| Project/Area Number |
10650041
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Applied optics/Quantum optical engineering
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| Research Institution | Shizuoka University |
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Principal Investigator |
KAWATA Yoshimasa Faculty of Engineering, Shizuoka University, Associate Professor, 工学部, 助教授 (70221900)
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| Project Period (FY) |
1998 – 2000
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| Project Status |
Completed (Fiscal Year 2000)
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| Budget Amount *help |
¥3,600,000 (Direct Cost: ¥3,600,000)
Fiscal Year 2000: ¥900,000 (Direct Cost: ¥900,000)
Fiscal Year 1999: ¥1,300,000 (Direct Cost: ¥1,300,000)
Fiscal Year 1998: ¥1,400,000 (Direct Cost: ¥1,400,000)
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| Keywords | microscopy / confocal microscopy / polarization microscopy / laser / polarization anlaysis / sigle molecular / biology / optical elasticity |
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| Research Abstract |
A confocal microscope for the use of three-dimensional polarization analysis was developed. Since the pinhole before the detector eliminates the light whose polarization is rotated by an imaging lens, the polarization properties of specimens are observed with high contrast. The pinhole size required to achieve high contrast was discussed. Three-dimensional resolution of the polarization microscope was also demonstrated.
The three-dimensional imaging analysis using the extended Mie scattering theory was developed. In the analysis, we calculated the images of a Mie particle whose diameter is comparable with the wavelength of confocal microscope. It was found that, when we observe a Mie particle, polarization confocal microscopy is not affected by the polarization distortion that is due to focusing with high-numerical-aperture lenses and does not produce pseudopeaks in the images in comparison with conventional polarization microscopy. The three-dimensional resolution of the polarization microscope and the verification of the proposed analysis method were also discussed.
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