Cette thèse de doctorat porte sur les fluctuations temporelles du flux lumineux des lampes LED, ce phénomène portant le nom de papilottement (flicker). Le papillotement est habituellement considéré comme une perturbation en raison de son impact négatif sur la santé. Pour les systèmes d'éclairage à base de diodes électroluminescentes (LED), sa définition vient d'être formalisée dans la norme IEEE 1789:2015 et a été décrite pour les appareils alimentés en courant alternatif (CA). Ce papillotement alternatif résulte des interactions entre l'impédance du réseau, l'onde de tension, les courants harmoniques et le convertisseur de courant alternatif en courant continu (CA - CC). L'alimentation en courant continu est généralement obtenue via des convertisseurs à découpage. Par conséquent, les mêmes facteurs perturbateurs sont également présents sur les réseaux à courant continu. Cette thèse résume les diférences entre les propriétés caractéristiques du papillotement sous alimentation en CA et en CC. Il a été montré dans la littérature et aussi dans cette thèse qu'avec les LED, le facteur clé qui affecte le papillotement réside dans la conception du driver de LED - une partie indispensable des systèmes d'éclairage à LED. Cette thèse décrit une méthodologie d'évaluation de la sensibilité au papillotement des lampes LED sous alimentation en CC et analyse la façon dont cette sensibilité se modifie lorsque les drivers de LED sont simplifiés et adaptés à des alimentations CC. La thèse présente un ensemble d'expériences de mesure visant à déterminer la réaction typique du papillotement des lampes LED à la fois sous alimentation CA et CC. D'autres expériences ont été efectuées pour révéler l'impact de l'adaptation du driver à l'alimentation CC (en enlevant le pont redresseur à diodes). On constate que certaines lampes présentent une meilleure résistance au papillotement, tandis que d'autres lampes présentent une moindre résistance. Ces expériences sont accompagnées de simulations de drivers pour les lampes LED visant à reproduire et à expliquer les résultats des mesures. La thèse décrit en outre une expérience de mesure visant à montrer la sévérité typique de la variation de tension dans un réseau CC à basse tension couplé au CA domestique et son impact sur le papillotement. On conclut qu'un tel système est suisamment robuste pour filtrer les perturbations provenant du CA, mais une interaction indésirable entre la lampe et l'alimentation peut se produire. / This dissertation thesis is concerned with temporal fluctuations of the luminous flux of LED lamps, a phenomenon referred to as flicker. Flicker is usually regarded as a disturbance due to its negative impact on human health. For lighting systems based on light emitting diodes (LED), its definition has recently been formalised in norm IEEE 1789-2015 and has been documented on devices supplied with AC voltage. AC flicker results from interactions between network impedance, voltage and current harmonics, and the AC to DC converter. DC supplies are generally obtained by switching converters. Consequently, the same perturbing factors are present on DC networks. The thesis summarises the differences between the characteristic properties of flicker under AC and DC supplies. It has been shown in the literature and also in this thesis that the key factor affecting flicker with LEDs is the design of the LED driver-a necessary part of the LED lighting systems. This thesis describes a methodology for the evaluation of the flicker sensitivity of DC supplied LED lamps and analyses how the sensitivity changes when the LED drivers are simplified and accustomed to DC supply. The thesis presents a set of measurement experiments aimed to determine the typical flicker response of LED lamps both under AC and DC supply. Further experiments were performed to reveal the impact of accustomising the driver to the DC supply (removing the diode rectifier). It was found that some lamps show better flicker immunity while other lamps show worse flicker immunity. These experiments are accompanied by LED driver simulations aiming to reproduce and explain the measurement results. The thesis further describes a measurement experiment aimed to show the typical severity of the voltage fluctuation in a low voltage DC network coupled to AC mains and its impact on the flicker. It is concluded that such a system is robust enough to filter out any perturbations coming from the AC supply, but an undesired interaction between the lamp and the supply may occur.

