Lab 1 Osmosis

 

Lab 1 Osmosis & Diffusion

osmosis lab

Osmosis Lab Introduction:

Cells have kinetic energy.  This causes the molecules of the cell to move around and bump into each other.  Diffusion is one result of this molecular movement.  Diffusion is the random movement of molecules from an area of higher concentration to areas of lower concentration.  Osmosis is a special kind of diffusion where water moves through a selectively permeable membrane (a membrane that only allows certain molecules to diffuse though).  Diffusion or osmosis occurs until dynamic equilibrium has been reached.  This is the point where the concentrations in both areas are equal and no net movement will occur from one area to another.
If two solutions have the same solute concentration, the solutions are said to be isotonic.  If the solutions differ in concentration, the area with the higher solute concentration is hypertonic and the area with the lower solute concentration is hypotonic.  Since a hypotonic solution contains a higher level of solute, it has a high solute potential and low water potential.  This is because water potential and solute potential are inversely proportional.  A hypotonic solution would have a high water potential and a low solute potential.  An isotonic solution would have equal solute and water potentials.  Water potential (y) is composed of two main things, a physical pressure component, pressure potential (yp), and the effects of solutes, solute potential (ys).  A formula to show this relationship is y = yp + ys.  Water will always move from areas of high water potential to areas of low water potential.
The force of water in a cell against its plasma membrane causes the cell to have turgor pressure, which helps maintain the shape of the cell.  When water moves out of a cell, the cell will loose turgor pressure along with water potential.  Turgor pressure of a plant cell is usually attained while in a hypotonic solution.  The loss of water and turgor pressure while a cell is in a hypertonic solution is called plasmolysis.
Hypothesis:
During these experiments, it will be proven that diffusion and osmosis occur between solutions of different concentrations until dynamic equilibrium is reached, affecting the cell by causing plasmolysis or increased turgor pressure during the process.
Materials:
Lab 1A – To begin Lab 1A, first collect the desired equipment.  The materials needed are dialysis tubing, Iodine Potassium Iodide (IKI) solution, 15% glucose/ 1% starch solution, glucose Testape or Lugol’s solution, distilled water, and a 250-mL beaker.
Lab 1B – For Lab 1B you will need to collect six presoaked dialysis tubing strips, distilled water; 0.2M, 0.4M, 0.6M, 0.8M, and a 1.0M sucrose solution; six 250-mL beakers or cups, and a scale.
Lab 1C – Lab 1C these items are needed: a potato, knife, potato core borers, six different solutions, and a scale.
Lab 1D – During Lab 1D, only paper, pencil, and a calculator will be needed to make the calculations.
Lab 1E – n Lab 1E these items are needed: a microscope slide, cover slip, onion cells, light microscope, and a 15% NaCl solution.
 Procedures:
Lab 1A – After gathering the materials, pour glucose/starch solution into dialysis tubing and close the bag.  Test the solution for presence of glucose.  Test the beaker of distilled water and IKI for presence of glucose.  Put the dialysis bag into the beaker and let stand for 30 minutes.  When time is up test both the bag and the beaker for presence of glucose.  Record all data in table.
Lab 1B – Obtain the six strips of dialysis tubing and fill each with a solution of a different molarity.  Mass each bag.  Put each bag into a beaker of distilled water and let stand for half and hour.  After 30 minutes is up, remove each bag and determine its mass.  Record all data in its appropriate table.
Lab 1C – sing the potato core borer, obtain 24 cylindrical slices of potato, four for each cup.  Determine the mass of the four cylinders.  Immerse four cylinders into each of the six beakers or cups.  Let stand overnight.  After time is up, remove the cores from the sucrose solutions and mass them.  Record all data in its appropriate table.
Lab 1D – Using the paper, pencil, and calculator collected, determine solute potentials of the solutions and answer the questions asked to better understand this particular part of the lab.
Lab 1E – Using the materials gathers, prepare a wet mount slide of the epidermis of an onion.  Draw what you see of the onion cell under the microscope.  Add several drops of the NaCl solution to the slide.  Now draw the appearance of the cell.
Data:
Lab 1A – Table 1.1

 

Contents  Initial Color Final Color Initial Presence of Glucose  Final Presence of Glucose
  Bag 15% Glucose/ 1% Starch Solution    clear Dark blue       + +
  Beaker  H2O+IKI Orange to brown Orange to brown      _ +

 

Lab 1A Questions
1)     Glucose is leaving the bag and Iodine-Potassium-Iodide is entering the bag.  The change in color of the contents of the bag and the presence of glucose in the bag prove this.
2)     In the results, the IKI moved from the beaker to the bag, this caused the change in the color of the bag.  The IKI moved into the bag to make the concentrations outside the bag equal to inside the bag.  The glucose solution moved out of the bag making glucose present in the beaker.  The glucose moved to make the solute concentration inside and out of the bag equal.
3)     If the initial and final percent concentration of glucose and IKI for in the bag and the beaker were given, they would show the differences and prove the movement of these substances to reach dynamic equilibrium.
4)     Based on my observations, the smallest substance was the IKI molecule, then the glucose molecules, water molecules, membrane pore, and then the starch molecules being the largest.
5)     If the experiment started with glucose and IKI inside the bag and starch in the beaker, the glucose and IKI would move out of the bag to make the concentrations equal, but the starch could not move into the bag because its molecules are too big to pass through the semipermeable membrane.

