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1zIUK2Y
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DIATOMS UNDER<br />
THE ELECTRON<br />
MICROSCOPE<br />
Diatoms are a great factor in the ecosystem yet<br />
they are too small to be visible with naked eye.<br />
Even with the best optical microscope, we cannot<br />
come near enough. The whole diversity and<br />
richness of complicated structures hidden in the<br />
siliceous skeleton of these algae could be revealed<br />
only by scanning electron microscope (SEM).<br />
There is no doubt SEM is a wonderful tool<br />
covering almost all the needs that appear in the<br />
research work on surface structures of diatoms.<br />
Modern commercial SEM microscopes enable<br />
magnifications from approximately 10 to<br />
1,000,000 times allowing image resolution to<br />
1 nm. However, it must be stressed that real magnification<br />
as well as real resolution of micrograph<br />
depend not only upon the capacity of the microscope<br />
but to a high degree also upon the sample<br />
quality as well as some other factors.<br />
Electronic microscope is sizable and complicated<br />
machine. Along with a number of electric and<br />
electronic complexes it includes also a complicated<br />
vacuum system. In the microscope column<br />
where is also a chamber for the sample, a series<br />
of pumps is maintaining vacuum which enables<br />
forming and managing of the electron beam. That<br />
fore the sample which we will investigate must be<br />
stable in vacuum, resistant to bombardment with<br />
electrons within electron beam and has to have<br />
a clean surface, while high magnifications reveal<br />
even the finest muck.<br />
In this kind of microscope the image doesn’t<br />
appear at a time like we are used in everyday life,<br />
rather it is appearing gradually, step by step. Electron<br />
beam is focused to a spot in the sample surface.<br />
Microscope tilting system scans the electron<br />
beam in a raster fashion over a rectangular area<br />
of the sample surface. The signal emerging from<br />
the collision of the beam with the surface of the<br />
sample investigated is transmitting from detectors<br />
via electronic amplifiers and filters to the<br />
screen where — point after point and row after<br />
row — the picture of the investigated structure is<br />
constituted. We could understand that the quality,<br />
resolution and communication value of the<br />
image are determined by the size of image points<br />
and by the density of the raster along which the<br />
beam is moving; magnification, however, results<br />
from the ratio of the dimensions of the raster on<br />
the specimen and the raster on the display device.<br />
In other words, magnification tells us, how many<br />
times alga, which we are observing is smaller<br />
from its image on the screen.<br />
Dr. Kazimir Drašlar<br />
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