Metabolic Processes — Making Food, Burning It, and Life in the Dark
Prove with iodine that a leaf needs light, chlorophyll and carbon dioxide to make starch. Count the oxygen bubbles a waterweed gives off and find what limits it. Catch seeds breathing in a sealed jar. Find the depth at which a seaweed can no longer pay its way, and meet the animals that live where sunlight never reaches.
Investigations column, block 36: "Investigate photosynthesis by showing that: starch is produced during photosynthesis; light is necessary for photosynthesis. The following investigations can be done by learners as experiments, or as demonstrations, as time permits: carbon dioxide is necessary for photosynthesis; chlorophyll is necessary for photosynthesis; oxygen is produced during photosynthesis. OR data can be provided and interpreted by learners. Design an investigation or demonstration to show that: oxygen is used by living organisms during respiration; carbon dioxide is produced by living organisms during respiration. OR provide relevant data that can be interpreted by learners (identify variables, suggest controls, and record observations). Internet research on extremophiles and chemosynthesis." Resources: "Living plants · Suitable equipment · Chemicals · Snails or seedlings."
CAPS offers the experiments or data. Because you have no school lab, this sheet gives you both. The starch tests are Investigation 1; oxygen and the rate of photosynthesis, Investigation 2; respiration, Investigation 3; the compensation depth (a key concept with its own zones diagram), Investigation 4; and the extremophile research, Investigation 5.
What you need
- 🟢 kitchen A potted geranium (Pelargonium) or other soft-leaved plant, and a variegated one (green-and-white leaves); a dark cupboard; aluminium foil and paper clips
- 🟡 pharmacy Tincture of iodine (dilute it 1 part to 10 parts water) and methylated spirits
- 🟢 kitchen A kettle, jars, a bowl, a white saucer, a straw, bicarbonate of soda, dishwashing liquid, and spinach leaves (for leaf discs, as in Practical 19)
- 🟡 aquarium shop A few stems of pondweed (Egeria or Elodea) — or 🌊 shore a frond of sea lettuce (Ulva) kept in sea water — plus a desk lamp, a kitchen thermometer, ice, a ruler and a stopwatch
- 🟢 kitchen Dried beans or peas, cotton wool, three jars with lids, a red cabbage (for indicator) — or 🟡 aquarium shop a pH test kit that uses bromothymol blue — a tea-light, a long wire or skewer, matches, dried yeast, sugar, a balloon and a small bottle
- 🔴 school lab Soda lime, hydrogencarbonate indicator, a respirometer — you will not have these at home. That's fine: their results are supplied.
- 🟢 kitchen Graph paper, a calculator and coloured pencils; internet access for Investigation 5 if you have it
Every investigation has a supplied results panel: four tested leaves and a soda-lime experiment, bubble counts at four light levels and five temperatures, three respiring jars, a respirometer and a yeast balloon, light-and-dark-bottle oxygen data from six depths, and six research cards on life at the vents. CAPS itself allows data instead of experiments — so the marks are all reachable.
Aim
To show that leaves make starch in photosynthesis, and that light, chlorophyll and carbon dioxide are all needed to make it.
Method
- De-starch both plants: put them in a dark cupboard for 48 hours.
- Fold a strip of foil over both sides of one leaf on the green plant and clip it. Draw the variegated leaf you will test, showing exactly which parts are green and which are white. Put both plants in bright light for 6 hours.
- Pick four leaves: (a) a leaf straight from the dark, before the light period (pick it in step 1's cupboard); (b) an uncovered leaf after 6 hours of light; (c) the foil-covered leaf; (d) the variegated leaf.
- The starch test. Dip each leaf in just-boiled water for 1 minute. Then stand it in a jar of methylated spirits, with the jar in a bowl of just-boiled water (never on a stove), for about 10 minutes until the leaf is pale and the spirits are green. Dip it in warm water to soften it, spread it on a white saucer, cover it with dilute iodine for 2 minutes, and rinse.
- Carbon dioxide, the kitchen way. Make leaf discs that sink (Practical 19, Test C). Put 10 in water with ¼ teaspoon of bicarbonate of soda, and 10 in water that has been boiled and cooled (boiling drives out the dissolved carbon dioxide), with no bicarbonate. Stand both under the lamp and count the floating discs after 20 minutes.
