228 resultados para Symphonia globulifera
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Se describen las características de las principales maderas tropicales con uso en España. La descripción incluye el nombre científico, sinonimias, nombres vulgares, su distribución en el mundo y en España, la descripción del fuste y de las trozas, con sus defectos más característicos, la descripción de la madera, sus características físicas, mecánicas, resistentes y durables. También se incluye sus aspectos tecnológicos, en el sentido de indicar que aspectos deben considerarse a la hora de trabajar estas maderas. Por último se indican los usos más comunes de las distintas maderas, las ventajas e inconvenientes frente a otras maderas Las especies principales que se describen son las siguientes: Algarrobo blanco, Prosopis alba, Grisebach Andiroba, Carapa guianensis, Aubl. Balsamo, Myroxylon balsamun, Harms. Sandwith. Barba jolote, Pithecolobium arboreum (L), Urban. Bubinga, Guibourtia tessmanii Caoba, Swietenia macrophylla, King. Cedro, Cedrela odorata, L. Cenizaro, Pithecellobium saman, (Jacq.) Benth Chinchon, Guarea grandiflora, A. DC. Cocobolo, Dalbergia retusa, Hemsl Cristobal, Platysmicium polystachyum Elondo o tali, Erythrophleum ivorensis Espavé, Anacardium excelsum, Skeels Gonzalo Alves, Astronium graveolens, Jacquin. Guayabillo, Terminalia lucida, Hoff. Guapaque, Dialium guianense, (Aubl.) Sandwith. Guayacán, Guaiacum sanctum, L. Huesito Homalium racemosum, Jacq. Ipe, Tabebuia guayacan, Hemsl. Iroko, Milicia excelsa Sim Jatoba, Hymenaea courbaril L. Machiche, Lonchocarpus castilloi, Standley. Manil, Symphonia globulifera, L. Marupa, Simarouba glauca, DC. Melina, Gmelina arborea, Roxb. Mongoy, Guibourtia ehie J. Léonard Nance, Byrsonima crassifolia (L.), H.B.K. Nazareno, Peltogyne purpurea Nispero, Manilkara zapota, (L.) Van royen. Palo blanco, Cybitax donnell- smith , Seibert. Pino amarillo, Erblichia odorata Piojo, Tapirira guianensis, Aubl. Quaruba, Vochysia guatemalensis, Donnell Smith Quira, Platysmicium pinnatum. Redondo, Magnolia yoroconte, Dandy. Rosul, Dalbergia tucurensis, Donn-Smith. Sande, Brossimiun ssp San juan areno, Ilex ssp. Saqui-saqui, Bombacopsis quinatum, (Jacq.) Dugand Santa maría, Calophyllum brasílíense Camb. Sapelly, Entandrophragma cylindricum Sprague Tamboril, Enterolobium cyclocarpum, Gris Teca, Tectona grandis, L.F.. Ukola, Tieghemella africana Ururucana, Hieronyma alchorneoides, Allem
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The areas of marine pollen deposition are related to the pollen source areas by aeolian and fluvial transport regimes, whereas wind transport is much more important than river transport. Pollen distribution patterns of Pinus, Artemisia, Chenopodiaceae-Amaranthaceae, and Asteraceae Tubuliflorae trace atmospheric transport by the northeast trades. Pollen transport by the African Easterly Jet is reflected in the pollen distribution patterns of Chenopodiaceae-Amaranthaceae, Asteraceae Tubuliflorae, and Mitracarpus. Grass pollen distribution registers the latitudinal extension of Sahel, savannas and dry open forests. Marine pollen distribution patterns of Combretaceae-Melastomataceae, Alchornea, and Elaeis reflect the extension of wooded grasslands and transitional forests. Pollen from the Guinean-Congolian/Zambezian forest and from the Sudanian/Guinean vegetation zones mark the northernmost extension of the tropical rain forest. Rhizophora pollen in marine sediments traces the distribution of mangrove swamps. Only near the continent, pollen of Rhizophora, Mitracarpus, Chenopodiaceae-Amaranthaceae, and pollen from the Sudanian and Guinean vegetation zones are transported by the Upwelling Under Current and the Equatorial Under Current, where those currents act as bottom currents. The distribution of pollen in marine sediments, reflecting the position of major climatic zones (desert, dry tropics, humid tropics), can be used in tracing climatic changes in the past.
