Professional Documents
Culture Documents
Aim
To identify the different phases of mitosis in a root tip squash.
Method
Apparatus Safety
● garlic clove with roots ● pencil with rubber end Do not touch hydrochloric acid
● distilled water ● dilute hydrochloric acid, or stain solution with bare
heated in bottles/tubes to hands. Wash immediately with
● paper towel
55 °C in water bath plenty of water if they touch skin
● microscope slides and or clothes, and tell your teacher.
coverslips ● bottle or tube of water
● toluidine blue stain in a Wear eye protection when
● watch glass or small dish
dropping bottle preparing the slide. Wear
● microscope with ×100 and gloves and dispose of these
×400 magnifications ● soft tissue paper
immediately after the slide has
● fine forceps ● beaker of tap water been prepared.
● eye protection ● gloves
A Use the forceps to gently place one glove of sprouted garlic into one of the bottles/tubes in the water bath.
The bottles/tubes contain hydrochloric acid.
B After 5 minutes, take your clove out of the acid and place it into the tube containing water.
C After another 5 minutes, remove the clove and dry it briefly on some pieces of paper towel.
D Find the creamy colour in the last 5 mm of a garlic root (which is the part containing rapidly dividing cells).
E Use the forceps to remove these last 5 mm from a root. Use the forceps to divide the piece of root into two.
F Place the two pieces of root in the centre of a slide. Carefully draw any excess water away from the root
pieces with the corner of a piece of tissue.
G Add one drop of toluidine stain to the root pieces.
H Carefully place a coverslip over the root pieces. With the rubber end of the pencil, touch the coverslip
gently and move it back and forth to squash the root pieces and spread them out. You will probably find
that some of the root tissue remains white and unstained.
I Place about six sheets of soft tissue paper in a stack and fold in half. Put the slide in the fold of the tissue
paper stack. Fold the top half over the slide and press gently to draw off any excess stain. Do not worry
about air bubbles – this is normal in this kind of preparation.
J View the slide under ×100 magnification on the microscope. Look for cells that are box shaped and in
chains. The cell cytoplasm should be nearly colourless and the nuclei dark blue. Change to ×400 and look
for dividing cells.
K If your preparation has not worked, put the slide in a beaker of water and try again. Adjust what you do to
avoid the problem. For example, if the cells were not spread out enough, squash the coverslip over cells a
little harder with the pencil end. Or, if the cells were too dark or light, adjust the amount of stain you use.
a b c d e
The A cell
chromosomes membrane
are pulled apart divides the cells.
by the spindles.
1 The stages of the cell cycle (below) are in the correct order. Draw lines to link the stages with what happens.
3 The cells produced by mitosis are diploid and genetically identical. Define each underlined term.
4 Suggest what will happen if cells keep dividing and do not stop.
1 State two parts of a cell that make copies of themselves before mitosis begins.
2 Look at the diagram below and draw what the cell looks like in the next stage of mitosis.
4 Why is mitosis important for organisms? Tick three boxes to show three reasons.
b Explain what ‘diploid’ means and why it is important to the cell. (Hint: What would happen to a cell if it
was not diploid and went through two rounds of the cell cycle?)
Extra challenge
5 Mitotic inhibitors are substances that are found naturally in plants. These substances stop the formation of
spindle fibres. Mitotic inhibitors can be used to treat some cancers.
a Explain why mitotic inhibitors can be used to treat cancers.
b Suggest one problem that might be caused by mitotic inhibitors.
c It is possible to watch some cells dividing, using certain types of microscope. Suggest what you might
see through this type of microscope if you looked at cancer cells that had just been treated with a
mitotic inhibitor.
Extra challenge
5 Mitotic inhibitors are substances that are found naturally in plants. These substances stop the formation of
spindle fibres. Mitotic inhibitors can be used to treat some cancers.
a Explain why mitotic inhibitors can be used to treat cancers.
b Suggest one problem that might be caused by mitotic inhibitors.
c It is possible to watch some cells dividing using certain types of microscope. Suggest what you might
see through this type of microscope if you looked at cancer cells that had just been treated with a
mitotic inhibitor.
Now circle the faces in the ‘Start’ row in the table showing how confident you are of your answers.
