My Science Box

This series of activities is designed to complement a semester long introductory biology course for non-majors (general education) at a 4 year university. These activities are designed to be used to review material from the week's lecture in an activity-based way that is practical to implement in a  section of 25-75 students.

The original course is structured in 3 segments:

Here's my current syllabus for an introductory college biology course for undergraduates planning on entering elementary teaching. This is NOT your traditionalcollege biology course. The goal of this course is to give students mastery over theconcepts required of K-8 students in California in a hands-on, experiential way.

Summary
Bubbling Yeast: Thanks to Ellen Loehman for creating this image.Yeast are a single celled fungi that are a great model organism for studying respiration in the classroom. The species Saccharomyces cerevisiae is commonly used for leavening bread and fermenting beer but other species such as Candida albicans are known to cause infections in humans (vaginal yeast infections and diaper rash being the most common). In this investigation, students fill the bulb of a disposable pipet (eyedropper) with yeast, then submerge the pipet in a test tube of water. They can then measure the rate of respiration by counting the number of bubbles of carbon dioxide gas that emerge from the tip of the pipet in a certain length of time. By varying the temperature and the nutrient source, students can discover what variables affect the rate of respiration in yeast. By submerging the pipet in bromthymol blue (see Colorful Respiration activity), students can identify the gas being produced as carbon dioxide.

Summary
Blow through a straw into bluish liquid and watch it turn green then yellow before your eyes. Put some plants into the yellow liquid, leave it in a sunny window, come back the next day and the liquid is green. What if you leave the plants in the dark? What if you put some pond snails in? What if you put both pond snails and plants? What’s going on?

The liquid is bromthymol blue (BTB) a non-toxic acid-base indicator that can be used to indirectly measure levels of dissolved carbon dioxide (CO₂). The amount of CO₂ in a solution changes the pH. An increase in CO₂ makes a solution more acidic (the pH gets lower). A decrease in CO₂ makes a solution more basic (the pH gets higher). The reason for this is that carbon dioxide that is dissolved in water is in equilibrium with carbonic acid (H₂CO₃).

CO₂ + H₂O ↔ H₂CO₃

In any solution, while the majority of CO₂ stays as CO₂, some of it is converted to H₂CO₃, turning the solution slightly acidic. If CO₂ is added to the water, the level of H₂CO₃ will rise and the solution will become more acidic. If CO₂ is removed from the water, the amount of H₂CO₃ falls and the solution becomes more basic. Thus, acid-base indicators such as BTB can indirectly measure the amount of CO₂ in a solution.

For more than you ever wanted to know about carbonic acid, see the Wikipedia article on carbonic acid. For the example lesson plans developed by Bob Culler through Access Excellence at the National Health Museum. For a great time lapse video showing BTB color changes using elodea and snails, see Activity C13 from Addison-Wesley’s Science 10 curriculum.

Materials

• Bromthymol blue (BTB can be ordered from any science supply company such as Flinn Scientific $9 for 1 liter 0.04% BTB solution).
• Several 2 liter soda bottles
• Test tubes
• 500 ml beakers or disposable plastic or paper cups
• Water (since the pH of tap water varies, you may wish to use distilled water for your master BTB solution)
• Drinking straws
• Plastic wrap
• Elodea
• Pond snails

Procedure

1. Before the lesson, the teacher should mix a master BTB solution in one or more 2 liter soda bottles. For each 2 liter bottle, mix 120 ml 0.04% BTB with 1800 ml water. The end result should be a medium blue master BTB solution, dilute enough to be safe for plants and snails but dark enough to see the color changes.
2. Pour 200 ml diluted BTB in a beaker or cup.
3. Take a deep breath then blow bubbles in the BTB solution through a drinking straw. What happened? Why?
4. Set up a test tube rack with 3 tubes. In tube #1 put unbubbled BTB solution (blue). In tube #2 put bubbled BTB solution (yellow). Tubes #1 and #2 will be your comparison tubes. In tube #3 you have a choice of what to do. Choose one option from each of the following columns:
   

   BTB solution	Living things	Light conditions
   bubbled BTB (yellow)	spring of Elodea	Sunny window/bright light
   unbubbled BTB (blue)	5 pond snails	Dark closet/drak heavy cloth
   	both Elodea and 5 pond snails

5. Make a hypothesis about what will happen to your tube.
6. After 24 hours, check the color of your tube. What happened? Why?