Supplied results — four leaves, a soda-lime experiment and leaf discs
| Leaf | Colour after iodine |
|---|---|
| (a) straight from the dark | yellow-brown all over |
| (b) 6 hours in light | blue-black all over |
| (c) foil strip, 6 hours in light | blue-black, except a sharp-edged yellow-brown band exactly where the foil was |
| (d) variegated, 6 hours in light | blue-black only where the leaf had been green; the white edge stayed yellow-brown |
Data set 1.2 — a school-lab result (soda lime). Two de-starched potted plants were each enclosed in a clear plastic bag. Bag A also held a dish of soda lime, which absorbs carbon dioxide; bag B held an identical dish of water. Both stood in the same bright light for 6 hours. A leaf from plant A stayed yellow-brown with iodine; a leaf from plant B turned blue-black.
Data set 1.3 — leaf discs after 20 minutes under the lamp. With bicarbonate: 10 of 10 floating. Boiled-and-cooled water, no bicarbonate: 0 of 10 floating.
Results
Analysis
- Why must the plants be de-starched first? What does leaf (a) prove? 3
- Why is the leaf dipped in boiling water, and why must the chlorophyll be removed before the iodine goes on? 2
- Why must the methylated spirits be heated in a bowl of hot water and never on a stove? 2
- State the conclusion from each of leaves (b), (c) and (d). For the foil leaf, name the independent variable and the control. 6
- Draw the variegated leaf before and after the test, labelled to show where starch was found and why. 4
- Explain the soda-lime result. Why did bag B need a dish of water and to be identical in every other way? 3
- Explain the leaf-disc result: why does boiled-and-cooled water make a fair "no carbon dioxide" treatment? 2
- Write the word equation and the balanced symbol equation for photosynthesis. Name the organelle where it happens and its two phases, and say what each phase needs. 4
- Photosynthesis makes glucose, not starch. Explain why a blue-black leaf is still good evidence of photosynthesis. 2
Aim
To show that photosynthesis gives off oxygen, and to measure how light, carbon dioxide and temperature change its rate.
Method
- Cut the end of a pondweed stem under water. Weight it with a paper clip, cut end up, in a jar of water at 20 °C with ¼ teaspoon of bicarbonate of soda. (Sea lettuce: use sea water and count bubbles rising from the frond.)
- Put the lamp 10 cm from the jar. Wait 5 minutes, then count the bubbles leaving the cut end in 1 minute, three times. Repeat at 20, 30 and 40 cm, and with the lamp off. Check the thermometer each time — stand a jar of plain water between lamp and plant if the water warms.
- Carbon dioxide: at 10 cm, repeat in boiled-and-cooled water with no bicarbonate.
- Temperature: at 10 cm, repeat in bicarbonate water at 10 °C (add ice), 30 °C, 35 °C and 45 °C (add hot water).
- The gas: stand a fresh plant under an upside-down water-filled bottle in sunshine for a day. With an adult, lower a glowing (not flaming) splint into the gas collected.
Supplied results — bubble counts, and the gas test
| Lamp distance | Count 1 | Count 2 | Count 3 |
|---|---|---|---|
| 10 cm | 42 | 45 | 43 |
| 20 cm | 23 | 21 | 22 |
| 30 cm | 11 | 12 | 10 |
| 40 cm | 6 | 7 | 6 |
| lamp off | 0 | 0 | 0 |
Data set 2.2 — carbon dioxide. At 10 cm in boiled-and-cooled water with no bicarbonate: 3, 2 and 3 bubbles per minute.
| Temperature (°C) | 10 | 20 | 30 | 35 | 45 |
|---|---|---|---|---|---|
| Bubbles per minute | 15 | 43 | 61 | 52 | 4 |
At 45 °C the leaves turned dark and limp, and they did not recover when the water was cooled.
Data set 2.4 — the gas. After a sunny day about 8 mL of gas had collected. A glowing splint lowered into it burst back into flame.
