May/June 2025 Paper 62 Worked Answers (IGCSE Biology 0610 Extended)
20 questions · 40 marks · 60 minutes
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Worked answers for 19 questions
- Step 1: Halving the concentration from 1.0 to 0.5 mol per dm3 means the stock must be diluted to twice its volume. Step 2: So half of the final 50 cm3 must be stock and half must be water. Step 3: That is 25 cm3 of salt solution S and 25 cm3 of distilled water W, which gives 50 cm3 in total.Method:Work out the dilution factor, then split the final volume between stock and water.Examiner tips
- To halve a concentration, use equal volumes of stock and water.
- Step 1: The discs are in pure water, which has a higher water potential than the potato cells. Step 2: Water moves into the cells by osmosis, so the discs swell slightly and the total length increases above the starting 100 mm. Step 3: Reading the ruler gives a final total length of about 102 mm.Method:Recall that pure water makes discs swell, then read the small increase above 100 mm.Examiner tips
- Read the ruler carefully; in pure water the discs swell a little above 100 mm.
- Step 1: A results table needs at least three ruled columns with a header line: one for the concentration and one each for the start and final lengths. Step 2: Every heading must include its unit, here mol per dm3 for concentration and mm for length. Step 3: The start and final lengths must be recorded against the correct concentration so the change can be found; only the first option does all of this.Method:Check the table has columns, units, and lengths matched to the right concentration.Examiner tips
- A good results table has ruled columns, headings with units, and every value in the right row.
- Step 1: The change in length is the final length minus the start length. Step 2: For S1, 94 minus 102 is minus 8 mm, a decrease of 8 mm. Step 3: For S2, 98 minus 103 is minus 5 mm, a decrease of 5 mm, because the salt solutions draw water out of the discs.Method:Subtract each start length from its final length and note the size and direction of change.Examiner tips
- Change in length = final length minus start length.
- Step 1: A more concentrated salt solution has a lower water potential than the potato cells. Step 2: So water moves out of the discs by osmosis, and the more concentrated the solution, the more water is lost and the greater the decrease in length. Step 3: In pure water the discs gain water instead, which fits the conclusion that water movement depends on the salt concentration.Method:Relate the size and direction of the length change to the salt concentration.Examiner tips
- A conclusion links the change in length to the salt concentration through osmosis.
- Step 1: The dependent variable is the one measured in response to the change. Step 2: Here the student measures the total length of the potato discs after they have been in each solution. Step 3: So the dependent variable is the total length of the potato discs.Method:Identify the quantity measured in response to the changing concentration.Examiner tips
- Dependent = measured; independent = changed; controlled = kept the same.
- Step 1: The change in length of one thin disc is very small and hard to measure precisely. Step 2: Measuring the total length of 10 discs gives a much larger change that can be measured more accurately. Step 3: This reduces the percentage error and the effect of any one unusual disc, making the result more reliable.Method:Explain how a larger total length improves the accuracy of the measured change.Examiner tips
- Measuring more units gives a larger change and a smaller percentage error.
- Step 1: The hazard here is the sharp blade used to cut the potato. Step 2: Cutting on a tile or flat surface and moving the blade away from the hand and body keeps the blade clear of the skin. Step 3: This reduces the risk of cutting yourself, which is the relevant safety precaution.Method:Pick the precaution that keeps the sharp blade away from the skin.Examiner tips
- Cut on a flat surface with the blade moving away from your hand and body.
- Step 1: A yellow-brown solution that turns blue-black on a food sample is iodine solution. Step 2: Iodine solution turns blue-black only when starch is present. Step 3: So the solution is iodine solution and the conclusion is that the potato disc contains starch.Method:Match the colour change to the food test and state the positive result.Examiner tips
- Iodine solution: yellow-brown to blue-black means starch is present.
- Step 1: Magnification = length of line PQ ÷ actual length. Step 2: Substitute the values: 63 ÷ 39 = 1.615... Step 3: To two significant figures this is ×1.6; magnification has no units.Method:Put the measured and actual lengths into the formula and round to two significant figures.Examiner tips
- magnification = image length ÷ actual length.
