Osmosis Lab Example 2

 

Lab 1: Osmosis & Diffusion

Introduction:
Kinetic energy, a source of energy stored in cells, causes molecules to bump into each other and move in new directions. Diffusion is the result of this contact. Diffusion is the random movement of molecules to an area of lower concentration from an area of higher concentration. Osmosis is a type of diffusion. This is the diffusion of water through a selectively permeable membrane from a region of higher water potential to a region of lower water potential. Water potential is the measure of free energy of water in a solution. A living system also contains an active transport to create movement of particles like ions that move against their concentration gradient. The energy source ATP is used during this process to move the particles across the cell membrane. This experiment takes place to measure the diffusion of small molecules through dialysis tubing. This tubing acts as a selectively permeable membrane, allowing larger molecules to pass through, but slowly. Dialysis is the movement of a solute through a selectively permeable membrane.

When the two solutions on either sides of the membrane are equal and no net movement is detected, the solutions are isotonic. This means that the solutions have the same concentration of solutes. If two solutions differ in the concentration of solutes that each has, the one with more solute is hypertonic. The solution that has less solute is hypotonic.

Water potential is predicting the movement of water into or out of plant cells. It is abbreviated by the Greek letter psi and has two components; a physical pressure component, pressure potential, and the effects of solutes, solute potential. Water always moves from an area of high to low water potential. The equation is water potential equals the sum of pressure potential and solute potential.

In a plant cell, turgor pressure is necessary. This is a pressure available to plants in a hypotonic environment. Turgor pressure gives plants their structure and strength. When a plant cell is in an isotonic solution, the turgor pressure decreases, causing wilting in the plant structure. In hypertonic solutions, plants plasma membrane shrinks away from the cell wall, an action termed plasmolysis.

 

Hypothesis:
Diffusion and osmosis occur between different molar solutions until the solutions are isotonic, effecting the turgor pressure of plant cells.

 

Materials:
Lab 1A – The materials used in conducting this experiment are as follows: one 30cm strip of dialysis tubing (presoaked), distilled water, 15%glucose/1%starch solution, 250mL beaker, Iodine Potassium Iodide solution, glucose Testape, and string.

Lab 1B – The materials used in conducting this experiment are as follows: six presoaked strips of dialysis tubing, distilled water, 0.2M, 0.4M, 0.6M, 0.8M, and 1.0M solutions of sucrose, six 250mL glass beakers, string, and an electronic balance.

Lab 1C – The materials used in conducting this experiment are as follows: six 250mL glass beakers, a potato, a core borer, a knife, distilled water, , 0.2M, 0.4M, 0.6M, 0.8M, and 1.0M solutions of sucrose, string, a ruler, and an electronic balance.

Lab 1D – The materials used in conducting this experiment are as follows: graph paper, pencil, a ruler, a calculator, and colored pencils.

Lab 1E – The materials used in conducting this experiment are as follows: a light microscope, microscope slide, cover slip, distilled water, NaCl solution, paper, pencil, and onion skin.

 

Procedure:
Lab 1A: Obtain a 30cm piece of dialysis tubing that has been presoaked in distilled water. Tie off one end securely. Open the other end of the dialysis tube and insert 15mL of 15%glucose/1%starch solution. Tie off the other end of the bag, leaving room for expansion. Record the color of the solution within the bag. Test the 15%glucose/1%starch solution for the presence of glucose using Testape. Fill a 250mL beaker with distilled water and add approximately 4mL of Lugol’s solution (IKI) to the distilled water. Test this solution for the presence of glucose as well with the Testape. Record the results in the data table. Immerse the bag in the beaker of solution. Let this stand for approximately 30min, or until distinct coloration is observed. Record final colors of solutions in the bag and in the beaker. Test both solutions once more for the presence of glucose with the Testape strips.