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No. of bitstreams: 2 license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) Dissertacao_EfeitosAdaptacaoFlicker.pdf: 2860740 bytes, checksum: f9abd8848d8f0d11bce4e73516f4fbe8 (MD5) Previous issue date: 2015-08-20 / CAPES - Coordenação de Aperfeiçoamento de Pessoal de Nível Superior / O potencial cortical provocado visual tem sido utilizado para avaliar a visão espacial de luminância. A observação prolongada de um estímulo visual leva a uma série de mudanças na resposta neural em diferentes níveis de processamento do sistema visual. Os resultados destes estudos tem levado à compreensão de como o córtex visual primário processa informações espaciais. Muito tem sido sugerido sobre a ativação das vias paralelas M e P para a contribuição das respostas visuais corticais à partir do uso de estímulos que ativariam preferencialmente uma ou outra via. Uma abordagem para se estudar as interações da atividade atribuída às vias paralelas visuais M e P sobre as respostas corticais poderia ser a aplicação de estímulos que promovessem a adaptação preferencial de uma das vias ou mesmo de ambas e deixar que a via remanescente pudesse se expressar na resposta visual cortical. O objetivo deste estudo é avaliar os efeitos da adaptação ao flicker para estímulos de contraste de luminância sobre respostas corticais visualmente provocadas em várias condições favoráveis à ativação diferencial ou conjunta das vias paralelas M e P, levando a um aumento ou diminuição das respostas corticais. Foram avaliados 8 sujeitos com visão normal e acuidade normal ou corrigida 20/20. Foram utilizadas várias condições de estimulação, as quais serão três condições de estimulação sem adaptação visual, contendo apenas os estímulos testes, redes senoidais em 0,4 cpg, 2 cpg e 10 cpg com taxa de reversão espacial de 180 graus de 1 Hz (condições controle). As demais condições apresentaram um estímulo de adaptação que será uma máscara gaussiana bidimensional que variará a luminância no tempo cosenoidalmente (flicker) com modulação temporal de 5 Hz, 10 Hz e 30 Hz. O experimento consistiu em apresentar um estímulo de adaptação durante 8 s seguido por um estímulo teste durante 2 s. As respostas corticais foram registradas sobre o couro cabeludo acima do córtex occipital e foram registradas apenas durante a apresentação do estímulo teste. As respostas corticais foram avaliadas no domínio do tempo e das frequências temporais. No domínio do tempo, medido a latência e a amplitude do componente P1 (pico-linha), enquanto no domínio das frequências temporais foram avaliadas as amplitudes das bandas de frequências alfa, beta e gama presentes no registro. As respostas para os estímulos testes foram comparadas entre as condições sem adaptação e com adaptação visual ao flicker. O principal resultado foi que a adaptação visual ao flicker ocorreu de forma diferenciada no domínio das frequências espaciais. Os resultados indicam que o componente P1 foi encontrado em todas as condições de estimulação e adaptação ao flicker na frequência espacial mais baixa (0,4 cpg) em todas as condições temporais. Os resultados também indicam que ocorreu uma diminuição da energia da banda alfa na mesma condição de 0,4 cpg e um aumento da banda gama. Este trabalho concluiu que a adaptação ao flicker levou à diminuição da amplitude do potencial cortical provocado visual causado pela diminuição da energia das oscilações alfa e aumento da energia na banda gama em 0,4 cpg, representando uma modificação do balanço entre as duas vias visuais M e P nas células do córtex. / Visual Evoked Potential (VEP) has been a useful method to evaluate spatial vision in humans. Sustained observation of a visual stimulus produces several changes in neural responses at different processing levels in visual system. Previous studies has elucidated how primary visual cortex processing spatial information. Many others studies has also suggested about the contribution of parallel pathways M and P activation on the visual cortical responses evoked by a stimuli that excite only one of these pathways. Cortical excitation through a kind of stimulus that promotes one or both preferential adaptation could be a valuable approach to study activity from M and P pathways interactions on the visual responses. The purpose of this study is to evaluate the effects of luminance flicker adaptation on cortical responses elicited under favorable conditions of joint or differential M and P pathways activation, leading to an increase or decrease cortical responses. Eight subjects (20.25 ± 1.5) with normal vision acuity or corrected to 20/20 were tested. VEPs were recorded under three conditions of visual stimulation with no adaptation: sinusoidal gratings at 0.4, 2 and 10cpd presented at 1 Hz pattern-reversal stimulus (test stimuli). Other conditions was elicited by two-dimensional Gaussian mask adaptation stimulus with luminance variation in time domain (flicker) presented at 5 Hz, 10 Hz and 30 Hz temporal modulation. The experiment consisted on VEPs records above occipital scalp elicited by 8 seconds of adaptation stimulus followed by 2 seconds test stimuli. Cortical responses were evaluated in the time and temporal frequencies domain. In the time domain were measured latency and the P1 component amplitude (peak-line), while in the temporal frequency domain were evaluated amplitudes of alpha, beta and gamma frequency bands present in the in the records. VEPs elicited by the test stimuli were compared between flicker adaptation and no adaptation conditions. Main findings consisted on flicker adaptation that occurred differently at spatial frequencies domain. Results showed P1 component in all stimulation conditions and flicker adaptation at lower spatial frequency (0.4 cpd) in all time conditions. It has also showed a reduction at alpha band energy and an increase in the gamma band at same condition. This study concluded that flicker adaptation led to VEP amplitude decreased due to loss of alpha oscillations energy and gamma band energy increased at 0.4 cpd, and it represented a modification on the balance between M and P visual pathways.

