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GROUP #1 ELS PeTa LifeinaBottle

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PONTIFICAL AND ROYAL
UNIVERSITY OF SANTO TOMAS
THE CATHOLIC UNIVERSITY OF THE PHILIPPINES
Senior High School – Science Department
2nd Term / SY 2021 – 2022
NAME OF MEMBERS:
PERFORMANCE TASK:
GROUP NUMBER: 1
SECTION: 11MAD-05
PETA 2:Life in a Bottle
Date of Implementation
October 2022
Date Submitted
November 29, 2022
Memoracion, Isah
Panaligan, Sofia
Perez, Kenizha
Sablan, Drei
Serrano, Elisha
Sunot, Mary Mitzi
Category
4
3
2
1
Weight
Analysis
The relationship
between the
variables is
discussed and
trends/patterns
logically analyzed.
Predictions are
made about what
might happen if part
of the lab were
changed or how the
experimental design
could be changed.
The
relationship
between the
variables is
discussed and
trends/patterns
logically
analyzed.
The relationship
between the
variables is
discussed but
no patterns,
trends or
predictions are
made based on
the data.
The
relationship
between the
variables is not
discussed.
6
/24
Professional
looking and
accurate
representation of
the data in tables.
Updates Data
weekly and gives
accurate
descriptions.
Accurate
representation
of the data in
tables. Data are
updated but
descriptions are
inaccurate.
Accurate
representation
of the data in
written form,
but not updated
regularly.
Data are not
shown OR are
inaccurate.
6
/24
Report illustrates an
accurate and
thorough
understanding of
scientific concepts
underlying the lab.
Report
illustrates an
accurate
understanding
of most
scientific
concepts
Report
illustrates a
limited
understanding
of scientific
concepts
underlying the
lab.
Report
illustrates
inaccurate
understanding
of scientific
concepts
underlying the
lab.
5
/20
Data
Scientific
Concepts
TOTAL
underlying the
lab.
Question/Pur
pose
Conclusion
The purpose of the
lab or the question
to be answered
during the lab is
clearly identified
and stated.
The purpose of
the lab or the
question to be
answered
during the lab
is identified,
but is stated in
a somewhat
unclear manner.
The purpose of
the lab or the
question to be
answered during
the lab is
partially
identified, and
is stated in a
somewhat
unclear manner.
The purpose of
the lab or the
question to be
answered
during the lab
is erroneous or
irrelevant.
4
/16
Conclusion includes
whether the
findings supported
the hypothesis,
possible sources of
error, and what was
learned from the
experiment.
Conclusion
includes
whether the
findings
supported the
hypothesis and
what was
learned from
the experiment.
Conclusion
includes what
was learned
from the
experiment.
No conclusion
was included in
the report OR
shows little
effort and
reflection.
4
/16
TOTAL
/100
PETA 2:
Life in a Bottle
INTRODUCTION:
Our planet supports a diverse form of life that thrives in all types of habitats, such as
soils, ocean water, clouds, and deep-sea sediments. We can see those different organisms in
all habitats, particularly microorganisms that interact and depend on each other. As
microorganisms grow, it consumes particular substrates, including carbon-rich fuels like
sugars and nutrients, vitamins, and respiratory gases like oxygen. Just like in any
environment, competition can arise when essential resources start to run out.
Microorganisms with different metabolic needs can bloom and thrive.
In the 1880s, Sergei Winogradsky developed a culturing device that supports a large
diversity of microorganisms. This device is the Winogradsky column of pond mud and water
mixed with a carbon source such as newspaper, eggshells, and gypsum. Incubating the
column in sunlight for months results in an aerobic/anaerobic gradient and a sulfide
gradient.
In this activity, your group will also take on the challenge of observing the interaction of
microorganisms and various microbial succession that can happen in your created
environment.
Key concepts
Microorganisms, Soil, Biology, Oxygen, Sunlight, Ecosystem
OBJECTIVES:
1. Describe the construction of a Winogradsky column.
2. Explain how this simulates a model ecosystem.
3. Explain the environmental factors that exist within each portion of the column.
4. Describe the bacteria capable of growing in each zone.
MATERIALS:
● soil or mud
● water (same source as the mud/soil or other tap water).
● latex gloves
● metal or plastic pans for mixing the materials
● spatulas/spoon
● sources of carbon (e.g., some, such as calcium carbonate and chalk, are rapidly
metabolized while others such as shredded paper and sawdust are metabolized
slowly)
● sources of sulfur (e.g., sodium sulfate, elemental sulfur, raw or hard-boiled eggs,
sodium sulfide)
● a bottle (2-liter soda bottle without the top) or other tall, clear container (wide mouth
containers are preferable).
