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Spec Mapping: This lesson is mapped to OCR H420 Module 2.1.5 — Biological membranes (refer to the official OCR H420 specification document for exact wording). It develops osmosis as the movement of water down a water potential gradient, the formal water-potential equation Ψ=Ψs+Ψp, and the responses of animal and plant cells to changes in external water potential.
Water is the most abundant molecule in living cells, and the movement of water across membranes is precisely controlled. In A-Level biology this movement is described using the formal language of water potential (Ψ). This lesson develops the OCR H420 Module 2.1.5 content on osmosis as the movement of water down a water potential gradient.
Key Definition — Osmosis: The net movement of water molecules from a region of higher water potential to a region of lower water potential, across a partially permeable membrane.
Osmosis is a special case of diffusion — but because water is such a small polar molecule, and membranes contain aquaporins, it has its own distinct vocabulary.
Three features define osmosis:
Water movement in osmosis is a result of random thermal motion — no ATP is used. It is a passive process.
In earlier years of secondary school you learned osmosis in terms of "concentrated" and "dilute" solutions. At A-Level we use water potential (symbol ψ, the Greek letter psi), measured in kilopascals (kPa). This is a more rigorous approach that accounts for both dissolved solutes and physical pressure.
Key Definition — Water Potential: The potential energy of water molecules in a solution compared with pure water at the same temperature and atmospheric pressure. Symbol ψ, units kPa.
Water always moves from higher (less negative) ψ to lower (more negative) ψ.
Exam Tip: When comparing, always say "higher (less negative) water potential" and "lower (more negative) water potential" — not "higher in number".
Water potential is the sum of two components:
ψ = ψ_s + ψ_p
Animal cells have no cell wall, so ψ_p ≈ 0 and water potential is driven almost entirely by solute content.
Plant cells have a strong cellulose cell wall. As water enters, the cell contents push against the wall, creating pressure potential (ψ_p). Pressure potential contributes to turgor, essential for plant support.
Animal cell membranes cannot withstand much osmotic stress. If placed in solutions of different water potential, red blood cells (erythrocytes) behave as follows:
| Solution type | Water potential | Net water movement | Result |
|---|---|---|---|
| Hypotonic (lower solute, higher ψ) | Higher ψ outside | Water moves into cell | Cell swells and bursts — haemolysis |
| Isotonic (same solute, same ψ) | Equal ψ | No net movement | Cell unchanged |
| Hypertonic (higher solute, lower ψ) | Lower ψ outside | Water moves out of cell | Cell shrinks — crenation |
graph TD
A[Red Blood Cell] --> B["Hypotonic solution<br/>psi outside higher<br/>water enters<br/>HAEMOLYSIS"]
A --> C["Isotonic solution<br/>psi equal<br/>no change"]
A --> D["Hypertonic solution<br/>psi outside lower<br/>water leaves<br/>CRENATION"]
Haemolysis is why intravenous fluids must be isotonic (0.9% saline, "physiological saline"). Pure water would cause red blood cells to burst within seconds.
Crenation gives the cell a wrinkled, shrivelled appearance because the cytoplasm pulls the membrane inward.
Plant cells behave differently because of the cell wall. Four key terms apply:
In a solution with higher water potential than the cell (e.g. pure water), water enters the cell by osmosis. The vacuole expands and the cytoplasm pushes against the cell wall. The cell becomes turgid — rigid and firm. The cell wall prevents bursting because it is strong and slightly elastic. Turgor pressure is essential for plant support, especially in herbaceous plants.
If water leaves until there is no net pressure on the wall, the cell becomes flaccid — limp but not yet damaged.
If the cell continues to lose water (e.g. in a strongly hypertonic solution), the cytoplasm shrinks away from the cell wall as the vacuole contracts. The point at which the plasma membrane just begins to pull away from the wall is called incipient plasmolysis; when the cytoplasm is entirely pulled away it is fully plasmolysed. The cell wall does not collapse — the gap between wall and membrane fills with the external solution.
Plasmolysis is usually reversible if the cell is returned promptly to water; prolonged plasmolysis damages the cell.
Wilting is the macroscopic drooping of a whole plant when large numbers of cells become flaccid. It does not necessarily involve plasmolysis — it can occur whenever water loss exceeds uptake.
| Plant cell state | Condition | Appearance |
|---|---|---|
| Turgid | Higher ψ outside; water in | Firm, wall under tension |
| Flaccid | ψ equal; no net water | Limp; wall not pushed |
| Incipient plasmolysis | Lower ψ outside | Membrane starts to pull away |
| Plasmolysed | Lower ψ outside; water out | Cytoplasm pulls away from wall |
A standard practical investigates the water potential of potato (or similar) tissue by placing chips in solutions of different known sucrose molarities and finding the one in which no mass change occurs.
Plot % change in mass (y-axis) against sucrose concentration (x-axis). The line crosses zero at the sucrose concentration whose water potential matches that of the potato tissue. Use a reference table to convert this sucrose concentration to a water potential in kPa.
Positive % change = water entered (sucrose solution had higher ψ than the tissue). Negative % change = water left (sucrose solution had lower ψ than the tissue).
Model answer for (3): "The cell (−500 kPa) has a lower (more negative) water potential than the solution (−200 kPa). Water therefore moves from the solution into the cell by osmosis across the partially permeable plasma membrane. The cell will gain water, the vacuole will expand, and the cytoplasm will press against the cell wall, making the cell turgid."
The OCR H420 specification expects mastery of the water-potential equation and its sign conventions:
Ψ=Ψs+Ψp
where:
For pure water at atmospheric pressure: Ψs=0, Ψp=0, so Ψ=0. This is the reference state — every aqueous solution has Ψ<0.
A plant cell with Ψs=−800 kPa and Ψp=+300 kPa has:
Ψ=−800+300=−500 kPa
Placed in a bathing solution of Ψ=−200 kPa, water moves from the solution into the cell (from higher Ψ, −200, to lower Ψ, −500). As the cell takes up water, Ψp rises and Ψs becomes slightly less negative (dilution) until Ψcell=Ψsolution=−200 kPa.
A-Level depth: Note that Ψ rises (becomes less negative) as the cell takes up water — both because Ψs dilutes and because Ψp rises. The reverse is true if a cell loses water: Ψs becomes more negative and Ψp falls (eventually to zero at incipient plasmolysis, beyond which Ψp=0 and further loss is driven by Ψs alone).
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