Question 1 2 3
Start
Assessment
Using a different colour, correct or add to your answers above. You may need to use the back of this sheet or
another piece of paper. Then circle the faces in the ‘Check’ row in the table.
Question 1 2 3
Check
Feedback
What will you do next? Tick one box.
Action
You may now be given another activity. After this, note down any remaining areas you need to improve and
how you will try to improve in these areas.
Introduction
Your teacher will display a list of specialised human cells that you will see in prepared microscope slides. You
should use the list to identify the cells on the slides, then draw and label one cell from each slide to show how it
is specialised.
Aim
To identify specialised human cells and describe how they are adapted to their function.
Method
Apparatus Safety
● prepared slides of human cells and tissues Eye protection should be worn at all
● light microscope and light source times.
Take care not to cut yourself when
using glass slides.
Do not angle microscope mirrors
towards the Sun.
A Move the low-power objective into position above the microscope stage.
B Place a slide on the stage, and focus on a part of the slide that shows cells clearly.
C Using your knowledge of cells and the list provided by your teacher, try to identify which type of specialised
cell is shown on the slide. Record the letter of the slide you are looking at, the type of cell that you think is
on the slide, and the reason why you think it is that type.
D Move the slide so that one of the cells is directly under the objective. Make sure the cell is in focus, then
move a higher power objective into position.
E Using the fine focusing wheel only, bring the cell clearly into focus.
F Draw one cell clearly using a sharp pencil, and label its specialised features.
G Repeat steps A to F for another slide.
Evaluation
3 Share your drawings with the rest of your group. For each drawing identify one good point, and one point
that could be improved to make sure the specialised features are shown clearly. For each of the drawings
you made, improve the drawing as discussed, and add notes to explain how the cell is adapted to its
function.
4 Use your findings to explain why it is important that animals have different types of cells in their bodies.
1 A human egg cell is a single unspecialised cell. After the cell is fertilised, two processes cause it to develop
into a large organism formed of billions of different types of cells.
a Name and describe the process that produces more cells from one cell.
S1 Describe how a single fertilised human egg cell develops into the billions of different cells in a human
adult.
Some robots can carry out many actions that humans can do, such as walk, or pick up and move other objects.
2 A robot arm is moved by pistons that can get longer and shorter. The pistons are attached to the outer shell
of the arm.
a Which organs in a human arm cause the arm to move?
b Which type of specialised human cell in those organs causes movement?
c How is the structure of those specialised human cells adapted to their function of causing movement?
3 To make a tall robot from a shorter one, you could remove the legs and replace them with longer ones.
Use the words in the box to help you write a sentence that explains how a child gets taller as they get older.
4 A baby's length is measured at 3 months old, and plotted on a percentile growth curve chart. The chart
shows that the baby's length lies on the 25th percentile curve. Explain what this means.
1 Growth of an animal can be defined as cell division followed by cell differentiation. Explain what the bold
words mean.
cell division
cell differentiation
Cell A B
b Suggest how old the boy was when the doctor became concerned about his growth. Explain your
answer.
The bones differ in size and shape. Use the information above about bone cells to help explain how the
changes from child to adult leg bone are brought about.
5 Use the example of osteoclasts and osteoblasts to explain why differentiation of cells is important in an
animal's body.
6 Imagine a space station was set up on Mars, and that people living there might have babies. Explain why a
new set of percentile growth curves would be needed to assess the growth of those babies.
Extra challenge
7 Suggest what the percentile growth curves for head circumference, mass and length for babies growing on
Mars might look like, bearing in mind that gravity on Mars is about one third that on Earth. Explain your
answer.
Now circle the faces in the ‘Start’ row in the table showing how confident you are of your answers.
Question 1 2 3
Start
Assessment
Using a different colour, correct or add to your answers above. You may need to use the back of this sheet or
another piece of paper. Then circle the faces in the ‘Check’ row in the table.
Question 1 2 3
Check
Feedback
What will you do next? Tick one box.
Action
You may now be given another activity. After this, note down any remaining areas you need to improve and
how you will try to improve in these areas.
Introduction
In this practical you will measure the mass of seedlings, and calculate the percentage gain in mass
over time. As seedlings vary in mass, each time you will take 10 seedlings and calculate the mean
mass of one seedling.
