• DocumentCode
    3359653
  • Title

    Optical sectioning and fast optical focussing in microscopy

  • Author

    Wilson, Tony

  • Author_Institution
    Dept. of Eng. Sci., Univ. of Oxford, Oxford, UK
  • fYear
    2011
  • fDate
    3-4 Dec. 2011
  • Firstpage
    1
  • Lastpage
    1
  • Abstract
    The fundamental property, which any optical microscope that is to be used to finally produce three-dimensional images of a volume specimen must possess, is the ability to image efficiently (and infocus) only those regions the specimen that lie within a thin section in the focal region of the microscope. In order to image a three-dimensional volume of a thick specimen it is necessary to take a whole series of such thin optical sections as the specimen is moved axially through the focal region. There are many methods to produce optical sectioning of which the confocal optical system is just one. We shall review these methods and describe a particularly convenient method of implementation that uses white light illumination and real-time image formation and can lead, amongst other things, to enhanced optical sectioning.
  • Keywords
    biomedical optical imaging; optical focusing; optical microscopy; confocal optical system; enhanced optical sectioning; fast optical focussing; focal region; fundamental property; microscopy; real-time image formation; thin optical sections; three-dimensional images; three-dimensional volume; volume specimen; white light illumination; Biological processes; Biomedical optical imaging; Focusing; Lead; Microscopy; Optical imaging; Optical microscopy;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Functional Optical Imaging (FOI), 2011
  • Conference_Location
    Ningbo
  • Print_ISBN
    978-1-4673-0452-8
  • Type

    conf

  • DOI
    10.1109/FOI.2011.6154833
  • Filename
    6154833