Practical Techniques Flashcards

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1
Q

Why does use of a colorimeter improve repeatability of results

A

It is quantitative and standardises the method

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2
Q

What’s one way a student could ensure a sample is kept at the same temperature the whole way through the experiment

A

Measure the temperature at intervals and use appropriate corrective measure

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3
Q

What’s the purpose of boiling the agar in the aseptic practical

A

So no contamination

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4
Q

What’s the purpose of transferring the same volume of liquid culture onto each agar plate in the aseptic practical

A

So same number of bacteria transferred to allow comparison

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5
Q

Describe how a student could make up a dilution series in bacteria practical

A
  1. Add 1 part bacteria culture to 9 parts sterile liquid
  2. Mix
  3. Repeat using 9 parts fresh sterile liquid and 1 part of 10^-1 and 10^-2 dilutions to make 10^-3 dilutions
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6
Q

Why does a student not use his preliminary dilution (aseptic practical)

A
  • count is unlikely to be reliable
  • because there’s too many cells
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7
Q

Describe method for potato osmosis practical

A

1) weight first and then put each cut cube in a test tube of sucrose and dilute water solution that you have made up.

2) at room temperature

3) dry the cubes with paper towel to remove excess water before measuring

4) measure mass of cubes every 10 mins

5) calculate percentage change in mass

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8
Q

In chromatography why is pencil used to mark and not ink

A

The ink and leaf pigments would mix

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9
Q

Describe the method to separate leaf pigments in chromatography

A
  • level of solvent below line
  • stop before solvent reaches the top
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10
Q

What is the purpose of incubating the root tip with HCl

A
  • stops cell division from occurring
  • hydrolyses the middle of the lamella so that the cells can be separated easily
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11
Q

How do you carry out a serial dilution?

A

1) Take original solution of known concentration
2) fill additional test tubes with the same volume of distilled water
3) transfer the same volume of solution from one test tube to the next and mix

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12
Q

Describe how to produce and use a calibration curve eg for concentration of protein in urine

A
  • use water and your protein solution to produce a dilution series of known concentrations protein
  • measure absorbance of each concentration using a colorimeter
  • plot a graph of absorbance on Y axis against concentration on X axis and draw a curve
  • use absorbance of samples to find protein conc from the curve
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13
Q

Why must a eyepiece graticule be calibrated when switching to a higher magnification

A

The stage micrometer will appear larger and so each eyepiece division will be a different value

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14
Q

Suggest why a stage micrometer and an eyepiece graticule are needed

A
  • the size of the units of the eyepiece graticule change depending on the magnification being used
  • a stage micrometer can be used to calibrate the graticule
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15
Q

Describe how a student could use an eyepiece graticule to determine the mean diameter eg of stomata

A
  • measure each stoma using eyepiece graticule
  • calibrate eyepiece graticule against stage micrometer
  • take a number of measurements to calculate a mean
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16
Q

Give two precautions the students should take when setting up a potometer

A
  • dry off leaves
  • ensure there are no air bubbles present
  • ensure it is airtight
17
Q

Why does a potometer not truly measure the rate of transpiration

A
  • water used in photosynthesis
  • apparatus is not sealed
  • water produced in respiration
18
Q

How does temperature/acidity effect the permeability of the cell surface membrane

A

Permeability increases
- the proteins in the membrane denature as heat damages the ionic bonds in their tertiary structure
- so more pigment is released

19
Q

How does conc of ethanol effect the permeability of the cell surface membrane

A

Increases permeability
- the alcohol starts to dissolve the phospholipid bilayer in the cell surface membrane
- releasing pigment from the cell

20
Q

When would you use Log10 and why

A
  • when you have a large range of data
  • so you can read the data points off the graph accurately
21
Q

How would you work out the original value from the log value

A

10^log

22
Q

How could you reset a potometer

A

Open the tap

23
Q

What variable should be controlled if you wanted to do the potometer experiment on two different plants

A

Surface area of leaves - Number and size of leaves

24
Q

How would you work out rate of transpiration from a potometer

A

Volume of cylinder/time taken

Volume = pie x r^2 x distance bubble travelled along tube

25
Q

What things are required for a good scientific drawing

A
  • no shading
  • draw all parts to the same scale
  • no overlapping lines/lines must be continuous
  • must have a scale or magnification indicator
  • diagram must have labels/a title
26
Q

Why is a mounted needle needed when using a microscope

A

To lower the cover slip and prevent air bubbles under the cover slip

27
Q

What are some safety precautions in the heart dissection practical

A
  • wash hands with soap and water
  • disinfect instruments/surfaces
  • carry sharp instruments by pointing away from your body
  • put gloves/paper towels in a separate bin to dispose
28
Q

How do you work out mitotic index

A

No. Of cells undergoing mitosis/total no. Of cells x 100

29
Q

Why would you stain the cells

A

To make chromosomes visible

30
Q

What’s the test for non-reducing sugars?

A
  • heat/with acid
  • cool and add an alkali to neutralise
  • heat with Benedict’s solution
  • turns red
31
Q

How do you calculate how many times bacteria divides in a certain amount of hours?

A
  • work out the number of divisions
  • 1 x 2^no. of divisions