Questions For AP Environmental Science Class

Questions For AP Environmental Science Class.

I need these questions answered in 3-5 sentences each. 7. Compare and contrast species richness and species evenness. Use an example to explain. 8. How are species phylogenies determined? 9. List the classification system from the most broad to the most specific. 10. Speciation is an example of microevolution or macroevolution? Explain. 11. Explain 2 ways mutations may occur. Are they good or bad? Explain. 12. Explain how recombination occurs. 13. Give 2 examples of how humans are purposefully or inadvertently directing evolution of organisms. 14. List the 5 key ideas of Darwin’s Theory of Evolution by Natural Selection. 15. Describe the 3 random evolutionary processes. 16. Give an example of how genetic drift may have a greater effect in small populations. 17. What are some ways the bottleneck effect may occur and why might this lead to an extinction of a population? Give an example of the founder effect. 18. Explain how Darwin’s finches are an example of allopatric speciation. 19. Give an example of sympatric speciation. 20. How long does evolution take? 21. Explain how the rate of environmental change, genetic variation, generation time and genetic engineering effect evolution. 22. Explain the difference between fundamental niche and realized niche. Give an example. 23. Would you rather be a niche generalist or niche specialist? Explain. 24. Can we predict future species distribution? Justify your answer. 25. What obstacles may prevent a species from being widely distributed? 26. Explain 3 reasons why species may go extinct when their habitat changes. 27. How can fossil records be useful for environmentalists? 28. What is the consensus on how the dinosaurs became extinct? 29. What is causing the 6th mass extinction?

Questions For AP Environmental Science Class

 
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Microscopy For Microbiology

Microscopy For Microbiology. Please note that I already have all the answers to this lab and the only thing I need is the PICTURES to go with it. I will not adjust the price of this post. Thank you!

I do not have my lab kit as yet and so the MICROSCOPE is what I do not have, so again all I need is the answers to the questions related to the pictures. I need the pictures of the magnified letter. PLEASE DO NOT GOOGLE THIS AND USE THEM, I WILL KNOW!!!!

Lab Reports:

You need to write:

1. Background

2. Procedure- can be in paragraph or step by step format.

3. Answer the Questions at the end.

Microscopy for Microbiology – Use and Function

Hands-On Labs, Inc. Version 42-0249-00-02

Lab Report Assistant

This document is not meant to be a substitute for a formal laboratory report. The Lab Report Assistant is simply a summary of the experiment’s questions, diagrams if needed, and data tables that should be addressed in a formal lab report. The intent is to facilitate students’ writing of lab reports by providing this information in an editable file which can be sent to an instructor.

 

Exercise 1: Getting to Know your Compound Microscope

Data Table 1. Microscope Components.

Letter Component Name Component Function
A    
B    
C    
D    
E    
F    
G    
H    
I    
J    
K    
L    
M    

 

 

 

 

Data Table 2. Total Magnification.

Lens Ocular Magnification Objective Magnification Total Magnification
Scanning      
Low Power      
High Power      
Oil Immersion      

Data Table 3. Field of View.

Lens Total Magnification Field of View (mm) Field of View (µM)
Scanning      
Low Power      
High Power      
Oil Immersion      

 

Data Table 4. Letter e Viewing Results.

Lens Photograph Observations
Scanning    
Low    
High    
Oil Immersion    

 

 

Questions

A. Describe the details in the slides “Letter e” that become visible as the power changed from scanning power, to low power, to high power.

B. Why is it important to calculate the diameter of the field when first using the microscope?

 

 

Exercise 2: Viewing Prepared Microbe Slides

Data Table 5. Prepared Slide Viewing Results.

Slide Photograph Total Magnification
Amoeba  

 

 

 
Penicillium  

 

 
Yeast  

 

 

 
Spirillium  

 

 

 
Bacillus  

 

 

 
Coccus  

 

 

 

 

Questions

A. Using the field of view calculated in Exercise 1 for the high power lens, approximately how far across are each of the cells in the Bacteria Coccus Form slide in Data Table 5? Show your calculations.