Lab 1B –  Table 1.2   Dialysis Bag Results

 

Contents in dialysis bag Initial mass Final mass Mass difference Percent change in mass
a) distilled       water 26.5g 26.6g 0.1g 0.4%

 

b)0.2M 28.1g 29.3g 1.2g 4.3%
c)0.4M 27.3g 30.1g 2.8g 10.3%
d)0.6M 28.3g 32.3g 4.0g 14.1%
e)0.8M 25.9g 30.7g 4.8g 18.5%
f)1.0M 26.7g 32.9g 6.2g 23.2%

 

Table 1.3     Dialysis Bag Results: Class Data

 

Group 1

Group 2

Group 3

Group 4 Total Class Average
Distilled Water 0.4% 1.16% 0.79% 1.54% 3.89% 1.0%
0.2M 4.3% 5.99% 6.44% 5.94% 22.67% 5.67%
0.4M 10.3% 10.49% 10.33% 8.45% 39.57% 9.89%
0.6M 14.1% 14.86% 16.04% 15.1% 60.1% 15.03%
0.8M 18.5% 19.80% 17.97% 20.0% 76.27% 19.07%
1.0M 23.2% 18.77% 23.55% 21.9% 87.42% 21.86%

 

Lab 1B Questions:
1)     The molarity of the sucrose in the bag determines the amount of water that either moves into or out of the bag, which changes the mass.  For example, when the bag contained a 0.2M solution, water entered the bag to make the concentrations inside and outside of the bag more equal.  As this happened, the mass rose 1.2g
2)     If each of the bags were placed into a 0.4M solution instead of distilled water, the masses of the bags would have changed in different ways.  The mass of the bags filled with distilled water and 0.2M sucrose would have gone down because water would have left the bag.  The mass of the 0.4M bag would have stayed the same because the concentrations are now equal.  The masses of the 0.6, 0.8, and 1.0M bags would have increased because water would have moved into the bag to equalize the concentrations.
3)     In the data collected, the percent change in mass was calculated to show how greatly the mass increased or decreased.  The difference in mass is not enough to go by because the initial masses of the dialysis bags were not all the same.
4)     If a dialysis bag’s initial mass was 20g and it’s final mass was 18g, the percent change in mass is 20%.
5)     The sucrose solution in the beaker would have been hypotonic to the distilled water in the bag.
Lab 1C        Table 1.4

 

Contents of Beaker Initial Mass Final Mass Difference in Mass % Change in Mass Initial Temp. Final Temp.
Distilled Water 1.5g 2.0g 0.5g 33% 20°C 20°C
0.2M 1.5g 1.6g 0.1g 7% 21°C 20°C
0.4M 1.5g 1.6g 0.1g 7% 20°C 20°C
0.6M 1.5g 1.5g 0.0g 0% 21°C 20°C
0.8M 1.5g 1.2g -0.3g -20% 21°C 20°C
1.0M 1.5g 1.4g -0.1g -7% 20°C 20°C

 

Lab 1C        Table 1.5     Class Results

 

Percent Change in Mass of Potato Cores
Group 1 Group 2 Group 3 Group 4 Total Class Average
Distilled Water 33% 35.29% 25% 31.25% 124.54% 31.14%
0.2M 7% 29.41% 25% 13.33% 74.74% 18.69%
0.4M 7% 11.11% -12.5% -12.5% -6.89% -1.7%
0.6M 0% -15.79% -18.75% -20% -54.54% -13.64%
0.8M -20% -15.79% -18.75% -25% -79.54% -19.89%
1.0M -7% 0% -18.75% -20% -45.75% -11.44%

 

Lab 1 D Questions:
1)  The water potential of the potato core after dehydrating will decrease because the water within the potato would evaporate and therefore lower the water potential.
2)     The solute concentration of the plant cell is hypertonic because the solute concentration is higher than the water concentration.  Because of this, water will diffuse into the cell to reach dynamic equilibrium.
3)     The pressure potential of the system is equal to 0.
4)     The water potential is greater in the dialysis bag.
5)     Water will diffuse out of the bag since the water potential is higher in the bag and water moves from areas of higher water potential to areas of lower water potential.
6)     Zucchini cores placed in sucrose solutions at 27°C resulted in the following percent changes after 24 hours:

Percent Change in Mass  Sucrose Molarity
20% Distilled Water
10% 0.2M
  -3% 0.4M
-17%  0.6M
 -25% 0.8M
-30% 1.0M

 

8)ys=-iCRT
ys=-(1)(0.35)(0.0831)(295)
ys=-8.580075

y=0+ys
y=0+(-8.580075)
y=-8.580075
9) Adding solute to a solution increases solute potential because the solute concentration increases.
10) The distilled water would have a higher concentration of water molecules and would also have a higher water potential.  The red blood cells would increase in size because water is moving from the area of higher water potential (the distilled water) to the area of lower water potential (the red blood cells) until dynamic equilibrium is reached.
Lab 1E Questions
1) After preparing a wet mount slide, I have observed the onion cells under magnification and they appear to be small, empty boxes pushed closely together.
2) By adding two or three drops of NaCl the cells should have shrunk, but no change took place.
3) The cells maintained the same shape.
4)  Plasmolysis is the lose of water and turgor pressure in a cell.
5)  The onion cells should have plasmolyzed because the area surrounding them had a lower water potential and water should have moved out of the cells.
6)  Grasses that live on the sides of roads that have been salted in the winter end to dies because the water is drained from the cells as it moves out of the grass cells into the hypertonic NaCl area around it.

