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Biology > 3.3 Exchange and Transport > Flashcards

3.3 Exchange and Transport Flashcards

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1
Q

What is digestion?

A

Larger biological molecules hydrolysed to smaller molecules that can be absorbed across cell membranes

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2
Q

How are carbohydrates digested?

A

•pancreatic and salivary gland amylase will hydrolyse starch into maltose
•membrane bound disaccharidases in ileum epithelial cells hydrolyse maltose into glucose (co-transport with Na+)

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3
Q

How are proteins digested?

A

•endopeptidases: hydrolyse peptide bonds between aa in middle of polypeptide chain (smaller peptide chains)
•exopeptidases: hydrolyse peptide bonds between aa at the end of a polypeptide chain (remove terminal aa)
•membrane bound dipeptidases: hydrolyse peptide bonds between 2 aa (dipeptides to aa)

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4
Q

How are lipids digested?

A

•bile salts emulsify lipids into smaller droplets- increase SA for faster hydrolysis action by lipase
•micelles form from bile salts, monoglycerides, glycerol=make them more soluble and they are absorbed by diffusion.

•inside cell: modified back into triglycerides by Golgi body and ER
•vesicle moves to cell surface membrane to be released by exocytosis

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5
Q

What is a chylomicron?

A

In the Golgi body, (modified) protein is added to the lipids and it is packed in a vesicle and released by exocytosis

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6
Q

Why are micelles important?

A

•micelles form from bile salts, monoglycerides, glycerol and fatty acids
•micelles make fatty acids more water soluble
•micelles carry fatty acids to epithelial cells of ileum
=fatty acids released from micelles are absorbed into cell by simple diffusion

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7
Q

What do very small organisms use for gas exchange compared to larger organism?

A

•small: have a very large SA:V + small distances so can do simple diffusion
•large: smaller SA:V + larger distances + higher metabolic rates so gas exchange systems

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8
Q

What is a consequence of a larger SA:V for small organism?

A

Lose heat more quickly so to compensate they have a higher metabolic rate. More Respiration so more heat energy to maintain temp.

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9
Q

How do terrestrial insects have an efficient gas exchange system?

A
  1. Large no. of tracheoles branching to each cell (large SA for rapid diffusion and short diffusion distance)
    2.thin tracheal walls (short diffusion distance)
    3.use of O2 and making of CO2 sets up steep conc. gradient
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10
Q

How do terrestrial insects minimise water loss?

A

1.have small SA:V less surfaces for evaporation
2.waterproof exoskeleton so less evaporation
3.spiracle valves close

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11
Q

What are the methods of gas exchange in terrestrial insects?

A
  1. Diffusion: conc. gradient when respiring

2.mass transport: abdominal muscles relax and contract to move gases on mass, so more air/O2 enters to maintain conc. gradient

3.anaerobic respiration: lactic acid lowers water potential of muscle cells so they gain water by osmosis from tracheoles=
•tracheole volume decreases so more air drawn in
•gases move faster in air than H2O
•greater SA exposed to air

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12
Q

How are insects able to obtain oxygen?

A

1.air enters through spiracles
2.travels down tracheae
3.diffusion gradient in tracheae as oxygen is used in respiration
4.tracheae associated with all cells (branching)
5.O2 diffuses into cells
6.ventilation replaces air in tracheae

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13
Q

What makes gas exchange in fish efficient?

A

•large SA:V=lots of gill filaments with lots of gill lamellae
•short diffusion distance=capillary network in every lamellae + very thin lamellae
•maintain conc. gradient=countercurrent flow, ventilation (fresh water), capillaries (good blood circulation)

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14
Q

What is the countercurrent flow in fish?

A

1.blood + water flow in opposite directions (blood always meets H20 with a higher O2 conc.)

2.equilibrium is not reached

3.diffusion gradient is maintained across the entire length of gill lamellae

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15
Q

What are the steps in inspiration?

A

1.external intercostal muscle contract
2. Diaphragm muscle contracts and flattens
3.Ribcage moves upwards + outwards
4. Volume of thoracic cavity increases
5.Pressure in thoracic cavity decreases
6.air moves into the lungs, down the pressure gradient

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16
Q

What are the steps in expiration?

A

1.internal intercostal muscles contract
2.Diaphragm muscle relaxes and domes
3. Ribcage moves downwards + inwards
4.Volume of thoracic cavity decreases
5. Pressure of thoracic cavity increases
6. Air is drawn out of the lungs, down pressure gradient

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17
Q

What features of the alveolar epithelium make it an efficient exchange surface? (+lungs?)

A

•thin epithelium - short diffusion distance
•each surrounded by a network of capillaries - steep conc. gradient
•many- large SA for rapid diffusion

Lungs:
•ventilation brings in air with higher O2 conc. and removed air with lower O2 conc. (conc. gradient of O2 maintained)
•good circulation of blood

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18
Q

What is the pathway taken by O2 from air to blood?

