C'est là que l'on joue la comédie: les casa da opera en Amérique Portugaise (1719-1819)

La présente thèse doctorale propose l’étude de l’activité théâtrale développée dans les théâtres permanents construits en Amérique Portugaise au long du XVIIIe et dans la première décennie du XIXe siècle, en mettant l’accent sur les idéalisateurs des Casas da Ópera et les moyens de financement utilisés dans l’édification et l’entretien de celles-ci, le répertoire mis en scène, les artistes composant les compagnies théâtrales, les spectateurs et les possibilités de sociabilité établies dans l’espace théâtrale et les modèles architectoniques qui ont inspiré la construction des bâtiments théâtraux au cours de la période mentionnée. Ces cinq axes principaux soulignent l’approche interdisciplinaire qui a orienté nos études, dans un souci de contribution à une plus complète compréhension de notre sujet de recherche. Mots clés : Théâtres, Amérique Portugaise, Comédiens Mulâtres, Théâtre Éphémère, Comédies Portugaises, Architecture théâtrale luso-américaine, Casa da Ópera de Vila Rica/Ouro Preto.

A importância de se chamar português: José Liberato Freire de Carvalho na direcção do investigador português, 1814-1819.

Tese apresentada para cumprimento dos requisitos necessários à obtenção do grau de Doutor em História e Teoria das Ideias, especialidade Pensamento, Cultura e Política

Encomenda, uso e coleccionismo de ourivesaria no século XVIII: a Mantearia da Casa de Aveiro em 1752

Neste artigo procuramos analisar a Mantearia da Casa de Aveiro em 1752. Através do inventário mandado realizar pelo 8.º Duque de Aveiro, logo no seu primeiro ano à frente da casa, permite‑se reflectir sobre a importação de obras de luxo dos grandes centros produtores da Europa para Portugal, ao longo do século XVIII: Augsburgo, Roma, Londres e Paris. As obras em prata pertencentes ao Museu Nacional de Arte Antiga, tomadas pela Casa Real na sequência do “processo dos Távoras” em 1759, apenas foram encomendadas após a realização deste inventário. Todavia podemos aferir a grande importância da Mantearia dos Duques de Aveiro, pela importância das obras de aparato, de que destacamos o conjunto de centros de mesa, e pelo coleccionismo de ourivesaria antiga, nomeadamente do período da renascença, que gozou de grande prestígio no Portugal de setecentos.

Os periódicos portugueses de emigração (1808-1822)

Esta dissertação analisa e compara os periódicos com uma componente de divulgação científica, editados por refugiados políticos em Londres e Paris, sendo o núcleo investigado composto por quatro títulos: o Correio Braziliense (1808-1822) e O Investigador Portuguez em Inglaterra (1811-1819), publicados em Londres, O Observador Lusitano em Pariz (1815) e os Annaes das Sciencias, das Artes, e das Letras (1818-1822), ambos com origem na capital francesa. Este estudo comporta uma discussão sobre questões historiográficas levantadas pelo estudo de periódicos de divulgação científica, nomeadamente num país com as particularidades de Portugal, a caracterização do período histórico em que decorreu a vida destas publicações, um panorama breve do estado das diversas ciências no plano internacional que nelas encontraram eco, seguidos da análise propriamente dita do núcleo de periódicos seleccionados. No âmbito desta última, deu-se particular destaque aos editores e ao seu percurso, ao lugar das ciências entre as matérias apresentadas por cada periódico, e aos temas e personalidades focadas. Foram identificadas as principais fontes citadas e analisou-se a participação dos leitores em cada periódico. Ressaltam como traços fundamentais destes periódicos o esforço desenvolvido pelos seus editores no sentido de sensibilizarem os governantes para a importância de alterarem práticas tradicionais e estruturas ultrapassadas, abrindo o país à informação proveniente do exterior e, em particular, ao desenvolvimento científico e económico.

