Bio Ciliate Lab #3
9/6/18 Lab #3
Compound Microscopy
Rationale: In this lab students learn about how to properly operate a compound microscope and work with concavity slides. Throughout this lab, students also gain experience with different stains and applying them to ciliates in order to see different aspects of the ciliates.
Experimental Procedure:
- First obtain a compound microscope, sample slides and ciliate samples.
- Then place a slide on the microscope to begin learning how to operate a compound microscope.
- Change the magnification to 40x to be able to see the sample clearly, while also adjusting the height of the stage and adjusting the fine tune.
- If the sample appears to bright, turn down the brightness of the light on the microscope to get a better look at the sample.
- A blue filter can be utilized on the microscope to change the coloring of the way the sample appears through the microscope; it can take away the orange tint and display the characteristics of the sample clearer.
- Next remove the sample slide and obtain a mini ruler to place onto the stage of the microscope in order to find the field of view.
- In order to find the field of view start with a magnification of 4x and count the hash marks while looking into the microscope.
- The amount of hash marks in mm that measure across the microscopes view at 4x is the field of view.
- You can then use this amount to find the fields of views at 10x and 40x by using the equation: Magnification (low) X FOV (low) = Magnification (high) X FOV (high)
- Next obtain a concavity slide and a ciliate sample
- Use a pipette to place a drop of the sample on the concavity slide and place it onto the microscope, then observe characteristics of ciliate. ( Record Data)
- Obtain a flat slide and get a new ciliate sample and put it onto the slide.
- Then insert a drop of iodine stain onto the sample and observe under microscope. (Record Data)
- Follow the same steps by getting a new flat slide and a new sample, then obtain a few drops of the second stain and observe. (Record data)
- Lastly clean off all of the slides with water and let dry, then put the microscope away and return samples to original place.
Sample Storage/ Label: NONE, cleaned slides and set to dry
Data Table/ Results:
UNKNOWN #5
Hanging Concavity |
Stain #1 Iodine |
Methyl Cellulose | |
Movement | Quick side to side movement | No Movement | Slow movement |
Shape | Long Oval | Long Oval | Long Oval |
Size | About 0.1 mm | About 0.1mm | About 0.1mm |
Characteristics |
-Twisting movement while moving side to side -transparent |
-No movement -Transparent |
-Slow movement, eventually die -able to see small vacuoles |
Sketch:
Interpretations, Conclusions and Next Steps:
Throughout this lab I learned how to properly use a compound microscope along with utilizing a blue filter which helped me see the ciliates clearer. I also learned how to calculate the field of view of a microscope which later on helped me describe the approximate size of my ciliate sample. To be able to analyze the ciliates correctly, I used a concavity slide which prevents the sample from being smashed between the top slide and the real slide. One form of error that could have occurred throughout this lab is during the transfer of the sample with the top slide to the concavity slide which can sometimes smash the sample preventing certain characteristics of the sample to be seen. I also learned how certain stains can affect the samples and show different aspects of the ciliate sample; the stains allowed for the ciliates to freeze and reveal certain properties not seen when they are in constant movement. Overall I was able to successfully carry out this experiment and in the future I hope to learn more about ciliate structure and what causes their specific movements and properties. `