A level Biology : Module 1 - Microscopes, Resolution and Magnification Flashcards

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1
Q

What is an Electron Micrograph?

A

Photo of an image seen under an electron microscope

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2
Q

What is Magnification?

A

Number of times larger an image appears compared to the actual size of the object

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3
Q

What are Organelles?

A

Small structures within cells, each one having a particular function

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4
Q

What is a photomicrograph?

A

Photo of an image seen under an optical microscope (light microscope)

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5
Q

What is resolution?

A

The ability to distinguish between 2 points on an image, i.e. the Detail, clarity and clearness of the image

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6
Q

Advantages of Light Microscopes

A
  • Cheap
  • Relatively easy to use
  • Portable, able to use in the field and in labs
  • Can be used to study whole living specimens
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7
Q

Disadvantages of Light Microscopes

A
  • Resolution is limited, so we cannot magnify any higher whilst giving a clear image
  • MAX magnification of 1500
  • Preparation could distort specimen
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8
Q

Information about Electron Microscopes

A
  • Use electrons to form an image
  • Higher resolution than light microscope
  • Beam of electrons has a far smaller wavelength than light, so can resolve (distinguish between) two objects extremely close together
  • Max resolution of around 0.2nm
  • 1,500,000 max useful magnification
  • Can observe the smaller organelles (ribosomes, ER, lysosomes)
  • 2 types (Transmission and Scanning)
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9
Q

Advantages of TEMs

A
  • Produce a high resolution image
  • Allows internal structures within cells and organelles to be seen
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10
Q

Disadvantages of TEMs

A
  • Can only be used with very thin specimens or thin sections of the object being observed
  • Can’t observe live specimens (vaccum, water is removed from specimen)
  • Lengthy treatment required to prepare specimens (so artefacts can be introduced, which are the result of preserving and staining and not the actual structures)
  • No colour image produced
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11
Q

How does a scanning electron microscope work

A
  • Scan a beam of electrons across the specimen
  • Beams bounce off the surface and electrons are detected which forms a 3D image of the surface of a specimen
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12
Q

Advantages of a Scanning electron microscope

A
  • Can be used on thick or 3D specimens to be observed
  • Can observe surface structure in 3D
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13
Q

Disadvantages of Scanning Electron Microscopes

A
  • Give lower resolution images (than TEMs)
  • Cannot observe live specimens
  • No colour images
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14
Q

How do Laser Scanning Confocal Microscopes work?

A
  • Relatively new technology
  • Cells viewed should be stained with florescent dyes
  • Thick section of tissue or small living organism is scanned with a laser beam
  • beam reflected by fluorescent dyes
  • Multiple depths of the tissue section / organism is scanned producing an image
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15
Q

Advantages of Laser Scanning Microcopes

A
  • Used on thick or 3D specimens
  • Allow external 3D structures of specimens to be observed
  • Clear images produced
  • STRUCTURE OF CYTOSKELETON CAN BE SEEN
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16
Q

Disadvantages of using Laser Scanning Microscopes

A
  • Slow process
  • Laser can cause photodamage to the cells
17
Q

What limits the resolution of an optical microscope?

A

The wavelength of light (400nm)

18
Q

How to calibrate microscope

A
  • Place stage micrometer on stage (each unit is 10nm)
  • Replace eyepiece on microscope with eyepiece graticule
  • Line up eyepiece graticule with stage micrometer
19
Q

Why do we stain in microscopy?

A
  • Tissues / organisms are often transparent
  • So coloured dyes absorb colours of light while reflecting others, so structures are visible
20
Q

What common stains are used in light microscopy?

A

Toluidine blue, Phloroglucinol (red/pink)