Analysis
- Calculate the mean number of bubbles per minute at each lamp distance. 2
- Plot the mean rate against the lamp distance and describe the pattern. 4
- Light intensity falls with the square of the distance. Taking the intensity at 10 cm as 100, calculate it at 20, 30 and 40 cm. Plot the rate against light intensity, describe the shape, and explain why the graph levels off at high intensity. 5
- What does Data set 2.2 show? Link it to CAPS's statement that "the amount of dissolved carbon dioxide will dictate the potential rate of photosynthesis". 2
- Plot the rate against temperature. Give the optimum temperature, and explain why the rate collapsed at 45 °C and did not recover. 4
- Why must the temperature stay the same while the light is varied, and how was this done? 2
- Counting bubbles is not a perfect measure of the oxygen produced. Give two reasons, and suggest a better measure. 3
- What does the glowing splint show about the gas? 1
- Off the Cape coast, kelp forests grow only in roughly the top 15–20 m. Use your light results to explain why. 2
Aim
To show that living seeds give off carbon dioxide and use up oxygen, to measure how temperature changes the rate, and to compare respiration with and without oxygen.
Method
- Soak 40 beans overnight, then keep them on damp paper towel for two days until they sprout. Boil 20 of them for 10 minutes and let them cool — these are dead.
- Red cabbage indicator: chop some red cabbage, pour just-boiled water over it, wait 10 minutes and strain. The purple liquid turns pinker in acid — and carbon dioxide dissolves to make a weak acid.
- Set up three jars, each with a small cup of indicator on the bottom and a wad of cotton wool above it: A — germinating seeds on the cotton wool; B — boiled seeds; C — no seeds. Seal them and keep them in the dark. Note the indicator colour at 0, 6 and 24 hours.
- After 24 hours, with an adult, open each jar and at once lower a lit tea-light on a wire to the bottom. Time how long the flame lasts.
- Without oxygen: in a small bottle, mix 1 teaspoon of dried yeast and 1 teaspoon of sugar in 200 mL of warm water; stretch a balloon over the neck. Set up a second bottle with no sugar. Leave both for an hour.
Supplied results — three jars, a respirometer and a yeast balloon
| Jar | 0 h | 6 h | 24 h | Tea-light lasted |
|---|---|---|---|---|
| A — germinating seeds | purple | pinkish purple | pink-red | 4 s |
| B — boiled seeds | purple | purple | purple | 13 s |
| C — no seeds | purple | purple | purple | 14 s |
Data set 3.2 — a school-lab respirometer. Germinating seeds sat in a sealed tube above soda lime, which absorbs carbon dioxide. A drop of coloured water in a thin glass tube attached to it moved towards the seeds as the air inside shrank.
| Tube | Trial 1 | Trial 2 | Trial 3 |
|---|---|---|---|
| germinating seeds, 20 °C | 17 | 19 | 18 |
| germinating seeds, 30 °C | 30 | 33 | 31 |
| boiled seeds, 20 °C | 0 | 0 | 1 |
| five small snails, 20 °C | 12 | 11 | 13 |
Data set 3.3 — yeast. After an hour the bottle with sugar was frothy, smelt of bread and alcohol, and its balloon had blown up to about 12 cm across. The bottle with no sugar was unchanged and its balloon stayed flat.
Analysis
- Explain the colour change in jar A. Why did jars B and C not change, and what does each of them rule out? 4
- Why were the jars kept in the dark? 1
- What do the tea-light times show? Which gas had the germinating seeds used, and why did the flame go out sooner? 3
- In the respirometer, explain why the drop moves towards the seeds, and why the soda lime is needed if the drop is to measure oxygen alone. 3
- Calculate the mean distance for seeds at 20 °C and at 30 °C, and explain the difference. 2
- For the 20 °C and 30 °C respirometer runs, name the independent variable, the dependent variable, and two variables that must be controlled. 4
- Name the process in the yeast bottle and the gas that filled the balloon. Write its word equation, and explain why the bottle with no sugar did nothing. 3
- The booklet's question 4: use a simple annotated flow diagram to show why oxygen is critical for aerobic respiration to take place. 6
- The booklet's question 5: marine reptiles and mammals sometimes rely on anaerobic respiration during long dives. Explain two disadvantages to someone who understands the chemistry of respiration. 4
- Draw the CAPS diagram of the relationship between photosynthesis and respiration, showing what each process takes in and gives out, and where the energy enters and leaves. 4
Aim
To find the compensation depth from real-style field data, using the method oceanographers have used since the 1920s, and to draw the light zones of the sea.
