Exchange of Substances (Topic 3) Flashcards

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1
Q

How does an organism’s size relate to
their surface area to volume ratio?

A

The larger the organism, the lower the
surface area to volume ratio.

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2
Q

How does an organism’s surface area to
volume ratio relate to their metabolic
rate?

A

The lower the surface area to volume
ratio, the lower the metabolic rate.

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3
Q

How might a large organism adapt to
compensate for its small surface area to
volume ratio?

A

Changes that increase surface area e.g.
folding; body parts become larger e.g.
elephant’s ears; elongating shape;
developing a specialised gas exchange
surface.

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4
Q

Why do multicellular organisms require
specialised gas exchange surfaces?

A

Their smaller surface area to volume ratio
means the distance that needs to be crossed
is larger and substances cannot easily enter
the cells as in a single-celled organism.

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5
Q

Name three features of an efficient gas
exchange surface.

A
  1. Large surface area, e.g. folded membranes
    in mitochondria.
  2. Thin/short distance, e.g. wall of capillaries.
  3. Steep concentration gradient, maintained
    by blood supply or ventilation, e.g. alveoli.
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6
Q

Why can’t insects use their bodies as an
exchange surface?

A

They have a waterproof chitin
exoskeleton and a small surface area to
volume ratio in order to conserve water.

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7
Q

Name and describe the three main
features of an insect’s gas transport
system.

A

• Spiracles= holes on the body’s surface which may be
opened or closed by a valve for gas or water exchange.
• Tracheae= large tubes extending through all body
tissues, supported by rings to prevent collapse.
• Tracheoles= smaller branches dividing off the tracheae.

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8
Q

Explain the process of gas exchange in
insects.

A

• Gases move in and out of the tracheae through
the spiracles.
• A diffusion gradient allows oxygen to diffuse into
the body tissue while waste CO2
diffuses out.
• Contraction of muscles in the tracheae allows
mass movement of air in and out.

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9
Q

Why can’t fish use their bodies as an
exchange surface?

A

They have a waterproof, impermeable
outer membrane and a small surface
area to volume ratio.

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10
Q

Name and describe the two main
features of a fish’s gas transport system.

A

Gills= located within the body, supported by arches, along
which are multiple projections of gill filaments, which are
stacked up in piles.
Lamellae= at right angles to the gill filaments, give an
increased surface area. Blood and water flow across them
in opposite directions (countercurrent exchange system).

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11
Q

Explain the process of gas exchange in
fish.

A

• The fish opens its mouth to enable water to flow
in, then closes its mouth to increase pressure.
• The water passes over the lamellae, and the
oxygen diffuses into the bloodstream.
• Waste carbon dioxide diffuses into the water
and flows back out of the gills.

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12
Q

How does the countercurrent exchange
system maximise oxygen absorbed by
the fish?

A

Maintains a steep concentration gradient, as
water is always next to blood of a lower
oxygen concentration. Keeps rate of diffusion
constant along whole length of gill enabling
80% of available oxygen to be absorbed.

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13
Q

Name and describe three adaptations of
a leaf that allow efficient gas exchange.

A
  1. Thin and flat to provide short diffusion pathway and large
    surface area to volume ratio.
  2. Many minute pores in the underside of the leaf (stomata)
    allow gases to easily enter.
  3. Air spaces in the mesophyll allow gases to move around
    the leaf, facilitating photosynthesis.
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14
Q

How do plants limit their water loss while
still allowing gases to be exchanged?

A

Stomata regulated by guard cells which
allows them to open and close as needed.
Most stay closed to prevent water loss
while some open to let oxygen in.

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15
Q

Describe the pathway taken by air as it
enters the mammalian gaseous
exchange system.

A

Nasal cavity → trachea → bronchi →
bronchioles → alveoli

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16
Q

Describe the function of the nasal cavity
in the mammalian gaseous exchange
system.

A

A good blood supply warms and moistens
the air entering the lungs. Goblet cells in
the membrane secrete mucus which traps
dust and bacteria.

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17
Q

Describe the trachea and its function in
the mammalian gaseous exchange
system.

