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Bio 137 Lab Manual
Bio 137 Lab Manual
Laboratory Manual
All Sections
Written and compiled by
Becky McCane
Lab Exercise 1
Measurements
Body Organization
Body Systems
What you need to be able to do on the exam after completing this lab exercise:
• Be able to identify each body cavity on the torso model and know which major
organs are housed within each cavity.
• Be able to identify the correct body systems and organs on the models or
diagrams.
1-1
Measurements
We will be using 3 base units: gram (to measure mass)
meter (to measure distance)
liter (to measure volume)
Giga- Mega- Kilo- Hecta- Deca- Base deci- centi- milli- micro- nano-
G X X M X X K H D(a) BU d c m X X µ X X n
Move decimal to the left (divide by 10) Move decimal to the right (multiply by 10)
Units get BIGGER as you go left Units get smaller as you go right
• Decimal begins at the unit you are given
• Move decimal to the unit you are asked
o Move decimal the number of spaces and the direction until you get to the unit you are asked
1-2
To convert from mm to m, move your decimal point 3 places to the left (since the base unit is
three places to the left of milli- on the chart).
46 mm = ____ m
46 mm = .046 m
To convert from cg to mg, move your decimal point 1 place to the right (since milli- is 1 place to
the right of centi- on the chart).
400 cg = ____ mg
400 cg = 4,000 mg
1-3
Body Organization
Anatomical Position
In Human Anatomy & Physiology, we refer to the body parts as if a person was standing in the
anatomical position.
_________________________________________
_________________________________________
_________________________________________
_________________________________________
_________________________________________
1-4
Directional Terminology
When comparing the location of one body part to another, we use directional terms.
D is ____________________ to C H is _________________________ to G
F is _____________________ to E 1-5
Planes of Reference
A Median (Midsagittal) plane divides the body/organ into equal Left/Right halves.
1-6
Frontal (Coronal) Section of Sheep Brain
1-7
Regional Terminology
In Human Anatomy & Physiology, we use scientific terms for various regions of the body.
1-8
1-9
Major Body Organs
A. ______________________________ E. ______________________________
B. ______________________________ G. ______________________________
D. ______________________________ H. ______________________________
1-10
B. ______________________________ I. ______________________________
C. ______________________________ J. ______________________________
F. ______________________________ K. ______________________________
1-11
Body Cavities
Body cavities are areas in the body that usually house an organ, bone, or other body part.
1-12
In addition to the information above:
1-13
Abdominopelvic Quadrants
In Human Anatomy & Physiology, we sometimes divide the abdominopelvic cavity into
quadrants to make studying the cavity easier.
1-14
Abdominopelvic Regions
In Human Anatomy & Physiology, we sometimes divide the abdominopelvic cavity into nine
regions to make studying the cavity easier.
1-15
Body Systems
For each of the following body systems, know the organs that are listed and to which body
system the organs belong:
Integumentary System
Know the parts of the Integumentary System (listed below) on the skin model in the lab.
A. ______________________________ D. ______________________________
B. ______________________________ E. ______________________________
C. ______________________________ F. _______________________________
A is ____________________ to B
B is ____________________ to A
1-16
Skeletal System
Know the parts of the skeletal system (listed below the picture) on the knee joint model in lab.
1-17
Muscular System
Know the parts of the Muscular System (listed below the picture) on the Muscle Man model in
the lab.
1-18
Nervous System
Know the parts of the Nervous System (listed below the picture) on the Nerve Man model in the
lab.
9. ______________________________
You will not need to know the Pineal Gland for the first lab exam. It will be covered when we
study the brain.
1-20
Cardiovascular System
Know the organs of the Cardiovascular System (listed below the picture) on the Heart model in
the lab.
A. Heart
C. Arteries
D. Veins
1-21
Lymphatic System
Know the following parts of the lymphatic system on the diagram displayed in the lab.
Note: The diagram in the lab looks different from this one, but has the same organs.
A. Lymph Nodes
B. Lymph Vessels
C. Spleen
D. Thymus
A. ___________________________________
B. ___________________________________
C. & D. _______________________________
12. ___________________________________
24. ___________________________________
37. ___________________________________
Urethra 1-25
Male Reproductive System
Know the parts of the Male Reproductive System (listed below the picture) on the Male
Reproductive system model in the lab.
38. ______________________________
40. ______________________________
1-26
Female Reproductive System
Know the parts of the Female Reproductive System (listed below the model) on the Female
Reproductive system model in the lab.
20. ____________________________________
21. ____________________________________
22. ____________________________________
29. _____________________________________
1-27
Lab Exercise 2
Microscopy
Cell Structure
What you need to be able to do on the exam after completing this lab exercise:
Be able to name the parts of the microscope and give the function of each part.
Be able to demonstrate the proper usage of the microscope by locating, focusing, and
identifying a specimen on a microscope slide.
Be able to explain how working distance, field size, brightness, and resolution change
with increasing magnification.
Be able to explain the lens effect and depth of field as it relates to microscope usage.
Be able to identify various cells and cell structures under the microscope.
2-1
The Microscope
We will be using a compound light microscope in this lab to view various cells and tissues. It is
very important that you learn to use the microscope correctly, and can efficiently get images into
the proper focus for study.
Know the following parts of the microscope and the function of each part.
2-2
Know the following functions of the microscope parts.
PART FUNCTION
Arm Used to carry the microscope; located between the body
tube and the base
Body tube (Head) Supports the objective lens system and the ocular lens;
directs light toward the ocular lens
Coarse focus (adjustment) Brings the specimen into focus by raising or lowering the
stage; never use the coarse focus on high power!
Fine focus (adjustment) Used for final focusing (fine-tuning the image)
Iris diaphragm Regulates the amount of light that passes through the stage;
located at the base of the condenser
Objective lenses Magnify the specimen for viewing; scanning lens (red ring)
magnifies 4X, low power lens (yellow ring) magnifies 10X,
high power lens (blue ring) magnifies 40X, oil immersion
lens (white ring) magnifies 100X
Ocular lens (eyepiece) The lens (or lenses) you look through; magnifies the
specimen 10X; monocular microscopes have one ocular
lens, binocular microscopes have two ocular lens
Revolving nosepiece Contains the objective lenses; use nosepiece to rotate the
correct objective lens into place over the opening in the
stage
Stage clips Hold the slide in place; two knobs below the stage control
the precise movement of the specimen on a mechanical
stage
Substage light Light source; a light dimmer dial on the base varies the
intensity of the light source
2-3
Use and Care of a Compound Microscope
1. Always use both hands when transporting the microscope. Place one hand on the arm
and the other hand under the base. Make sure the cord is not hanging down so you don’t
trip over it.
4. Place the cord behind the microscope then plug it into the outlet. Be very careful not to
trip over the cord or pull on it.
5. Once you have the microscope plugged in, sit down and find the light switch. The light
switch on your microscope is located on the side of the base (see microscope picture
above). Turn on the light switch and adjust the intensity of the light with the light
dimmer dial (see microscope picture above).
6. Turn and “lock” the scanning lens (4X objective) in place above the opening in the stage. If
the lens is in the correct place, you should see a bright circle of light when you look through
the eyepiece. This circle of light is your field of view.
7. Without looking through the eyepiece, lower the stage completely and carefully place the
microscope slide on the microscope stage with the specimen on the slide directly over the
opening in the stage. If your microscope has stage clips, secure the slide under the stage
clips. If your microscope has a mechanical stage, turn the control knobs (below one side
of the stage) to position the specimen directly over the opening in the stage.
8. While looking through the eyepiece, carefully turn the coarse adjustment knob to raise the
stage until the specimen comes into view.
9. Use the fine adjustment knob for final focusing of the image.
10. Since the scanning lens allows you to see a larger portion of your slide in less detail, you
may need to increase your magnification. To switch to the next magnification, carefully
turn the revolving nosepiece until the low power lens (10X objective) is locked in place.
11. Your compound light microscope is parfocal. If your image was in proper focus before
you changed the objective lens, you should only have to do minimal focusing to get the
image in focus with the new objective. You should only have to use the fine focus knob
on low power to get the image in proper focus.
12. If you need to increase your magnification to the high power lens (40X objective), simply
turn the revolving nosepiece until the 40X objective is locked in place. Make sure your
image is in proper focus on low power before switching to the high power objective.
2-4
13. Use ONLY the fine adjustment knob to focus on high power. NEVER USE THE
COARSE FOCUS KNOB ON HIGH POWER! The high power lens should be very
close to your slide when in proper focus. If you turn the coarse adjustment knob while on
high power, the objective could easily break your slide.
NOTE: If you lose the image on high power, go back to low power and find/focus it
before going up to high power again.
14. When you are finished with the microscope, return the scanning lens (4X) to place.
Lower the stage completely, remove the slide, and carefully place into the correct box.
