BNWL7-SCI TB C06 QR11 Laboratory-Activities
BNWL7-SCI TB C06 QR11 Laboratory-Activities
BNWL7-SCI TB C06 QR11 Laboratory-Activities
Objectives MATERIALS
1. State the function of each part of a compound microscope alcohol or xylene
2. Handle the microscope properly and carefully prepared slide of any
specimen
3. Properly focus a specimen under the microscope compound microscope
4. Compute the total magnification of a specimen lens paper or cotton
swab
5. Observe proper care of the microscope
Procedure
1. Identify the parts of the microscope and list down their functions
in table 12-1.
2. In using the microscope, observe the following:
a. Carry the microscope with both hands. Grasp the arm with
one hand and support the base with the other hand.
b. Gently place the microscope on the laboratory table, with its
arm facing you.
c. Clean the lenses with lens paper or cotton swab for a clear
view of your specimen. You may need to moisten the lens
paper with alcohol or xylene to remove grease or oil, which
can blur the image of the specimen. (Caution: Xylene is
hazardous.)
d. Examine the eyepiece or ocular lens and take note of the
number followed by ×. This refers to the magnification of
the eyepiece, which tells how many times it can magnify the
specimen. For example, 5× means the eyepiece can magnify
an object five times its original size.
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e. Look for the objective lenses. There may be three or four of them. Notice that each objective
has a number followed by ×. Each objective magnifies the object by the factor marked
on the particular lens. For example, a scanner objective, which is usually the shortest, has
5×, a low-power objective (LPO) has 10×, a high-power objective (HPO) has 40×, and an
oil-immersion objective (OIO) has 100×. Objective lenses should be used in the following
order: scanner, low, high, and oil-immersion.
If you multiply the magnification of the ocular lens by the magnification of the
objective lens, you will get the total magnification of the specimen under the microscope.
For example, if you are using the LPO with 10×, multiply this with the magnification
number of the ocular lens, which is 5×, and you get a total magnification of 50×. With this
information, fill in table 12-2.
f. Turn the coarse adjustment knob to raise the body tube away from the stage. In some
microscopes, the body tube is fixed and the coarse adjustment knob is used to lower or
raise the stage.
g. Rotate the revolving nosepiece and select the objective lens with the lowest magnification.
Continue rotating until the objective lens sets into place.
h. Place a prepared slide on the stage and secure it with the stage clips. If your microscope
uses a mirror for illumination, position the mirror at an angle that allows it to catch and
reflect a sufficient amount of light. If it has a built-in light source, switch it on.
i. Adjust the iris diaphragm located under the stage of the microscope to control the amount
of light that passes through the specimen and the lens, thus making the microscope’s field
of view bright.
j. In focusing the specimen, use the objective lens with the lowest magnification first. This
may be a scanner or an LPO. Turn the coarse adjustment knob until the specimen comes
into focus. To use the HPO, rotate the revolving nosepiece until the HPO sets into place.
Focus the specimen using the fine adjustment knob. Do not use the coarse adjustment
knob in focusing specimens under HPO or OIO to avoid damaging the specimen and the
objective lenses.
k. The OIO is used for very small organisms, such as bacteria. To use it, locate first the specimen
to be observed using the scanner, then the LPO, then the HPO. Place a drop of cedarwood
oil on the coverslip at the center of the viewing area. Rotate the nosepiece until the OIO
is in contact with the oil. Only use the fine adjustment knob in focusing your specimen.
After examining your specimen, lower the stage before removing the slide. Be sure to wipe
off the oil from the coverslip and the OIO lens with a lens paper or cotton swab dipped in
xylene.
l. After using the microscope, lower the stage and set the revolving nosepiece to its shortest
objective. Return it to its storage box or cabinet. Do not forget to carefully hold it by its arm
and support the base with your palm.
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Name Date Performed
Groupmates Date Submitted
Mark/Grade
REPORT SHEET 12
Parts of a Compound Microscope
Data and Results
Table 12-1. Parts of a Compound Microscope and Their Fuctions
Draw tube
Body tube
Revolving nosepiece
Objective lenses
Stage
Stage clips
Condenser
Iris diaphragm
Arm
Base
10× 100×
10× 40×
10× 100×
10× 50×
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Analysis and Interpretation
1. How should you carry a microscope?
4. When do you use the coarse adjustment knob? the fine adjustment knob?
5. What are the essential parts of the microscope for you to see a specimen?
6. How do you compute the total magnification of a specimen viewed under a microscope?
Generalization
Application
1. Why are microscopes important in science?
2. If the microscope had not been invented, what would be some of the possible setbacks this
would have brought to humanity?
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EXPERIMENT 13
Focusing Specimens
under the Compound Microscope
Sample specimens to be examined under the microscope are generally prepared in two ways:
prepared slides or wet mounts. Prepared or permanent slides can last for a long time. They are
purchased from biological supply stores, or may be made by teachers. Wet mounts, on the other
hand, are temporary, usually lasting for one laboratory period.