A

• Wide tube supported by C-shaped cartilage to keep
the air passage open during pressure changes.
• Lined by ciliated epithelium cells which move
mucus towards the throat to be swallowed,
preventing lung infections.
• Carries air to the bronchi.

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18
Q

Describe the bronchi and their function in
the mammalian gaseous exchange
system.

A

• Like the trachea they are supported by rings of
cartilage and are lined by ciliated epithelium cells.
• However they are narrower and there are two of
them, one for each lung.
• Allow passage of air into the bronchioles.

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19
Q

Describe the bronchioles and their
function in the mammalian gaseous
exchange system.

A

• Narrower than the bronchi.
• Do not need to be kept open by cartilage, therefore
mostly have only muscle and elastic fibres so that
they can contract and relax easily during ventilation.
• Allow passage of air into the alveoli.

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20
Q

Describe the alveoli and their function in
the mammalian gaseous exchange
system.

A

• Mini air sacs, lined with epithelium cells, site of
gas exchange.
• Walls only one cell thick, covered with a
network of capillaries, 300 million in each lung,
all of which facilitates gas diffusion.

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21
Q

Explain the process of inspiration and
the changes that occur throughout the
thorax.

A

• External intercostal muscles contract (while internal
relax), pulling the ribs up and out.
• Diaphragm contracts and flattens.
• Volume of the thorax increases.
• Air pressure outside the lungs is therefore higher than
the air pressure inside, so air moves in to rebalance.

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22
Q

Explain the process of expiration and the
changes that occur throughout the
thorax.

A

• External intercostal muscles relax (while internal
contract), bringing the ribs down and in.
• Diaphragm relaxes and domes upwards.
• Volume of the thorax decreases.
• Air pressure inside the lungs is therefore higher than the
air pressure outside, so air moves out to rebalance.

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23
Q

What is tidal volume?

A

The volume of air we breathe in and out
during each breath at rest.

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24
Q

What is breathing rate?

A

The number of breaths we take per minute.

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25
Q

How do you calculate pulmonary
ventilation rate?

A

Tidal volume x breathing rate. These can
be measured using a spirometer, a device
which records volume changes onto a
graph as a person breathes.

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26
Q

Define digestion.

A

The hydrolysis of large, insoluble
molecules into smaller molecules that
can be absorbed across cell
membranes.

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27
Q

Which enzymes are involved in
carbohydrate digestion? Where are they
found?

A

• Amylase in mouth
• Maltase, sucrase, lactase in
membrane of small intestine

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28
Q

What are the substrates and products of
the carbohydrate digestive enzymes?

A

• Amylase → starch into smaller polysaccharides
• Maltase → maltose into 2 x glucose
• Sucrase → sucrose into glucose and fructose
• Lactase → lactose into glucose and galactose

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29
Q

Where are lipids digested?

A

The small intestine.

30
Q

What needs to happen before lipids can
be digested?

A

They must be emulsified by bile salts
produced by the liver. This breaks down
large fat molecules into smaller, soluble
molecules called micelles, increasing
surface area.

31
Q

How are lipids digested?

A

Lipase hydrolyses the ester bond
between the monoglycerides and fatty
acids.

32
Q

Which enzymes are involved in protein
digestion? What are their roles?

A

• Endopeptidases= break between specific
amino acids in the middle of a polypeptide.
• Exopeptidases= break between specific amino
acids at the end of a polypeptide.
• Dipeptidases= break dipeptides into amino
acids.

33
Q

How are certain molecules absorbed into
the ileum despite a negative
concentration gradient?

A

Through co-transport.

34
Q

Which molecules require co-transport?

A

Amino acids and monosaccharides.

35
Q

Explain how sodium ions are involved in
co-transport.

A

Sodium ions (Na+
) are actively transported
out of the cell into the lumen, creating a
diffusion gradient. Nutrients are then taken
up into the cells along with Na+
ions.

36
Q

Why do fatty acids and monoglycerides
not require co-transport?

A

The molecules are nonpolar, meaning
they can easily diffuse across the
membrane of the epithelial cells.

37
Q

Describe the structure of haemoglobin.

A

Globular, water soluble. Consists of four
polypeptide chains, each carrying a
haem group (quaternary structure).

38
Q

Describe the role of haemoglobin.

