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THE MICROSCOPE 3.

Clean the mechanical parts with soft tissue paper and the
lenses with lens paper before and after using it.
4. Avoid wetting any part of the microscope wit h water or
Light Microscope chemicals when suing temporary mounts. Wipe off dry any
 Operate through reflection of light from the object to part that accidentally gets wet with appropriate wiper.
our eyes 5. If and only when a dry preparation or mount is to be
studied, tilting the microscope may be allowed provided it is
Types tilted only to a comfortable angle of not more than 30
 Simple microscopes degrees from the vertical. Use the inclination joint in the
– Made of one lens process and don’t fail to return the microscope to its original
– Hand lenses up-right position after use.
 Compound microscopes 6. Do not remove any part of the microscope, unless
– Has a heavy metal foot specifically directed to do so, and ascertain that no part is
– Platform on which to place what is being examined missing or damaged before and after use. Report immediately
– Nosepiece that platform any observed irregularity of the microscope.
– Long tube at the top which is the eyepiece
MECHANICAL PARTS OF THE MICROSCOPE
Dark field microscope  Base –Heavy “Y” shaped foot on which the microscope
 Specimen is illuminated by a special condenser that stands
provides oblique lights  Pillar –Short supporting piece arising from, the base
 Light will not pass up into the tube of the microscope  Arm –Short curved handle used in carrying the
unless it is deflected or scattered by the object microscope
 Objects show up as brightly illuminated bodies  Inclination joint –Joint between the pillar and the arm
 Focuses a hollow cone of light in the plane of the used to tilt the upper part
specimen  Body tube –Attached to the arm and which bears the
lenses
Phase Contrast microscope  Draw tube –Upper portion of the upper lenses or the
 Enables contrast to be added to the normally eyepiece
invisibles objects  Rotating nosepiece –Revolving structure at the lower
 Depends on the ability of the specimen to alter the and of the body tube
wave form by retardation or absorption  Dust shield –Metallic structure above the nosepiece
 Light passing through the denser parts of the which protects the lower lenses.
specimen will appear dark  Coarse adjustment screw –Knob geared to the tube
 Light passing directly thought the specimen and the use to bring the object into focus
channel is retarded a quarter of wave length less  Fine adjustment screw –Knob below the coarse
than of the plate adjustment screw, used for more delicate focusing
 Interference of the deviated and undedicated rays  Stage – Platform with a central aperture and two clips to
produces the phase contrast effect hold the slide being studied.
 Mechanical stage –Moves the slide into focus
Stereoscopic Microscope
 Designed to produce a three-dimensional image OPTICAL PARTS OF THE MICROSCOPE
 Two low power microscopes set side by side at a  Mirror –Found below the stage with concave and flat
light angle to each other so a stereoscopic effect to surfaces use to gather; directs the light to illuminate the
the image object
 Restricted to quite low magnification  Iris diaphragm – Found above the mirror consisting of
– Used in dissecting work several metal blades which forms a circular opening;
 Only occasional focusing necessary controls the amount of light reaching the object
 Condenser –Further to concentrate the light rays into
Fluorescence Microscope the specimen
 Used to detect chemical bonding between certain  Low Power Objective –shorter lens screwed to the
substances rotating nosepiece; bring the object into focus
 Treating one of the substances in the reaction with a  High Power Objective –longer lens screwed to the
fluorescent dye rotating nosepiece; serves to form a larger image of the
 Detection of antigen-antibody reactions. object
 Labeled by chemically combining them with  Ocular (Eyepiece) –found in the draw tube; for further
fluorescent dyes magnification of the object

Electron Microscope TERMS RELATED TO MICROSCOPE USE


 Equipped with a binocular light microscope • Magnification –ability of the microscope to render the
 Magnifies about ten times and is used to view the fine detail of an object visible
fluorescent screen where ether image is formed  Resolving Power –depends upon two factors
 Magnification in millions of times – numeric aperture
 High-resolution electron microscopes – wavelength of light
 Top screen magnification in the region of 250,000  Numerical Aperture – designation of the amount of
times light entering the objective from a point in the
microscopic field
CARE OF THE MICROSCOPE  Refractive Index – Ratio of the velocity of light in a
1. Carry the microscope properly by keeping it in an up-right medium as compared with that in a vacuum
position as close to the body as possible with one hand grasps –Amount of refraction of ray upon entering the medium
the arms securely and the other hand supporting the base –Expression of the light-bending capacity of the medium
firmly.  Depth of Focus – Capacity of the objective lens to
2. Be sure that it is placed squarely in front of your and kept render details of an object in different planes clearly at
at a safe distance of about 3-4 inches from the edge of the the same time
table.

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