Mammalians process their photoreceptions through lateral eyes; however, non-mammalian vertebrates and invertebrates possess additional extraretinal photoreceptors over their bodies to detect light stimuli. Chromatophores, i.e. dermal specialized pigment cells, play important roles in the regulation of body patterns. Since chromatophores derive from neural crest, they share the common embryonic origin with retina. Recent evidence shows that they are light-sensitive due to opsin expression. In the present study, the expression of seven cone opsins was detected in tilapia caudal fin tissues. Moreover, distinct photoresponses were found in two chromatophore types. Regardless of stimulating wavelengths, melanophores tend to disperse and maintain cell shape at dispersion stage by shuttling pigment granules. Conversely, erythrophores respond to light in a wavelength-dependent manner. The opsin expression profiles of melanophores and erythrophores imply SWS1 and RH2 group genes may play important roles in chromatophore photoresponses. Through measuring photosensitivity, I suggest the two opsins play opposite roles in light-induced translocations of pigment granules within erythrophores: SWS1 for aggregations at UV and short wavelength regions and RH2b for dispersion in middle/long wavelengths. An antagonistic interaction occurs in the overlapping of the absorbance spectra of the two opsins. I also found that the photoresponses take place along with the occurrence of the change of cell membrane potential. In addition, the effect of different light backgrounds (broad spectrum, short wavelength-rich, and red-shifted light conditions) on the photosensitivity of tilapia erythrophores was investigated. I found that the major opsin classes (SWS1 and RH2b) responsible for photoresponses remain constant in three groups of erythrophores. Together, I postulate that melanophores may serve as a light filter in integumentary tissues, and the chromatically antagonistic mechanism enables tilapia erythrophores to sense the subtle change of environmental photic condition and to fine-tune pigmentation. I also investigated the ontogenetic change of photoresponses of rainbow trout melanophores. Distinct photoresponses were found in parrs and smolts. Furthermore, smolt melanophores responded to light in a wavelength-dependent manner. Since the change of coloration and visual system during smoltification of salmonids is regulated by thyroid hormone (TH), I suggest that the development of melanophore photosensitivity is associated to TH as well. / Thesis (Ph.D, Biology) -- Queen's University, 2013-08-27 09:57:22.907

Mammalians process their photoreceptions through lateral eyes; however, non-mammalian vertebrates and invertebrates possess additional extraretinal photoreceptors over their bodies to detect light stimuli. Chromatophores, i.e. dermal specialized pigment cells, play important roles in the regulation of body patterns. Since chromatophores derive from neural crest, they share the common embryonic origin with retina. Recent evidence shows that they are light-sensitive due to opsin expression. In the present study, the expression of seven cone opsins was detected in tilapia caudal fin tissues. Moreover, distinct photoresponses were found in two chromatophore types. Regardless of stimulating wavelengths, melanophores tend to disperse and maintain cell shape at dispersion stage by shuttling pigment granules. Conversely, erythrophores respond to light in a wavelength-dependent manner. The opsin expression profiles of melanophores and erythrophores imply SWS1 and RH2 group genes may play important roles in chromatophore photoresponses. Through measuring photosensitivity, I suggest the two opsins play opposite roles in light-induced translocations of pigment granules within erythrophores: SWS1 for aggregations at UV and short wavelength regions and RH2b for dispersion in middle/long wavelengths. An antagonistic interaction occurs in the overlapping of the absorbance spectra of the two opsins. I also found that the photoresponses take place along with the occurrence of the change of cell membrane potential. In addition, the effect of different light backgrounds (broad spectrum, short wavelength-rich, and red-shifted light conditions) on the photosensitivity of tilapia erythrophores was investigated. I found that the major opsin classes (SWS1 and RH2b) responsible for photoresponses remain constant in three groups of erythrophores. Together, I postulate that melanophores may serve as a light filter in integumentary tissues, and the chromatically antagonistic mechanism enables tilapia erythrophores to sense the subtle change of environmental photic condition and to fine-tune pigmentation. I also investigated the ontogenetic change of photoresponses of rainbow trout melanophores. Distinct photoresponses were found in parrs and smolts. Furthermore, smolt melanophores responded to light in a wavelength-dependent manner. Since the change of coloration and visual system during smoltification of salmonids is regulated by thyroid hormone (TH), I suggest that the development of melanophore photosensitivity is associated to TH as well. / Thesis (Ph.D, Biology) -- Queen's University, 2013-08-27 09:57:22.907

This study describes the creation of various furfural derivatives and their respective light sensitivity.