A

Present in red blood cells. Oxygen
molecules bind to the haem groups and
are carried around the body to where
they are needed in respiring tissues.

39
Q

Name three factors affecting
oxygen-haemoglobin binding.

A
  1. Partial pressure/concentration of oxygen.
  2. Partial pressure/concentration of carbon
    dioxide.
  3. Saturation of haemoglobin with oxygen.
40
Q

How does partial pressure of oxygen
affect oxygen-haemoglobin binding?

A

As partial pressure of oxygen increases, the
affinity of haemoglobin for oxygen also
increases, so oxygen binds tightly to
haemoglobin. When partial pressure is low,
oxygen is released from haemoglobin.

41
Q

How does partial pressure of carbon
dioxide affect oxygen-haemoglobin
binding?

A

As partial pressure of carbon dioxide increases, the
conditions become acidic causing haemoglobin to
change shape. The affinity of haemoglobin for
oxygen therefore decreases, so oxygen is released
from haemoglobin. This is known as the Bohr effect.

42
Q

How does saturation of haemoglobin
with oxygen affect oxygen-haemoglobin
binding?

A

It is hard for the first oxygen molecule to bind. Once
it does, it changes the shape to make it easier for
the second and third molecules to bind, known as
positive cooperativity. It is then slightly harder for
the fourth oxygen molecule to bind because there is
a low chance of finding a binding site.

43
Q

Explain why oxygen binds to
haemoglobin in the lungs.

A

• Partial pressure of oxygen is high.
• Low concentration of carbon dioxide in the lungs,
so affinity is high.
• Positive cooperativity (after the first oxygen
molecule binds, binding of subsequent molecules
is easier).

44
Q

Explain why oxygen is released from
haemoglobin in respiring tissues.

A

• Partial pressure of oxygen is low
• High concentration of carbon dioxide
in respiring tissues, so affinity
decreases.

45
Q

What do oxyhaemoglobin dissociation
curves show?

A

Saturation of haemoglobin with oxygen
(in %), plotted against partial pressure of
oxygen (in kPa). Curves further to the left
show the haemoglobin has a higher
affinity for oxygen.

46
Q

How does carbon dioxide affect the
position of an oxyhaemoglobin
dissociation curve?

A

Curve shifts to the right because
haemoglobin’s affinity for oxygen has
decreased.

47
Q

Name some common features of a
mammalian circulatory system.

A
  1. Suitable medium for transport, water-based to
    allow substances to dissolve.
  2. Means of moving the medium and maintaining
    pressure throughout the body, such as the heart.
  3. Means of controlling flow so it remains
    unidirectional, such as valves.
48
Q

Relate the structure of the chambers of the heart to
their function. (Draw it out too if you have spare paper)

A

• Atria: thin-walled and elastic, so they can
stretch when filled with blood
• Ventricles: thick muscular walls pump blood
under high pressure. The left ventricle is
thicker than the right because it has to pump
blood all the way around the body.

49
Q

Relate the structure of the vessels to
their function.

A

• Arteries have thick walls to handle high pressure
without tearing, and are muscular and elastic to
control blood flow.
• Veins have thin walls due to lower pressure,
therefore requiring valves to ensure blood doesn’t
flow backwards. Have less muscular and elastic
tissue as they don’t have to control blood flow.

50
Q

Why are two pumps (left and right)
needed instead of one? (In the heart)

A

To maintain blood pressure around the whole body.
When blood passes through the narrow capillaries of
the lungs, the pressure drops sharply and therefore
would not be flowing strongly enough to continue
around the whole body. Therefore it is returned to the
heart to increase the pressure.

51
Q

Describe what happens during cardiac
diastole.

A

The heart is relaxed. Blood enters the atria,
increasing the pressure and pushing open the
atrioventricular valves. This allows blood to
flow into the ventricles. Pressure in the heart
is lower than in the arteries, so semilunar
valves remain closed.

52
Q

Describe what happens during atrial
systole.

A

The atria contract, pushing any
remaining blood into the ventricles.

53
Q

Describe what happens during
ventricular systole.

A

The ventricles contract. The pressure
increases, closing the atrioventricular
valves to prevent backflow, and opening
the semilunar valves. Blood flows into
the arteries.

