Exchange Flashcards

1
Q

What kind of SA:V ratio do small organism have

A

A large one

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2
Q

Gas exchange in single celled organisms

A

Substances just diffuse across body surface

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3
Q

What features does insects have for gas exchange

A
  • Trachea
  • Tracheoles w/ water in the ends
  • Spiracles
  • Muscle fibre
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4
Q

What supports the trachea

A

Rings of cartilage so it doesn’t collapse

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5
Q

Why are do the tracheoles allow quick diffusion

A

Because they are directly next to cells allowing air to be directly brought to the respiring tissue

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6
Q

What 3 ways are gases moved in the insect tracheal system

A
  • along a diffusion gradient
  • mass transport
  • the ends of the tracheoles are filled with water
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7
Q

How do gases move in the insect tracheal system along a diffusion gradient

A
  • when cells are respiring, oxygen is used up decreasing its concentration at the ends of tracheoles -> this creates a diffusion gradient causing oxygen to diffuse from the atmosphere to the tracheoles
  • carbon dioxide is produced in cells during respiration -> this creates a diffusion gradient in the opposite direction so it’s taken out into the atmosphere
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8
Q

How do gases move in the insect tracheal system by mass transport

A

The contraction of muscles in insects can squeeze the trachea -> this allows mass movements of air in and out of

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9
Q

How do gases move in the insect tracheal system due to tracheoles being water filled

A
  • when insects undergo major activity, some anaerobic respiration takes places producing lactate
  • this lactate is soluble and lowers the water potential of the muscle cells
  • so water moves into cells from tracheoles by osmosis
  • the water in tracheoles ends decreases in volume allowing more air to be drawn in
  • this increases rate of air moved in but leads to greater water evaporation
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10
Q

What are spiracles

A

Pores on the body surface of an insect which open and close by a valve to let substances in and out of the

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11
Q

What are the limitations of the insect tracheal system

A
  • relies mostly on diffusion for gas exchange
  • and for diffusion to be effective the diffusion pathway must be short
  • so insects have to be of a small size
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12
Q

Structure of the gills

A

They are made up of gill filaments which have gill lamellae at a right angle
-> these increase surface area

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13
Q

What is the countercurrent flow

A

The flow of water over the gill lamellae and the flow of blood within them are in opposite directions

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14
Q

Why is the countercurrent so important

A
  • it means that the blood is already full of oxygen when it meets water which has its maximum concentration of water
    -> therefore diffusion of oxygen from the water to the blood takes place
  • blood with little oxygen in it meets water which has had most of its oxygen removed
    -> so diffusion of oxygen from the water to blood takes place
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15
Q

What is flow in the same direction called

A

Parallel flow

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16
Q

Why is countercurrent flow better than parallel flow

A

Parallel flow would mean the diffusion gradient would only be maintained across part of the length of the gill lamellae and only half the available oxygen would be absorbed by the blood

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17
Q

What adaptations do plant leaves have for gas exchange

A
  • many stomata
  • many air spaces throughout the mesophyll
  • large SA of mesophyll cells for rapid diffusion
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18
Q

What do the stomata do

A
  • each stoma is surrounded by guard cells which can open and close the stomata and so can control the rate of gas exchange and control water loss
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19
Q

What adaptations do insects have to reduce water loss

A
  • small SA:V ratio
  • waterproof cuticle
  • spiracles -> can open and close
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20
Q

What are xerophytes

A

Plants that have many adaptations to limit water loss through transpiration

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21
Q

Adaptations of xerophytes

A
  • thick cuticle -> waterproof barrier
  • rolling up of leaves -> protects lower epidermis of stomata + traps moist air with high water potential so there’s no movement of water
  • hairy leaves -> traps moist air so water potential gradient is decreased
  • stomata in pits -> traps moist air
  • small SA:V ratio
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22
Q

What do all aerobic organisms require a constant supply of and why

A

Oxygen to release energy in the form of ATP in respiration

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23
Q

What supports lungs

A

Ribcage

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24
Q

Why are lungs inside the body opposed to outside

A
  • air isn’t dense enough to support and protect the delicate structures
  • the body would lose a lot of water and dry out
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25
Q