Lab 1D Plasmolysis of Cells – Drawings of onion cells

100X
Onion Cells in Distilled Water

*Picture Of onion cells in saline not available.
Error Analysis:
Lab 1A – The data collected in this lab experiment did not seem to contain any inconsistencies, so therefore no human error is detected.
Lab 1B – In this lab experiment, the data seems to be compliant with the data collected by the other lab groups, so no human error was thought to have happened.
Lab 1C – There was some discrepancy in this experiment in the 1.0M solution’s percent change in mass of potato cores.  The data decreases consistently until the 1.0M solution, so human error is thought to be a factor in this.  Some mistakes that could have taken place are miscalculations in initial and final masses or problems with the molarity of the solution itself.
Lab 1D – In this part of the lab, only calculations were made, so no human error probably occurred during this time.
Lab 1E – In part 1E, after adding the NaCl solution to the onion cells, the cells should have reduced in size, but no reaction took place.  This may have occurred in part because the onion itself was already dried out and dehydrated, or while the onion was being looked at through the microscope, the heat from it may have caused the cells to loose water.
Conclusion:
During the experiment conducted in Lab 1A, the results and data collected make it possible to conclude that glucose and Iodine Potassium Iodide can pass through a selectively permeable membrane and will if the concentrations on either side are not equal. In Lab 1B, it can be concluded that sucrose cannot pass over a selectively permeable membrane, but instead water molecules will move across the membrane to the area of lower water potential to reach dynamic equilibrium. Lab 1C provided information that helps to conclude that potatoes do contain sucrose molecules.  This can be stated because the cores took in water while they were emerged in the distilled water.  This means they had a lower water potential and higher solute potential than the distilled water.  The solute potential is equal to about a 0.6M solution of sucrose according to the data collected. During Lab 1D calculations were made and questions were answered to help give a better understanding of water and solute potential. If the onion cell experiment in part 1E of the lab would have produced correct results, conclusions could have been made.  It is thought that the onion cells would have plasmolyzed due to the addition of NaCl to the cells.  This shows how the onion cells had high water potential and moved to the area outside the cell with lower water potential.  Then, after adding water back to the cells, water would have moved back into the cells increasing turgor pressure.
The water potential played an enormous role in each part of this lab.  Since water moves areas of high water potential to areas of low water potential, reactions took place in each part resulting in different conclusions being derived from them.  Water potential was a key element in each part of the experiment. In plant and animal cells, loss or gain of water can have different effects.  In a plant cell, it is ideal to have an isotonic solution.  If the solution is hypertonic, the cell will shrivel from lack of water intake.  Inversely, if the solution is hypotonic the cell could take in too much water and the cell will lyse and break open.  For a plant cell, the ideal solution is a hypotonic solution because the cell takes in water increasing turgor pressure which keeps the cells tightly packed and keep their shape.  If the solution is hypertonic, the cell will plasmolyze and died from lack of water.  In an isotonic solution, the plant cell does not have enough turgor pressure to keep is shape.


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Lab 11a Behavior Ap

 

Lab 11   Animal Behavior

Introduction:

 

Ethology is the study of animal behavior. An animal’s behavior is its response to sensory input. There are three types of behaviors: orientation, agonistic, and mating.

Orientation behaviors take the animal to its most favorable environment. Taxis is when an animal moves toward or away from a stimulus. Taxis is often characterized by light, heat, moisture, sound, or chemicals. Kinesis is another type of movement that involves orientation. Kinesis is a movement that is random and doesn’t involve a stimulus. So an animal would respond to light by moving everywhere in random directions.

Agonistic behavior is when animals respond to each other in aggressive or submissive movements. Like the hair on dogs backs when they get ready to fight. Another excellent example is the Betta fish, which is sometimes studied in labs.

Mating behaviors are activities that involve finding, courting, and mating with a member of the same species. An example would be a peacock fluffing up its feathers to attract females.

 

Hypothesis:

 

Pill bugs will prefer the wet side to the dry side of the petri dishes because they are used to living in dark moist conditions, such as under rocks or in rotting trees.

 

Materials:

 

Materials used in this experiment involved: a double petri dish combination, 10 pillbugs, bedding material, scissors, pencils, 2 pieces of filter paper, a piece of black construction paper, and a watch.

 

Methods:

Place 10 pillbugs in the petri dishes along with a little bedding material in each container. Observe them for about 10 minutes noting any observations that are characteristic to the bugs. Once that is done, take a piece of filter paper and soak it in water, then put the wet piece in the bottom of one of the containers. Put the other dry paper in the bottom of the other container. Put 5 pillbugs on each side and count how many bugs there are on each side every 30 seconds for 10 minutes.

