Question 127 marks
Question
You are going to investigate the effect of surface area on the rate of diffusion. You will be preparing different sized blocks of agar. The agar contains universal indicator. The blocks of agar have different surface areas. You will place the blocks of agar into hydrochloric acid and measure the time taken for the acid to diffuse to the centre of the agar block. The agar block will change colour as the acid diffuses through it. Read all the instructions but DO NOT CARRY THEM OUT until you have drawn a table for your results in the space provided in 1(a)(i). You should use the safety equipment provided while you are carrying out the practical work. Step 1 Use the measuring cylinder to put 10 cm3 of hydrochloric acid into each of the four test‑tubes. Place the test‑tubes in the test‑tube rack. Step 2 You are provided with a large piece of agar which is approximately 1.0 cm thick. Use the knife and the ruler to cut two blocks from the large piece of agar, that each measure approximately 1.0 cm × 1.0 cm × 1.0 cm, as shown in Fig. 1.1. 1.0 cm 1.0 cm agar block 1.0 cm 1.0 cm white tile 1.0 cm 1.0 cm Fig. 1.1 Step 3 Put one of the 1.0 cm × 1.0 cm × 1.0 cm blocks of agar into one of the test‑tubes containing hydrochloric acid and immediately start the stop‑clock. Step 4 Observe the colour of the agar block. You may find it easier to observe the colour change if you hold the white card behind the test‑tube. Record in your table in 1(a)(i) the time taken, in seconds, for the block to become completely red. If the agar block in the test‑tube has not become completely red after five minutes, stop observing and record the time as >300 in your table. Step 5 Cut the second 1.0 cm × 1.0 cm × 1.0 cm block into two blocks that are each 1.0 cm × 1.0 cm x 0.5 cm. Step 6 Put one of the 1.0 cm × 1.0 cm × 0.5 cm blocks from step 5 into the second test‑tube containing hydrochloric acid and immediately start the stop‑clock. Repeat step 4. Step 7 Cut the second 1.0 cm × 1.0 cm × 0.5 cm block into two blocks that are each 1.0 cm × 0.5 cm × 0.5 cm. Step 8 Put one of the 1.0 cm × 0.5 cm × 0.5 cm blocks from step 7 into the third test‑tube containing hydrochloric acid and immediately start the stop‑clock. Repeat step 4. Step 9 Cut the second 1.0 cm × 0.5 cm × 0.5 cm block into two blocks that are each 0.5 cm × 0.5 cm × 0.5 cm. Step 10 Put one of the 0.5 cm × 0.5 cm × 0.5 cm blocks from step 9 into the fourth test‑tube containing hydrochloric acid and immediately start the stop‑clock. Repeat step 4. (a) (i) Prepare a table to record your results. [4] (ii) State a conclusion for your results. …… [1] (iii) State the variable that you changed (independent variable) in this investigation. …… [1] (iv) State two variables that were kept constant in this investigation. 1 …… 2 …… [2] (v) Suggest two ways you could improve the method used in this investigation. 1 …… 2 …… [2] (vi) Describe how you carried out step 2 safely. …… [1] (b) Table 1.1 shows the surface areas and volumes of the blocks of agar that you used in your investigation. Table 1.1 surface area to length of sides / cm surface area / cm2 volume / cm3 volume ratio 1.0 × 1.0 × 1.0 6.00 1.000 6:1 1.0 × 1.0 × 0.5 4.00 0.500 8:1 1.0 × 0.5 × 0.5 2.50 0.250 0.5 × 0.5 × 0.5 1.50 0.125 12:1 Calculate the surface area to volume ratio for the 1.0 cm × 0.5 cm × 0.5 cm block of agar. …… [1] (c) (i) Many organisms have adaptations that increase the area of their gas exchange surfaces. Fig. 1.2 is a photomicrograph of part of a fish gill. P Q magnification ×550 Fig. 1.2 Draw a large diagram of the part of the fish gill shown in the box in Fig. 1.2. [4] (ii) Measure the length of line PQ in Fig. 1.2. length of line PQ …… mm Calculate the actual length of the part of the fish gill using the formula and your measurement. length of line PQ magnification = actual length of the part of the fish gill Give your answer to three decimal places. Space for working. …… mm [3] (d) Fish is a source of protein in the diet. State how you could test a sample of food to show that it contains protein. Include the result of a positive test. …… [2] (e) Photographic film consists of a plastic sheet coated in crystals. The crystals are fixed to the plastic sheet by gelatin, which is made of protein. If the gelatin is digested by protease enzymes the crystals fall off and the film will become transparent, as shown in Fig. 1.3. before protease treatment after protease treatment Fig. 1.3 Plan an investigation to determine the effect of temperature on the activity of a protease enzyme, using photographic film. …… [6] [Total: 27]
Mark scheme
1(a)(i) table drawn with a minimum of two columns and a header 4 line ; appropriate headings with units ; recording of four readings (for time) ; suitable trend in data ; check supervisor’s report 1(a)(ii) the time taken (for the agar block to change colour) increases 1 as the, side length / diffusion distance / surface area, increases ; ora 1(a)(iii) size of block / AW ; 1 1(a)(iv) any two from: 2 concentration of acid ; volume of acid ; type of acid ; agar (cut from) same (block) / type of indicator ; (block) starting colour / green at the start ; 1(a)(v) any two from: 2 repeat the investigation ; control the temperature ; standardise the cutting procedure ; AVP ;; 1(a)(vi) cut away from body / cut towards tile / cut on flat surface 1 / AW ; 1(b) 10 (:1) ; 1 1(c)(i) outline single clear line no shading ; 4 size larger than image ; details ;; e.g. proportion, filaments and lamellae shown, 14–8 branches, at least one alternation of branches 1(c)(ii) line PQ 90±1(mm) ; 3 MP1 measurement of line PQ 0.162 / 0.164 / 0.165 ;; MP2 correct calculation MP3 correct rounding to three decimal places ecf MP2 and MP3 1(d) (add) biuret (solution) ; 2 purple / AW ; 1(e) independent variable: 6 1 (at least) two different temperatures ; 2 method of maintaining temperature ; dependent variable: 3 measuring time for film, to become transparent / to become clear / for crystals to fall off ; method: 4 use of a buffer ; 5 equilibration to correct temperature ; 6 shaking ; constant variables ;; 7,8 concentration of protease / volume of protease / type of protease / type of film / pH / size of film pieces / light (intensity) / volume of buffer / consistent shaking 9 two or more replicates or repeat investigation twice ; 10 valid safety precaution ;