B. Detail techniques you found helpful for focusing on the various slides in this exercise.

 

 

 

Exercise 3: Preparing Wet-Mount Slides

Data Table 6. Wet-Mount Viewing Results.

Slide Photograph Total Magnification
Cheek Cell Smear  

 

 

 
Dental Tatar Smear  

 

 

 

 

Questions

A. Describe the similarities and differences between the cheek cell wet mount and dental plaque wet mount.

B. How did the process of preparing wet-mount slides become easier as you prepared the second wet-mount slide of this exercise?

Microscopy For Microbiology

 
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Fermentation Post Lab Questions

Fermentation Post Lab Questions. BIOL 102: Lab 7

Yeast Fermentation

PRE-LAB ASSIGNMENT:

Students are expected to read pages 1-2 before coming to the lab to complete the experiments.

Print this entire lab packet and bring it to the laboratory.

Please provide a FULL lab report for this experiment following the “Lab Report Guidelines”.

Please note that this lab report WILL include a HYPOTHESIS.

Objectives:

· Observe yeast fermentation

· Determine the optimum conditions for yeast fermentation

Background:

All fungi are eukaryotes. Although they vary in size and shape, fungi share key characteristics including their way of obtaining nutrients for growth and energy. Fungi are heterotrophs and they depend on preformed carbon molecules produced by other organisms. However, fungi do not ingest food and then digest it using enzymes; instead they invade -think of a moldy piece of bread-a food source and secrete digestive enzymes onto it. The digestion occurs outside the body. When the polymers are broken down into monomers, the fungi absorb the predigested food into its body.

Yeast are microscopic, unicellular organisms in the Kingdom Fungi. Like other fungi, yeast are incapable of making their own food, but like any other organism, need food for energy. They rely on carbohydrates (usually sugars) found in their environment to provide them with this energy so that they can grow and reproduce. There are many species of yeast, and each has a particular food source.

Regardless of the food source, yeast perform fermentation which does not utilize oxygen. In fermentation, the only energy extraction pathway is glycolysis, with one or two extra reactions tacked on at the end, but no electron transport chain. Therefore, only 2 ATPs are formed per glucose.

Fermentation and cellular respiration begin the same way, with glycolysis. In fermentation, however, the pyruvate made in glycolysis is not completely oxidized because it does not continue through the citric acid cycle and the electron transport chain does not run. Because the electron transport chain is not functional, the NADH cannot drop its electrons off to the electron transport chain, and thus very few ATP molecules are synthesized because the ATP synthase is not running.

Based on the end products, fermentation can be of two types: ALCOHOLIC fermentation (the subject of this lab) and LACTIC ACID fermentation.

image1.png

Regardless of the type of fermentation, the purpose of the extra reactions in fermentation, is to regenerate (recycle) the electron carrier NAD+ from the NADH produced in glycolysis. The extra reactions accomplish this by letting NADH drop its electrons off with an organic molecule such as acetaldehyde to produce ethanol (alcoholic fermentation), or pyruvate to produce lactic acid (lactic acid fermentation). This “drop-off” of electrons allows glycolysis to keep running by ensuring a steady supply of NAD+.

Going from pyruvate to ethanol is a two-step process. In the first step, a carboxyl group is removed from pyruvate and released as carbon dioxide, producing a two-carbon molecule called acetaldehyde. In the second step, NADH passes its electrons to acetaldehyde, regenerating NAD+ and forming ethanol.

Yeast breaks down glucose into ethanol, 2 carbon dioxide molecules, and 2 ATP molecules. The formula for the yeast fermentation reaction is:

Reactant Products

C6H12O6 >>>>>>> 2CH3CH2OH + 2CO2 + 2 ATP molecules

For the yeast cell, this chemical reaction is necessary to produce the energy for life. The ethanol and the carbon dioxide are waste products. It is these waste products that we take advantage of: we use the ethanol in alcoholic beverages and the carbon dioxide makes bread rise when baking.