15. Carefully clean all the lenses with lens paper. Never use paper towels or any other kind
of paper/cloth on your microscope lenses as it may scratch the glass.
16. Carefully unplug the microscope and wrap the cord snugly around the base.
17. Place the dust cover over the microscope and carefully carry it with both hands back to
where you got it.
NOTE: Most likely your microscope will already be set up on your lab bench before you get to
the lab. If so, do not worry about Steps 1 - 3 and 17 when working in the BIO 137 lab.
2-5
Viewing Objects Through the Microscope
Procedure:
2. Bring the slide into focus using the scanning (4X) lens.
3. Observe how much of the paramecium you can see. Make a drawing of your paramecium below.
4. Now, switch to low power (10X) and use the fine adjustment knob to focus the image.
Note: Before switching to the low power lens, make sure your paramecium is in the center of
your field of view.
5. Observe how much of the paramecium you can see. Make a drawing below.
6. Lastly, switch to high power (40X). Make sure your paramecium is in the center of your low power
field of view before you switch to the high power lens. If you lose the image, go back to the low
power lens, focus it, put it in the center, switch to the high power lens, and use fine focus only.
7. Observe how much of the paramecium you can see now. Make a drawing below.
2-6
Answer the parts of Question #8 with either “Increased” or “Decreased”
1. Switch to the scanning lens on your microscope, lower the stage, and remove the slide.
2. Obtain a metric ruler and place it under the stage clips with the millimeters (smallest marks)
over the opening in the stage.
3. Switch to the low power lens and raise the stage until the millimeters are in focus.
4. Count the number of millimeters that will fit in your low power field of view. The
millimeters are counted as the spaces between the dark lines. Record the number below.
5. To calculate the diameter of your low power field of view in micrometers, multiply your
answer in #4 by 1,000.
7. Place the paramecium slide on the microscope and bring into focus using the low power
lens.
8. Choose one paramecium cell and estimate its length and width in µm (based on the diameter
of the entire field of view).
Example: if the low power field of view was 1000µm and the paramecium cell occupied
one-half of the field of view, you could estimate the length to be 500µm. If it occupied
one-fourth of the field of view, you could estimate the length to be 250µm.
1. Place the “Letter e” slide in the stage clips (slide label right side up).
2. Get the letter “e” in focus using the low power lens.
4. How does the position of the letter viewed through the microscope differ from the actual
position of the letter on the slide?
6. Looking through the microscope, move your slide forward (away from you).
The mirrors in the microscope flip and reverse the image before it reaches your eyes. This is
called the lens effect. This may be a little confusing at first, but with practice you will learn to
move the slide in the desired direction with no problem.
2-8
Perceiving Depth and the Depth of Field
1. Obtain a slide with three colored threads crossed and get the image into focus on low power.
2. Adjust the light with the diaphragm, if necessary, to increase the contrast of the threads.
3. Move the slide so that the area where all three threads overlap is in the center of your field of
view and adjust the image so that it is in clear focus.
4. Switch to the high power lens and use the fine adjustment knob to fine-tune the image. Move
the slide so you can see all three colors at once. Note: you will only be able to see a very
small portion of each color.
5. Looking through the microscope, turn the fine adjustment knob to lower the stage just until
the threads are out of focus. Now, slowly roll the stage back up noting which color thread
comes into clear focus first, then second, then last. The first thread to come into focus when
you raise the stage is the one that is on top. The second thread to come into focus is the one
in the middle.
Record your observations, relative to which color of thread is uppermost, middle, and lowest.
There is always a certain amount of distance between the cover glass and the slide. This distance
becomes more apparent when you increase the magnification of the specimen.
Put out your hand in front of you so you can see your hand and the wall behind it. Can you get
your hand and the distant wall into clear focus at the same time? No. This is similar to what you
are experiencing when trying to view a specimen on high power. You cannot get the entire
specimen into focus at the same time. The portion of the slide that is in clear focus at any given
time is the depth of field.
When you view the various tissue slides in upcoming lab exercises, you will likely be viewing
more than one layer of cells. When viewing these slides on high power, you will need to move
the fine adjustment back and forth slowly to view the entire slide.
2-9
Determining Total Magnification
Total magnification is the total number of times the specimen you are viewing is magnified. To
determine the total magnification you multiply the ocular lens magnification times the
objective lens magnification. On your microscopes, the ocular lens always magnifies 10X.
Magnification of
Ocular Lens
Total
Magnification
2. Place a small drop of methylene blue stain on the clean microscope slide.
3. Take a clean toothpick and gently scrape the inside of your cheek.
4. Roll the toothpick with the cheek scrapings into the drop of stain on your slide and stir the contents
gently.
5. Put the toothpick into the coffee can provided on your lab bench.
Note: Slowly lowering the cover slip at about a 450 degree angle helps avoid air bubbles getting
trapped beneath the cover slip.
This is called a temporary, wet mount, since a cover slip was placed over a specimen within a
liquid.
2-10
7. Observe your cheek scrapings under the scanning lens (4X), the low power lens (10X), and the
high power lens (40X). Remember to put the cells in the center of your field of view before
increasing magnification.
8. Find a few isolated cheek cells. You may see clumps of cells and/or crumpled cells. Try to find a
few whole, flat cells out by themselves and focus on them. You should see roundish cells, with a
stained nucleus in the center.
10. When you are finished, return the scanning lens to position, lower the stage, remove the slide and
place the slide in the coffee can provided on your lab bench.
Scanning Observation:
2-11
Cell Structure
All living organisms are composed of cells. The cell is the basic unit of structure and function
for all living things.
Know the following parts of the cell on the cell model. You do not need to know the functions
in lab. You will learn those in lecture.
Procedure:
1. Obtain prepared slides of simple squamous epithelium, cardiac muscle cells, human blood,
and sperm.
2. Observe each slide under the microscope with the scanning lens, low power lens, and high
power lens. Carefully note the similarities and differences between the different cell types.
Note the sizes and shapes of the cells and the position of the nucleus.
3. Make a drawing of each type of cells, as seen on high power. Label the visible cell parts.
Note: You will not see very much detail due to the small size of the cells.
What you need to be able to do on the exam after completing this lab exercise:
Be able to identify each type of epithelial tissue on a microscope slide (or photo) and give
its location and function in the body
Be able to identify the specified features for each epithelial tissue on a microscope slide
or photo
Be able to identify each type of connective tissue proper on a microscope slide (or photo)
and give its location and function in the body
Be able to identify the specified features for each connective tissue proper on a
microscope slide or photo
NOTE: On the exam, you may be asked to give the name, location, and function of the tissues.
If you miss the name of the tissue, you may also miss the location and function. Make sure you
can correctly identify all 12 tissues in this lab!
3-1
Epithelial Tissues
Epithelial tissue covers surfaces/organs, and lines cavities, organs, and tubules.
Epithelial tissue is classified by the cell shape and by the number of cell layers.
Cell Shapes:
Squamous cells are flat.
Cell Layers:
Simple epithelial tissue has one layer of cells.
3-2
Simple Cuboidal Epithelium
3-3
Pseudostratified Columnar Epithelium
3-4
Transitional Epithelium
You will NOT need to know anything about stratified cuboidal or stratified columnar
epithelium in this lab.
Procedure:
1. Obtain a simple squamous (or lung) slide and bring into focus using the scanning lens
(4X). Look for flattened rings of cells around white spaces.
2. Focus on the cells, position them to the center of your field of view, and switch to the low
power lens (10X).
3. Focus on a few cells, position them to the center of your field of view, and switch to the high
power lens (40X). Notice that the cells are flattened and irregular in shape with a prominent
nucleus.
4. Make a drawing of the tissue on high power in the space below. Label the nucleus.
3-5
Simple Cuboidal Epithelium
1. Obtain a simple cuboidal (kidney) slide and bring into focus using the scanning lens
(4X). Look for squarish cells with dark nuclei, arranged in a circle.
2. Focus on the cells, position them to the center of your field of view, and switch to the low
power lens (10X).
3. Focus on a few cells, position them to the center of your field of view, and switch to the high
power lens (40X).
4. Make a drawing of the tissue on high power in the space below. Label the nucleus.
1. Obtain a simple columnar (jejunum) slide and bring into focus using the scanning lens
(4X). Look for column-like cells with large, dark nuclei arranged in a neat row.
2. Focus on the cells, position them to the center of your field of view, and switch to the low
power lens (10X).
3. Focus on a few cells, position them to the center of your field of view, and switch to the high
power lens (40X).
4. Make a drawing of the tissue on high power in the space below. Label the microvilli, goblet
cells, and nuclei.
3-6
Pseudostratified Columnar Epithelium
1. Obtain a pseudostratified columnar (trachea) slide and bring into focus using the scanning
lens (4X). Look for many dark nuclei toward the outer edge of the tissue.