PROCEDURES:
NOTE:
Each member of the group will make his/her own experimental set-up.
1. Mix the collected mud/soil with the desired carbon and sulfur sources.
Possible carbon sources:
Vegetable materials such as shredded hay, newspaper or sawdust, grass clippings, corn
starch, and oatmeal will work fine. These materials release carbon relatively slowly.
Fast release carbon sources include sodium carbonate (soda ash), sodium bicarbonate
(baking soda), and calcium carbonate (chalk).
Possible sulfur sources:
Elemental sulfur, calcium sulfate (gypsum), magnesium sulfate (Epsom salt), raw or
hard-boiled eggs, and cheese can work in this experiment.
SAFETY NOTE: It is uncertain if the mud is contaminated with sewage, waste, heavy
metals, or other toxic materials. Wear latex gloves in mixing materials and putting
them in the column. Add a minimal amount of water to the container and add the
mud/soil mixture a little at a time using a stick or rod to push the material in the
bottom of the column. Make sure that air bubbles are excluded as much as possible.
*** The nutrient source weight may vary per student.
2. Add water and soil mixture until the bottle/container is about three-fourths full. Rinse
the excess mud/soil mixture from the container above the soil level and then add
additional water to produce a water column. Leave some space above the surface of the
water and cover the column with plastic wrap. Be sure to cut a slit or put some small
holes in the plastic wrap to permit an exchange of gases.
3. Place your column near a window/balcony with good ventilation. (You may also use a
tungsten lamp. Your setup can produce a strong or pungent smell until they stabilize.
Ensure that the column is not exposed to too much heat or not heated by the tungsten
bulb. The temperature must be maintained and does not rise to exceed much above
room temperature.
4. Observe changes in the column (color, gas bubbles, odor). Record these observations.
Note: Photographs taken at regular intervals are a great way to record color and color
distribution changes within the column.
5. Record the date and the observations of your setup.
6. Collate all data from all members of the group and summarize results.
NOTE: Your Winogradsky column must be placed in an area that is not easily disturbed. It
is important not to vigorously move or shake the column in doing your observations.
The success of your column will be evident within a few weeks. Colored patches can appear
just under the glass or plastic layer of the column (phototrophic green and purple sulfur
bacteria). Green patches (algae and cyanobacteria) will likely appear at the top of the
water column.
WEEKLY DATA and RESULTS
NAME: Isah Memoracion
WEEK
1
11/04/22
_______
Date
2
11/11/22
_______
Date
3
11/18/22
_______
Date
4
11/25/22
_______
Date
PHOTO
DESCRIPTION
In the first week, there are no visible
and major changes. The color of the
water is still brown, the soil is still the
same, and there is no odor yet.
By week 2, I can already see visible
changes such as the water turning
green and a bit of smell. However,
there were no changes in the soil.
By week 3, the soil darkened, and the
water also turned into a darker green.
There were also spots of green
moss-like patches and the smell got
stronger.
Week 4 was the time that the typhoon
Paeng hit so the bottle overflowed. I
removed some of the excess water. By
this week, the soil darkened even more
and the water was greenish and
brownish. There were more moss-like
patches and the smell really got
stronger, and you can smell it from
afar, especially when I poured the
overflowing water. I also noticed I bit
of a red-ish spots on the bottom part of
the soil.
NAME (STUDENT 2): Sofia Isabel Panaligan
WEEK
1
10/08/22
_______
Date
2
10/14/22
_______
Date
3
10/21/22
_______
Date
4
10/28/22
_______
Date
PHOTO
DESCRIPTION
It was still moist at first, and then
the bad odor started to come in
after a few days.
The bad odor was now bearable,
but still smells bad. There were
changes with the water.
There were movements around
the water and the soil, still the bad
odor stays.
The odd smell was still there but
there were bits of color green seen
when you looked closely.
5
11/04.22
_______
Date
6
11/11/22
_______
Date
7
11/18/22
_______
The small movements were still
there and the greenish stuff on the
soil is now around the bottle if I
look close enough.
There were still small bubbles, but
the green particles are now also
around the top of the cover of my
bottle.
There were not many changes.
Date
8
11/25/22
_______
Date
The water has now turned brown,
still not much changes.
NAME: KENIZHA CHLOE PEREZ
WEEK
PHOTO
DESCRIPTION
1
10/10/22
Nothing much really changed
since the day I made it and I can
still see through the water.
2
10/17/22
Smells bad and there are some
floating particles on top of the
water. The water was also getting
dirty.
3
10/24/22
Still smells pretty bad and the
floating particles on top look like
it’s sticking together. Still no
result on the soil.
4
10/31/22
There were some bubbles under
the soil and on top of the water.