How the method works
At each depth, two bottles are filled with seawater and its plankton. One is clear (the light bottle); the other is painted black (the dark bottle). Both are hung back at that depth for 24 hours, and the oxygen in each is measured before and after. In the dark bottle nothing can photosynthesise, so its oxygen falls by the amount used in respiration. In the light bottle, photosynthesis and respiration both happen, so its change is the net result. This is the light-and-dark-bottle method, first used by Norwegian scientists Gaarder and Gran in 1927.
Supplied results — oxygen change over 24 hours at six depths
| Depth (m) | 0 | 5 | 10 | 15 | 20 | 30 |
|---|---|---|---|---|---|---|
| Light bottle | +4.2 | +3.0 | +1.6 | +0.6 | −0.2 | −0.7 |
| Dark bottle | −1.0 | −1.0 | −1.0 | −0.9 | −0.9 | −0.9 |
| Light (% of surface) | 100 | 29 | 8 | 2.4 | 0.7 | 0.06 |
Analysis
- Explain what the dark bottle measures, and why its oxygen falls. 2
- Calculate the gross photosynthesis at each depth (light-bottle change minus dark-bottle change). 3
- Plot the light-bottle and dark-bottle changes against depth on one graph, with depth increasing downwards. 5
- Find the compensation depth from your graph. What percentage of surface light reaches it, and how does that compare with CAPS? 3
- Explain why a seaweed whose fronds lived permanently below this depth could not survive. 2
- In Practical 19 you used the rule of thumb that the euphotic zone reaches about 2.7 × the Secchi depth. Estimate the Secchi depth of this water, and predict how the compensation depth would change a week after a river flood. 3
- Draw and label a diagram of the photic, euphotic, disphotic and aphotic zones for clear open ocean, marking the compensation depth and giving approximate depths. 5
Aim
To research how life can run on chemical energy instead of sunlight, and to keep a record of where each fact came from.
Method
- If you have internet access, find: three kinds of extremophile and the extreme each survives; one named hydrothermal vent field and where it is; one animal that lives there and how it feeds.
- For every fact, write down the website or book, its author or organisation, and the date you read it. Prefer a university, a museum, a research institute or a science magazine to a forum.
- No internet? Use the research cards below — they are written to answer every question.
| Fact | Source (site or book, author or organisation) | Date read |
|---|---|---|
Supplied research cards — six cards on life in the dark
Analysis
- Complete a table comparing photosynthesis and chemosynthesis under five headings: energy source, raw materials, products, the organisms that do it, and where in the sea it happens. 5
- Name three kinds of extremophile and the extreme condition each survives. 3
- Riftia has no mouth or gut. Explain how it gets its food, and why its red plume matters. 3
- CAPS writes chemosynthesis as CO₂ + H₂S + O₂ → (CH₂O)x + SO₄. Taking x = 1, count the atoms of each element on each side to show that it does not balance. Then show that adding one H₂O on the left and writing the sulphate as H₂SO₄ makes it balance. 3
- CAPS says chemosynthesis was "thought to be insignificant until the early 1990s" — yet vent communities were found in 1977, and chemosynthetic bacteria were discovered in the 1880s. Use card 5 to explain what changed in the 1990s. 2
- The booklet says vents are found in "deep ocean trenches". Use Topic 11 to say where most hydrothermal vents are actually found, and why there. 2
- Explain why a vent community at 2 500 m holds far more life than the abyssal plain around it. 2
- The booklet's questions 1 and 2. Give the term for: (a) the upper region of the ocean, exposed to sufficient light for photosynthesis to take place; (b) any process which takes place in the absence of oxygen; (c) organisms, normally Archaea, capable of living in extreme conditions. Then define: (d) chemosynthesis; (e) compensation depth; (f) glycolysis. 6
Memo — worked answers and mark allocation (does not print)
Total: 136 marks — Investigation 1: 28 · Investigation 2: 25 · Investigation 3: 34 · Investigation 4: 23 · Investigation 5: 26.
