Microscopes Flashcards

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1
Q

How do you convert from millimetres to micrometers ??

A

X1000

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2
Q

How do you convert from micrometers to manometers ?

A

X1000

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3
Q

What is the resolution of a light microscope ??

A

0.17 micrometers or around 200 manometers.

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4
Q

What is he definition for magnification ?

A

How many times larger an image appears.

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5
Q

What is the definition for resolution ?

A

The minimum distance between two objects before they appear as one.

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6
Q

What are light microscopes often used to explore ?

A

Cell division or movement of cells.

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7
Q

Name some issues with Light microscopes.

A

You often need stain to see the cells and this can kill the cells.

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8
Q

How do lenses make an image visible in an optical/ light microscope ?

A

They converge the light rays to the specimen.

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9
Q

Compare the different views of a SCanning electron microscope and a transmission electron microscope.

A

SEM -3D

TEM - 2D

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10
Q

Compare how the SEM and TEM create images using electrons.

A

SEM - bounce off.
TEM- electron beam passes through a think sample. Passes through denser parts less easily creating contrasting black and white shades.

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11
Q

Compare the thickness of specimens used in SEMs and TEMs.

A

TEM needs to be thin.

SEM can be thick or thin.

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12
Q

Why is resolution often limited on an optical or light microscope ?

A

The wavelength of light is too long to resolve between close objects.

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13
Q

Compare the resolution of all 3 microscopes.

A

Light - low

SEM & TEM - high

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14
Q

Compare the types of specimens used in each microscope.

A

Light - living or dead

SEM & TEM - dead only

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15
Q

How is magnification calculated ?

A

Magnification = image length / actual length.

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16
Q

Explain how light microscopes and electron microscopes show a different image.

A

Electron microscopes only just a short beam of electrons which creates a high resolution.

Light microscopes use light - the wave length of light is often too long to distinguish between close together objects so a lower resolution image is shown.

17
Q

Explain the meaning of resolving power.

A

The ability to distinguish between points which are close together.

18
Q

Explain the reason for the difference in resolving power between light and electron microscopes.

A

Electrons have a shorter wave length. The wave length of light is too long to distinguish between close together points.

19
Q

Care must be taken in interpreting electron micrograph a. Some features visible in an electron micrograph may not be present in a living cell. Explain why.

A

Processes involved in preparation alter and distort the contents of the cell.

20
Q

Give one advantage of using a TEM rather than an SEM.

A

Higher resolution.

21
Q

Name two structures in a eukaryotic cell that cannot be identified using a light microscope.

A

Ribosomes , Centrioles, ER, lysosomes.

22
Q

Describe how you could make a temporary mount of a piece of plant tissue to observe the position of starch grains in the cells when using an optical light microscope.

A

Place one drop of water on a clean slide.
Take a thin slice of epithelial tissue from the plant using tweezers and place this on the slide ensuring this is completely flat.
Cover the specimen with a solution of iodine in potassium iodide.
Cover the specimens with a thin glass cube and wipe away any excess liquid on the slide.
Place the slide on the microscope stage and adjust the view.

23
Q

Describe how you would use a microscope to find the mean diameter of triglyceride droplets on a cell.

A

Use an eyepiece graticule to accurately measure he radius of each triglyceride to 1 micrometer. Calibrate the graticule using a stage micrometer scale and repeat to calculate a mean.
Then divide the radius value for each triglyceride and divide this answer by the number of triglycerides investigated.