« Back to Course Test Your Knowledge Flash Cards ๐Ÿ”’Play Lemonaire ๐Ÿ”’Play Last Stand

Cell Structure ยป Required Practical: Looking at Cells Under a Microscope

What you'll learn this session

Study time: 30 minutes

AQA spec: Required practical activity 1 (8.2.1)

  • How to prepare a slide of plant or animal cells and stain it
  • How to focus a light microscope from low power to high power
  • How to make a clear, labelled scientific drawing with a magnification scale
  • The safety rules and the mistakes examiners see most

๐Ÿ”’ Unlock Full Course Content

Sign up to access the complete lesson and track your progress!

Unlock This Course

The aim of the practical

In this required practical you use a light microscope to observe, draw and label a selection of plant and animal cells. A common pair is onion epidermis (a plant tissue) and cheek cells (an animal cell). A magnification scale must be included on your drawing.

Plant cells show a cell wall and sometimes a permanent vacuole. Animal cells show a nucleus inside a thin cell membrane. You met these parts in Animal and Plant Cells. Here the focus is on the skill of looking at them properly.

Key terms:

  • Epidermis: a thin layer of cells that covers the surface of a plant or animal.
  • Stain: a coloured liquid that soaks into cells so that their parts are easier to see.
  • Slide: a thin piece of glass that holds the specimen.
  • Coverslip: a very thin square of glass or plastic placed over the specimen.

Parts of the light microscope

🔍 Lenses

The eyepiece lens is the one you look through. The objective lenses sit on a turret just above the slide. They come in different strengths, such as x4, x10 and x40. The turret is the rotating part that holds them.

⚙ Controls

The coarse focus wheel moves the stage a long way. The fine focus wheel makes small changes to sharpen the image. The stage holds the slide, and light shines up through it from a lamp or mirror.

Total magnification is the eyepiece magnification multiplied by the objective magnification. An eyepiece of x10 with an x10 objective gives x100.

Preparing a slide

The specimen is the thing you are looking at. It must be thin enough for light to pass through it. If it is too thick, you see a dark blur.

Onion epidermis

  1. Cut a small piece from the inside of an onion and peel off a very thin, see-through layer.
  2. Place the layer flat on a clean slide.
  3. Add a drop of iodine solution as the stain.
  4. Hold the coverslip at an angle with one edge touching the liquid. Lower it slowly with a mounted needle.

Lowering the coverslip slowly stops air bubbles being trapped. Bubbles look like dark circles and hide the cells.

Cheek cells

  1. Gently rub the inside of your cheek with a clean cotton bud.
  2. Smear the cotton bud on a clean slide.
  3. Add a drop of stain, for example methylene blue, then lower a coverslip over it.

Cheek cells are colourless and almost invisible without a stain. The stain makes the nucleus show up clearly.

Focusing the microscope

  1. Turn the turret to the lowest power objective lens.
  2. Place the slide on the stage and clip it in place.
  3. Look from the side and use the coarse focus wheel to bring the objective lens close to the slide, without touching it.
  4. Look through the eyepiece and turn the coarse focus wheel slowly the other way until the cells come into view.
  5. Use the fine focus wheel to make the image sharp.
  6. Move the slide so the cells you want are in the middle of the view.
  7. Only then switch to a higher power objective lens and sharpen the image with the fine focus wheel only.

Always start on low power because the field of view (the circle of the slide you can see) is larger, so it is much easier to find the cells. Never use the coarse focus wheel on high power, because the lens could hit the slide and crack the coverslip.

Safety

Stains such as iodine and methylene blue can mark skin and clothes, so wipe up spills. Slides and coverslips are glass and can break, so tell your teacher if one does. Use only your own cheek cells and a clean cotton bud, then put the used cotton bud in disinfectant. Wash your hands afterwards. If the microscope has a mirror, never point it at the Sun, because strong light can damage your eyes.

Making a scientific drawing

A scientific drawing is a record of what you see. It is not a work of art. Follow these rules:

  • Use a sharp pencil and a clean eraser. Draw single, clear lines with no sketching and no shading.
  • Do not colour in the drawing.
  • Make the drawing large. Use at least half the space on the page.
  • Draw only what you see. Show a few cells, not the whole view, and keep the proportions correct.
  • Use a ruler to draw label lines. They must touch the part and must not cross each other.
  • Write labels horizontally, away from the drawing.
  • Give the drawing a title that says what it is, and write the magnification beside it.

🌱 Onion cells

Label the cell wall, cytoplasm and nucleus. The cells are joined side by side in a regular, brick-like pattern.

🔬 Cheek cells

Label the cell membrane, cytoplasm and nucleus. There is no cell wall, and the cells are irregular in shape and are not joined in a regular pattern.

Magnification scale and relative size

Your drawing must show how much bigger it is than the real cell. Work out the magnification of the drawing and write it next to the title, for example "x300". You can also draw a scale bar, which is a short line labelled with a real length such as 50 µm.

Worked example

A drawing of an onion cell is 45 mm wide. The real cell is 0.15 mm wide.
Magnification = image size ÷ real size = 45 ÷ 0.15 = x300.
The magnification is x300.

The spec also asks you to use estimations to judge relative size. You do not need exact measurements. Compare one length with another, for example "one onion cell is about three times as long as it is wide". That relative size is the same on the drawing and in the real cell.

Use a ruler to record the length of the drawing, and the area of a cell if you are asked, in millimetres, and always write the units.

Common mistakes

Drawing with shaded areas or colour, so the lines are not clear. Label lines that cross each other. Leaving out the title or the magnification. Moving to high power without focusing on low power first. Using the coarse focus wheel on high power. A thick specimen or air bubbles on the slide. Drawing the cells too small, so the labels are squashed.

Exam-style question

A student looked at onion epidermis cells under a light microscope.

(a) Describe how the student should prepare the slide. [3 marks]

(b) Why is it important to start by focusing on low power? [1 mark]

(c) The student made a drawing 72 mm wide of a cell that is 0.12 mm wide. Calculate the magnification. [2 marks]

Model answer

(a) Peel a thin layer of epidermis from the onion and place it flat on a slide (1). Add a drop of stain such as iodine (1). Lower a coverslip slowly at an angle so no air bubbles are trapped (1).
(b) The field of view is larger, so it is easier to find the cells (1).
(c) Magnification = 72 ÷ 0.12 (1) = x600 (1).

Exam tip

For a "describe how" question about preparing a slide, give the steps in order and mention the coverslip and air bubbles. Those are the details that earn the marks.

Test Your Knowledge
Chat to Biology tutor