water potential of potato tuber cells

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DAVOR ZIBAR

WATER POTENTIAL OF POTATO

TUBER CELLS

INTRODUCTION:

AIM:

To find the water potential of potato tuber cells.

HYPOTHESIS:

When cells are put in a solution with a different water potential than inside of them, cells will gain or loose water. If concentration of solution is the same, there will be no change in mass.

THEORETICAL BACKGROUND:

If a sample of tissues immersed in solution of varying water potential (concentration of water molecules), the cells will loose or gain water by osmosis. If the cell is put into solution of higher water potential (hypotonic solution), water will go inside the cell. As the pressure potential rises inside the cell it becomes turgid. In the plant cells turgidity is rising up the moment when cell can’t take more water because of cell wall. Animal cells don’t have cell wall so water is constantly going inside the cell until it lyses.

If the cell is put into solution of lower water potential (hypertonic solution) the water will go out of cell and cell will be plasmolysed. In both ways cell will gain or loose mass.

 


APPARATUS AND MATERIALS:

  • Cork borer
  • Scalpel
  • Syringe
  • Digital balance
  • Filter paper
  • Forceps
  • Blue ink

EXPERIMENT 1:

METHOD:

  1. In 6 test tubes labelled: distilled water, 0.1, 0.2, 0.3, 0.4, 0.5 mol dm3; place10 ml of appropriate solution.
  2. Using a cork borer and scalpel cut 6 cylinders of 10mm diameter and 1,2 cm length. All cylinders should be cut into six discs of approximately equal thickness (2mm). When they are cut place each group on a separate filter paper.
  3. Weight each group of discs accurately with filter paper and then only weight filter paper. Calculate mass of potato.
  4. Put each group of potato discs in one of the 6 test tubes and watch out that all discs are immersed in a solution. Stopper the test tubes firmly and leave them still for 24 hours.
  5. After 24 hours remove the discs from solution and dry them with filter paper.  Do the same process with all discs. Repeat weighting as in step 3.
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EXPERIMENT 2:

METHOD

  1. Put 3 ml of 0.1, 0.15, 0.2, 0.25, 0.3, 0.5, 1 mol dm3 sucrose  in different test tubes and label them.
  2. Make potato discs as in experiment 1.
  3. Put the discs in the solutions and leave them for 30 min.
  4. Put 2 ml of same solutions again in test tubes and put 3 drops of blue ink in them and label them.
  5. After 30 min remove the potato discs from solutions.
  6. With a syringe take some coloured solution (e.g. 0.1 mol dm3) and carefully put one drop of it in ...

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