Avaliação da instabilidade de vertentes e processos de erosão superficial na zona de Castelo Branco, Furnas, ilha de São Miguel, Açores

A presente dissertação tem como objetivo identificar e avaliar os elementos de instabilidade geotécnica das vertentes e terrenos da zona do Vanzinho (Castelo Branco, Furnas, ilha de São Miguel), com vista a propor medidas de estabilização das vertentes e controlo da erosão superficial dos terrenos. Com este objetivo foi definida uma metodologia de trabalho em cinco etapas que consistiu: (i) a primeira etapa, no levantamento de dados bibliográficos, integração da informação geológica/geomorfológica em SIG (sistema de informação geográfica) e na observação e levantamento de campo das superfícies de instabilidade geotécnica; (ii) a segunda etapa, na recolha de amostras de solo, remexidas e não remexidas, para caracterização das propriedades físicas e mecânicas dos materiais; (iii) a terceira etapa, na realização de ensaios laboratoriais para a determinação das propriedades físicas e mecânicas dos solos e respetiva classificação; (iv) uma quarta etapa, que consistiu no tratamento estatístico multivariado de dados, nomeadamente, a aplicação dos métodos de análise fatorial das correspondências e de classificação hierárquica com vista à caracterização da tipologia dos materiais e eventual correlação com as evidências de instabilidade; (v) a quinta etapa consistiu na projeção de um conjunto de medidas estruturais e não estruturais (medidas biológicas) a implementar para a estabilização de vertentes e controlo dos processos de erosão superficial observados na área do Vanzinho. Para a estimação da distribuição espacial das diferentes tipologias de solo foi utilizado o método geoestatístico da krigagem multifásica. Para cada elemento de instabilidade cartografado foi criada uma ficha que caracteriza a tipologia da ocorrência, a dimensão, a forma e o coberto vegetal do meio envolvente. O trabalho realizado teve por base a integração de toda a informação num SIG, o que possibilita a atualização de eventuais novas ocorrências, bem como o fácil manuseamento e análise dos dados, a utilizar em trabalhos futuros.

Análise experimental das condições de escoamento superficial em zonas urbanas na presença de viaturas

As cheias em zonas urbanas representam um fenómeno natural que parece ocorrer cada vez com mais frequência, provocando muitas vezes a inundação de caves, estações de metropolitano e, em alguns casos extremos, a perda de vidas humanas. Estas cheias ocorrem quando os sistemas artificiais de recolha de águas pluviais deixam de ter capacidade de vazão suficiente para os caudais afluídos e parte do escoamento começa a fazer-se à superfície. Deste modo, o objetivo principal deste trabalho consiste na avaliação da influência que o grau de obstrução, causado pela presença de viaturas nas vias públicas, tem no agravamento das alturas de água nos arruamentos. Para isso, foram realizados ensaios laboratoriais num modelo à escala 1:12, nos quais se procurou simular as condições reais de escoamento de caudais de cheia, em vias urbanas. Os ensaios foram feitos para 20 cenários, para os quais se combinaram diferentes quantidades e disposições de veículos, a que correspondem diferentes graus de obstrução ao escoamento. Durante as medições das alturas de água, em todos os cenários, fizeram-se variar as inclinações do fundo entre 0,005 e 0,030 m/m para uma gama de caudais compreendida entre 10 e 40 m3/h. Posteriormente, com os valores das medições obtidas, inferiram-se quais os cenários mais críticos, ou seja, quais as situações onde se observaram maiores incrementos nas alturas de água de escoamento nos arruamentos. A partir da variação entre as alturas de escoamento do cenário base, sem a presença de veículos, e as alturas dos diferentes cenários com obstáculos, obtiveram-se as sobrelevações da altura de água, tanto em valor absoluto como em valor relativo. Por fim, mas não menos importante, procurou-se obter padrões e consequentemente relações entre os diversos parâmetros em estudo, principalmente a relação entre a percentagem de obstrução e a sobrelevação da altura de água nos arruamentos. Da análise dos resultados obtidos procurou-se por último extrair conclusões e tecer algumas recomendações tendo em vista a minimização de algumas consequências deste tipo de situações extremas.

