Topic 2 - Microscopes Flashcards

1
Q

What is the formula for magnification?

A

Magnification = size of image/size of real object

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2
Q

What is magnification?

A

How much bigger the image can be enlarged compared to its actual size

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3
Q

What is resolution?

A

The ability to distinguish between two objects as separate. Defined as the minimum distance at which two objects can still be seen as distinct.

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4
Q

What is the limiting factor of resolution?

A

The wavelength of light limits resolution which cannot resolve structures smaller than 0.2 µm

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5
Q

What are the uses of a light microscope?

A

Suitable for observing life specimens and used for general cellular observations.

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6
Q

How do electron microscopes work?

A

– They use a beam of electrons focused by electromagnets.
– Operate in a vacuum to prevent air particles from scattering the electrons.
– Can resolve objects a small as 0.1 nm providing a much greater resolution than light microscopes.

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7
Q

What are the two types of electron microscope and what is the difference?

A

Transmission electron microscope (TEM): a beam of electrons passes through a specimen and produces a detailed 2-D image of the internal structure areas absorbing more electrons appear darker.

Scanning electron microscope: a beam of electrons scans, the surface of the specimen and produces a detailed 3-D image of the specimens surface.

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8
Q

What is the main advantage of the TEM?

A

Extremely high resolution for internal details.

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9
Q

What is the main advantage of the SEM?

A

Produces 3-D images useful for understanding surface textures.

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10
Q

What are the limitations of transmission electron microscopes?

A
  • require a vacuum so living specimens cannot be observed.
  • a complex staining process is required which may introduce artefacts.
    – Specimens must be thin.
    – SEM has a lower resolving than TEM but both are far superior light microscope.
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11
Q

Compare the light and electron microscopes.

A

Source of light is visible light - electrons
Resolution is 0.2 µm - 0.1 nm
Magnification is up to x1500 - up to x2000000
Simple specimen preparation can view live samples- complex specimen cannot view live samples
Image produced is @-D - @-D or £-D

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12
Q

What are the guidelines for drawing a scientific diagram?

A
  • use a sharp pencil to clear lines
  • Avoid shading or colouring
  • Ensure diagrams are large and clear
  • Labels structures with straight lines not crossing one another
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13
Q

How should you label your scientific diagram?

A
  • include the name of the specimen and magnification used
  • label should: be horizontal and include specific terms.
  • use a scale bar to indicate actual size
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14
Q

How should the proportions be done on a scientific diagram?

A
  • Accurately represent the relative size of structures
  • Use grid paper if necessary to maintain proportions.
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15
Q

How would you prepare the specimen to identify starch grains in a plant cell?

A

– A thin section of the plant tissue is prepared and placed on a slide.
– A drop of iodine solution is added to the tissue to stain the grains.
– The slide is covered with a cover slip and observed under a light microscope.

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16
Q

How would you be able to detect starch grains in a plant cell?

A

– When iodine binds to start grains the grains turn blue – black
– The colour change is due to the formation of an iodine starch complex

17
Q

What three steps should you ensure for microscope calculations?

A
  1. Make sure the units are consistent; convert the measurements to the same unit
  2. Apply the formula; use the given data to calculate the required value
  3. Label answers; always include correct units in your answer
18
Q

The image of a cell measures 50 mm and the magnification is x500. What is the actual size of the cell?

A

50 mm/500 = 0.1 mm
0.1 mm = 100 nm