Features of the lungs

A
  • trachea
  • tracheoles
  • bronchi
  • bronchioles
  • alveoli
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26
Q

Structure of trachea

A
  • supported by rings of cartilage that prevents it from collapsing as air pressure inside falls when breathing in
  • tracheal walls are made up of muscle, lined with ciliated epithelium and goblet cells
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27
Q

Structure of bronchi

A
  • 2 divisions of the trachea that each lead to one lung
  • produce mucus to trap dirt
  • have cilia to move mucus towards throat
  • larger bronchi are supported by cartilage -> but amount decreases as bronchi gets smaller
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28
Q

Structure of bronchioles

A
  • walls are made of muscles lined with epithelial cells
    -> this muscles lets them construct so they can control the flow of air in and out of the alveoli
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29
Q

Structure of alveoli

A
  • have collagen and elastic fibres between alveoli -> elastic fibres allow them to stretch as they fill with air and then spring back during exhalation to get rid of carbon dioxide rich air
  • lined with epithelium
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30
Q

What is the scientific word for breathing

A

Ventilation

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31
Q

What is the other word for inhalation and what is it

A

Inspiration
- when the atmospheric pressure is greater than pulmonary pressure and air is forced into the lungs

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32
Q

What is the other word for exhalation and what is it

A

Expiration
- when pulmonary pressure is greater than atmospheric pressure and air is forced out of the lungs

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33
Q

What muscles cause pressure changes in lungs

A
  • diaphragm
  • intercostal muscles
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34
Q

What are the types of intercostal muscles

A
  • internal intercostal muscles -> contract during expiration
  • external intercostal muscles -> contract during inspiration
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35
Q

Process of inspiration

A

• The external intercostal muscles contract, while the internal intercostal muscles relax

• The ribs are pulled upwards and outwards, increasing the volume of the thorax

• The diaphragm muscles contract, causing it to flatten, which also increases the volume of the thorax

• The increased volume of the thorax results in reduction of pressure in the lungs

• Atmospheric pressure is now greater than pulmonary pressure, and so air is forced into the lungs

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36
Q

Process of expiration

A

• The internal intercostal muscles contract, while the external intercostal muscles relax

• The ribs move downwards and inwards, decreasing the volume of the thorax

• The diaphragm muscles relax and so it is pushed up again by the contents of the abdomen that were compressed during inspiration

The volume of the thorax is therefore further decreased

• The decreased volume of the thorax increases the pressure in the lungs

• The pulmonary pressure is now greater than that of the atmosphere, and so air is forced out of the lungs

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37
Q

What types of processes are inspiration and expiration

A

Inspiration is an active process (uses energy)

Expiration is a largely passive process (doesn’t require much energy)

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38
Q

What is the main cause of air being forced out during breathing

A

The recoil of elastic tissue
BUT under more strenuous conditions, various muscles start to play a major part

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39
Q

Why is diffusion of gases between the alveoli and blood very rapid

A
  • RBCs are slowed as they pass through the pulmonary capillaries -> allowing more time for diffusion
  • the distance between the alveolar air and RBCs is reduced as the RBCs are flattened against the capillary walls
  • the walls of the alveoli and capillaries are very thin
  • large SA of alveoli and pulmonary capillaries
  • well ventilated + rich blood supply -> maintains steep concentration gradient
  • blood flow through the pulmonary capillaries maintains a concentration gradient
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40
Q

Why is the diffusion pathway in alveoli short

A

Because the alveoli only have a single layer of epithelial cells and the blood capillaries only have one layer of cells

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41
Q

What is a correlation

A

When a change in one of two variables is reflected by a change in the other variable

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42
Q

Vital capacity

A

the maximum volume of air that can be inhaled or exhaled in a single breath.
Varies depending on gender, age, size as well as height

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43
Q

Tidal volume

A

the volume of air we breathe in and out at each breath at rest

44
Q

Breathing rate

A

the number of breaths per minute, can be calculated from the spirometer trace by counting the number of peaks or troughs in a minute

45
Q

What is digestion

A

the hydrolysis of large biological molecules into smaller molecules which can be absorbed across cell membranes