2. Focus on the cells, position them to the center of your field of view, and switch to the low
power lens (10X).
3. Focus on a few cells, position them to the center of your field of view, and switch to the high
power lens (40X).
4. Make a drawing of the tissue on high power in the space below. Label the cilia, goblet cells,
and nuclei.
Transitional Epithelium
1. Obtain a transitional (urinary bladder) slide and bring into focus using the scanning
lens (4X). Look for many layers of cells surrounding the central white area.
2. Focus on the cells, position them to the center of your field of view, and switch to the low
power lens (10X).
3. Focus on a few cells, position them to the center of your field of view, and switch to the high
power lens (40X).
4. Make a drawing of the tissue on high power in the space below. Label the nuclei.
3-7
Connective Tissue Proper
While epithelial tissue has a high degree of cellularity, connective tissue has more extracellular
matrix between the cells.
Fibroblasts
Lymphoblasts
Adipocytes
Connective tissue also consists of fibers in the matrix The fibers found in connective tissue
include:
Collagen fibers
Elastic fibers
3-8
Reticular Connective Tissue
Identification: dark-staining
reticular fibers (2), many
nuclei of lymphoblasts and
other cells (1); overall
brownish color is characteristic
of this tissue
Features to know:
lymphoblasts (1)
3-9
Dense Regular Connective Tissue
3-10
Elastic Connective Tissue
Location: aorta
Function: elasticity
Procedure:
1. Obtain an areolar connective tissue slide and bring into focus using the scanning lens
(4X). Look for criss-crossing fibers of thick and thin fibers with much space around the
fibers.
2. Focus on the tissue, position it in the center of your field of view, and switch to the low
power lens (10X).
3. Focus on the tissue, position it in the center of your field of view, and switch to the high
power lens (40X).
4. Make a drawing of the tissue on high power in the space below. Label the fibroblast nuclei,
collagen fibers, and elastic fibers.
3-11
Reticular Connective Tissue
1. Obtain a reticular connective tissue slide and bring into focus using the scanning lens
(4X). Look for a brownish tissue with many nuclei and dark fibers.
2. Focus on the tissue, position it in the center of your field of view, and switch to the low
power lens (10X).
3. Focus on the tissue, position it in the center of your field of view, and switch to the high
power lens (40X).
4. Make a drawing of the tissue on high power in the space below. Label the fibroblast nuclei,
and reticular fibers.
1. Obtain an adipose connective tissue slide and bring into focus using the scanning lens
(4X). Look for thin cells surrounding a large, round fat vacuole.
2. Focus on the tissue, position it in the center of your field of view, and switch to the low
power lens (10X).
3. Focus on the tissue, position it in the center of your field of view, and switch to the high
power lens (40X).
4. Make a drawing of the tissue on high power in the space below. Label the adipocyte nuclei.
3-12
Dense Regular Connective Tissue
1. Obtain a dense regular connective tissue (tendon or ligament) slide and bring into focus
using the scanning lens (4X). Look for many fibers running in the same direction.
2. Focus on the tissue, position it in the center of your field of view, and switch to the low
power lens (10X).
3. Focus on the tissue, position it in the center of your field of view, and switch to the high
power lens (40X).
4. Make a drawing of the tissue on high power in the space below. Label the fibroblast nuclei
and collagen fibers.
1. Obtain a dense irregular connective tissue (skin) slide and bring into focus using the
scanning lens (4X). Look for scattered patches of collagen fibers.
2. Focus on the tissue, position it in the center of your field of view, and switch to the low
power lens (10X).
3. Focus on the tissue, position it in the center of your field of view, and switch to the high
power lens (40X).
4. Make a drawing of the tissue on high power in the space below. Label the fibroblast nuclei
and collagen fibers.
3-13
Elastic Connective Tissue
1. Obtain an elastic connective tissue (aorta) slide and bring into focus using the
scanning lens (4X). Look for the dark-stained elastic fibers.
2. Focus on the tissue, position it in the center of your field of view, and switch to the low
power lens (10X).
3. Focus on the tissue, position it in the center of your field of view, and switch to the high
power lens (40X).
4. Make a drawing of the tissue on high power in the space below. Label the fibroblast nuclei
and elastic fibers.
3-14
Bio137 — Human Anatomy & Physiology I
Epithelial Tissues
Fill in the following table.
Simple
Squamous
Stratified
Squamous
Simple
Cuboidal
Stratified
Cuboidal
(Not in lab!)
Simple
Columnar
Pseudostratified
Columnar
Stratified
Columnar
(Not in lab!)
Transitional
Areolar
(Loose) CT
Adipose
Tissue
Reticular CT
Dense
Regular CT
Dense
Irregular CT
(Dense
Irreg.)
Elastic CT
1
Cell types that are present in tissue may include: adipocytes, fibrocytes/fibroblasts, lymphoblasts
2
Collagen, elastic, and/or reticular
3
Any features that would be helpful in remembering this tissue
Lab Exercise 4
Membrane Transport Mechanisms and Osmosis
The Cell Cycle
What you need to be able to do on the exam after completing this lab exercise:
Be able to explain the criteria for passive transport and how certain factors influence it
Be able to explain osmosis and explain which way water will move in or out of a cell
Be able to define hypotonic, hypertonic, and isotonic, and explain what happens to a cell
when placed in each of these solutions
Be able to name all phases in the cell cycle and explain what happens in each phase
Be able to identify the phases of the cell cycle on the lab models
4-1
Membrane Transport Mechanisms & Osmosis
Brownian Motion
In 1827, the English botanist Robert Brown noticed that pollen grains suspended in water jiggled
about under the lens of the microscope, following a zigzag path. This zigzag motion of the
particles resulted from collisions with smaller particles and is referred to as Brownian motion.
Although the individual molecules cannot be seen, the random motion of the molecules colliding
with one another can be observed. The higher the temperature of the liquid, the faster the
movement of the particles.
We will not be observing Brownian motion in this lab, but know the definition of Brownian
motion.
Passive Transport
Passive transport involves the movement of particles from an area of higher concentration to an
area of lower concentration, without the input of energy.
Simple diffusion: Simple diffusion is a type of passive transport. Molecules simply move from
where they are more concentrated to where they are less concentrated, down the concentration
gradient (the difference between high and low concentration).
In simple diffusion, molecules may move through a solid (such as gel-like agar), a liquid (such as
water or blood), or a gas (such as the air).
Several factors can affect the rate of diffusion. Some of these include temperature, particle size,
molecular weight, and concentration of particles.
4-2
Observing the Simple Diffusion of Dye Through Water
1. Your instructor will place a few crystals of potassium permanganate dye into a large beaker of
water.
2. Observe the movement of the dye in the water. At first you can differentiate between the dye
and the water. As the dye continues to diffuse through the water (down the concentration
gradient), the dye particles move from where they are more concentrated to where they
are less concentrated, without an input of energy.
3. Observe the beaker again toward the end of the lab period. The dye molecules should have
reached equilibrium and are now equally concentrated throughout the water.
4. How does the temperature of the water affect the movement of the dye molecules?
_________________________________________________________________________
_________________________________________________________________________
Facilitated Diffusion
To travel in or out of a cell, molecules must move across the plasma membrane.
The plasma membrane is selectively permeable. It acts as a barrier to the movement of some
molecules, but allows other molecules to pass through. You could say it “selects” what
ions/molecules can enter and leave the cell.
If the ions/molecules require the aid of a membrane-protein to move in or out of the cell, we call
the movement facilitated diffusion. The movement is facilitated (or “helped”) by membrane-
proteins.
4-3
Osmosis
The diffusion of water through a selectively permeable membrane is called osmosis. Water will
move from where it is more concentrated to where it is less concentrated across the plasma
membrane.
Since most solvents contain water, osmosis is the movement of solvent across the membrane.
Water moves from the side of the membrane that has a lower solute concentration to the side of
the membrane that has a higher solute concentration.
Hypotonic describes the solution with a lower solute concentration; higher water concentration
Hypertonic describes the solution with a higher solute concentration; lower water concentration
Isotonic describes the solution with an equal solute concentration; equal water concentration
Water moves from a hypotonic solution to a hypertonic solution (Hypo Hyper) across a
selectively permeable membrane.
If you place a cell (70% water/30% solute) in a hypotonic solution (90% water/10% solute), the
cell will gain water and swell. Water moves by osmosis from the solution (which has a higher
water concentration) into the cell (which has a lower water concentration).
If you place a cell (70% water/30%solute) in a hypertonic solution (40% water/60% solute), the
cell will lose water and shrink (crenate). Water moves by osmosis from the cell (which has a
higher water concentration) into the solution (which has a lower water concentration).
If you place a cell (70% water/30% solute) in an isotonic solution (70% water/30% solute), the
cell will not gain or lose water and will stay the same. Water moves in and out of the cell at
the same rate, so there is no net gain or loss of water.
