Floating Leaf Disk Assay

 

The Floating Leaf Disk Assay for Investigating Photosynthesis

Brad Williamson

 

Introduction:

 

Trying to find a good, quantitative procedure that students can use for exploring photosynthesis is a challenge. The standard procedures such as counting oxygen bubbles generated by an elodea stem tend to not be “student” proof or reliable. This is a particular problem if your laboratory instruction emphasizes student-generated questions. Over the years, I’ve found that the floating leaf disk assay technique to be reliable and understandable to students. Once the students are familiar with the technique they can readily design experiments to answer their own questions about photosynthesis. I plan to add to this page as I have time to elaborate on the technique and provide suggestions for modifications.

 

Materials:

 

1.                Sodium bicarbonate (Baking soda)

2.               Liquid Soap

3.               Plastic syringe (10 cc or larger)—remove any needle!

4.               Leaf material

5.               Hole punch

6.               Plastic cups

7.               Timer

8.               Light source

 

Optional:

 

Buffer Solutions

Colored Cellophane or filters

Leaf material of different ages

Variegated leaf material

Clear Nail polish

 

 

 

Procedure:

 

 

  1. Prepare 300 ml of bicarbonate solution for each trial.
    1. The bicarbonate serves as an alternate dissolved source of carbon dioxide for photosynthesis. Prepare a 0.2% solution. (This is not very much—it’s about 1/8 of a teaspoon of baking soda in 300 ml of water.) Too much bicarbonate will cause small bubbles (CO2)to form on the surface of the leaf which will make it difficult to sink the leaf disk.
    2. Add 1 drop of dilute liquid soap to this solution. The soap wets the hydrophobic surface of the leaf allowing the solution to be drawn into the leaf. It’s difficult to quantify this since liquid soaps vary in concentration. Avoid suds. If your solution generates suds then dilute it with more bicarbonate solution.

 

  1. Cut 10 or more uniform leaf disks for each trial

    1. Single hole punches work well for this but stout plastic straws will work as well
    2. Choice of the leaf material is perhaps the most critical aspect of this procedure. The leaf surface should be smooth and not too thick. Avoid plants with hairy leaves. Ivy, fresh spinach, Wisconsin Fast Plant cotyledons—all work well. Ivy seems to provide very consistent results. Any number of plants work. My classes have found that in the spring, Pokeweed may be the best choice.
    3. Avoid major veins.

 

  1. Infiltrate the leaf disks with sodium bicarbonate solution.
    1. Remove the piston or plunger and place the leaf disks into the syringe barrel. Replace the plunger being careful not to crush the leaf disks. Push on the plunger until only a small volume of air and leaf disk remain in the barrel (< 10%).

    1. Pull a small volume of sodium bicarbonate solution into the syringe. Tap the syringe to suspend the leaf disks in the solution.

 

    1. Holding a finger over the syringe-opening, draw back on the plunger to create a vacuum. Hold this vacuum for about 10 seconds. While holding the vacuum, swirl the leaf disks to suspend them in the solution. Let off the vacuum. The bicarbonate solution will infiltrate the air spaces in the leaf causing the disks to sink. You will probably have to repeat this procedure several times in order to get the disks to sink. You may have difficulty getting the disks to sink even after applying a vacuum three or four times. Generally, this is usually an indication that you need more soap in the bicarbonate solution. Some leaf surfaces are more water repellent than others are. Adding a bit more soap usually solves the problem.

 

  1. Pour the disks and solution into a clear plastic cup. Add bicarbonate solution to a depth of about 3 centimeters. Use the same depth for each trial. Shallower depths work just as well.

    1. This experimental setup includes a control. The leaf disks in the cup on the right were infiltrated with a water solution with a drop of soap—no bicarbonate.

 

  1. Place under the light source and start the timer. At the end of each minute, record the number of floating disks. Then swirl the disks to dislodge any that are stuck against the sides of the cups. Continue until all of the disks are floating.

    1. The control is on the left in each image. In the experimental treatment, on the right, leaf disks are rising and floating on the surface.

 

  1. Sample results:

 

Time (minutes)Disk Floating
10
20
30
40
50
60
71
81
91
101
114
127
138
1410

 

  1. The point at which 50% of the leaf disks are floating is the point of reference for this procedure. By interpolating from the graph, the 50% floating point is about 11.5 minutes. Using the 50% point provides a greater degree of reliability and repeatability for this procedure.

 

Only You Can Help Save Sam

 

Only You Can Help Save Sam!

 

 

Sam has been spending his summer boating on the great lakes.  However, he’s not too bright (after all, the brains of worms are pretty small).  He’s never learned how to swim, and he never wears his life preserver.  The worst has happened!  His boat has capsized and he’s stuck!  Fortunately, his life preserver is in the boat, but unfortunately he does not know how to reach it without falling off and drowning.