Thesis (Magister Technologiae - Discipline Electrical Engineering, Faculty of Engineering) -- Vaal University of Technology / Discomfort glare is a topic that has been investigated for many years without any reasonable explanation regarding its effect on the human visual system. Results of previous research concluded that established methods have a lot of similarities in implementation; but a number of differences when comparing the results of observer's evaluations with the mathematically calculated glare ratings. Therefore, an alternative method of evaluating the influence of exposure to an unshielded light source was investigated to establish a more reliable and realistic response from observers. In order to address the discrepancies of previous evaluation systems concerning observer's varying opinions regarding the level of discomfort experienced, it was decided to investigate the feasibility of evaluating the brain activity of the observers exposed to an unshielded incandescent lamp. This was done in order to facilitate the differences in each individual observer's sensitivity to bright light sources and the influence of personal taste therefore, eliminating the effect of personal interpretation. The main purpose of this study was to determine whether it would be possible to get any response regarding brain functions when an observer is exposed to a bare light source. In order to determine the pathway of visual stimuli it was necessary to investigate the operating principles of the human eye in detail. Because the eye is only an instrument that makes seeing possible; it was also important to investigate the brain and all its different functions. The part of the brain where visual interpretation takes place was indicated as the occipital lobe. This is the part of the brain monitored for any change of functional status by taking measurements with an electroencephalogram (EEG). Measurements were indeed possible; it was presented as a suppression of the alpha brain activity. During the testing procedure it was observed that the observers were not equally photosensitive. There was also a difference in the amount of alpha suppression with the observer's eyes open and closed respectively. Because the alpha rhythm has a tendency to increase with closed eyes it was much easier to notice the suppression.

Many of us can relate to being tired and maybe even feel down during the winter months. Reports show that we spend more and more time indoors and with that, problems linked to low daylight exposure increases. The main recommendation from doctors is to try to spend more time outdoors to really get that dosage of the sun that one needs. Research also shows that people are not aware of the actual amount of time they spend either indoors or in their cars.  With this in mind, what could we do to create a healthier way of living?  In this project, I have chosen to explore how we can motivate and inspire people with a sensitivity to light to spend more time outdoors and help them stimulate their circadian rhythm. People that suffer from symptoms could in worst cases not even leave their bed making them unable to cope with their life. Using natural ways of changing habits could in most cases have a better effect than what heavy medication does.

Organic bioelectronics develops electronic devices at the interface with living systems using organic electronic materials. These devices can identify various chemical species and regulate the operation of individual cells, tissues, or organs. A famous organic bioelectronic device is the organic electrochemical transistor (OECT), a highly versatile circuit component that has been used in applications spanning from biosensing to neuromorphic computing. OECTs can be operated in aqueous electrolytes and use organic mixed ionic-electronic conductors (OMIECs) in their channel (and sometimes as gate electrode coating) that can transport electronic and ionic charges, making them ideal for bridging biological systems and silicon-based electronic devices. Electron-transporting (n-type) OMIEC materials have received particular attention because high-performance n-type OECTs can be used to build inverters, sensors, and complementary amplifiers. However, electron transport in an aqueous and ambient environment under the application of electrical fields is a complex phenomenon that requires in situ investigation techniques. Understanding how films operate in such media can allow to construct novel sensors and eliminate the loss processes. This Ph.D. dissertation focuses on the impact of the environment, specifically oxygen, and light, on the performance of n-type OECTs and shows how to use this knowledge to develop OECT-based glucose sensors and photodetectors. Chapter 1 introduces the mixed charge transport phenomenon in conjugated polymers and how to use it in OECT operation. OECT fabrication and various designs are described, setting the ground for the sensors we will show in the following chapters. The experimental procedures used to evaluate the critical figures of merit of the materials and the transistor performance are described in detail. Chapter 2 introduces how OECTs can be used to transduce biochemical binding events. When employing the OECT platform for biochemical sensing, it is essential to differentiate between the faradaic, capacitive, and potentiometric contributions to the sensor response. Understanding the underlying mechanisms is critical for optimizing performance. This chapter explains these different sensing mechanisms with literature examples. Chapter 3 compiles all experimental details relevant to the investigations presented in Chapters 4 and 5. Chapter 4 investigates the working mechanism of a novel n-type OECT-based glucose sensor relying on an enzymatic reaction. This chapter shows the oxygen reaction reactions and the importance of monitoring contact potentials during device operation to understand how detection occurs. The work unveils the role of the oxygen sensitivity of the n-type material on the sensor operation and suggests paths to improve performance. Chapter 5 explores the interactions of light with n-type OMIECs and how to utilize them to build water-compatible phototransistors. The first part of the chapter involves a characterization of the light/matter interplay of an n-type film and a demonstration of how to use it to build a photoelectrochemical transistor. The second part of the chapter expands this work to other n-type materials and assesses their light sensitivity, building a relationship between material property and device performance. Since most detection events lead to a change in the surface of materials, techniques that monitor surface roughness and profile changes in situ can be useful. Chapter 6 describes an atomic force microscopy (AFM) setup that can be used to investigate binding events and electrochemical doping and de-doping dynamics of OMIEC films. This chapter is intended to assist researchers in developing in-operando AFM procedures studying OMIEC films.