Lab 1B: Before starting this lab, wash your hands. Obtain six 30cm dialysis strips that have been presoaked in distilled water. Tie off each end securely. Pour approximately 25mL of each sucrose molar solution into its respective bags (that should be labeled, but not on the tubing itself). Tie off the other ends securely with string, careful to get any air bubbles out and leaving room for expansion. Rinse off each bag and blot off the water. Weigh and record the initial mass of the dialysis bags in the data table. Fill six 250mL glass beakers 2/3 full of distilled water and label each beaker with its respective bag’s molarity of sucrose. Immerse each bag into the distilled water. Allow this to stand for thirty minutes. Remove each bag, blot the sides to get off extra solution and weigh and record mass in grams each bag and determine the mass difference and percent change in mass. Next, compare the group percentages to the class.

Lab 1C: Pour 100mL of the assigned sucrose solutions into their 250mL beakers (pre-labeled). Obtain a large potato. Using a core borer, take 24 samples out of the potato, and measure each in centimeters so that they are all equal in length (use the knife to slice off ends). Make sure not to leave any skin with the samples. Place these cores in a covered beaker until an electronic balance can be obtained. Determine the mass of four cores at a time, placing the four in their sucrose solutions. Record this data for each of the six beakers. Allow these potato samples to sit immersed in the solutions overnight, covered. Remove the cores, blot off excess solution, and weigh the samples, recording the mass in the data table. Determine the mass difference, the percent change in mass and the class average percent change in mass. Graph the increase and decrease in mass of the potato cores according to the molarity of the solutions they were placed in on graph 1.2.

Lab 1D: Using paper, a pencil, and a calculator determine the solute potential of the sucrose solution, the pressure potential, and the water potential. Also, obtain graph paper and graph the values given for the zucchini percent change in mass and molarity of sucrose solutions in the graph 1.3.

Lab 1E: Prepare a wet mount slide of onion skin. Observe under a light microscope and sketch what you see. Add a few drops of the NaCl solution, observe, and sketch what you see there as well.

 

Data:
Table 1.1 The presence of glucose in beaker and bag solutions

 

Initial Contents

 

Initial Solution Color

 

Final Solution Color

 

Initial Presence of Glucose

 

Final Presence of Glucose

 

Bag

15%glucose/1%starch solution Clear Midnight blue + +
 

Beaker

Water and IKI indicator Amber Amber +

Table 1.2 Dialysis Bag Results: Individual Data

 

Contents in Bag

 

Initial Mass

 

Final Mass

 

Mass Difference

 

Percent Change in Mass

 

Distilled water

28 g 28g 0g 0%
 

0.2M sucrose

26.9g 28.5g 1.6g 5.95%
 

0.4M sucrose

27.0g 29.4g 2.4g 8.89%
 

0.6M sucrose

28.4g 32.6g 4.2g 14.79%
 

0.8M sucrose

28.2g 32.0g 3.8g 13.48%
 

1.0M sucrose

29.9g 34.8g 4.9g 16.39%

Bags immersed @ 12:01pm, removed at 12:31pm.

Table 1.3 Dialysis Bag Results: Class Data

 

Group 1

 

Group 2

 

Group 3

 

Group 4

 

TOTAL

 

Class Average

 

Distilled water

0% 0% .71% .38% 1.09% 0.27%
 

0.2M sucrose

5.95% 4.01% 5.41% 1.75% 17.12% 4.28%
 

0.4M sucrose

8.89% 8.63% 8.89% 8.42% 34.83% 8.71%
 

0.6M sucrose

14.79% -8.06% 10.69% 9.61% 27.03% 6.76%
 

0.8M sucrose

13.48% 15.19% 12.33% 15.70% 56.70% 14.10%
 

1.0M sucrose

16.39% 7.29% 15.13% 12.50% 51.31% 12.83%

Table 1.4: Potato Core: Individual Data

 

Contents in Beaker

 

Initial Mass

 

Final Mass

 

Mass Difference

 