Alcoholic fermentation, can be observed and measured by using the amount of carbon dioxide gas that is produced from the breakdown of glucose. In this exercise, you will observe alcoholic fermentation by yeast. To do so you will add the same amounts of yeast and water to different amounts of sugar in Erlenmeyer flasks and cap them with a balloon to see how much carbon dioxide gas is produced. You will also use water at two different temperatures and determine how much carbon dioxide is produced. The more fermentation that occurs, the more carbon dioxide will be produced, and the more the balloon will expand.

Information adapted from:

Solomon, Eldra P. et al. Biology. 10th ed. Cengage, 2015.

https://www.khanacademy.org/science/biology/cellular-respiration-and-fermentation

LAB DATASHEET

Determine the optimum conditions for yeast fermentation.

Think Scientifically:

Please explain your rationale to which flask or test variable will produce the most CO2. Look at the various bottles below and state whether bottle A-F will produce the most CO2 and explain why.

Materials:

Sugar

Dry yeast

Warm water

Ice cold water

Balance scale

Measuring spoons

100 mL Graduated Cylinder

6 Erlenmeyer flasks

6 Rubber bands

6 Balloons

Ruler

Procedure:

1. Obtain 6 labeled Erlenmeyer flasks.

2. Fill each flask accordingly:

· Bottle A – 5 mL sugar, 3 grams of dry yeast

· Bottle B – 10 mL sugar, 3 grams of dry yeast

· Bottle C – 15 mL sugar, 3 grams of dry yeast

· Bottle D – 5 mL sugar, 3 grams of dry yeast

· Bottle E – 3 grams of dry yeast

· Bottle F – 15 mL sugar

3. Fill all flasks except D with 100 mL of warm water. Fill flask D with 100 mL of ice cold water.

4. Place a balloon over the top of each flask and tighten it with a rubber band.

5. Swirl flask to mix contents. Wait 20-30 minutes.

6. Record observations in Table 1.

7. Measure the width and height of the balloon (from the top of the flask to the top of the balloon) with a ruler, and record it in Table 1.

8. Graph the Sugar Quantity vs. Balloon Height in an X-Y Scatterplot. Insert DIGITAL scatterplot only. Written graphs and/or pictures of written graphs will not be accepted.

Table 1: Observations and Measurements of Balloon height in cm
Flask Observations Height Width
A 1st to rise 4.5inch 2inch
B 3rd to rise 3.8inch 1.5inch
C 2nd to rise 4.2inch 1.8inch
D Did not rise 0 0
E Did not rise 0 0
F Did not rise 0 0

Conclusion:

Be sure to address the following:

· How did your original rationale compare to the data collected? If your rationale was incorrect, why do you think it did not produce the most CO2?

· Describe what happened in this reaction using the following terms: yeast, warm water, cold water, sugar, anaerobic respiration, and carbon dioxide.

· Compare what happened to each of the balloons for flasks A through F. Which flask had the most CO2 production? Least? How do you know? Be sure to describe WHY!

· There were four experimental flasks and two control flasks in this exercise. Which flasks were the experimental and which were the control flasks? Explain how each determination was made.

Fermentation Post Lab Questions

 
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Lab 5: Meiosis

Lab 5: Meiosis.

Your Full Name:

UMUC Biology 102/103

Lab 5: Meiosis

INSTRUCTIONS:

 

· On your own and without assistance, complete this Lab 5 Answer Sheet electronically and submit it via the Assignments Folder by the date listed in the Course Schedule (under Syllabus).

· To conduct your laboratory exercises, use the Laboratory Manual located under Course Content. Read the introduction and the directions for each exercise/experiment carefully before completing the exercises/experiments and answering the questions.

· Save your Lab 5 Answer Sheet in the following format: LastName_Lab5 (e.g., Smith_Lab5).