46
Q

What enzymes digest carbohydrates

A
  • Amylases in the mouth digest larger polymers
  • Maltases in the ileum break down monosaccharides
  • Sucrases and lactases break down the dissacharides sucrose and lactose
47
Q

What enzymes digest lipids and how

A
  • Lipases by hydrolysing the ester bond between the monoglycerides and fatty acid.
  • Before being broken down in the ileum, lipids are emulsified into micelles by bile salts released by the liver
48
Q

What does emulsification do

A

Emulsification increases the surface area and speeds up the chemical reaction

49
Q

What enzymes digest proteins and what are the 3 types:

A
  • Peptidases of which they are divided into 3 main groups:
    • endopeptidases
    • exopeptidases
    • dipeptidases
50
Q

What does an endopeptidase do

A

hydrolyse peptide bonds between specific amino acids in the middle of a polypeptide

51
Q

What does an exopeptidase do

A

hydrolyse bonds at ends/terminals of a polypeptides

52
Q

What does a dipeptidase do

A

break dipeptides into individual amino acids

53
Q

How are amino acids transported

A

Via co transport

54
Q

How does the co transport of amino acids work

A
  • Amino acids are absorbed by facilitated diffusion through specific carrier molecule in the surface membrane of epithelial cells.
  • With each amino acid, one Na+ is also taken up, therefore amino acid absorption occurs via a process known as co-transport.
  • A diffusion gradient for Na+ is maintained by their active transport through the base of epithelial cells where amino acids pass by facilitated diffusion.
55
Q

Why can monoglycerides and fatty acids easily diffuse across the cell membrane

A

Because they are polar

56
Q

Where do monoglycerides and fatty acids go once through the cell membrane

A
  • into the epithelial cells lining the epithelium
  • then are transported to the endoplasmic reticulum where they are reformed into triglycerides again
  • then they leave the cells via vesicles into the lymph system
57
Q

Where does lipid digestion occur

A

Only in the lumen of the small intestine

58
Q

What happens in the stomach

A

Lipids are churned to turn them into a fatty liquid

59
Q

What does bile contain

A

Bile salts

60
Q

What is emulsification

A

When lipids are broken down (by binding to bile salts) into small droplets giving them a large SA

61
Q

Where is lipase secreted from and to

A

From the pancreas to the small intestine

62
Q

What do bile salts do

A

Bind to fat droplets and break them down into smaller fat droplets (emulsification)

63
Q

What are micelles

A

Droplets that are smaller than fat droplets in emulsified lipids

64
Q

How are micelles formed

A

When monoglycerides and fatty acids associate with bile salts and phospholipids

65
Q

What does micelles do

A

Transport the poorly soluble monoglycerides and fatty acids to the surface of the epithelial cells where they can be absorbed

66
Q

How do the micelles get the monoglycerides and fatty acids in the cell

A
  • they are constantly breaking down and reforming producing a small pool of monoglycerides and fatty acids that are in solution
  • only the freely dissolved monoglycerides and fatty acids can be absorbed -> not the micelles because they are non-polar
67
Q

Where do short chain fatty acids diffuse into

A

Directly into the blood from the lumen of the small intestine via the epithelial cells

68
Q

How do longer chain fatty acids diffuse into the blood

A
  • monoglycerides and glycerol diffuse into the epithelial cells where they recombine to form triglycerides again
  • these triglycerides are packed with cholesterol and phospholipids to form water soluble fat droplets called chylomicrons
  • these are then transferred to a lymph vessel and then eventually into the blood system
69
Q

How are chylomicrons transferred

A

By exocytosis
- when a small piece of cell surface membrane is wrapped around the lipid droplet and pinched off so that the fatty droplets are now wrapped in membrane as they enter the lymph vessels

70
Q

Where are the triglycerides reformed in the epithelial cell

A

At the endoplasmic reticulum

71
Q

What is a lacteal

A

A lymph vessel

72
Q

How is a lipid droplet formed

A

By lipids being churned in the stomach and then emulsified by binding to bile salts from bile made in the liver and stored in the gallbladder

73
Q

What happens after lipids are emulsified

A

The droplets are hydrolysed into fatty acids and glycerol by lipase from the pancreas in the small intestine