Percent Change in Mass

 

Class Average % Change

 

Distilled water

3.4g 4.1g .7g 20.59% 15.93%
 

0.2M sucrose

3.4g 3.5g .1g 2.94% -2.77%
 

0.4M sucrose

6.2g 5.3g 0.9g -14.52% -16.55%
 

0.6M sucrose

6.3g 4.8g 1.5g -23.81% -22.83%
 

0.8M sucrose

6.2g 4.4g 1.8g -29.03% -25.72%
 

1.0M sucrose

6.0g 4.3g 1.7g -28.33% -28.17%

Table 1.5: Potato Core Results: Class Data

 

Group 1

 

Group 2

 

Group 3

 

Group 4

 

TOTAL

 

Class Average

 

Distilled water

20.59% 13.33% 14.81% 15.00% 63.73% 15.93%
 

0.2M sucrose

2.94% -3.39% -7.69% -2.94% -11.08% -2.77%
 

0.4M sucrose

-14.52% -18.64% -15.38% -17.65% -66.19% -16.55%
 

0.6M sucrose

-23.81% -26.23% -23.08% -18.18% -91.30% -22.83%
 

0.8M sucrose

-29.03% -26.32% -26.92% -20.59% -102.86% -25.72%
 

1.0M sucrose

-28.33% -29.31% -30.78% -24.24% -112.66% -28.17%

Questions:

Which substance(s) are entering the bag and which are leaving the bag? What experimental evidence supports your answer? Iodine Potassium Iodide is entering the bag because the indicator’s color is concentrated in the bag when the IKI started only in the beaker. Glucose and water left the bag, the evidence was the Testape color.

 

Explain the results you obtained. Include the concentration differences and membrane pore size in your discussion. The results simply state that the water, glucose, and IKI were small enough molecules to pass through the selectively permeable membrane. The starch didn’t leave the beaker because its color was amber and the starch molecule was much too large to pass through the selectively permeable membrane.

 

Quantitative data uses numbers to measure observed changes. How could this experiment be modified so that quantitative data could be collected to show that water diffused into the dialysis bag? Quantitative data would include the initial and final percent concentrations of the glucose, therefore showing the concentration of water by the change of percent in glucose. The movement would be noticeable in the concentration because it is known that water moves from high water potential to a low water potential.

 

Based on your observations, rank the following by relative size, beginning with the smallest: glucose molecules, water, IKI, membrane pores, and starch molecules. The smallest substance was IKI, followed by water, glucose, the membrane pores, then the starch molecules.

 

What results would you expect if the experiment started with a glucose and IKI solution inside the bag and only starch and water outside? Why? Based on the size of the molecules, the glucose and IKI would move out of the bag, the water in, and the starch left in the beaker again.

 

Explain the relationship between the change in mass and the molarity of sucrose within the dialysis bags. These two things are directly proportional. As the mass increases, so does the molarity.

 

Predict what would happen to the mass of each bag in this experiment if all the bags were placed in a 0.4M sucrose solution instead of distilled water. Explain your response. These are inversely proportional because whenever the sucrose molarity inside the bag is more concentrated, it will become more dilute and vise versa. The solutions will reach equilibrium somewhere between the two concentrations.

 

Why did you calculate the percent change in mass rather than simply using the change in mass? The differences in mass don’t deal with the proportional aspect of the solutions, making the real results less accurate. The percent was calculated to give the exact difference, along with considering the quantities of solution.

 

A dialysis bag is filled with distilled water and then placed in a sucrose solution. The bag’s initial mass is 20g, and its final mass is 18g. Calculate the percent change of mass, showing your calculations in the space below. 18g(final mass) – 20g(initial mass)=-2/20g(initial mass) x 100, which gives you a 10% change of mass.

