Core practical 1 - analysing biological specimens using microscopes
Investigating biological specimens using microscopes
Aims
- To use a light microscope to examine animal and/or plant cells.
- To make observations and draw scale diagrams of cells.
Method
Image caption, Rotate the objectives so that the low power objective lens, eg ×10, is in line with the stage.
Image caption, Turn the coarse focus to adjust the space between the stage and the objective lens.
Image caption, Place the microscope slide on the stage. Line it up so that the specimen is in the centre of the stage, where the light passes through.
Image caption, Focus the slide by turning the coarse focus adjustment.
Image caption, Draw a low power image. Rotate the objectives so that the high power objective, eg ×40, is in line with the stage.
Image caption, Bring the slide back into focus using the fine focus adjustment. If you do not succeed, go back to low power and re-focus and start again.
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Risks
- Care must be taken when looking down the microscope that the illumination is not too bright as eye damage could be caused.
- Care when using microscope stains as some are harmful.
- Care when handling coverslips and microscope slides as broken glass could cut skin.
Drawing the image
A low power magnification is used to show the arrangement of cells in a tissue. This includes regions of the tissue but not individual cells.
A diagram of the slide under high power will be a detailed image of a part of the specimen which shows individual cells.
Measuring cell size
Cell size can be measured using an eyepiece graticule, which is a glass or plastic disc fitted into the eyepiece. The graticule has a scale ruled on it.
You must find out the distance measured for each division of the graticule. You can then use the graticule to measure cells. The distance will be different for each objective.
To do this, you will use a stage micrometer. This is a glass slide etched with an accurate scale on it. You will use this to calibrateTo set an instrument or scale against a standard. the eyepiece graticule. Once it's calibrated, you can use the eyepiece graticule every time you use the microscope.
- Place a stage micrometer on the stage of the microscope.
- Line up one of the divisions on the eyepiece graticule with a fixed point on the stage micrometer.
- Count the number of divisions on the eyepiece graticule that correspond with a set measurement on the stage micrometer.
- Calculate the distance in micrometres of one division on the eyepiece graticule.
In the diagram:
61 − 10 = 51 divisions on the eyepiece graticule are equivalent to 250 μm on the stage micrometer.
1 division on the eyepiece graticule is equivalent to 250/51 μm on the stage micrometer:
= 4.9 μm (to two significant figureGiving a number to a specified number of significant figures is a method of rounding. For example, in the number 7483, the most significant, or important, figure is 7, as its value is 7000. To give 7483 correct to one significant figure (1 sf), would be 7000. To 2 sf, it would be 7500.)
Using the calibrated eyepiece graticule to measure a cell:
The width of the cell shown = 52 − 40 = 12 eyepiece graticule divisions.
The real width of the cell is 12 × 4.9 μm = 59 μm (to two significant figures).
Question
What would be the length of a plant cell, to two significant figures, that was 35 divisions on this graticule?
170 μm
Each eyepiece graticule division is 4.9 μm
The real width of the cell is 35 × 4.9 μm = 171.5 μm
To two significant figures, this is 170 μm
Question
How many graticule divisions would a single celled organism that was 240 μm take up?
49
Each graticule division is 4.9 μm
An organism that measured 240 μm would take up \(\frac{240}{4.9}\) divisions = 49 divisions