Preparation of temporary mount of onion peel
Answers
Answer:
Pour some distilled water into a watch glass.
Peel off a leaf from half a piece of onion and using the forceps, pull out a piece of transparent onion peel (epidermis) from the leaf.
Put the epidermis in the watch glass containing distilled water.
Take a few drops of safranin solution in a dropper and transfer this into another watch glass.
Using a brush, transfer the peel into the watch glass containing the safranin solution.
Let this remain in the Safranin solution for 30 seconds, so that the peel is stained.
Take the peel from the Safranin solution using the brush and place it in the watch glass containing the distilled water.
Take a few drops of glycerine in a dropper and pour 2-3 drops at the center of a dry glass slide.
Using the brush, place the peel onto the slide containing glycerine.
Take a cover slip and place it gently on the peel with the aid of a needle.
Remove the extra glycerine using a piece of blotting paper.
Place this glass side on the stage of the compound microscope and view it.
Observations
There are a large number of regularly shaped cells lying side by side and each cell has a distinct cell wall.
A distinct nucleus is present on the periphery of each cell.
Lightly stained cytoplasm is observed in each cell.
A large vacuole is present at the centre of each cell, and is surrounded by the cytoplasm.
Conclusion
As cell walls and large vacuoles are clearly observed in all the cells, the cells placed for observation are plant cells.
Precautions
Use a brush to transfer the peel from one apparatus to another.
Staining of peel should neither be too dark, nor too light.
Extra glycerine stain should be removed using blotting paper.
To Prepare Stained Temporary Mount of Human Cheek Cells
Materials Required
Real Lab Procedure
Gently scrape the inner side of the cheek using a toothpick, which will collect some cheek cells.
Place the cells on a glass slide that has water on it.
Mix the water and the cheek cells using a needle and spread them.
Take a few drops of Methylene blue solution using a dropper and add this to the mixture on the slide.
After 2-3 minutes remove any excess water and stain from the slide using a blotting paper.
Take a few drops of glycerine using a dropper and add this to the test mixture.
Take a clean cover slip and lower it carefully on the mixture with the aid of a needle.
Using a brush and needle, press the cover slip gently to spread the epithelial cells.
Remove any extra liquid around the cover slip using a blotting paper.
Place this glass side on the stage of the compound microscope and view it.
Observations
A large number of flat and irregular-shaped cells are observed.
The cells do not have a cell wall. However, each cell has a thin cell membrane.
A deeply stained nucleus is observed at the centre of each cell.
No prominent vacuoles are observed in the cells.
Conclusion
As the cells observed do not have a cell wall, nor a prominent vacuole, the cells of the specimen on the slide are animal cells.
Simulator Procedure (as performed through the Online Labs)
The ‘Select view’ drop down list allows you to select either the Microscope or Binocular View (It is the 'Binocular view' through which you can see the cell structure as viewed through the microscope).
To select the sample, you can use the ‘Select sample’ drop down list.
To change the power of the lens, you can choose a lens from the ‘Select objective lens’ drop down list.
For coarse adjustments, you can either click on the up and down arrow of ‘Coarse adjustment’ knob, or click on the left and right arrows of 'Course Adjustment' seen on the left controls panel.
For fine adjustments, you can click on the left and right arrows of ‘Fine adjustment’ seen on the left controls panel.
You can redo the experiment by clicking on the ‘Reset’ button.
Precautions
Ensure toothpick used to scrape the cheek is clean, so it does not cause infection to the cheek.
Extra glycerine stain should be removed using blotting paper.
Answer:
Aim
To study mitosis by preparing a temporary mount of an onion root tip.
Necessary Materials & Apparatus
Onion
Watch glass
Glass slide
Filter paper
Aceto-alcohol
Coverslip
Water
N/10 Hydrochloric acid
Acetocarmine Stain
Burner
Forceps
Dropper
Blade
Needle
Compound microscope
Procedure
Place the onion on a tile
Using the blade, remove the dry roots
Regrow the root tips by placing the bulbs in a water-filled beaker
After 3 to 6 days, new roots may emerge
Slide 2 to 3 cm off freshly grown roots and place them on a watch glass
Use a forceps to transfer the freshly cut tips to a test tube containing Aceto-alcohol (1:3 = anhydrous acetic acid: ethanol)
Submerge the root tips in the solution for 24 hours
Use the forceps to take out a single root and place it on a glass slide.
Put a single drop of N/10 HCl on the root tip
Then, put 2-3 drops of acetocarmine stain
Use a burner to warm it, and ensure that the stain does not dry up.
Use a filter paper to blot out the excess stain, if any
Cut the significantly stained portion of the root using a blade and place it on a slide. Discard the rest of the root
Put a drop of water on the root tip
Place a coverslip using a needle
Tap the coverslip such that the meristematic tissue of the root tip is compressed and spread out as a thin layer.
The preparation is ready for studying mitosis.
Observation
Use the compound microscope to study the various phases of mitosis