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The deep-sea cores M 16415-2 and M 16416-2 at about 9°N off Sierra Leone were analysed palynologically for the time interval 140,000-70,000 yr B.P. Results were presented in absolute (pollen concentration and pollen influx) and relative diagrams (pollen percentage). In a previous study it was evidenced that in northwest Africa pollen is mainly transported to the Atlantic by wind, so that the efficiency of aeolian pollen transport (pollen flux) could be used to evaluate changes in the intensity of the northeast trade winds. The glacial episodes (represented by the oxygen isotope stages 6 and 4) are characterized by strong northeast trade winds, whereas the last interglacial (stage 5) is characterized by weak trade winds. The pollen influx diagram shows that the intensity of the trade winds increased slightly during the relatively cool intervals of stage 5 (viz. 5.4 and 5.2). Tropical forest had maximally expanded around 124,000 yr B.P. (stage 5.5), around 98,000 yr B.P. (transition of stage 5.3 to 5.2), and around 70,000 yr B.P. (first part of stage 4): an increasing delay of the response of tropical forest to global intervals with maximum temperature is apparent during the last interglacial. As tropical forests need continuous humidity, the record of tropical forest monitors changes in climatic humidity south of the Sahara. During the last interglacial, the southern boundary of the Sahara shifted only little: expansions and contractions of the tropical forest area are correlated with contra-oscillations of the grass-dominated savanna zone. Great latitudinal shifts of the desert savanna boundary, on the contrary, occurred during the penultimate glacial interglacial transition (around 128,000 yr B.P.) to the north, and during the last interglacial-glacial transition (around 65,000 yr B.P.) to the south.
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Palynological data of the marine core M 16415-2 show latitudinal shifts of the northern fringe of the tropical rain forest in north-west Africa during the last 700 ka. Savanna and dry open forest expanded southwards and tropical rain forest expanded northwards during dry and humid periods, respectively. Until 220 ka B.P., the tropical rain forest probably kept its zonal character in West Africa during glacials and interglacials. It is only during the last two glacial periods that the rain forest possibly fragmented into refugia. Throughout the Brunhes chron, pollen and spore transport was mainly by trade winds.
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1974
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Mode of access: Internet.
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The relationship between the religious and political fields in the Orthodox Church is defined by the concept of symphonia which dates back to the Byzantine Empire. The concept suggests that the religious and political authorities should work together in a symphonic agreement towards achieving the material and spiritual welfare of the faithful. This article argues that an investigation of the theory of sign and symbol offers a better understanding of symphonia and, in particular, of its relationship with the nation-building process. From this perspective, by corroborating the data provided by the European Values Survey from 1990 to 2000 with this theory, this article demonstrates that the enlargement of the European Union represents the most significant challenge to symphonia, shifting its national focus to a supranational level. © 2011 Taylor & Francis.
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Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
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Pós-graduação em Letras - IBILCE
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Vorlage d. Digitalisats aus d. Besitz d. Theol. Hochschule St. Georgen
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Benthic foraminifers of the Coniacian-Santonian through the Paleocene were recovered from a continuous pelagic carbonate section from Hole 516F on the Rio Grande Rise. Sixty-five genera and 153 species have been identified, most of which have been reported from other localities. Bathyal depths are reflected in the benthic assemblages dominated by gavelinellids (Gavelinella beccariiformis, G. velascoensis), Nuttallides truempyi, and various gyroidinids and buliminids. Rapid subsidence during the Coniacian-Santonian from nearshore to upper to middle bathyal depths was followed by much reduced subsidence, with the Campanian-Paleocene interval accumulating at middle bathyal to lower bathyal depths. A census study based on detailed sampling reveals major changes in benthic faunal composition at the Cretaceous/Tertiary boundary transition. It was a time of rapid turnover, with the extinctions of numerous species and the introduction of many new species. Overall, species diversity decreases about 20%, and approximately one-third of latest Maestrichtian species do not survive to the end of the Cretaceous. This shift indicates a significant environmental change in the deep sea, the precise nature of which is not apparent from the foraminifers or their enclosing sediments.