Gas tungsten arc welding of NiTi shape memory alloy

Shape memory alloys are characterized by the ability of recovering their initial shape after being deformed and by superelasticity. Since the discovery of these alloys, a new field of interest emerged not only for the scientific community but also to many industries. However, these alloys present poor machinability which constitute a constrain in the design of complex components for new applications. Thus, the demand for joining techniques able to join these alloys without compromising their properties became of great importance to enlarge the complexity of existing applications. Literature shows that these alloys are joined mainly using laser welding. In the present study, similar NiTi butt joints, were produced using TIG welding. The welds were performed in 1.5 mm thick plates across the rolling direction. A special fixture and gas assist device was designed and manufactured. Also a robot arm was adapted to accommodate the welding torch to assure the repeatability of the welding parameters. Welds were successfully achieved without macroscopic defects, such as pores and distortions. Very superficial oxidation was seen on the top surface due to insufficient shielding gas flow on the weld face. The welded joints were mechanically tested and structurally characterized. Testing methods were used to evaluate macro and microstructure, as well as the phase transformation temperatures, the mechanical single and cyclic behaviour and the shape recovery ability. Differential Scanning Calorimetry (DSC), Scanning Electron Microscopy (SEM), Energy Dispersive Spectroscopy (EDS), microhardness measurements were techniques also used to evaluate the welded joints. A depletion in Ni in the fusion zone was seen, as well as a shift in Ms temperature. For strain values of 4% the accumulated irrecoverable strain was of about 30% and increased with the strain imposed during cycling. Nevertheless, a complete recovery of initial shape was observed when testing the shape memory effect on a dedicated device that introduces a deformation of 6.7%. That is, the welding procedure does not remove the ability of the specimens to recover their initial shape.

Relações entre fluxos de água subterrânea e superficial em bacia hidrográfica caracterizada por cobertura florestal amazônica.

O experimento foi conduzido em uma bacia hidrográfica de 1,3 km2, drenada pelo igarapé Barro-Branco, localizada na Reserva florestal Ducke, à cerca de 30 km de Manaus. A cobertura vegetal dessa bacia e caracterizada, em quase sua totalidade, por floresta amazônica do tipo "Terra-firme". A coleta de dados e respectivos cálculos estenderam-se no período de maio de 1981 a dezembro de 1983. Para o período em questão, os resultados obtidos mostraram que, em termos médios, o escoamento total do igarapé representou 32,3% da chuva, dos quais apenas 2,8% se deram na forma de escoamento superficial direto, implicando numa evapotranspiração da ordem de 67,7% do total precipitado. Considerando-se um valor médio de 22% para o total da chuva interceptada pela cobertura florestal, a transpiração dada pela floresta pode ser estimada como sendo de cerca de 45,7% da precipitação. Acredita-se que o corte indiscriminado e irracional da Floresta Amazônica, visando-se a sua ocupação, deverá alterar significativamente as relações encontradas, trazendo como conseqüências, sérios problemas de erosão, transporte de sedimentos, menor tempo de residência da água na bacia e outros problemas que certamente irão interferir no atual equilíbrio ecológico da maior reserva florestal do mundo.

Acellular Gellan-gum based bilayered structures for the regeneration of osteochondral defects: a preclinical study

