Skip to main content Accessibility help
×
Hostname: page-component-76fb5796d-vfjqv Total loading time: 0 Render date: 2024-04-26T17:53:47.164Z Has data issue: false hasContentIssue false

Chapter F1 - Light microscopy

from Part F - Optical microscopy

Published online by Cambridge University Press:  05 November 2012

Igor N. Serdyuk
Affiliation:
Institute of Protein Research, Moscow
Nathan R. Zaccai
Affiliation:
University of Bristol
Joseph Zaccai
Affiliation:
Institut de Biologie Structurale, Grenoble
Get access

Summary

Historical review

Light microscope

Mid-fifteenth century

The simple one-lens microscope was available at this time, with low-power magnifiers being used for the examination of insects. From these early beginnings, glass lenses of increased power were developed. A. Leeuwenhoek (1632– 1723) produced remarkable microscopes. One of them had a resolving power of 1.35 μm, which was enough for basic cytology. About the same time the basic idea for the compound microscope, in which two or more lenses are arranged in such way to form an enlarged image of an object, occurred independently to several people in the Netherlands (H. Jansen, his son Zacharias and H. Lippershey). Subsequently, compound microscopes became widely available.

1830

J. Lister published the first work in which the construction and design of achromatic microscope lenses was placed on theoretical bases. He showed how two separate achromatic lenses could be combined to act as a single lens so that the image rendered would be completely free from chromatic aberration and from distortion caused by curvature of the lenses. This discovery opened the way to the construction of high-power microscope lenses over the next 50 years. The first achromatic microscope lenses appeared in the Netherlands at about the end of the eighteenth century.

The latter part of the nineteenth century

E. Abbe was the outstanding figure in development of the microscope. Abbe placed the theory of microscopic image formation on a sound basis by emphasising the importance of the light diffracted by the object in resolving its fine details.

Type
Chapter
Information
Methods in Molecular Biophysics
Structure, Dynamics, Function
, pp. 627 - 640
Publisher: Cambridge University Press
Print publication year: 2007

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Kino, G. S., and Corle, T. R. (1989). Confocal scanning optical microscopy. Physics Today, 42, 55–62.CrossRefGoogle Scholar
Lichtman, J. W. (1994). Confocal microscopy. Sci. Am., 271, 40–45.CrossRefGoogle Scholar
Bergethon, P. R. (1995). In The Physical Basis of Biochemistry. The Foundation of Molecular Biophysics. Ch. 16. New York: Springer.Google Scholar
Webb, R. H. (1996). Confocal optical microscopy. Rep. Prog. Phys., 59, 427–471.CrossRefGoogle Scholar
Lemasters, J. J., Chacon, E., Zahrebelski, G., Reece, J. M., and Nieminen, A.-L. (1993). Laser scanning confocal microscopy of living cells. In Optical Microscopy. Emerging Methods and Application. eds. Herman, B. and Lemasters, J. J.. San Diego: Academic Press.Google Scholar
Webb, R. H. (1999). Theoretical bases of confocal microscopy. Meth. Enzymol., 307, 3–20.CrossRefGoogle Scholar
Betzig, E., and Trautman, J. K. (1992). Near-field optics: microscopy, spectroscopy, and surface modification beyond the diffraction limit. Science, 257, 189–195.CrossRefGoogle ScholarPubMed
Shiku, H., and Dunn, R. C. (1999). Near field scanning optical microscopy. Analytical Chem., 23A–29A.CrossRefGoogle ScholarPubMed
Kino, G. S., and Corle, T. R. (1989). Confocal scanning optical microscopy. Physics Today, 42, 55–62.CrossRefGoogle Scholar
Lichtman, J. W. (1994). Confocal microscopy. Sci. Am., 271, 40–45.CrossRefGoogle Scholar
Bergethon, P. R. (1995). In The Physical Basis of Biochemistry. The Foundation of Molecular Biophysics. Ch. 16. New York: Springer.Google Scholar
Webb, R. H. (1996). Confocal optical microscopy. Rep. Prog. Phys., 59, 427–471.CrossRefGoogle Scholar
Lemasters, J. J., Chacon, E., Zahrebelski, G., Reece, J. M., and Nieminen, A.-L. (1993). Laser scanning confocal microscopy of living cells. In Optical Microscopy. Emerging Methods and Application. eds. Herman, B. and Lemasters, J. J.. San Diego: Academic Press.Google Scholar
Webb, R. H. (1999). Theoretical bases of confocal microscopy. Meth. Enzymol., 307, 3–20.CrossRefGoogle Scholar
Betzig, E., and Trautman, J. K. (1992). Near-field optics: microscopy, spectroscopy, and surface modification beyond the diffraction limit. Science, 257, 189–195.CrossRefGoogle ScholarPubMed
Shiku, H., and Dunn, R. C. (1999). Near field scanning optical microscopy. Analytical Chem., 23A–29A.CrossRefGoogle ScholarPubMed

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

  • Light microscopy
  • Igor N. Serdyuk, Institute of Protein Research, Moscow, Nathan R. Zaccai, University of Bristol, Joseph Zaccai, Institut de Biologie Structurale, Grenoble
  • Book: Methods in Molecular Biophysics
  • Online publication: 05 November 2012
  • Chapter DOI: https://doi.org/10.1017/CBO9780511811166.029
Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

  • Light microscopy
  • Igor N. Serdyuk, Institute of Protein Research, Moscow, Nathan R. Zaccai, University of Bristol, Joseph Zaccai, Institut de Biologie Structurale, Grenoble
  • Book: Methods in Molecular Biophysics
  • Online publication: 05 November 2012
  • Chapter DOI: https://doi.org/10.1017/CBO9780511811166.029
Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

  • Light microscopy
  • Igor N. Serdyuk, Institute of Protein Research, Moscow, Nathan R. Zaccai, University of Bristol, Joseph Zaccai, Institut de Biologie Structurale, Grenoble
  • Book: Methods in Molecular Biophysics
  • Online publication: 05 November 2012
  • Chapter DOI: https://doi.org/10.1017/CBO9780511811166.029
Available formats
×