Going Further

Summary
These experiments use a bell jar (or any other very large, clear, glass jar) to determine the identity of the gas produced by plants. It mirrors the famous experiments of Joseph Priestley and Jan Ingenhousz from the 1700’s that first demonstrated the existence of oxygen and its importance to plants and animals.

In 1771 and 1772, Priestly conducted a series of experiments using a bell jar. It was known that a candle placed in a sealed bell jar would eventually burn out and could not be relighted while still in the jar. Priestly discovered that a plant can survive indefinitely within a jar. Thus, he tried placing a plant into the jar with the burning candle. The candle went out as before and could not be relit right away. Priestly waited several days and tried again. The candle could be relit! The plant had restored the air inside the jar! (Do not try the next series of experiments since it harms animals!) Next priestly investigated what would happen to animals. He found that a mouse placed inside a sealed jar will eventually collapse. However, a mouse can survive in a sealed jar with a plant since the plant restores the air. Priestly was the first to demonstrate that oxygen is necessary for fire and animals but that given time, plants can create oxygen, allowing fires to burn and animals to breathe.

Elodea nuttallii: Image courtesy of Christopher Fischer.Summary
Students often believe that only animals “breathe”, but all things exchange gases with their environment. It’s just that the process is not so obvious in plants. Elodea is a very common water plant that can be found in aquarium stores. As photosynthesis occurs, oxygen is produced as a by-product. Elodea releases bubbles of oxygen as it photosynthesizes. In fact, the number or volume of bubbles in a certain amount of time can be used as a rough measure of photosynthetic rate.

Chlorophyll extractionSummary
Chlorophyll is the pigment in plants that captures sunlight energy and uses it to drive photosynthesis. While chlorophyll does give plants their characteristic green color, chlorophyll actually comes in many colors and subtypes ranging from green to yellow to orange to red. In this experiment, students use paper chromatography to separate the many pigments from one another. First the pigments are extracted from the plants by simply crushing the plant cells open on the filter paper with the edge of a penny. When the filter paper is then immersed in rubbing alcohol, the pigments are carried upwards through capillary action. The smallest pigments travel more quickly and thus separate from the larger pigments that remain closer to the origin line.

Summary
Here you will find a toolbox full of inquiry investigations on photosynthesis and respiration. Rather than the detailed lesson plans provided elsewhere at My Science Box, each experiment only contains a short background, materials, procedure, and going further section. It is up to you to decide which of the many experiments you wish to try with your students and how to sequence them. You will find everything from descriptions for how to extract chlorophyll, discover that plants “breathe”, recreate the experiments of Priestly and Ingenhousz, detect carbon dioxide production, and measure the rate of yeast respiration. None of these experiments require expensive equipment such as metabolism chambers or oxygen meters although those are great tools if you can afford them.

Summary
To solidify students’ conceptualization of cells, students build a model of a cell in a ziplock bag using polyvinyl alcohol slime as cytoplasm. So far, students’ experience with cells has been 2 dimensional – diagrams and microscopic slides. The 3 dimensional nature of cells comes to life as students use everyday objects to represent the many parts of a cell. In addition, students can use this activity to develop a sense of scale, calculating how big a human would be if the ziplock bag cell model were really the size of a cheek cell.

Summary
The invisibly small world of the cell comes to life as students look at plant and animal cells through a microscope. Students create wet-mount slides of onion skin, elodea leaf, and human cheek cells. They learn some of the gross differences between plant and animal cells (cell walls are present in plant but not in animal cells), and even some of the differences between different plant cells (chloroplasts are found in the leaves but not in the roots). It is suggested that this lesson take place after students learn the parts of a cell and their functions. Resources for good cell diagrams are provided in the Sources section. This lesson may be used in conjunction with the Pond Water activity for students to get a sense of the diversity of microscopic life, both single celled and multi-celled.