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Prepare the specified concentration series and equal comparable plant-tissue pieces. Record the initial mass of each piece, expose it to a defined solution for the same interval, and measure the final mass using the approved method. Keep tissue source, dimensions, solution volume and temperature comparable.
Video by Malmesbury Education. The demonstration is labelled A-level. Use it for the shared tissue-preparation and weighing methods; this GCSE guide focuses on controlled concentrations, percentage mass change and interpretation.
Viewing focus: Design a controlled solution-concentration comparison
After watching, attempt these questions before opening the answers. You can also use the written lesson below.
After watching 1: Why blot consistently before weighing?
To reduce the contribution of surface solution. The mass should primarily represent the tissue.
After watching 2: What is the denominator in percentage mass change?
Initial mass. Relative change is based on the starting value.
What you'll be able to do
Prepare the specified concentration series and equal comparable plant-tissue pieces. Record the initial mass of each piece, expose it to a defined solution for the same interval, and measure the final mass using the approved method. Keep tissue source, dimensions, solution volume and temperature comparable.
The pieces must be immersed consistently, and the starting solution should not be changed substantially by the tissue itself. Use appropriate independent pieces at each concentration. Several readings of one piece check weighing consistency but do not replace separate biological samples.
Pearson CP1.16 specifies potato in sucrose solutions, with known starting and final masses used to obtain percentage mass change. The zero-change solution is an external comparison under the tissue’s conditions, not an exact assay of every intracellular solute.
Use a consistent gentle blotting method before weighing so liquid on the outside does not dominate the apparent change. Do not squeeze water from the tissue or leave it drying for different intervals. Record raw initial and final masses with the balance’s supported precision.
Percentage mass change = (final − initial mass) ÷ initial mass × 100. Positive values indicate gain and negative values loss. Percentage change allows fairer comparison when initial masses differ, but it does not remove every effect of unequal dimensions or preparation.
Plot concentration against percentage mass change with suitable axes and use a justified best-fit relationship. An estimated zero-change point identifies an external solution producing no net measured mass change under those conditions. Interpolation between measured points is more defensible than extrapolating far outside the range.
Osmosis explains net water movement across partially permeable membranes. A zero final change does not mean individual water molecules stopped moving, nor does it give the exact concentration of every solute inside every cell. Tissue variation, equilibration time and measurement uncertainty limit the inference.
| External concentration / mol dm⁻³ | Mean mass change / % |
|---|---|
| 0.00 | +14 |
| 0.20 | +6 |
| 0.40 | −4 |
| 0.60 | −12 |
Attempt these problems on paper before opening the worked reasoning. Explain your steps as well as giving a final answer.
Common mistakes to avoid
Key takeaways
Question 1: Mean changes are +6% at 0.20 mol dm⁻³ and −4% at 0.40 mol dm⁻³. Estimate the zero-change concentration assuming a straight relationship locally.
About 0.32 mol dm⁻³; it is a local interpolation.
Check the assessed scope and practical or mathematical requirements.
An external explanation or interactive activity to use alongside the lesson. It may include extension material.
Close the notes and answer from memory. Revisit any explanation you cannot yet reconstruct.
Test yourself
Answer a few questions, then review anything you missed.
Start with the quiz above to check the key ideas. You can also choose another topic from the practice library.