Save Sam!!

 

 

 

Use the Scientific Method to:

 

Problem:

How can you and your partner save Fred using only 4 paper clips. You may not touch Fred, the boat, or the life preserver directly with your hands.

 

Materials:

·        Gummy Worm

·        Gummy life preserver

·        1 Plastic Cup

·        4 Paper Clips

 

Procedures:

1.      Work with your partner and “Save Fred”.

2.    Follow the rules.

§        Fred, the boat, the life preserver can be touched only with the paper clips.  NO HANDS.

3.    Develop a data section that includes

§        Diagrams of how you saved Fred

§        A detailed protocol describing the diagrams.

4.    Homework:

§        Analyze and conclude the experiment.

·        This means that you must discuss (tell me what you think) about the difficulty of the task, what other strategies you and your partner worked on before you succeeded, and what you think the critical steps were for solving this problem.

§        Although this is working backwards, and not how scientists normally work, please develop a hypothesis for this lab.  (Remember that a hypothesis is an ‘if-then’ statement: if I do this, then this will happen)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Teacher Notes:

Fred sits on the inverted cup.  The cup sits covering the life preserver on the tabletop.  No real water is involved.  If the group size is 3 or 4, each person gets only 1 paper clip. Have a camera ready.

There are not any real answers – since it’s more of a team-building problem solving initiative rather than a yes/no answer.  However, what they need to figure out is that if they work together, then one person maneuvers Fred (without hooking him) and the other uses the paper clips to stretch the gummy lifesaver for him to slip on.  (The lifesaver will have a smaller inner diameter than Fred’s outer diameter by a fairly obvious amount.)

Ask them typical debriefing-type questions: what worked, what didn’t, did you plan, did you share ideas, did you just mangle poor Fred trying to make it work?, etc.

Groups of 3 and make it more of a challenge by allowing only 1 paperclip per student – that takes more thought and coordination to save Fred without drowning him.  (No mouth-to0mouth resuscitation allowed!)

 

 

 

 

 

Organism Classification Webquest

 

Living Thing #1

Color: Black
Location: in forest on a rotting tree
Eats decaying plant material
Has many cells
Releases spores to reproduce.
Stays in one spot (immobile)
Cells have no chlorophyll
Feels soft and smooth

 

BACK

LIVING THING #2

Cells  have chlorophyll
Is autotrophic (produces its own food) and heterotrophic (eats insects) to supplement its diet
Has many cells
Lives in swampy areas
Immobile though catches prey as shown.
Reproduces by seeds

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Living Thing #3


Adults live underground or under logs and rocks
They breed and lay eggs in the water
Young live in the water, have external gills, budding arms and legs and a fish like tail
Adults must keep skin moist
Ectothermic (an animal whose body temperature is determined by the temperature of its immediate environment.)
Do not have scales
Have Slimy skin

No external ears

Eats insects and small fish

BACK

Living Thing #4

Has webbed feet
Lays eggs
50 cm long and weighs 1.5 kilograms
Covered with 2 layers of waterproof hair
Eats insects, frogs and fish
Has no external ears
Lives in fresh water lakes
Endothermic an animal whose body temperature is determined by its own metabolic heat production)
Bill has two nostrils
Care for their young and have mammary glands
Sounds like a puppy barking

 

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Living Thing #5

 

Click on picture to hear its call

 

Has rough, shaggy hair-like feathers

Tiny wings

Sharp claws

Endothermic (an animal whose body temperature is determined by its own metabolic heat production)

Lays eggs

Eats insects and worms

Has whiskers to find way in the dark

 

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Living Organism #6

 


Click on picture to view video and see sight about these amazing creatures.

Breathe air

Has tough wrinkly skin

Bristled hairs cover entire body

Eats algae and crustaceans

Has teeth

Babies are born live and cared for by mother for up to 2 years

Have mammary glands

Live in warm coastal waters

Are Endothermic.

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Osmosis

Osmosis
Osmosis: the movement of water molecules from an area of high concentration to an area of low concentration.

Cell membranes are completely permeable to water, therefore, the environment the cell is exposed to can have a dramatic effect on the cell.

Hypertonic Solutions: contain a high concentration of solute relative to another solution (e.g. the cell’s cytoplasm). When a cell is placed in a hypertonic solution, the water diffuses out of the cell, causing the cell to shrivel.

Hypotonic Solutions: contain a low concentration of solute relative to another solution (e.g. the cell’s cytoplasm). When a cell is placed in a hypotonic solution, the water diffuses into the cell, causing the cell to swell and possibly explode.

Isotonic Solutions: contain the same concentration of solute as an another solution (e.g. the cell’s cytoplasm). When a cell is placed in an isotonic solution, the water diffuses into and out of the cell at the same rate. The fluid that surrounds the body cells is isotonic.

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© Copyright 1999 Terry Brown. All rights reserved.