Master of Science / Department of Architectural Engineering and Construction Science / Raphael A. Yunk / Autism Spectrum Disorders, (ASD) are being diagnosed at an alarming rate. Students with ASD face many challenges in educational environments and struggle to overcome daily distractions. Students with ASD have variances in neuron connections that cause them to receive and understand their environment differently than a student without special needs. In the educational classrooms, fluorescent lighting is a significant source of extraneous stimuli that not only a source of annoyance but can also trigger common symptoms of ASD. Fluorescent fixtures economically provide an acceptable uniformity and quality of illumination, but also have disadvantages that can aggravate symptoms in students with ASD. Ballasts are required for the operation of fluorescent fixtures. These ballasts, especially if not replaced at the end of their usable life, can generate an audible hum and cyclical flickering of light. Alternative light sources, such as incandescent lamps and fixtures should be evaluated and installed not only in special needs classrooms but standard group classrooms as well. Providing additional sources or quality sources of light may help students with ASD focus on the information presented in the classroom. Traditional classroom design needs to be re-evaluated to accommodate the needs of those students with ASD to better provide a comfortable and less distracting learning environment. It is difficult to establish rigid standards for lighting designs sensitive to individuals and special needs occupants'. By understanding the symptoms of ASD and taking into account the occupants needs lighting designers will be better able to design an environment that is both comfortable and educational. This report will address the classroom environment and student considerations in order to develop parameters and design practices that will assist new lighting designers.

Sixteen Nerodia rhombifera were used in each of two experiments investigating operant conditioning of the tongue flicker response. A yoked pair design was utilized throughout phases of baseline, continuous reinforcement, partial reinforcement, and extinction. During partial reinforcement, one-half of the experimental animals were reinforced FR-4 and the other half were reinforced continuously. Control subjects were treated as were their experimental partners, with the exception of noncontingent reinforcement. Statistical comparisons between means for groups during the CRF phase, partial reinforcement phase, and extinction phase were nonsignificant. However, because some snakes in the experimental groups appeared to show increases in response rate during CRF and FR conditions, the possibility exists that modification of task parameters will produce positive results in future research.

Master of Science / Department of Electrical and Computer Engineering / William B. Kuhn / A technique for measuring and characterizing transistor noise is presented. The primary goal of the measurements is to locate the 1/f noise corner for select transistors in Silicon-on-Sapphire processes. Additionally, the magnitude of the background channel noise of each transistor is measured. With this data, integrated circuit (IC) engineers will have a qualitative and quantitative resource for selecting transistors in designs with low noise requirements. During tests, transistor noise behavioral change is investigated over varying channel lengths, device type (N-type and P-type), threshold voltage, and bias voltage levels. Noise improvements for increased channel lengths from minimal, 1.0μm, and 4.0μm are measured. Transistors with medium and high threshold voltages are tested for comparison of their noise performance. The bias voltages are chosen to represent typical design values used in practice, with approximately 400 mV overdrive and a drain-to-source voltage range of 0.5 to 3.0V. The transistors subjected to tests are custom designed in Peregrine’s 0.5μm (FC) and 0.25μm (GC) Silicon-on-Sapphire (SOS) processes. In order to allow channel current noise to dominate over other circuit noise, the transistors have extraordinarily large aspect ratios (~2500 - 5000). The transistor noise produced is amplified and measured over a frequency range of 1kHz - 100MHz. This range allows the measurement of each device’s low and high frequency noise spectrum and resulting noise corner.

