Photosynthesis and Respiration: Experiment
Photosynthesis and Respiration: Experiment
Photosynthesis and Respiration: Experiment
Cellular respiration refers to the process of converting the chemical energy of organic molecules
into a form immediately usable by organisms. Glucose may be oxidized completely if sufficient
oxygen is available by the following equation:
C6H12O6 + 6 O2 → 6 H2O + 6 CO2 + energy
All organisms, including plants and animals, oxidize glucose for energy. Often, this energy is
used to convert ADP and phosphate into ATP.
OBJECTIVES
In this experiment, you will
• use an O2 Gas Sensor to measure the amount of oxygen gas consumed or produced by a
plant during respiration and photosynthesis.
• use a CO2 Gas Sensor to measure the amount of carbon dioxide consumed or produced by
a plant during respiration and photosynthesis.
• determine the rate of respiration and photosynthesis of a plant.
Figure 1
MATERIALS
LabPro or CBL 2 interface 250-mL respiration chamber
TI Graphing Calculator plant leaves
DataMate program 500-mL tissue culture flask
Vernier O2 Gas Sensor lamp
Vernier CO2 Gas Sensor aluminum foil
CO2–O2 Tee forceps
PROCEDURE
1. Plug the O2 Gas Sensor into Channel 1 and the CO2 Gas Sensor into Channel 2 of the
LabPro or CBL 2 interface. Use the link cable to connect the TI Graphing Calculator to the
interface. Firmly press in the cable ends.
2. Turn on the calculator and start the DATAMATE program. Press CLEAR to reset the program.
3. Set up the calculator and interface for an O2 Gas Sensor and CO2 Gas Sensor.
a. Select SETUP from the main screen.
b. If the calculator displays an O2 Gas Sensor in CH 1 and a CO2 Gas Sensor in CH2, proceed
directly to Step 4. If it does not, continue with this step to set up your sensors manually.
c. Press ENTER to select CH 1.
d. Select OXYGEN GAS from the SELECT SENSOR menu.
e. Select parts per thousand (PPT) as the unit.
f. Press once, then press ENTER to select CH2.
g. Select CO2 GAS from the SELECT SENSOR menu.
h. Select parts per thousand (PPT) as the unit.
4. Set up the data-collection mode.
a. To select MODE, press (the up arrow key) twice and press ENTER .
b. Select TIME GRAPH from the SELECT MODE menu.
c. Select CHANGE TIME SETTINGS from the TIME GRAPH SETTINGS menu.
d. Enter “15” as the time between samples in seconds.
e. Enter “40” as the number of samples (data will be collected for 10 minutes).
f. Select OK twice to return to the main screen.
5. Obtain several leaves from the resource table and blot them dry, if damp, between two pieces
of paper towel.
6. Place the leaves into the respiration chamber, using forceps if necessary. Wrap the
respiration chamber in aluminum foil so that no light reaches the leaves.
7. Insert the CO2–O2 Tee into the neck of the respiration chamber. Place the O2 Gas Sensor into
the CO2–O2 Tee as shown in Figure 1. Insert the sensor snugly into the Tee. The O2 Gas
Sensor should remain vertical throughout the experiment. Place the CO2 Gas Sensor into the
Tee directly across from the respiration chamber as shown in Figure 1. Gently twist the
stopper on the shaft of the CO2 Gas Sensor into the chamber opening. Do not twist the shaft
of the CO2 Gas Sensor or you may damage it.
8. Wait two minutes, then select START to begin data collection. Data will be collected for 10
minutes.
9. When data collection has finished, remove the aluminum foil from around the respiration
chamber.
10. Fill the tissue culture flask with water and place it between the lamp and the respiration
chamber. The flask will act as a heat shield to protect the plant leaves.
11. Turn the lamp on. Place the lamp as close to the leaves as reasonable. Do not let the lamp
touch the tissue culture flask.
12. Press ENTER to view the graph of O2 GAS VS. TIME. Sketch a copy of your graph in the Graph
section below. When finished, press ENTER to return to the graph menu.
