Topic 2A: Cell Structure And Division Flashcards
Define magnification:
How many times bigger an image appears compared to the objects actual size.
Define resolution:
The minimum distance apart two objects need to be in order to appear as separate items.
Optical (light) microscopes:
• Use light to form an image.
• Maximum resolution of around 0.2 micrometers.
• Maximum useful magnification of around x1500.
Electron microscopes:
• Use electrons to form an image.
• Higher resolution and magnification than optical microscopes, so give more detailed images.
• Maximum resolution of around 0.0002 micrometers.
• Maximum useful magnification of around x1,500,000
• Give a black and white image (but is often coloured using a computer).
Transmission electron microscopes (TEM):
• Use electromagnets to focus a beam of electrons, which is then transmitted through the specimen.
• Denser parts of the specimen absorb more electrons, so appear darker in the image you end up with.
• Give higher resolution images, so you can see the internal structures of organelles e.g. chloroplasts.
• Specimen must be viewed in a vacuum, so must be a non-living organism.
• TEM’s can only be used on thin specimens.
• 2-D image
Scanning electron microscopes (SEM):
• Scan a beam of electrons across the specimen - knocking off electrons from the specimen, which are gathered in a cathode ray tube to form an image.
• Must be used on non-living organisms.
• Produces a 3-D image.
• Can be used on thicker specimens.
• Gives a lower resolution image than TEM’s.
How to prepare a optical microscope slide:
- Start by pipetting a small water droplet onto the centre of the microscope slide.
- Use tweezers to place a thin section of your specimen on top of the water droplet, your specimen needs to be thin to allow light to pass through it.
- Add a drop of stain - stains highlight objects in a cell.
- Place your cover slip on top of the specimen. To do this: stand your coverslip upright on the slide, next to the water droplet, then carefully tilt and lower your specimen so it covers the specimen. Don’t get any bubbles under your cover slip, they’ll obstruct your view of the specimen.
What are artefacts?
Things that you can see when you look down a microscope that aren’t part of the cell or specimen you are looking at.
Examples of microscope artefacts:
• Dust particles
• Fingerprints
• Inaccuracies caused by squashing or staining your sample.
When are artefacts most commonly made?
During the preparation of your specimen.
Where are artefacts most common?
In electron micrographs because specimens require a lot of preparation when they are viewed under an electron microscope.
How were the first scientists who used electron microscopes able to distinguish between artefacts and organelles?
By using several different sample preparation techniques. If an object can be found using one preparation technique but not another, it is more likely an artefact.
Compare the advantages and disadvantages of TEM’s and SEM’s:
TEM’s
Advantages:
• Gives a high resolution image, so shows small objects.
Disadvantages:
• Can only be used on thin specimens and non-living organisms.
• Only produces a 2-D image.
SEM’s:
Advantages:
• Can be used on thicker organisms.
Disadvantages:
• Gives a lower resolution image than TEM’s.
• Can only be used on non-living organisms.
What are the 4 examples of eukaryotic cells?
Animal, plant, algal and fungal cells.
Describe the structure and function of the mitochondrion:
• Structure - Oval shape, contains a double membrane: an outer and inner membrane. The inner membrane is folded to create a structure called crista, inside the inner membrane is the matrix which contains enzymes for respiration.
• Function - Site for aerobic respiration. Aerobic respiration produces ATP (a common energy source in the cell). Mitochondria are found in large numbers in cells that are very active and require a lot of energy.