4-4
Observing Osmosis Through a Selectively Permeable Membrane
Your instructor will do this activity as a class demonstration. You will record the data on your
“Membrane Transport & Osmosis” homework sheet (Question #7).
Procedure:
1. On the front desk, you should see three beakers with the following solutions:
2. Your instructor will fill the first bag of dialysis tubing (a selectively permeable membrane)
with 40% sucrose solution. The bag will be weighed on the balance before the instructor
places it into Beaker #1.
3. Next, your instructor will fill the second bag with a 0% sucrose solution. The bag will be
weighed on the balance before being placed into Beaker #2.
4. Finally, your instructor will fill a third bag with 0% sucrose solution. The bag will be
weighed on the balance before being placed into Beaker #3.
5. Your instructor will leave the bags in the beakers for approximately 1 hour.
6. After 1 hour, your instructor will take each bag out of the beaker one-by-one, dry off the
excess water on the outside of the bag, and weigh each bag on the balance.
Answer Questions 6 & 8 – 11 on your “Membrane Transport & Osmosis” homework sheet.
Filtration
Filtration is a passive transport process where water and solutes move from an area of higher
hydrostatic (fluid) pressure to an area of lower hydrostatic (fluid) pressure. The water and
solutes will move through pores in the membrane, down a pressure gradient.
Example: Coffee moves by filtration through the pores of a coffee filter from the side of the
filter that has the highest (gravitational) pressure to the side of the filter that has the lowest
pressure.
4-5
The Cell Cycle
Most of your cells divide for growth and repair. The stages that a cell goes through from the
time it is formed until it divides is called the cell cycle.
In G1 of interphase, the cell is growing and doing its job – making proteins and undergoing
routine metabolism
The duplicated chromosomes are held together by a structure called a centromere. As long as
the duplicated chromosomes are held together by the centromere, they are referred to as sister
chromatids.
4-6
In G2 of interphase, the cell continues to make proteins, undergo routine metabolism, and also
prepares the cell for division by making more cytoplasm and replicating the centrioles.
Metaphase sister chromatids line up at the metaphase plate (equator) of the cell
Anaphase sister chromatids separate and are pulled toward opposite poles of the cell
Cytokinesis is the division of the cytoplasm. As the cleavage furrow pinches the cell in two, the
cytoplasm divides so that each new daughter cell has enough cytoplasm to begin it’s life as a
new cell.
The formation of the cleavage furrow and cytokinesis begin at the end of anaphase and continue
to the end of telophase.
4-7
Identifying Interphase and the Mitotic Stages on Mitosis Models
In the lab are interphase and mitosis models. Know the name of the stage represented by each
model.
4-8
Early Anaphase Late Anaphase
Telophase Interphase
C = Cytoplasm N = Nucleolus
Ch = Chromosome Z1, Z2 = Centrosome (Centrioles)
E = Cleavage Furrow AF, AS = Mitotic Spindle (Spindle Microtubules)
K = Nucleus
4-9
Identifying Interphase and the Mitotic Stages on Onion Root (Allium) Tip Slides
Procedure:
1. Place the onion root tip slide on the microscope and position the specimen over the opening in
the stage.
2. Using the scanning lens (4X), bring one of the root tips into focus (there may be 2 -3 onion
root tips on your slide). It is best to look toward the bottom of your onion root tip, but not at
the very tip.
3. You should see vertical columns of cells. Each small box-like structure is a cell. The cells
will be in various stages of the cell cycle.
4. Position the root tip in the center of your field of view and switch to the low power lens
(10X). You should be able to see the cells a bit more clearly now. The dark structures around
the center of each cell (box) is either the nucleus or the visible chromosomes, depending upon
the stage.
5. Position the cells in the center of your field of view and switch to the high power lens (40X).
7. Locate cells in each of the following stages on your slide: interphase, prophase, metaphase,
anaphase, telophase.
Note: You may have to move your slide around while viewing it to find all 5 phases. You
should be able to find all 5 phases on one root tip, but if not, look at the other root tips on
your slide.
Examples:
4-10
In these onion root tip cells, 1-2 are in
Interphase, 3-5 are in Prophase, 6-7 are in
Metaphase, 8 is in Anaphase, 9-10 are in
Telophase.
8. Make a drawing of a cell from your onion root tip slide in each of stages of the cell cycle.
Anaphase Telophase
4-11
Bio 137 — Human Anatomy & Physiology I
Directions: Before lab, answer questions 1 – 9. During lab, answer questions 10-14.
1. The zigzag motion of particles resulting from collisions with smaller particles is called:
_____________________________
3. Define diffusion:
5. For molecules with a given amount of kinetic energy, small molecules move more rapidly
than large molecules. This difference is even more pronounced when diffusing through
a semi-solid substance, such as agar, that can hinder the movement of molecules: small
molecules can slip through the gaps more easily than large ones.
Which would move the slowest and go the furthest through agar? _____________________
8. Define osmosis:
10. Record the results from your instructor’s demonstration of osmosis in the table below:
11. Predict which bag(s) will gain weight and which should lose weight:
b) If the observed results did not match your prediction, explain some possible reasons.
A B
13. The two artificial cells above are separated by a selectively permeable membrane that is
permeable to water but impermeable to sodium chloride (NaCl). Cell A contains a 30% NaCl
solution, while cell B contains a 20% NaCl solution.
a. Cell A is hypotonic / hypertonic / isotonic compared to cell B.
b. Draw an arrow on the diagram to indicate in which direction water would move.
14. If you were hospitalized and needed to be given fluids intravenously (IV), would you
want that fluid to be hypertonic to your cells? (circle one) Yes No
Explain what would occur if you were to receive hypertonic IV fluid, including the
direction of fluid movement and how it would affect the cell.
Lab Exercise 5
Axial Skeleton
What you need to be able to do on the exam after completing this lab exercise:
Be able to name all the listed bone and bone features on the skull models.
Be able to name the listed parts of the ribcage and sternum on the models in the lab.
Be able to name the hyoid bone, if shown individually.
Be able to name the different vertebrae, if shown individually, as given in this lab exercise.
Be able to name the listed features of each vertebra on the vertebrae in the lab.
Be able to name the sacrum and the listed parts of the sacrum on the models in the lab.
Be able to name the coccyx, if individually shown.
5-1
The following tables contain terms that are useful when learning the various bone features. The
terms will NOT be on the test. They are simply here for you to use when learning the names of
the bone features.
5-2
Axial Skeleton
The axial skeleton consists of the skull, the ribcage, and the vertebrae.
The Skull
Know the following bones/bone features on the skull models.
5-5
1. frontal bone 15. ethmoid bone 39b. inferior orbital fissure
10. sphenoid bone 16. vomer 52. mental foramen
11. zygomatic bone 20. mandible 62. greater wing
12. nasal bone 30. zygomatic arch
13. maxilla 39a. superior orbital fissure
5-6
2. parietal bone
3. occipital bone
24. sagittal suture
25. lambdoid suture
5-7
Rib Cage
Know the following bones of the ribcage on the ribcage model:
The first seven pairs of ribs are true ribs because they attach directly to the sternum via the costal
cartilage.
The last five pairs of ribs are false ribs because they either attach indirectly to the sternum or not at all.
The last two pairs of false ribs are floating ribs because they do not attach to the sternum at all.
5-8
The Sternum
The anterior end of a rib is the end that articulates with the costal cartilage.
The rib head articulates with the thoracic vertebra of the spinal column.
The tubercle is a small bump on the posterior end of the rib that articulates with the vertebra below the
vertebra which with the head articulates.
The hyoid bone is found between the chin and the thyroid gland on the anterior neck. This U-shaped
bone serves as an attachment site for several muscles that help elevate the larynx during swallowing. It
also supports the tongue. The hyoid bone is the only bone in the body that does not articulate with
another bone. During an autopsy, a fractured hyoid bone is an indicator of strangulation.
5-10
The Vertebrae
There are 7 cervical vertebrae, 12 thoracic vertebrae, 5 lumbar vertebrae, 1 sacrum, and 1 coccyx.
Cervical vertebrae
The atlas, the first cervical vertebra (C1), articulates with the occipital condyles of the skull. It is
the only vertebra without a body. It has a very large vertebral foramen through which the dens of
the axis protrudes at the anterior end. It is also the only vertebra that does not have a spinous
process. Instead, it has a posterior tubercle.
The axis, the second cervical vertebra (C2), articulates with the atlas. It has a prominent,
toothlike process, called the dens, that projects superiorly from the body of the vertebra and fits
into the anterior portion of the vertebral foramen of the atlas.