A
  1. Trachea, bronchi, bronchioles
  2. Down pressure gradient
  3. Down diffusion gradient
  4. Across alveolar epithelium
  5. Across capillary endothelium
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19
Q

How is pulmonary ventilation calculated?

A

PV= tidal volume * ventilation rate
Tidal volume:vol of air enters+leaves at normal resting breath (0.5dm3)
Ventilation rate:breaths per minute

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20
Q

What are adaptations of xerophytic plants to reduce water loss?

A

•sunken stoma with hairs traps water vapor and increases humidity to lower water potential gradient
•curled leaves to protect from wind
•reduced no. of open stomata
•thick waxy cuticle to reduce evaporation

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21
Q

How are plants adapted for efficient gas exchange?

A

•short diffusion distance: thin leaves
•steep diffusion gradient: palisade use up CO2 for photosynthesis
•large SA: spongy mesophyll has lots of air space

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22
Q

How could you find the surface area of a leaf?

A

1.draw around leaf on graph paper
2.count squares
3.multiply by 2 (2 sided)

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23
Q

Why might the rate of H2O uptake not be the same as the rate of transpiration by a plant?

A

Water used in photosynthesis , hydrolysis, for turgid, made in respiration

24
Q

What is the structure of haemoglobin?

A

•quaternary protein= 4 polypeptide chains (more than 1)
•each chain has haem group (Fe2+) which binds to O2 to become oxyhaemoglobin

25
Q

Explain a oxyheamoglobin dissociation curve

A

•Low PO2 = low affinity = O2 unloaded for respiration
•High PO2 = high affinity = O2 loaded in e.g alveoli

26
Q

What is cooperative binding?

A

When 1st O2 binds, haemoglobin changes shape (changes quaternary structure of hb) and it is easier for further O2 to bind as it uncovers more haem group binding sites.

27
Q

What is the Bohr effect?

A

•High PCO2 will decrease affinity for O2 as acidic CO2 (Ph) will change the shape of haemoglobin so more oxygen is unloaded.
•High PCO2 will shift oxyhaemoglobin curve to the right

Right= release
Left= load

28
Q

When will oxyhaemoglobin curve shift to the left? (E.g)

A

•higher affinity for O2
E.g
•high altitudes + underground have lower PO2 so higher affinity of O2 needed to load more o2

29
Q

When will oxyhaemoglobin curve shift to the right? (E.g)

A

•lower affinity for O2
E.g
•faster metabolism so need more O2 for more respiration so more ATP/heat energy for more muscle contraction or to maintain body temp. So have lower O2 affinity to unload more O2 in respiring cells

30
Q

What do the coronary arteries do?

A

Supply oxygenated blood and glucose to cardiac muscles to respire and release ATP energy for contractions

31
Q

What is the pathway of blood circulation?

A

Vena cava, right atrium/ventricle, pulmonary artery to lungs, pulmonary vein, left atrium/ventricle, aorta to body

32
Q

What are valves and what types are there?

A

Valves prevent back flow of blood as they only open when pressure is higher behind.
•atrioventricular valves between atrium and ventricles
•semi lunar valves between ventricle and aorta/pulmonary artery

33
Q

What is a septum and why is it helpful?

A

It separates oxygenated and deoxygenated blood which will maintain a high concentration gradient of oxygen

34
Q

Why is a double circulatory system useful?

A

•blood flows to the lungs at a lower pressure to prevent damage to capillaries in alveoli + reduces speed of blood flow to give time for gas exchange

•blood flows to body at higher pressure to ensure it reaches all respiring cells

35
Q

What are the blood vessels in lungs and kidneys?

A

Lungs: pulmonary artery/vein
Kidney: renal vein (out)/ renal artery (in)

36
Q

Why are arterioles different to arteries?

A

•thicker muscle layer to help restrict blood flow into capillaries
•thinner elastic layer as lower pressures
•muscle contracts and lumen narrows to reduce blood flow into capillary

37
Q

What is the structure of the artery and why?

A

•thicker muscle layer to allow constriction/dilation to control blood volume
•thicker elastic muscle layer to maintain blood pressure. The walls can stretch and recoil in response to a heart beat
•thicker wall to prevent it bursting at high pressure

38
Q

What is the structure of the vein and why?

A

•thin muscle/elastic layer as pressures are much lower, so low risks of bursting
•valves to prevent back-flow of blood

39
Q

What is the structure and function of capillaries?

A

•form capillary beds as exchange surfaces= narrow diameter to slow blood flow and maximise diffusion of O2 from RBC
•one cell thick= short diffusion distances

40
Q

How is tissue fluid formed?