Our designed experiment involved the same methods except substituting filter paper with a piece of black construction paper. Cut out the circular paper from a sheet of black paper and put it in one of the containers along with some bedding material. Place 5 pillbugs on each side and count how many there are on each side every 30 seconds for 10 minutes.

 

Results:

Table 11.1

 

 

Time (mins)

 

Number in wet Chamber

 

Number in dry Chamber

0 5 5
.5 9 1
1.0 8 2
1.5 8 2
2.0 9 1
2.5 10 0
3.0 9 1
3.5 7 3
4.0 9 1
4.5 9 1
5.0 8 2
5.5 7 3
6.0 9 1
6.5 7 3
7.0 7 3
7.5 7 3
8.0 8 2
8.5 9 1
9.0 7 3
9.5 8 2
10.0 9 1

 

 

Table 11.2

 

Time (Mins) Number in wet Chamber Number in dry Chamber
0 5 5
.5 9 1
1.0 6 4
1.5 7 3
2.0 5 5
2.5 6 4
3.0 5 5
3.5 7 3
4.0 6 4
4.5 8 2
5.0 3 7
5.5 2 8
6.0 6 4
6.5 0 10
7.0 2 8
7.5 5 5
8.0 0 10
8.5 2 8
9.0 1 9
9.5 5 5
10.0 7 3

 

 

 

1. What conclusion do you draw from your data? Explain physiological reasons for the behavior observed in this activity.

– The bugs preferred it in the wet conditions. They probably like it there because they live in place like that, under rocks or in trees or just in the soil. That is probably the only way they can keep cool and obtain moisture.

 

2. Obtain results from all lab groups in your class. With respect to humidity, light temperature, and other environmental conditions, which types of environment do isopods prefer? How do the data support these conclusions? Give specific examples.

– Our class didn’t exchange data with each other.

 

3. How do isopods locate appropriate environments?

– They use their antennae for a lot of their locating. One thing that I observed was they did use their antennae when they were walking around. They probably don’t have very good eyesight.

 

4. If you suddenly turned a rock over and found isopods under it, what would you expect them to be doing? If you watched the isopods for a few minutes, how would you expect to see their behavior change?

– I would expect them to scurry around, probably find and tunnel and go down it to keep out of the sunlight. If you found one that wasn’t already underground, I would probably see it walking out in the grass, looking for another object to go under.

 

5. Is the isopod’s response to moisture best classified as kinesis, or taxis? Explain your response.

– I think it’s best classified as kinesis because they moved around in random directions. Some of them just sat there while the others were moving around.

 

1. Select one of the variable factors above, and develop a hypothesis concerning the pillbug’s response to the factor.

– Background Color- I hypothesize that the pillbugs will prefer the dark background color over the light background color because they are used to living in dark places for most of their lives.

 

2. Use the material available in your classroom to design an experiment. Remember that heat is generated by lamps.

A) State the objective of your experiment.

– To see if background color has anything to do with behavioral responses in pillbugs to their environment.

 

B) List the materials you will use.

– Scissors, black construction paper, pillbugs, petri dish containers, and bedding material, as well as a watch.

 

C) Outline your procedure in detail.

– Our designed experiment involved the same methods as the real experiment except substituting filter paper with a piece of black construction paper. Cut out the circular paper from a sheet of black paper and put it in one of the containers along with some bedding material. Place 5 pillbugs on each side and count how many there are on each side every 30 seconds for 10 minutes.

 

 

Error Analysis:

 

Not many things could have drastically changed our results. All we had to do was to watch them and watch the time. If the bugs were forced into one of the chambers then that could have changed our results. Also if we hadn’t had kept a good time method then we could have been lost.

 

Conclusions:

 

The bugs like it in the wet environment because that is what it’s used to. It’s an easy way to get water and stay cool in their environment. They also liked the dark background because, again, that is what they are used to in their environment, under rocks or other things.

 

 

Lab 10 – Physiology of the Circulatory System

 

 

Lab 10   Physiology of the Circulatory System

 

 

 

Introduction: The human circulatory system is a collection of structures thorough which oxygen and nutrient rich blood flows to all tissues of the body for metabolism and growth, and to remove metabolic wastes. The blood is pumped to these tissues by the heart through a circuit composed of arteries, arterioles, capillaries, venules, and veins. Oxygenated blood is pumped to the tissues from the left side of the heart, whereas deoxygenated blood is pumped to the lungs from the right side of the heart. This circuit where gas exchange takes place within the alveoli of the lung is very important and is known as the pulmonary circuit. When the body is exercised changes can take place in the circulatory system that allow more blood to pass to actively respiring muscle cells and less to nonmuscular tissue. Increased heart rate, arterial pressure, body temperature, and breathing rate also occur during exercise.

