Pasteur Experiment

Recreation of Pasteur’s Experiment

Introduction:

Today, we take many things in science for granted. Many experiments have been performed and much knowledge has been accumulated that people didn’t always know. For centuries, people based their beliefs on their interpretations of what they saw going on in the world around them without testing their ideas to determine the validity of these theories — in other words, they didn’t use the scientific method to arrive at answers to their questions. Rather, their conclusions were based on untested observations.

Among these ideas, for centuries, since at least the time of Aristotle (4th Century BC), people (including scientists) believed that simple living organisms could come into being by spontaneous generation. This was the idea that non-living objects can give rise to living organisms. It was common “knowledge” that simple organisms like worms, beetles, frogs, and salamanders could come from dust, mud, etc., and food left out, quickly “swarmed” with life. For example:

Observation: Every year in the spring, the Nile River flooded areas of Egypt along the river, leaving behind nutrient-rich mud that enabled the people to grow that year’s crop of food. However, along with the muddy soil, large numbers of frogs appeared that weren’t around in drier times. Conclusion: It was perfectly obvious to people back then that muddy soil gave rise to the frogs.

Objective:

In this experiment, you will conduct an experiment similar to the one done by Pasteur whenever he disproved spontaneous generation.

 

Materials Needed:Experiment Set-Up

  • Low-salt broth (chicken or beef, home-made or purchased)
  • 2  250-mL Erlenmeyer flasks
  • 2  1-hole rubber stoppers with bent glass tubing inserted (see diagram)
  • Glycerine
  • Hot plate & pot holders
  • 50-ml Graduated Cylinder
  • Marker

Procedure:

  1. Students should work in teams of 2 to 3 people. Each team should perform the following steps.
  2. Use glycerine and a twisting motion to insert glass tubing into the stoppers. be sure to rinse off excess glycerine with water.
  3. Mark Erlenmeyer flasks accordingly:
    1. Flask 1 with stopper and glass tube going straight up
    2. Flask 2 with stopper and glass tube bent in S-curve
  4. Using a graduated cylinder, place about 50-mL of broth in each Erlenmeyer flask.
  5. Place appropriate lids on flasks.
  6. Use a hot plate to boil broth in flasks with appropriate lids on them for 30 min., then let cool.
  7. For the next ten days, observe the flasks and record any changes in color, turbidity, smell, etc. (Be careful to NOT remove the stoppers from the flasks.)

Data:

Microbial Growth Record
Record the appearance of the flask contents.

Day Flask 1 with Straight Tubing Day Flask 2 with S-shaped Tubing
1 1
2 2
3 3
4 4
5 5
6 6
7 7
8 8
9 9
10 10

Conclusion:

  1. What was the appearance on the broth in each flask on Day 1?
  2. Was their an observed appearance change in flask 1 over the 10 days? Describe the change, if any.
  3. Was their an observed appearance change in flask 2 over the 10 days? Describe the change, if any.
  4. Explain why there was or was not a change in the appearance of the broth in each flask.
  5. Why do you think the idea of spontaneous generation was believed to be true for so long (1000+ years)?
  6. Did your experiment support spontaneous generation of organisms? Explain why or why not?

Metric Measurement Lab

 

Metric Measurement Lab

 

Part A: Count your drops!

 

Take a guess – How many drops of water will it take to equal 1 milliliter? _____ drops

Follow the directions to find the number of drops in 1 milliliter of water, then answer the questions. You will need a small graduated cylinder (25 ml), a beaker of water, and an eyedropper for this section.  Remember to read the bottom of the meniscus when you are reading the volume of a liquid in a graduated cylinder.

 

  1. Fill a small graduated cylinder with 10 ml of water.
  2. Count the number of drops it takes to raise the water to 11 ml. Record the number in the chart.
  3. Leave the water in the graduated cylinder and count the number of drops it takes to raise the water to 12ml. Record the number in the chart.
  4. Leave the water in the graduated cylinder and count the number of drops it takes to raise the water to 13ml. Record the number in the chart.
  5. Calculate your average and round to the nearest tenth.

 

Picture of graduated cylinder

 

# of drops to 11 ml # of drops to 12 ml # of drops to 13 ml Average
 

 

 

Based on your average, how close were you to your guess?________

Based on your average, how many drops would it take to make 1 liter? _______

Part B: Water Displacement

 

Follow the directions to find the volume of three marbles using water displacement.

  1. Add 20 ml of water to a 100 ml graduated cylinder. Record this amount in the chart.
  2. Add three marbles to the cylinder and measure the volume. Record this amount in the chart.
  3. Find the difference between the two measurements and record in the chart. The difference between the two measurements will be the volume of the three marbles.
Volume of Water Before adding Marbles (ml) Volume of Water After Adding Marbles (ml) Difference in Volume (ml) Volume of 3 Marbles
 

 

 

Part C: Mass Mania

 

The gram is the standard unit of mass in the metric or SI system. The basic instrument used to measure mass is the mass balance.  Some mass measurements can be made using an electronic balance.

