0610/61 May/June 2025 Worked Answers (IGCSE Biology 0610 Extended)
17 questions · 40 marks · 60 minutes
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Worked answers for 16 questions
- Step 1: A results table needs ruled columns with a header line and headings that include units, here the concentration of acid in mol per dm3 and the time to turn red in seconds. Step 2: A converted time must be recorded for all four concentrations so they can be compared. Step 3: A higher acid concentration speeds up diffusion, so the time to turn red falls as the concentration rises.Method:Recall the features of a good results table, then use diffusion to predict the trend with concentration.Examiner tips
- Tables need ruled columns, a header line, headings with units, and every converted value.
- Step 1: A shorter time to turn red means the acid has diffused to the centre of the agar faster. Step 2: The most concentrated acid gave the shortest time, so a higher concentration gave a faster rate of diffusion. Step 3: The conclusion is that increasing the concentration of acid increases the rate of diffusion.Method:Translate the times into rate of diffusion and relate it to the acid concentration.Examiner tips
- A conclusion links the measured result (time) to the variable changed (concentration).
- Step 1: The independent variable is the one deliberately changed, here the concentration of hydrochloric acid. Step 2: The dependent variable is the one measured in response, here the time for the agar to turn red. Step 3: So acid concentration is the independent variable and the time is the dependent variable.Method:Decide which variable is deliberately changed and which is measured in response.Examiner tips
- Independent = changed; dependent = measured; controlled = kept the same.
- Step 1: Cutting the agar into equal-sized pieces means each piece has the same surface area and distance to the centre, making the comparison fair. Step 2: Using a white background makes the colour change easier to judge, giving a more accurate end-point. Step 3: Together these improve the reliability and accuracy of the results.Method:Pick changes that make the test fairer or the measurement more accurate.Examiner tips
- Good improvements keep the test fair or make the end-point easier to judge.
- Step 1: A hazard is something that could cause harm. Step 2: The knife can cut the skin and hydrochloric acid is corrosive and can irritate or burn, so both are hazards. Step 3: Distilled water, a stop-clock, a rack, a tile and a scale are not harmful, so they are not hazards.Method:Pick the two items that could actually cause harm.Examiner tips
- Hazards are things that could cause harm, such as sharp tools or corrosive acids.
- Step 1: Temperature is the independent variable, so it must be changed over several values while everything else is held constant. Step 2: Osmosis is measured by the change in mass (or length) of equal-sized potato pieces before and after a fixed time in the same solution. Step 3: The concentration of solution and the size of the pieces are kept constant and the readings repeated; only the first plan does all of this.Method:Check each plan changes only the temperature, measures the change in mass and is repeated.Examiner tips
- A valid plan changes one variable, measures a relevant response, controls the rest and repeats.
- Step 1: DCPIP is a blue dye. Step 2: Adding vitamin C decolourises it, so it becomes colourless only at the end-point. Step 3: Before any vitamin C is added the DCPIP is still blue.Method:Recall the starting colour of DCPIP before it is decolourised.Examiner tips
- DCPIP is blue and turns colourless when decolourised by vitamin C.
- Step 1: A controlled variable is kept the same in every test so the comparison is fair. Step 2: The volume and concentration of the DCPIP must be the same each time, otherwise different amounts of vitamin C would be needed for reasons other than the vitamin C concentration. Step 3: So the volume and concentration of DCPIP are the controlled variables.Method:Pick the conditions that must stay the same so only the vitamin C concentration changes.Examiner tips
- Controlled variables are kept the same in every test; here that is the DCPIP.
- 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 through the points; only the first approach meets all of these requirements.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 volume of 1.2 cm3 lies between the 500 mg per dm3 point (1.1 cm3) and the 250 mg per dm3 point (1.4 cm3). Step 2: Reading along the line, a volume of 1.2 cm3 corresponds to a concentration a little below 500 mg per dm3. Step 3: Interpolating between the points gives an estimate of about 420 mg per dm3.Method:Use the line to read the concentration that corresponds to a volume of 1.2 cm3.Examiner tips
- Read across from the given volume to the line, then down to the concentration axis.
- Step 1: Each stored sample has a lower vitamin C concentration than when it was fresh. Step 2: This pattern holds across all the samples. Step 3: So the conclusion is that storing the apple juice decreases its vitamin C concentration.Method:Compare the fresh and stored values and state the overall trend.Examiner tips
- A conclusion compares the measured values before and after the change.
- Step 1: An anomalous result stands out from the others. Step 2: It does not follow the pattern or trend that the rest of the data show. Step 3: So an anomalous result is one that does not fit the pattern of the other results.Method:Define an anomaly as a result that breaks the trend of the others.Examiner tips
- An anomalous result is the one that does not fit the trend of the rest.
- Step 1: Two of the stored results, 96 and 104 mg per dm3, are close together and form a clear pattern. Step 2: The value 170 mg per dm3 is much higher than these two. Step 3: Because it does not fit the pattern of the others, 170 mg per dm3 is the anomalous result.Method:Compare the three stored values and pick the one that does not fit the pattern.Examiner tips
- The anomaly is the value that sits well away from the cluster of the others.
- Step 1: Change in concentration = stored − fresh = 104 − 272 = −168 mg per dm3. Step 2: Percentage change = (change ÷ fresh value) × 100 = (−168 ÷ 272) × 100. Step 3: This gives −61.76… = −61.8 % to one decimal place; the minus sign shows it is a decrease.Method:Find the change, divide by the fresh value, multiply by 100 and keep the negative sign.Examiner tips
- Percentage change = (final − initial) ÷ initial × 100; a fall gives a negative answer.
- Step 1: Rearrange magnification = length of PQ ÷ actual diameter to give actual diameter = length of PQ ÷ magnification. Step 2: Actual diameter = 61 ÷ 1.8 = 33.88… mm. Step 3: To three significant figures this is 33.9 mm.Method:Rearrange the magnification formula, divide 61 by 1.8 and round to three significant figures.Examiner tips
- actual size = image length ÷ magnification.
- Step 1: Reducing sugars are tested for with Benedict’s solution. Step 2: The mixture must be heated in a hot water-bath for the reaction to take place. Step 3: A positive result is a colour change from blue to brick-red; iodine tests for starch, biuret for protein and the ethanol emulsion test for fats.Method:Recall the reagent and the heating step needed to test for reducing sugars.Examiner tips
- Benedict’s solution plus heat tests for reducing sugars (blue to brick-red).
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