Arterial blood pressure is directly dependant on the amount of blood pumped by the heart per minute and the resistance to blood flow through the arterioles. This is an important measurable aspect of the circulatory system and it is measured using a sphygmomanometer. This device has an inflatable cuff that connects to a hand pump and a pressure gauge, graduated in millimeters of mercury, by rubber tubing. The cuff is wrapped around the upper arm and inflated, the person taking the pressure then listens for two sounds and observes the gauge to determine what the blood pressure is. The systolic number is determined by the first noise heard as the cuff is deflated, and the diastolic number is determined by the last distinct noise heard.

Hypothesis: From this experiment it is expected that a subject’s heart rate and blood pressure will change during rest and exercise based on how physically fit they are. If the subject is in good shape the heart rate will not increase significantly and the blood pressure will increase. The opposite is true of someone in poor shape.

Materials: The materials used in this experiment include a blood pressure kit, alcohol swabs, a stopwatch, two depression slides, a cotton ball, four rubber bands, a pipet, a petri dish, a Daphnia culture, a stereomicroscope, and some ice.

Methods:

A. Measuring Blood Pressure: To measure blood pressure, one member of the lab group sat down in a chair, rolled up his sleeve, and then the sphygmomanometer cuff was placed around his upper left arm at heart level. The cuff was then pumped to 200mm Hg, which is safely higher than the blood pressure of the subject. The stethoscope was then placed in the well of the subject’s elbow, where the brachial artery is located, and pressure was slowly released as the taker listened for a pulse. The pressure on the gauge was noted when first sound of Korotkoff was heard, which is the pressure that blood is first able to pass through the artery during systole, representing systolic pressure. The sounds of Korotkoff are heard between the systolic and diastolic blood pressures. The diastolic pressure is the reading of the gauge at the time the sounds of Korotkoff can no longer be heard. The subject’s blood pressure was taken two more times and an average was calculated and recorded in Table 1.

 

Average Blood Pressure

 

 

 

Systolic Pressure

 

Diastolic Pressure

Age in Years Men Women Men Women
10 103 103 69 70
11 104 104 70 71
12 106 106 71 72
13 108 108 72 73
14 110 110 73 74
15 112 112 75 76
16 118 116 73 72
17 121 116 74 72
18 120 116 74 72
19 122 115 75 71
20-24 123 116 76 72
25-29 125 117 78 74
30-34 126 120 79 75
35-39 127 124 80 78
40-44 129 127 81 80
45-49 130 131 82 82
50-54 135 137 83 84
55-59 138 139 84 84
60-64 142 144 85 85
65-69 143 154 83 85
70-74 145 159 82 85

 

B. Physical Fitness Test: The first numbers recorded from this section of the experiment were those of standing vs. resting blood pressure. To do this a member of the lab group had to lie down on a table for five minutes. After five minutes the subject’s blood pressure was taken while he was still lying down and the numbers were recorded in Table 2. The subject remained lying down for another two minutes, stood up, and their blood pressure was taken again. The standing systolic pressure was subtracted from the resting systolic pressure and recorded in Table 2. A chart was used to determine the number of points received by the subject and recorded in Table 3.

The next part of this section is where the subject’s standing heart rate was determined. Taken by the subject was the radial artery pulse by counting the number of beats for 30 seconds. That number was multiplied by 2 to obtain the number of beats per minute. That number was recorded in Table 3. Another chart was used to determine the amount of points the subject received for this section and that number was also recorded in Table 3.

Next the resting heart rate was determined by having the subject lie down on a table for five minutes. After five minutes the subject’s pulse was taken and recorded in Table 3. Once again a chart was used to determine the number of points the subject received for this section of the experiment and the number was recorded in Table 3.

Next the Baroreceptor reflex test was given to the subject. The subject had to lie down for five minutes, stand up quickly, and record the pulse. From this number the resting heart rate was subtracted and recorded in Table 3. A chart was then used to determine the number of points the subject received for this section and recorded in Table 3.

The endurance test was the last leg of this section of the experiment. To do this the subject stepped up with one foot onto an 18 inch high surface and then brought up the other foot onto the surface. This was continued for 15 seconds, and then his pulse was taken at several intervals. First the pulse was taken right after the exercise for 15 seconds and multiplied by four. This was repeated one more time after that as well. Then the pulse was taken every 30 seconds for 120 seconds after that. The data was recorded in Table 4. The amount of time it took for the subject’s heart rate to return to normal was figured and a chart was used to award points. These heart rates were then compared to the standing heart rate. Next, the standing heart rate was subtracted from the rate taken right after exercise, and yet another chart was used to award points.

 

C. Investigating Heart Rate in Daphnia: Two depression slides were obtained and a small piece of cotton was placed in the center of one of the slides. Several Daphnia were placed on the slide with a pipet and the other slide was placed on top of this slide and wrapped together with a rubber band on each end. A petri dish was filled with room-temperature water, 1cm deep and the slides were placed into it. The heart of the largest Daphnia was then located under the stereomicroscope and the number of beats in 15 seconds was determined, multiplied by four, and the results placed in Table 5. Into the dish was then added ice water and the same Daphnia’s heart rate was determined and recorded in Table 5. Gradually warm water was added and the heart rate was taken at five minute intervals until the normal heart rate is noted. These results were put in Table 5.