 

 

  1. Check to see that the Pointer is pointing to zero.
  2. If it is not, check to see that all the Riders (weights) are all the way to the left at the Zero mark.
  3. Adjust the balance by turning the Adjustment Screw slowly until it points to zero.
  4. Place your metric ruler on the pan and read & record the ruler’s mass.
  5. After resetting the balance to Zero, measure and record the mass of the empty 50-ml graduated cylinder and then the 3 marbles.
  6. Reset the balance to ZERO when all items have been massed.

 

 

 

Mass of Metric Ruler (g) Mass of Empty 50-ml graduated cylinder (g) Mass of 3 Marbles (g)
 

 

 

Part D: Volume by Formula

 

Use the formula to find the volume of the box. Measure to the nearest centimeter before calculating your answer.  If necessary, Round your answer to Two Decimal places.

 

Volume = length x width x height

__________ x __________ x __________ =________________cm3

 

Part E: Color Challenge

 

1. Obtain the following items from your teacher:

  • 3 beakers with colored water- 25 ml of each color (red, blue, and yellow)
  • 1 graduated cylinder (25 ml – 50 ml)
  • 1 eyedropper
  • 6 test tubes labeled A, B, C, D, E, and F

2. Perform each step outlined below using accurate measurements.

  1. Measure 17 ml of RED water from the beaker and pour into test tube A.
  2. Measure 21 ml of YELLOW water from the beaker and pour into test tube C
  3. Measure 22 ml of BLUE water from the beaker and pour into test tube E.
  4. Measure 5 ml of water from test tube A and pour it into test tube B.
  5. Measure 6 ml of water from test tube C and pour it into test tube D.
  6. Measure 8 ml of water from test tube E and pour it into test tube F.
  7. Measure 5 ml of water from test tube C and pour it into test tube B.
  8. Measure 2 ml of water from test tube A and pour it into test tube F.
  9. Measure 4 ml of water from test tube E and pour it into test tube D.

3. Complete the chart.

Test Tube Color Final Volume (ml)
A
B
C
D
E
F

Click HERE for Notebook Copy

 

Mitosis Activity

 

Stages of Mitosis

Introduction

Mitosis, also called karyokinesis, is division of the nucleus and its chromosomes.  It is followed by division of the cytoplasm known as cytokinesis.  Both mitosis and cytokinesis are parts of the life of a cell called the Cell Cycle.  Most of the life of a cell is spent in a non-dividing phase called Interphase.  Interphase includes G1 stage in which the newly divided cells grow in size, S stage in which the number of chromosomes is doubled and appear as chromatin, and G2 stage where the cell makes the enzymes & other cellular materials needed for mitosis.

Mitosis has 4 major stages — Prophase, Metaphase, Anaphase, and Telophase. When a living organism needs new cells to repair damage, grow, or just maintain its condition, cells undergo mitosis.

During Prophase, the DNA and proteins start to condense. The two centrioles move toward the opposite end of the cell in animals or microtubules are assembled in plants to form a spindle. The nuclear envelope and nucleolus also start to break up.


Prophase

During Metaphase, the spindle apparatus attaches to sister chromatids of each chromosome. All the chromosomes are line up at the equator of the spindle. They are now in their most tightly condensed form.


Metaphase

During Anaphase, the spindle fibers attached to the two sister chromatids of each chromosome contract and separate chromosomes which move to opposite poles of the cell.


Anaphase

In Telophase, as the 2 new cells pinch in half (animal cells) or a cell plate forms (plant cells), the chromosomes become less condensed again and reappear as chromatin. New membrane forms nuclear envelopes and the nucleolus is reformed.


Telophase

Objective: 

In this lab, you will determine the approximate time it takes for a cell to pass through each of the four stages of mitosis. You may use your textbook and class notes to help you identify the stages of mitosis as seen under the microscope. 

Materials:

Microscope, prepared slide onion root tip or whitefish blastula, textbook, lab worksheet, pencil

Procedure:

  1. Set up a compound light microscope and turn on the light.
  2. Place a slide containing a stained preparation of the Allium (onion root tip) or Whitefish blastula.
  3. Locate the meristematic or growth zone, which is just above the root cap at the very end of the tip or
  4. Focus in on low power, and then switch to medium or high power. Below find micrographs of the four stages of mitosis. Use them to help you identify the stages on the microscope slide.


