This instruction manual has been written for the use of the Olympus System Microscope Model
BHT.
It is recommended that you read the manual carefully in order to familiarize yourself fully
with the use of the microscope, so that you can obtain optimum performance from it.
IMPORTANT
0
bserve the following points carefully:
Operation
Always handle the microscope with the care it deserves, and avoid abrupt motions.
1.
Avoid the use and maintenance of the microscope in direct sunlight, high temperature and
2.
humidity, dust and vibration.
3.
Only use the tension adjustment ring for altering the tension of the coarse adjustment
knobs. (Do not twist the two coarse adjustment knobs in opposite directions simultaneously, as this will cause damage.)
4.
Make sure that the voltage selector switch on the base plate is set to conform with the local
mains voltage.
Make it a point of grounding the microscope to prevent electric accidents.
5.
Maintenance
1.
Lenses must always be kept clean. Carefully wlpe off oil or fingerprints deposited on the
a
lens surfaces with gauze moistened with
Do not use organic solutions to wipe the surfaces of various components. Plastic parts,
2.
especially, should be cleaned with neutral detergent.
3.
Never disassemble the microscope for repair. Only authorized Olympus service personnel
should make repairs.
The microscope should be covered with the vinyl dust cover provided and stored in a place
4.
free from humidity and fungi. For extended storage it is recommended to keep objectives
and eyepieces in desiccators, containing desiccants such as silica gel.
small amount
of
xylene, alcohol or ether.
CONTENTS
STANDARD EQUIPMENT
II.
NOMENCLATURE
Ill. ASSEMBLY
IV. IDENTIFICATION AND FUNCTION OF VARIOUS COMPOhlENTS
V. OPERATION
A. Switching on the Light Source
1
voltage Adjustment and Light Intensity
Placement of a Specimen Slide
B.
pizGq
kwecimen Slide
C. Observation Tube
1.
2.
3.
D.
Condenser Adjustment
1.
Field lris Diaphragm
Aperture lris Diaphragm
...................................
..................................
...............
1
lnterpupillary Distance Adjustment
Diopter Adjustment
Light Path Selector
Condenser Centration
...
I
..............
.
I
I
. .
E.
Focusing Adjustment
1.
Tension
l~se of Rubber Cap for Fine Adjustment Knob
2.
Pre-Focusing Lever
3.
Adjustment
F. Use of Immersion Objectives
G.
Photomicrography
VI. OPTICAL DATA
VII. TROUBLESHOOTING
of
Coarse Adjustment Knobs and Fine Adjustment
of
............................
/
Stage Block Height
.....
. .
I.
STANDARD
EQUIPMENT
Component
Microscope stand BHT-F
I
Line cord UYCP
Binocular tube BH2-B 130
Observation tubes
I
Quintuple revolving nosepiece BH2-5RE
Square mechanical stage with right-hand
wide variety of combinations, standard or optional, is available according to your
of
various components and interchangeable accessories as shown in the
Observation tube
Microscope stand
"I
Stage
Condenser
Base
Halogen lamp
holder
-
-
Ill.
ASSEMBLY
This picture illustrates the sequential procedure of assembly. The numbers indicate the
order of assembly of various components. Remove dust caps before mounting components.
Take care to keep all glass surfaces clean, and avoid scratching the glass surface.
NOTE:
For numbers
O
@
and 0 please refer to explanations in detail on the next page.
Eyepiece
Condenser clamping screw
Condenser
(The
N.A.
should
scale
face
engraved on the con-
denser
microscope front.)
the
Microscope stand
Halogen bulb
Line cord
0
Outlet
Explanations in detail
@
Mounting the stage
1)
Loosen the stage clamping screw @ by
rotating counterclockwise. (Fig.
2)
Insert the stage into the mounting dovetail of the microscope stand slowly and
lock with clamping screw.
@
Mounting the revolving nosepiece
1)
L-oosen the nosepiece clamping screw
(Fig.
2)
2)
Aligning the nosepiece dovetail slide to
@
,
the mounting block
piece slowly all the way.