All 7 cervical vertebrae have a vertebral foramen that is larger than the body (with the
exception of the atlas, which has no body). The spinous process of the cervical vertebrae
(except the atlas) is short and bifid (forked). Another distinctive feature of cervical vertebrae are
the transverse foramina, two additional openings in the transverse processes.
The thoracic vertebrae are a bit larger than the cervical vertebrae (to support more body
weight). The vertebral foramen is round, and the body is usually heart-shaped. The thoracic
vertebrae become larger as they get closer to the lumbar vertebrae. They have a distinctively
long, slender (triangular) spinous process. The transverse processes are long, thick, and
strong. When viewed from the side, thoracic vertebrae resemble an elephant.
The lumbar vertebrae have large, thick bodies (to support much body weight). The large body
has a wide oval shape. The vertebral foramen is small and somewhat triangular. The spinous
process is thick, broad, flattened, and rounded at the tip. When viewed from the side, the lumbar
vertebrae resemble a moose.
The sacrum is a large, triangular bone that articulates with the fifth lumbar vertebra. It consists
of five fused vertebrae. It is concave on the anterior side, to give increased capacity to the pelvic
cavity. There are four pairs of sacral foramina, for the passage of spinal nerves. The dorsal
(posterior) side of the sacrum is convex. At the top of the dorsal side is the superior sacral
canal, which forms a passageway for the spinal cord. At the inferior end is the sacral hiatus,
which is an opening for the exit of inferior spinal nerves.
The coccyx consists of four (or five) fused vertebrae below the sacrum. They diminish in size
from the first to the fourth. The coccyx is also known as the “tailbone”.
5-11
5-12
The Vertebrae
5-13
The Sacrum and Coccyx
5-14
Bio 137 — Human Anatomy & Physiology I
Articulations (Joints)
What you need to be able to do on the exam after completing this lab exercise:
Be able to name all the listed bones and bone features of the shoulder girdle.
Be able to differentiate between a right scapula and a left scapula.
Be able to name all the listed bones and bone features of the proximal limbs (humerus and femur).
Be able to differentiate between a right humerus and a left humerus.
Be able to differentiate between a right femur and a left femur.
Be able to name all the listed bones and bone features of the distal limbs (radius, ulna, tibia, and fibula).
Be able to identify/name the three bones that make up the pelvis.
Be able to name all the listed bone features of the pelvis.
Be able to differentiate between a male pelvis and a female pelvis.
Be able to name all the listed bones of the hands and feet.
Be able to name all the listed parts of a synovial joint on the synovial joint model of the knee joint.
Be able to name the listed ligaments of the shoulder joint, hip joint, knee joint, and elbow joint.
6-1
Appendicular Skeleton
The Appendicular Skeleton includes the shoulder girdle, upper limbs, pelvic girdle, and lower limbs.
**Know all the listed bones and bone features on the bones in the lab.
The Shoulder (Pectoral) Girdle includes the scapula (shoulder blade) and the clavicle (collar bone).
Right Scapula
Clavicle
Acromial end Sternal end
**Be able to distinguish the right scapula from the left scapula.
In order to determine if a scapula is right or left, orient it so the glenoid fossa (articulating surface)
faces laterally (outward) and the spine is posterior (toward back) and superior (upper). The coracoid
process should be superior and anterior.
6-2
Proximal Limbs (Femur – 2 on left and Humerus – 2 on right)
**Be able to distinguish the right femur and humerus from the left femur and humerus.
Identification: These two bones both are large and have a distinct rounded head, allowing for a great
range of movement. The femur has a distinct neck separating the head from the rest of the bone, while
the humerus lacks such a neck.
Determining side: In order to distinguish right from left, first orient the bones so that the rounded head
is superior (up) and pointing medially (toward the body's midline). Then you will need to determine the
anterior vs. posterior side. On the femur, look for the patellar surface, which is anterior. Also note how
the articulating surfaces of the condyles extends far back on the posterior side (since the knee bends
back but not forward). On the humerus, look for the deep olecranon fossa on the posterior side (where
the olecranon process of the ulna fits in when the elbow is straightened). Both specimens above are
from the right side.
6-3
Distal Limbs (from left to right – Tibia, Fibula, Ulna Radius)
Identification: The tibia is a large, heavy bone and thus potentially confused with the femur or
humerus. Note that its superior end is rather flat-topped and lacks any sort of a rounded head. The other
three bones are more slender and could be confused with each other. The fibula is distinguished by
being longer and proportionately more slender than any other bone (the specimens are not quite to scale
here). Also note that it is enlarged and pointed at both ends. The ulna is best identified by the
distinctive U-shaped notch made by the olecranon and coracoid processes (think U for Ulna). The
radius' most distinctive feature is the nearly perfectly round, flat-topped head (think radial).
Determining side: You only need to tell right from left for the tibia, not the smaller bones. To do so,
first orient the tibia so that the larger flatter end is superior (up). The anterior crest (shin) should of
course be anterior (front). Finally, the medial side can be determined by the medial malleolus
(remember that the malleoli bracket the ankle and since the tibia is the medial bone of the lower limb,
its malleolus must be medial). A right tibia is shown.
6-4
Pelvis – Ilium, Ischium, and Pubis
The photo below indicates the three fused bones that make up the pelvis.
6-5
Pelvis
**Know the bone features of the pelvis listed in the picture below.
In order to determine if a pelvis is right or left, hold it with acetabulum facing laterally and the
obturator foramen inferior (down). Now all you need to do is determine which side is anterior vs
posterior, which can be done by looking for the pubic symphysis (anterior) or the sciatic notches
(posterior). The specimen in the photo is a right pelvic bone.
6-6
The Difference Between a Male Pelvis and a Female Pelvis
**Know the difference between a male pelvis and a female pelvis.
In the pictures below, the male pelvis is on the left and the female pelvis is on the right.
6-7
Hands and Feet
**Know the bones of the hands and feet, as shown in the pictures below.
6-8
Articulations/Joints
1. Fibrous joints – sutures, tibiofibular joints, radioulnar joints, and gomphosis joints (between tooth
and jaw)
2. Cartilaginous joints – intervertebral joints, pubic symphysis, joint between manubrium and
sternum, and epiphyseal plate
1. Coracohumeral Ligament
2. Glenohumeral Ligament
6-10
Hip Joint
**Know the following ligaments of the hip joint.
1. Iliofemoral Ligament
2. Ischiofemoral Ligament
3. Pubofemoral Ligament
6-11
Knee Joint
6-13
Bio 137 — Human Anatomy & Physiology I
Bones and Markings of the Appendicular Skeleton
UPPER LIMB LOWER LIMB
Metatarsals
Phalanges
________________________________ ________________________________
* Need to know right from left * Need to know right from left
† Need to distinguish male from female (on
intact pelvis only)
Lab Exercise 7
Cartilage, Bone and Blood Tissues
Integumentary System
Textbook Reference: See Chapter 5 for Cartilage, Bone, and Blood Tissue
See Chapter 6 for the Integumentary System
See Chapter 7 for Introduction of the Skeletal System
What you need to be able to do on the exam after completing this lab exercise:
Be able to recognize/name all three types of cartilage, and give the locations and functions of
each type.
Be able to recognize/name the chondrocytes in lacunae and the visible fibers.
Be able to recognize bone tissue and list its functions.
Be able to name the visible cells and structures on a ground bone microscope slide, as listed in
this lab exercise.
Be able to name the parts of an osteon on the osteon model in the lab (picture not in this lab
exercise).
Be able to recognize blood tissue and give its function.
Be able to name the plasma and the cells on a blood smear slide.
Be able to name all the listed parts of the integumentary system on the skin models.
Be able to name the listed parts of the skin slides.
Be able to give examples of each bone shape and when given a bone be able to give its shape, as
listed in the lab exercise.
Be able to name the parts of a long bone on a bone or picture.
7-1
Cartilage, Bone, & Blood Tissues
Cartilage is a tough, but flexible, tissue in the body. It contains collagen fibers and elastic
fibers. The cells, called chondrocytes, are located in depressions, called lacunae, in the matrix.
There are 3 types of cartilage: hyaline cartilage, elastic cartilage, and fibrocartilage.
Hyaline Cartilage
lacuna (arrow)
7-2
Elastic Cartilage
Function: flexibility
Fibrocartilage
7-3
Identifying Cartilage Tissues Under the Microscope
Procedure:
Hyaline Cartilage
1. Obtain a hyaline cartilage slide and bring into focus using the scanning lens (4X).
Look for the large chondrocytes and lacunae.
2. Focus on the cells, position them to the center of your field of view, and switch to the low
power lens (10X).
3. Focus on a few cells, position them to the center of your field of view, and switch to the
high power lens (40X). Notice the smooth background and the large, distinctive
chondrocytes in their lacunae.
4. Make a drawing of the tissue on high power in the space below. Label the chondrocytes
and lacunae.