 

If a potato is allowed to dehydrate by sitting in the open air, would the water potential of the potato cells decrease or increase? Why? The water potential of the potato would decrease because water moves from a high water potential region to a low potential region, and a dehydrated potato cell is hypertonic in comparison with the environment, forcing water to come into the cell. The moving in part shows that the potato cell had a low water potential.

 

If a plant cell has a lower water potential than its surrounding environment, and if pressure is equal to zero, is the cell hypertonic or hypotonic to its environment? Will the cell gain water or lose water? Explain your response. If the plant cell has lower water potential, that means the water will come into the cell, the cell is hypertonic to its environment. This cell will gain water because water follows its concentration gradient.

 

In figure 1.5, the beaker is open to the atmosphere. What is the pressure potential of the system? The pressure potential in this figure is equal to zero.

 

In figure 1.5, where is the greatest water potential? The greatest water potential is within the dialysis bag.

 

Water will diffuse__the bag. Why? Water will diffuse out of the bag because the highest water potential is inside the bag, forcing the water out.

 

Calculate solute potential of the sucrose solution in which the mass of the zucchini cores does not change. Show work. Y s =iCRT therefore Y s=(1)(1.0mole/liter)(0.0831 liter bar/mole degrees K)(295 degrees K) Y s=-24.51 bars.

 

Calculate the water potential of the solutes within the zucchini cores. Show work. Y =Y s+Y p so Y =0+-24.51 , Y =-24.51bars

 

What effect does adding solute have on the solute potential component of that solution? Why? Adding solute to a solution would increase the solute potential and decrease the water potential.

 

Consider what would happen to a red blood cell placed in distilled water:
Which would have the higher concentration of water molecules?The distilled water would have the higher concentration of water molecules.

 

Which would have the higher water potential? The red blood cell would have the higher water potential.

 

What would happen to the red blood cell? Why? The red blood cell would take in a lot of water and might lyse due to pressure inside. This is a possibility because animal cells have no tolerance under hypotonic situations.

 

Describe the appearance of the onion cells. The onion cells appear to have great turgor pressure, spread out, thick and bright in the inside. The cell walls were very defined and it was clear where one cell ended and another began.

 

Describe the appearance of the onion cells after the NaCl was added. The plasma membrane shriveled from the cell wall, causing plasmolysis. The cells looked wrinkly or weak. The turgor pressure dropped tremendously.

 

Remove the cover slip and flood the onion with fresh water. Observe and describe what happened. The onion cells were again hypertonic to their environment, and gathered water, increasing in turgor pressure and restoring themselves to the normal state of being.

 

What is plasmolysis? Plasmolysis is the separation of the plasma membrane from the cell wall in a plant cell.

 

Why did the onion cell plasmolyze? The environment became hypertonic to the cell and the water left the cell running with its concentration gradient due to the NaCl. With all the water leaving the cell, it shrank, leaving behind its cell wall.

 

In the winter, grass often dies near roads that have been salted to remove ice. What causes this to happen. The salt causes the grass’s environment to become hypertonic, and the water leaves the plant cells, causes withering and eventually death of the plant.

 

Error Analysis:
Lab 1A: One possible source of error could be the tightness of the string that tied off the dialysis tubing. If there was a leak or a break in the dialysis tubing, all of the data would be off.

Lab 1B: A possible source of error in this lab could have been in the first step. If the handler of the dialysis tubing did not wash their hands and accidentally touched the sac part of the tubing, the oils from their hands could have blocked some of the pores on the tubing, distorting the data.

Lab 1C: A piece of potato skin could have been left in the beakers along with the potato. This causes problems in the data tables. Another possible source of error could be that the students did not pat dry the potato sample well enough causing drops to be left on the electronic balance, tarring it incorrectly, causing all other data to be off slightly.

Lab 1D: Simple mathematical errors always occur, so there is always room for simple algebraic mistakes in this section of the lab.