54
Q

Name the nodes involved in heart
contraction and where they are situated.

A

• Sinoatrial node (SAN)= wall of right
atrium.
• Atrioventricular node (AVN)= in
between the two atria.

55
Q

What does myogenic mean?

A

The heart’s contraction is initiated from
within the muscle itself, rather than by
nerve impulses.

56
Q

Explain how the heart contracts.

A

• SAN initiates and spreads impulse across the
atria, so they contract.
• AVN receives, delays, and then conveys the
impulse down the bundle of His.
• Impulse travels into the Purkinje fibres which
branch across the ventricles, so they contract
from the bottom up.

57
Q

Why does the impulse need to be
delayed?

A

If the impulse spread straight from the
atria into the ventricles, there would not
be enough time for all the blood to pass
through and for the valves to close.

58
Q

How is the structure of capillaries suited
to their function?

A

• Walls are only one cell thick; short diffusion pathway.
• Very narrow, so can permeate tissues and red blood
cells can lie flat against the wall, effectively delivering
oxygen to tissues.
• Numerous and highly branched, providing a large
surface area.

59
Q

What is tissue fluid?

A

A watery substance containing glucose,
amino acids, oxygen, and other
nutrients. It supplies these to the cells,
while also removing any waste materials.

60
Q

How is tissue fluid formed?

A

As blood is pumped through increasingly
small vessels, this creates hydrostatic
pressure which forces fluid out of the
capillaries. It bathes the cells, and then
returns to the capillaries when the hydrostatic
pressure is low enough.

61
Q

How is water transported in plants?

A

Through xylem vessels; long, continuous
columns that also provide structural
support to the stem.

62
Q

Explain the cohesion-tension theory.

A

Water molecules form hydrogen bonds with
each other, causing them to ‘stick’ together
(cohesion). The surface tension of the water
also creates this sticking effect. Therefore as
water is lost through transpiration, more can be
drawn up the stem.

63
Q

What are the three components of
phloem vessels?

A

• Sieve tube elements= form a tube to transport
sucrose in the dissolved form of sap.
• Companion cells= involved in ATP production for
active loading of sucrose into sieve tubes.
• Plasmodesmata= gaps between cell walls where
the cytoplasm links, allowing substances to flow.

64
Q

Name the process whereby organic
materials are transported around the
plant.

A

Translocation

65
Q

How does sucrose in the leaf move into
the phloem?

A

Sucrose enters companion cells of the phloem
vessels by active loading, which uses ATP and
a diffusion gradient of hydrogen ions. Sucrose
then diffuses from companion cells into the
sieve tube elements through the
plasmodesmata.

66
Q

How do phloem vessels transport
sucrose around the plant?

A

As sucrose moves into the tube elements, water potential
inside the phloem is reduced. This causes water to enter
via osmosis from the xylem and increases hydrostatic
pressure. Water moves along the sieve tube towards
areas of lower hydrostatic pressure. Sucrose diffuses into
surrounding cells where it is needed.

67
Q

Give evidence for the mass flow
hypothesis of translocation.

A

• Sap is released when a stem is cut, therefore there
must be pressure in the phloem.
• There is a higher sucrose concentration in the
leaves than the roots.
• Increasing sucrose levels in the leaves results in
increased sucroses in the phloem.

68
Q

Give evidence against the mass flow
hypothesis of translocation.

A

• The structure of sieve tubes seems to hinder mass flow.
• Not all solutes move at the same speed, as they would in
mass flow.
• Sucrose is delivered at the same rate throughout the
plant, rather than to areas with the lowest sucrose
concentration first.

69
Q

How can ringing experiments be used to
investigate transport in plants?

A

The bark and phloem of a tree are removed in a ring,
leaving behind the xylem. Eventually the tissues
above the missing ring swells due to accumulation of
sucrose as the tissue below begins to die. Therefore
sucrose must be transported in the phloem.

70
Q

How can tracing experiments be used to
investigate transport in plants?

A

Plants are grown in the presence of radioactive
CO2
, which will be incorporated into the plant’s
sugars. Using autoradiography, we can see
that the areas exposed to radiation correspond
to where the phloem is.