Automatic learning for the classification of chemical reactions and in statistical thermodynamics

This Thesis describes the application of automatic learning methods for a) the classification of organic and metabolic reactions, and b) the mapping of Potential Energy Surfaces(PES). The classification of reactions was approached with two distinct methodologies: a representation of chemical reactions based on NMR data, and a representation of chemical reactions from the reaction equation based on the physico-chemical and topological features of chemical bonds. NMR-based classification of photochemical and enzymatic reactions. Photochemical and metabolic reactions were classified by Kohonen Self-Organizing Maps (Kohonen SOMs) and Random Forests (RFs) taking as input the difference between the 1H NMR spectra of the products and the reactants. The development of such a representation can be applied in automatic analysis of changes in the 1H NMR spectrum of a mixture and their interpretation in terms of the chemical reactions taking place. Examples of possible applications are the monitoring of reaction processes, evaluation of the stability of chemicals, or even the interpretation of metabonomic data. A Kohonen SOM trained with a data set of metabolic reactions catalysed by transferases was able to correctly classify 75% of an independent test set in terms of the EC number subclass. Random Forests improved the correct predictions to 79%. With photochemical reactions classified into 7 groups, an independent test set was classified with 86-93% accuracy. The data set of photochemical reactions was also used to simulate mixtures with two reactions occurring simultaneously. Kohonen SOMs and Feed-Forward Neural Networks (FFNNs) were trained to classify the reactions occurring in a mixture based on the 1H NMR spectra of the products and reactants. Kohonen SOMs allowed the correct assignment of 53-63% of the mixtures (in a test set). Counter-Propagation Neural Networks (CPNNs) gave origin to similar results. The use of supervised learning techniques allowed an improvement in the results. They were improved to 77% of correct assignments when an ensemble of ten FFNNs were used and to 80% when Random Forests were used. This study was performed with NMR data simulated from the molecular structure by the SPINUS program. In the design of one test set, simulated data was combined with experimental data. The results support the proposal of linking databases of chemical reactions to experimental or simulated NMR data for automatic classification of reactions and mixtures of reactions. Genome-scale classification of enzymatic reactions from their reaction equation. The MOLMAP descriptor relies on a Kohonen SOM that defines types of bonds on the basis of their physico-chemical and topological properties. The MOLMAP descriptor of a molecule represents the types of bonds available in that molecule. The MOLMAP descriptor of a reaction is defined as the difference between the MOLMAPs of the products and the reactants, and numerically encodes the pattern of bonds that are broken, changed, and made during a chemical reaction. The automatic perception of chemical similarities between metabolic reactions is required for a variety of applications ranging from the computer validation of classification systems, genome-scale reconstruction (or comparison) of metabolic pathways, to the classification of enzymatic mechanisms. Catalytic functions of proteins are generally described by the EC numbers that are simultaneously employed as identifiers of reactions, enzymes, and enzyme genes, thus linking metabolic and genomic information. Different methods should be available to automatically compare metabolic reactions and for the automatic assignment of EC numbers to reactions still not officially classified. In this study, the genome-scale data set of enzymatic reactions available in the KEGG database was encoded by the MOLMAP descriptors, and was submitted to Kohonen SOMs to compare the resulting map with the official EC number classification, to explore the possibility of predicting EC numbers from the reaction equation, and to assess the internal consistency of the EC classification at the class level. A general agreement with the EC classification was observed, i.e. a relationship between the similarity of MOLMAPs and the similarity of EC numbers. At the same time, MOLMAPs were able to discriminate between EC sub-subclasses. EC numbers could be assigned at the class, subclass, and sub-subclass levels with accuracies up to 92%, 80%, and 70% for independent test sets. The correspondence between chemical similarity of metabolic reactions and their MOLMAP descriptors was applied to the identification of a number of reactions mapped into the same neuron