Aim
To calculate percentage gain in the mass of seedlings.
Method
Apparatus Safety
● tray of seedlings Wash hands thoroughly after handling plant
● forceps material.
● accurate balance
● beaker of water
● sheet of paper towel
● Petri dish
A Look at the tray of seedlings and select 10 that show a range of heights. Use the forceps to carefully
remove each of the 10 seedlings from the tray. Gently rinse the roots in the beaker of water to remove any
support medium. Lay the seedlings out to dry on a piece of absorbent paper towel.
B Measure the mass of the Petri dish to two significant figures and record it.
C Place the 10 seedlings on the Petri dish and measure the total mass to two significant figures. Record this
in Table 1 below.
D Gently water the remaining seedlings in the tray so that they are moist but not soggy. Return them to a well-
lit area until the next lesson.
E Repeat steps A to D every three to four days until you have four sets of measurements.
3 Calculate the mass of the 10 seedlings on each date in your copy of Table 1 using this formula:
mass of 10 seedlings = mass of dish + 10 seedlings (row B) – mass of Petri dish (row A)
Use these values to complete column 1 of your Table 2.
4 Calculate the mean mass of one seedling for each date using:
mass of 10 seedlings
mean mass of one seedling =
10
Use these values to complete column 2 of your Table 2.
5 Calculate the increase in mass of one seedling for each day after the start using:
increase in mass = mass in column 2 for that day – mass in column 2 on day 0
Use these values to complete column 3 of your Table 2.
6 Calculate the percentage increase since day 0 for each day using:
increase in mass (column 3)
percentage increase = 100 %
starting mass (day 0, column 2)
Use these values to complete column 4 of Table 2.
7 Use the values in column 4 to draw a graph of percentage increase in mass (on y-axis) against time (on x-
axis).
8 Describe and explain the shape of your graph.
Evaluation
9 Describe any problems that you had with carrying out this experiment.
10 Suggest one way of improving the practical so that you could get better results another time.
1 Use the diagram below to map where in a plant you can find the following cells:
meristem cells xylem vessels root hair cells palisade cells guard cells
Think carefully before you start about how best to do this, as the cells may be found in more than one part
of a plant.
S1 The tree in photo A grew from a small seedling. Use bullet points to describe how the seedling increased
in size and developed into the tree.
d Explain why the adaptation of these cells is important for the plant.
3 One month after germination the tree seedling has a mass of 65 g. One year later it has a mass of 345 g.
Use this formula to calculate the percentage gain in mass of the tree seedling:
final mass - starting mass
percentage change in mass = 100 %
starting mass
1 Select the statement that best describes how plants grow. Tick one.
3 Explain why measuring the change in mass of a plant over time can be used to measure the plant’s growth.
a Add labels to the lines to describe the features of a xylem vessel that are not found in other plant cells.
b Describe the function of a xylem vessel.
c Explain how the features of a xylem vessel help it to carry out its function.
5 Describe one other kind of specialised plant cell and explain how it is adapted to carry out its function.
Carbon dioxide concentration Dry mass at 30 days (mg) Dry mass at 100 days (mg)
root stem leaf root stem leaf
normal atmospheric 0.005 0.001 0.009 0.298 0.069 0.595
high 0.009 0.002 0.015 0.428 0.069 0.656
6 Calculate the percentage gain in mass of roots between 30 and 100 days for normal and high carbon
dioxide concentrations.
Extra challenge
7 Calculate the percentage gain in mass of stem and of leaf between 30 and 100 days at the high carbon
dioxide concentration. Use your calculation to identify which part of the plant grew fastest when carbon
dioxide concentrations were increased.
Now circle the faces in the ‘Start’ row in the table showing how confident you are of your answers.
Question 1 2 3
Start
Assessment
Using a different colour, correct or add to your answers above. You may need to use the back of this sheet or
another piece of paper. Then circle the faces in the ‘Check’ row in the table.
Question 1 2 3
Check
Feedback
What will you do next? Tick one box.
Action
You may now be given another activity. After this, note down any remaining areas you need to improve and
how you will try to improve in these areas.
