Chapter 2.1 Basic components of living systems Flashcards
What is a microscope
A microscope is an instrument that enables you to magnify and observe an object which are not visible by the naked eye.
What makes up the cell theory
Both plant and animal tissue are composed of cells.
Cells are the basic unit of life
Cells only develop from existing cells.
What is a light microscope/ optical microscope?
Type of microscope that uses visible light and a system of lenses to generate magnified images of small objects
How to prepare a light microscope (6 marker)?
- Specimens are prepared on a microscope slide therefore, a stain is used to highlight structures within the cells and this is typically methylene blue
2.Clip the microscope slide onto the stage - Ensure that the lowest-powered objective lens is over the slide.
- Use coarse adjusting knob to bring the stage up just below the lens.
- Look down the eyepiece and move stage downwards using coarse adjusting knob then stop when image is roughly in focus.
- To ring image into focus, use fine-adjusting knob until clear image is obtained.
- Observe image at a higher magnification by changing objective lens to a higher power therefore, readjust the stage using the coarse and fine adjusting knobs.
What are the 4 types of sample preperation in OCR biology?
Dry Mount, Wet Mount, Squash Slides and Smear Slides.
What is Dry Mount?
In a dry mount, the specimen is placed directly on the slide. A cover slip may be used to keep the specimen in place and to help protect the objective lens. Dry mounts are suitable for specimens such as samples of pollen, hair, feathers or plant materials
What is Wet Mount?
Specimens are suspended in a liquid such as water or an immersion oil. A cover slip placed at an angle so that aquatic samples are viewed this way.
What is a Squash Slide?
Squash slide is where an entire cells are pressed flat on a piece of glass and observed through a microscope technique.
Why is staining used within microscopy? (2 marks)
Staining is used to enhance visualization of the cell or certain cellular components under a microscope. As well as this some organelles absorb the stain and can increase contrast between components therefore, can identify organelles structure and function more easily.
What is a gram staining technique?
Gram staining is a common technique used to differentiate two large groups of bacteria based on their different cell wall constituents. The Gram stain procedure distinguishes between Gram positive and Gram negative groups by coloring these cells red or violet.
What is the difference between Gram positive and Gram negative bacteria? (2 marker)
Gram positive bacteria have a thick peptidoglycan layer and no outer lipid membrane whilst Gram negative bacteria have a thin peptidoglycan layer and have an outer lipid membrane.
What is the difference between magnification and resolution? (2 marker)
Resolution is the ability to distinguish two seperate points from being seperate entities whereas, magnification is the Magnification is how many times bigger the image of a specimen observed is in compared to the actual (real-life) size of the specimen.
What is the formula for manification? (2 marker)
magnification = imge size/ actual size.
What is the metric conversion? for example how do you get from metres to mm?
1m - 1000mm
1mm - 1000micrometers
1micrometers-1000nanometers.
What is an eyepiece graticule?
An eyepiece graticule and stage micrometer are used to measure the size of the object when viewed under a microscope.
What is the stage micrometer?
A stage graticule is a microscope slide with an accurate measuring scale – this is used to calibrate the value of the eyepiece divisions at different magnifications.
What is a laser confocal microscope?
Confocal laser scanning microscopy is a technique for obtaining high-resolution optical images with depth selectivity and allows protein localisation in specific cellular compartments.
How is a specimen viewed under a laser scanning confocal microscope?
The cells being viewed must be stained with fluorescent dyes
A thick section of tissue or small living organisms are scanned with a laser beam
The laser beam is reflected by the fluorescent dyes
Multiple depths of the tissue section/organisms are scanned to produce an image
Think of it like the laser beam is building up the image layer by layer
Advantages of a laser scanning confocal microscope?
They can be used on thick or 3-D specimens
They allow the external, 3-D structure of specimens to be observed
Very clear images are produced. The high resolution is due to the fact that the laser beam can be focused at a very specific depth
You can even see the structure of the cytoskeleton in cells
Disadvantages of a laser scanning confocal microscope?
It is a slow process and takes a long time to obtain an image
The laser has the potential to cause photodamage to the cells
What is an electron microscope?
Electron microscopes use electrons to form an image
This greatly increases the resolution of electron microscopes compared to optical microscopes, giving a more detailed image. There are also two types of electron microscopes which are TEM and SEM.
What are TEM (Transmission electron microscope)?
TEMs use electromagnets to focus a beam of electrons
This beam of electrons is transmitted through the specimen
Denser parts of the specimen absorb more electrons
This makes these denser parts appear darker on the final image produced (produces contrast between different parts of the object being observed) as well as this, produces a 2D image.
Advantages of a TEM?
They give high-resolution images (more detail)
This allows the internal structures within cells (or even within organelles) to be seen
Disadvantages of TEM?
They can only be used with very thin specimens or thin sections of the object being observed
They 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, meaning that specimens must be dead, unlike optical microscopes that can be used to observe live specimens)
The lengthy treatment required to prepare specimens means that artefacts can be introduced (artefacts look like real structures but are actually the results of preserving and staining)
They do not produce a colour image (unlike optical microscopes that produce a colour image).