944 resultados para Medium Access Control (MAC)


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A presente dissertação insere-se no âmbito da unidade curricular “ Dissertação” do 2º ano do mestrado em Engenharia Eletrotécnica – Sistemas Elétricos de Energia. Com o aumento crescente do número de consumidores de energia, é cada vez mais imperioso a adoção de medidas de racionalização e gestão dos consumos da energia elétrica. Existem diferentes tipos de dificuldades no planeamento e implementação de novas centrais produtoras de energia renovável, pelo que também por este motivo é cada vez mais importante adoção de medidas de gestão de consumos, quer ao nível dos clientes alimentados em média tensão como de baixa tensão. Desta forma será mais acessível a criação de padrões de eficiência energética elevados em toda a rede de distribuição de energia elétrica. Também a economia é afetada por uma fraca gestão dos consumos por parte dos clientes. Elevados desperdícios energéticos levam a que mais energia tenha que ser produzida, energia essa que contribui ainda mais para a elevada taxa de dependência energética em Portugal, e para o degradar da economia nacional. Coloca-se assim a necessidade de implementar planos e métodos que promovam a eficiência energética e a gestão racional de consumos de energia elétrica. Apresenta-se nesta dissertação várias propostas, algumas na forma de projetos já em execução, que visam sensibilizar o consumidor para a importância da utilização eficiente de energia e, ao mesmo tempo, disponibilizam as ferramentas tecnológicas adequadas para auxiliar a implementação dos métodos propostos. Embora os planos apresentados, sobejamente conhecidos, tenham imensa importância, a implementação nos vários consumidores de sistemas capazes de efetivamente reduzir consumos tem um papel fundamental. Equipamentos de gestão de consumos, que são apresentados nesta dissertação, permitem ao consumidor aceder diretamente ao seu consumo. Podem aceder não apenas ao consumo global da instalação mas também ao consumo específico por equipamento, permitindo perceber onde se verifica a situação mais desfavorável. Funcionalidades de programação de perfis tipo, com limitações de potência em vários períodos horários, bem como possibilidades de controlo remoto com recurso a aplicações para Smartphones permitem a redução de consumos ao nível da rede de distribuição e, desta forma, contribuir para a redução dos desperdícios e da dependência energética em Portugal. No âmbito do trabalho de dissertação é desenvolvida uma metodologia de comercialização de potência, que é apresentada nesta tese. Esta metodologia propõem que o consumidor, em função dos seus consumos, pague apenas a quantidade de potência que efetivamente necessita num certo período de tempo. Assim, o consumidor deixa de pagar uma tarifa mensal fixa associada á sua potência contratada, e passará a pagar um valor correspondente apenas à potência que efetivamente solicitou em todas as horas durante o mês. Nesta metodologia que é apresentada, o consumidor poderá também fazer uma análise do seu diagrama de cargas e simular uma alteração da sua tarifa, tarifa esta que varia entre tarifa simples, bi-horária semanal, bi-horária diária, tri-horária semanal ou tri-horária diária, de forma a perceber em qual destas pagará um menor valor pela mesma energia. De forma a que o consumidor possa perceber se haverá vantagem de uma alteração para uma potência contratada flexível, ou para uma outra tarifa associada á energia, tem ao seu dispor uma ferramenta, que em função dos seus consumos, permite retirar conclusões sobre o preço final a pagar na fatura, após cada tipo de alteração. Esta ferramenta foi validada com recurso a várias simulações, para diferentes perfis de consumidores. Desta forma, o utilizador fica a perceber que realmente pode poupar com uma potência contratada flexível, ao mesmo tempo que pode identificar-se com um perfil de simulação e, mais facilmente, perceber para que alteração tarifária pode usufruir de uma maior poupança.

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Tese apresentada como requisito parcial para obtenção do grau de Doutor em Gestão de Informação

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Patients who develop a severe stenosis in biological pulmonary conduits previously implanted for pulmonary outflow trunk reconstructions are treated either by surgical re-replacement, or by transcatheter stent-valve implantation through a femoral vein access. A catheter-based sub-xyphoidian access through the right ventricle for stent-valve positioning in a pulmonary conduit has rarely been proposed. We describe the case of a 20-year-old man who underwent a pulmonary trunk reconstruction for a congenital pulmonary valve dysplasia and a few years later developed a stenosis in the pulmonary conduit. He was successfully treated with a 23 mm Edwards Sapien stent-valve implantation in pulmonary position, through an unusual right ventricular, sub-xyphoidian access and without contrast medium injections and pleura opening.

