topic 2 - cell division (investigating mitosis) Flashcards
cgp (topic 2A) 36 - 37
what’s the first step to using a root tip to observe mitosis
cut 1cm from the tip from a growing root - it needs to be the tip as that’s where growth occurs (so that’s where mitosis takes place)
what’s the second step to using a root tip to observe mitosis
prepare a boiling tube containing 1M hydrochloric acid and put it in a water bath at 60C
what’s the third step to using a root tip to observe mitosis
transfer the root tip into the boiling tube and incubate for about 5 minutes
what’s the fourth step to using a root tip to observe mitosis
use a pipette to rinse the root tip well with cold water - leave the tip to dry on a paper towel
what’s the fifth step to using a root tip to observe mitosis
place the root tip on a microscope slide and cut 2mm from the very tip of it - get rid of the rest
what’s the sixth step to using a root tip to observe mitosis
use a mounted needle to break the tip open and spread the cells out thinly
what’s the seventh step to using a root tip to observe mitosis
add a few drops of stain and leave it for a few minutes - the stain will make the chromosomes easier to see under a microscope
what’s the eighth step to using a root tip to observe mitosis
place a cover slip over the cells and push down firmly to squash the tissue - this will make the tissue thinner and allow light to pass through it - don’t smear the cover slip sideways
what’s the ninth step to using a root tip to observe mitosis
now you can look at all the stages of mitosis under an optical microscope
what’s the first step of using an optical microscope to observe your prepared root cell
start by clipping the slide you’ve prepared onto the stage
what’s the second step of using an optical microscope to observe your prepared root cell
select the lowest powered objective lens
what’s the third step of using an optical microscope to observe your prepared root cell
use the coarse adjustment knob to bring the stage up to just below the objective lens
what’s the fourth step of using an optical microscope to observe your prepared root cell
look down the eyepiece (which contains the ocular lens) - use the coarse adjustment knob to move the stage downwards, away from the objective lens until the image is roughly in focus
what’s the fifth step of using an optical microscope to observe your prepared root cell
adjust the focus with the fine adjustment knob, until you get a clear image of what’s on the slide
what’s the sixth step of using an optical microscope to observe your prepared root cell
if you need to see the slide with greater magnification, swap to a higher powered objective lens and refocus
how do you calculate the mitotic index
number of cells with visible chromosomes ÷ total number of cells observed
what is the mitotic index
the proportion of cells undergoing mitosis
what does the mitotic index let you know
how quickly the tissue if growing and if there’s anything weird going on
what does it mean if a plant has a high mitotic index
a plant root tip is constantly growing so you’d expect a high mitotic index - in other tissue samples a high mitotic index could mean that tissue repair is taking place or that there’s cancerous growth in tissues
what is a stage micrometre
a microscope slide with an accurate scale and it used to work out the value of the divisions on the eyepiece graticule at a particular magnification
what equipment do you use to calculate the size of cells
graticule and micrometre
where is the stage micrometre placed on
the stage
where is the eyepiece graticule fitted onto
the eyepiece
how do you calculate the actual size
size of image ÷ magnification
what are artifacts
things you can see down the microscope that aren’t part of the cell or specimen that you’re looking at
what are four examples of artifacts
(1) dust
(2) air bubbles
(3) fingerprints
(4) inaccuracies caused by squashing and staining your sample
where are artefacts especially common, why
in electric micrographs because specimens need a lot of preparation before you can view them under an electric microscope
if an object could be seen with one preparation technique but not another, what is it likely to be
an artefact rather than an organelle