Investigation 1 — the starch tests
- Q1 (3): Leaves store starch from earlier photosynthesis; it must be used up first (1), or starch found later might have been made before the experiment (1). Leaf (a) shows the de-starching worked — there was no starch at the start, so any starch found later was made during the experiment (1).
- Q2 (2): Boiling water kills the cells, stops all reactions and softens the leaf so the spirits and iodine can get in (1). Chlorophyll's green colour would hide the iodine colour change, so it is removed to see the result clearly (1).
- Q3 (2): Methylated spirits are highly flammable and boil at a lower temperature than water (1); the hot water warms them safely without any flame or hot element that could ignite the vapour (1).
- Q4 (6): (b) Starch was made in the light — the leaf photosynthesised (1). (c) Only the uncovered parts made starch: light is necessary for photosynthesis (1). (d) Only the green parts made starch: chlorophyll is necessary (1). Foil leaf: independent variable — whether the leaf received light (light vs no light) (1); the control — the uncovered part of the same leaf (or leaf b), which had light and was treated the same way in every other respect (2).
- Q5 (4): Two outline drawings of the same leaf (1); "before" showing green and white areas, labelled (1); "after" showing blue-black exactly where it was green and yellow-brown where it was white, labelled (1); a caption: no chlorophyll, so no photosynthesis, so no starch (1).
- Q6 (3): Soda lime removed the carbon dioxide from bag A, so plant A could not photosynthesise or make starch (1); plant B had carbon dioxide and made starch, so carbon dioxide is necessary (1). Bag B is the control: it must be identical — same plant type, light, time, a similar dish — so that the presence of carbon dioxide is the only difference (1).
- Q7 (2): Gases are less soluble in hot water, so boiling drives the dissolved carbon dioxide out, and it does not return quickly on cooling (1). With no carbon dioxide the discs could not photosynthesise, make oxygen and float — carbon dioxide is necessary (1).
- Q8 (4): Carbon dioxide + water → glucose + oxygen, with light energy and chlorophyll (1). 6CO₂ + 6H₂O → C₆H₁₂O₆ + 6O₂ (1). In the chloroplast (1). The light phase (in the grana) needs light — it splits water, releasing oxygen; the dark phase (light-independent, in the stroma) does not need light directly — it uses carbon dioxide to make glucose (1). No biochemical detail is required.
- Q9 (2): Glucose made in photosynthesis is converted to insoluble starch for storage (1), so starch builds up only where glucose has been made — it is a stored record of photosynthesis (1).
Investigation 2 — oxygen and the rate
- Q10 (2): 10 cm: 43.3; 20 cm: 22.0; 30 cm: 11.0; 40 cm: 6.3 bubbles per minute (2 for all four; 1 for two or three).
- Q11 (4): Axes labelled with units (1); points accurate (1); a smooth curve (1); the rate falls as the lamp moves further away, steeply at first, then more gently (1).
- Q12 (5): Intensities: 20 cm → 25; 30 cm → 11; 40 cm → 6.25 (1). Graph plotted correctly (1). At low intensity the rate rises in proportion — 6.25 → 6.3, 11 → 11, 25 → 22 (1); between 25 and 100 the rate only doubles while the light quadruples, so the curve levels off (1). At high light intensity light is no longer the limiting factor; something else — carbon dioxide or temperature — limits the rate (1).
- Q13 (2): Without dissolved carbon dioxide the rate fell from about 43 to about 3 bubbles per minute, even in bright light (1) — carbon dioxide is a raw material, so its supply sets how fast photosynthesis can go (1).
- Q14 (4): Graph plotted (1). The optimum is about 30 °C (1). Photosynthesis is controlled by enzymes; above the optimum they begin to denature (1); at 45 °C they were denatured — their shape permanently changed — so the rate collapsed and could not recover on cooling (1).
- Q15 (2): Temperature also changes the rate, so it must be kept constant for light to be the only variable (1); by checking with the thermometer and standing a jar of water between the lamp and the plant to absorb heat (or using a cool LED lamp) (1).