- Step 1: A valid difference compares a visible feature, here the potato leaf has more, and more branched, veins than the tomato leaf. Step 2: A valid similarity is a feature both leaves share, such as a midrib and a leaf stalk. Step 3: Only the first option pairs a true difference with a true similarity; the others contain statements that are not correct.Method:Pick a true visible difference and a true shared feature of the two leaves.Examiner tips
- Compare a visible feature for the difference and a shared feature for the similarity.
- Step 1: A constant temperature needs a source that holds the same temperature throughout. Step 2: A thermostatically controlled water-bath set to 40 C keeps the mixture at that exact temperature. Step 3: A Bunsen flame, the open bench or a refrigerator would all let the temperature change, so they do not keep it constant at 40 C.Method:Choose the method that holds the mixture at a steady, set temperature.Examiner tips
- A thermostatically controlled water-bath holds a set temperature constant.
- Step 1: A controlled variable is kept the same in every test so the comparison is fair. Step 2: The mass of crushed apple and the volume of pectinase solution must be the same each time, so only the pectinase concentration differs. Step 3: The concentration of pectinase is the variable being changed and the volume of juice is the result, so neither of those is controlled.Method:Pick the conditions that must stay the same so only the pectinase concentration changes.Examiner tips
- Keep everything the same except the one variable you are testing.
- Step 1: Both axes are labelled with units and an even scale is chosen so the plotted points fill at least half the grid. Step 2: All five points are plotted accurately, to within half a small square. Step 3: A single suitable line is then drawn; only the first approach meets every requirement for a line graph.Method:Recall the rules for a line graph and pick the approach that meets all of them.Examiner tips
- Line graphs need labelled axes with units, an even scale filling the grid, accurate points and a single line.
- Step 1: A concentration of 0.5% lies just above the 0.4% point (12 cm3) and well below the 0.8% point (22 cm3). Step 2: Reading up from 0.5% to the line and across to the volume axis gives a value a little above 12 cm3. Step 3: Interpolating between the points gives an estimate of about 15 cm3.Method:Use the line to read the volume that corresponds to a concentration of 0.5%.Examiner tips
- Read up from the given concentration to the line, then across to the volume axis.
- Step 1: From 0.1% to 0.8% the volume of juice rises as the concentration increases. Step 2: From 0.8% to 1.6% the volume stays at 22 cm3, so it has stopped increasing. Step 3: So increasing the concentration increases juice production up to a point, after which it levels off.Method:State the trend, then note where the volume stops changing.Examiner tips
- Describe both the rise and the levelling off shown by the data.
- Step 1: The optimum is the lowest concentration that gives the maximum juice, somewhere between 0.4% and 1.6%. Step 2: The gap between 0.4% and 0.8% is large, so the exact turning point is not known. Step 3: Testing more concentrations in small steps between these values, such as 0.7% and 0.9%, would show whether 0.8% is truly the optimum.Method:Identify the region of interest and add closely spaced concentrations there.Examiner tips
- To find an optimum, test more values in small steps around the suspected best point.
- Step 1: To separate the juice from the pulp the mixture is poured through a funnel lined with filter paper. Step 2: The filtered juice must run into a measuring cylinder so that its volume can be read from the scale. Step 3: So the correct apparatus is a funnel with filter paper over a measuring cylinder, with the parts labelled.Method:Pick apparatus that both separates the juice and measures its volume.Examiner tips
- Filter paper in a funnel separates the juice; a measuring cylinder reads its volume.
- Step 1: Light intensity is the independent variable, so it must be changed over several values, for example by altering the lamp distance, while everything else is held constant. Step 2: The colour of the hydrogencarbonate indicator around the submerged plant is the dependent variable, and a heat screen keeps the temperature constant so only light intensity changes. Step 3: The rate of photosynthesis equals the rate of respiration at the intensity where the indicator stays red; only the first plan changes one variable, controls the rest and repeats the readings.Method:Check the plan changes only the light intensity, follows the indicator colour and controls the other variables.Examiner tips
- A valid plan changes one variable, measures a relevant response, controls the rest and repeats.
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