974 resultados para 317-U1353B


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A presente dissertação tem dois objetivos, o primeiro é a realização de uma auditoria energética e avaliação da qualidade do ar às instalações de uma Piscina Municipal, permitindo a sua classificação energética, e o segundo é o estudo de propostas de melhoria que contribuam para uma melhor eficiência energética do edifício. Na análise à qualidade do ar interior os parâmetros avaliados encontravam-se todos dentro dos limites estabelecidos por lei, com exceção dos valores de COVs que em dois pontos de medição (ambos na nave) ultrapassaram os limites estabelecidos por lei. A auditoria ao edifício permitiu verificar que o caudal mínimo de água nova nas piscinas imposto por lei é cumprido pela instalação. No que diz respeito ao caudal de ar novo introduzido, este apenas é respeitado quando a unidade de tratamento de ar está a debitar 100% da sua capacidade. Quando a unidade opera a 50% da sua capacidade apresenta um défice de 5% do valor mínimo estabelecido. Relativamente às perdas energéticas associadas aos tanques de natação, estas apresentam um valor de 95,89 kW, em que 59,09 kW dizem respeito às perdas por evaporação. Foi também possível concluir que as perdas por evaporação representam cerca de 39% da energia calorifica produzida nas caldeiras. O edifício apresenta um consumo anual de eletricidade de 166 482 kWh em que 69% deste valor é provocado pelas unidades de tratamento de ar e a iluminação apresenta apenas um peso de 3%. Em relação ao gás natural consumido pelas caldeiras o seu valor anual é de 1 317 240 kWh. A simulação dinâmica do edifício permitiu concluir que este apresenta um IEE de 1 269,9 kWh/m2.ano. O rácio de classe energética (RIEE) é de 1,24 o que significa que o edifício pertence à classe energética C. As medidas estudadas para a melhoria da eficiência energética, nomeadamente integração energética com uma central de ciclo combinado, aplicação de cobertura isotérmica nas piscinas e substituição do telhado na zona da nave, mostraram-se viáveis. O estudo da possibilidade da realização de uma integração energética permitiu concluir que a poupança anual é de 9 374 € e o investimento é recuperado em menos de 1,5 anos. Relativamente à aplicação de cobertura isotérmica o investimento é de 14 000 € e é recuperado em 2 anos. A substituição do telhado na zona da nave tem um investimento de 20 500 € e a recuperação realiza-se num período de 3,5 anos.

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This work describes the ab initio procedure employed to build an activation model for the alpha 1b-adrenergic receptor (alpha 1b-AR). The first version of the model was progressively modified and complicated by means of a many-step iterative procedure characterized by the employment of experimental validations of the model in each upgrading step. A combined simulated (molecular dynamics) and experimental mutagenesis approach was used to determine the structural and dynamic features characterizing the inactive and active states of alpha 1b-AR. The latest version of the model has been successfully challenged with respect to its ability to interpret and predict the functional properties of a large number of mutants. The iterative approach employed to describe alpha 1b-AR activation in terms of molecular structure and dynamics allows further complications of the model to allow prediction and interpretation of an ever-increasing number of experimental data.

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The Mont Collon mafic complex is one of the best preserved examples of the Early Permian magmatism in the Central Alps, related to the intra-continental collapse of the Variscan belt. It mostly consists (> 95 vol.%) of ol+hy-nonnative plagioclase-wehrlites, olivine- and cpx-gabbros with cumulitic structures, crosscut by acid dikes. Pegmatitic gabbros, troctolites and anorthosites outcrop locally. A well-preserved cumulative, sequence is exposed in the Dents de Bertol area (center of intrusion). PT-calculations indicate that this layered magma chamber emplaced at mid-crustal levels at about 0.5 GPa and 1100 degrees C. The Mont Collon cumulitic rocks record little magmatic differentiation, as illustrated by the restricted range of clinopyroxene mg-number (Mg#(cpx)=83-89). Whole-rock incompatible trace-element contents (e.g. Nb, Zr, Ba) vary largely and without correlation with major-element composition. These features are characteristic of an in-situ crystallization process with variable amounts of interstitial liquid L trapped between the cumulus mineral phases. LA-ICPMS measurements show that trace-element distribution in the latter is homogeneous, pointing to subsolidus re-equilibration between crystals and interstitial melts. A quantitative modeling based on Langmuir's in-situ crystallization equation successfully duplicated the REE concentrations in cumulitic minerals of all rock facies of the intrusion. The calculated amounts of interstitial liquid L vary between 0 and 35% for degrees of differentiation F of 0 to 20%, relative to the least evolved facies of the intrusion. L values are well correlated with the modal proportions of interstitial amphibole and whole-rock incompatible trace-element concentrations (e.g. Zr, Nb) of the tested samples. However, the in-situ crystallization model reaches its limitations with rock containing high modal content of REE-bearing minerals (i.e. zircon), such as pegmatitic gabbros. Dikes of anorthositic composition, locally crosscutting the layered lithologies, evidence that the Mont Collon rocks evolved in open system with mixing of intercumulus liquids of different origins and possibly contrasting compositions. The proposed model is not able to resolve these complex open systems, but migrating liquids could be partly responsible for the observed dispersion of points in some correlation diagrams. Absence of significant differentiation with recurrent lithologies in the cumulitic pile of Dents de Bertol points to an efficiently convective magma chamber, with possible periodic replenishment, (c) 2005 Elsevier B.V. All rights reserved.

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Presentan datos de variables físicas, químicas y biológico-pesqueras correspondientes al período 1989-1991 en las áreas del norte y para 1986-88 en el área del Callao.

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TAT-RasGAP317-326, a peptide corresponding to the 317-326 sequence of p120 RasGAP coupled with a cell-permeable TAT-derived peptide, sensitizes the death response of various tumor cells to several anticancer treatments. We now report that this peptide is also able to increase cell adherence, prevent cell migration and inhibit matrix invasion. This is accompanied by a marked modification of the actin cytoskeleton and focal adhesion redistribution. Interestingly, integrins and the small Rho GTP-binding protein, which are well-characterized proteins modulating actin fibers, adhesion and migration, do not appear to be required for the pro-adhesive properties of TAT-RasGAP317-326. In contrast, deleted in liver cancer-1, a tumor suppressor protein, the expression of which is often deregulated in cancer cells, was found to be required for TAT-RasGAP317-326 to promote cell adherence and inhibit migration. These results show that TAT-RasGAP317-326, besides its ability to favor tumor cell death, hampers cell migration and invasion.

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TAT-RasGAP317-326, a cell-permeable 10-amino acid-long peptide derived from the N2 fragment of p120 Ras GTPase-activating protein (RasGAP), sensitizes tumor cells to apoptosis induced by various anticancer therapies. This RasGAP-derived peptide, by targeting the deleted in liver cancer-1 (DLC1) tumor suppressor, also hampers cell migration and invasion by promoting cell adherence and by inhibiting cell movement. Here, we systematically investigated the role of each amino acid within the RasGAP317-326 sequence for the anticancer activities of TAT-RasGAP317-326. We report here that the first three amino acids of this sequence, tryptophan, methionine, and tryptophan (WMW), are necessary and sufficient to sensitize cancer cells to cisplatin-induced apoptosis and to reduce cell migration. The WMW motif was found to be critical for the binding of fragment N2 to DLC1. These results define the interaction mode between the active anticancer sequence of RasGAP and DLC1. This knowledge will facilitate the design of small molecules bearing the tumor-sensitizing and antimetastatic activities of TAT-RasGAP317-326.

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