NOTE:
Do not tilt or rock the nosepiece while inserting into the
mounting block.
push in the nose-
1)
a.
Fig.
1
@
Mounting the observation tube
1)
Loosen the clamping knob @ fully. Pull
spring-loaded clamping knob
will cause the locating pin
3)
(Fig.
screw further until the pin withdraws.
2)
With clamping knob @ pulled out, insert
the circular dovetail of the observation
tube into the ring dovetail.
Voltage lowers
pulled toward the microscope
front.
as
the lever is
Photo tube
Condenser height
adjustment knob
Pre-focusing lever
adjustment
L~ne cord
7
Arrow mark
increase
Filter mount
6
+O
in
diaphragm diameter.
indicates
Summary of Putting
the
Microscope into Operation
Match the voltage selector switch to local mains voltage (page
Switch on the light source (page
Place a specimen slide on the mechanical stage (page
Coarse focus with the
Make interpupillary distance and diopter adjustments (page
Adjust the condenser position (page
Swing in the desired objective.
Adjust light intensity.
Fine focus.
Adjust aperture iris diaphragm and field iris diaphragm (page
1
OX
9).
objective (page
12).
10.
9).
13).
9).
11).
12).
Adjustment of Illumination System for Various Objective Powers
I
Objective
1
magnification
1
Achromatic-
condenser
B H2-AAC
condenser
BH2-CD
Abbe
Condenser
Swing-out
condenser
BH2-SC
Model
Low power
condenser
BH2-UL-C
BHT
1
Compatible
*N.A.
is somewhat low, but st111 compatible with
(Cut off this page at dotted line and put it on the wall near the microscope for
scopic procedure.)
Swing in top
a
100X
lens
objective.
OLYMPUS
use
as a reminder
of
micro-
V.
OPERATION
A. Switching on the Light Source
1)
Ascertain that the voltage selector switch
is set to conform with the local mains volt-
age. (Fig.
If the switch is not correctly set, adjust it by
means of the Allen wrench provided or a
screwdriver.
2) Place the sliding voltage control lever on the
right side of the microscope base to
tion closest to you (low voltage position).
Switch on the light source. (Fig. 4)
4)
a
@
posi-
I
-
Fig. 4
Voltage Adjustment and Light Intensity
As you push the control levera in the direc-
tion of the arrow in order to obtain increas-
ing intensity (Fig.
will display the lamp voltage.
Placement of a Specimen Slide
B.
1)
Rotate the coarse adjustment knobs in
the direction of the arrow to rack down the
stage so that a specimen slide can be placed
on the stage. (Fig.
NOTE:
2)
Opening the spring-loaded finger of the
specimen holder with one hand, place a
specimen slide inside the holder. (Fig. 7)
When the slide comes in contact with the
back of the specimen holder, slowly return
the spring-loaded finger.
WARNING:
The rotation of the coarse and fine
adjustment knobs in the direction of
the arrow will rack down the stage.
5),
the
LED
readout
6)
If
the spring-loaded finger is
returned quickly, it may cause
damage to the specimen slide.
1
@
Fig.
Fig.
5
6
Fig. 7
I
Cover Glass
An Olympus objective engraved "160/0.17" requires a cover glass of 0.17mm thickness.
If the numerical aperture of the objective is 0.7 or higher (except immersion objectives) and
no correction collar is provided, the resolving power deteriorates to a great extent if cover
glass thickness deviates from the above listed value.
IVOTE: In some countries a 0.17mm cover glass corresponds to a designation of #I%.
A cover glass (0.4mm thick) for blood counting, etc. can be used with Olympus objectives
except
1
Specimen Slide
I
D
Plan 40X, S Plan Apo 40X and S Plan 100X.
(
Specimen slides 0.8 mm to
recommended for Olympus objectives.
Specimen slides 0.8 mm to
recommended for the darkfield condenser
and the differential interference contrast condenser.
3)
Bring the portion of the specimen for observation into the light path by means of the
low drive control knobs. (Fig.
*
Tighten the stage clamping screw @ in the
microscope front.
1
stage
1
The specimen holder can accommodate two
standard specimen slides simultaneously.