Introduction
Tissue culture is the production of new complete plants from tiny pieces (explants) of meristems in adult plants.
In this practical you will use explants of meristems in cauliflower florets (pieces of the white part that we eat).
The plant material must be kept as clean as possible, using aseptic (sterile) techniques, to reduce the risk of
contamination by mould (fungus), which can kill the explants.
Aim
To grow new cauliflower plants from explants.
Method
Apparatus Safety
● forceps in beaker of Eye protection should be worn at all
sterilising solution (SDICN) times.
● 70% ethanol Sterilising solution (SDICN) is toxic
● paper towel and a bleach that removes colour
● small piece of cauliflower from clothing. Wear a protective
apron/lab coat and gloves when
● scalpel
handling SDICN, in case of leaks or
● screw-lid jar of sterilising splashes. Do not breathe in the
solution (SDICN) vapours from the SDICN.
● empty beaker (for collecting
Take care when using sharp scalpels.
waste)
Wash hands thoroughly after handling
● tube containing growth plant material.
medium
● clean tile
● marker pen
A Wipe down the surface of the bench and the tile using the paper towel and a small amount of ethanol.
B Use the scalpel to carefully cut the piece of cauliflower lengthways into small 3–5 mm3 pieces. These are
your explants.
C Use the forceps from the sterilising solution to place the explants in the jar of SDICN to sterilise them. Put
the lid on and swirl the jar gently for 5 seconds.
D Every 2–3 minutes, swirl the jar gently for 5 seconds. Repeat until 15 minutes have passed.
E Carefully strain the liquid from the jar into a waste beaker. Use the forceps to stop the explants falling into
the beaker. Put the forceps back in the beaker of sterilising solution.
F Take the lid off the tube containing the agar plant growth medium. Put the lid face down on a clean tile.
G Using the forceps, pick up the best explant from the jar and transfer it to the agar, pressing the stalk end
into the agar slightly. Replace the lid and use the pen to label the tube with your name and the date. Try not
to lean over your working area, to minimise contamination.
H Incubate the tube in a warm place near to a window or light bank. Examine the tube weekly and record any
details of growth or greening. Do not open the tube during these checks.
3 Explain your results, using the terms ‘meristem’ and ‘stem cells’ in your answer.
4 Explain why it was important to use aseptic (sterile) methods to prepare the explants.
Evaluation
5 Describe any problems that you had with this practical.
6 Suggest ways of improving the method to reduce the problems you had.
1 a Complete the table to show where the different kinds of stem cell are found and what range of
specialised cell they can produce.
b For each statement, tick one box to show whether it is a benefit or a risk of using stem cells.
● Stem cells can be used to replace damaged or diseased cells. benefit risk
● Stem cells can be used for testing new drugs before they are tried
on people. benefit risk
S1 a Describe the functions of the different kinds of stem cell in animals and plants.
b Describe one benefit and one risk of using stem cells in medicine.
3 Use one of the risks and one of the benefits from the bullet list in question 1b to explain why you are or are
not in favour of using stem cells.
E many F few
E1 In 2014, scientists studying zebrafish discovered that ‘buddy' cells are needed to help one type of stem
cell become blood stem cells.
a Suggest how this research could lead to new treatments for people with diseases.
b Suggest what risks must be overcome before these treatments can be given to patients.
6 One problem with using stem cells from one person to treat another person is rejection by the immune
system. Explain what this means.
7 Construct an argument for or against the use of stem cell treatments in humans.
6 Leukaemia is a disease of the blood, which produces faulty blood cells that replace healthy blood cells. This
causes many problems in the body. Blood stem cells can be used to treat leukaemia. Complete the
sentences below to show how this can be done.
a Healthy blood stem cells are taken from .
b The healthy blood stem cells are inserted into .
c The healthy blood stem cells produce .
7 Explain how treatment with stem cells could cause each of the following problems:
a cancer
These phrases may help you with the answers to questions 4, 5 and 6.
the bone marrow of the patient with leukaemia to repair diseased or damaged cells
the bone marrow of a healthy person to produce new cells for growth.
new cells that differentiate into healthy blood cells they can produce a wider range of specialised cells
1 Three different sources of stem cells are embryos, stem cells in specialised tissue, and reprogrammed
specialised cells (iPSCs). Compare the ranges of specialised cells that these stem cells can produce.