· You should submit your document as a Word (.doc or .docx) or Rich Text Format (.rtf) file for best compatibility.

 

Pre-Lab Questions

1. Compare and contrast mitosis and meiosis.

 

 

 

2. What major event occurs during interphase?

 

 

 

Experiment 1: Following Chromosomal DNA Movement through Meiosis

Data Tables and Post-Lab Assessment

Trial 1 – Meiotic Division Without Crossing Over Beads Diagram:

Take pictures of your beads for each phase of meiosis I and II without crossing over. Include notes with your name, date and meiotic stage on index cards in the pictures. Please use the lowest resolution possible so that your file does not become too large to submit.

Insert pictures here:

 

Prophase I

Metaphase I

Anaphase I

Telophase I

Prophase II

Metaphase II

Anaphase II

Telophase I

Cytokinesis

Trial 2 – Meiotic Division with Crossing Over Beads Diagram:

Take pictures of your beads for each phase of meiosis I and II with crossing over.  Include notes with your name, date and meiotic stage on index cards in the pictures.  Please use the lowest resolution possible so that your file does not become too large to submit.

Insert pictures here:

 

Prophase I

Metaphase I

Anaphase I

Telophase I

Prophase II

Metaphase II

Anaphase II

Telophase I

Cytokinesis

 

Post-Lab Questions

 

1. What is the ploidy of the DNA at the end of meiosis I? What about at the end of meiosis II?

 

 

 

2. How are meiosis I and meiosis II different?

 

 

 

3. Why do you use non-sister chromatids to demonstrate crossing over?

 

 

 

4. What combinations of alleles could result from a crossover between BD and bd chromosomes?

 

 

5. How many chromosomes were present when meiosis I started?

 

 

 

6. How many nuclei are present at the end of meiosis II? How many chromosomes are in each?

 

 

 

7. Identify two ways that meiosis contributes to genetic recombination.

 

 

 

8. Why is it necessary to reduce the number of chromosomes in gametes, but not in other cells?

 

 

 

9. Blue whales have 44 chromosomes in every cell. Determine how many chromosomes you would expect to find in the following:

 

i. Sperm Cell:

 

ii. Egg Cell:

 

iii. Daughter Cell from Mitosis:

 

iv. Daughter Cell from Meiosis II:

 

10. Research and find a disease that is caused by chromosomal mutations. When does the mutation occur? What chromosomes are affected? What are the consequences?

 

 

 

11. Diagram what would happen if sexual reproduction took place for four generations using diploid (2n) cells.

 

Experiment 2: The Importance of Cell Cycle Control

For each of the five abnormalities you find online, copy and paste a picture of it (and be sure to cite the URL for the picture)—you will not be photographing your own results for this section of lab, because you’re doing your research online for the questions below.

Data Tables and Post-Lab Assessment

1.  [paste in your online picture and cite the URL]

 

 

2.  [paste in your online picture and cite the URL]

 

 

3.  [paste in your online picture and cite the URL]

 

 

4.  [paste in your online picture and cite the URL]

 

 

5. [paste in your online picture and cite the URL]

 

 

Post-Lab Questions

1. Record your hypothesis from Step 1 in the Procedure section here.

 

 

 

 

2. What do your results indicate about cell cycle control?

 

 

 

3. Suppose a person developed a mutation in a somatic cell which diminishes the performance of the body’s natural cell cycle control proteins. This mutation resulted in cancer, but was effectively treated with a cocktail of cancer-fighting techniques. Is it possible for this person’s future children to inherit this cancer-causing mutation? Be specific when you explain why or why not.

 

 

 

4. Why do cells which lack cell cycle control exhibit karyotypes which look physically different than cells with normal cell cycle.

 

 

 

5. What are HeLa cells? Why are HeLa cells appropriate for this experiment?

© eScience Labs, LLC 2014

Lab 5: Meiosis

 
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