The specimen holder is removable to obtain
a large unobstructed stage surface to hold
specimens up to
To rotate the stage loosen the stage clamping
@
screw
stage into the desired direciton. (Fig.
Q
Stage clips for use with immersion objectives.
(Fig. 10)
A
pair of stage clips are optionally available
to hold the specimen on the stage, eliminating a specimen drag caused by immersion oil
between slide and stage surface. The clips
can be inserted into the holes
on the specimen holder.
2) Looking through the eyepieces with both
eyes, adjust the interpupillary distance of
the binocular tube by adjusting the
@
knurled dovetail slides
left eyepiece tubes with both hands until
perfect binocular vision is obtained. (Fig.
11)
Diopter Adjustment
1)
Look at the image through the right eyepiece with your right eye and focus on
the specimen with the fine adjustment
knobs.
2) Next, look at the image through the left
eyepiece with your left eye and rotate the
diopter adjustment ring
the specimen without using the coarse
and fine adjustment knobs.
Light Path Selection
1)
The trinocular tube is provided with a
light path selector knob to direct the light
to the observation tube andlor to the
photo tube in 3 positions. (Fig.
of the right and
@
to focus on
(Fig.
12)
13)
Fig. 12
Fig. 13
I
Pushed in all the way
(V)
/
1
Application
The indicator plate is provided at the knob port to summarize the usage of the above
table; it can be consulted before operating the knob.
The colors of the letters correspond with the color bands on the knob shaft.
100% into binocular tube
@
Observation
@
Dark specimens
V:
Viewer (white letter)
&
CV: Camera
C: Camera (red letter)
viewer (yellow-green letters)
Knob Position
Pulled out halfway
(C. V.)
20% into binocular tube
80% into ~hoto tube
Photomicrography (fo-
Pulled out all the way
(C)
1
into
photo
tube
1
I
D.
Condenser Adjustment
1.
Condenser Centration
1)
Stop down the field iris diaphragm with
knurled ring
tion of the arrow.
2)
Use the condenser height adjustment
knob
@
down until an image of the field diaphragm can be seen clearly in the eyepieces. The rotation of the knob in the
direction of the arrow lowers the condenser.
Field iris
diaphragm image Field of view
@
to move the condenser up and
,
by rotating in the direc-
(Fig.
14)
-7g+('J
Fig. 15
3)
Bring the field iris diaphragm image into the center of the field of view with the two con-
denser centering knobs
4)
Widen the diameter of the iris diaphragm progressively. If the polygonal image of the iris
diaphragm becomes inscribed in the field it means that the field diaphragm
(Fig. 15)
@.
(Fig. 14)
is
centered.
Field Iris Diaphragm
The field iris diaphragm controls the diameter of the ray bundle impining on the speci-
is
men surface and therefore, by stopping down the field diaphragm until it
larger than the field of view, it can reduce stray light, which in turn increases image defi-
nition and contrast.
In order to achieve optimum objective performance, the opening of the aperture iris
diaphragm should be matched to the numerical aperture of the objective in use. It is
often preferable, however, to stop down the aperture diaphragm slightly more than indicated by the objective N.A. This will result in better image contrast, increased depth of
focus and a flatter field.
After completing focus adjustment, remove one of the eyepieces from the observation tube and look into the empty
eyepiece tube. As you stop down the
aperture iris diaphragm, the image of the
iris diaphragm can be seen in the objective pupil. Adjust the opening of the
diaphragm to match the N.A. of the objective in use. If the specimen is low in
contrast, it is recommended to stop down
70%
--
80%
to
16)
of the objective
N.A.
Opening of the
aperture diaphragm
Objective exit pupil
(Fig.
I
Fig. 16
slightly
Focus Adjustment
Tension
Fine Adjustment.
Although the tension of the coarse adjust-
ment knobs has been already adjusted for
optimum performance by the manufacturer,
it is possible to personally adjust the tension
of the coarse adjustment for either heavy or
light movement depending on the operator's
preference by rotating the tension adjustment ring
The ring can be rotated by inserting a screwdriver into one of the holes on the periphery of
the ring. The clockwise rotation (in the direction of the arrow) tightens the coarse adjustment knobs. Do not loosen the ring too much, because the stage may drop or the fine
adjustment knobs may slip.
