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R V Shack

Publications and source records attributed to R V Shack.

5 recordsLinked to original sources

Measurement of the three-dimensional microscope point spread function using a Shack-Hartmann wavefront sensor.

We present a technique to measure the wavefront in the exit pupil of a microscope to determine the microscope's three-dimensional point spread function (PSF) experimentally. The wavefront yields the microscope PSF through a Fourier transform that models propagation of light from the exit pupil to the image plane. A Shack-Hartmann wavefront sensor is used to measure the wavefront shape by recording lateral displacements of a grid of focused spots created by a lenslet array. The displacement of each spot is related to the local wavefront slope. Thus, with appropriate sampling across the exit pupil, the entire wavefront can be reconstructed. This technique does not require the use of a sub-resolution object to obtain the three-dimensional microscope PSF. Consequently, larger, brighter fluorescent objects may be imaged, thereby reducing the requirements for detector sensitivity and leading to a three-fold increase in the axial range over which the PSF is measured. The Shack-Hartmann technique results in a description of the PSF as a continuous function whose sampling is not dependent on the size of the CCD pixels. The Shack-Hartmann sensor is not limited by the numerical aperture of the objective and can easily be calibrated to measure the PSF at any wavelength.

Image Processing, Computer-Assisted↗

Design for a fast fluorescence laser scanning microscope.

The design of a fast fluorescence laser scanning microscope is described and illustrated, with discussion of the design consideration of the principal components, including the optical elements. The system, now under construction at the Optical Sciences Center of the University of Arizona, is expected to provide very-high-speed scanning, at a high spatial sampling density, of large object areas while retaining a flexibility of applications. The projected scanning rate approximates the rate achieved by flow cytometry; the projected rates of information generation should be orders of magnitude higher.

Equipment Design↗

A novel method of focus sensing for the laser scanner microscope.

An unconventional approach to the focus-sensing problem in a high-speed cell scanner has resulted in a method of directly detecting the position of the cell layer. This is done by using two coaxial but axially shifted beams, one focused on either side of the cell layer. The modulation induced in each beam by the cell's fine structure is compared electronically to yield the focus-error signal. The beams are orthogonally polarized, therefore separable, and are independently detected. The two detector-output signals are used to form both the focus-error signal and the scanner's primary data signal. This focus-sensing technique has been analytically modeled and experimentally demonstrated for a high-numerical-aperture system. In that system, the depth of focus is less than the thickness of the cell layer. It is shown that a lens fabricated from a birefringent crystal is an attractive means of forming the required orthogonally polarized axially shifted beams.

Cytological Techniques↗

Ultrafast laser scanner microscope: design and construction.

The design of an ultrafast laser scanner microscope has been completed, and an experimental model has been constructed. Details of the novel objective lens design, the automatic focus system, the high-speed polygon scanner and the fast clock system are given. Results from initial tolerance testing as well as the first recorded images are presented.

Microscopy↗