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Dissertação apresentada para cumprimento dos requisitos necessários à obtenção do grau de Mestre em História Moderna e dos Descobrimentos

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MARQUES, B.P. (2014) From Strategic Planning to Development Initiatives: a first reflection on the situation of Lisbon and Barcelona, in 20th APDR Congress Proceddings, APDR and UÉvora, Évora, pp. 850-857, ISBN 978-989-8780-01-0.

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The agroindustrial residues including plant tissues rich in polyphenols were explored for microbial production of potent phenolics under solid state fermentation processes. The fungal strains capable of hydrolyzing tannin-rich materials were isolated from Mexican semidesert zones. These microorganisms have been employed to release potent phenolic antioxidants during the solid state fermentation of different materials (pomegranate peels, pecan nut shells, creosote bush and tar bush). This chapter includes the critical parameters for antioxidants production from selective microbes. Technical aspects of the microbial fermentation of antioxidants have also been discussed.

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El desarrollo de actividades industriales, contribuye cada vez más a la generación de residuos con elementos potencialmente tóxicos que en concentraciones altas (fijadas por ley nacional 24051) pueden tener efectos nocivos a la salud de la población y afectaciones al equilibrio ecológico y el ambiente. Hoy existen estudios tendientes a resolver la contaminación originada por metales pesados en suelos, mediante estrategias basadas en el uso de plantas que tienen la propiedad de acumular metales pesados; proceso denominado “fitoremediación” que consiste en la remoción, transferencia, estabilización y/o degradación y neutralización de compuestos orgánicos, inorgánicos y radioactivos que resultan tóxicos en suelos y agua. Esta novedosa tecnología tiene como objetivo degradar y/o asimilar, los metales pesados, presentes en el suelo, lo cual tiene muchas ventajas con respecto a los métodos convencionales de tratamientos de lugares contaminados; en 1º lugar es una tecnología económica, de bajo costo, en 2º lugar posee un impacto regenerativo en lugares en donde se aplica y en 3º lugar su capacidad extractiva se mantiene debido al crecimiento vegetal (Harvey et al., 2002). La fitoremediación no es un remedio para todos los suelos contaminados y antes que esta tecnología pueda volverse técnicamente eficiente y económicamente viable, hay algunas limitaciones que necesitan ser superadas como por ejemplo la falta de pruebas a escala industrial (Freitas et al., 2004). Para la realización del trabajo se utilizarán las instalaciones de la empresa FACSA S.A ubicada en Avda. De las Quintas y De los Hornos de barrio villa Esquiú de Córdoba, empresa operadora de residuos de plomo autorizada por la Secretaría de Ambiente de la Provincia de Córdoba. Se utilizarán dos hectáreas de terreno de la empresa en la que se acumulará un máximo 1 metro cúbico por cada metro cuadrado de superficie. Previamente al deposito de suelo contaminado, el terreno será impermeabilizado con suelo cemento y cal para evitar lixiviaciones de plomo y luego se cercará para evitar ingreso de personal no autorizado. En las hectáreas preparadas se aplicarán capas sucesivas de suelo contaminado con suelo natural en la mitad del terreno y en la otra mitad capaz sucesivas de suelo contaminado y suelo fertilizado con lombricompuesto, ambos sectores serán sembrados con pasto Rye Grass. Durante el proceso se medirá la concentración de Pb por FRX cada tres meses, en tres profundidades para cada preparados de campo. Las muestras serán compuestas y se corresponderán a un mínimo de 5 puntos para cada profundidad. Lo mismo se realizará para medir la concentración de Pb en el pasto. Las cosechas o cortes de pasto serán trimestrales y el pasto cortado se recogerá, secará e incinerará en el propio horno de FACSA S.A. Se evaluarán las siguientes variables. Salinidad: Se realizará antes y al final del año, tomando muestras compuestas de 100g de suelo c/u a las cuales se le agregarán 100 ml de agua destilada, se deja reposar y luego se toma la lectura con la ayuda de un conductímetro calibrado. Acumulación de Pb en tejido vegetal: Se considerará como variable principal la acumulación de Pb en tejido vegetal, ya que integra tanto el grado de absorción del metal por las plantas, así como el efecto negativo que las concentraciones excesivas del metal sobre la producción de materia seca. Para el estudio de esta variable, se captarán y prepararán muestras trimestrales. Secado y protocolo para el análisis de Pb por FRX. Pb en Suelo:Esta variable se examinará trimestralmente, mediante mezcla compuesta de cada sector tomada como mínimo en cinco puntos. Se tomarán muestras a tres profundidades distintas. Ph en Suelo:Se tomarán partes de las muestras para análsis de ph. El experimento culminará a los dos años con análisis de las 9 tandas de mediciones (La 1º corresponde a la determinación de la línea de base). Se realizará la prospección para determinar el momento de perfecta recuperación del suelo.

