lab report: respiration
TRANSCRIPT
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CELL BIOLOGY LABORATORY REPORTSubject : Cell Biology LaboratoryLecturer : Dr.rer.nat. Maruli PandjaitanInstructor : Ms. Nani Pasaribu, M. Si; Ms. Sylvia Yusri, S. SiFaculty/Class : Life Science/LS 1 ADate of Experiment : 25 September 2013Date of Lab. Report : 9 October 2013Semester : 1Time of Experiment : 14-00 16.00 pm
Experiment:Cellular Respiration
Photosynthesis
NAME : Felicia Melissa, KristaniaHadhiwaluyo, Chita Sakina Putrianti,Jonathan Winarno,Nabila Putri
Group : 4
Campus BSD CityBumi Serpong DamaiTangerang 15321 Indonesia
Tel. +62 21 537 6221Fax. +62 21 537 6201
S W I S S G E R M N U N I V E R S I T Y
mailto:[email protected]:[email protected]://www.sgu.ac.id/http://www.sgu.ac.id/http://www.sgu.ac.id/mailto:[email protected] -
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I. Objectives
To examine the factors affecting respiration in plants, state of cell and carbon
dioxide concentration, and their effect to the rate of cellular respiration of mung
beans (Vigna radiate).
To examine the factors affecting the rate of photosynthesis and their effect,
particularly the light intensity.
II. Theoretical Background
Experiment 1: Cellular Respiration
Cellular respiration
Process of cellular respiration
Factors affecting cellular respiration and their effects
Respirometer
Mung beans (Vigna radiate)
Experiment 2: Photosynthesis
Photosynthesis
Process of photosynthesis
Factors affecting photosynthesis and their effects
III. Apparatus and Materials
Apparatus
o Experiment 1: Cellular Respiration
Bent pipes, 2
Rubber tubing,2, each was attached to a syringe and rubber stopper
Large test tubes, 4
Stopwatch
Hotplate
Beaker glass, 1
o Experiment 2: Photosynthesis
Leaves, 2 Water, 100 cm
3
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Stopwatch
Beaker glasses, 2
Materials
Mung beans (Vigna radiate), 16.22 g
Cotton, for each test tubes
KOH(s)(Potassium Hydroxide)
Phenol Red, powder
Distilled water, H2O
Vanillin (in a wax form)
DC Power Source
Light, 300 Watt
IV. Procedure
Experiment 1: Cellular Respiration
1. All materials and apparatus used for the first experiment was prepared
2. Preparation of the Mung beans (Vigna radiate)
1. 16.22 g was measured and divided evenly in such a way that those 4
test tubes would have the same amount of Mung beans
2.
A small amount of the Mung beans was filled evenly into two testtubes
3.
The Mung beans that were left was filled into one beaker, and half of
the beaker glass was filled by distilled water, H2O
4. The Mung beans were boiled in a hot water on the hotplate for 10
minutes
5. The water from the beaker was rinsed leaving the hot, boiled Mung
beans behind
6. The hot, boiled Mung beans were put evenly into the other 2 test
tubes
3. Each test tubes was labeled with Test Tube 1, 2, 3, and 4
4. Cotton was placed above the beans in each test tubes
5. KOH(s)(Potassium Hydroxide) flakes were into the first and second test
tubes, located directly above the cotton
6. For each test tubes one rubber tubing that each was attached to a syringe and
rubber stopper was attached
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7.
Bent pipette was also attached to each test tubes by inserted them into
another hole in the rubber stopper
8.
Some amount of the wax containing vanillin was rubbed on the surrounding
surface of the rubber stopper to ensure that the system was in a vacuum state
when the investigation process began
9. Some phenol red powder was mixed with small amount of distilled water,
H2O leaving a liquid in a form similar to a red paint
10.
Each bent pipette attached to each test tubes was put into contact with the red
paint-like solution
11.Syringe was pulled to suck in phenol red solution into the bent pipe
12.The initial location of the phenol red solution was indicated using a black
marker13.Using a stopwatch, the movement of the phenol red solution inside the bent
pipe for 10 minutes was observed and recorded in the data table as shown
below
Time
(minutes)
Tube 1
(with KOH
boiled Mung
Beans)
Tube 2
(without KOHnon-
boiled Mung Beans)
Tube 4
(without KOH
boiled Mung
Beans)
Tube 5
(with KOHnon-
boiled Mung
Beans)
0 0 0.5 0 0.5
10.85
(1 minute 30 seconds)
2
3
4
0.25
(4 minutes 28
seconds)
5
6
7
8
9
10
Experiment 2: Photosynthesis
1. Two glass beakers were prepared and filled with 100 cm3of Distilled water,
H2O
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2.
One leave sample was put into each glass beakers but make sure that the
leave sample did not sink into the distilled water
3.
The 300 watt lamp was connected to the DC power source
4. Arrange both glass beakers in such a way that one was located at 30 cm and
50 cm from the lamp.
5. With the help of a stopwatch the time of the formation of bubbles was
observed until it reaches time where formation of bubbles from each of the
leaves stopped, and the observation was recorded in the data table as shown
below
Table 2.1Beaker 1
Distance: 50 cm
1
st
bubble formation: 00:45 (45 seconds)Time (minutes) Number of bubbles
00:0001:45 2
01:4502:45 1
02:4503:45 0
03:4504:45 1
04:4505: 45 1
05:45
06:45 206:4507:45 2
07:4508:45 1
08:4509:45 2
09:4510:45 2
Table 2.2Beaker 2
Distance: 30 cm1
stbubble formation: 01:34 (1 minute 34 seconds)
Time (minutes) Number of bubbles
01:3402:34 2
02:3403:34 3
03:3404:34 3
04:3405:34 4
05:34
06:34 506:3407:34 7
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07:3408:34 8
08:3409:34 9
09:3410:34 14
10:3411:34 16
V. Data
Experiment 1: Cellular Respiration
o Mass of Mung beans : 16.22 g
Time
(minutes)
Tube 1
(with KOH
boiled Mung
Beans)
Tube 2
(without KOHnon-
boiled Mung Beans)
Tube 4
(without KOH
boiled Mung
Beans)
Tube 5
(with KOHnon-
boiled Mung
Beans)
0 0 0.5 0 0.5
1 -0:85
(1 minute 30 seconds)- -
2 - - - -
3 - - - -
4 - - -
0:25
(4 minutes 28
seconds)
5 - - - -6 - - - -
7 - - - -
8 - - - -
9 - - - -
10 - - - -
Experiment 2: Photosynthesis
Table 2.1Beaker 1
Distance: 50 cm
1stbubble formation: 00:45 (45 seconds)
Time (minutes) Number of bubbles
00:0001:45 2
01:4502:45 1
02:4503:45 0
03:4504:45 1
04:4505: 45 1
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05:4506:45 2
06:4507:45 2
07:4508:45 1
08:4509:45 2
09:45
10:45 2
Table 2.2Beaker 2
Distance: 30 cm
1stbubble formation: 01:34 (1 minute 34 seconds)
Time (minutes) Number of bubbles
01:3402:34 2
02:34
03:34 3
03:3404:34 3
04:3405:34 4
05:3406:34 5
06:3407:34 7
07:3408:34 8
08:3409:34 9
09:34
10:34 14
10:3411:34 16
VI. Discussion
VII. Conclusion
VIII. References