Elastic Cartilage
1. Obtain an elastic cartilage slide and bring into focus using the scanning lens (4X). Look
for the dark elastic fibers and large chondrocytes in lacunae.
2. Focus on the cells, position them to the center of your field of view, and switch to the low
power lens (10X).
3. Focus on a few cells, position them to the center of your field of view, and switch to the
high power lens (40X). Notice the dark elastic fibers and the large, distinctive chondrocytes
in their lacunae.
4. Make a drawing of the tissue on high power in the space below. Label the chondrocytes,
lacunae, and elastic fibers.
7-4
Fibrocartilage
1. Obtain a fibrocartilage slide and bring into focus using the scanning lens (4X).
Look for the nearly parallel collagen fibers and chrondrocytes in lacunae.
2. Focus on the cells, position them to the center of your field of view, and switch to the low
power lens (10X).
3. Focus on a few cells, position them to the center of your field of view, and switch to the
high power lens (40X). Notice the collagen fibers and the distinctive chondrocytes in
their lacunae.
4. Make a drawing of the tissue on high power in the space below. Label the chondrocytes,
lacunae, and collagen fibers.
7-5
Bone Tissue
Bone tissue is a living tissue consisting of three types of cells. The mature bone cells are called
osteocytes. The osteocytes are located within shallow depressions, called lacunae, in the hard,
bony matrix.
The basic structural unit of compact bone is called the Haversian system, or osteon. It consists of
a central opening, called the Haversian (or central) canal. Surrounding this canal are concentric
rings of bony matrix. These concentric rings are called lamellae. Between the lamellae are the
osteocytes within lacunae. Very small canals run perpendicular to the lamellae. These tiny
canals are called canaliculi.
Bone tissue
Identification: large, dark circles with
concentric circles surrounding it,
much like tree rings
Location: bones
7-6
Identifying Bone Tissue Under the Microscope
Procedure:
1. Obtain a ground bone slide and bring into focus using the scanning lens (4X). Look for the
circular osteons.
2. Focus on an osteon, position it to the center of your field of view, and switch to the low
power lens (10X).
3. Focus on the lamellae, position them to the center of your field of view, and switch to the
High power lens (40X). Notice dark osteocytes in the lacunae and the tiny canaliculi.
4. Switch back to the low power lens and make a drawing of the tissue in the space below.
Focus on an osteon and label the Haversian (central) canal, lamellae, osteocytes in lacunae,
and canaliculi.
Blood Tissue
Blood tissue consists of a liquid matrix, called plasma, and formed elements. The formed elements
include erythrocytes (red blood cells), leukocytes (white blood cells), and platelets
(thrombocytes).
The erythrocytes are small and pink. They lack a nucleus. The center is depressed and usually
appears lighter than the rest of the cell.
The leukocytes are usually stained purple. They are fewer and larger than the erythrocytes. Most
leukocytes have either a bi-lobed or multi-lobed nucleus.
The platelets are small cell fragments that are stained blue or purple. They are smaller than the
erythrocytes and are scattered between the cells in the tissue.
7-7
Blood
Procedure:
1. Obtain a blood smear slide and bring into focus using the scanning lens
(4X). Look for numerous, very small pink circles with larger purple cells scattered
throughout.
2. Focus on the cells, position them to the center of your field of view, and switch to the low
power lens (10X).
3. Focus on a few cells, position them to the center of your field of view, and switch to the high
power lens (40X).
4. Make a drawing of the tissue on high power in the space below. Label the plasma,
erythrocytes, and leukocytes.
7-8
The Integumentary System
Three main layers of the skin include the epidermis (outermost layer), dermis (main middle layer),
and the hypodermis (innermost layer).
The epidermis is stratified squamous epithelial tissue consisting of 4-5 distinct layers.
The layers of the skin, other than the palms and soles, include:
Stratum corneum – outermost layer consisting of several layers of flattened dead cells
Stratum granulosum – second, thin, layer consisting of cells with keratin granules
Stratum spinosum – thickest layer of the epidermis
Stratum basale – bottom-most dark, thin layer consisting of pigmented cells
The dermis is dense irregular connective tissue. It consists of two main layers: (1) the thin
uppermost papillary layer is folded into peg-like projections called dermal papillae; and (2) the
thick reticular layer, which accounts for the majority of the dermis, consists of several appendages,
including hair follicles, sebaceous glands, arrector pili muscles, sweat glands, Meissener’s
corpuscles, and Pacinian corpuscles.
Most sebaceous glands are formed from the hair follicle and are located beside the hair follicle.
The hair follicle produces the hair. The arrector pili muscle is attached to the hair follicle. When
it contracts, it pulls the hair follicle up and forms a “goose bump”. The sweat glands are located
throughout the dermis and have a duct that leads to the outside of the skin. Meissener’s corpuscles
are small, encapsulated sensory nerve endings located near the top of the dermis. Pacinian
corpuscles are larger plate-like sensory nerve endings located near the bottom of the dermis.
The hypodermis consists of adipose tissue and is not considered part of the skin. It is below the
skin.
7-9
Know the following parts of the skin model:
7-10
7-11
Microscopic Investigation of the Skin
Bald Scalp
7-12
Identifying Skin Tissue Under the Microscope
Procedure:
1. Obtain a skin (scalp) slide and bring into focus using the scanning lens (4X). Look for the
epidermal layers, the hair follicles, and sebaceous glands.
2. Focus on the tissue, position it to the center of your field of view, and switch to the low
power lens (10X).
3. Make a drawing of the tissue on low power in the space below. Label the epidermis, dermis,
hair follicle, and sebaceous gland (if visible). You may need to move the slide around while
viewing it to see all the features.
7-13
Introduction to the Skeletal System
Bone Shape
The Skeletal system consists of bones and ligaments. Human bones come in different sizes and
shapes. Bones can be classified on the basis of shape. Common bone shapes include long bones,
short bones, flat bones, and irregular bones.
Long bones are longer than they are wide. Long bones include all bones of the limbs, except the
patella (kneecap), wrist bones, and ankle bones.
Short bones are smaller than long bones and many are roughly cube-shaped. Short bones include
the wrist bone and ankle bones.
A sesamoid bone is a type of short bone that is shaped like a sesame seed and form in a
tendon. The patella is an example of a sesamoid bone.
Flat bones are flattened bones. Flat bones include the sternum (breastbone), scapulae (shoulder
blades), ribs, and most skull bones.
Irregular bones are irregularly shaped and do not fit into any of the preceding categories. Irregular
bones include the vertebrae and hip bones.
**Know the examples of each type of bone shape on display in the lab
The shaft of a long bone is called the diaphysis. Each knob-like end is called an epiphysis. The
canal that runs through the diaphysis is called the medullary cavity. It is surrounded by a thin
layer of porous spongy bone, which is surrounded by a thicker layer of hard compact bone. The
epiphyses contain spongy bone.
**Know the following parts of a long bone on the long bone model in the lab.
7-14
BIO 137 — Human Anatomy & Physiology I Lab
Connective Tissues
Fill in the following table.
Visible Distinctive
Tissue Cell Types1 Fibers2 Features3 Functions Locations
Hyaline
Cartilage
Elastic
Cartilage
Fibrocartilage
Bone
Blood
Muscles
What you need to be able to do on the exam after completing this lab exercise:
Be able to answer questions covering the Muscle Physiology Pre-Lab Assignment.
Be able to identify the three types of muscle tissue on microscope slides.
Be able to name the distinguishing features of each type of muscle tissue, including nuclei,
striations, and intercalated disks.
Be able to identify the listed muscles on the head/neck model, the muscle man model, the arm
models, and the leg models.
Be able to give the listed functions of the muscles.
8-1
Muscle Physiology Pre-Lab Assignment
8-2
Muscle Tissue
There are three types of muscle tissue: skeletal muscle, cardiac muscle, and smooth muscle.
Skeletal Muscle
Cardiac Muscle
8-3
Smooth Muscle
1. Obtain a skeletal muscle slide and bring into focus using the scanning lens (4X).
Look for long, cylindrical muscle fibers with fine stripes and many nuclei.
2. Focus on the cells, position them to the center of your field of view, and switch to the
low power lens (10X).
3. Focus on a cell or two and position them to the center of your field of view, and switch to
the high power lens (40X).
4. Make a drawing of the tissue on high power in the space below. Label the striations and
nuclei.
Cardiac Muscle Tissue
1. Obtain a cardiac muscle slide and bring into focus using the scanning lens
(4X). Look for cells with fine stripes and dark pink intercalated disks between
them.
2. Focus on the cells, position them to the center of your field of view, and switch to the low
power lens (10X).
3. Focus on a cell or two and position them to the center of your field of view, and switch to the
high power lens (40X).
4. Make a drawing of the tissue on high power in the space below. Label the striations,
intercalated disks, and nuclei.
