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STPM Biology
FOCUS ON ESSAY
BIOLOGY SEMESTER 3
Chapter 3: Control and Regulation
Learning objective:
Organisation of nervous system.
1.
Explain the organisation of sympathetic and parasympathetic nervous
systems and their relationship with the central nervous system.
[9]
-
Learning objectives:
Formation of resting potential and action potential.
Characteristics of nerve impulses.
2.
(a) Explain how resting potential and action potential are generated on an
axon.
[8]
(b) State the mechanism presents in the nerve to allow only unidirectional
impulses and prevent fatigue.
[7]
-
While the sodium-potassium pumps (Na+/K+ ATPase) are always working. For
every 2K+ pumped into the cell, 3Na+ will be actively transported out of the cell.
- The axon membrane is more permeable to K+ than Na+ due to the presence of more
K+ non-voltage gated dependent channels than Na+ non-voltage gated channels.
More K+ diffuse out of the cell faster than Na+ can diffuse back in.
- The net result is the outside of the membrane is more positive compared to the inside
of axon. The axon membrane is polarised.
Formation of action potential:
- Some sodium gated channels in the stimulated region of the axon open.
- Na+ diffuse into the axon (facilitated diffusion) down an electrochemical gradient.
- When the potential difference across the membrane reaches a threshold value, many
more sodium gated channels open, results in influx of Na+.
- The sodium-potassium pump is inactive.
- The influx of Na+ leads to a sudden increase in the cell potential difference which
becomes positive (+40 mV).
- The reversal in the potential difference is known as depolarization, an action
potential is generated.
-
After an action potential for about 5 to 10 ms, the portion of axon undergoes a
refractory period.
Refractory period allows impulses to travel only in one direction and limits the
frequency at which successive impulses can pass along an axon.
During the absolute refractory period (~ 1 ms), the axon membrane is unable to
respond to another stimulus, no matter how strong it is.
An action potential cannot be produced due to a conformational change in sodiumgated channels which are still in a closed, inactive state. This also prevents the
action potential from travelling backwards.
Following the absolute refractory period, there is relative refractory period (~ 5 ms).
During this period, the resting potential is gradually restored by the Na+/K+ pumps
and the relative permeability of membrane of facilitated diffusion of ions is also
restored.
A new action potential then can be produced if the stimulus is greater than the usual
one.
The refractory period is also a limiting factor in the speed of conduction of the nerve
impulses.
Under the all or nothing law, an action potential can only be generated after the
threshold value is exceeded.
After the threshold is reached, the size of the action potentials produced remains
constant and is independent of the intensity of the stimulus. All action potentials are
of the same amplitude.
Learning objective:
Structure of a synapse.
3.
With the aid of a labelled diagram, describe the structure of a synapse. [8]
Synapse is the junction between two neurons with the presynaptic knob located at
the end of the axon.
In each synaptic knob, there are many mitochondria and sac-like vesicles.
These vesicles contain neurotransmitters which play an important role in the
transmission of impulses across synapse, eg: acetylcholine.
Between the end of the synaptic knob and the neuron membrane that connects to it,
is a small space called synaptic cleft.
This cleft is bordered by the presynaptic membrane of the synaptic knob and
postsynaptic membrane of the neuron that connects to it.
The postsynaptic membrane contains many receptors which allow the
neurotransmitters from presynaptic knob to bind to them.
This results in the sodium-potassium gated channels found on the postsynaptic
membrane to open and allow influx of Na+ leading to depolarisation of postsynaptic
membrane.
Learning objective:
Impulse transmission along axon and across a synapse.
4.
(a)
(b)
axon.
(c)
When the node of Ranvier of a myelinated axon receives a strong stimulus, it causes
the sodium gated-channel to open and allow the influx of sodium ions into the axon.
This causes the axon membrane at the node to depolarise and generate an action
potential.
Once initiated, the action potential is self-propagating.
During depolarisation, the axoplasm at a particular node is more positive relative to
the axoplasm of the adjacent node which is at its resting potential.
The difference in potential causes ions to flow in the axoplasm between the nodes.