Press once, then press ENTER to view the graph of CO2 GAS VS. TIME. Sketch a copy of
your graph in the Graph section below. When finished, press ENTER to return to the graph
menu. Select MAIN SCREEN from the graph menu.
13. Perform a linear regression to calculate the rate of respiration/photosynthesis.
a. Select ANALYZE from the main screen.
b. Select CURVE FIT from the ANALYZE OPTIONS menu.
c. Select LINEAR (CH 1 VS TIME) from the CURVE FIT menu.
d. The linear-regression statistics for these two lists are displayed for the equation in the
form:
Y=A∗X+B
e. Enter the value of the slope, A, as the rate of respiration/photosynthesis in Table 1.
f. Press ENTER to view a graph of the data and the regression line.
g. Press ENTER to return to the ANALYZE menu.
h. Repeat Steps 13b – 13g to calculate the respiration/photosynthesis rate using the data
from the CO2 Gas Sensor (CH 2 VS TIME).
i. Select RETURN TO MAIN SCREEN from the ANALYZE menu.
14. Repeat Steps 8 – 13 to collect data with the plant exposed to light.
15. Remove the plant leaves from the respiration chamber, using forceps if necessary. Clean and
dry the respiration chamber.
DATA
Table 1
In the light
GRAPHS
Darkness
QUESTIONS
1. Were either of the rate values for CO2 a positive number? If so, what is the biological
significance of this?
2. Were either of the rate values for O2 a negative number? If so, what is the biological
significance of this?
3. Do you have evidence that cellular respiration occurred in leaves? Explain.
4. Do you have evidence that photosynthesis occurred in leaves? Explain.
5. List five factors that might influence the rate of oxygen production or consumption in leaves.
Explain how you think each will affect the rate?
EXTENSIONS
1. Design and perform an experiment to test one of the factors that might influence the rate of
oxygen production or consumption in Question 5.
2. Compare the rates of photosynthesis and respiration among various types of plants.
2. A fluorescent ring lamp works very well since it bathes the plant in light from all sides and it
gives off very little heat. When using a ring lamp as shown below, it is not necessary to use a
heat shield.
3. If tissue culture flasks are not available, a beaker or flask of water will also work. The tissue
culture flask is very thin, however, and will allow leaves to receive much more light from the
same lamp.
4. To extend the life of the O2 Gas Sensor, always store the sensor upright in the box in which
it was shipped.
5. The waiting time before taking data may need to be adjusted depending on the rate of
diffusion of the oxygen gas and the carbon dioxide gas. Monitor the gas concentrations and
start collecting data when the levels of gas begin to move in the correct direction.
6. The stopper included with the CO2 Gas Sensor is slit to allow easy application and removal
from the probe. When students are placing the probe in the CO2–O2 Tee, they should gently
twist the stopper into the adapter opening. Warn the students not to twist the probe shaft or
they may damage the sensing unit.
7. To conserve battery power, we suggest that AC Adapters be used to power the interfaces
rather than batteries when working with the CO2 Gas Sensor. An AC Adapter is shipped
with each LabPro interface at the time of purchase. If you are using the CBL 2, you can
purchase a Vernier AC Adapter for $10 (order code–IPS).
SAMPLE RESULTS
Table 1
GRAPHS
Darkness
ANSWERS TO QUESTIONS
1. The CO2 rate value for leaves in the dark was a positive number. The biological significance
of this is that CO2 is produced during respiration. This causes the concentration of CO2 to
increase, as sugar is oxidized and broken into CO2, water, and energy.
2. The O2 rate value for leaves in the dark was a negative number. The biological significance
of this is that O2 is consumed during cellular respiration. This causes the concentration of O2
to decrease as glucose is oxidized for energy.
3. Yes, cellular respiration occurred in leaves, since O2 decreased when leaves were in the dark
and photosynthesis was not possible.
4. Yes, photosynthesis occurred in leaves, since O2 increased when leaves were exposed to
light.