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Columnar cell apical membranes (CCAM) in series with goblet cell apical membranes (GCAM) form an electroosmotic barrier separating the midgut lumen from epithelial cell cytoplasm. A unique K+ ATPase in GCAM generates three gradients across this barrier. A greater than 180 mV electrical gradient (lumen positive) drives amino acid uptake through voltage-dependent K+ symports. A greater than 1000-fold [H+] gradient (lumen alkaline) and a greater than 10-fold [K+] gradient (lumen concentrated) are adaptations to the high tannin and high K+ content, respectively, in dietary plant material. Agents which act on the apical membrane and disrupt the PD, H+, or K+ gradients are potential insecticides. Insect sensory epithelia and mammalian stria vascularis maintain similar PD and K+ gradients but would not be exposed to ingested anti-apical membrane insecticides. Following the demonstration by Sacchi et al. that Bacillus thuringiensis delta-endotoxin (Bt) induces specifically a K+ conductance increase in CCAM vesicles, we find that the K+ channel blocking agent, Ba2+, completely reverses Bt inhibition of the K+-carried short circuit current in the isolated midgut of Manduca sexta. Progress in characterizing the apical membrane includes finding that fluorosulfonylbenzoyladenosine binds specifically to certain GCAM polypeptides and that CCAM vesicles can be mass produced by Ca2+ or Mg2+ precipitation from Manduca sexta midgut.

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OBJECTIVE: To provide an update to the original Surviving Sepsis Campaign clinical management guidelines, "Surviving Sepsis Campaign Guidelines for Management of Severe Sepsis and Septic Shock," published in 2004. DESIGN: Modified Delphi method with a consensus conference of 55 international experts, several subsequent meetings of subgroups and key individuals, teleconferences, and electronic-based discussion among subgroups and among the entire committee. This process was conducted independently of any industry funding. METHODS: We used the Grades of Recommendation, Assessment, Development and Evaluation (GRADE) system to guide assessment of quality of evidence from high (A) to very low (D) and to determine the strength of recommendations. A strong recommendation (1) indicates that an intervention's desirable effects clearly outweigh its undesirable effects (risk, burden, cost) or clearly do not. Weak recommendations (2) indicate that the tradeoff between desirable and undesirable effects is less clear. The grade of strong or weak is considered of greater clinical importance than a difference in letter level of quality of evidence. In areas without complete agreement, a formal process of resolution was developed and applied. Recommendations are grouped into those directly targeting severe sepsis, recommendations targeting general care of the critically ill patient that are considered high priority in severe sepsis, and pediatric considerations. RESULTS: Key recommendations, listed by category, include early goal-directed resuscitation of the septic patient during the first 6 hrs after recognition (1C); blood cultures before antibiotic therapy (1C); imaging studies performed promptly to confirm potential source of infection (1C); administration of broad-spectrum antibiotic therapy within 1 hr of diagnosis of septic shock (1B) and severe sepsis without septic shock (1D); reassessment of antibiotic therapy with microbiology and clinical data to narrow coverage, when appropriate (1C); a usual 7-10 days of antibiotic therapy guided by clinical response (1D); source control with attention to the balance of risks and benefits of the chosen method (1C); administration of either crystalloid or colloid fluid resuscitation (1B); fluid challenge to restore mean circulating filling pressure (1C); reduction in rate of fluid administration with rising filing pressures and no improvement in tissue perfusion (1D); vasopressor preference for norepinephrine or dopamine to maintain an initial target of mean arterial pressure > or = 65 mm Hg (1C); dobutamine inotropic therapy when cardiac output remains low despite fluid resuscitation and combined inotropic/vasopressor therapy (1C); stress-dose steroid therapy given only in septic shock after blood pressure is identified to be poorly responsive to fluid and vasopressor therapy (2C); recombinant activated protein C in patients with severe sepsis and clinical assessment of high risk for death (2B except 2C for postoperative patients). In the absence of tissue hypoperfusion, coronary artery disease, or acute hemorrhage, target a hemoglobin of 7-9 g/dL (1B); a low tidal volume (1B) and limitation of inspiratory plateau pressure strategy (1C) for acute lung injury (ALI)/acute respiratory distress syndrome (ARDS); application of at least a minimal amount of positive end-expiratory pressure in acute lung injury (1C); head of bed elevation in mechanically ventilated patients unless contraindicated (1B); avoiding routine use of pulmonary artery catheters in ALI/ARDS (1A); to decrease days of mechanical ventilation and ICU length of stay, a conservative fluid strategy for patients with established ALI/ARDS who are not in shock (1C); protocols for weaning and sedation/analgesia (1B); using either intermittent bolus sedation or continuous infusion sedation with daily interruptions or lightening (1B); avoidance of neuromuscular blockers, if at all possible (1B); institution of glycemic control (1B), targeting a blood glucose < 150 mg/dL after initial stabilization (2C); equivalency of continuous veno-veno hemofiltration or intermittent hemodialysis (2B); prophylaxis for deep vein thrombosis (1A); use of stress ulcer prophylaxis to prevent upper gastrointestinal bleeding using H2 blockers (1A) or proton pump inhibitors (1B); and consideration of limitation of support where appropriate (1D). Recommendations specific to pediatric severe sepsis include greater use of physical examination therapeutic end points (2C); dopamine as the first drug of choice for hypotension (2C); steroids only in children with suspected or proven adrenal insufficiency (2C); and a recommendation against the use of recombinant activated protein C in children (1B). CONCLUSIONS: There was strong agreement among a large cohort of international experts regarding many level 1 recommendations for the best current care of patients with severe sepsis. Evidenced-based recommendations regarding the acute management of sepsis and septic shock are the first step toward improved outcomes for this important group of critically ill patients.