In this experiment, you will learn how to prepare slides for observation, and focus and observe
specimens under the microscope.
Objectives MATERIALS
1. Prepare slides for examination under the microscope water
2. Locate the specimen of interest and focus it under LPO and HPO letter e
(cut from a magazine or
3. Calculate the magnification of an image observed under the newspaper)
microscope hair strand with follicle
compound microscope
Procedure medicine dropper
lens paper or cotton
1. Place the cutout letter e at the center of the glass slide. Using swab
the medicine dropper, drop a small amount of water on it. Put a scissors or cutter
coverslip over the specimen, starting from the edge to prevent the coverslip
formation of bubbles. ruler
2. Place the slide at the center of the stage and secure it with the glass slide
stage clips.
3. Set the LPO in place and use the coarse adjustment knob to lower
the objective as close as possible to the slide.
4. Keeping both of your eyes open, focus the specimen carefully
using the coarse adjustment knob. If you do not see anything with
both eyes open, cover one eye with your palm. Sharpen the focus
with one eye.
5. Using the iris diaphragm, regulate the amount of light that
illuminates the specimen. You cannot see clearly the details of the
specimen under examination with too much light.
6. Once the specimen is in focus, move the slide slightly to the left
and then to the right. Note the position and orientation (upright or
inverted) of the specimen. Draw your observations under Data and
Results.
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7. Set the HPO in place and focus the specimen using the fine adjustment knob. Draw your
observations under Data and Results. Compare the appearance of the letter e under LPO and
HPO.
8. Replace the letter e specimen with a 1 cm piece of hair strand with follicle.
9. Focus the hair follicle under LPO, then HPO. Take note of its size. Draw your observations in Data
and Results. Compare the appearance of the follicle under LPO and HPO.
10. Once you are done, clean the ocular and the objective lenses. Make sure that the stage is dry
before returning the microscope into the storage box or cabinet.
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Name Date Performed
Groupmates Date Submitted
Mark/Grade
REPORT SHEET 13
Focusing Specimens under the Compound Microscope
Hair follicle as seen under LPO Hair follicle as seen under HPO
Magnification: Magnification:
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b. In what objective lens did you see the whole mount of the letter e?
2. Hair follicle
a. Did you see the whole specimen?
b. Differentiate the image of the hair follicle when focused under LPO and HPO.
3. Why should you put the specimen at the center of the field of view before changing the objective
lens?
4. Why must you use the fine adjustment knob in focusing the specimen under HPO?
Generalization
Application
1. If the ocular lens can magnify an object 10×, and the objective lens 100×, what is the total
magnification of the specimen under the microscope?
2. What are the possible reasons a specimen may not be focused clearly under the microscope?
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EXPERIMENT 14
Objectives MATERIALS
1. Examine plant and animal cells under the microscope water
2. Describe the structures found in plant and animal cells iodine solution
or methylene blue
3. Compare and contrast plant cells and animal cells compound microscope
forceps
Procedure medicine dropper
glass slide
A. Plant cells
coverslip
1. Select a young Hydrilla leaf. Using the forceps, mount this toothpick
carefully onto the slide. Drop a small amount of water on the Hydrilla (digman) leaf
specimen and put a coverslip.
2. Observe the specimen under LPO, and identify the visible cell
parts. Put a check mark in the appropriate boxes in the table
under Data and Results to indicate these visible parts.
3. Repeat step 2, but use HPO instead.
4. Describe the shape of the cells of the leaf. Record your
description under Data and Results.
5. Draw the leaf cells as observed under LPO and HPO.
B. Animal cells
1. Using the flat or round end of a toothpick, gently scrape the
inner lining of your cheeks.
2. Carefully smear the scrapings onto a clean glass slide and
drop a very small amount of iodine solution or methylene
blue on the specimen. Put a coverslip over the specimen.
3. Observe the specimen under LPO, then HPO. Take note of
the cell parts visible under LPO and HPO. Put a check in the
appropriate boxes.
4. Draw the cheek cells as observed under LPO and HPO.
© Sibs Publishing House, Inc.
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Name Date Performed
Groupmates Date Submitted
Mark/Grade
REPORT SHEET 14
Comparing Plant and Animal Cells
Data and Results
A. Observed cell parts
Cell wall
Cell membrane
Cytoplasm
Chloroplast
Nucleus
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C. Drawings
Hydrilla leaf cells observed under LPO Hydrilla leaf cells observed under HPO
Cheek cells observed under LPO Cheek cells observed under HPO
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Analysis and Interpretation
1. What organelles in plant cells were visible under the compound microscope?
3. How did cheek cells look like? Were the scraped cheek cells compactly arranged?
5. Why are stains such as iodine solution or methylene blue used when observing cells under the
microscope?
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Generalization
Application
1. What are the advantages of having a cell wall in plant cells?
2. Would it be possible in the future for human cells to perform the biochemical processes that
only plant cells are capable of doing? If so, how do you suppose it would be done?