NOTE: Do not rotate the right and left coarse adjustment knobs in the opposite directions
I
Use of Rubber Cap for Fine Adjustment Knob
of
Coarse Adjustment Knobs and
'3
'i
la
rr
Fig.
@.
(Fig.
17)
simultaneously. If the stage drops and the specimen goes out of focus, the tension
adjustment ring is too loose. Tighten the ring.
I
Attaching this cap over the fine adjustment
knob increases the sensitivity of the fine focusing motion. (The rubber cap is optionally available.)
17
-b
2.
Pre-Focusing Lever
@
This lever
contact between specimen and objective as
well as to simplify coarse focusing. (Fig.
The lever is locked after coarse focus has
been accomplished. This prevents further
upward travel of the stage by means of the
coarse adjustment knobs, and automatically
provides a limiting stop if thestage is lowered
and then raised again. The pre-focusing lever
does not restrict fine focusing.
3.
Adjustment
In addition to the vertical movement of the
stage by means of coarse and fine adjust-
ments, the stage block height can be changed
for observation of specimens 'which are
thlcker than standard slides, e.g. chambers,
flasks, etc. with much larger thickness.
The stage block height can be adjusted by
loosening the stage block locking screw
with the Allen wrench provided and retightening it at the upper position. Then, dislocate the
lower limit stop pin beneath the stage block into a lower tapped hole. After lowering the
stage block, reclamp the stage block locking screw
is provided to prevent possible
of
Stage Block Height
18)
@
a.
(Fig.
19)
Fig.
Fig.
10
19
F.
Use of Immersion Objectives
1)
Focus the specimen with a low power objective.
2)
Put a drop of immersion oil on the specimen slide and the front lens of the immersion
objective.
3) Turn the revolving nosepiece to bring the immersion objective into the light path, and focus
with the fine adjustment knobs.
NOTE:
G.
Photomicrography
The Olympus Photomicrographic Equipment Model PM-IOAD is uniquely qualified to be
used with the BHT microscope for routine and advanced photomicrography. A separate,
detailed instruction manual
For quick reference, however, you may want to refer to the following pointers when using
the PM-IOAD.
1.
Photographic Eyepiece
Use
graphy.
Insert the eyepiece into the eyepiece tube of
the photo tube. (Fig.
@
For immersion condensers such as an achromatic-aplanatic condenser or Abbe
condenser, remove the specimen from the mechanical stage and place a drop of
immersion oil on the front lens of the condenser. Then, place the specimen on
the stage and slowly raise the condenser until firm contact with the underside of
the specimen slide
@Care should be taken to prevent oil bubbles from forming in the oil
condenser and specimen slide. If any, re-apply immersion oil, for these bubbles
greatly deteriorate the lens performance.
@After use carefully wipe off the immersion oil deposited on the lens surfaces
with gauze moistened with xylene. Never leave oil on the lens surfacesafter use
as oil remnants will seriously impair the performance of the lens system.
NF
K
photo eyepieces for photomicro-
is
made.
is
available for the PM-TOAD camera system.
film
20)
between
2.
Mounting the Photographic Unit
Slip the body of the photographic unit over the
photo tube. Align the dots on photo tube and
the PM-1 OAD body and clamp the camera unit
to the photo tube. (Fig.
3.
Setting the Light Path Selector
Refer to section C.3. on page
21)
11.
Fig.
Fig.
20
21
4.
Focusing Procedure
Use the field of view eyepieces for focusing on the fi Im plane. Each field of view eyepiece
has a focusing front lens and a reticle with
by a specific power NFK photo eyepeice. (Fig.
The number at each frame indicates the
magnification of the photo eyepiece. The
i,mage in the field of view eyepiece and the
image on the film plane are in focus at the
same time. Several type field of view eyepieces are available, according to the film
size employed.
4
frames, each frame indicating the area covered
22).
,:f;~l
i')
&.'