 In orthopaedics, the management and treatment of osteochondral (OC) defects remains an ongoing clinical challenge. Autologous osteochondral mosaicplasty has been used as a valid option for OC treatments although donor site morbidity remains a source of concern [1]. Engineering a whole structure capable of mimicking different tissues (cartilage and subchondral bone) in an integrated manner could be a possible approach to regenerate OC defects. In our group we have been proposing the use of bilayered structures to regenerate osteochondral defects [2,3]. The present study aims to investigate the pre-clinical performance of bilayered hydrogels and spongy-like hydrogels in in vivo  models (mice and rabbit, respectively), in both subcutaneous and orthotopic models. The bilayered structures were produced from Low Acyl Gellan Gum (LAGG) from Sigma-Aldrich, USA. Cartilage-like layers were obtained from a 2wt% LAGG solution. The bone-like layers were made of 2wt% LAGG with incorporation of hydroxyapatite at 20% and 30% (w/v). Hydrogels and spongy-like were subcutaneouly implanted in mice to evaluate the inflammatory response. Then, OC defects were induced in rabbit knee to create a critical size defect (4 mm diameter and 5 mm depth), and then hydrogels and sponges implanted. Both structures followed different processing methods. The hydrogels were injected allowing in situ  crosslinking. Unlike, the spongy-like were pre-formed by freeze-drying. The studies concerning subcutaneous implantation and critical size OC defect were performed for 2 and 4 weeks time, respectively. Cellular behavior and inflammatory responses were assessed by means of histology staining and biochemical function and matrix deposition by immunohistochemistry. Additionally, both OC structures stability and new cartilage and bone formation were evaluated by using vivo- computed tomography (Scanco 80). The results showed no acute inflammatory response for both approaches. New tissue formation and integration in the adjacent tissues were also observed, which present different characteristic behaviors when comparing hydrogels and sponges response. As future insights, a novel strategy for regeneration of OC defects can be designed encompassing both, hydrogels and spongy-like structures and cellular approaches. References: 1. Espregueira-Mendes J. et al. Osteochondral transplantation using autografts from the upper tibio-fibular joint for the treatment of knee cartilage lesions. Knee Surgery, Sports Traumatology, Arthroscopy 20,1136, 2012. 2. Oliveira JM. et al, Novel hydroxyapatite/chitosan bilayered scaffold for osteochondral tissue-engineering applications: Scaffold design and its performance when seeded with goat bone marrow stromal cells. Biomaterials 27, 6123, 2006. 3. Pereira D R. et al. Gellan Gum-Based Hydrogel Bilayered Scaffolds for Osteochondral Tissue Engineering. Key Engineering Materials 587, 255, 2013.

Bioactive nanocomposite spheres with proved shape memory capability in bone defects

Bioactive glass nanoparticles (BGNPs) promote an apatite surface layer in physiologic conditions that lead to a good interfacial bonding with bone.1 A strategy to induce bioactivity in non-bioactive polymeric biomaterials is to incorporate BGNPs in the polymer matrix. This combination creates a nanocomposite material with increased osteoconductive properties. Chitosan (CHT) is a polymer obtained by deacetylation of chitin and is biodegradable, non-toxic and biocompatible. The combination of CHT and the BGNPs aims at designing biocompatible spheres promoting the formation of a calcium phosphate layer at the nanocomposite surface, thus enhancing the osteoconductivity behaviour of the biomaterial. Shape memory polymers (SMP) are stimuli-responsive materials that offer mechanical and geometrical action triggered by an external stimulus.2 They can be deformed and fixed into a temporary shape which remains stable unless exposed to a proper stimulus that triggers recovery of their original shape. This advanced functionality makes such SMPs suitable to be implanted using minimally invasive surgery procedures. Regarding that, the inclusion of therapeutic molecules becomes attractive.  We propose the synthesis of shape memory bioactive nanocomposite spheres with drug release capability.3   1.  L. L. Hench, Am. Ceram. Soc. Bull., 1993, 72, 93-98. 2.  A. Lendlein and S. Kelch, Angew Chem Int Edit, 2002, 41, 2034-2057. 3.  Ã . J. Leite, S. G. Caridade and J. F. Mano, Journal of Non-Crystalline Solids (in Press)

Uma comparação entre diferentes estimativas da condutância superficial numa floresta primária na Amazônia Central

