecology 73:1943–1967. AGRADECIMENTOS Manifestar a gratidão às tantas pessoas que fizeram parte direta ou indiretamente do processo que culmina nesta tese não é tarefa trivial. -
Tansley Review Evolution of Development of Vascular Cambia and Secondary Growth
New Phytologist Review Tansley review Evolution of development of vascular cambia and secondary growth Author for correspondence: Rachel Spicer1 and Andrew Groover2 Andrew Groover 1The Rowland Institute at Harvard, Cambridge, MA, USA; 2Institute of Forest Genetics, Pacific Tel: +1 530 759 1738 Email: [email protected] Southwest Research Station, USDA Forest Service, Davis, CA, USA Received: 29 December 2009 Accepted: 14 February 2010 Contents Summary 577 V. Evolution of development approaches for the study 587 of secondary vascular growth I. Introduction 577 VI. Conclusions 589 II. Generalized function of vascular cambia and their 578 developmental and evolutionary origins Acknowledgements 589 III. Variation in secondary vascular growth in angiosperms 581 References 589 IV. Genes and mechanisms regulating secondary vascular 584 growth and their evolutionary origins Summary New Phytologist (2010) 186: 577–592 Secondary growth from vascular cambia results in radial, woody growth of stems. doi: 10.1111/j.1469-8137.2010.03236.x The innovation of secondary vascular development during plant evolution allowed the production of novel plant forms ranging from massive forest trees to flexible, Key words: forest trees, genomics, Populus, woody lianas. We present examples of the extensive phylogenetic variation in sec- wood anatomy, wood formation. ondary vascular growth and discuss current knowledge of genes that regulate the development of vascular cambia and woody tissues. From these foundations, we propose strategies for genomics-based research in the evolution of development, which is a next logical step in the study of secondary growth. I. Introduction this pattern characterizes most extant forest trees, significant variation exists among taxa, ranging from extinct woody Secondary vascular growth provides a means of radially lycopods and horsetails with unifacial cambia (Cichan & thickening and strengthening plant axes initiated during Taylor, 1990; Willis & McElwain, 2002), to angiosperms primary, or apical growth. -
Temporal and Spatial Origin of Gesneriaceae in the New World Inferred from Plastid DNA Sequences
bs_bs_banner Botanical Journal of the Linnean Society, 2013, 171, 61–79. With 3 figures Temporal and spatial origin of Gesneriaceae in the New World inferred from plastid DNA sequences MATHIEU PERRET1*, ALAIN CHAUTEMS1, ANDRÉA ONOFRE DE ARAUJO2 and NICOLAS SALAMIN3,4 1Conservatoire et Jardin botaniques de la Ville de Genève, Ch. de l’Impératrice 1, CH-1292 Chambésy, Switzerland 2Centro de Ciências Naturais e Humanas, Universidade Federal do ABC, Rua Santa Adélia, 166, Bairro Bangu, Santo André, Brazil 3Department of Ecology and Evolution, University of Lausanne, CH-1015 Lausanne, Switzerland 4Swiss Institute of Bioinformatics, Quartier Sorge, CH-1015 Lausanne, Switzerland Received 15 December 2011; revised 3 July 2012; accepted for publication 18 August 2012 Gesneriaceae are represented in the New World (NW) by a major clade (c. 1000 species) currently recognized as subfamily Gesnerioideae. Radiation of this group occurred in all biomes of tropical America and was accompanied by extensive phenotypic and ecological diversification. Here we performed phylogenetic analyses using DNA sequences from three plastid loci to reconstruct the evolutionary history of Gesnerioideae and to investigate its relationship with other lineages of Gesneriaceae and Lamiales. Our molecular data confirm the inclusion of the South Pacific Coronanthereae and the Old World (OW) monotypic genus Titanotrichum in Gesnerioideae and the sister-group relationship of this subfamily to the rest of the OW Gesneriaceae. Calceolariaceae and the NW genera Peltanthera and Sanango appeared successively sister to Gesneriaceae, whereas Cubitanthus, which has been previously assigned to Gesneriaceae, is shown to be related to Linderniaceae. Based on molecular dating and biogeographical reconstruction analyses, we suggest that ancestors of Gesneriaceae originated in South America during the Late Cretaceous. -