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EXPERIMENT 15
Objectives MATERIALS
1. Observe how diffusion and osmosis take place water
2. Compare diffusion and osmosis potassium
permanganate (KMn04)
solution
Procedure perfume
20% sugar solution
A. Diffusion
large potato
1. Fill a 100 mL beaker with water. Slowly add a small amount 100 mL beaker
of potassium permanganate (KMnO4) to the beaker. Observe. potato peeler
Write down your observation under Data and Results. knife or scalpel
2. Spray the perfume in one corner of your classroom or cork borer
laboratory. Go to another corner of the room. Observe what pins
happens to the scent of the perfume after a few seconds. stopwatch or timer
Note your observation under Data and Results.
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B. Osmosis
1. Peel the potato and cut off one of its ends to get a flat base.
2. Using a cork borer, carefully bore a cavity in the potato. Make sure not to bore through the
base.
3. Pour the 20% sugar solution into the cavity, filling it about one-third.
5. Mark this initial level of sugar solution with a small pin.
6. Carefully transfer the potato to the beaker filled about halfway with water.
7. Observe the level of the sugar solution in the cavity.
8. After 30 min, mark the final level of the sugar solution in the cavity using another small pin.
pin beaker
potato
sugar solution
water
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Name Date Performed
Groupmates Date Submitted
Mark/Grade
REPORT SHEET 15
Diffusion and Osmosis
Data and Results
A. Diffusion
1. Mixing of water and potassium permanganate (KMnO4)
2. Spraying of perfume
B. Osmosis
Volume of sugar solution in the cavity of potato =
2. Which of the two diffused faster—potassium permanganate (KMnO4) in water or the perfume in
air? Why do you think so?
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3. What happened to the volume of the sugar solution in the cavity of the potato? What process
took place? Why do you say so?
Generalization
Application
1. Cite at least two common kitchen activities or chores that show diffusion.
2. Cite at least two common kitchen activities or chores that show osmosis.
3. Why do the vegetables in salads become soft and watery when salt or sugar is added?
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EXPERIMENT 16
Objectives MATERIALS
1. Examine examples of plant and animal tissues whole herbaceous dicot
plants (e.g., pansit-
2. Compare plant and animal tissues
pansitan, mayana)
water
Procedure prepared slides of
animal tissues (muscle,
A. Plant tissues blood, and epithelial)
1. Obtain young, herbaceous dicot plants from the school sharp blade or scalpel
grounds. compound microscope
glass slide
2. Examine the internal parts of the stems by making freehand
medicine dropper
cross sections using the sharp blade or scalpel. Make sure
coverslip
that the cross sections are thin so that you can see the cells in
detail.
3. Examine the plant cells or tissues under the compound
microscope. Take note of the many visible cells or tissues,
especially on the outermost layer (epidermis). The big, round,
thin-walled cells found after the epidermis are parenchyma
tissues. Notice also the presence of the vascular tissues
arranged circularly along the center. Draw these tissues in
Data and Results.
B. Animal tissues
1. Focus each prepared slide of muscle, blood, and epithelial
tissues under the microscope. Observe them under LPO, then
under HPO. Draw your observations in Data and Results.
2. Compare the animal tissues with the plant tissues.
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Name Date Performed
Groupmates Date Submitted
Mark/Grade
REPORT SHEET 16
Comparing Plant and Animal Tissues
Data and Results
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2. What group of plant tissue did you see in your specimen?
3. How do cells that function together look in the specimen that you used?
B. Animal tissues
1. How would you describe the shape of the muscle tissue that you examined? Was it striated
or not?
2. What type of blood cell was the most abundant in the blood smear that you examined?
3. How were epithelial cells arranged? How did they look like?
Generalization
Application
1. Which has more tissues—plants or animals? Why do you say so?
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Open-ended activity 2
TASK
1. Using a dialysis membrane, design an experiment that will prove that semipermeable
membranes allow some, but not all, substances to pass through.
2. Know the following:
• semipermeable • 5% sugar solution
• selective membrane • osmosis
• dialysis membrane • diffusion
• thistle tube • Benedict’s solution
3. Plan the experiment:
a. List, gather, and use all the materials for the experiment.
b. Write a brief and concise experimental design or procedure.
c. Describe and analyze what you tested.
d. Report the results of your experiment.
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Name Date Performed
Groupmates Date Submitted
Mark/Grade
REPORT SHEET 33
The Selective Semipermeable Membrane
I. Objectives
II. Materials
III. Hypothesis
IV. Procedure
V. Illustration
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VI. Data and Results
VIII. Generalization
IX. Application
ENRICHMENT QUESTIONS
1. How important is the semipermeable membrane to the cell?
2. What pieces of evidence proved that some substances passed through the dialysis membrane
that you used?
4. What are some of the sources of error that might have led to inaccurate results in the experiment?
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