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Observing Plasmolysis Using The Veho VMS-001 USB Microscope

This document provides instructions for observing plasmolysis in red onion cells under a microscope. The method involves: 1) preparing a thin slice of onion epidermis, 2) placing it on a slide and covering it with a coverslip propped up on blu tack, 3) flooding the area with distilled water, 4) adding salt crystals to draw water from the cells, causing them to shrink away from their walls and demonstrating plasmolysis. Diagrams are included to illustrate the process. Tips are given to optimize viewing the effects of plasmolysis and rehydration of the cells.

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53 views

Observing Plasmolysis Using The Veho VMS-001 USB Microscope

This document provides instructions for observing plasmolysis in red onion cells under a microscope. The method involves: 1) preparing a thin slice of onion epidermis, 2) placing it on a slide and covering it with a coverslip propped up on blu tack, 3) flooding the area with distilled water, 4) adding salt crystals to draw water from the cells, causing them to shrink away from their walls and demonstrating plasmolysis. Diagrams are included to illustrate the process. Tips are given to optimize viewing the effects of plasmolysis and rehydration of the cells.

Uploaded by

Zico
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Observing plasmolysis using the Vehotm VMS-001 USB Microscope

Materials:

1 x red onion Distilled water

1 pair forceps Rock salt crystals

1 scalpel Petri-dish or gallipot

Microscope slides and coverslips USB microscope and PC

Blu tacktm

Method:

1. Remove the two ends of the onion and as many layers as is necessary to
expose a fresh and unblemished layer.
2. Using the scalpel, cut a square shape approximately 0.25cm x 0.25cm in the
fresh layer of onion.
3. Using the forceps tease away the red epidermis from the onion tissue and
place this explant onto a microscope slide (figure 1).
4. Make four small pieces of Blu tack and work them into spheres. Place the
spheres at the four corners of a coverslip and place over the onion tissue
(figure 2).
5. Using a Pasteur pipette, flood the gap between the slide and the coverslip
with distilled water. The piece of onion tissue will move when this is done. If it
settles near any of the Blu tack, use one arm of the forceps to move it to a
more central position.
6. Using the USB microscope, locate the piece of tissue and focus on the edge.
The cell walls and cytoplasm of individual cells are easily observable at a
magnification of around x 200 (figure 3).
7. Pour rock salt crystals into a Petri-dish or gallipot and select 4-6 which are flat
enough to fit through the gap between the slide and the coverslip.
8. Slip the crystals into the distilled water between the microscope slide and the
coverslip (figure 4). This will result in the tissue being surrounded by a strong
sodium chloride solution, allowing the observation of plasmolysis within a few
minutes.
9. As water leaves the onion cells, the cytoplasm of cells will shrink away from
the cell wall (figure 5).
Hints and Tips

The larger the piece of onion tissue, the longer the effects of plasmolysis may take to
become visible, so smaller pieces are more desirable.

The field of view of the microscope, as displayed on the laptop, is in a different


orientation to the slide that you are looking at. As a consequence, it is not always
easy to know which side of the coverslip is closest to the tissue edge that is in view.
In order to minimise the time taken for the effects of plasmolysis to be seen, sliding
rock salt crystals under the coverslip on all four sides is recommended.

Rehydration can also be observed with this set up. The salt solution should be bled
out, using an absorbent paper towel, while at the same time adding more distilled
water from the opposite side of the coverslip. This process will move the onion
tissue. It is important to find it with the microscope again as quickly as possible or the
phenomenon can be missed.

Figure 1: Removal of onion epidermis.


Figure 2: Coverslip on Blu-tack.

Figure 3: Red onion epidermis cells (x 200 magnification).


Figure 4: Salt crystal insertion.

Figure 5: Plasmolysed cells.

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