74
Q

What is a chylomicrons

A

A water soluble fat droplet

75
Q

Why are micelles used in lipid digestion

A

Because the components on their own are portly soluble and can’t move very well

76
Q

Explain the sodium potassium pump

A
  • not all available glucose can be absorbed because there’s no concentration gradient
  • so sodium ions are actively transported out of epithelium cells into the lumen -> takes place in a protein carrier molecule in the surface membrane
  • now there’s a higher concentration of sodium ions in the lumen of the intestine than inside the cells
  • the sodium ions now diffuse back into the cells down a concentration gradient through a different type of protein carrier
  • as the sodium ions go back they couple with glucose molecules which are carried with them
  • the glucose passes into the blood by facilitated diffusion using another type of carrier
77
Q

What powers the movement of glucose into cells

A

The sodium ion concentration gradient rather than ATP directly
-> this makes it an indirect rather than a direct form of active transport

78
Q

Insect adaptations to limit water loss

A
  • Spiracles
  • Small SA:V ratio (of tracheal system not whole insect)
  • Waterproof exoskeleton
79
Q

Adaptations for quick diffusion in insects

A
  • steel diffusion gradient
  • large number of tracheoles -> increases SA
  • short diffusion pathway
80
Q

Why do fish need an exchange surface

A

Because they are waterproof and have a small SA:V ratio

81
Q

Gas exchange surface features

A
  • large SA:V ratio
  • short diffusion distance
  • maintained concentration gradient
82
Q

Fick’s Law

A

Diffusion = SA x difference in conc / length of diffusion pathway

83
Q

Adaptations in fish for efficient gas exchange

A
  • large SA:V ratio created by many gill filaments cover in gill lamellae
  • short diffusion pathway due to capillary network in lamellae and thin lamellae
  • maintains concentration gradient by countercurrent flow
84
Q

Countercurrent and what it does

A

When water flows over the gills in the opposite direction to the flow of blood in the capillaries

-> ensures that equilibrium isn’t reached
-> ensures that a diffusion gradient is maintained across the entire length of the gill lamellae

85
Q

How do stomata reduce water floss

A

Close at night when photosynthesis wouldn’t be happening

86
Q

What are xerophytic plants

A

Plants adapted to survive in environments with limited water

87
Q

What is the compromise in xerophytes

A

They have structure features to allow efficient gas exchange whilst also limiting water loss

88
Q

Xerophyte adaptations

A
  • Curled leaves to trap moisture to maintain water potential
  • hairs to trap moisture
  • sunken stomata to trap moisture
  • thicker cuticle to reduce evaporation
  • longer root network to reach more water
89
Q

What do carbohydrates need to be hydrolysed

A

2 enzymes
- amylases
- membrane-bound disaccharides

90
Q

What produces amylase

A

The pancreas and salivary glands

91
Q

What does amylase do

A

Hydrolyses polysaccharides into the disaccharide maltose by hydrolysing the glycosidic bonds

92
Q

Where does protein digestion start and end

A

Starts in stomach and ends in ileum where it’s fully digested

93
Q

What are lipids digested by

A

Lipase and bile salts

94
Q

Where is lipase produced

95
Q

What does lipase do

A

Hydrolyses the ester bond in triglycerides to form monoglycerides and fatty acids

96
Q

Where are bile salts produced

97
Q

What do bile salts do

A

Emulsify lipids to form micelles -> increases SA for lipase to act on

98
Q

What are the 2 stages of digestion of lipids

A

Physical: emulsification and micelle formation

Chemical: lipase

99
Q

What is the physical stage of lipid digestion

A
  • lipids bind to bile salts to be emulsified
  • micelles provide larger SA for faster hydrolysis by lipase
101
Q

What is the chemical stage of lipid digestion

A
  • lipase hydrolyses lipids in glycerol and fatty acids (some monoglycerides)
102
Q

What are micelles

A

Vesicles formed from fatty acids, monoglycerides and bile salts

103
Q

Where are products of digestion absorbed

A

across the cells lining the ileum

104
Q

What is the ileum wall covered in

A

Villi
-> which have thin walls surrounded by a network of capillaries
-> epithelial cells have even smaller microvilli

105
Q

Why is active transport and co-transport required for glucose and amino acid absorption

A

Because there is usually more glucose in the epithelial cells