- Q16 (3): Any two: bubbles are not all the same size; some oxygen dissolves in the water instead of forming bubbles; the plant uses some of its oxygen in respiration; bubbles may contain other gases; counting fast bubbles is error-prone (2). Better: collect the gas in a measuring tube or a syringe and measure its volume per minute (1).
- Q17 (1): A glowing splint relights in oxygen — the gas given off in photosynthesis is oxygen.
- Q18 (2): Light is absorbed as it passes down through the water, so the rate of photosynthesis falls with depth (1); below about 15–20 m in coastal water too little light reaches the kelp for it to make more food than it uses, and the light that remains is mostly blue (1).
Investigation 3 — respiration in a jar
- Q19 (4): The germinating seeds respired and gave off carbon dioxide (1), which dissolved in the indicator as a weak acid, so it turned pink (1). Jar B: dead seeds do not respire, so it rules out the seeds' material itself causing the change — it was living seeds (1). Jar C: with nothing in it there was no change, so it rules out the jar, the air or the indicator changing by themselves (1).
- Q20 (1): In the dark the seedlings cannot photosynthesise, which would use up the carbon dioxide and hide the respiration.
- Q21 (3): The flame lasted 4 s in jar A against 13–14 s in B and C (1). The germinating seeds had used up some of the oxygen in jar A (1). A flame needs oxygen; with less oxygen left it went out sooner (1).
- Q22 (3): The seeds take in oxygen and give out carbon dioxide (1); the soda lime absorbs the carbon dioxide, so the air in the tube shrinks by the volume of oxygen used, pulling the drop towards the seeds (1). Without soda lime the carbon dioxide given out would replace the oxygen used, and the drop would hardly move (1).
- Q23 (2): 20 °C: 18 mm; 30 °C: 31.3 mm (1). Respiration is controlled by enzymes, which work faster at the higher temperature (up to their optimum), so oxygen was used faster (1).
- Q24 (4): Independent: temperature (1). Dependent: the distance the drop moved in 10 minutes — the oxygen used (1). Controlled — any two: the number or mass of seeds; the type and age of seeds; the amount of soda lime; the size of the tube; the time; the same start position of the drop (2).
- Q25 (3): Anaerobic respiration (alcoholic fermentation) — the balloon filled with carbon dioxide (1). Glucose → ethanol (alcohol) + carbon dioxide + a little energy (1). Without sugar the yeast had no glucose to break down, so no carbon dioxide was produced (1).
- Q26 (6): Diagram (4): glucose → glycolysis (cytoplasm, 2 ATP) → pyruvic acid → Krebs cycle (mitochondrion matrix, CO₂ released, energised H atoms) → oxidative phosphorylation (cristae, about 36 ATP) → H combines with O₂ to form H₂O; arrows and annotations. Explanation (2): oxygen collects the depleted hydrogen at the end of the chain to form water (1); without oxygen the hydrogen cannot be removed, so the Krebs cycle and oxidative phosphorylation stop and only the 2 ATP of glycolysis are made (1).
- Q27 (4): Any two, each explained (2 each): anaerobic respiration releases only about 2 ATP per glucose instead of about 38, so the muscles quickly run short of energy or use up glucose stores fast; lactic acid builds up in the muscles, which is harmful and causes fatigue; the lactic acid must be broken down with oxygen afterwards, so the animal must spend time at the surface recovering (an oxygen debt) before it can dive again.
- Q28 (4): A cycle: photosynthesis takes in carbon dioxide and water and gives out glucose and oxygen (1); respiration takes in glucose and oxygen and gives out carbon dioxide and water (1); light energy enters at photosynthesis (1); energy (ATP) is released in respiration for life processes, and lost as heat (1).
Investigation 4 — the compensation depth
- Q29 (2): Respiration only — no light, so no photosynthesis (1). The plankton and bacteria in the bottle use oxygen to respire, so the oxygen falls (1).
- Q30 (3): 0 m: 5.2 · 5 m: 4.0 · 10 m: 2.6 · 15 m: 1.5 · 20 m: 0.7 · 30 m: 0.2 mg/L per 24 h (3 for all six; 2 for four or five; 1 for two or three).
- Q31 (5): Depth on the vertical axis, increasing downwards (1); oxygen change on the horizontal axis with zero marked (1); both lines plotted accurately (2); a key (1).
