LOGIC LAB · UNITS 3 AND 6

Design an
investigation.

Unit 3 (WBI13) and Unit 6 (WBI16) both ask you to plan an experiment. Build the plan on CORMMSS: seven points, one sentence each. Then add the A level extras that turn a method into a plan you can defend.

What the two units ask

Unit 3 (WBI13), AS

Planning is based on the practical work in Units 1 and 2. Expect parts that ask you to name the variables, say how to control them, describe how to measure, deal with safety, and say how you would use the data and reduce uncertainty.

Unit 6 (WBI16), A level

Planning draws on practical work from Units 1, 2, 4 and 5, and often starts from a hypothesis. On top of the Unit 3 skills, expect a null hypothesis, calibration, ethics for living organisms and a statistical test. A full plan can be a long answer, so structure matters.

These are Scholar Lab study notes, written to help you plan. They are not Pearson’s wording or an official mark scheme.

The backbone: CORMMSS

Write the seven points in this order and you will not miss a basic mark. At A level, each one needs a number, a unit or a method, not just a name.

  1. Change

    Name the independent variable, how each value is produced and the values themselves: usually five or more, at even intervals, for example 20 to 60 °C in 10 °C steps from a thermostatically controlled water bath, or a serial dilution. Add a control when it shows the effect comes from the treatment, such as boiled enzyme or no inhibitor.

  2. Organism

    For organisms, name the species and match them on age, size, sex, developmental stage or source. For tissue or extracts, take them from the same organism or batch. Say how you would choose them, for example at random from one population.

  3. Repeat

    Give the number of repeats, for example at least three at each value, and calculate a mean. At this level, say why: repeats show variation, let you spot anomalies and allow a standard deviation or a statistical test.

  4. Measure (what)

    Name the dependent variable, the instrument and the unit, and say how the reading becomes a rate or a result: time to a colour end-point compared with a standard, volume of gas in a gas syringe, mass change as a percentage, or 1/time.

  5. Measure (when)

    State the time interval or end-point: readings every 30 s for 5 minutes, or after a stated number of days. Include an equilibration time before you start, so every tube begins at the planned value.

  6. Same (1)

    Name the most important variable that could also affect the result, give its value and how it is controlled and checked: “pH 7, kept with a buffer solution”.

  7. Same (2)

    Name a second, different controlled variable in the same way: “the same volume and concentration of substrate, measured with a graduated pipette”. Monitoring counts too: check the water bath with a thermometer during the run.

The A level extras

These sit on top of CORMMSS. Unit 3 plans often need risk, uncertainty and data use. Unit 6 plans add the null hypothesis, ethics and the statistical test.

Hypothesis and null hypothesis

Unit 6 plans often start with a testable hypothesis, and a null hypothesis for the statistical test. The null hypothesis says there is no difference or no correlation.

Write both in terms of the actual variables, not “the factor affects the result”.

For example: Null hypothesis: there is no correlation between the distance from the woodland edge and the mean leaf area of the plants.

Choosing the range and the intervals

Choose a range wide enough to show the pattern, and include values on both sides of any optimum. Five or more values at even intervals make a line graph worth drawing.

Justify the range with biology: enzymes denature above about 60 °C, and most organisms die well before that.

For example: 20, 30, 40, 50 and 60 °C, so that the rise, the optimum and the fall are all visible.

Pilot study

A pilot study is a quick trial before the real run. It checks that the method gives readings you can measure and lets you fix the range, the intervals, the timing or the concentrations.

Say what the pilot will decide, not just “do a pilot study”.

For example: Run a pilot at 20 °C and 60 °C to check that the colour change takes between 30 s and 10 min, then adjust the enzyme concentration if it does not.

Risk assessment

Name a specific hazard, the harm it could cause and a precaution that reduces the risk. Generic safety rules (“wear a lab coat”) earn little on their own.

Match the precaution to the hazard: eye protection for an irritant splashing, aseptic technique and disinfectant for microorganisms, heat-proof gloves for a hot water bath.

For example: Trypsin is an irritant if it gets on the skin or in the eyes, so wear eye protection and gloves, and wash off any splashes at once.

Ethics

If the plan uses living organisms, say how you will look after them: use the fewest you need, avoid harm and stress, return animals to their habitat, and keep the time they are out of it short.

If people are involved, ask for informed consent and let them stop at any time. Do not use intensities that could harm them.

For example: Keep the water fleas at each temperature for only 5 minutes, use the smallest number that still allows repeats, and then return them to the culture.

The statistical test

Choose the test from the type of data and the question you are asking: Student’s t-test for a difference between two means, a correlation coefficient (such as Spearman’s rank) for a relationship between two variables, and chi-squared for observed and expected frequencies.

Say how you will use it: compare the calculated value with the critical value at p = 0.05, then accept or reject the null hypothesis. Plan enough repeats or pairs for the test to work.

For example: Collect at least 10 pairs of readings, so a Spearman’s rank correlation coefficient can be tested at p = 0.05.

