Lesson 3.2.1.3.1
3.2.1.3.1 Microscopy, magnification and cell fractionation Quiz: AQA Biology, Unit 2
20 questions
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Lesson 3.2.1.3.1, Microscopy, magnification and cell fractionation: 20 multiple choice questions for the AQA Biology (7402), Unit 2: Cells, written with Revision Ninja.
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The 20 questions
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What is the formula for magnification?
- Magnification = size of image + size of real object
- Magnification = size of real object / size of image
- Magnification = size of image / size of real object
- Magnification = size of image x size of real object
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What is meant by the resolution of a microscope?
- The brightness of the image that is produced by the light source inside the microscope body
- The size of the smallest object that can be seen as a single point when viewed under the lens
- The maximum magnification that the microscope is able to produce while keeping the image in focus
- The minimum distance between two points that can still be seen as two separate points
-
Which type of microscope gives the highest resolution?
- Optical microscope
- Transmission electron microscope
- Scanning electron microscope
- Light microscope with a digital camera
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What does a scanning electron microscope mainly show?
- The three-dimensional surface of a specimen
- The internal structure of a thin section of a cell
- Only the nucleus of a cell, stained with a dye
- Living cells at high resolution in their natural colour
-
What is the approximate resolution limit of a light microscope?
- About 20 mm
- About 200 nm
- About 0.02 nm
- About 2 nm
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Why is the homogenisation step performed in cell fractionation?
- To stain the organelles so they can be seen under a microscope with no exceptions
- To separate the organelles by their density in a gradient
- To break open the cells and release the organelles into a solution
- To make the organelles soluble in ethanol
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Why is the solution used in cell fractionation kept cold and isotonic?
- To encourage the organelles to dissolve in the solution so that they can be separated more easily
- To prevent organelles from being damaged, and to avoid their swelling or shrinking by osmosis
- To make the organelles denser so that they settle out of solution more quickly in the tube
- To allow the organelles to synthesise ATP during the separation process in the centrifuge tube
-
What is the unit conversion for 1 micrometre expressed in nanometres?
- 100 nm
- 1000 nm
- 10000 nm
- 1 nm
-
A cell has an image length of 40 mm when viewed at a certain magnification. Its actual length is 0.02 mm. What is the magnification?
- 4000
- 200
- 20
- 2000
-
An image of a cell is 16 mm wide at a magnification of x800. What is the actual width of the cell?
- 0.2 mm
- 0.002 mm
- 12.8 mm
- 0.02 mm
-
A mitochondrion appears 60 mm long in a micrograph at a magnification of x30000. What is its actual length?
- 20 micrometres
- 0.2 micrometres
- 200 micrometres
- 2 micrometres
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In a centrifuge, which cell component sediments first when a homogenate is spun at a low speed?
- Ribosomes, which are the lightest components
- Nuclei and large unbroken cell fragments
- Mitochondria, which need the highest speed
- Lysosomes, which have a density lower than water
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Why do ribosomes need to be separated by ultracentrifugation at a higher speed than mitochondria?
- Ribosomes are much smaller than mitochondria, so they need a greater centrifugal force to sediment
- Ribosomes contain DNA, which makes them heavier than mitochondria
- Ribosomes are larger than mitochondria, so they need more force to move
- Ribosomes are membrane-bound, so they stick to the tube and must be spun harder
-
A light microscope cannot show individual ribosomes clearly. Why?
- Ribosomes are too heavy to be placed on a slide
- Ribosomes are smaller than the resolution limit of a light microscope
- Ribosomes absorb all the light so that no image is produced
- Ribosomes are colourless and cannot be stained
-
Why does increasing magnification without increasing resolution produce a less useful image?
- The image becomes sharper, but the actual object becomes smaller
- The image becomes smaller and darker, which hides the detail
- The image becomes larger but blurred, so no additional detail can be seen
- The image shows more colour, which reduces the detail visible
-
A student says that doubling the magnification of a light microscope doubles the amount of detail that can be seen. Which evaluation is correct?
- Correct, because doubling the magnification always doubles the number of organelles that can be seen clearly
- Correct, because magnification and resolution are the same property of the microscope and always rise together
- Incorrect, because detail depends on resolution, and beyond the resolution limit more magnification gives only a larger blurred image
- Incorrect, because magnification has no effect on the image itself, but only changes the brightness of the view
-
Explain why artefacts can appear in electron micrographs, and how scientists distinguish them from genuine organelles.
- Artefacts are always organelles that have been stained by the dye, so they must be counted as genuine structures
- Artefacts come from the preparation process, so they are checked by comparing images prepared in different ways and other evidence
- Artefacts appear only in living cells that are viewed without any fixing, so they can be avoided by fixing the cell
- Artefacts are caused by the light source of the microscope, so they can be removed by using a higher magnification
-
A student claims that a scanning electron microscope shows internal structure better than a transmission electron microscope. Which evaluation is correct?
- Incorrect, because neither type of electron microscope can produce any usable image of the internal structure of cells
- Correct, because the scanning electron microscope has a higher resolution than every other type of microscope available
- Correct, because the scanning electron microscope passes the electron beam through the whole specimen to show the interior
- Incorrect, because the scanning microscope shows surface detail, whereas the transmission microscope shows internal structure
-
Explain why the principle of cell fractionation depends on organelles having different densities or sizes.
- Organelles of different density and size sediment at different rates during centrifugation, so they can be separated into layers
- Organelles are separated by their colour, which changes at different centrifugal speeds
- Organelles of the same density all sediment at the same rate, so they can be separated only by staining
- Organelles are separated by their electric charge, which makes them move in a magnetic field
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Explain why a student would not expect to see the internal structure of a living cell in a transmission electron micrograph.
- The specimen must be thinly sliced, fixed and placed in a vacuum, which kills the cell
- Living cells cannot be stained, so they show no contrast in an electron micrograph with no exceptions
- The electron beam is too weak to pass through any cell structure
- Transmission electron microscopes can only image the outer surface of the cell
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