Neste trabalho foi realizada a estimativa da condutância superficial para transferência de vapor d'agua, característica de uma floresta primária próxima a Manaus, à partir de dois diferentes métodos baseados em equações de regressão que procuram associar essa condutância a diferentes variáveis físicas. A equação proposta por Allen (1986) foi estabelecida através da correlação com a radiação líquida média diária, enquanto a estimativa proposta por Roberts et al. (1990) procurou correlacionar a condutância estomática com o déficit de umidade específica e a radiação solar, utilizando dados médios horários e, neste caso, estes valores foram reunidos para representar a média diária correspondente. Uma comparação entre os resultados estimados por tais métodos apresentou o primeiro (Allen) com estimativas sempre inferiores ao segundo (Roberts), da ordem de 30%(±8) na média. Os desvios de ambos também foram relativamente diferentes e, embora tivesse apresentado índices mais elevados de condutância, os desvios do método de Roberts foram de magnitude inferior aos do método de Allen c, portanto, seus valores mostraram-se mais estáveis. As diferenças menores foram observadas no período relativo à estação seca, principalmente nos meses de agosto, setembro e outubro, quando estiveram dentro do limite determinado pela soma dos desvios padrões de ambos.

Electronic transport across linear defects in graphene

We investigate the low-energy electronic transport across grain boundaries in graphene ribbons and infinite flakes. Using the recursive Green’s function method, we calculate the electronic transmission across different types of grain boundaries in graphene ribbons. We show results for the charge density distribution and the current flow along the ribbon. We study linear defects at various angles with the ribbon direction, as well as overlaps of two monolayer ribbon domains forming a bilayer region. For a class of extended defect lines with periodicity 3, an analytic approach is developed to study transport in infinite flakes. This class of extended grain boundaries is particularly interesting, since the K and K0 Dirac points are superposed.

Modelo de escoamento superficial em bacia experimental da Reserva Florestal Adolpho Ducke

Neste estudo, a experimentação e a modelagem hidrológica de eventos de precipitação transformada em escoamento superficial em sistemas naturais de floresta são investigadas, contemplando os seguintes tratamentos: construção de algoritmo computacional iterativo de otimização para a identificação do hidrograma unitário médio (função de transferência chuva-descarga) da bacia e para o cálculo das precipitações efetivas adequadas à cada evento chuva-escoamento; aplicação da metodologia à bacia hidrográfica do igarapé Bolívia, situada no interior da Reserva Florestal Adolpho Ducke; análise e interpretação do algoritmo criado, enfocando a sua convergência e o significado dos resultados desse processo de otimização; e comparação com outros estudos em pequenas bacias da Amazônia Central. O período de medidas de chuva e de vazões estende-se de julho de 2004 a setembro de 2006, incluindo a fase de preparação da curva-chave do igarapé Bolívia e a formação de um conjunto amplo e diversificado de eventos de chuva e de escoamento no curso d'água.

Percutaneous closure of atrial septal defects. The role of transesophageal echocardiography

PURPOSE: Evaluation of the role of transesophageal echocardiography in percutaneous closure of atrial septal defects (ASD) with the Amplatzer septal occluder. METHODS: Patients were selected for percutaneous closure of ASD by transesophageal echocardiography (TEE), which was also used to monitor the procedure, helping to select the appropriate size of the Amplatzer device, to verify its position, and to access the immediate results of the procedure. During the follow-up, TEE was used to evaluate the presence and magnitude of residual shunt (RS), device position, and right cardiac chamber diameters. RESULTS: Twenty-two (40%) of a total of 55 studied patients were selected. Thirteen underwent Amplatzer device implantation, eight are still waiting for it, and one preferred the conventional surgical treatment. All procedures were successful, which was mainly due to proper patient selection. Six (23%) patients acutely developed RS, which spontaneously disapeared at the three-month follow-up examination in three patients. There was a significant reduction in the right ventricle diastolic diameter, from 27mm (average) to 24mm and 20mm, one and three months after the procedure, respectively (p<0.0076). CONCLUSION: With the aid of TEE, percutaneous closure of ASD can be successfully, safely, and effectively performed.

