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Magnification and Resolution

Light Microscopes

Electron Microscopes

Of all the techniques used in biology microscopy is probably the most important. The vast majority of living organisms are too small to be seen in any detail with the human eye, and cells and their organelles can only be seen with the aid of a microscope. Cells were first seen in 1665 by Robert Hooke (who named them after monks' cells in a monastery), and were studied in more detail by Leeuwehoek using a primitive microscope.  

 Units of measurement 



= 1 m



= 10-3 m



= 10-6 m



= 10-9 m



= 10-12 m



= 10-10 m  (obsolete)

Magnification and Resolution  [back to top]

By using more lenses microscopes can magnify by a larger amount, but this doesn't always mean that more detail can be seen. The amount of detail depends on the resolving power of a microscope, which is the smallest separation at which two separate objects can be distinguished (or resolved).

The resolving power of a microscope is ultimately limited by the wavelength of light (400-600nm for visible light). To improve the resolving power a shorter wavelength of light is needed, and sometimes microscopes have blue filters for this purpose (because blue has the shortest wavelength of visible light).  


Magnification is how much bigger a sample appears to be under the microscope than it is in real life.

Overall magnification = Objective lens x Eyepiece lens

Resolution is the ability to distinguish between two points on an image i.e. the amount of detail

Different kinds of Microscopes:  [back to top]

Light Microscopy: This is the oldest, simplest and most widely-used form of microscopy. Specimens are illuminated with light, which is focussed using glass lenses and viewed using the eye or photographic film. Specimens can be living or dead, but often need to be stained with a coloured dye to make them visible. Many different stains are available that stain specific parts of the cell such as DNA, lipids, cytoskeleton, etc. All light microscopes today are compound microscopes, which means they use several lenses to obtain high magnification. Light microscopy has a resolution of about 200 nm, which is good enough to see cells, but not the details of cell organelles. There has been a recent resurgence in the use of light microscopy, partly due to technical improvements, which have dramatically improved the resolution far beyond the theoretical limit. For example fluorescence microscopy has a resolution of about 10 nm, while interference microscopy has a resolution of about 1 nm.  

Preparation of Slide Samples

Electron Microscopy. This uses a beam of electrons, rather than electromagnetic radiation, to "illuminate" the specimen. This may seem strange, but electrons behave like waves and can easily be produced (using a hot wire), focused (using electromagnets) and detected (using a phosphor screen or photographic film). A beam of electrons has an effective wavelength of less than 1 nm, so can be used to resolve small sub-cellular ultrastructure. The development of the electron microscope in the 1930s revolutionised biology, allowing organelles such as mitochondria, ER and membranes to be seen in detail for the first time.

The main problem with the electron microscope is that specimens must be fixed in plastic and viewed in a vacuum, and must therefore be dead. Other problems are that the specimens can be damaged by the electron beam and they must be stained with an electron-dense chemical (usually heavy metals like osmium, lead or gold). Initially there was a problem of artefacts (i.e. observed structures that were due to the preparation process and were not real), but improvements in technique have eliminated most of these.

There are two kinds of electron microscope. The transmission electron microscope (TEM) works much like a light microscope, transmitting a beam of electrons through a thin specimen and then focusing the electrons to form an image on a screen or on film. This is the most common form of electron microscope and has the best resolution. The scanning electron microscope (SEM) scans a fine beam of electron onto a specimen and collects the electrons scattered by the surface. This has poorer resolution, but gives excellent 3-dimentional images of surfaces.

Transmission Electron Microscope (TEM)

Scanning Electron Microscope (SEM)
  • Pass a beam of electrons through the specimen. The electrons that pass through the specimen are detected on a fluorescent screen on which the image is displayed.

  • Thin sections of specimen are needed for transmission electron microscopy as the electrons have to pass through the specimen for the image to be produced.

  •  This is the most common form of electron microscope and has the best resolution 


Bacterium (TEM)
(Image provided by: ceiba.cc.ntu.edu.tw)

  • Pass a beam of electrons over the surface of the specimen in the form of a ‘scanning’ beam.

  • Electrons are reflected off the surface of the specimen as it has been previously coated in heavy metals.

  • It is these reflected electron beams that are focussed of the fluorescent screen in order to make up the image. 

  • Larger, thicker structures can thus be seen under the SEM as the electrons do not have to pass through the sample in order to form the image.  This gives excellent 3-dimensional images of surfaces

  • However the resolution of the SEM is lower than that of the TEM.

A head and the right eye of a fly
(Image provided by: Goran Drazic)


Four conodont elements stuck on a pin head (SEM)
(Image provided by
Mark Purnell)


Comparison of the light and electron microscope  [back to top]

Light Microscope Electron Microscope
Cheap to purchase (£100 – 500) Expensive to buy (over £ 1 000 000).
Cheap to operate. Expensive to produce electron beam.
Small and portable. Large and requires special rooms.
Simple and easy sample preparation. Lengthy and complex sample prep.
Material rarely distorted by preparation. Preparation distorts material.
Vacuum is not required. Vacuum is required.
Natural colour of sample maintained. All images in black and white.
Magnifies objects only up to 2000 times Magnifies over 500 000 times.
Specimens can be living or dead Specimens are dead, as they must be fixed in plastic and viewed in a vacuum
Stains are often needed to make the cells visible The electron beam can damage specimens and they must be stained with an electron-dense chemical (usually heavy metals like osmium, lead or gold).


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Last updated 18/06/2004