cell structure Flashcards
magnification defintion
the number of times larger an image appears compared to its actual size
resolution definition
the ability to distinguish between 2 separate points in an image
measure of clarity
microscopes allow us to ______ objects and therefore study organisms at a ______ level
magnify
cellular
magnification equation?
what is the total magnification?
eyepiece magnification x objective magnification
which type of microscope was the first to be developed?
light microscope
light microscope magnification range
4x to 2000x
light microscope resolution
200nm
3 advantages of using light microscopes
easy to section and stain specimen
easy to use
both dead and living samples can be viewed
chepa
path of light in a microscope
light from source travel through the specimen, through the objective lens, through the eyepiece lens, to your eye
eyepiece lens magnification and what does it contain?
x10
contains eyepiece graticule
turret function
rotates to bring the objective lenses into place
objective lenses powers/magnifications
low=x4
medium=x10
high=x40
stage function
where the microscopic slide is placed
condenser function
used to vary intensity of light reaching the object
fine focus function
used to focus high-power objective lens
coarse focus function
used to focus low and medium-power objective lenses
3 advantages of staining specimens to be viewed under a microscope
increases contrast in the slide
easier to distinguish between different organelles
stains bind to particular molecules e.g. toluidine blue binds to chromosomes, iodine solution binds to cellulose
what is Gram’s stain used for?
classifying bacterial species into 2 large groups: gram-positive and gram-negative
this helps doctors prescribe correct medicine
Gram’s stain steps
stain bacteria
fix colour
decolourise cells
apply counterstain
Gram’s stain colour
pink and purple
wet mounting meaning and steps
involves water/ stain
1)put a drop of water/stain onto specimen
2)lower a cover slip onto the specimen
dry mounting meaning and steps
does not involve any water/ stain
1)observe specimen on a slide
assume specimen is cut very thinly so light can pass through
a lot of biological tissue is transparent ; why is this a problem when using microscopy to view it and how can it be overcome?
would not show up clearly
stain specimen to increase contrast between cells/organelles and increase ability to distinguish between them
why must specimens be thin on a slide
light must be able to pass through the specimen
for clarity you want to be able to only see a single layer of cells
why should the refractive index of media when wet mounting be about equal to glass
if light is refracted too much or too little, the image is distorted
describe how a slide to show onion cells could be prepared
a layer of onion cells removed from epidermis using mounted needle/forceps
placed onto slide, ensuring it does not fold
stained with 1 drop of iodine solution
cover slip placed on at angle so no air bubbles form
ready to be viewed
why should a cover slip be placed onto a wet mount at an angle
it prevents air bubbles forming, which can distort the image
what is laser scanning confocal microscopy
a light microscope that sues lasers and fluorescence to create a 3D image of a sample
what type of image does laser scanning confocal microscopy form
a 3D image with depth selectivity
how does laser scanning microscopy differ from conventional light microscopy?
uses lasers instead of visible light
higher magnification
builds up image thorough computer which is 3D
higher resolution
how is an image formed in laser scanning confocal microscopy
laser beam is focussed onto a sample by mirrors. the sample, stained by fluorescent dyes, reflects the laser back through a pinhole to a detector. This is attached to a computer which builds up the image one pixel at a time.
what is laser scanning confocal microscopy used to observe and why
living organisms/species because it is non-invasive
you can watch a process taking place
what are the 2 types of electron scanning microscopy?
scanning electron microscopy (SEM)
transmission electron microscopy (TEM)
how does a scanning electron microscope work
electrons are fired at a specimen and bounce off the surface
these are detected by a compute and an image is built up
scanning electron microscopy magnification range
100x-100,000x
scanning electron microscopy resolution range
3-10nm
advantages of scanning electron microscopy
3D image formed
surface detail
how does a transmission electron microscope work
electrons are fired through a specimen
these are detected by a computer and an image is built up
transmission electron microscopy magnification range
100x-2,000,000x
transmission electron microscopy resolution range
0.2-1.0nm
disadvantages of electron microscopy
highly specialist training is required for use
complex slide preparation means artefacts can be produced so the image is distorted
electron beam can damage the specimen
specimens must be dead because the images are viewed under a vacuum so you cannot observe live processes
TEM is 2D
advantages of electron microscopy
3D for SEM
surface detail
high magnification and resolution, but TEM>SEM
advantages of laser scanning confocal microscopy
depth selectivity
3D image
observe living organisms and processes taking place
disadvantages of laser scanning confocal microscopy
limited magnification and resolution (not as high as electron microscopy)
success criteria for biological sketches
plain paper; use over half
single, clear, continuous line with a sharp pencil
no shading or colour
correct proportions
label lines in pencil with a ruler; start at structure, do not cross and are horizontal
horizontal labels
no arrowheads
title at top
scale bar in pencil with ruler at the bottom
what makes up a nucleus?
nucleolus
chromatin
nuclear envelope
nuclear pores
where is the nucleolus located?
in the centre of the nucleus