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Specific metabolic pathways are activated by different nutrients to adapt the organism to available resources. Although essential, these mechanisms are incompletely defined. Here, we report that medium-chain fatty acids contained in coconut oil, a major source of dietary fat, induce the liver ω-oxidation genes Cyp4a10 and Cyp4a14 to increase the production of dicarboxylic fatty acids. Furthermore, these activate all ω- and β-oxidation pathways through peroxisome proliferator activated receptor (PPAR) α and PPARγ, an activation loop normally kept under control by dicarboxylic fatty acid degradation by the peroxisomal enzyme L-PBE. Indeed, L-pbe(-/-) mice fed coconut oil overaccumulate dicarboxylic fatty acids, which activate all fatty acid oxidation pathways and lead to liver inflammation, fibrosis, and death. Thus, the correct homeostasis of dicarboxylic fatty acids is a means to regulate the efficient utilization of ingested medium-chain fatty acids, and its deregulation exemplifies the intricate relationship between impaired metabolism and inflammation.

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Whereas the role of the anterior cingulate cortex (ACC) in cognitive control has received considerable attention, much less work has been done on the role of the ACC in autonomic regulation. Its connections through the vagus nerve to the sinoatrial node of the heart are thought to exert modulatory control over cardiovascular arousal. Therefore, ACC is not only responsible for the implementation of cognitive control, but also for the dynamic regulation of cardiovascular activity that characterizes healthy heart rate and adaptive behaviour. However, cognitive control and autonomic regulation are rarely examined together. Moreover, those studies that have examined the role of phasic vagal cardiac control in conjunction with cognitive performance have produced mixed results, finding relations for specific age groups and types of tasks but not consistently. So, while autonomic regulatory control appears to support effective cognitive performance under some conditions, it is not presently clear just what factors contribute to these relations. The goal of the present study was, therefore, to examine the relations between autonomic arousal, neural responsivity, and cognitive performance in the context of a task that required ACC support. Participants completed a primary inhibitory control task with a working memory load embedded. Pre-test cardiovascular measures were obtained, and ontask ERPs associated with response control (N2/P3) and error-related processes (ERN/Pe) were analyzed. Results indicated that response inhibition was unrelated to phasic vagal cardiac control, as indexed by respiratory sinus arrhythmia (RSA). However, higher resting RSA was associated with larger ERN ampUtude for the highest working memory load condition. This finding suggests that those individuals with greater autonomic regulatory control exhibited more robust ACC error-related responses on the most challenging task condition. On the other hand, exploratory analyses with rate pressure product (RPP), a measure of sympathetic arousal, indicated that higher pre-test RPP (i.e., more sympathetic influence) was associated with more errors on "catch" NoGo trials, i.e., NoGo trials that simultaneously followed other NoGo trials, and consequently, reqviired enhanced response control. Higher pre-test RPP was also associated with smaller amplitude ERNs for all three working memory loads and smaller ampUtude P3s for the low and medium working memory load conditions. Thus, higher pretest sympathetic arousal was associated with poorer performance on more demanding "catch" NoGo trials and less robust ACC-related electrocortical responses. The findings firom the present study highlight tiie interdependence of electrocortical and cardiovascular processes. While higher pre-test parasympathetic control seemed to relate to more robust ACC error-related responses, higher pre-test sympathetic arousal resulted in poorer inhibitory control performance and smaller ACC-generated electrocortical responses. Furthermore, these results provide a base from which to explore the relation between ACC and neuro/cardiac responses in older adults who may display greater variance due to the vulnerabihty of these systems to the normal aging process.

