Photosynthesis Lab

Photosynthesis in Leaf Disk
Name: ______________________________________________________________________ Date: __________________________________________ Section: __________
rocess in which plants convert light energy (sunlight) into
usable chemical energy
Photosynthesis in Leaf Disks
otosynthesis involves two simultaneous processes: the light dependent reactions
Introduction:
ndent reactions (Calvin Cycle). In the light dependent reactions, light energy is
Photosynthesis is a process in which plants convert light energy into the usable chemical energy of glucose. Photosynthesis
ted to high
energy
and NADPH
molecules.
In the light independent
reactions
involves
two ATP
simultaneous
processes:
the light-dependent
reactions and
the light-independent reactions (Calvin Cycle). In the
olecules
are used to reduce
CO2 light
and eventually
form carbohydrates
as glucose.
light-dependent
reactions,
energy is captured
and convertedsuch
to high
energy ATP and NADPH molecules. In the lightindependent reactions these high-energy molecules are used to reduce CO2 and eventually form glucose.
balanced): CO2 + H2O + light energy Overall
Glucose
+ O2 6CO2 + 6H2O + light energy  C6H12O6 + 6O2
reaction:
Photosynthesis
occurs
in the chloroplast
the filled
plant with
cell. Most
of thebicarbonate
chloroplasts in a plant are located in the cells of the
he spaces
in the spongy
mesophyll
of leaf disksofare
a sodium
mesophyll, the green tissue in the center of the leaf. The cells of the mesophyll have air spaces around them used for gas exchange.
es themYou
to will
sinkuse
in the
solution. The leaf disks are then exposed to light and
these characteristics of leaf structure and function to measure and compare the rates of photosynthesis in different
de as the
cells
undergo
photosynthesis.
leaves.
tivity you should be able to:
reactants and products of photosynthesis and the
ctants from the environment.
elationship of photosynthesis to the observations
the experiment.
her variable that might affect photosynthesis and
Mesophyll Tissue in Plant Leaf
Spongy Mesophyll
periment that uses leaf disks to test your ideas.
As oxygen gas is a product of photosynthesis, the rate of photosynthesis in a leaf can be determined by measuring the amount of
heses about
of environmental
on the
of photosynthesis.
oxygenthe
theeffects
leaf produces
in a certain variables
period of time.
In rate
this investigation,
you will measure oxygen production indirectly. You will
suspend leaf disks in a solution and apply a vacuum. The air spaces inside each leaf disk will become filled with liquid and the leaf
disks will sink downward. You will then measure how quickly the leaf disks float upward. When the light-dependent reactions
produce oxygen, liquid is forced out of the air spaces and the leaf disks become more buoyant. In general, the more quickly the
leaf disks
become
buoyant enough to float, the faster they are photosynthesizing.
bicarbonate
(baking
soda)
ap
Materials:
• 1.5 g sodium bicarbonate (baking soda)
e (20-65• Plastic
mL)—no
needle!
syringe
(10-65 mL)—no needle!
•
Plastic
spoon
or
or straw (for stirring) straw (for stirring)
• Leaf material
• Hole punch
• 1 beaker
rynthesis
or plastic
cup
in
Leafwith
Discs
• Timer
or clock
second hand
ers or plastic
• Lightcups
source
kewith
secondgloves.
hand
without
Procedure:
Leaf Disks Lesson
Wear Goggles!
1.
Using a one-hole punch, punch 10 leaf disks from young actively growing leaves.
2.
Prepare a 0.2% solution of sodium bicarbonate (NaHCO3) and water in the beaker by adding approximately 1.5 g sodium
bicarbonate to 300 mL of water. Stir until dissolved.
from young actively growing leaves.
onate (NaHCO3) and water in the large beaker or clear
3. Remove the plunger from a large clean syringe (no needle). Place 10 leaf disks into the body of the syringe. Be sure the
odium bicarbonate
to near
300the
mLtipof
leaf disks are
of water.
the syringe as you reinsert the plunger so as not to damage the disks.
dd about 2 drops of dish detergent to the
o bubbles afterward.
ringe (no needle). Place 20 leaf disks into
ks are near the tip of the syringe as you redisks. (A)
of 0.2% sodium bicarbonate solution and
ks should be floating at this time. If your
third full.
e air by depressing the plunger carefully.
4.
A
Insert the tip of the syringe into a beaker of 0.2% sodium bicarbonate solution and draw the liquid into the syringe until it
is about one third full.
finger of your left hand and hold
artial vacuum within the syringe. If
nge into a beaker of 0.2% sodium bicarbonate solution and
ringe. The leaf disks should be floating at this time. If your
A
ml fill it about one third full.
5. Hold the syringe tip upward and expel the air by depressing the plunger carefully. Stop before solution comes out the tip.
6. Seal
the by
tip depressing
of the syringe
using
the index
finger of your left hand and hold tightly. Pull back on the plunger creating a
ward and expel
the air
the
plunger
carefully.
s out the tip. partial vacuum within the syringe. If you have a good seal it should be hard to pull on the plunger and you should see
bubbles coming from the edge of the leaf disks. Hold for a count of ten and then with your finger still on the tip of the
syringe,
firmly
pushleft
up hand
on theand
plunger.
e using the index
finger
of your
hold
unger creating a partial vacuum within the syringe. If
ould be hard to pull on the plunger and you should see
edge of the leaf disks. Hold for a count of ten. (B)
your index finger and the plunger. Some of the leaf
Tap the side of the tube or shake gently to break any
e disks.
til all the disks sink. Do not overdo these steps!! You
e disks sink to the bottom. Don't repeat "just to be
B
mage the cells of the leaves.
7. Release your index finger and the plunger. Some of the leaf disks should start to sink. Tap the side of the tube or shake
gently
to break
any bubbles
on the edges
of theinto
disks.
m the syringe and
pour
the solution
containing
the disks
2 plastic cups or
8. solution
Repeat steps
6 and
untilbeakers.
all the disks
sink.should
Do not be
overdo
theseper
steps! You have been successful if the disks sink to the
inder of your
equally
to7both
There
10 disks
bottom.
Don't
repeat
"just
to
be
sure"
as
it
is
possible
to
damage
the
cells of the leaves.
o the bottom.
9. Remove the plunger from the syringe and pour the solution containing the disks into the beaker. Make sure the leaf disks
ers to block light
from
the
leaf disks. Place the second beaker under a light
sink
to the
bottom.
inches below
the
light.
The
lights
are
bestsource,
held inapproximately
a clamp on a 6ring
stand.
10. Place the beaker
under
a light
inches
below the light. Begin timing the experiment as soon as the
nt as soon as the
light
is
turned
on.
Record
your
observations
on
page
4.
light is turned on.
11. Each
a leaf disk floatsproceeds.
to the surface
of the beaker
record
the time in your data table. When 5 of the 10 leaf disks have
ing to the leaf
diskstime
as photosynthesis
Continue
to record
your
reached the top of the beaker the experiment is complete.
n page 4. After each time check, tap the side of the beaker to make sure the
12. Discard the leaf disks in the trash and rinse out your beaker and syringe in the sink.
13. Repeat steps 1-12 but this time turn off the light and cover the beaker with paper to block light from reaching the leaf
disks.
Data: Time for Leaf Disks to Rise
Number of
Light
Disks Risen
(minutes)
Dark
(minutes)
1
2
3
4
5
(After 15 minutes consider the experiment over and that no more disks will rise)
Analysis:
1.
Explain the changes that occurred within the leaf tissue that allowed the leaf disks to rise to the surface.
2.
In which environment did leaf disks float faster – light or dark? How would you explain this result?