but belonging to different EC classes, which demonstrated the ability of the MOLMAP/SOM approach to verify the internal consistency of classifications in databases of metabolic reactions. RFs were also used to assign the four levels of the EC hierarchy from the reaction equation. EC numbers were correctly assigned in 95%, 90%, 85% and 86% of the cases (for independent test sets) at the class, subclass, sub-subclass and full EC number level,respectively. Experiments for the classification of reactions from the main reactants and products were performed with RFs - EC numbers were assigned at the class, subclass and sub-subclass level with accuracies of 78%, 74% and 63%, respectively. In the course of the experiments with metabolic reactions we suggested that the MOLMAP / SOM concept could be extended to the representation of other levels of metabolic information such as metabolic pathways. Following the MOLMAP idea, the pattern of neurons activated by the reactions of a metabolic pathway is a representation of the reactions involved in that pathway - a descriptor of the metabolic pathway. This reasoning enabled the comparison of different pathways, the automatic classification of pathways, and a classification of organisms based on their biochemical machinery. The three levels of classification (from bonds to metabolic pathways) allowed to map and perceive chemical similarities between metabolic pathways even for pathways of different types of metabolism and pathways that do not share similarities in terms of EC numbers. Mapping of PES by neural networks (NNs). In a first series of experiments, ensembles of Feed-Forward NNs (EnsFFNNs) and Associative Neural Networks (ASNNs) were trained to reproduce PES represented by the Lennard-Jones (LJ) analytical potential function. The accuracy of the method was assessed by comparing the results of molecular dynamics simulations (thermal, structural, and dynamic properties) obtained from the NNs-PES and from the LJ function. The results indicated that for LJ-type potentials, NNs can be trained to generate accurate PES to be used in molecular simulations. EnsFFNNs and ASNNs gave better results than single FFNNs. A remarkable ability of the NNs models to interpolate between distant curves and accurately reproduce potentials to be used in molecular simulations is shown. The purpose of the first study was to systematically analyse the accuracy of different NNs. Our main motivation, however, is reflected in the next study: the mapping of multidimensional PES by NNs to simulate, by Molecular Dynamics or Monte Carlo, the adsorption and self-assembly of solvated organic molecules on noble-metal electrodes. Indeed, for such complex and heterogeneous systems the development of suitable analytical functions that fit quantum mechanical interaction energies is a non-trivial or even impossible task. The data consisted of energy values, from Density Functional Theory (DFT) calculations, at different distances, for several molecular orientations and three electrode adsorption sites. The results indicate that NNs require a data set large enough to cover well the diversity of possible interaction sites, distances, and orientations. NNs trained with such data sets can perform equally well or even better than analytical functions. Therefore, they can be used in molecular simulations, particularly for the ethanol/Au (111) interface which is the case studied in the present Thesis. Once properly trained, the networks are able to produce, as output, any required number of energy points for accurate interpolations.

Construir testes on-line

Este guião de apoio à formação tem como objectivo apoiar docentes na (1) configuração e utilização da actividade teste do moodle e (2) criação de bancos de perguntas.

A idealização de dois projectos para o teatro régio e um novo desenho do arquitecto Filippo Juvarra para a corte portuguesa

Na Biblioteca Nacional Universitária de Turim, no álbum Ris. 59-17 de Ignazio Agliaudi Baroni di Tavigliano, estão guardados cinco desenhos de grande interesse para o estudo da actividade portuguesa de Filippo Juvarra. Estes fólios representam dois projectos de teatro régio destinados à corte lusitana e são cópias de originais perdidos do arquitecto siciliano. Este ensaio estabelece uma maior fluidez entre a experiência artístico-musical da primeira metade do século xviii e o reinado de D. José I, a quem, tradicionalmente, os estudos críticos atribuem o ‘acto político’ de ter introduzido na corte portuguesa o melodrama face à aversão obstinada do pai. A problematização desta dicotomia permite criar uma liaison entre a chamada, em 1752, do cenógrafo e arquitecto teatral Giovanni Carlo Sicinio Bibiena por parte de D. José I com a memória do acontecido anteriormente, aquando jovem.