The flow of sodium ions into the adjacent nodes induces the opening of sodiumgated channels and causes the influx of sodium ions.
This action is repeated in a wave of depolarisation till the end of the myelinated
axon with depolarization only occur at the nodes.
The impulse seems to leap from one node to another during its transmission along
a myelinated axon.
Such a transmission is known as the salutatory conduction which helps to spped up
its transmission.
When a non-myelinated neurone is sufficiently stimulated, an action potential is
generated.
This sets up a local current which depolarizes the adjacent region.
The influx of sodium ions from the extracellular fluid into one region of the axon
creates a local circuit in that region.
The increase in sodium ions in the axoplasm repels the cations to move to the
adjacent region which is more negatively-charged.
This increases the membrane potential in the adjacent region and open up sodiumgated channels.
Sodium ions diffuse into the neurone and the membrane is depolarized.
When the threshold level is exceeded, a new action potential is generated.
The local current at one region, therefore, induces a new action potential in the
adjacent region which keeps moving in a forward direction.
When a nerve impulse arrives at the synaptic knob, calcium gated channels in the
presynaptic membrane open.
Ca2+ ions diffuse quickly from the synaptic cleft or extracellular fluid into the
synaptic knob.
The influx of Ca2+ ions causes the synaptic vesicles to fuse with the presynaptic
membrane.
The vesicles release neurotransmitters into the synaptic cleft by exocytosis.
Neurotransmitters diffuse across the cleft and bind to the receptors on postsynaptic
membrane.
SMKSI Kulai Johor | 4
Learning objective:
Structure of a neuromuscular junction (NMJ) and sarcomere.
5.
The sarcomere is the basic unit of the myofibril between two Z lines.
The myofibril is made up of thick filament of myosin and thin filaments of actin.
The thick filament corresponds to the dark band, and the thin filament corresponds
to the light band as seen in the electron micrograph.
The thick and thin filaments overlap to form the darker band.
The darker inner part of H zone indicates the presence of entirely thick filaments,
explaining this zone is darker than the outer part of the dark band.
During muscle contraction, the position of thick filaments remains unchanged.
The thin filaments slide pass one another.
Myofibril becomes shorter and shorter.
During muscle relaxation, the position of thick filaments remain unchanged.
The thin filament slides out to the original position.
The muscle reverts to its original position.
Learning objective:
Explain the mechanism of muscle contraction using the sliding filament
theory.
6. Describe the sequence of events occurring during skeletal muscle contraction,
starting from when a motor neurone is stimulated.
[10]
-
Learning objective:
Compare sympathetic and parasympathetic nervous systems.
7.
(a)
(b)
system.
-
Learning objective:
Effects of cocaine and curare.
8.
(a)
(b)
Curare binds to the receptors on motor end plate where acetylcholine supposed to
bind to.
Depolarization of the motor end plate is prevented.
No sodium gated channels in the motor end plate are stimulated to open.
Impulse transmission across the neuromuscular junction is blocked.
No impulse is transmitted to the skeletal muscle.
This results in paralysis of muscle.
A high concentration of curare might be fatal as the breathing process is blocked.
Learning objective:
Mechanism of action of steroid and non-steroid hormones.
9.
(a) Name two main types of human hormones and give an example for
each.
[2]
(b) Explain the mechanism of action of a non-steroidal hormone, taking
adrenaline as example.
[13]
(c) Describe the differences in mechanism of action between both types of
human hormones.
[10]
-
Non-steroid hormones are insoluble in lipid and thus cannot diffuse across the
plasma membrane.
Non-steroid hormone act via the activation of cyclic AMP pathway.
The hormone acts as first messenger and binds to a specific receptor protein in the
plasma membrane of a particular cell.
The binding of hormone to the receptor triggers a conformational change of the
receptor.
The hormone-receptor complex formed increases the affinity of the receptor to bind
with and activate G protein.
Once G protein is activated, it stimulates enzyme adenylyl cyclase.
Adenylyl cyclase converts ATP into cAMP.
cAMP acts as a second messenger, which then activates other enzymes.