Epidemiological study of congenital heart defects in children and adolescents: analysis of 4,538 cases

OBJECTIVE: To analyze the frequency and prevalence of congenital heart defects in a tertiary care center for children with heart diseases. METHODS: We carried out an epidemiological assessment of the first medical visit of 4,538 children in a pediatric hospital from January 1995 to December 1997. All patients with congenital heart defects had their diagnoses confirmed at least on echocardiography. The frequency and prevalence of the anomalies were computed according to the classification of sequential analysis. Age, weight, and sex were compared between the groups of healthy individuals and those with congenital heart defects after distribution according to the age group. RESULTS: Of all the children assessed, 2,017 (44.4%) were diagnosed with congenital heart disease, 201 (4.4%) with acquired heart disease, 52 (1.2%) with arrhythmias, and 2,268 (50%) were healthy children. Congenital heart diseases predominated in neonates and infants, corresponding to 71.5% of the cases. Weight and age were significantly lower in children with congenital heart defects. Ventricular septal defect was the most frequent acyanotic anomaly, and tetralogy of Fallot was the most frequent cyanotic anomaly. CONCLUSION: Children with congenital heart defects are mainly referred during the neonatal period and infancy with impairment in gaining weight. Ventricular septal defect is the most frequent heart defect.

Initial experience in Brazil with the Helex septal occluder for percutaneous occlusion of atrial septal defects

OBJECTIVE: To evaluate the initial clinical experience with the Helex septal occluder for percutaneous closure of atrial septal defects. METHODS: Ten patients underwent the procedure, 7 patients with ostium secundum atrial septal defects (ASD) with hemodynamic repercussions and 3 patients with pervious foramen ovale (PFO) and a history of stroke. Mean age was 33.8 years and mean weight was 55.4 kg. Mean diameter by transesophageal echocardiography and mean stretched ASD diameter were 11.33 ± 3.3mm, and 15.2 ± 3.8mm, respectively. The Qp/Qs ratio was 1.9 ± 0.3 in patients with ASD. RESULTS: Eleven occluders were placed because a patient with 2 holes needed 2 devices. It was necessary to retrieve and replace 4 devices in 3 patients. We observed immediate residual shunt (< 2mm) in 4 patients with ASD, and in those with patent foramen ovale total occlusion of the defect occurred. No complications were noted, and all patients were discharged on the following day. After 1 month, 2 patients with ASD experienced trivial residual shunts (1mm). In 1 patient, we observed mild prolapse in the proximal disk in the right atrium, without consequences. CONCLUSION: The Helex septal occluder was safe and effective for occluding small to moderate atrial septal defects. Because the implantation technique is demanding, it requires specific training of the operator. Even so, small technical failures may occur in the beginning of the learning curve, but they do not involve patient safety.

Investigación de defectos genéticos en el sistema de la fosforilasa hepática en pacientes argentinos. Definición nosológica mediante una estrategia de análisis molecular. Investigation of genetic defects in the hepatic phosphorylase system in Argentinean patients. Nosological definition by molecular analysis strategy.

