Explain how the internal structure of a leaf is adapted for photosynthesis and describe the basic processes, products and factors involved in photosynthesis as required by the Cambridge IGCSE (0610) syllabus.
1. Definition & Equations
Definition: Photosynthesis is the process by which green plants use light energy to convert carbon dioxide (CO₂) and water (H₂O) into carbohydrate (glucose) and oxygen (O₂).
Word equation: CO₂ + H₂O → glucose + O₂
Balanced chemical equation: 6 CO₂ + 6 H₂O + light energy → C₆H₁₂O₆ + 6 O₂
2. Role of Chlorophyll & Other Pigments
Chlorophyll a & b: Located in thylakoid membranes; absorb mainly blue (≈ 430 nm) and red (≈ 660 nm) light, reflect green.
Carotenoids (β‑carotene, lutein, etc.): Extend the range of usable light (blue‑green) and protect chlorophyll from photodamage.
Absorbed photons raise electrons to a higher energy level, initiating the light‑dependent reactions that produce ATP and NADPH.
3. Main Products of Photosynthesis & Their Uses
Product
Primary Use in the Plant
Glucose
Immediate energy source for cellular respiration.
Sucrose
Transport form of carbohydrate; moves through the phloem to growing tissues.
Starch
Long‑term storage in roots, tubers, seeds and some leaves.
Cellulose
Structural component of cell walls.
Nectar
Produced in specialised glands to attract pollinators.
4. Supporting Nutrients (Core Requirements)
Nutrient
Why It Is Needed for Photosynthesis
Nitrogen (NO₃⁻, NH₄⁺)
Component of amino acids, proteins (e.g., Rubisco) and chlorophyll.
Magnesium (Mg²⁺)
Central atom of the chlorophyll molecule; essential for light capture.
Phosphorus (P)
Part of ATP, NADPH and nucleic acids.
Potassium (K⁺)
Regulates stomatal opening and activates many enzymes.
5. Leaf Structure – Adaptations for Efficient Photosynthesis
5.1 Epidermis & Cuticle
Upper (adaxial) and lower (abaxial) epidermal layers protect the leaf.
Cells are thin and transparent, allowing maximum light penetration.
The cuticle is thin enough not to impede light yet waxy enough to minimise water loss.
5.2 Stomata
Pores surrounded by guard cells that open/close to regulate CO₂ uptake and water‑vapour loss.
Most abundant on the lower epidermis to avoid direct sunlight and reduce transpiration.
Guard‑cell turgor is controlled by K⁺ ions, linking water status to gas exchange.
5.3 Mesophyll
Palisade mesophyll: Columnar cells tightly packed beneath the upper epidermis; high chloroplast density and elongated shape maximise light capture – the main site of the light‑dependent reactions.
Spongy mesophyll: Loosely arranged cells with large intercellular air spaces; facilitate rapid diffusion of CO₂ to, and O₂ from, photosynthetic cells – important for the Calvin cycle (light‑independent reactions).
5.4 Chloroplasts
Abundant in both mesophyll layers, especially palisade cells.
Thylakoid membranes are organised into stacks (grana) that increase surface area for light‑absorbing pigments and the electron‑transport chain.
The stroma contains the enzymes of the Calvin cycle.
5.5 Vascular Bundles (Veins)
Xylem: Transports water and mineral nutrients from the roots to the mesophyll – essential for the light‑dependent reactions.
Phloem: Carries the sugars (mainly sucrose) produced in the mesophyll to other parts of the plant.
Veins run close to the mesophyll to minimise diffusion distances for both water and photosynthates.
5.6 Leaf Shape, Thickness & Surface Area
A broad, thin lamina maximises light interception while keeping the diffusion path for gases short.
In most dicots the leaf is dorsiventral (different upper and lower sides) to optimise light capture and gas exchange.
6. Light‑Dependent Reactions (Supplementary)
Location: Thylakoid membranes of the chloroplasts.
Key steps:
Photolysis of water (H₂O) – light energy splits water, releasing O₂, electrons and H⁺ ions.
Photosystem II (PSII): Absorbs photons, excites electrons which pass to the plastoquinone pool.
Electron transport chain: Energy from electrons pumps H⁺ into the thylakoid lumen, creating a proton gradient.
ATP synthesis: H⁺ flow back through ATP synthase drives formation of ATP (photophosphorylation).
Photosystem I (PSI): Re‑excites electrons; final electron acceptor NADP⁺ is reduced to NADPH.
Outputs: O₂ (released to the atmosphere), ATP and NADPH (used in the Calvin cycle).
Pigment roles: Chlorophyll a is the primary electron donor; chlorophyll b and carotenoids broaden the range of usable wavelengths.
Carbon fixation: CO₂ combines with ribulose‑1,5‑bisphosphate (RuBP) – catalysed by Rubisco – to form two molecules of 3‑phosphoglycerate (3‑PGA).
Reduction: ATP and NADPH from the light‑dependent reactions convert 3‑PGA into glyceraldehyde‑3‑phosphate (G3P). One G3P leaves the cycle to form glucose and other carbohydrates.
Regeneration: The remaining G3P molecules are rearranged, using ATP, to regenerate RuBP, allowing the cycle to continue.
Overall outcome: For every 3 CO₂ fixed, one G3P is exported; six G3P molecules are needed to synthesise one molecule of glucose (C₆H₁₂O₆).
8. Limiting Factors (Core)
Factor
How It Limits the Rate of Photosynthesis
Light intensity
Insufficient photons reduce ATP & NADPH production; very high intensity can cause photoinhibition.
Carbon‑dioxide concentration
Low CO₂ limits the Calvin cycle; higher CO₂ can increase rate up to a saturation point.
Temperature
Enzyme activity (e.g., Rubisco) rises with temperature to an optimum; beyond that enzymes denature.
Water availability
Water stress triggers stomatal closure, reducing CO₂ entry and thus photosynthetic rate.
Photoinhibition: Excessive light (especially high‑energy blue light) damages the D1 protein of PSII, decreasing the efficiency of the light‑dependent reactions.
Wavelength effectiveness:
Blue (≈ 430 nm) and red (≈ 660 nm) photons are most efficiently absorbed by chlorophyll a and b.
Green light (≈ 550 nm) is largely reflected, contributing little to photosynthesis.
Carotenoids absorb in the blue‑green region, extending the usable spectrum and providing photoprotection.
Starch test (iodine colour change): Dark‑adapt leaves for 24 h, expose one leaf to strong light for 2 h while keeping another in darkness. Boil, de‑colourise with alcohol, add iodine. The light‑exposed leaf turns blue‑black (starch present), confirming the need for light.
Floating leaf‑disc assay (CO₂ effect): Punch uniform leaf discs, place them in sodium bicarbonate solution, and expose to different light intensities. Measure the time for discs to rise (oxygen production). Vary CO₂ by adding more NaHCO₃ to see the effect.
Temperature experiment: Use a water bath to keep leaf samples at 10 °C, 20 °C, 30 °C and 40 °C while measuring oxygen evolution with a gas‑collection apparatus.
Wavelength experiment (supplementary): Shine monochromatic light (blue, green, red) on identical leaf sections and compare the rate of oxygen evolution to illustrate wavelength effectiveness.
Cross‑section of a typical dicot leaf (from top to bottom): cuticle, upper epidermis, palisade mesophyll, spongy mesophyll with air spaces, lower epidermis with stomata, and a vascular bundle (xylem and phloem). Chloroplasts are shown within mesophyll cells, and thylakoid stacks (grana) are indicated inside the chloroplasts.
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