Prophase (onion)

 


Metaphase (onion)

 


Anaphase (onion)

 


Telophase (whitefish)

 

  1. Now count the number of cells found in each stage of mitosis and place the data in the chart below.
  2. Determine the percentage of time each cell will spend in each stage of mitosis. Divide the number of each cell by the total number of cells and multiply by 100 to determine the percentage. Place these values in the chart below.

 

Stage of Mitosis Number of Cells Percent of time in each stage =

# of cells in stage     X  100%
Total # of Cell

Prophase %
Metaphase %
Anaphase %
Telophase %
Interphase
(Not a Mitotic Stage)
%
Total # cells 100%

 

  1. Line graph the data you have just collected.  Be sure to label the X and Y axis & include the units of measurement.

Title: __________________________________________________

Graph Legend:

 

Questions:

1. Of the four stages of mitosis, which one takes the most time to complete? 

 

2. Which is the shortest stage in duration?

 

3. What would happen if the process of mitosis skipped metaphase?  telophase?

Further Study:

Normal Cell Division may be observed in onion root tips. Many of the processes are similar to those in animal cells. However, in plant cells, the cell plate between daughter cells forms from the Golgi.

Find all of the stages of mitosis and  interphase in the above picture. Make a sketch of each stage and briefly describe what is occurring. Count and record the number of cells you see in each stage.

Projects
Notes

 

Mitosis PPT Questions

Cell Cycle and Mitosis
ppt Questions

Cell Cycle

1.Prokaryotic organisms include ___________, while plants and animals are ____________.

2. Describe prokaryotes.

 

3. How do bacteria asexually reproduce?

4. Name the 3 main steps of binary fission in bacteria.

    a.

    b.

     c.

5. Name a bacterial cell that reproduces by binary fission.

6. Describe eukaryotes.

 

7. How do eukaryotes asexually reproduce cells?

8. The stages in the growth and reproduction of a cell are called the __________ ___________.

9. List the 5 stages in the cell cycle.

 

10. What does G1 stage stand for?

11. Name two things that happen to a cell during G1?

 

12. What is the S stage of the cell cycle?

13. _________ instructions are copied in the S phase as ___________ are duplicated.

14. _______ stands for second growth stage.

15. G2 is the time between ____________ and ___________.

16. Cells continue to _________ during G2 and to make __________ that will be needed for mitosis or cell division.

17. Mitosis or cell division is known as the ________ stage.

18. How does a cell use its energy during the M phase?

19. Does a cell continue growing & making proteins in the M phase?

20. Mitosis is also called _______________ which means division of the ____________.

21. ____________ is called the resting stage and makes up the longest part of a cell’s life cycle.

22. What happens to cells during interphase?

 

23. Are chromosomes visible during interphase?

Mitosis

24. Name the 4 stages of mitosis.

 

25. Name 2 things that happen to a cell during prophase.

     a.

     b.

     c.

     d.

     e.

26. Can chromosomes be seen during prophase?

27. Sketch a eukaryotic chromosome and label the centromere and kinetochore fiber that attaches to it.

 

 

28. How many pairs of chromosomes are found in humans?

29. List 3 things that occur during metaphase.

     a.

     b.

     c.

30. Where are chromosomes located during metaphase of a cell?

31. What stage occurs after metaphase?

32. List 2 things that happen to cells during anaphase.

     a.

     b.

33. Sketch and label the mitotic spindle and attached chromosomes.

 

 

 

 

34. What is the last stage of mitosis?

35. Where are the two sets of chromosomes located at Telophase?

36. What two things reform during Telophase?

37. Chromosomes ___________ during Telophase so they are no longer visible.

38. In plants, what begins to form that will separate the two cells?

39. How are the two cells separated from each other in animals?

 

40. _____________ or division of the cytoplasm follows ___________, division of the nucleus, and forms ____________ daughter cells.

41. How do the two, new daughter cells compare to each other?

 

42. Label the following stages of mitosis.

 

Printable Copy

Leaf Collection Instructions

Arkansas is essentially a forest state because more than half of the state is covered with trees.  The climate and soils of Arkansas also support a great variety of trees, both conifers and deciduous.  Trees are one of Arkansas’ most important crops.  Forests are also valuable in preventing erosion, in offering parks and recreational areas, and in providing homes for wildlife.  In addition, many trees have been introduced into the state as ornamentals.

Leaf collecting is a good way to learn the trees native to your area.  Collecting leaves will also help you to learn leaf margins, shapes, and  venations and how to use different taxonomic keys to identify trees.