Lighting is one of the most important issues for the perception of the physical environment and the ability to perform. Lighting design of classrooms is therefore crucial to achieve the goals of education. The Swedish school aim to provide a working environment supporting every child. As children are individuals their perceptions and light preferences differ just as adults do. Accessibility to tools to be able to customize for the individual child are therefore important. To support our planet, every new product developed should be considered regarding sustainability.  This is particularly important of products designed for children as they are our future. This thesis will focus on finding a task light option suitable for the classroom environment. By researching literature, performing market research and conducting interviews with school professionals, important characteristics of a school task light were established. Based on the findings, a task light proposal was developed including the defined properties.

During the industrialization of the 19th century the negative health effects of vitamin D was discovered as children in the cities developed osteomalacia or more commonly known as rickets caused by vitamin D deficiency. Vitamin D is produced in the skin from 7-dehydrocholesterol during sun-exposure and enhances intestinal phosphor and calcium absorption thus enhancing the bone remodeling process. Now, in the 21st century, Vitamin D is still relevant as positive health effects have been recognized and with it an increased number of samples and a demand for accurate analyzing. Vitamin D is commonly believed to be sensitive to ultraviolet radiation in serum and blood samples and therefore have traditionally been kept protected from light exposure from the time of sampling until the finished analyze. However recent studies have proven 25- hydroxyvitamin D (25[OH]D) to be stable in both whole blood and serum. As previous studies have been primarily conducted in research laboratories with the aim to study vitamin D under specific research-laboratory conditions the aim of this study was to study the stability of 25[OH]D in serum and whole blood within both primary care- and hospital laboratories under normal and exaggerated conditions with the purpose to evaluate possible pre-analytical issues with everyday handling processes. The assay used was high pressure liquid chromatography-tandem mass spectrometry, HPLCMS/MS, and the sought analytes 25-hydroxyvitamin D2 and 25-hydroxyvitamin D3, 25[OH]D2 and 25[OH]D3. The results showed that 25-hydroxyvitamin D is stable in serum for 24 hours at room temperature whilst exposed to light both ultraviolet and fluorescent. The analyte is also stable for up to four freeze-thaw cycles rendering the process of light-protection and samples frozen immediately after centrifugation superfluous. The results also ensure reliable results even if samples are accidently left on benchtops or saved refrozen to be reanalyzed at a later date. / Under den industriella revolutionen på 1800 talet upptäcktes de negativa hälsoeffekterna av vitamin D-brist då barnen i städerna utvecklade rakit (osteomalaci) eller engelska sjukan som sjukdomen också kallas på grund av brist på sol och D-vitamin. Vitamin D produceras i huden från 7-dehydrokolesterol vid solexponering och ökar upptaget av fosfor och kalcium i tarmen som i sin tur förbättrar återuppbyggnaden av skelettet. Vitamin D är fortfarande aktuell även nu i vår tid men då för dess nyupptäckta hälsofrämjande egenskaper som till exempel förebyggandet av coloncancer. Detta medför även en ökning av antalet analyser och kräver därmed en adekvat analysmetod. Traditionellt har det antagits att vitamin D är ljuskänsligt i alla former därför har blod och serum ljusskyddats, från provtagningstillfället fram tills dess att analysen är utförd. Dock har nya studier visat att 25-hydroxyvitamin D (25[OH]D) är mycket stabilt bundet till vitamindbindande protein i både serum och helblod. Syftet med studien var att utvärdera om 25[OH]D i serum och helblod behöver ljusskddas genom att studera stabiliteten hos 25[OH]D i både serum och helblod under normala primärvårdslaboratorie- och sjukhuslaboratorieförhållanden samt under extrema förhållanden för att utvärdera eventuella preanalytiska problem eller fel relaterade till den vardagliga hanteringen av vitamin D prover. Proverna analyserades med högupplösande vätskekromatografi-tandem masspektrometri, HPLC-MS/MS, och de sökta analyterna var 25-hydroxyvitamin D2 and 25-hydroxyvitamin D3, 25[OH]D2 och 25[OH]D3. Resultat från studien visade att 25-hydroxyvitamin D är stabilt i serum i 24 timmar i rumstemperatur med ljusexponering från både ultraviolett och fluorescerande ljus. 25-hydroxyvitamin D är även stabil i serum upp till fyra frys- och tiningscykler. Detta gör att provhanteringen kan förenklas genom att dessa prover inte behöver ljusskyddas samt att serumet ej behöver frysas in direkt efter centrifugering. Resultatet säkerställer även tillförlitliga resultat om prover lämnas framme på bänken av misstag eller om prover behöver sparas och frysas om för att analyseras vid senare tillfälle.