- - - -
JJLll
Fig. 22
Field of view eyepiece
Attachment camera
1) Select the field of view eyepiece matching the camera back in use and insert it into the
right eyepiece tube of the trinocular tube, aligning locating groove and locating pin.
2)
While looking through the field of view eyepiece, rotate the eyepiece front lens in screw
mount to focus on the double cross lines in the field. For sharp focusing with objectives
4X or lower, the focusing magnifier FT is recommended.
3) Bring the specimen detail to be photographed within the frame corresponding to the
power of the NFK eyepiece in use and focus on the specimen with the microscope fine
adjustment knobs. Make sure the light path selector knob on the observation tube is
either on the white (V) or yellow-green (CV) band.
4)
It is recommended to tighten the tension adjustment ring considerably to prevent the
stage from dropping during long exposures.
35WH K10X
35 mm Back
PWH KIOX
3%"
x
4%"
Polaroid
Back
4X5WHKlOX
4" x 5"
Sheet Film or
Polaroid Film
Holder
MHWHKIOX
16 mm Bolex
camera
120 Roll Film
Holder
VI.
OPTICAL
DATA
D
Achromat
D
Plan
Ach.
(mm)
W.D.
Focal
length
Eyepiece
WHKlOX
(Field
number
20)
*
Resolving
power
Total
mag.
Focal
depth
.
Field of
(mm)
view
Immersion objectives
0.10
18.2
30.03
(fi)
(PI
3.36
40X 100X 400X
171.6
10X
0.25
7.2
16.9
1.34
27.45
2
40X
0.65
0.6
4.58
0.52
3.0
lOOX*
1.30
0.20
1.91
0.26
0.7 171.6
34.23
4X
0.10
7.03
3.36
1OX
0.25
7.4
17.5
1.34
27.45
40X
0.65
0.27
4.67
0.52
3.0 0.7
10OX1
The resolving power and focal depth are obtained with fully opened aperture diaphragm.
Technical terms:
Working distance: The distance from the cover glass to the nearest point of the
objective.
Numerical aperture: The N.A. represents a performance number which can be com-
pared to the relative aperture (f-number) of a camera lens. The
N.A. values can be used for directly comparing the resolving
powers of all types of objectives. The larger the N.A., the higher
resolving power.
Resolving power:
The ability of a lens to register small details. The resolving power
of a lens is measured by its ability to separate two points.
Focal depth:
The distance between the upper and lower limits of sharpness in
the image formed by an optical system. As you stop down the
aperture iris diaphragm, the focal depth becomes larger. The
larger the N.A. of an objective the shallower the focal depth.
Field number:
A number that represents the diameter in mm of the image of
the field diaphragm that is formed by the lens in front of it.
Field of view diameter: The actual size of the field of view in mm on the object surface.
1.25
0.17
1.75
0.27
VII.
TROUBLESHOOTING
If you are unable to obtain full performance from your microscope, please consult with the
table below as pointers for troubleshooting.
front
Remedy
lenses.
I
I
1.
a) With illuminator switched I Field iris diaphragm is not I Open diaphragm to proper
I
b)
Phenomenon
Optical System
on, the field of view is
dark.
Field of view is cut off or
illuminated irregularly.
pulled out to C position.
Light path selector lever is
stopped m idway.
Nosepiece is not clicked into
place.
Nosepiece is not correctly
1
mounted.
1
The power of objective used
exceeds the illumination ca-
pacity of condenser.
1
Condenser is not centered. ( Center condenser.
Field iris diaphragm is stopped Open diaphragm to proper
down excessively. diameter.
c) Dust or dirt is visible in Remove dust, etc.
the field of view.
1
Dirty specimen.
I
~ust on eyepiece.
d) Excessive image contrast.
Condenser is lowered too Adjust condenser height.
much.
Aperture iris diaphragm is
stopped down excessively.
Cause
position.
Click it into proper position
according to your purpose.
Slightly rotate nosepiece until
it clicks into place.
Insert nosepiece dovetail into
I
microscope frame all the way,
I
then lock.
Choose a condenser to meet
your purpose.