Bosque Pehuén Park's Flora: a Contribution to the Knowledge of the Andean Montane Forests in the Araucanía Region, Chile Author(S): Daniela Mellado-Mansilla, Iván A
Bosque Pehuén Park's Flora: A Contribution to the Knowledge of the Andean Montane Forests in the Araucanía Region, Chile Author(s): Daniela Mellado-Mansilla, Iván A. Díaz, Javier Godoy-Güinao, Gabriel Ortega-Solís and Ricardo Moreno-Gonzalez Source: Natural Areas Journal, 38(4):298-311. Published By: Natural Areas Association https://doi.org/10.3375/043.038.0410 URL: http://www.bioone.org/doi/full/10.3375/043.038.0410 BioOne (www.bioone.org) is a nonprofit, online aggregation of core research in the biological, ecological, and environmental sciences. BioOne provides a sustainable online platform for over 170 journals and books published by nonprofit societies, associations, museums, institutions, and presses. Your use of this PDF, the BioOne Web site, and all posted and associated content indicates your acceptance of BioOne’s Terms of Use, available at www.bioone.org/page/terms_of_use. Usage of BioOne content is strictly limited to personal, educational, and non-commercial use. Commercial inquiries or rights and permissions requests should be directed to the individual publisher as copyright holder. BioOne sees sustainable scholarly publishing as an inherently collaborative enterprise connecting authors, nonprofit publishers, academic institutions, research libraries, and research funders in the common goal of maximizing access to critical research. R E S E A R C H A R T I C L E ABSTRACT: In Chile, most protected areas are located in the southern Andes, in mountainous land- scapes at mid or high altitudes. Despite the increasing proportion of protected areas, few have detailed inventories of their biodiversity. This information is essential to define threats and develop long-term • integrated conservation programs to face the effects of global change. -
Preliminary Phytochemistry, Antibacterial and Antifungal Properties of Extracts of Asystasia Gangetica Linn T. Anderson Grown in Nigeria
Available online a t www.pelagiaresearchlibrary.com Pelagia Research Library Advances in Applied Science Research, 2011, 2 (3): 219-226 ISSN: 0976-8610 CODEN (USA): AASRFC Preliminary Phytochemistry, Antibacterial and Antifungal Properties of extracts of Asystasia gangetica Linn T. Anderson grown in Nigeria A. A. Hamid 1* , O. O. Aiyelaagbe 2, R. N. Ahmed 3, L. A. Usman 1 and S. A. Adebayo 1 1Department of Chemistry, University of Ilorin, P.M.B. 1515, Ilorin, Nigeria 2Department of Chemistry, University of Ibadan, Ibadan, Nigeria 3Department of Microbiology, University of Ilorin, P.M.B. 1515, Ilorin, Nigeria ______________________________________________________________________________ ABSTRACT The hexane, ethylacetate and methanol extracts obtained from the whole plant of Asystasia gangetica were evaluated invitro to determine inhibition of human pathogenic microorganisms made up of six bacteria and six fungi. The crude extracts inhibited the growth of twelve test organisms to different degrees. All the bacteria strains were sensitive to all the extracts at concentration ranging from 50 to 200mg/mL using the agar diffusion pour plate method. The inhibition of these test organisms were concentration dependent, activity being higher at higher concentrations of all the three extracts. The extracts showed higher antifungal properties on Candida albicans, Penicillum notatum, Tricophyton rubrum and Epidermophyton floccosum with activity comparable to that of the reference drug, Tioconazole. Preliminary phytochemical investigation of the extracts revealed the presence of saponins, reducing sugar, steroids, glycosides, flavonoids and anthraquinones. Keywords: A. gangetica, bioactivity, phytochemical screening, agar diffusion method. _____________________________________________________________________________ INTRODUCTION Asystasia comprises about 50 species, and is distributed in tropics of the old world, with about 30 species in tropical Africa [1,2,3 ]. -