Validity, reliability and accuracy

Validity: the method measures what it sets out to measure, and only the independent variable is changing the result. Controlled variables protect validity.

Reliability: repeated readings agree. Repeats, means and standard deviations show this. Accuracy: readings are close to the true value. Calibration (checking a meter reads zero, or using a colour standard) protects accuracy. Precision is how closely repeats cluster, and it is limited by the resolution of the instrument.

For example: A colorimeter is set to zero with a blank before each reading, so the results are more accurate. Taking three repeats and a standard deviation shows how reliable they are.

Limitations and how the data will be used

Name a source of uncertainty or systematic error in your own plan, say how it affects the results and how to reduce it. Then say what you will do with the data: the table, the graph and the test.

An end-point judged by eye, temperature drift and natural variation between organisms are common limitations. Each needs its own fix.

For example: Judging the end-point by eye is subjective, so compare each tube with a colour standard or use a colorimeter.

Putting a long plan in order

  1. Hypothesis and null hypothesis, if the question gives a hypothesis or asks for a test.
  2. Change: the values, how you make them and any control.
  3. Organism: which ones, and how you make them alike.
  4. Same: each controlled variable with its value and how it is kept and checked.
  5. Measure: what, how, the unit, and when.
  6. Repeat: how many, and the mean.
  7. Pilot, risk and ethics, each linked to this method.
  8. Data: the table, the graph and the statistical test, and what result would support the hypothesis.

This order follows how you would run the experiment, which keeps a 10-line answer readable. CORMMSS is still the checklist.

Worked plan · illustrative values

Worked plan 1, Unit 3 style: temperature and an enzyme

The question

Plan an investigation into the effect of temperature on the rate at which trypsin breaks down the protein in milk. The milk goes from cloudy to clear as the protein is digested.

Change
Temperature: 20, 30, 40, 50 and 60 °C, each set with a thermostatically controlled water bath. A control tube at each temperature has boiled and cooled trypsin, to show that clearing depends on active enzyme.
Organism
Use trypsin from one batch and milk from one carton, so the enzyme and substrate source are the same in every tube.
Repeat
Three repeats at each temperature; calculate the mean time and the standard deviation.
Measure (what)
Time, in s, for the milk to clear, judged against a cross on white card seen through the tube. Convert to a rate with rate = 1/time (s⁻¹).
Measure (when)
Leave the trypsin and the milk in separate tubes in the water bath for 5 minutes to reach the temperature, then mix them and start the stopwatch. Stop at 10 minutes if the milk has not cleared, and record “no clearing”.
Same (1)
pH 7, kept with 2 cm³ of the same buffer solution in every tube.
Same (2)
The same volume and concentration of trypsin (2 cm³ of 1%) and of milk (5 cm³), measured with graduated pipettes.

On top of CORMMSS

Pilot study
Try 20 °C and 60 °C first. If any tube takes longer than 10 minutes, raise the trypsin concentration and repeat the pilot.
Risk
Trypsin is an irritant: wear eye protection and gloves. Take care with the hot water bath at 60 °C.
Accuracy
Check each water bath with a thermometer during the run. Use the same card and lighting, so the same person judges every end-point the same way.
Data use
Tabulate the times and the mean rates, plot the mean rate against temperature, add standard deviation error bars, and read off the optimum.

The CORMMSS rows carry the method. The extras add what Unit 3 also asks for: safety, a way to reduce uncertainty, and how the data will be used. All values are illustrative.

Worked plan · illustrative values

Worked plan 2, Unit 6 style: a field study with a statistical test

The question

A student thinks ivy leaves are larger in shade. Plan an investigation to test whether there is a correlation between light intensity and the surface area of ivy leaves at the edge of a wood.

Change
You cannot set light intensity in a field, so you sample along it. Place a tape from open ground into the wood and sample at 12 points, 2 m apart, recording the light intensity at each point with a light meter.
Organism
Ivy (one species) only. At each point take the fifth fully opened leaf from the shoot tip, so that the leaves are the same age.
Repeat
Take five leaves at each point and calculate the mean surface area. Twelve points give 12 pairs of readings for the test.
Measure (what)
Leaf surface area in cm², found by drawing round each leaf on 1 cm² squared paper and counting squares (counting a square when at least half of it is covered).
Measure (when)
Take every light reading on the same day, within one hour around midday, with the meter held at leaf height and facing up.
Same (1)
Height above the ground: take every leaf from between 0.5 and 1.0 m, checked with a metre rule.
Same (2)
The aspect: sample only along the south-facing edge of the wood. Record the soil moisture at each point as a variable you cannot control.