The side of the container starts
getting dirty. There were some
green particles forming on top of
the soil.
5
11/07/22
Lots of green particles started
appearing on top of the water and
soil and sticks on the side of the
container.
6
11/14/22
Nothing much has changed since
last week. Still the same.
7
11/21/22
The green particles on the side of
the column are much lighter than
last week.
8
11/28/22
No changes.
WEEKLY DATA & RESULTS
NAME:JULI DREIANN LEIE P. SABLAN
WEEK
1
10/22
PHOTO
DESCRIPTION
-
Not much changes.
Odor is a bit smelly.
-
Odor is pungent.
Air bubbles forming on the
sides.
-
Water and soil turned a bit
greenish.
Pungent odor has subsided.
Date
2
10/27
Date
3
11/1
Date
-
4
11/7
Date
5
11/13
-
Water turned black.
Soil turned grayish.
Thin white fungi layer start to
form.
-
Soil & water are still the same.
Red fungus start to form on
one spot.
-
White layer has become
brownish.
Cracks and a lump start to
form from the red fungus.
Roots are visible under the
fungus.
Date
6
11/20
Date
-
7
11/28
Date
-
Not much changes.
brown layers cracked.
green splotches on the side of
the column.
Elisha Maura Serrano
WEEK
PHOTO
DESCRIPTION
●
Week 1
OCT 8
●
●
●
●
Week 2
●
OCT 15
●
The water is really dark but starting to
clean up a little after the water and
mud separated.
There is no strange odor.
On the water's surface, a layer and
some bubbles are beginning to
appear.
Maggots were seen in the column.
The abundance of maggots rose, and
they appeared to be attempting to exit
the column.
The water is now clearer and seems
lighter than it did earlier.
There is still no strange odor
emanating from the column.
●
Week 5
NOV 5
●
●
●
Week 5
●
NOV 12
The water darkened and the layer on
top turned reddish.
At the center of the column, something
reddish-brown is developing.
At the base of the column, some dark
green specks may be seen.
The water has cleared up so much and
the color lightened and became a bit
orange.
In the middle of the column, there’s
more of the reddish-brown thing
forming
WEEKLY DATA & RESULTS
NAME: Mary Mitzi Jim Sunot
WEEK
1
10/20
Date
PHOTO
DESCRIPTION
First day.
2
10/24
4 days later. Starting to see changes,
though they’re not major.
Date
3
10/27
Date
After 3 days, I was shocked to see
maggots in my plant. I kept it for
like one more week but I had to put
it in our bathroom, and there were
flies roaming around. I had to throw
it away.
GUIDE QUESTIONS:
1. What changes did you see in the column at the end of your observation period?
Are there also sections in the column that remain unchanged?
At the end of our observation period we noticed changes with the odor (the odor
got stronger as time passed by), color of the water (first it turned green then turned into
dark brown), for some members there were green particles on the side of the bottle in the
water column and for others the green particles were on the top of their water, the sides,
and on top of the soil. A member noticed that there were small red particles on her soil
column. The small bubbles at first were visibly seen, but as the week passes by it
gradually decreases. Both the water and the soil column have changed, but the changes
in the soil column were only minimal.
2. Explain how the biodiversity found on Earth is demonstrated through the
Winogradsky Column in terms of the niches they occupy.
The Winogradsky column served as a mini ecosystem because microorganisms
grew and multiplied from the closed system of the column. The microorganisms created
a suitable environment for them inside the closed system just like how organisms on
Earth shape the environment to be suitable for our needs.
3. Why does the Winogradsky column require sunlight? How does it illustrate the
sun as the primary source of energy on Earth?
The Winogradsky column requires sunlight because it is their primary source for
their energy to make food. Microbes need sunlight to provide them food and energy
through photosynthesis, so the Winogradsky column should be placed in an area where
they get sunlight.
CONCLUSION:
All life on earth can be classified through the organism's carbon and energy source, like
sunlight and the carbon and sulfur sources incorporated in the soil to make our column. As a
student it enables us to observe the growth and changes in microbial populations. The
Winogradsky column is also a unique microbial ecosystem that has various advantages for use
as a model system to study microbial and viral dynamics, interactions, and diversity. The
Winogradsky column shows how different the microorganisms perform their roles while
depending on each other. The processes of a microorganism can be used by other
microorganisms to grow. The Winogradsky is a closed system, driven by sunlight that provides
them energy and food. We therefore conclude that the Winogradsky column is a demonstration
of the biodiversity that can be found on Earth and that we should appreciate the small things
even if we aren’t meant to see them.
REFERENCES:
Scientific American (2021). Soil Science: Make a Winogradsky Column.
https://www.scientificamerican.com/article/bring-science-home-soil-column/
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