Results:

Table 1

 

 

Blood Pressure Systolic Diastolic
Trial 1 115 72
Trial 2 115 70
Trial 3 115 74
Average 115 72

 

Table 2

Standing vs. Resting Blood Pressure

 

Position Systolic Diastolic
Lying Down 5 min. 110 72
Lying to Standing 120 72
Change 10 0

 

 

Table 3

Fitness Points

 

Activity Result Fitness Points
Change in Blood Pressure 10 3
Standing Pulse Rate 78 3
Resting Pulse Rate 64 3
Baroreceptor Reflex 76 3
Heart Rate Recovery After Exercise 28 4
Heart Rate Increase After Exercise 18 2
Total Points – 18

 

 

Table 4

Heart Rate After Exercise

 

Interval No. of Beats Heart Rate
0 to 15 sec. 24 X4= 96
16 to 30 sec. 19 X4= 76
31 to 60 sec. 35 X2= 70
61 to 90 sec. 35 X2= 70
91 to 120 sec. 35 X2= 70

 

 

 

Total Score Cardiovascular Fitness
17 to 18 Excellent
14 to 16 Good
8 to 13 Fair
7 or less Poor

 

 

 

Questions:

1. What changes occur in the circulatory system when a person stands up from a prone position? How do these changes affect the heart rate and blood pressure of the individual?

 

The circulatory system is not working very hard when a person is at rest so when that person stands up suddenly the blood pressure and heart rate of that person increase.

 

2. How does the circulatory system, and the heart in particular, of a conditioned athlete differ from that of a person in poor shape?

 

The heart of a conditioned athlete is stronger because it has been worked harder pumping more blood when that person exercises. The heart of a person in poor shape has not been worked as hard.

 

3. Why is high blood pressure dangerous? What health problems does it lead to?

 

High blood pressure is dangerous because the heart has to work to hard to push the blood through the various veins and arteries and a heart attack can occur.

 

4. What sort of behaviors encourage high blood pressure? Why?

 

Eating fatty foods and not exercising cause high blood pressure because the heart is not working hard to pump the blood, which makes it weak.

 

Table 5

 

 

Temperature (C) Heartbeats per Minute
Room Temperature 200
0 to 5 84
10 160
15 152
20 204
25 200
30 212
35 216

 

 

Change in Metabolic Rate

 

 

Temperature Range Rate of the reaction (change in heart rate)
0-10 Q10 =1.9
10-20 Q10 =1.275
20-30 Q10 =1.04

 

 

 

Questions:

1. Why does the rate of activity of ectothermic organisms increase with a rise in the temperature of its environment? How is this different from an endothermic organism?

 

Ectothermic organisms’ body heat is determined by the environment, so their metabolic rates also change with this. Endotherms have a constant body temperature and do not change their metabolic rate strictly based on environmental conditions.

 

2. If this experiment were performed on a human subject, what results would you expect? Explain.

 

A human’s heart would also be affected by the temperature changes, but not to the extent that the Daphnia heart did.

Error Analysis: The only possible source of error in this lab would have been the slight misreading of the gauge on the sphygmomanometer.

Conclusions: Cardiovascular fitness is very important to living a healthy life. If one doesn’t exercise and eat healthy foods they run a risk of being in poor shape and having a heart attack or other serious things. Heart rate and blood pressure readings can give a person a good idea about how healthy they are or how healthy they need to be. Blood pressure is so important to a person’s health it is checked at every visit to the doctor or hospital.

 

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Lab8 Requirements

Lab 8   Population Genetics Write Up

Introduction:

Read and summarize the lab introduction being sure to include both HW equations and what each variable stands for, explain what a population is and what type of population HW applies to, list and explain the 5 assumptions necessary for HW to be true, and be sure to give a brief description (not the procedures) for each of the 4 cases in the lab.

Hypothesis:

Use the objective (s) for the lab and write them into a single statement for your hypothesis.

Materials:

In sentence form list the materials you will need including paper, pencil, PTC paper, index cards, and calculator.

Procedure:

Type 4 paragraphs, one for each case study. Remember to write in paragraph form without numbering steps.

Data & Analysis:

·        Include the 4 case study sheets with all calculations completed

·        Write out and answer the questions from your lab sheet. Remember to underline the question, but not the answer.

·        Write out and answer the questions at the end of Lab 8 in your lab manual.  Remember to underline the question, but not the answer.

Conclusion:

·        Explain the effect each of the situations had on the allele frequencies and genotypic frequencies (include supporting data)

·        Explain why each condition could or could not actually occur in nature

·        Explain the effect natural selection has on recessive traits

·        Explain how the HW law helps determine whether evolution is occurring

Click Here For Case Study Sheets

 

Lab 7 Sample 3 Fruitflies

Drosophila Genetics

Introduction

Drosophila Melanogaster, the fruit fly, is a great organism for genetic use because it has simple food requirements, occupies little space, is hardy, completes its life cycle in 12 days, makes a large number of offspring, can be knocked out easily, and it has many types of hereditary variations that can be seen with low power microscopes. Drosophila has a small number of chromosomes, four pairs. They are easily located in the large salivary glands. The Drosophila can be obtained from many places. Research of Drosophilae has led to a lot of knowledge about many of its genes.