Lab 1E: If the wet sample was not prepared correctly, or the salt solution added to fast not giving the cells time to react, this lab would have different results. The sources of error also include the possible concept that the onion cells might have dried out by the time the observer got around to sketching. This could cause error in observances, and data in conclusion.

 

Discussion and Conclusion:
During Lab 1A, the data suggests what molecules can and cannot diffuse across a selectively permeable membrane. The coloration showed that the Iodine Potassium Iodide was small enough to pass through the pores of the membrane because the color of this indicator moved from within the beaker to in the bag. Water and glucose moved out because water is small enough to pass through the membrane and the glucose tested positive with the Testape inside the beaker. The glucose at the beginning was only in the bag, so it obviously moved out.

Lab 1B proved that water moves across the selectively permeable membrane of the dialysis tubing much easier than sucrose sugar does. The water moved to reach equilibrium between the solutions. Sucrose must be too large a molecule to pass through the membrane quickly.

Lab 1C showed that the potato samples took in water when immersed in a distilled water solution. Potatoes must contain sucrose molecules due to the conclusion of this lab because the potatoes take in water in the distilled water beaker. Potatoes had a lower water potential and higher solute potential than the distilled water. It is just the opposite inside the beaker.

 

Lab 1D’s calculations made it evident that all of the results could be determined and proved correct with simple algebra equations and formulas. This gives the lab much better illustration and a stable understanding of diffusion and osmosis.

Lab 1E showed the plasmolysis clearly and allowed the student to see exactly what goes on in this action. This particular part of the lab illustrated the shrinking of the plasma membrane from the cell wall in a plant cell. It shows how plant cells react in a hypertonic environment. The turgor pressure decreases a lot, and the cells become very weak when the water leaves the cell.

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Osmosis Lab3 Sample

 

Osmosis Through the Cell Membrane of an Egg
by Brett Helms

Introduction:
An egg can be used to show the process of osmosis through the egg’s cell membrane. Osmosis is the process in which water diffuses across a cell membrane from an area of high concentration to an area of low concentration. Osmosis occurs when the cell needs to release water to the exterior of the cell membrane or it can occur when water needs to diffuse into the cell. Diffusion is the movement of molecules from an area of high concentration to an area of lower concentration. Diffusion and osmosis are both types of passive transport. A passive transport is the movement of molecules across a cell membrane without the cell having to exert any energy. Water will move into the cell when the solution is hypotonic to the cytosol. A hypotonic solution is defined as a solution whose solute concentration is lower than that inside a cell. The cell membrane is the thin outer layer of a cell. It allows certain substances to diffuse across, into and out of the cell. When a solution is hypertonic the solute concentration is higher than that inside a cell. This would result in molecule movement into a cell. When a solution is isotonic, the solute concentration equals that inside a cell. This would result into no movement of molecules across the cell membrane. Molecules that are very small but not soluble in lipids may diffuse across the membrane by moving through the pores of the cell membrane.

 

Hypothesis:
The water and the vinegar will diffuse through the cell membrane more easily then the syrup.

 

Materials:
The materials used included paper, pencil, 200ml beakers, vinegar, distilled water, syrup, 2 eggs, tray, plastic wrap, colored marker, tape, and a digital balance.

 

Methods:
The two eggs were weighed on a digital balance and their initial masses were recorded. The eggs were then placed in a beaker of vinegar to dissolve the calcium shell and leave the cell membrane exposed. The eggs were weighed after they were removed from the vinegar and their masses were recorded. The two eggs were then placed in a beaker of syrup.  The eggs were once again weighed on the digital balance and their masses recorded. The eggs were then placed a beaker of distilled water. After the eggs were removed and their weights and appearance recorded.

