scholarly journals Erratum to: The Influence of the Numerical Aperture of a Beam Probing an Object on the Determination of the Thickness of a Layered Object in Confocal Microscopy

2019 ◽  
Vol 127 (3) ◽  
pp. 586-586
Author(s):  
D. V. Lyakin ◽  
L. A. Maksimova ◽  
A. Yu. Sdobnov ◽  
V. P. Ryabukho
2012 ◽  
Vol 35 (1) ◽  
pp. 135-145 ◽  
Author(s):  
Leonilde Roselli ◽  
Elena Stanca ◽  
Francesco Paparella ◽  
Annunziata Mastrolia ◽  
Alberto Basset

2010 ◽  
Vol 98 (3) ◽  
pp. 493-504 ◽  
Author(s):  
Yong Wu ◽  
Mansoureh Eghbali ◽  
Jimmy Ou ◽  
Rong Lu ◽  
Ligia Toro ◽  
...  

2012 ◽  
Vol 4 (2) ◽  
pp. 66 ◽  
Author(s):  
DShyam Prasad Reddy ◽  
HeraldJ Sherlin ◽  
Pratibha Ramani ◽  
PAjay Prakash

Author(s):  
Shuangmu Zhuo ◽  
Liqin Zheng ◽  
Xiaoqin Zhu ◽  
Jianxin Chen ◽  
Shusen Xie ◽  
...  

2005 ◽  
Vol 44 (11) ◽  
pp. 2072 ◽  
Author(s):  
Tom Collier ◽  
Michele Follen ◽  
Anais Malpica ◽  
Rebecca Richards-Kortum

Author(s):  
Alan Bearden ◽  
Terrence L. Wong ◽  
Morgan W. Mitchell ◽  
Leslie C. Osborne ◽  
Michael P. O’Neill

As discovered by Abbé, a fundamental limit to the lateral resolution of a conventional optical microscope is produced by “far-field” aperture diffraction at the objective lens. This limitation can be expressed in terms of the Airy disc which relates the obtainable resolution to the wavelength of light used and the objective’s numerical aperture (NA). In scanning confocal microscopy with a laser-produced Gaussian profile illumination beam, the lateral resolution in given by 1.22λ/NA. The axial resolution in this design is improved by the use of a pinhole aperture to pass light only from the objective’s focal plane. Typical best values for lateral (x,y) and axial (z) resolution for visible wavelength scanning confocal microscopy are ~200nm and ~300nm with a NA=1.4 oil immersion objective.Although optical microscopy displays limited resolution when compared to some forms of electron and scanning-probe microscopies (STM, AFM), the convenience of sample preparation and its ease in performing in vivo studies has given rise to new methods of increased resolution (e.g., “near field” techniques, photon-tunneling, phase interference contrast).


2005 ◽  
Vol 13 (1) ◽  
pp. 30-31
Author(s):  
RA McLeod ◽  
P Jacquemin ◽  
S Lai ◽  
RA Herring

Confocal Holography is a combination of two well known concepts: confocal microscopy and light (laser) holography. Confocal microscopy places an aperture at a conjugate focus to the specimen focus. This filters any rays that are not on the focus plane, allowing a 3-dimensional image of the specimen to be built up over a set of planes.Holography is the measurement of both the amplitude and phase characteristics of light. Typically most methods only measure the amplitude of the image. The phenomenon of interference allows the determination of the phase shift for a coherent source as well. The phase information is directly related to the index of refraction of a material, which in turn is a function of the temperature and composition.


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