1. Obtain a smooth muscle slide and bring into focus using the scanning lens (4X). Look for
long cells with many nuclei.
2. Focus on the cells, position them to the center of your field of view, and switch to the low
power lens (10X).
3. Focus on a cell or two and position them to the center of your field of view, and switch to the
high power lens (40X).
4. Make a drawing of the tissue on high power in the space below. Label the nuclei.
Muscles
8-10
**Know the following muscles on the models in the lab and the function of each.
Torso Muscles
Trapezius Shrug shoulders
Latissimus dorsi Extends, adducts, and medially rotates arm
Pectoralis major Flexes, adducts, and medially rotates arm
External oblique Lateral rotation of the vertebral column; twisting
Rectus abdominis Flexion of the vertebral column; sit ups
Define “fatigue.”
Phase 1: ______________________________
Phase 2: ______________________________
Phase 3: ______________________________
9. What are the three factors that determine the strength of a muscle contraction?
.
Muscle Tissues
Fill in the following table.
Skeletal
Cardiac
Smooth
Nervous Tissue
Fill in the following table.
Nervous
1
Describe shape (cylindrical, branching, spindle); use to identify tissue type
2
Number of nuclei per fiber (1 or multiple); use to identify tissue type
3
Special features include any additional identifiable structures except nuclei (which you should be able to identify
for all tissues). These may include striations, intercalated discs, axon/dendrites, cell body, and glial cells.
4
Voluntary or involuntary
Lab Exercise 9
Nervous Tissue
Brain
Cranial Nerves
Spinal Cord
Spinal Nerves
Textbook Reference: See Chapter 11 for histology of nerve tissue and spinal cord
See Chapter 12 for brain and spinal cord anatomy
See Chapter 13 for cranial nerves and spinal nerves
What you need to be able to do on the exam after completing this lab exercise:
Be able to identify nerve tissue and identifying features, such as nerve cell body, nuclelus,
nucleolus, processes, supporting cell nuclei, etc.
Be able to identify the listed parts of the brain on the brain models.
Be able to identify the listed parts of the brain on the sheep brains.
Be able to identify the cranial nerves by name, Roman numeral, and function on the brain and
brainstem models.
Be able to identify the listed parts of the spinal cord on the spinal cord models.
Be able to identify the listed parts of the spinal cord on the spinal cord microscope slides.
Be able to identify the listed plexuses and major spinal nerves on the nerve man model.
For a handy supplemental study guide, please print the “Nervous System Handout” under
“Virtual Lab Nine” on the Virtual Lab website.
9-1
Nervous Tissue
Nervous tissue is composed of two major cell types: supporting cells and neurons.
Supporting cells are non-conducting cells that far outnumber the neurons and function to protect,
support, and insulate the neurons.
Neurons are the large conducting cells of nervous tissue. They all have a nucleus-containing cell
body, and their cytoplasm is drawn out into long extensions (processes). There are two types of
neuron processes, dendrites and axons. Dendrites deliver the nerve impulse to the cell body and the
axon carries the nerve impulse away from the cell body.
Nervous Tissue
9-2
Identifying Nervous Tissue Under the Microscope
Procedure:
1. Place the neuron smear slide on the microscope and bring it into focus using the scanning
objective lens (4X).
2. Locate a large neuron and move it to the center of your field of view.
3. Switch to the low power lens (10X), get the neuron into focus, and move it to the center of your
field of view.
4. Note the processes extending from the cell body. On the slide, you cannot distinguish the
dendrites from the axon. Also, note the small dark spots around the neuron cell bodies. These
are the supporting cell nuclei.
4. Switch to the high power lens (40X) and get into focus using the fine adjustment knob ONLY!
5. Locate the nerve cell body. Identify the nucleus and the nucleolus. The nucleolus will stain
very dark and the nucleus will appear as a lighter halo around it.
6. Make a drawing of a neuron in the space below and label the following: cell body, nucleus,
nucleolus, processes, and supporting cell nuclei.
9-3
The Brain
**Know the following parts of the human brain on the brain models in the lab.
9-4
1. Frontal lobe 20. Hypothalamus 35. Cerebellum
15. Parieto-occipital sulcus 32. Midbrain (includes 30 & 31) II. Optic nerve
19. Thalamus
9-5
Sheep Brain
**Know the following parts of the sheep brain on the sheep brains in the lab.
9-6
9-7
Cranial Nerves
There are 12 pairs of cranial nerves that branch from the brain.
**Know the 12 pairs of cranial nerves by name, Roman numeral, and function on the
brainstem models and brain models.
“On Occasion Our Trusty Truck Acts Funny Very Good Vehicle Any How”
“On Old Olympus’ Towering Tops A Friendly Viking Grew Vines And Hops”
9-8
Brainstem Model
**Know the cranial nerves by name, Roman numeral, and function on the brainstem models
The olfactory nerves lie on the anterior inferior surface of the brain and are not present on the
brainstem models.
9-9
Spinal Cord
**Know the following parts of the spinal on the spinal cord models in the lab.
9-10
1. Posterior funiculus* 9. Central canal
*White Matter
** Gray Matter
9-11
**Know the following parts of the spinal cord on the hanging spinal cord model.
9-12
Spinal Cord
** Know the following parts of the spinal cord on the spinal cord microscope slide.
Gray Matter:
5. Posterior Horn
6. Lateral Horn
7. Anterior Horn
9-13
Structures: White Matter:
1. Posterior Median Sulcus 8. Posterior Funiculus
2. Gray Commissure 9. Lateral Funiculus
3. Central Canal 10. Anterior Funiculus
4. Anterior Median Fissure
9-14
Spinal Nerves
**Know the following plexuses and spinal nerves on the nerve man model.
9-15
Bio 137 — Human Anatomy & Physiology I Lab
II
III
IV
VI
VII
VIII
IX
XI
XII
Bio 137 — Human Anatomy & Physiology I
Nervous System Lab
Students will be responsible for the structures and features listed below
Cranial Nerves (brain stem model): Know number (Roman), name, and function for each and be
able to identify them on the brain stem model (or brain model for olfactory nerve).
III Oculomotor Nerve Superior, inferior and medial movement of the eye
Eye Anatomy
Vision Tests
Ear Anatomy
Hearing Tests
What you need to be able to do on the exam after completing this lab exercise:
Be able to answer any question regarding the reflex/sensory tests, including the name of the
reflex/sensory test, how it is performed, and what it is testing. For example, the patellar reflex
test is testing the conduction of the femoral nerve.
Be able to identify the listed parts of the eye on the eye models.
Be able to answer any question regarding the vision tests, including the name of the test, how the
test is performed, and what the results mean.
Be able to identify the listed parts of the ear on the ear models.
Be able to answer any question regarding the hearing tests, including the name of the test, how
the test is performed, and what the results mean.
10-1
Sensory Tests
Reflexes are involuntary, instantaneous movements in response to stimuli. Reflexes are
mediated via a reflex arc, which includes a receptor, sensory neuron, integration center,
motor neuron, and effector.
Stretch Reflexes
Patellar Reflex
The patellar (knee-jerk) reflex is an example of a stretch reflex. The patellar reflex tests the
conduction of the femoral nerve.
2. Have your lab partner tap the patellar ligament with the blunt side of a patellar reflex hammer.
The tap should be 3-4 inches below the kneecap, and firm, but not hard enough to hurt.
The calcaneal (Achilles) tendon reflex tests the tibial nerve. It is a reflex bending of the foot
resulting from the contraction of the calf muscles when the Achilles tendon is tapped.
1. Kneel on a chair (backwards) with your foot hanging over the front edge.
2. Have your lab partner tap your calcaneal tendon (Achilles tendon).
Corneal Reflex
The corneal reflex involves the automatic blinking of the eye, which is important to keep
material, such as dust and debris, away from the outer layer of the eye, known as the cornea.
1. Have your lab partner try to make you blink by carefully flicking his/her fingers near your
eyes. He/she should come close to the eye without actually touching it.
2. Can you prevent the corneal (blinking) reflex? _______ Yes _______ No
3. Have your lab partner take a clean rubber squeeze bulb and squirt a blast of air across the
surface of the eye.
Foot Reflex
The Babinski reflex involves the extension of the big toe in response to stroking the plantar
surface of the foot. The response is perfectly normal in infants under the age of one. A plantar
response in adults may occur due to damage to the pyramidal tracts and is important in
determining spinal damage. A normal response in adults is to flex the toes.
2. Kneel in a chair (backwards) with the bare foot hanging off the front edge.
3. Have your lab partner stroke your foot from the heel along the lateral, inferior surface and
then toward the ball of the foot using the metal end of the patellar hammer. The pressure
should be firm, but not uncomfortable.
10-3
Sensory Receptors
The two-point discrimination test is the most frequently used test for the assessment of the
sensory outcome after nerve repair. It measures the sensitivity of an area on the skin. It tests the
ability to distinguish between two points.