Orientadora: Ahda Piorkoski Grilo Pavani / Dissertação (mestrado) - Universidade Federal do ABC. Programa de Pós-graduação em Energia.

Sensory deficits represent a major global public health problem. According to the World Health Organization, vision impairment affects an estimated 300 million people worldwide, and hearing impairment affects an estimated 360 million people worldwide. Consistent clinical evaluations for all individuals with sensory deficits cannot be practically realized due to the rising costs of healthcare, capital and labor limitations, and inaccessibility to healthcare due to a multitude of factors including proximity. The high prevalence of visual and hearing deficits can be lessened through consistent, comprehensive, at-home testing which can allow a larger amount of the affected and at-risk populations to be screened for abnormal function earlier and prior to permanent loss, and provide a wealth of patient-specific data that can be used to understand the time-scale of diseases and monitor the effectiveness of clinical interventions in unprecedented detail. While health-oriented smartphone applications exhibit a strong presence on the app stores, these applications are seldom vetted by expert scientists, engineers, and clinicians, and there are considerable opportunities for methodological improvements. The present work discusses the creation, calibration, and proof-of-concept, preliminary validation of a suite of psychophysical tests implemented as smartphone applications that can be utilized to rapidly and objectively quantify several functional sensory behaviors including flicker sensitivity, contrast sensitivity, visual acuity, and hearing-in-noise. Rigorous steps were undertaken to perform the necessary calibrations (a feat not routinely achieved by the creators of existing medical smartphone applications), and ensure the technical validity of the varying stimuli presented. Preliminary tests in the clinic have documented the potential of these tests to objectively provide numerous quantifications of, but not limited to, individual visual and hearing function, and variation between normal and abnormal subjects and function. The foundation laid by this work allows novel psychophysical tests to rapidly be implemented, vetted, and added to this battery of publicly and universally accessible medical smartphone applications.

The bounded-hybrid superiority hypothesis (BHSH) predicts stable hybrid zones are characterized by hybrids having the highest fitness within the zone. The dynamic-equilibrium hypothesis (DEH) predicts hybrids to have the lowest fitness and mating should be strongly assortative in the hybrid zone. I used phenotypic-based hybrid indices (HI) to assess mating patterns, reproductive success, and survival of hybridizing northern flickers (Colaptes auratus) within the hybrid zone at Riske Creek, British Columbia. Contrary to the BHSH, flickers showed significant assortative pairing (P = 0.038) which may result via passive mate choice if yellow and red flickers migrate from allopatric winter ranges. North American band recoveries show red-shafted and yellow-shafted flickers winter on different sides of the Rocky Mountains while red-orange hybrids from Riske Creek winter in the range of red-shafted flickers. Arrival dates of phenotypes did not support the idea that mating patterns are caused passively via different arrival schedules. However, assortative mating patterns did correlate with regional weather patterns along flicker migration routes as well as the North Atlantic Oscillation (NAO) a continental weather pattern that has been shown to influence various aspects of the annual cycle in other birds. If variable weather patterns result in different mating patterns by affecting migration, the geographic location of the northern portion of the zone may be variable due to the migratory behaviour of individuals.<p>There were no differences among yellow, orange and red flickers to win more agonistic contests or have earlier nest initiation dates, larger clutch sizes, greater hatching success, or produce more fledglings. No colour group had a higher likelihood of having a successful compared to a depredated nesting attempt. Aggression was similar between red (N = 21) and yellow flickers (N = 20) during taxidermy model presentations of pure red-shafted and yellow-shafted flickers. Using Akaikes information criterion (AIC) in Program MARK, I determined survival was best modeled as either constant between males and females or varying annually according to weather. Models incorporating HI had less support but suggested that survival is best modeled as a linear relationship where red-shafted flickers have the highest survival. Survival modeled in quadratic relationships found hybrid flickers to have the highest apparent survival estimates in support of the BHSH. Overall there was no support for reduced hybrid fitness, but survival appears to be influenced more by annual variation rather than strictly by an individuals HI. Overall, I failed to find reduced hybrid fitness in support of the DEH but also failed to find increased hybrid fitness as predicted by the BHSH. Annual changes in selection pressure could prevent introgression of hybrid genes throughout the zone if selection favours red-shafted genes in some years and yellow-shafted genes in other years.

