Collecting Data in Biology (DP IB Biology): Revision Note

Ruth Brindle

Last updated

Collecting data in Biology

  • This is the "doing" phase of your investigation where you perform the experiment you have carefully designed

  • Your goal is to gather high-quality raw data that is both accurate and sufficient to answer your research question

  • This involves making precise measurements and recording all relevant information, including both numbers and observations

Principles of data collection

Collect and record sufficient relevant quantitative data

  • Quantitative data is numerical data that you measure in your experiment

  • The foundation of your report is a raw data table.

    • This should be the first table you present and must contain only the direct measurements you take, with no calculations

  • Designing your raw data table before you start is crucial

  • A well-designed table must include:

    • A specific title that describes the experiment.

    • Clearly labelled columns for your independent and dependent variables

    • Units and uncertainties in the column headers, not in the body of the table

  • Data must be recorded to the correct precision of the instrument

    • This is a common place where students lose marks

      • For a digital balance that reads to two decimal places, all masses must be recorded to two decimal places (e.g., 1.50 g, not 1.5 g)

      • For a graduated cylinder with 1 cm3 divisions, a volume should be recorded to the nearest 0.5 cm3

  • Sufficient data means collecting enough data points to see a trend

    • This includes:

      • collecting data for at least five increments of your independent variable

      • carrying out at least three replicates (and ideally five or more in biology) for each increment to ensure reliability

Identify and record relevant qualitative observations

  • Qualitative data is non-numerical data that you observe during the experiment

    • These observations provide context and are crucial for your final analysis and evaluation

  • Do not underestimate the importance of qualitative data

    • It can help explain unexpected results or errors

  • Examples of important qualitative data in biology include:

    • the turgidity of plant tissue (e.g. potato cylinders feeling firm and stiff or soft and limp).

    • the colour of leaves (e.g. yellowing due to a mineral deficiency).

    • behavioural responses of organisms (e.g. woodlice moving away from a light source).

    • the texture or appearance of a substance (e.g. a cloudy solution of milk turning clear in an enzyme experiment).

Identify and address issues that arise during data collection

  • Biological experiments rarely go perfectly to plan

    • A key scientific skill is to notice and respond to issues as they happen

  • If you encounter a problem, do not ignore it

    • Record the issue in your lab notes

  • Examples of issues and how to address them:

    • The reaction is too fast or slow:

      • You may need to adjust the concentration of an enzyme or substrate to get a measurable rate

      • Record the change and the reason for it

    • An anomalous result (outlier):

      • If one of your repeat trials gives a result that is very different from the others, record it, and then conduct an additional trial to get a reliable set of concordant results

      • Do not erase the outlier; you will justify its exclusion later

    • Organisms are not behaving as expected

      • In an ecological study, if you find no organisms in your quadrats, you may need to reconsider your sampling location

      • Record this decision and your reasoning

Worked Example

Research question:

  • "What is the effect of pH (from pH 4 to pH 10) on the rate of activity of the enzyme trypsin in breaking down casein protein?"

Quantitative data:

  • The time taken for a casein suspension to become transparent after adding trypsin solution

pH (±0.1)

Time (Trial 1) /s (±0.2)

Time (Trial 2) /s (±0.2)

Time (Trial 3) /s (±0.2)

Time (Trial 4) /s (±0.2)

4.0

185.4

182.9

184.1

5.0

158.3

160.2

159.0

6.0

102.5

101.8

103.1

7.0

63.4

62.8

63.0

8.0

46.9

52.6 (anomalous)

47.0

47.1

9.0

65.1

64.8

65.9

10.0

150.5

148.8

149.3

Qualitative data:

  • At pH 4.0 and 5.0, the casein suspension remained cloudy for a long time, showing low enzyme activity

  • Between pH 6.0 and 8.0, the solution cleared much more rapidly, with the fastest reaction at pH 8.0 — suggesting this is near the optimum pH for trypsin

  • At higher pH values (9.0–10.0), the reaction slowed again, and the solution stayed slightly opaque, indicating that trypsin was beginning to denature

Issue addressed during collection:

  • At pH 8.0, Trial 2 gave a time of 52.6 s, which was noticeably longer than the other two (46.9 s and 47.0 s)

  • A fourth trial was performed, giving 47.1 s, confirming that Trial 2 was an anomalous result, likely caused by incomplete mixing when the enzyme was first added

Worked Example

Research question:

  • "What is the effect of sucrose concentration (from 0.0 M to 1.0 M) on the percentage change in mass of potato (Solanum tuberosum) cylinders after 24 hours?"

Quantitative data:

  • The raw data would be recorded in a table like the one below, showing all initial and final mass readings for each replicate cylinder

Sucrose Conc. / M

Replicate

Initial Mass / g (±0.01)

Final Mass / g (±0.01)

0.0

1

1.85

2.12

2

1.88

2.16

3

1.86

2.14

0.2

1

1.91

2.02

2

1.89

1.99

3

1.87

1.98

...

...

...

...

Qualitative data:

  • The potato cylinders placed in the 0.0 M sucrose solution (distilled water) felt very firm and stiff (turgid) after the 24-hour period

  • The potato cylinders placed in the 1.0 M sucrose solution felt very soft and limp (flaccid)

Issue addressed during collection:

  • When cutting the potato cylinders, one cylinder for the 0.4 M solution was accidentally cut too short (2.5 cm instead of 3.0 cm)

  • This cylinder was discarded and a new one was cut to the correct dimensions before the experiment began to ensure all cylinders had the same surface area to volume ratio

Examiner Tips and Tricks

  • Record raw data directly

    • Never perform calculations in your head or on scrap paper

    • Your raw data table must show the actual measurements you took (e.g., initial and final mass, not just the change in mass)

  • Units and uncertainties belong in the headers

    • This is the correct scientific convention and makes your tables clear and easy to read

    • Avoid writing units after every number in the table body

  • Your observations are evidence

    • Don't treat qualitative data as an afterthought

    • Good observations can be used as evidence in your conclusion and evaluation to explain why your results might differ from what you expected

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Ruth Brindle

Author: Ruth Brindle

Expertise: Biology Content Creator

Ruth graduated from Sheffield University with a degree in Biology and went on to teach Science in London whilst also completing an MA in innovation in Education. With 10 years of teaching experience across the 3 key science disciplines, Ruth decided to set up a tutoring business to support students in her local area. Ruth has worked with several exam boards and loves to use her experience to produce educational materials which make the mark schemes accessible to all students.