Many factors combine to affect the length of the Drosophila life cycle. Temperature affects the life cycle the most. At room temperature the average life cycle of the Drosophila is about 12 days. Eggs of the Drosophila are small, oval shaped, and have two filaments at one end. They are usually laid on the surface of the culture medium, and with practice, can be seen with the naked eye. After one day the eggs hatch into the larva.

The larval stage of the Drosophila eats all the time. Larvae tunnel into the culture medium when they eat. The larva will shed its skin as it increases in size. In the last of the three larval stages, the cells of the salivary glands contain giant chromosomes that can be seen under low power in a microscope.

The pupal stage. Before a larva becomes a pupa it climbs the side of the container. The last larval covering then becomes harder and darker, forming the pupal case. Through this case the later stages of metamorphosis to an adult fly can be seen. In particular, the eyes, the wings, and the legs become visible.

The adult stage. When metamorphosis is over, the adult fly emerges form the pupal case. They are fragile and light in color and their wings are not fully expanded. They get darker in about an hour. They live about a month and then die. A female refrains from mating for about 12 days after she emerges from the pupal case. After she mates her receptacles contain large amounts of sperm and she lays her eggs. Make sure that the first flies you use are virgins.

The experiment will take several weeks. You will be assigned Drosophila with well-defined mutant traits by your teacher. You will keep a close record of what happens as each of these flies mate and pass there traits off to their offspring over a few generations.

There are three types of crosses that are studied in this lab. In monohybrid crosses the mode of inheritance is determined when a single contrasting pair of characteristics is involved. In a dihybrid cross the mode of inheritance is determined when the two pairs of contrasting of characteristics are considered simultaneously. In a sex-linked cross the mode of inheritance is determined when the mutant characteristic is associated with the X chromosome.

Hypothesis

In the sex linked cross of Drosophila Melanogaster, a phenotypic ratio of 1:1 will be obtained.

Materials

The materials used in this lab are as follows: a vile of Drosophilia with c designated trait, vials containing a medium, a refrigerator, ice packs, Petri dishes, a light microscope, a vial of wild type flies, an incubator, a pencil and paper.

Methods

Begin by obtaining a vial of wild type flies. Practice immobilizing and sexing these flies. Make sure to examine the flies and determine the characteristics of their eyes, wings, bristles, and antennae. Next, these are the steps for immobilizing the flies. Hold the vial containing the flies at an angle and place it in a refrigerator for several minutes. When the flies are immobilized, place them into a small plastic Petri dish. Then place the Petri dish on top of the icepack in order to maintain the cool temperature necessary to keep flies immobilized. Use the dissecting microscope to view the flies. Make sure to top the petri dish on when viewing the flies.

You can easily distinguish male flies from females by looking for the following characteristics: males are usually smaller than the females, males have dark blunt abdomens and females have lighter pointed abdomens. The males have sex combs, which are black bristles on the uppermost joint of the forelegs. Next, get a vial containing experimental flies. Make sure to write down the number of the vial that you have. The flies you now have are the P1 generation. The females should have laid eggs. The eggs and larvae are the F1 generation. Then after there are eggs present knock out remove the adult flies from the vial. Sex the adult flies and write down any mutations. Place the flies in the morgue that contains alcohol. Make sure to label the vial with the symbols for the mating.

After about another week has passed knock out and record characteristics of the remaining F1 flies and record the results in table 7.1. Then place the six pairs of these flies in a new vial and place the remaining flies in the morgue. Label the new vial F1, and tell the cross, date and your name.

After another week has passed, remove the F1 flies and put them in the morgue. The F2 generation are the eggs and larvae in the vial. Place the vial back into the incubator. Once again, after another week has passed remove the F2 flies and record their sex and characteristics and place the results in Table 7.2. Recording a greater number of F2 flies will make your results more accurate. Try to collect at least 200 flies. In order to analyze your data you will first have to be able to be able to complete Chi-Square Analysis.

Results

Table 7.1 F1 Generation

 

Phenotype females males
Red eyes 33 0
White eyes 0 31
 

Table 7.2 F2 Generation

Phenotype Male Female
Red eyes 50 52
White eyes 56 67

 

 

1. Describe the observed mutations? In the F1 generation the males had white eyes and the females had red eyes. In the F2 generation the males and females could have had either red or white eyes.

2. Write a hypothesis which describes the mode of inheritance of the trait you studied. This is your null hypothesis ( as described in the Statistical Analysis Section). For a sex linked cross there will always be a one to one ratio of the phenotypes. In the F1 generation there will be a one to one ratio of red eyed females to the number of white eyed males. In the F2 generation there will be a one to one ratio of red eyed females to white eyed females. There will also be a one to one ratio of red eyed males to white eyed males.

3. Refer to a textbook and review Punnett squares. In the space below construct two Punnett squares to predict the expected results of both the parental and F1 crosses from your null hypothesis.

Parental cross

 

Y Xr
Xr YXr Xr Xr
Xr YXr Xr Xr

 

 

F1 cross

 

Y Xr Y XR
XR YXR XR Xr YXR XRXR
XR YXR XR Xr YXr XR Xr
Xr YXr XrXr YXr X RXr
Xr YXr XrXr YXr XRXr

 

 

4. Refer to the Punnett squares above. Record the expected ratios for the genotypes and phenotypes of the F1 and F2 in the experiment below.

