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Give the method for RP 1 microscopy (measuring the size of cells)
Place the sample on a slide with a drop of water/stain and place a cover slip at an angle to avoid air bubbles
Use the lowest magnification objective lens first to locate the sample
Adjust the focus with the coarse and dune focus knobs
Use an eyepiece graticule to calibrate measurements
Calculate actual size using:
Actual size= image size/magnification
Give the method for RP 2 preparing a root tip squash (mitosis)
Cut 1-2cm of a root tip
Place in HCl at 60°C for 5 minutes to break down cell walls
Rinse in distilled water and place on a slide
Stain with toluidine blue or acetic ore in to highlight chromosomes
Use a mounted needle to spread the root tip and squash with a coverslip avoiding sideways movement
Examine under a microscope and count cells in each mitotic stage
Give the method for RP3 investigating water potential in plant tissues
Cut equal sized potato cylinders and blot dry
Weigh each before placing them in different concentrations of sucrose solution
Leave for at least 20 minutes
blot dry and re weigh
Calculate the % change in mass using: (final mass -initial mass)/initial mass x100
Plot a graph of % change in mass against sucrose concentration to estimate water potential
Give the method for RP4 investigating membrane permeability
Use a cork border to cut beetroot cylinders equally
Rinse to removes excess pigment
Place in a test tube with water at different temperatures
Leave for 10 minutes
Use a colorimeter to measure absorbance of the solution
Higher absorbanve = more pigment released = greater membrane permeability
Give the method for RP5 the effect of enzyme concentration on a rate of reaction
Prepare different enzyme concentrations using serial dilution
Add enzymes to substrate in a test tube
Use a stopwatch to record time taken for a visible change
Repeat at least 3 times and calculate a mean
Control temperature using a water bath
Give the method for RP6 investigating the rate of photosynthesis
Place pondweed in a test tube of sodium hydrogen carbonate solution
Place a light source at a set distance
Leave to acclimate for 5 minutes
Count oxygen bubbles produced per minute or collect oxygen using a capillary tube and measure the volume
Repeat with different light intensities
Give the method for RP7 chromatography of photosynthetic pigments
Grind the leaf sample with propanone
Use a capillary tube to place a concentrated spot of pigment onto chromatography paper
Place in a beaker with solvent
Allow the solvent to rise up the paper
Calculate the Rf value
Rf= distance moved by pigment/distance moved by solvent
Give the method for RP8 investigation of the rate of respiration in yeast
Place yeast and glucose solution in a sealed test tube
Connect to a respirometer with a drop or coloured liquid in the capillary tube
Leave in a water bath at a controlled temp
Measure the movement of lieuqid over time
Use rate=distance moved by liquid/time
Repeat at different temps to compare
Give the method for RP9 investigating the effect of a named growth factor in bacteria growth
Pour sterile nutrient agar into Petri dishes
Use a sterile pipette to spread bacteria culture evenly
Place paper discs soaked in different antibiotics onto the agar
Seal the petri dish with tape and incubate at 25°C
Measure the clear zone around each disc
Give the method for RP10 investigating the effect of an abiotic factor on organism distribution
Use a random sampling method
Place a quadrat and count the number of organisms inside
Repeat multiple times for reliability
Use a transect for systematic sampling along and environmental gradient
Calculate mean density or percentage cover