BIOLOGY Practicals EOY Flashcards
(44 cards)
Microscopy
use a light microscope to observe, draw and label a selection of plant and animal cells.
MICROSCOPY: Purpose of practical / Background
Light microscopes are really useful for studying cells. In the past they have been used to learn about how cells work. Scientists often produce drawings of what they see down a microscope
MICROSCOPY: Safety
Stains may irritate skin/eyes - wear protection
Don’t use direct sunlight as a source of light
If using a lamp be aware it may get hot.
Take care when cutting plant tissue samples.
Swabs used to collect cheek cells should be sterile and disposed of properly.
MICROSCOPY: Sample method / Apparatus
Place a tissue sample on a microscope slide.
Add a few drops of a suitable stain
Lower the coverslip (at an angle) onto the tissue
Place the slide on the microscope stage and focus on the cells using the lower power objective lens (+ the coarse and fine focus knobs)
Change to higher powered objective lens and focus
Draw any types of cells that cann be seen
Add a magnification scale to the diagram.
MICROSCOPY: Why do you need a stain?
To make certain structures visible
MICROSCOPY: Why lower the coverslip and press carefully?
To remove any bubbles
MICROSCOPY: Why can you see the nucleus and cell wall but not the mitochondria?
They’re too small
MICROSCOPY: How could we see the smaller structures (e.g. ribosomes)?
You would need to use an electron microscope which has a higher magnification and higher resolution.
MICROSCOPY: You must be able to remember, use and rearrange the magnification equation
You might need to use your ruler to measure the size of images and work out their real size or magnification
Measure carefully and remember it’s usually best to work in mm rather than cm
Make sure you can convert between units. The important ones are 1mm = 1000 um and 1um = 1000nm
MICROSCOPY: Drawings (there are rules to scientific drawings)
no shading, no broken/sketchy/overlapping lines, labels should be added with ruled lines (NOT ARROWS) and there should be a magnification/scale bar
OSMOSIS
Investigate the effect of a range of concentrations of sugar or salt solutions on the mass of plant tissue
OSMOSIS: Calculate the change in mass as a percentage change
change in mass / starting mass x 100
OSMOSIS: Purpose of practical / Background
Osmosis is the movement of water molecules from a more dilute solution to a more concentrated solution through a partially permeable membrane.
Sugar and salt are examples of solutes (they dissolve in water). The more solute dissolved, the more concentrated the solution is. Potatoes are often used for this investigation.
OSMOSIS: Variables
IV - The concentration of sugar/salt
DV - The change in mass of the potato
CVs - The temperature, the length of time the cylinders are left for, the shape of the cylinders, drying the cylinders before re-weighing, skin should be removed from cylinders, the cylinders should be fully submerged in the solution.
OSMOSIS: other information
Length could be used instead of mass
A bung might be used to prevent the water from the solutions evaporating (as this would change the concentration)
OSMOSIS: Safety
Care must be taken when cutting the cylinders of potato
OSMOSIS: Sample method / apparatus
Cut some cylinders of potato tissue using a cork borer and measure their mass.
Submerge the cylinders in different concentrations of salt/sugar (e.g. 0.0 molar, 0.2 molar, 0.4 molar, 0.6 molar, 0.8 molar, 1 molar)
After 30-60 minutes, remove the cylinders, dab them dry and reweigh them
Calculate the change in mass or length.
OSMOSIS: Results
High concentration of salt/sugar in solution = water moves out of potato cells into solution by osmosis. Potato loses mass
Low concentration of salt/sugar in solution = water moves into potato cells from solution by osmosis. Potato gains mass
If no water goes into or out of the potato overall and it doesn’t change mass,, then the solution is exactly the same concentration as inside the potato.
OSMOSIS: You should be able to use a table or a graph to calculate the concentration of the cytoplasm of the plant tissues
This will be when there is no overall movement of water into or out of the cell so there will be no change in mass (on a graph this might be where the line crosses the axis)
OSMOSIS: Why is it better to measure the change in mass/percentage change in mass rather than just the final mass?
This allows a clear comparison to be made even if the starting masses are slightly different
OSMOSIS: How to calculate the rate of water uptake?
The water uptake is measured by recording the time taken for a bubble in the tube to move a set distance
FOOD TESTS:
Use qualitative reagents to test for a range of carbohydrates, lipids and proteins
FOOD TESTS: purpose of practical / background
to find out whether starch, sugars or protein are present in samples
FOOD TESTS: other information
food samples might need to be chopped up or crushed to release the substance being tested for
it’s important to refer to “iodine solution” not just iodine
Don’t forget to mention that for the test for sugars, the sample needs to be heated