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Both learning and basic biological mechanisms have been shown to play a role in the control of protein int^e. It has previously been shown that rats can adapt their dietary selection patterns successfully in the face of changing macronutrient requirements and availability. In particular, it has been demonstrated that when access to dietary protein is restricted for a period of time, rats selectively increase their consumption of a proteincontaining diet when it becomes available. Furthermore, it has been shown that animals are able to associate various orosensory cues with a food's nutrient content. In addition to the role that learning plays in food intake, there are also various biological mechanisms that have been shown to be involved in the control of feeding behaviour. Numerous studies have documented that various hormones and neurotransmitter substances mediate food intake. One such hormone is growth hormone-releasing factor (GRF), a peptide that induces the release of growth hormone (GH) from the anterior pituitary gland. Recent research by Vaccarino and Dickson ( 1 994) suggests that GRF may stimulate food intake by acting as a neurotransmitter in the suprachiasmatic nucleus (SCN) and the adjacent medial preoptic area (MPOA). In particular, when GRF is injected directly into the SCN/MPOA, it has been shown to selectively enhance the intake of protein in both fooddeprived and sated rats. Thus, GRF may play a role in activating protein consumption generally, and when animals have a need for protein, GRF may serve to trigger proteinseeking behaviour. Although researchers have separately examined the role of learning and the central mechanisms involved in the control of protein selection, no one has yet attempted to bring together these two lines of study. Thus, the purpose of this study is to join these two parallel lines of research in order to further our understanding of mechanisms controlling protein selection. In order to ascertain the combined effects that GRF and learning have on protein intake several hypothesis were examined. One major hypothesis was that rats would successfully alter their dietary selection patterns in response to protein restriction. It was speculated that rats kept on a nutritionally complete maintenance diet (NCMD) would consume equal amount of the intermittently presented high protein conditioning diet (HPCD) and protein-free conditioning diet (PFCD). However, it was hypothesized that rats kept on a protein-free maintenance diet (PFMD) would selectively increase their intake of the HPCD. Another hypothesis was that rats would learn to associate a distinct marker flavour with the nutritional content of the diets. If an animal is able to make the association between a marker flavour and the nutrient content of the food, then it is hypothesized that they will consume more of a mixed diet (equal portion HPCD and PFCD) with the marker flavour that was previously paired with the HPCD (Mixednp-f) when kept on the PFMD. In addition, it was hypothesized that intracranial injection of GRF into the SCN/MPOA would result in a selective increase in HPCD as well as Mixednp-t consumption. Results demonstrated that rats did in fact selectively increase their consumption of the flavoured HPCD and Mixednp-f when kept on the NCMD. These findings indicate that the rats successfully learned about the nutrient content of the conditioning diets and were able to associate a distinct marker flavour with the nutrient content of the diets. However, the results failed to support previous findings that GRF increases protein intake. In contrast, the administration of GRF significantly reduced consumption of HPCD during the first hour of testing as compared to the no injection condition. In addition, no differences in the intake of the HPCD were found between the GRF and vehicle condition. Because GRF did not selectively increase HPCD consumption, it was not surprising that GRF also did not increase MixedHP-rintake. What was interesting was that administration of GRF and vehicle did not reduc^Mixednp-f consumption as it had decreased HPCD consumption.

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Affiliation: Paul Allard : Département de kinésiologie, Université de Montréal

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Affiliation: Mark Daniel : Département de médecine sociale et préventive, Faculté de médecine, Université de Montréal

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Affiliation: Département de Psychologie, Université de Montréal

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Affiliation: Louise Potvin: Groupe de recherche interdisciplinaire en santé, Faculté de médecine, Université de Montréal

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Affiliation: Faculté de médecine, Université de Montréal & CANVAC

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Affiliation: André Dagenais: Centre hospitalier de l'Université de Montréal/ Hôtel-Dieu, Département de médecine, Université de Montréal. Yves Berthiaume: Médecine et spécialités médicales, Faculté de médecine

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Affiliation: Faculté de pharmacie, Université de Montréal & Institut de recherches cliniques de Montréal

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Affiliation: Pascal Michel : Département de pathologie et microbiologie, Faculté de médecine vétérinaire, Université de Montréal

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Affiliation: Maude Loignon, Lise Cyr & Emil Toma : Département de microbiologie et immunologie, Faculté de médecine, Université de Montréal