The cascade effect occurs to produce a large amount of cAMP from a small amount
of non-steroid hormone.
cAMP catalyzes the conversion of inactive protein kinase A into active protein
kinase A via the cascade effect.
The active protein kinase A then activates phosphorylase kinase via the cascade
effect.
Phosphorylase kinase then further activates glycogen phosphorylase, which will
then catalyses the phosphorylation of glycogen to glucose-1-phosphate.
The effect of non-steroid hormone is fast but last for a short duration.
Steroid hormone
Can easily pass through the lipoprotein
membrane of target cells
Binds to receptor in the cytoplasm or
nucleoplasm
The complex formed does not activate
adenylyl cyclase
No cAMP is produced
No cascade effect occurs
Non-steroid hormone
Cannot pass through the lipoprotein
membrane of target cells
Bind to receptors found on the plasma
membrane of cell
The complex formed activates adenylyl
cyclase
cAMP is produced
Cascade effect occurs and effects take
place immediately
The complex enters the nucleus
The complex does not enter the nucleus
Gene transcription is accelerated by the No gene is involved by the complex
complex
Transcription takes place followed by No transcription take place and no
protein production
protein is produced
Effects take place through the protein Effects take place through the activated
formed
enzymes and their products
Effects are usually long term such as Effects are short term such as in blood
muscular body by testosterone
glucose level by insulin and adrenaline
Learning objectives:
Roles of plant hormones.
Plant growth regulators.
9.
(a)
(b)
Name five plant hormones and explain the functions of each hormone.
[10]
Explain how phytochrome regulates flowering in plants.
[5]
PFR
Far red light
(rapid conversion)
The active PFR form converts an inactive hormone precursor in the leaf into
hormone florigen.
Florigen is transported by phloem to the floral buds. This promotes flowering in
long day plants.
In dark, PFR is converted to PR.
Increase in concentration of PR and decrease in concentration of PFR promotes
florigen production causing flowering in short day plants.
10.
Auxin and gibberellins help in stimulating fruit development and increase fruit yield.
Promotes parthenocarpy (seedless tomatoes and citrus fruits), seedless grape.
Auxin prevents premature fruit drop.
Ethene is used to stimulate ripening of some commercial fruits such as bananas,
papayas, mangoes and apples are often picked green and unripe.
Cytokinin spray is used on cut flowers, vegetables and fruits to keep them fresh and
to extend shelf life.
Cytokinin and gibberellins break dormancy.
Abscisic acid can be sprayed on fruit trees to regulate fruit drop at the end of the
season.
Copyright: ccy/SMKSI/2015
STPM-format Question
1.
(a)
(b) The graph below shows the generation and transmission phases of an
impulse along an axon.
Membrane
potential /
mV
+50
0
Q
-50
|
2.5
P:
Q:
|
5
|
7.5
|
10
Time / ms
2.
The graph below shows the potential difference across an axon membrane.
+60
+40
+20
0
-20
-40
-60
-80
-100
X
Z
Time / ms
(a)
3.
Different plants require different daylengths or period of daylight for flowering.
These plants can be classified into three groups.
(a)
(i) Using a suitable example, explain what is meant by day-neutral
plants.
[2 marks]
_____________________________________________________________________
_____________________________________________________________________
(ii) An experiment was carried out to investigate the relationship between
the period of daylight and flowering on a particular plant. The results of the experiment
are as below.
100
50
10
12
14
16
Period of daylight
No flowering
Flowering
No flowering
0
6
12 18
Time / hours
24
Keys:
Dark
Light
(i) From the data given, state which is crucial in determining flowering:
light period or dark period?
[1 mark]
_____________________________________________________________________
(ii) Use the results from the experiment to deduce the photoperiodic
group to which this plant belongs.
[1 mark]
_____________________________________________________________________
What is your conclusion about the effects of the two types of light on
flowering?
[4 marks]
_____________________________________________________________________
_____________________________________________________________________
_____________________________________________________________________
_____________________________________________________________________
_____________________________________________________________________