Light microscopes use visible light and a combination of lenses to magnify images of mounted specimens
Most light microscopes include both an ocular lens (~10×) and objective lens (~10×; 40×; 100×)
When using a light microscope to view biological specimens, the following conventions should be followed:
The image should initially be resolved at the lowest magnification using the coarse focus mechanism
Higher magnifications are then obtained by changing the objective lens (via the revolving nosepiece) and making fine focus adjustments
The total magnification of the image is calculated by multiplying the magnification of both lenses (ocular and objective) together
If the eyepiece has a measurement scale on its surface (eyepiece graticule), this can be used to determine sizes of biological structures
To calculate the linear magnification of a drawing or image, the following equation should be used:
Magnification = Image size (with ruler) ÷ Actual size (according to scale bar)
In order to calculate magnification, both image size and actual size must be in the same units
Metric conversions can be applied according to the following table:
Unit
Metre
Centi-
Milli-
Micro-
Nano-
Sign
m
cm
mm
μm
nm
Size
1 (100)
10–2
10–3
10–6
10–9
Unit
Sign
Size
Metre
m
1 (100)
Centi-
cm
10–2
Milli-
mm
10–3
Micro-
μm
10–6
Nano-
nm
10–9