Problématique : Certaines personnes souffrent d'avoir un horaire de sommeil trop tardif qu'elles n'arrivent pas à modifier pour satisfaire les exigences liées à leur emploi ou à leurs études. Ces individus souffrent de privation de sommeil et de somnolence lorsqu'ils doivent se conformer à un horaire socialement acceptable. Malgré sa prévalence importante, l’étiologie d’un horaire trop tardif reste méconnue. Objectif: Évaluer des facteurs pouvant contribuer au maintien d’un horaire de sommeil tardif chez des jeunes adultes. Méthodes : Quatorze jeunes adultes se plaignant d’un horaire de sommeil trop tardif ont été comparés à des sujets appariés qui avaient un horaire de sommeil adapté. L’heure de coucher (HC) était après minuit pour les sujets tardifs et avant minuit pour les sujets adaptés. Les sujets étaient admis au laboratoire 5h avant l’HC et garder en obscurité pour 6h. Ils étaient ensuite exposés à 1,5h de lumière bleue. La mélatonine salivaire et la vigilance subjective étaient mesurées aux 30 minutes. La suppression de mélatonine a été utilisée pour déterminer la sensibilité circadienne à la lumière. Le dim light melatonin onset (DLMO) a été utilisé pour déterminer la phase circadienne. Résultats : Le DLMO survenait plus tard dans le groupe tardif que dans le groupe adapté. Il n’y avait pas de différence de suppression de mélatonine après 1,5h d’exposition à la lumière. Néanmoins, une corrélation entre la sensibilité à la lumière et la phase circadienne a été trouvée dans le groupe tardif. Les sujets tardifs présentaient aussi une augmentation plus lente de la somnolence subjective en soirée. Conclusion : Nos résultats suggèrent qu’une phase circadienne en délai, une augmentation plus lente du besoin de dormir et une sensibilité circadienne à la lumière accrue contribuent à la plainte d’un horaire de sommeil trop tardif. / Problem: Some people suffer from having a delayed sleep schedule that they can’t modify to satisfy school/work requirements. These individuals suffer from sleep deprivation and sleepiness when they have to comply with a socially acceptable schedule. Despite its high prevalence, the etiology of a delayed schedule remains unknown. Objective: This study aims to elucidate factors that might contribute to the maintenance of a delayed sleep schedule in young adults. Methods: Fourteen young adults (8 women) complaining of delayed sleep schedule were compared to matched subjects with an adapted sleep schedule. Habitual bedtime (HB) was after midnight in all delayed subjects and before midnight in all adapted subjects. Subjects were admitted 5h before HB and kept in dim light for 6h. They were then exposed for 1.5h to blue light. Salivary melatonin and subjective sleepiness were assessed every 30 min. Melatonin suppression was used to measure circadian sensitivity to light. Dim light melatonin onset (DLMO) was used to estimate circadian phase. Results: DLMO was later in the delayed than in the adapted group. There was no difference for melatonin suppression over the 1.5h of light exposure. However, in the delayed group, there was a significant correlation between DLMO and melatonin suppression. There was a smaller increase of subjective sleepiness in the delayed subjects than in the adapted subjects before HB. Conclusions: Our results suggest that a delayed circadian phase, a slower build-up of sleep propensity and an enhanced circadian sensitivity to evening light contribute to the complaint of a delayed sleep schedule.

No description available.