Good power quality is not only determined by uninterruptable power supply, voltage deviations also affect the function of the network and the equipment connected. Electromagnetic disturbances as flicker, harmonics, interharmonics and unbalance are decreasing the power quality. How are the measurement methods and restrictions stated, to keep the voltagedeviations within reasonable limits and thereby maintaining the networkfunction? Lillgrund wind farm has power quality restrictions set by E.ON Elnät to fulfil in the connection point to the subtransmission network. In addition isa fault ride through requirement set by SVK. All equipment connected tothe network are introducing voltage changes, which can be measured at the point of connection. The scope of the thesis has been to explicitly determine Lillgrund‟s emissions. Three-phase voltage and current measurements have been performed, with measurement systems comprising different bandwidth, to analyse the power quality parameters.Comparisons between standard documentation and technical specifications have been made in order to precise what is considered as good power quality and how it can be measured accurately.

The bounded-hybrid superiority hypothesis (BHSH) predicts stable hybrid zones are characterized by hybrids having the highest fitness within the zone. The dynamic-equilibrium hypothesis (DEH) predicts hybrids to have the lowest fitness and mating should be strongly assortative in the hybrid zone. I used phenotypic-based hybrid indices (HI) to assess mating patterns, reproductive success, and survival of hybridizing northern flickers (Colaptes auratus) within the hybrid zone at Riske Creek, British Columbia. Contrary to the BHSH, flickers showed significant assortative pairing (P = 0.038) which may result via passive mate choice if yellow and red flickers migrate from allopatric winter ranges. North American band recoveries show red-shafted and yellow-shafted flickers winter on different sides of the Rocky Mountains while red-orange hybrids from Riske Creek winter in the range of red-shafted flickers. Arrival dates of phenotypes did not support the idea that mating patterns are caused passively via different arrival schedules. However, assortative mating patterns did correlate with regional weather patterns along flicker migration routes as well as the North Atlantic Oscillation (NAO) a continental weather pattern that has been shown to influence various aspects of the annual cycle in other birds. If variable weather patterns result in different mating patterns by affecting migration, the geographic location of the northern portion of the zone may be variable due to the migratory behaviour of individuals.<p>There were no differences among yellow, orange and red flickers to win more agonistic contests or have earlier nest initiation dates, larger clutch sizes, greater hatching success, or produce more fledglings. No colour group had a higher likelihood of having a successful compared to a depredated nesting attempt. Aggression was similar between red (N = 21) and yellow flickers (N = 20) during taxidermy model presentations of pure red-shafted and yellow-shafted flickers. Using Akaikes information criterion (AIC) in Program MARK, I determined survival was best modeled as either constant between males and females or varying annually according to weather. Models incorporating HI had less support but suggested that survival is best modeled as a linear relationship where red-shafted flickers have the highest survival. Survival modeled in quadratic relationships found hybrid flickers to have the highest apparent survival estimates in support of the BHSH. Overall there was no support for reduced hybrid fitness, but survival appears to be influenced more by annual variation rather than strictly by an individuals HI. Overall, I failed to find reduced hybrid fitness in support of the DEH but also failed to find increased hybrid fitness as predicted by the BHSH. Annual changes in selection pressure could prevent introgression of hybrid genes throughout the zone if selection favours red-shafted genes in some years and yellow-shafted genes in other years.