2 Identify the advantages and disadvantages of developing cell lines from each source of stem cell.
3 Describe one medical treatment that is currently carried out using stem cells.
4 Describe two other medical treatments that could be carried out in the future using stem cells. Explain your
answers.
5 Scientists are trying to produce iPSCs from the skin cells of patients who have diseases of other cells.
Explain why this treatment could be more successful than using stem cells from the other two sources.
6 Describe one other problem with using stem cells in medical treatments that is different from the problem
you identified in question 5.
7 Why do differentiated cells have the potential to be ‘reprogrammed’ and become stem cells?
Extra challenge
8 Money for scientific research is limited. Imagine you are the director of a research institute that wishes to
carry out stem cell research. You have only enough budget to fund research into one source of stem cells
for developing new medical treatments. Which source would you choose as the most promising and why?
3 What are the advantages and risks of using stem cells in medicine?
Now circle the faces in the ‘Start’ row in the table showing how confident you are of your answers.
Question 1 2 3
Start
Assessment
Using a different colour, correct or add to your answers above. You may need to use the back of this sheet or
another piece of paper. Then circle the faces in the ‘Check’ row in the table.
Question 1 2 3
Check
Feedback
What will you do next? Tick one box.
Action
You may now be given another activity. After this, note down any remaining areas you need to improve and
how you will try to improve in these areas.
Introduction
Your skin can detect many different stimuli, including touch, pressure, pain, heat and cold. For each of these
stimuli there is a different sort of receptor cell. You are going to find out if these receptors are spread evenly
through your skin.
Aim
To test the hypothesis that the skin on different parts of the arms and hands contains different densities of
touch receptors.
Method
Apparatus Safety
● blindfold Do not touch the sharp points on the touch tester
● ruler when pressing objects into sticky tack or cork.
● touch tester (e.g. U-shaped piece of wire, or Do not press down hard when placing the points
two cocktail sticks pressed into sticky tack or onto your partner’s skin.
cork)
A With your partner, decide who will be tested
and who will do the testing. If there is time you
may be able to swap roles and repeat the
experiment.
B Decide on five or six areas on the arms and
hands to test (e.g. tip of middle finger, upper
arm). You will also need to decide on the
number of gap sizes (the distance between the
points on the touch tester) that you are going
to try.
C Blindfold your partner.
D Alter the touch tester so that there is a gap of
1 mm between the two points.
E Place the two points onto your partner’s skin
and ask how many points can be felt, one or
two. Repeat this for the different areas of skin
that you have decided to test. Your partner will
know that there are two points, so sometimes
use one point instead. Do not record the
results when using one point, but doing this
helps to prevent bias.
F Repeat step E using different gap sizes.
upper arm
c Why do you think this part should be more sensitive than other parts?
4 How sensitive a part of the skin is depends on the density of the receptor cells.
a What does the phrase ‘density of receptor cells’ mean?
Evaluation
5 a How would you improve the way in which you tested your partner’s skin?
1 The sentences below describe how you feel something that touches the heel of your foot. Write in numbers
1 to 7, to show the order in which the events occur.
S1 Draw a flow chart to show how information about something touching the heel of your foot gets to your
brain.
2 Unmuddle the letters to show the names of the three main parts of the nervous system.
REV ENS
RANCID SLOP
IN BAR
1 On the diagram, label the two parts of the body in the central
nervous system.
2 Certain cells in your body detect changes in your surroundings
(stimuli). They send information in electrical signals to the
brain. Rearrange the letters on the lines to answer the
questions.
(SCEPTRE OR CELL)
(SUMS PILE)
(ONE RUNE)
(ROSE SPECS)
b Add arrows below the diagram to show the direction in which electrical signals are transmitted.
c What substance is the sheath made out of? Tick one.
4 Anthony picks up an ice cube. Explain how Anthony can feel that the ice cube is cold.
2 a Your skin contains receptor cells for different stimuli. What is a stimulus?
b What is an organ that contains receptor cells called?
c Name one area of your body where you would expect to find many touch receptors. Explain your
answer.
d You touch a cold stone. Which receptor cells would be activated?
e In what form is information from receptor cells carried to the brain?
