microscopes Flashcards

1
Q

magnification

A

how many times bigger the image produced by the microscope is than the real-life object you are viewing

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2
Q

resolution

A

the ability to distinguish between objects/points that are close together

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3
Q

what do optical microscopes use?

A

they use light to form an imagr

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4
Q

resolution of optical microscopes

A

-using light, can’t distinguish between two objects that are closer than half the wavelength of light → low resolution
-maximum resolution of around 0.2
micrometres

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5
Q

what can optical microscopes be used to observe?

A

-eukaryotic cells, their nuclei (possibly mitochondria and chloroplasts)
-living specimens

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6
Q

maximum magnification of optical microscopes:

A

1500x

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7
Q

what do electron microscopes use?

A

they use electrons to form an image

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8
Q

resolution of electron microscopes

A

-high resolution
-a beam of electrons has a much smaller wavelength than light
-maximum resolution of 0.0002 pm

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9
Q

what can electron microscopes be used to observe?

A

small organelles

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10
Q

what is the maximum magnification of electron microscopes?

A

×1,500,000

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11
Q

what are the two types of electron microscopes?

A

trasmission electron microscopes:
(TEMs)
scanning electron microscopes:
(SEMs)

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12
Q

how do TEMS work?

A

-use electromagnets to focus a beam of electrons
-beam of electrons is transmitted through the specimen
-denser parts of the specimen absorb more electrons & appear darker on the final image produced

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13
Q

advantages of TEMs

A

-give high-resolution images
-allows small organelles to be seen

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14
Q

disadvantages of TEMs

A

-can only be used with very thin specimens

-cannot be used to observe live specimens (as there is a vacuum inside a TEM, all the water must be removed from the specimen and so living cells cannot be observed)

-the lengthy treatment required to prepare specimens means that artefacts can be produced (artefacts look like real structures but are actually the results of preserving and staining)

-do not produce a colour image

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15
Q

how do SEMS work?

A

-scan a beam of electrons across the specimen
-beam bounces off the surface of the specimen and the electrons are detected, forming an image
-this means SEMs can produce 3D images that show the surface of specimens

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16
Q

advantages of SEMs:

A

-can be used on thick or 3-D specimens
-allow the 3-D structure of specimens to be observed

17
Q

disadvantages of SEMs:

A

-lower resolution images than TEMs
-cannot be used to observe live specimens
-no colour image

18
Q

electron microscope vs light microscope (basic differences)

A

large and can’t be moved (e) v small and easy to carry (l)
-vacuum needed (e) v no vacuum needed (l)
-complicated sample preparation (e) v simple sample preparation (I)
-over 500,000x magnification (e) v up to 2,000x magnification (l)
-specimens are dead (e) v specimens can be living (l)

19
Q

the start of using an optical microscope:

A

start with the low power objective lens
→ it’s easier to find what you’re looking for in the field of view
→ this helps to prevent damage to the lens or coverslip, incase the stage has been raised too high

20
Q

where & how can graticules be used?

A

they can be placed into the eyepiece of a microscope to act as a ruler in the field of view

21
Q

what must be done with a graticule?

A

it must be calibrated for the objective lens that is in use

22
Q

how is calibration done?

A

this is done by using a stage micrometer
-by using the two scales together, you can find out how many micrometers each graticule unit is worth

23
Q

rules of biological drawings:

A

-the drawing must have a title
-the magnification under which the observations were made must be recorded
-no shading
-label lines should be kept to one side of the drawing

24
Q

how many different lenses does a light microscope have?

A

two:
-an eyepiece lens
-an objective lens

25
Q

objective lenses on a microscope:

A

a series of objective lenses, each with a different magnification

26
Q

magnification formula

A

I.A.M

image size/actual size = magnification

27
Q

mm → um

A

x1000

28
Q

um → nm

A

x1000

29
Q

the actual thickness of the leaf below is 2000um, but the image size of the leaf in the diagram is 50mm. what is the magnification of the diagram?

A

2000 / 1000 = 2, so the actual thickness of
the leaf is 2 mm and the image size is 50 mm

magnification = image size / actual size
50 / 2 = 25

magnification = x25