'lean
I
I
Open diaphragm to proper
diameter.
I
I
1
Phenomenon
e) Resolution problems:
lmage is not sharp.
Insufficient contrast.
lmage details lack definition.
f)
Field of view is partially
out of focus, or image is
partly out of focus.
g) Specimen image is partial-
ly out of focus.
h) Field of view becomes
only slightly brighter by
increasing voltage.
Cause
Non Olympus objectives are
used.
positioned in the light path.
I
Objective correction collar is I Rotate correction collar, keep-
I
not adjusted.
I
used with immersion oil.
Bubbles in immersion oil.
Immersion oil designated by
1
Olympus is not used.
Dirty specimens.
Dust on condenser lens.
Nosepiece is not correctly
1
mounted.
1
Objective is not correctly
positioned in the light path.
Specimen is not correctly
positioned on stage.
Nosepiece is not correctly
mounted.
Objective is not correctly
positioned in the light path.
Condenser is not centered.
Condenser is not correctly
centered.
Condenser is lowered too
Use Olympus
tives.
microscope frame all the way,
1
ing specimen in fine focus
until optimum resolution is
1
Remove bubbles (and reapply oil).
Use Olympus immersion oil.
1
Clean.
lnsert nosepiece dovetail into
(
microscope frame all the way,
1
then lock.
Slightly rotate nosepiece until
it clicks in place.
Place specimen slide correctly
on stage, and place stage clips
open it.
lnsert nosepiece dovetail into
microscope frame all the way,
then lock.
Slightly rotate nosepiece until
it clicks into place.
Center condenser.
Center condenser.
Adjust condenser height.
Remedy
LB
series objec-
1
1
2.
Electric System
I
a) Illuminator
(or too dark) even when I is not matched with local
I
b) Voltage for illuminator
cannot be raised.
is
too bright I Line voltage selector switch
mains voltage
Match selector switch to
mains voltage.
I
1
C)
d) Bulb burns out frequently.
1
3.
a) Coarse adjustment knob is
b)
C) Stage cannot be raised to
d) Stage cannot be lowered
e) Objective front lens hits
1
4.
a) l ncomplete binocular vi-
Phenomenon
Lamp &off and
on
1
I
r
Coarse and Fine Adjustments
too tight.
Stage drops or specimen
goes out of focus during
observation due to slipping
fine adjustment knobs.
the upper limit.
to the lower limit.
specimen before coming
into focus.
Observation Tubes
sion.
1
1
I
Cause
Bulb filament is likely to / Replacebulb.
burn out.
Loose electric connections. I Check all connections.
Line voltage selector switch is
not matched with local mains mains voltage.
voltage.
Bulb is not standard one.
Tension adjustment ring is
tightened too much.
User is trying to raise stage
above the focusing limit imposed by the engaged prefocusing lever.
Tension adjustment ring is
too loose.
Pre-focusing lever is engaged
in lower than focusing position.
Stage is mounted too low.
1
I I
I
I
Specimen is placed on stage
upside down.
l nterpupillary distance is not
correctly adjusted.
Diopter adjustment is incom- I Complete the diopter adjustplete.
Right and left eyepieces are
not matched.
User is unaccustomed to binocular vision.
I
1
1 1 1
1
5.
Stage
a) l mage easily goes out of
focus when you touch the
stage.
b)
Specimen stops midway
on the east-west traverse. I sitioned.
1
Stage is not correctly locked.
Specimen is not correctly po- Adjust specimen position.
1
Remedv
Match selector switch to
Use standard bulb.
Loosen ring properly.
Unlock lever.
Tighten ring properly.
Unlock lever.
Raise stage mount with Allen
wrench.
Reverse specimen
Correct the interpupillary distance.
ment.
Use a pair of matched eye-
pieces.
Prior to looking into the bi-
nocular observation tube, look
at a far away obiect.
Clamp stage securely.
-
1
I
1
1
I
1
1
I
I
I
SAN-El BUILDING,
1
-CHOME,
SHINJUKU-KU,
22-2,
NlSHlSHlNJUKU
TOKYO,
JAPAN
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