 

Results:

 

Results of Osmosis
Table for Egg 1

 

Solutions Egg Mass Before in Grams Observations Before Placed in Solution Egg Mass After in Grams Observations After removed from Solution
Vinegar 56.9g Hard exterior 84.3g Egg lost shell
Syrup 84.3g Shell had a firm jelly-like membrane 48.4g Outside not firm anymore, very shriveled
Water 48.5g The jelly-like membrane was soft and not firm at all 77.9g Egg firmed up and looked like the shell just came off

 

 

Results of Osmosis
Table for Egg 2

 

 

Solutions

 

Egg Mass Before in Grams

 

Observations Before placed in solution

 

Egg Mass After in Grams

 

Observations After removed from solution

Vinegar 60.5g Hard exterior 87.65g Egg Lost Shell
Syrup 87.65g Shell had a firm jelly-like membrane 54.4g Outside not firm anymore
Water 54.4g The jelly-like membrane was soft and not firm at all 79.3g Egg firmed up and looked like the shell just came off

 

1. When the egg was placed in the water, in which direction did the water molecules move? The water molecules moved into the egg.

2. On what evidence do you base this? The egg mass increased.

3. How do you explain the volume of liquid remaining when the egg was removed from the syrup? It was less because some had moved into the egg.

4. When the egg was placed in the water after being removed from the syrup, in which direction did the water move? The water moved into the egg.

 

Error Analysis:
This experiment is based upon changes in egg mass in various solutions. The balance used was not checked for accuracy with two standard masses. The changes in masses may or may not be correct.

 

Discussion and conclusion:
There were significant increases in egg mass when the eggs were submerged in vinegar and water. However there was a significant decreased in egg mass when the eggs were submerged in syrup causing the egg to appear shriveled. The reason for the increasing and decreasing is called diffusion, which is the movement of molecules from an area of high concentration to an area of lower concentration. That is why when the egg was submerged in syrup much of the water in the egg diffused out because of the higher amount of water in the egg compared to the smaller amount in the syrup. That is also why when the egg was placed in vinegar and in distilled water its mass increased meaning that more water molecules moved into the eggs because the solution outside the egg was lower in water than that inside the egg. These results support the hypothesis that water diffuses from an area of high to an area of low concentration across a cell membrane. This experiment demonstrated the process of osmosis through the egg cell membrane.

BACK

 

Osmosis & Diffusion in Egg Lab

 

Osmosis & Diffusion in an Egg

 

Objective:
In this investigation, you will use a fresh hen’s egg to determine what happens during osmosis & diffusion across membranes.

Materials: (per lab group)
1-2 fresh hen eggs in their shells, masking tape & marker, distilled water, clear sugar syrup (Karo, for example), vinegar, clear jar with lid, tongs, electronic balance, paper towels, paper, pencil

Procedure:

Day 1   

  1. Label the jar with your lab group & the word “vinegar”.
  2. Mass the egg with the electronic balance & record in the data table.
  3. Carefully place the raw egg into the jar & cover the egg with vinegar.
  4. Loosely re-cap the jar & allow the jar to sit for 24 to 48 hours until the outer calcium shell is removed.

Day 2   

  1. Open the jar & pour off the vinegar.
  2. Use tongs to carefully remove the egg to a paper towel & pat it dry.
  3. Record the size & appearance of your egg in your data table.
  4. Mass the egg on an electronic balance & record.
  5. Clean and re-label the jar with your lab group & the word “distilled water”.
  6. Carefully place the egg into the jar & cover the egg with distilled water.
  7. Loosely re-cap the jar & allow it to sit for 24 hours.

Day 3   

  1. Open the jar & discard the distilled water.
  2. Use tongs to carefully remove the egg to a paper towel & pat it dry.
  3. Record the size & appearance of your egg in your data table.
  4. Mass the egg on an electronic balance & record.
  5. Clean and re-label the jar with your lab group & the word “syrup”.
  6. Carefully place the egg into the jar & cover the egg with clear syrup.
  7. Loosely re-cap the jar & allow it to sit for 24 hours.

