The microscopes ability to distinguish details of a sample or specimen
In 1609, an italian scientist called Galileo Galilei developed his first compound microscope
In the mid 17th century, Robert Hooke, the English father of microscopy made improvements to Galileo's design. He was the first person to observe and describe a cell
In the mid 19th century, Charles A Spencer produced microscopes that could magnify objects up to 5000 times their normal size with blue light
Light microscopes cannot be used to view objects that are smaller than half the wavelength of light. This is because the objects are not large enough to interfere with the passage of the light waves
Light wavelength varies between 400nm (nanometers) for violet light and 700nm for red light
The resolving power of a microscope refers to its ability to differentiate between closely spaced objects
Transmission Electron Microscope
TEM allows electrons to be transmitted through the specimen before viewing
Sections that are more dense and absorb more electrons appear blacker in the image
Dense areas appear more black or dark on an electron graph
Scanning Electron Microscope
IN SEM, specimens are frozen, fractured and coated in gold atoms
They are used to form a TV image on a cathode ray tube
A beam of electrons is scanned to and fro across the specimen. The electrons that are reflected off the surface area collected
Advantages of TEM over SEM
Transmission electron microscope has a greater resolving power
TEM has a resolution of 0.5nm, whereas SEM has a resolution between 5nm and 20nm
Advantages of SEM over TEM
Surface structures of specimens can be seen easily
Structures can be seen in 3D
Scanning electron microscopes can view much larger samples than the TEM can
Limitations of electron microscopy
Expensive to buy and run
Preparations of material is time consuming, expensive and technical
Preservation and staining can damage tissue structure