Las Enfermedades de Atesoramiento de Glucógeno (EAGs) también llamadas Glucogenosis comprenden un grupo de entidades causadas por una deficiencia enzimática específica relacionada con la vía de síntesis o degradación de esta macromolécula. La heterogeneidad fenotípica de los pacientes afectados dificulta la identificación de las diferentes variantes de EAG y por ende la correcta definición nosológica. En el Centro de Estudio de las Metabolopatías Congénitas, CEMECO, se fueron definiendo los diferentes tipos de Glucogenosis a través de una estrategia multidisciplinaria que integra distintos niveles de investigación clínica y complementaria, laboratorio metabólico especializado, enzimático, histomorfológico y de análisis molecular. Sin embargo, en algunos enfermos, entre los que se encuentran aquellos con defectos en el sistema de la fosforilasa hepática (EAG-VI y EAG-IX), la exacta definición nosológica aún no está resulta. La EAG-VI se refiere a un defecto en la fosforilasa hepática, enzima codificada por el gen PYGL, mientras que la EAG-IX es causada por un defecto genético en una de las subunidades de la fosforilasa b quinasa hepática codicadas por los genes PHKA2, PHKB y PHKG2, respectivamente. El objetivo del presente trabajo es propender a la definición nosológica de pacientes con defectos en el sistema de la fosforilasa mediante una estrategia de análisis molecular investigando los genes PYGL, PHKA2, PHKB y PHKG2. Los pacientes incluidos en este estudio deberán ser compatibles de padecer una EAG-VI o EAG-IX sobre la base de síntomas clínicos y hallazgos bioquímicos. La metodología incluirá la determinación de la enzima fosforilasa b quinasa en glóbulos rojos y dentro del análisis molecular la extracción de DNA genómico a partir de sangre entera para la amplificación por PCR de los exones más las uniones exon/intron de los genes PHKG2 y PYGL y la extracción de RNA total y obtención de cDNA para posterior amplificación de los cDNA PHKA2 y PHKB. Todos los fragmentos amplificados serán sometidos a análisis de secuencia de nucleótidos. Resultados esperados. Este trabajo, primero en Argentina, permitirá establecer las bases moleculares de los defectos del sistema de la fosforilasa hepática (EAG-VI y EAG-IX). El poder lograr este nivel de investigación traerá aparejado, una oferta integrativa en el vasto capítulo de las glucogenosis hepáticas, con extraordinaria significación en la práctica asistencial para el manejo, pronóstico y correspondiente asesoramiento genético. Hepatic glycogen storage diseases (GSDs) are a group of disorders produced by a deficiency in a specific protein involved in the metabolism of glycogen causing different types of GSDs. Phenotypic heterogeneity of affected patients difficult to identify the different GSD variants and therefore the correct definition of the disease. In the “Centro de Estudio de las Metabolopatías Congénitas”, CEMECO, were defined the different GSD types by a protocol which included complex gradual levels of clinical, biochemical, enzymatic and morphological investigation. However, in some patients, like those one with defects in the hepatic phosphorylase system (GSD-VI and GSD-IX) the exact definition of the disease has not yet been resolved. The GSD-VI is produced by a defect in the PYGL gen that encode the liver phosphorylase, while the GSD-IX is caused by a genetic defect in one of the Phosphorylase b kinase subunits, encoded by the PHKA2, PHKB and PHKG2 genes, respectively. The aim of the present study is to define the phosphorylase system defects in argentinian patients through a molecular strategy that involve the investigation of PYGL, PHKA2, PHKB and PHKG2 genes. Patients included in the present study must be compatible with a GSD-VI or GSD-IX on the bases of clinical symptoms and biochemical findings. The phosphorylase b kinase activity will be assay on in blood red cells. The molecular study will include genomic DNA extraction for the amplification of PHKG2 and PYGL genes and the total RNA extraction for amplification of the PHKA2 and PHKB cDNA by PCR. All PCR-amplified fragments will be subjected to direct nucleotide sequencing. This work, first in Argentina, will make possible to establish the molecular basis of the defects on the hepatic phosphorylase system (GSD-VI and GSD IX). To achieve this level of research will entail advance in the study of the hepatic glycogen storage disease, with extraordinary significance in the treatment, prognosis and the genetic counselling.

Investigation of Copy Number Variation in Children with Conotruncal Heart Defects

Background:Congenital heart defects (CHD) are the most prevalent group of structural abnormalities at birth and one of the main causes of infant morbidity and mortality. Studies have shown a contribution of the copy number variation in the genesis of cardiac malformations.Objectives:Investigate gene copy number variation (CNV) in children with conotruncal heart defect.Methods:Multiplex ligation-dependent probe amplification (MLPA) was performed in 39 patients with conotruncal heart defect. Clinical and laboratory assessments were conducted in all patients. The parents of the probands who presented abnormal findings were also investigated.Results:Gene copy number variation was detected in 7/39 patients: 22q11.2 deletion, 22q11.2 duplication, 15q11.2 duplication, 20p12.2 duplication, 19p deletion, 15q and 8p23.2 duplication with 10p12.31 duplication. The clinical characteristics were consistent with those reported in the literature associated with the encountered microdeletion/microduplication. None of these changes was inherited from the parents.Conclusions:Our results demonstrate that the technique of MLPA is useful in the investigation of microdeletions and microduplications in conotruncal congenital heart defects. Early diagnosis of the copy number variation in patients with congenital heart defect assists in the prevention of morbidity and decreased mortality in these patients.