Day 4   

  1. Open the jar & pour off the syrup.
  2. Use tongs to very carefully remove the egg & rinse off the excess syrup under slow running water.
  3. Pat the egg dry on a paper towel.
  4. Record the size & appearance of your egg in your data table.
  5. Mass the egg on an electronic balance & record.
  6. Clean up your work area & put away all lab equipment.

Data:

 

RESULTS OF DIFFUSION

Original Mass Final Mass Appearance of Egg
VINEGAR
WATER
SYRUP

 

 

Questions & Conclusion:

1. Vinegar is made of acetic acid & water. Explain how it was able to remove the calcium shell.

 

2. (a) What happened to the size of the egg after remaining in vinegar?

(b) Was there more or less liquid left in the jar?

   (c) Did water move into or out of the egg? Why?

 

3. (a) What happened to the size of the egg after remaining in distilled water?

(b) Was there more or less liquid left in the jar?

   (c) Did water move into or out of the egg? Why?

 

4. (a) What happened to the size of the egg after remaining in syrup?

(b) Was there more or less liquid left in the jar?

   (c) Did water move into or out of the egg? Why?

 

5. Was the egg larger after remaining in water or vinegar? Why?

 

6. Why are fresh vegetables sprinkled with water at markets?

 

7. Roads are sometimes salted to melt ice. What does this salting do to the plants along roadsides & why?

 

 

 

 

Origin of life PPT Qs

Origin Of Life
ppt Questions

Early Thoughts on Life

1. What was Aristotle’s idea about how life arose called?

2. What is another name for spontaneous generation?

3. Explain spontaneous generation of life.

 

4. How long did the idea of abiogenesis or spontaneous generation last?

5. The idea of abiogenesis lasted so long because, instead of testing their ideas, people based their beliefs on what?

 

6. Were their observations tested?

7. Did they use the scientific method for their observations?

Examples of Spontaneous Generation

8. What observation about new life did Egyptians make when the Nile River flooded each year?

 

9. What observation about new life did Medieval farmers make when they stored their grain each year?

 

10. The English people centuries ago, threw their garbage and sewage out on the streets. What observation about new life did these people make?

 

 

11. This practice led to a plague that killed many Europeans. What was this plague called and what carried the disease organism?

 

 

 

12.Before refrigerators, large slabs of meat were hung after being purchased. What observation about new life was made from this practice?

 

 

13. People believed so strongly in abiogenesis that they had recipes for making living things. Name two organisms that had accepted recipes.

 

Disproving Spontaneous Generation

14. Francesco ____________ was an early scientists who conducted experiments to try and disprove spontaneous generation.

15. What was Redi’s hypothesis?

 

16. Explain how Redi tried to prove this.

 

 

 

17. What were the results Redi found in the closed jars & why?

 

18. What were the results in the open jars?

 

19. How did maggots appear in the open jars?

 

20. Complete this table summarizing Redi’s experiment:

 

Evidence Against Spontaneous Generation
Unsealed Jar
Sealed Jar
Gauze Covered jar

 

21. Redi’s experiment disproved spontaneous generation for _____________ organisms.

Use of the Scientific Method

22. Did Francesco Redi use the scientific method in his experiment?

23. What served as the control in Redi’s experiment?

 

24. What jars served as the experimental groups?

25. What was Redi’s conclusion?

 

Disproving Spontaneous Generation of Microbes

26. Anton Van _______________ made one of the first simple microscopes.

27. Leeuwenhoek called the living things he saw in pond water ______________.

28. By the end of the 19th century, these organisms were known as ______________.

29. John _____________ did experiments with microorganisms growing in broths.

30. Needham believed there was a __________ __________ present in nonliving substances like air.

31. Why were bacteria able to grow in Needham’s soups?

 

32. What could have been done to the broths to kill the bacteria already present?

33. What scientists repeated this experiment but with boiled broth?

34. After boiling, what did Spallanzani do to the tops of the bottles? how did this help?

 

35. Critics of Spallanzani’s experiment said there was not enough _______ for the bacteria to survive and that boiling had destroyed the _________ __________.

