Preparation of Tissue: Use a cork borer to cut cylinders of plant tissue (e.g., potato) to ensure a uniform diameter and surface-area-to-volume ratio. Trim the cylinders to the same length using a scalpel and a ruler to maintain consistency across all samples.
Initial Measurements: Carefully dry each cylinder with a paper towel to remove excess surface moisture and record the initial mass using a high-precision digital balance. It is vital to label each sample or container to track which cylinder corresponds to which concentration.
Incubation: Place the cylinders into boiling tubes containing equal volumes of different solute concentrations (e.g., to mol/dm of sucrose). Leave the samples for a set period, typically at least 30 minutes, to allow sufficient time for osmosis to occur.
Final Measurements: Remove the cylinders, gently blot them dry to remove surface liquid that is not part of the tissue mass, and re-weigh them. Calculate the percentage change in mass for each sample to account for variations in the starting mass.
Percentage Change Formula: Because it is nearly impossible to cut every cylinder to the exact same starting mass, the relative change must be calculated. The formula used is:
Graphing Results: Plot a scatter graph with the independent variable (solute concentration) on the x-axis and the dependent variable (percentage change in mass) on the y-axis. Draw a line of best fit, which typically shows a negative correlation as concentration increases.
Determining Concentration: Identify the point where the line of best fit crosses the x-axis (where y = 0). This x-intercept represents the concentration of the solution that is isotonic to the plant tissue, revealing its internal solute concentration.
| Condition | External Concentration | Water Movement | Mass Change |
|---|---|---|---|
| Hypotonic | Lower than cell | Into the cell | Increase |
| Isotonic | Equal to cell | No net movement | No change |
| Hypertonic | Higher than cell | Out of the cell | Decrease |
Variable Identification: Always be ready to identify the independent variable (concentration), the dependent variable (percentage change in mass), and control variables (temperature, volume of solution, time, and surface area of tissue).
The Importance of Blotting: Examiners frequently ask why cylinders are blotted dry. The answer is to remove surface water that would artificially increase the final mass reading, leading to an inaccurate calculation of water gained or lost by the cells.
Interpreting the Intercept: If a graph shows the line crossing the x-axis at mol/dm, the student must conclude that the internal concentration of the potato is mol/dm. If the line never crosses the axis, the range of concentrations used was insufficient.
Anomalous Results: If one data point deviates significantly from the line of best fit, it should be identified as an anomaly. Common causes include improper drying of the tissue or errors in weighing.