Pollen Morphology of Fridericia Mart. (Bignoniaceae) from Brazilian Forest Fragments
Braz. J. Bot (2014) 37(1):83–94 DOI 10.1007/s40415-013-0042-1 Pollen morphology of Fridericia Mart. (Bignoniaceae) from Brazilian forest fragments Cintia Neves de Souza • Eduardo Custo´dio Gasparino Received: 18 October 2013 / Accepted: 3 December 2013 / Published online: 17 December 2013 Ó Botanical Society of Sao Paulo 2013 Abstract A pollen morphology study of 10 Brazilian Introduction native species of Fridericia (Bignoniaceae) from forest fragments was performed using light microscopy and The fragmentation process of forest habitats has increased scanning electron microscopy, in search of new characters in most ecosystems particularly in the tropics, so this has that might increase knowledge of pollen morphology of the caused, in general, the loss of the biodiversity (Turner species, and also to help the taxonomic characterization of 1996; Myers et al. 2000). The northwestern of Sa˜o Paulo the genus. The pollen grains were acetolysed, measured, State, Brazil, is a region consisting of vegetation that photographed, and described qualitatively. The quantitative includes small fragments of semideciduous forest and large data were analyzed by descriptive statistics and multivar- areas of Cerrado (Kronka et al. 1993). This structure is a iate statistics. Non-acetolysed pollen grains were observed result of fragmentation in natural forest (Atlantic Forest of under scanning electron microscopy for further details of Brazil), which currently only take up 5 % of the original exine and pollen surface. The pollen grains are isopolar, forest -
Bignoniaceae 1.3.3.3.6.A
111 1.3.3.3.6. Bignoniaceae 1.3.3.3.6.a. Características ¾ Porte: árboles, arbustos y lianas, ramas a menudo lenticeladas. ¾ Hojas: generalmente opuestas, decusadas, a menudo compuestas, con un folíolo en las hojas de las trepadoras, transformado en un zarcillo. ¾ Flores: perfectas, muy vistosas, apenas zigomorfas hasta sub-bilabiadas generalmente en inflorescencias cimosas. ¾ Perianto: cáliz 5-mero, tubuloso, acampanado, espatiforme, truncado o acodado a veces bilabiado, corola 5-lobulada, acampanada-embudada algo doblada, con la misma estructura básica. ¾ Androceo: 4 (2) estambres didínamos, insertos en el tubo corolino, estaminodio 1 (rara vez 3), más cortos que los estambres (en Jacaranda más desarrollado y barbado), con los filamentos recurvos (los estambres ausentes pueden estar reemplazados por estaminodios); anteras con 2 tecas característicamente divergentes. ¾ Gineceo: ovario súpero, 2 carpelos soldados, 2 (1-3) locular con numerosos óvulos axilares, generalmente con largo estilo y estigma bilobado, a menudo papiloso, se puede presentar un disco nectarífero. ¾ Fruto: cápsula septicida o loculicida, rara vez baya. ¾ Semilla: sin endosperma, aplanadas, aladas, con ala lateral o circular, hialina o laciniada. Jacaranda mimosifolia Handroanthus heptaphyllus Flor con pétalos y sépalos soldados Corola Corte longitudinal de la flor con estambres y estaminodio Corte longitudinal de la flor Semilla alada Cáliz con ovario Fruto Semilla alada Detalle del estaminodio Cáliz y gineceo Dibujos: Daniel Cian 3.3.6.b. Biología Floral: Tecoma stans posee polinización entomófila u ornitófila (Lahitte et al., 2001). Diversidad Vegetal- Facultad de Ciencias Exactas y Naturales y Agrimensura (UNNE) CORE EUDICOTILEDÓNEAS- Asterídeas-Euasterídeas I: Lamiales: Bignoniaceae 112 1.3.3.3.6.c.