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Measurement uncertainty and percentage error
Edexcel IAL Biology · WBI13 Practical Skills in Biology I
Every measurement has an uncertainty. Unit 3 asks you to identify it, calculate percentage uncertainty or percentage error, and explain how to reduce it.
Uncertainty of a reading
- For a scale you read by eye (ruler, measuring cylinder, thermometer), the uncertainty is usually half the smallest division: a measuring cylinder graduated in 0.2 cm³ gives ±0.1 cm³.
- For a digital display, it is usually ± the last digit (a balance reading to 0.01 g gives ±0.01 g).
- When a value comes from two readings (a burette titre = final reading minus initial reading, or a length from two ends of a ruler), add the uncertainties: a burette read to ±0.05 cm³ gives a titre of ±0.10 cm³.
Percentage uncertainty and percentage error
Percentage uncertainty = (uncertainty / measured value) x 100
The same uncertainty is a smaller percentage of a larger reading, so measuring a larger volume, longer time or longer length lowers the percentage uncertainty.
Percentage error = (difference between measured and true value / true value) x 100
Percentage error compares your result with an accepted or known value (for example the known vitamin C content of a standard solution).
If a result is calculated by multiplying or dividing two measurements, add their percentage uncertainties.
Random and systematic error
- Random errors make repeated readings scatter either side of the true value (judging a colour end point, reaction time). Reduce their effect by repeating and calculating a mean, or by using a better method (colorimeter, data logger).
- Systematic errors shift every reading the same way (a balance not zeroed, reading a meniscus from above, a colorimeter not zeroed with a blank). Repeating does not remove them; find and correct the cause, or calibrate.
- Accuracy is how close a result is to the true value; precision is how close repeated results are to each other (small spread, small standard deviation).
Worked example
A burette is read to ±0.05 cm³. The initial reading is 0.50 cm³ and the final reading is 12.90 cm³. Calculate the percentage uncertainty in the titre.
- Titre = 12.90 - 0.50 = 12.40 cm³
- Two readings, so uncertainty = 2 x 0.05 = ±0.10 cm³
- Percentage uncertainty = 0.10 / 12.40 x 100 = 0.81%
Answer: 0.81% (about 0.8%)
Check yourself
- A 10 cm³ measuring cylinder is graduated in 0.2 cm³ divisions. Calculate the percentage uncertainty when measuring 5.0 cm³.
Show answer
2.0 %. Uncertainty = half of 0.2 = 0.1 cm³; 0.1 / 5.0 x 100 = 2%.
- A root is measured as 24 mm with a ruler; the uncertainty is ±0.5 mm. Calculate the percentage uncertainty to 2 significant figures.
Show answer
2.1 %. 0.5 / 24 x 100 = 2.1%.
- A student's titration gives a vitamin C concentration of 0.86 mg cm⁻³ for a standard that is really 0.80 mg cm⁻³. Calculate the percentage error to 2 significant figures.
Show answer
7.5 %. (0.86 - 0.80) / 0.80 x 100 = 7.5%.
- A burette titre of 6.20 cm³ comes from two readings, each ±0.05 cm³. Calculate the percentage uncertainty to 2 significant figures.
Show answer
1.6 %. 2 x 0.05 = 0.10; 0.10 / 6.20 x 100 = 1.6%.
- How could the percentage uncertainty in measuring the volume of oxygen collected be reduced?
- Repeat with a smaller volume
- Use a measuring cylinder with larger divisions
- Round the answer to fewer figures
- Collect gas for longer so a larger volume is measured
Show answer
Collect gas for longer so a larger volume is measured. A larger reading makes the same uncertainty a smaller percentage.
- A colorimeter is not zeroed with a blank, so every absorbance is 0.05 too high. What type of error is this?
- Random error
- Systematic error
- Percentage error
- Anomalous error
Show answer
Systematic error. The same shift in every reading is systematic; repeats will not remove it.
- Five repeats give 4.1, 4.2, 4.1, 4.2, 4.1 s, but the true value is 5.0 s. How are these results best described?
- Accurate but not precise
- Accurate and precise
- Neither accurate nor precise
- Precise but not accurate
Show answer
Precise but not accurate. They are close together (precise) but far from the true value (not accurate).
- Which method best reduces the effect of random error in judging a colour end point?
- Zero the balance
- Change the independent variable
- Repeat several times and calculate a mean, or use a colorimeter
- Use a smaller sample
Show answer
Repeat several times and calculate a mean, or use a colorimeter. Repeats average out random error; a colorimeter removes the judgement.
Sources
- Pearson Edexcel International Advanced Level in Biology specification (XBI11/YBI11, first teaching 2018): Unit 3, Unit 6 and Appendix 6 mathematical skills
- Pearson mark scheme WBI13/01, June 2024 (via Physics & Maths Tutor)
Last updated 8 November 2026. Spotted a mistake? Tell us.