Materials needed:

  • leaf press
  • black ink pen
  • pencil
  • small notebook
  • scissors
  • Elmer’s glue
  • art paper, poster board, etc. for mounting
  • labels
  • taxonomic keys (Trees of Arkansas published by the Arkansas Forestry Commission)

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Directions for making a leaf press:
1.   Cut 15 – 20 pieces of corrugated cardboard 30 cm by 50 cm in size.
2. Cut several sheets of newspaper the same size as the cardboard.
3. Lay 10 or 12 sheets of newspaper between each cardboard layer sandwich style.  These sheets will need to be changed every couple of days as they absorb moisture from your leaves; therefore, cut extra sheets.
4. Use one, preferably two, stretch belts to bind the press together.
5. Leave the press in an area so that air can circulate &  more quickly dry the leaves.

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Getting started with your collection:
1. Study the shapes, margins, venations, tips, bases, etc. in your Trees of Arkansas book.

Click here to view reference page

2. Learn to distinguish simple leaves from compound leaves and conifers from deciduous trees.
3. Learn to distinguish a tree from a shrub.
4. Gather your collecting materials together – press, pencil, scissors, & small notebook.
6. Always get permission before collecting leaves on someone else’s property.
7. Be sure to collect at least
two of each type of leaf so both the bottom & top side of the leaf can be shown in your collection.
8. Place leaves in your press immediately after collecting them so they do not start to dry out and wrinkle.
9. Record the name of each leaf, date collected, and place collected in your notebook as you collect.  Also record tree characteristics such as shape of the crown, color and type of bark, etc.

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Collecting:
1. Remember to collect two of every type of leaf!
2. Carefully remove an entire leaf, not a leaflet, from the tree, and place this in your press between newspaper layers.
3. If leaves are damaged or torn, don’t use them because you will not receive credit.
4. Make sure that none of the leaf parts extend beyond the edge of the press.
5. You may also collect &press seeds and/or fruits from some trees if they fit in your press.
6. Leave the leaf in the press for 3 – 5 days depending on its thickness and moisture content.  Remember to change the newspaper when needed.
7. Keep the press in an area where air is circulating (in front of a fan).

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Labeling and identifying:
1. Obtain printed labels from your teacher.
2. Use only black ink to write labels, & do not mark out or white out mistakes on the labels; rewrite them.
3. Use taxonomic keys to identify each leaf, and include both the scientific & common name of the tree on the label.
4. Determine the shape, margin, tip, base, and venation of your leaf and whether it is a simple or compound leaf; record this on your label.
5. Use you key to give a description of the tree, not the leaf.
6. Research uses for the tree, its fruit, etc. and record on your label.
7. Tell if the leaf is deciduous or coniferous.

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Mounting leaves:
1. Use pieces of cut poster board or art paper to mount your leaves.  Make sure all sheets are uniform in size! (The size of your sheets will be determined by your largest leaf.)
2. Use Elmer’s glue to adhere two leaves to each page — one showing the upper surface of the leaf and the other showing the underside of the leaf.
3. Each page should have only one type of leaf on it.
4. Arrange the leaves so they do not overlap each other and so there is room to glue the label in the lower right hand corner.  The leaves should look nice on the page.
5. On compound leaves, mount the topside of the complete leaf and then mount the underside of a single leaflet. Make sure the leaflet comes from another leaf to receive credit!
6. Use a small amount of Elmer’s glue to adhere the completed label in the lower right hand corner of the page.
7. LET THE PAGES DRY COMPLETELY BEFORE ASSEMBLING THEM TOGETHER IN YOUR COLLECTION OR THE PAGES WILL STICK TOGETHER!!!!!
8. Once the pages are dry, lay them in the correct order (see your list of required leaves), and then number the pages in the lower right corner with black ink.
9. Make a stiff front and back cover for your collection from poster board, cardboard, wood, etc.  Include the following items on your cover:

  • title (Tree Identification Through Leaves)
  • your complete name
  • date collection turned into teacher
  • class period
  • subject
  • teacher’s name

10. Use ribbon, string, etc. to bind the pages together or assemble the collection in a scrapbook.  DO NOT COVER THE LEAVES WITH PLASTIC!!!

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Required leaves:
1. Only native, Arkansas trees may be used.  Refer to your Trees of Arkansas book.
2. Leaves must be in perfect condition without damage or tears.
3. No more then 4 oaks are allowed in the collection.
4. No fruit trees such as apple, pear, orange, peach, etc. are allowed.
5. Place the following leaves in your collection first and in this order:

  • sweet gum
  • American sycamore
  • pine (any type)
  • flowering dogwood
  • redbud
  • ash (any type)
  • persimmon
  • Eastern red cedar
  • red or silver maple
  • hickory (any type)
  • pecan
  • pin oak
  • willow oak
  • water oak
  • elm (any type)

6. The remaining leaves that you include must be trees native to Arkansas!

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*Pre AP Biology is required to collect 30 leaves including the 15 required.

 *Biology I is required to collect 20 leaves including the 15 required.

   Pre AP      Biology I