Dark Field Viewing
Dark field optics are a low cost alternative
to phase contrast optics. The contrast and
resolution obtained with inexpensive dark field
equipment may be superior to what you
have with student grade phase contrast equipment.
It is surprising that few manufacturers and vendors
promote the use of dark field optics.
A dilute suspension of yeast
cells makes a good practice
specimen for
dark field optics, particularly when cultured with
living Paramecium.
Principle
To view a specimen in dark field, an opaque
disc is placed underneath the condenser lens,
so that only light that is scattered by objects
on the slide can reach the eye (figure 2).
Instead of coming up through the specimen,
the light is reflected by particles on the
slide. Everything is visible regardless of
color, usually bright white against a dark
background. Pigmented objects are often seen
in "false colors," that is, the reflected light
is of a color different than the color of the
object. Better resolution can be obtained using
dark field as opposed to bright field viewing.

You don't need sophisticated equipment to
get a dark field effect, although the effect
is most dramatic when the occulting disk is
built into the condenser itself. You do need
a higher intensity light, since you are seeing
only reflected light. At low magnification
(up to 100x) any decent optical instrument
can be set up so that light is reflected toward
the viewer rather than passing through the
object directly toward the viewer.

To set up a dissecting microscope
for "dark field" viewing, the specimen should
be placed over an opening so that light reflects
only from surfaces between cover slip and slide,
not from a surface beneath the slide. You may
need to make a stand to hold the slide. The
surface beneath the opening should be a flat
black. Turn off any built-in illuminator. Aim
a high-intensity light source toward the specimen
at an angle, from the top or side through a
glass dish or jar.
With a compound microscope, dark
field is obtained by placing an occulting disk
in the light path between source and condenser.
A cheap set of occulting disks can be prepared
by cutting circular pieces of black electrical
tape ranging from dime-size up to a diameter
that equals the width of the slide, and sticking
them to the slide in a row. The circles should
be spaced well apart. A specimen is placed
on the microscope stage as usual, and the illumination
should be made as uniform as possible. If there
is an aperture diaphragm in the condenser (contrast
lever), it should be opened up wide. After
focusing at low power, the slide with occulting
disks is placed in the light path between source
and condenser, bringing it as close to the
bottom of the condenser as it will go.
I would start with the largest
disk, sliding it around until it is directly
in the center of the light path. Increasing
the illumination should then produce a good
dark field effect. To optimize, first try stopping
down the field diaphragm to get the best contrast
between background and specimen. Try to match
the size of the occulting disk to the field
diameter, so that the edge of the disk is just
outside the field of veiw - smaller disks are
appropriate for higher power objectives. Vertically,
the disk should be a close to the condenser
as possible, to make the contrast the greatest.
On microscopes with built-in dark field equipment,
the view is so impressive because the occulting
disk is built into the condenser - very close
and focused. After testing the set-up this
way, a stand might be rigged to fit under the
microscope, so the slide can be placed in position
without holding it. Something that 'grabs'
the condenser and supports the occulting disks
would be ideal. The less the students have
to mess with, the better.
I set this up on the crummiest
little piece of garbage microscope I could
find, and it looked very good. A relatively
new student-model microscope should give a
much better effect.
Suspensions of cells and samples
of pond water look spectacular in dark field.
While specimens may look washed out and lack
detail in bright field, protists, metazoans,
cell suspensions, algae, and other microscopic
organisms are clearly distinguished and their
details show up well. At 100x you can readily
see bacteria, even distinguish some structure
(rods, curved rods, spirals, or cocci) and
movement. Non-motile bacteria look like vibrating
bright dots against a dark background. Motile
bacteria can be seen moving in a definite direction,
sometimes remarkably fast. In pond water samples
you may find Spirillum volutans, a very large
(up to 0.5 mm) motile spiral bacterium.
When to use dark field illumination
Dark field illumination is most
readily set up at low magnifications (up to
100x), although it can be used with any dry
objective lens. Any time you wish to view everything
in a liquid sample, debris and all, dark field
is best. Even tiny dust particles are obvious.
Dark field is especially useful for finding
cells in suspension. Dark field makes it easy
to obtain the correct focal plane at low magnification
for small, low contrast specimens. Use dark
field for
-
Initial examination of suspensions
of cells such as yeast, bacteria, small protists,
or cell and tissue fractions including cheek
epithelial cells, chloroplasts, mitochondria,
even blood cells (small diameter of pigmented
cells makes it tricky to find them sometimes
despite the color).
-
Initial survey and observation
at low powers of pond water samples, hay
or soil infusions, purchased protist or metazoan
cultures.
-
Examination of lightly stained
prepared slides. ? Initial location of any
specimen of very small size for later viewing
at higher power.
-
Determination of motility
in cultures
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