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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 />

9

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