3 In glabrous skin, some receptors detect light pressure and others detect stronger pressure. Which of the
receptors in the diagram do you think detect light pressure and which detect strong pressure? Explain your
answers.
4 Meissner corpuscles are not found in hairy skin. Suggest why they are not needed.
5 Receptor cells link to sensory neurones. Explain a function of each of these sensory neurone adaptations:
a long axons and dendrons
b many dendrites and axon terminals
c myelin sheath.
Extra challenge
6 a Name one area of your body where you would find a mucous membrane.
b Name one receptor cell you would not expect to find in a mucous membrane.
2 How does the nervous system allow the body to respond to stimuli?
Now circle the faces in the ‘Start’ row in the table showing how confident you are of your answers.
Question 1 2 3
Start
Assessment
Using a different colour, correct or add to your answers above. You may need to use the back of this sheet or
another piece of paper. Then circle the faces in the ‘Check’ row in the table.
Question 1 2 3
Check
Feedback
What will you do next? Tick one box.
Action
You may now be given another activity. After this, note down any remaining areas you need to improve and
how you will try to improve in these areas.
Introduction
You are going to try to find out how fast impulses travel through someone by measuring the time it takes for
someone to feel a squeeze in one elbow and pass the squeeze on to a neighbour.
Prediction
1 a Describe the route impulses will take through each person in this experiment.
b How long do you think the ‘squeezing message’ will take to go through one person?
c Why do you think this?
Aim Apparatus
To work out the mean speed of impulses through the human body. ● stop clock
● tape measure
Method
A Stand in a circle in your group. Each person holds their neighbour’s right elbow with their left hand.
B Get one person to be the ‘timer’ and hold a stop clock in their right hand.
C The ‘timer’ squeezes the elbow of the person to their left at the same time as starting the stop clock.
D As soon as the next person feels their elbow being squeezed, they squeeze the person on their left.
E When the person with the stop clock feels the squeeze, they stop the stop clock and record the time.
F Calculate the time taken for the impulses to travel through one person.
G Measure the route an impulse takes from the right elbow to the brain and to the left hand. This gives an
idea of the distance travelled through a person. Multiply this value by the number of people in your group.
total distance
H Calculate average speed (in m/s), using: average speed =
total time taken
I Repeat the experiment several times and record all your results.
2 a Descriptions of some human neurones taken from different places in the body are given in the tables
below. Some impulse speeds are also given. Use your findings from question 1 and your own
knowledge about neurones to match each description with a speed.
b Cut out and place your neurone and speed cards in an ordered list (slowest at the top). Discuss in your
group how you each arranged the cards and then reach a final decision about the order.
E connecting 100 13 no
100 m/s
neurone
1 Add numbers (1−5) next to these sentences to show the order in which the events occur:
S1 Draw a flow chart to show how an impulse in a relay neurone causes an impulse in a motor neurone.
2 Sasha picked up her scarf. She felt that it was cold and wet, and so she dropped it again.
What effectors did Sasha use?
3 Look at the cells A and B.
A B
c Look at the axons in the diagrams. In which cell would you expect impulses to be slowest? Explain your
reasoning.
Cell P is a Cell Q is a
c Which cell, P or Q, would connect to light receptor cells in the retina of the eye?
d Which cell, P or Q, would connect to a muscle cell?
e Which cell, P or Q, would connect to an adrenal gland cell?
f The diagram here on the right shows three cells in a
reflex arc. Label cells P and Q.
g State the name of the other neurone.
h Describe the function of a reflex arc.
i Explain how the structure of the reflex arc helps with this function.
3 This statement is incorrect: ‘Impulses travel through synapses to get from one neurone to another.’
a Explain why this is incorrect.
so that one impulse can generate many impulses so that impulses do not travel too quickly through
with equal ‘strength’ the nervous system
so that neurotransmitters can be released so that neurones are separated from each other
Inside all your muscles are muscle spindles that contain receptor cells. The muscle spindles are stretched
when a muscle is stretched. When this happens an impulse is generated, which is sent along a sensory
neurone. The impulse is transmitted through a reflex arc, causing the muscle to contract (or contract even
more). Even if you are standing still, minute variations in position are occurring all the time, and these are
detected by muscle spindles and cause reflexes that automatically make slight alterations to muscle tensions,
so that you stay upright.