The Theory Changes

36. What did the Paris Academy of Science do in 1860 to solve the problem?

 

37.Who won the prize? 

38. What was Pasteur’s experimental hypothesis?

 

39. What was the shape of Pasteur’s flasks? Include a sketch.

 

 

40. What was the special S-shaped neck intended to do?

 

41. Did Pasteur boil the broth in his flasks? Why?

 

42. The flasks were left at ___________ locations.

43. Did the broth change cloudy because microbes were growing in it?

 

44. What was visible in the neck of the flask after collecting there?

45. Once the S-shaped stem was broken off the top of the flasks, what happened to the broth and why?

 

46. Pasteur’s S-shaped flasks kept ___________ out but let ______ inside.

47. Pasteur’s experiment proved that living things only come from other _________ ___________.

48. What is the name of Pasteur’s theory?

Review

49. Where did the maggots come from in Redi’s experiment?

50. What was the purpose of the sealed jars?

51. Redi was trying to disprove – spontaneous generation or biogenesis?

52. Where did the microbes come from in Needham’s broth?

53. Needham & Spallanzani were trying to disprove – spontaneous generation or biogenesis?

54.Who proved biogenesis?

 

 

 

Organic Model Project Bi

 

Constructing Monomers of Organic Molecules

 

 

 

Introduction

Almost all molecules made by cells are composed of carbon atoms bonded to one another and to atoms of other elements (especially H, O, N). Compounds made by cells and containing carbon are known as organic compounds. Carbon can form four covalent bonds with other carbons or other types of atoms. Cells make a huge number of large molecules from a small set of small molecules. These smaller molecules are called monomers and are linked together to make larger molecules known as polymers. Four main groups of organic compounds exist — carbohydrates, lipids, proteins, and nucleic acids.

The monomers of carbohydrates are called monosaccharides or simple sugars. the 3 monosaccharides, glucose, fructose, and galactose, all have the same chemical formula, C6H12O6, but their structural formulas are different.

Glucose Fructose
Galactose

 

The monomers monomers that make up lipids are glycerol and fatty acid chains. Saturated fatty acid chains have all single bonds between carbons, while unsaturated fatty acids will have 1 or more double bonds between carbons in the chain.

Glycerol Fatty Acid
[Glycerol]

The monomers making up proteins are called amino acids. Twenty different amino acids exist, but they all have the same basic structure — a central carbon has a single hydrogen , an amine group (-NH2), a carboxyl group (-COOH), and a side or R group attached. The side group determines the difference in properties.

Basic Amino Acid Structure

Two Simple Amino Acids

 

Glycine Alanine

 

Nucleic acids include DNA and RNA. The monomers of nucleic acids are called nucleotides and are composed of a pentose (5-sided sugar), a nitrogen containing base, and a phosphate group (-PO4). The sugar found in DNA is called deoxyribose, while the sugar in RNA is called ribose.

 

Deoxyribose Ribose

 

Objective

Each student will construct a monomer of an organic compound found within organisms. You may construct one of the following — glucose, fructose, galactose, glycine, alanine, glycerol, saturated or unsaturated fatty acid, deoxyribose, or ribose.

Materials

Various materials may be used for the atoms that make up a nucleotide such as styrofoam balls, plastic coke bottle caps, beads, etc. Bonds between atoms may be made from toothpicks, plastic stirring sticks, popsicle sticks, etc. Single & double bonds must be represented by the correct number of “sticks”. The atoms and bonds may NOT be made of any food item. Your model should be glued together to make the model rigid for hanging. Attach string and a label with the nucleotide’s name to your model. Models must be sturdy, light weight, and small enough to hang from the ceiling.

Color Code for atoms:

CARBON – BLACK
HYDROGEN – YELLOW
OXYGEN – RED
NITROGEN – BLUE