The translated conceptual survey of physics / stablization of the focal plane in two photon excitation fluorescence microscopy

As a reflection of my career to be an effective college physics teacher, my thesis is in two parts. The first is in education research, the focus of this part is to have a tool to evaluate pedagogies I have learned at the school and plan to apply in my classrooms back home. Consequently, this resulted in the development of the translated conceptual survey of physics ( TCSP).;(TCSP) was designed by combining some questions from the Force Conceptual Inventory (FCI), and the Conceptual Survey of Electricity and Magnetism (CSEM) to assess student's understanding of basic concepts of Newtonian mechanics and electricity and magnetism in introductory physics. The idea of developing this questionnaire is to use it in classrooms back home as a part of a long term objective to implement what has been realized in the area of education research to improve the quality of teaching physics there. The survey was initially written in English, validated with interviews with native English speakers, translated into Arabic, and then validated via an interview with a native Arabic speaker. We then administered the survey to two different English-speaking intro physics courses and analyzed the results for consistency.;The objective of the second part in my thesis is to expand my knowledge in an area of physics that I have interest in, and getting involved in a scientific research to develop skills I need as a teacher. My research is in optical physics, in particular, I am working on one of the challenges in implementing two photon excitation luorescence (TPEF) microscopy in imaging living systems. (TPEF) microscopy has been shown to be an invaluable tool for investigating biological structure and function in living organisms. The utility of (TPEF) imaging for this application arises from several important factors including it's ability to image deep within tissue, and to do so without harming the organism. Both of these advantages arise from the fact that (TPEF) imaging is done with excitation wavelengths in the near infrared (NIR). The (NIR) wavelength regime, 750- 1100nm, penetrates deep (>100 &mgr;m) into tissue, and has been used to image to depths of up to 1 mm. Further, the longer excitation wavelengths are less absorbing than the traditional ultraviolet wavelengths used in confocal microscopy, and are consequently less damaging. As a result, (TPEF) is presently the preferred tool for visualizing dynamics by biologists. One important aspect of imaging living systems, however, is that they move! This adds to the challenge of trying to study some particular biological function(s). This thesis begins to address this issue by combining a simple micro controller circuit that can be linked to a remote focusing scheme that will make it possible to lock a focal plane to a specific depth inside a living, moving specimen.