- Q32 (3): The light-bottle line crosses zero at about 19 m (accept 18–20 m) (1). About 1 % of surface light reaches it (between 2.4 % at 15 m and 0.7 % at 20 m) (1) — matching CAPS's "approximately 1 % of surface light" (1).
- Q33 (2): Below the compensation depth the seaweed uses more food and oxygen in respiration over 24 hours than it makes in photosynthesis (1), so it runs down its stores and cannot grow or survive (1).
- Q34 (3): Secchi depth ≈ 19 ÷ 2.7 ≈ 7 m (1). After a flood the water would be muddier, light would be attenuated faster (1), so the compensation depth would become shallower (1).
- Q35 (5): Euphotic zone from the surface to the compensation depth, about 150–200 m in clear open ocean (1); compensation depth marked at its base, about 1 % of surface light (1); disphotic zone below it, to about 1 000 m (1); aphotic zone below 1 000 m, no light (1); photic shown as the lit layer — either the euphotic zone alone (booklet) or euphotic plus disphotic (accept either if labelled consistently) (1).
Investigation 5 — life without sunlight
- Q36 (5): Energy source: sunlight / chemical energy from oxidising hydrogen sulphide (1). Raw materials: CO₂ + H₂O / CO₂ + H₂S + O₂ (1). Products: glucose + oxygen / carbohydrate + sulphate (1). Organisms: plants, seaweeds, phytoplankton, cyanobacteria / bacteria and archaea (1). Where: the euphotic zone / hydrothermal vents, sea-floor sediments and the crust (1).
- Q37 (3): Any three, one mark each: hyperthermophiles or thermophiles — heat; piezophiles (barophiles) — pressure; halophiles — salt; acidophiles — acid; psychrophiles — cold.
- Q38 (3): Chemosynthetic bacteria living inside its body make its food (1). The red plume's haemoglobin collects oxygen and hydrogen sulphide from the water (1) and carries them to the bacteria, which need both to make carbohydrates (1).
- Q39 (3): Left: C 1, O 4, H 2, S 1. Right: C 1, O 5, H 2, S 1 — the oxygen does not balance (1). With H₂O added on the left: C 1, O 5, H 4, S 1 (1). With H₂SO₄ on the right: C 1, O 5, H 4, S 1 — balanced: CO₂ + H₂S + O₂ + H₂O → CH₂O + H₂SO₄ (1).
- Q40 (2): Before the 1990s chemosynthesis was known, but thought to happen only in a few special places such as vents (1). In the 1990s drilling showed living microbes hundreds of metres down in sea-floor sediments and crust all over the ocean, so chemosynthesis was found to be widespread and significant (1).
- Q41 (2): Most vents are on mid-ocean ridges (and at other spreading centres), not trenches (1). There the plates move apart, magma lies close below the sea floor, and seawater seeps into the cracks, is heated and comes back out loaded with dissolved minerals and hydrogen sulphide (1).
- Q42 (2): On the abyssal plain the only food is the little that sinks from the sunlit surface (1); at a vent, chemosynthetic bacteria produce food on the spot from the chemicals in the vent water, so a whole food chain can be supported (1).
- Q43 (6): (a) photic or euphotic zone · (b) anaerobic · (c) extremophiles (3). (d) Chemosynthesis — a process in which certain bacteria use the energy in locally abundant compounds to make energy-rich compounds for their own use and storage (1). (e) Compensation depth — the depth at which the CO₂ used and O₂ produced by a photosynthetic organism by day equals the CO₂ produced and O₂ used at night (1). (f) Glycolysis — the breakdown of a glucose molecule, releasing two ATP and energised hydrogen atoms, and passing the residue (pyruvic acid) to a mitochondrion (1).
Marking note. CAPS allows experiments or data for every photosynthesis and respiration investigation; this sheet gives both, and marks only the reasoning, so a learner who used the supplied panels loses nothing. Q12 is the hardest question: the levelling-off is a limiting factor, and the learner should name what might be limiting it. Q39–Q41 check CAPS and the booklet against the evidence — the chemosynthesis equation as printed does not balance, the "early 1990s" claim needs card 5 to make sense, and vents are on ridges, not in trenches.