Olympus SZX16 Руководство по эксплуатации - Страница 8

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OBSERVATION

CAUTION

Fig. 1

Fig. 2

Fig. 3

Fig. 4

Always use a zoom magnification of 1X or more. The peripheral part of the illumination field will be

shaded under lower magnifications.

For the operating methods of the controls on the zoom microscope body, refer to the instruction

manual for the SZX16.

1. Pull out the shutter slider @ fully to the "shutter in" condition for the sake

of safety.

2. Rotate the filter turret ² to engage the desired filter in the light path. The

filter being engaged in the light path can be confirmed at position ³.

}See "

Combinations and Applications of Fluorescence Filters"

on page 6.

3. Set the main switch | of the power supply unit to " I " (ON).

The arc will stabilize in 5 to 10 minutes after ignition of the burner.

If you have not yet adjusted the centering of the mercury burner, center it

now (pages 13 to 15).

4. Place the specimen on the center of the stage plate 5.

}If transmitted light observation is not required, set the stage plate so that

the black side faces up.

If autofluorescence is noticeable, use the black plate of the optional SP-

FL fluorescence center plate.

If transmitted light observation is also performed, use a glass center plate.

If autofluorescence is noticeable during this, use the glass plate of the

optional SP-FL .

5. Push in the shutter slider @ to the empty or either ND filter position, bring

the specimen into focus and observe it.

}Adjust the collector lens focusing knob 6 as required.

}If the illumination is too bright, engage an ND filter in the shutter slider

into the light path.

}When fluorescence microphotography is required, all of the observation

light can be led to the TV/photo light path by using the optional SZX2-

TR30PT or SZX2-TTRPT trinocular observation tube with the 100% TV/

photo light path.

1. Pull out the shutter slider @ fully to the "shutter in" condition.

2. Rotate the filter turret ² to engage the dummy filter position in the light

path.

3. Bring the specimen into focus and observe it.

(Figs. 1 to 3)

(Fig. 4)