Effect of Sodium Hydrogen Carbonate Concentration on the Rate of Photosynthesis

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Effect of Sodium Hydrogen Carbonate Concentration on the Rate of Photosynthesis

Method

           Firstly I will attach a capillary tube to the nozzle of end of a 20cm3 syringe by means of rubber tubing. I shall push the end of the capillary tube to the tip of the nozzle of the syringe, ensuring that the rubber tubing provides an airtight seal. Using razor blade I will cut three sections of the Elodea stem and after removing the plunger I shall place the cuttings into the nozzle. I will also make certain that the cut ends of the Elodea are facing upwards away from the nozzle end. After this is prepared I can then place the different concentrations of sodium hydrogen carbonate solutions into the barrel. The solutions that are to be used are 0.0100, 0.0125, 0.0166, 0.0250, 0.0500, 0.1000 mol dm-3. To do this I will place my finger over the open end of the capillary tube. Then slowly I will pour one of the concentrations of sodium hydrogen carbonate into the barrel. I will add the solution until the Elodea is covered to the 20cm3 marking. I will then invert the apparatus and slowly push the plunger to push out all the air bubbles from the capillary tube and also makes certain no air is trapped between the plunger and solution in the barrel. Then I will gradually pull back the plunger drawing up a meniscus to a point near the top of the capillary tube. I will then using a clamp and boss, clamp the capillary tube around the rubber tube and not over the syringe or the capillary tube. This is done so none of the Elodea is covered, so light can reach it and also if over the capillary tube is covered it is difficult to see if there is any movement of the meniscus. I will mark the initial point of the meniscus with a marker. A lamp will be placed exactly 8cms from the Elodea and parallel to it so the whole of the Elodea is able to receive enough light. The laboratory lights will be switched off and the blinds closed so no other source of light except the one from the lamp interferes with the experiment. The temperature will also be recorded using a thermometer before the start of each new concentration. At every three minute intervals I will record how far the meniscus has moved and note this in a results table. This will then be displaced in a graph of rate of photosynthesis against the concentration of sodium hydrogen carbonate.

Results

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Analysis and Conclusion

           The resulting tabular and graphical evidence show some good results. From the data collected and collated I plotted the points on a graph of the rate of photosynthesis (mm) against the concentration of sodium hydrogen carbonate (mol dm-3). This gave me one graph from the data collected. The graph shows the whole range of sodium hydrogen carbonate concentrations used and the average distance the meniscus moved in millimetres during nine minutes, for each concentration. The graph shows the trend that as the concentration increases, the average distance the meniscus ...

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