Terminal ballistics study multivariate behavior and aftermath of projectile and target interactions. Tests and models are often based on monolithic armors, however, layered and spaced armors are common in real world applications. Such configurations add complexities that require research to understand their effects on terminal ballistics. The ballistic limit velocity (V50) represents the speed where armor perforation probability is 50%. It is used for quantitative comparison of protection capabilities for different armors. This research studied the V50 of spaced and layered A36 steel armors against fragment simulating projectiles (FSPs). Four methods for estimating armor V50 were evaluated and compared to experimental data. The first two methods were analytical methods from literature, the third was finite element (FE) simulations in EPIC, and the fourth was a Monte Carlo method developed in this research. The Monte Carlo method using 100,000 iterations was the most accurate and efficient of all methods.

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The task of medicinal chemists in a drug discoveryproject is to synthesize/design analogues to the screening hits, simultaneouslyincreasing target potency and optimizing the pharmacological properties.  This requires a wide selection of moleculesto be synthesized, where both synthetic feasibility and price of startingmaterials are of great importance. In this work, a synthetic pathway from cheapand readily available starting materials to highly modifiable 2,4-disubstitutedpyrrolidines is demonstrated. Previously reported procedures to similarpyrrolidines use expensive catalysts, requires harsh conditions and requiresnon-commercially available starting materials. The suggested pathway herein has demonstrated great possibility forvariation in the 4-position, including fluoro, difluoro, nitrile and alcoholfunctional groups. There are several areas in which the synthesis can beimproved and expanded upon. Improvements can be made by optimizing thedescribed reaction conditions and further expansion of possible modificationsin both 2- and 4-position could be explored.

[pt] Avanços tecnológicos recentes, tanto nos métodos de sequenciamento quanto nos algoritmos de montagem de fragmentos, têm facilitado a reconstrução de todo o DNA de espécies sem a necessidade de um genoma de referência. A montagem da cadeia completa envolve a leitura um grande volume de fragmentos do genoma (short reads), um desafio significativo em termos computacionais. Todos os principais algoritmos de montagem de fragmentos existentes têm como gargalo principal o alto consumo de memória principal. Consonante a isso, essa dissertação de mestrado visa estudar a implementação de um destes algoritmos, Velvet, que é amplamente usado e recomendado. A mesma possuiu um módulo, VelvetH que realiza um pré-processamento dos dados com o intuito de reduzir o consumo de memória principal. Após um estudo minucioso do código e alternativas de melhorias, foram feitas alterações pontuais e proposta uma solução com persistência de dados em memória secundária visando obter eficácia e robustez. / [en] Recent technological advances, both in assembly algorithms and in sequencing methods, have enabled the reconstruction of whole DNA even without a reference genome available. The assembly of the complete chain involves reading a large volume of genome fragments, called short-reads, which makes the problem a significant computational challenge. A major bottleneck for all existing fragmentassembly algorithms is the high consumption of RAM. This dissertation intends to study the implementation of one of these algorithms, called Velvet, which is widely used and recommended. The same possessed a module, VelvetH that performs a pre-processing data with the aim of reducing the consumption of main memory. After a thorough study of code improvements and alternatives, specific changes have been made and proposed a solution with data persistence in secondary memory in order to obtain effectiveness and robustness.

Fusarium head blight (FHB) is one of the most economically important diseases of small grains and continues to impact crops when environmental conditions are favorable to Gibberella zeae (Fusarium graminearum), the causal agent of the disease. Corn residues are considered to be primary sources of inoculum for epidemics of FHB. Therefore, knowledge of the movement of Gibberella zeae from a local source of infested corn residue is critical to the management of FHB in wheat and barley. Previous research made significant progress in defining the spatial dissemination of inoculum sources of G. zeae within agricultural fields, but was unable to clearly distinguish between within-field and background sources. Using amplified fragment length polymorphism, released clones of G. zeae were tracked within wheat and barley fields. This strategy allowed the distinction between the contributions of released clones to FHB, compared to that of background inocula. Corn residue infested with clones of G. zeae was placed into small replicated plots in winter wheat fields in New York and Virginia in 2007 and 2008 and wheat spikes were collected at 0, 3, 6, and ≥24 m from the inoculum sources. Recovery of released clones decreased an average of 90% between 3 and 6 m from inoculum sources. Various amounts of corn residue infested with a single clone of G. zeae were placed into small replicated plots in winter wheat and barley fields in Virginia from 2008 to 2010. The use of minimal or conventional tillage and a moderately resistant cultivar of wheat or barley may reduce the contribution of within-field inocula to FHB; however, environmental conditions play an important role in the effectiveness of these management strategies. With the increase of corn production due to incentives for ethanol-based fuel, overwintering sites for G. zeae on corn residue are likely to increase. Our work contributes to an increased understanding of the influence of overwintered corn residue to FHB which will also direct future research on how to reduce the inoculum potential from within-field sources. / Ph. D.

Mémoire numérisé par la Direction des bibliothèques de l'Université de Montréal.

Hypertrophic cardiomyopathy (HCM), a heart-related abnormality, is the most prevalent cause of sudden death in young athletes at sporting events. A cluster of cardiomyopathy mutations are localized in β-cardiac myosin at the N-terminal region of subfragment-2. Using resonance energy transfer probes, a synthetic peptide model system was developed to study stability of the coiled coil (S2 fragment) structure by determining monomer-dimer equilibrium of the peptide. Fluorescence resonance energy transfer and MacroModel software suite were used to obtain distance measurements along with measurement of coiled coil formation. The model peptide was used to characterize the effects of disease-causing-mutations and examine potential candidate drugs (polyamines) to counteract effects of mutations causing HCM. Distance measurements between donor and acceptor probes obtained by computational simulation and fluorescence resonance energy transfer (FRET) were consistent. Measurements also agreed with simulations of unlabeled wildtype, indicating coiled coil structural stability of the peptide. Interaction of the site-specific antibody with the peptide strongly inhibited dimerization and destabilized coiled coil structure of the peptide. Presence of negatively charged glutamate residues in the region of subfragment-2 strongly suggested a potential interaction site for positively charged polyamines. Binding of certain polyamines, such as poly-L-Lysine 11 residues and poly-D-Lysine 17 residues, demonstrated the ability to enhance dimerization and improve stability of the coiled coil structure, while some other polyamines were shown to have insignificant impact on the structure. In an attempt to characterize the effect of HCM-causing-mutations, peptides containing E924K mutation and lethal mutation E930 deletion were synthesized. Fluorescence resonance probes were conjugated to the mutant peptides to determine coiled coil formation. Results obtained from both dynamic simulations and resonance energy transfer experiments indicated that these mutations strongly inhibit dimerization, and thus, destabilize coiled coil structure of the peptide. Further experiments were conducted using heterodimers containing a chain of wildtype and a chain of mutant peptide. Both E924K & Edel930 mutations destabilized coiled coil formation and prevented dimerization. This peptide model system would provide a promising tool for drug development targeting HCM-causing-mutations along the S2 region of myosin.