On top of CORMMSS

Null hypothesis
There is no correlation between light intensity and the mean surface area of ivy leaves.
Statistical test
Spearman’s rank correlation coefficient on the 12 pairs. Compare it with the critical value at p = 0.05 and accept or reject the null hypothesis.
Ethics
Pick only the leaves you need, spread across several plants, and do not damage the plants’ growing tips. Ask the landowner for permission.
Risk
Uneven ground and thorny plants: wear gloves and stout shoes, and work in pairs.
Limitation
Light changes as clouds pass. Take three meter readings at each point and use the mean, or take the readings at the same time on a fully overcast day.

CORMMSS still works when you cannot set the variable: “Change” becomes the gradient you sample along, and “Same” includes the factors you record but cannot fix. The Unit 6 extras, a null hypothesis, a statistical test and ethics, sit on top. All values are illustrative.

Practice

Three original prompts. Plan each one on paper, then check it against the points. The points are Scholar Lab guidance, not an official mark scheme.

Practice 1

Unit 3 style: yeast and sugar concentration

Your turn

Plan an investigation into the effect of sucrose concentration on the rate of respiration of yeast. Use a redox indicator, methylene blue, which loses its blue colour as it is reduced.

Write your plan on paper first, one sentence per letter. Then open the hints or the points.

Hints
  1. C: how will you make the concentrations, and which values?
  2. M1 and M2: what is the end-point, how will you judge it, and how do you turn a time into a rate?
  3. S: which two factors most affect the rate of yeast respiration besides sucrose?
Points a strong plan includes
  • C: at least five sucrose concentrations, for example 0, 2, 4, 6 and 8%, made by diluting a stock solution with distilled water.
  • O: yeast suspension from one batch, stirred before each sample is taken.
  • R: three repeats at each concentration; calculate the mean time.
  • M1: time, in s, for the methylene blue to lose its colour, judged against a colour standard; rate = 1/time.
  • M2: leave the tubes in the water bath for 5 minutes before you add the methylene blue, then start the timer.
  • S1: temperature, for example 35 °C, in a thermostatically controlled water bath checked with a thermometer.
  • S2: the same volume of yeast suspension and of methylene blue, measured with a syringe or pipette. Do not shake the tubes, which would reoxidise the dye.
  • Extras: a no-yeast control; eye protection, because methylene blue stains and irritates; plot the mean rate against concentration.

Practice 2

Unit 6 style: water flea heart rate and temperature

Your turn

Plan an investigation to test the hypothesis that temperature affects the heart rate of water fleas (Daphnia). Include a null hypothesis, how you would analyse the data, and any ethical issues.

Write your plan on paper first, one sentence per letter. Then open the hints or the points.

Hints
  1. C: how will you change and check the temperature of the water under the microscope?
  2. O and ethics: how do you choose the fleas fairly, and how do you keep harm to a minimum?
  3. Statistics: is this a difference between two means or a correlation, and how many readings does the test need?
Points a strong plan includes
  • Null hypothesis: there is no correlation between temperature and the heart rate of Daphnia.
  • C: five temperatures, for example 10 to 30 °C at 5 °C intervals, using water baths, then a cavity slide with a thermometer or temperature probe in the water.
  • O: Daphnia of the same species and similar size, chosen at random from one culture.
  • R: at least five fleas at each temperature; calculate the mean.
  • M1: count heartbeats under a microscope, for example with a tally counter, and convert to beats per minute.
  • M2: leave each flea for 5 minutes at the temperature before you start; count for 20 s and multiply by 3.
  • S1 and S2: the same volume of culture water, the same light intensity from the microscope lamp (use a heat filter or limit the time under the lamp), and no caffeine or other chemicals.
  • Pilot study: check that the heartbeat can be counted at the highest temperature.
  • Statistics: Spearman’s rank correlation coefficient on temperature and heart rate, compared with the critical value at p = 0.05.
  • Ethics: use as few fleas as possible, keep them out of the culture for only a short time, avoid temperatures that harm them, and return them afterwards.

Practice 3

Unit 6 style: limpet shells on two shores

Your turn

Plan an investigation to find out whether the mean height of limpet shells differs between an exposed and a sheltered rocky shore.

Write your plan on paper first, one sentence per letter. Then open the hints or the points.

Hints
  1. C: the variable here is two places, not a range. What test compares two means?
  2. R: how will you choose the limpets so that the samples are not biased?
  3. S: which other factors change across a shore?
Points a strong plan includes
  • C: two sites, one exposed and one sheltered; the comparison is between the two means.
  • O: one limpet species, and only adults, for example with a shell length above a stated minimum.
  • R: random sampling: place quadrats at random coordinates and measure at least 20 limpets per site.
  • M1: shell height in mm, from the rock to the shell tip, measured with calipers, without removing the limpet.
  • M2: sample both sites at low tide on the same day, or within a few days.
  • S1: the same zone of the shore at both sites, for example the same height above low water.
  • S2: the same rock type and a similar slope at both sites.
  • Statistics: Student’s t-test, with the null hypothesis that there is no difference between the mean shell heights. Compare the result with the critical value at p = 0.05.
  • Ethics and risk: do not pull limpets off the rock; check the tide times, wear non-slip footwear, and work in pairs.