A

1.blood enters capillaries from arterioles. As is enters a small diameter, there is high hydrostatic pressure which is higher than osmotic effect (increase in outward pressure) due to contraction from left ventricle so H2O and small molecules forced
2.large plasma proteins too big to leave capillary and lower the water potential + hydrostatic pressure at venule end (in the blood) is very low so water re-enters capillary by osmosis

41
Q

What happens to excess tissue fluid and why?

A

•Not all liquids can be reabsorbed by osmosis as equilibrium is reached
•rest of the tissue fluid is absorbed into the lymphatic vessel/capillaries and will drain back into the bloodstream near the heart

42
Q

How is one way blood flow maintained in the heart? (Route)

A
  1. Diastole: atria and ventricular muscles relax so blood enters the atria (pressure increases)

2.atrial systole: atria muscle walls contract (++pressure), so AV valve opens and blood flows into ventricles (ventricular diastole)

  1. Ventricular systole: after short delay, ventricle muscle walls contract and its pressure is higher that in atria so AV valve closed and semi lunar valves will open to allow blood to be pushed out of ventricles to arteries

4.semi lunar valves will close when the pressure in the arteries is higher than in the ventricles

43
Q

How is a heartbeat initiated and coordinated?

A

1.sino atrial node (SAN) will send wave of electrical excitation across atria, atrial contraction happens
2.layer of non-conducting tissue prevents immediate contraction of ventricles , as impulse doesn’t reach it
3.atrioventricular node (AVN) delays impulses whilst blood leaves atria
4. AVN sends wave of electrical excitation down Bundle of His (into purkyne fibres)
5.this causes ventricles to contract from base up

44
Q

Why is there a short delay of electrical activity after SAN?

A

It allows atria to be fully empty of blood and the ventricles fully full before the ventricles contract

45
Q

Why are electrical impulses passed to the base of the ventricles?

A

So that ventricles contract from base upwards, which makes sure all the blood can be pushed out of the ventricles and into the arteries (aorta or pulmonary artery)

46
Q

How is cardiac output measured?

A

Stroke volume x heart rate
(dm3) (bpm)

Cardiac output (dm3/min) amount of blood pumped by the left ventricle in one minute

47
Q

What is the structure of the xylem?

A

•waterproof lignin to withstand tension
•no organelles to allow easy flow of water
•no end walls to allow continuous water columns
•pits in walls to allow lateral movement

48
Q

Describe the cohesion-tension theory of transpiration

A

1.water evaporates in the leaf via stomata
2.water potential gradient across cells of the leaf produced
3.this causes water to be drawn out of the xylem and creates tension in the xylem
4.hydrogen bonds cause a cohesive force between molecules so water gets pulled up the xylem as a continuous column

49
Q

Why are there larger fluctuations in blood pressure in the aorta that the small arteries?

A

1.aorta is close to the heart
2.it has elastic tissue
3.it has stretch/recoil

50
Q

How is directional flow of blood maintained?

A

1.valves stop backflow of blood
2.pressure gradient/moves from high to low pressure

51
Q

What affects rate of transpiration?

A

1.light intensity as + so more stomata open
2.humidity as + water potential gradient reduced
3.wind as + water potential gradient maintained
3.temperature as + more evaporation

52
Q

What is the structure of the phloem?

A

•cellulose cell wall-resist high pressure in sieve tubes
•sieve plates-provide structural strength but pores allow flow of sap
•plasmodesmata-connects sieve tube elements and companion cells
•companion cells-provide metabolic support
•few organelles-hollow to let sap through

53
Q

What is the mass flow hypothesis? (Translocation)

A

1.in source cell, companion cells use active transport to load sucrose into the sieve tube elements
2.water potential of sieve tube is reduced
3.water moves into the tubes from the xylem by osmosis, causing a high hydrostatic pressure

4.in the sink cell, sucrose is unloaded from the sieve tubes using active transport
5.water potential is increased in the tubes
6.water moves back into the xylem by osmosis, reducing the hydrostatic pressure

(Sucrose will move down its pressure gradient from source to sink)
*sugars used/converted in root for respiration/storage

54
Q

Why does diameter decrease when transpiration increases?

A

Increase in transpiration produces a higher tension in the xylem. There is adhesive forces between xylem and water and this will pull the walls inward

55
Q

How can we prove that the phloem is the site of translocation?

A

•radioactively labelling carbon which can traced to show that sugars are transported in the phloem in the stem
•ringing- ring of phloem removed and it swells above due to sugar build up (test it) as no phloem to transport it
•aphids will penetrate into phloem, we cut its stylet and test the sap flowing out

56
Q

What is the advantage of giving data as %?

A

•allows comparison
•as different initial no. /value

57
Q

Why does uptake of CO2 fall to zero when light is turned off?

A

1.no use of CO2 in photosynthesis when no light
2.no diffusion gradient for CO2 into the leaf

Biology (8 decks)

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