The knee jerk reflex (or patellar reflex) is one of these reflexes and it occurs using a monosynaptic (single
synapse) reflex arc. However, it is not quite as simple as that!
Another sensory neurone runs from a receptor called the Golgi tendon organ. As the quadriceps muscle
contracts, it pulls on the tendon and stretches it. If the quadriceps muscle contracts too much, and there is a
danger that the tendon could be damaged, the Golgi tendon organ sends impulses to a relay neurone, which
connects to the motor neurone going to the quadriceps. This relay neurone uses a neurotransmitter called
glycine in its synapse with the motor neurone, and this inhibits (decreases the chances of) an impulse being
generated in the motor neurone. Most synapses use a neurotransmitter called acetylcholine (ACh) that
stimulates (increases the chances of) impulses being generated.
1 a What is a monosynaptic reflex arc?
b State a purpose of reflex arcs.
c Explain what happens at a synapse.
d State one drawback of synapses in the nervous system.
e State one benefit of synapses in the nervous system.
2 What part of a muscle detects stretching?
3 a What is the effect on the quadriceps muscle when the tendon is stretched too much?
b Why is this useful?
c Weightlifters have been known to inject themselves with local anaesthetic near their Golgi tendon
organs. Why do you think they do this?
4 a Name each type of neurone labelled P to U in the diagram.
b State whether each neurone is inhibitory or stimulatory.
5 Describe, in as much detail as you can, what happens when the muscle spindle is stretched.
Extra challenge
6 If a bacterium called Clostridium tetani gets into humans it can produce a poison that causes a serious
condition called tetanus. The poison blocks the release of glycine into synapses. What do you think the
symptoms of tetanus are? Explain your reasoning.
3 How does the structure of a reflex arc allow faster reactions to stimuli?
Now circle the faces in the ‘Start’ row in the table showing how confident you are of your answers.
Question 1 2 3
Start
Assessment
Using a different colour, correct or add to your answers above. You may need to use the back of this sheet or
another piece of paper. Then circle the faces in the ‘Check’ row in the table.
Question 1 2 3
Check
Feedback
What will you do next? Tick one box.
Action
You may now be given another activity. After this, note down any remaining areas you need to improve and
how you will try to improve in these areas.
CB2a Mitosis
Word Pronunciation Meaning
anaphase an-na-fays The stage of mitosis in which the separated
chromosomes move away from each other.
asexual reproduction Producing new organisms from one parent only.
These organisms are genetically identical to the
parent.
cancer cell Cell that divides uncontrollably.
cell cycle A sequence of growth and division that happens in
cells. It includes interphase and mitosis, and leads to
the production of two daughter cells that are identical
to the parent cell.
clone Offspring from asexual reproduction. All the cells in a
clone are genetically identical to each other and to
the parent’s cells.
cytokinesis site-O-kY-nee-sis When the cytoplasm of the cell is separated as the
cell membrane is pinched to divide the cell into two
daughter cells.
daughter cell New cell produced by cell division.
diploid dip-loyd A cell with two sets of chromosomes.
DNA replication rep-li-kay-shun The copying of the DNA within a cell.
haploid hap-loyd A cell with one set of chromosomes.
interphase in-ter-fays The stage when the cell prepares itself for the
process of cell division, and DNA replication takes
place. The cell also makes more of its sub-cellular
structures.
metaphase met-a-fays The stage of mitosis when the chromosomes line up
across the middle of the cell.
mitosis my-toe-sis The process of cells dividing to produce two daughter
cells that are genetically identical to the parent.
multicellular mul-tee-sell-U-lar An organism that is made of many cells.
prophase prO-fays The stage of mitosis in which the nucleus starts to
break down and spindle fibres appear.
spindle fibre spin-del fY-ber Filament formed in a cell during mitosis, which helps
to separate chromosomes.
telophase tee-lO-fays The stage of mitosis in which the chromosomes
arrive at opposite ends of the cell and the nucleus
membrane reforms.
tumour tyoo-mer Lump formed of cancer cells.