1. Using a blue caliper and a metric ruler, test your ability to differentiate between two distinct
sensations when the skin is touched simultaneously by two points.
2. Close your eyes and have your partner test the following areas of your body listed in the
following table.
3. Starting the test with the caliper arms completely together, you should feel only ONE point
touch you. Have your partner gradually increase the distance between the two arms, touching the
same area of skin each time, until you feel TWO distinct points touch you. This measurement,
the smallest distance at which you could distinguish two separate points of contact, is the two-
point discrimination threshold. (Your partner should randomly touch you with just one point to
discourage you from guessing.)
4. As soon as you feel TWO distinct points touch you, measure the distance between the two
caliper arms and record the results in the table below.
Back of Hand
Palm of Hand
Fingertip
Back of Neck
Posterior Forearm
10-4
Locating Stimulus with Proprioception
Proprioception is the awareness of the position of one’s body. It is the sense of the orientation
of one’s limbs in space. It is what police officers test for when they pull someone over and
suspect they are drunk.
1. Sit in a chair, rest your forearm on the lab table and close your eyes.
2. Have your lab partner touch your forearm with a felt marker.
3. Keep your eyes closed and with a different color felt marker, try to locate (touch) the same
spot on your arm.
4. Test at least five locations on various parts of the forearm and repeat each location at least
twice.
6. Measure the distance error with a metric ruler and record the result.
Another test:
1. Close your eyes and gently try to touch the lateral corner of your own eye with your fingertip.
2. Have your lab partner watch you and determine the accuracy of your attempt.
3. While your eyes are still closed, bring your hand far behind your head and try to touch the
bottom part of your earlobe or the exact tip to your chin.
Earlobe: _________________________________________________________________
10-5
Eye Anatomy
**Know the following parts of the eye on the eye models in the lab.
10-6
10-7
Vision Tests
Vision Tests
Visual Tracking
Your six extrinsic eye muscles precisely control eye movements. You can test the effectiveness
of these muscles.
2. Have your lab partner move his/her finger slowly from side-to-side while you follow the
finger with your eyes.
3. Ask your lab partner to tell you if your eye movement was smooth or jerky and record below.
The elasticity of the lens is responsible for being able to see clearly far away or close up. The
near point of vision, which is how close you can see something clearly, is about 10cm from the
eye in adults. It is closer in children and farther in old age.
The elasticity of the lens decreases dramatically with age, resulting in difficulty in focusing for
near (or close) vision. You can test the lens elasticity by measuring the near point of
accommodation.
1. Sit in a chair and hold this lab exercise page at arm’s length in front of
one eye.
2. Slowly move the paper toward that eye until the words becomes distorted.
3. Have your lab partner use a metric ruler to measure the distance from your eye to the paper at
this point and record the distance below.
Visual acuity is the sharpness of vision. It is generally tested with a Snellen eye chart, which
consists of letters of various sizes printed on a white card. This test is based on the fact that
letters of a certain size can be seen clearly by eyes with normal vision at a specific distance. The
distance at which the normal eye can read a line of letters is printed at the end of that line.
1. Stand 20 feet in front of the posted Snellen eye chart (hanging on the back wall). There is a
strip of masking tape on the lab floor that marks the 20 foot distance.
2. Have your lab partner stand at the Snellen eye chart. Cover one eye with your hand and read
each consecutive line on the chart aloud and have your lab partner check for accuracy. If you
wear glasses, take the test twice – first with glasses off and then with glasses one. Do not
remove contact lenses, but note that they were in place during the test.
3. Record the number of the line with the smallest-sized letters read correctly.
If the second number is more than 20, you have less than the normal visual acuity. If it is
20/40, you can see at 20 feet what a person with normal vision can see at 40 feet. If it is
20/60, you can see at 20 feet what a person with normal vision can see at 60 feet, and so on.
If the visual acuity is 20/15, your vision is better than normal. You can see at 20 feet what a
person with normal vision can see at 15 feet.
4. Repeat the above process with the other eye and record the results below.
10-9
Pupillary Light Reflex
The pupil of the eye reacts to light. In response to low light, the pupil will enlarge (to allow
more light to enter the eye). In response to brighter light, the pupil will constrict (get smaller to
prevent too much light from entering the eye).
Pupils that dilate in response to bright light, or are sluggish to close, are abnormal and may
indicate a neurological disorder (such as autism, Alzheimer’s disease, etc), or it may indicate
drunkenness.
1. Sit in a chair and have your lab partner shine a pen light quickly in your right eye. Record the
response of the pupil below.
2. Have your lab partner shine the pen light quickly in your left eye and record the response of
the pupil below.
People who are colorblind cannot see certain colors. There are many different types of color
blindness, but red-green color blindness is the most common. There are color vision tests that
can assess if a person has normal color vision or not. Ishihara plates are a common test for color
blindness.
2. Read the plate interpretation instructions for each plate to see if you have a type of color
blindness.
10-10
Ear Anatomy
**Know the following parts of the ear anatomy on the ear models in the lab.
10-11
10-12
Hearing Tests
Hearing Tests
Weber Test
The Weber test is a quick test for determining a hearing impairment. It can differentiate
between conductive hearing loss and sensorineural hearing loss.
1. Sit in a chair and have your lab partner strike a tuning fork and while it is vibrating hold the
handle of the tuning fork to your forehead.
2. Is the sound the same in both ears or is it louder in the left or right ear?
_______________________________________________________
Rinne Test
The Rinne test is a hearing test that compares hearing through the air and bone conduction
hearing through the mastoid process.
1. Sit in a chair and have your lab partner strike a tuning fork and while it is vibrating hold the
handle of the tuning fork on your mastoid process for a few seconds. After the sound
diminishes, hold the fork a few centimeters from the external auditory canal.
10-13
Criteria:
Standing Erect
Facing Forward
Arms at Sides
Palms Forward
1-4
Directional Terminology
When comparing the location of one body part to another, we use directional terms.
Know the following directional terms on Muscle Man:
D is Posterior to C H is Distal to G
F is Lateral to E 1-5
Planes of Reference
A Median (Midsagittal) plane divides the body or an organ into equal Left/Right halves.
1-6
Frontal (Coronal) Section of Sheep Brain
1-7
Regional Terminology
In Human Anatomy & Physiology, we use scientific terms for various regions of the body.
Know the following regional terms on the baby doll:
1-8
1-9
Major Body Organs
1-10
B. Lung I. Kidney
C. Heart J. Adrenal Gland
F. Pancreas K. Urinary Bladder
1-11
Body Cavities
Body cavities are open areas in the body that usually house an organ, bone, or other body part.
1-12
The diagram below lists the organs housed within the body cavities.
1-13
Abdominopelvic Quadrants
In Human Anatomy & Physiology, we sometimes divide the abdominopelvic cavity into
quadrants to make studying the cavity easier.
1-14
Abdominopelvic Regions
In Human Anatomy & Physiology, we sometimes divide the abdominopelvic cavity into nine
regions to make studying the cavity easier.
1-15
Body Systems
For each of the following body systems, know the organs that are listed and to which body
system those organs belong:
Integumentary System
Know the parts of the Integumentary System (listed below) on the skin model in the lab.
A. Epidermis D. Hair
Know the parts of the Skeletal System (listed below the picture) on the knee joint model in lab.
1-17
Muscular System
Know the parts of the Muscular System (listed below the picture) on the muscle man model in
the lab.
1-18
Nervous System
Know the parts of the Nervous System (listed below the picture) on the nerve man model in the
lab.
C. Peripheral Nerves (yellow on diagram; extend from brain/spinal cord) Endocrine System
1-19
Know the listed glands of the Endocrine System on the model board in the lab.
9. Adrenal Gland
You will not need to know the Pineal Gland for the first lab exam. It will be covered when we
study the brain.
1-20
Cardiovascular System
Know the organs of the Cardiovascular System (listed below the picture) on the heart model in
the lab.
A. Heart
C. Arteries
D. Veins
1-21
Lymphatic System
Know the following parts of the Lymphatic System on the diagram displayed in the lab.
Note: The diagram in the lab looks different from this one, but has the same organs.
A. Lymph Nodes
B. Lymph Vessels
C. Spleen
D. Thymus
A. Larynx
B. Trachea
C. & D. Lungs
1-23
Digestive System
Know the parts of the Digestive System (listed below the picture) on the digestive system model
in the lab.
12. Kidney
24. Ureter
Urethra
1-25
Male Reproductive System
Know the parts of the Male Reproductive System (listed below the picture) on the male
reproductive system model in the lab.
1-26
Female Reproductive System
Know the parts of the Female Reproductive System (listed below the model) on the female
reproductive system model in the lab.
21. Ovary
22. Uterus
29. Vagina
1-27