TY - JOUR
T1 - Polarization Modulation Differential Interference Contrast (Pol Mod Dic) Microscopy
T2 - An Improvement for Video Microscopy
AU - Stromgren Allen, N.
AU - Moxley, D.
AU - Collings, D.
AU - Holzwarth, G.
N1 - Publisher Copyright:
© 1998 Microscopy Society of America.
PY - 1998/7/1
Y1 - 1998/7/1
N2 - Differential interference contrast (DIC) light microscopy, particularly when coupled with digital image processing, is a powerful tool for the high-resolution microscopy of unstained, transparent biological specimens and can equally well be applied to semiconductor measurements. We show analytically, and with images of diatoms, plant cells and protoplasts, that switching the polarization of the incident light by 90 degrees, changes the image highlights found in conventional DIC images into shadows and vice versa (1). Using a ferroelectric liquid-crystal modulator, this switching can be done at frame rates, synchronized to the camera. By subtracting alternate frames, a stream of difference DIC images is created. We call this technique Pol Mod DIC. Subtraction of alternate images is carried out efficiently by frame buffer operations and amounts to massively parallel synchronous detection. A similar method has been applied to confocal microscopy (2).
AB - Differential interference contrast (DIC) light microscopy, particularly when coupled with digital image processing, is a powerful tool for the high-resolution microscopy of unstained, transparent biological specimens and can equally well be applied to semiconductor measurements. We show analytically, and with images of diatoms, plant cells and protoplasts, that switching the polarization of the incident light by 90 degrees, changes the image highlights found in conventional DIC images into shadows and vice versa (1). Using a ferroelectric liquid-crystal modulator, this switching can be done at frame rates, synchronized to the camera. By subtracting alternate frames, a stream of difference DIC images is created. We call this technique Pol Mod DIC. Subtraction of alternate images is carried out efficiently by frame buffer operations and amounts to massively parallel synchronous detection. A similar method has been applied to confocal microscopy (2).
UR - http://www.scopus.com/inward/record.url?scp=85180092088&partnerID=8YFLogxK
U2 - 10.1017/S1431927600020778
DO - 10.1017/S1431927600020778
M3 - Article
AN - SCOPUS:85180092088
SN - 1431-9276
VL - 4
SP - 130
EP - 131
JO - Microscopy and Microanalysis
JF - Microscopy and Microanalysis
ER -