 

 

Expected Genotypic Ratio Expected Phenotypic ratio
F1 1:1 1:1
F2 1:1 1:1

 

        5. Do the actual results deviate from what was expected? If so, explain how.
No my results do no deviate much from what was expected. However in the F2 generation there were 67 white females and 52 red females.

6. For the results describe your cross? My cross is a sex linked cross.


7. Are the deviations for the phenotypic ratio of the F2 generation within the limits expected by chance?
To answer this question, statistically analyze the data using the Chi-Square-Analysis. Calculate the Chi-Square for the F2 generation in the chart below. Refer to the critical values of the Chi Square distribution table to determine the P value that is associated with your statistic.

 

 

Observed Phenotypes (o) Expected (e) (o-e) (o-e)2 (o-e)2

e

67 Xr Xr 56 11 121 2.16
52 XR XR 56 -4 16 .28
50 YXR 56 -6 36 .64
56YXr 56 0 0 0
3.02

 

(a) Calculate the Chi-Square value for these data.

1. How many degrees of freedom are there? 3 degrees of freedom

2. Chi Square=2.52

3. Referring to the critical values chart what is the probability value for these data? Greater than .05 probabilities that the null hypothesis is right.

(b) According to the probability value, can you accept or reject your null hypothesis? Explain why. I can accept the null hypothesis because my Chi-Square answer is less than the critical value form the table. I have 3 degrees of freedom and my Chi- Square answer was3.0 which is less than 7.82.

        1. Why was it necessary for the females of the parental generation to be virgins? The females store sperm in their receptacles and if they were not virgins we would not be able to tell who the fathers were.

2. Why was it not necessary to isolate virgin females for the F1 cross? The females store sperm in their receptacles and if they were not virgins we would not be able to tell who the fathers were

3. Why the adult flies were removed from the vials at weeks 2 and 4? So, they are not be able to mate with the next generation.

Chi-Square Analysis

Introduction

Statistics can be used to determine if differences among groups are significant, or simply the result of predictable error. The statistical test most frequently used to determine whether data obtained experimentally provide a good fit, or approximation to the expected or theoretical data is the Chi-square test. This test can be used to determine if deviations from the expected values are due to chance alone or to comeother circumstance.

To determine if the observed data fall with in acceptable limits, a Chi-Square analysis is performed to test the validity of a null hypothesis; that there is no statistically significant difference between the observed and expected data. If the Chi-Square analysis indicates that the data vary too much from the expected 3: 1 an alternative hypothesis is accepted.

Methods

The formula for Chi-square is:

X2=E(o-e)2
E

O= observed number of individuals

e= expected number of individuals

E= the sum of the values

The (df) are determined by taking the number of possible phenotypes and subtracting one from it. If the Chi- Square answer is greater than the number from the critical values chart then the null hypothesis is incorrect. The results are said to be significant at .05. This means that only 5 % of the time you would expect to see similar data if the null hypothesis were correct. The probability can also be rejected at .001. This time it means that less than 1 % of the time would you expect to see similar data.

Results

Critical Values Chart

 

Degrees of Freedom (df)

1 2 3 4 5
.05 3.84 5.99 7.82 9.49 11.1
.01 6.64 9.21 11.3 13.2 15.1
.001 10.8 13.8 16.3 18.5 20.5

 

Practice Problem

An investigator observes that when pure-breeding long winged Drosophila are mated with pure breeding short wing flies the F1 have an intermediate wing length. When several intermediate wing length flies are allowed to interbreed the following results are obtained. 230 long wings. 510 intermediate length wings. 260 short wings.

a. What is the genotype of the F intermediate wing length flies? The genotype is Ll.

b. Write a hypothesis describing the mode of inheritance of wing length in Drosophila. There will be 333 long winged flies. 666 intermediate winged flies. There will be 33 short wing flies.

c. Complete the table

Table 7.8

 

Observed Phenotypes Expected (e) (o-e) (o-e)2 (o-e)2/ e
LL 333 -103 10609 31.86
Ll 666 -156 24336 36.54
ll 333 -73 5329 16.00

84.4

 

1. How many degrees of freedom are there? There are 2 degrees of freedom.

2. Chi-Square= 84.4

3. Referring to the critical values chart, what is the probability value for these data? Less than .001.

4. According to the probability value can you except or reject the null hypothesis? 

I can reject the null hypothesis because the Chi-square answer is greater than the critical value from the table.

Error Analysis

Results from this lab could have been affected by many things. The constant knocking out of flies could have caused some of the larvae to not hatch therefore affecting our numbers. Also, incorrectly identifying the characteristics of the flies could have also greatly affected the results received. Improper calculation of numbers could have also caused inaccurate results. Finally, some flies could have gotten stuck in the medium and could have been identified.

Conclusion

From the results of the experiment I can conclude that I received results that were close to a 1:1 ratio. The Chi- Square worked from my data was accepted at a possibility greater than .05. The null hypothesis in this case can be accepted.

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