Animal Transport Flashcards

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1
Q

What is an open circulatory system?

A

A circulatory system with a heart or pump but few vessels to contain the transport medium.

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2
Q

What is a closed circulatory system?

A

A circulatory system where blood is enclosed in blood vessels and does not come into direct contact with body cells.

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3
Q

What is a single circulatory system?

A

A circulatory system where the blood flows through the heart once with each full circuit.

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4
Q

What is a double circulatory system?

A

A circulatory system where the blood flows through the heart twice with each full circulation.

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5
Q

What is haemolymph?

A

The transport medium found in insects.

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6
Q

What is a mass transport system?

A

A transport system where substances are transported in a mass of fluid.

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7
Q

What is oncotic pressure?

A

The tendency of water to osmose into the blood from surrounding tissues.

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8
Q

At which ends are oncotic pressure and hydrostatic pressure higher?

A

Hydrostatic pressure highest at arterial end, oncotic pressure higher at venous end.

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9
Q

What causes oncotic pressure? Why does it remain constant (3.3kPa)?

A

Large, dissolved proteins decrease the water potential of blood. These proteins cannot diffuse out, too large.

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10
Q

What is the role of tissue fluid?

A

Bathes cells in required nutrients/reactants for metabolic processes e.g oxygen and glucose. Waste diffuses into it.

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11
Q

How does the tissue fluid composition compare to plasma composition?

A

Less dissolved substances (e.g large proteins), higher proportion of it is water. No blood structures can move across (e.g erythrocytes), some leukocytes can.

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12
Q

What % of tissue fluid returns to the capillary? Why?

A

Oncotic pressure begins to overcome hydrostatic pressure as the blood in the capillary travels toward the venous end, so fluid moves back in. 90% returns. The other 10% becomes lymph.

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13
Q

Why is the lymphatic system so important?

A

Prevents accumulation of unnecessary tissue fluid. Contains leukocytes. Drainage system, gets rid of cellular waste products.

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14
Q

Relate the structure of arteries to their function.

A

Thick muscular walls to maintain high pressure without tearing. elastic tissue allows recoil to prevent pressure surges. Narrow lumen to maintain pressure.

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15
Q

Relate the structure of veins to their function.

A

Thin walls due to low pressure. Valves to ensure blood doesn’t flow backwards. Less muscular and elastic tissue as they don’t have to control blood flow.

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16
Q

Relate the structure of capillaries to their function.

A

One cell thick walls; 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 to provide a large SA.

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17
Q

Relate the structure of arterioles and venues to their function.

A

Branch off of arteries and veins in order to feed blood into capillaries. Smaller than arteries and veins so that the change in pressure is more gradual as blood passes through increasingly small vessels.

18
Q

How does tissue fluid differ from blood and lymph?

A
  • Tissue fluid is formed from blood, but does not contain red blood cells, platelets, and various other solutes usually present in blood.
  • After tissue fluid has bathed cells 10% becomes lymph, and therefore this contains less oxygen and nutrients and more waste products.
19
Q

Describe what happens during cardiac diastole.

A
  • Ventricles and atria relax.
  • Pressure inside the chambers drops below that in the arteries because they are not contracted (higher volume).
  • Blood under high pressure in arteries cause semi-lunar valves to shut. (DUB).
20
Q

Describe what happens during atrial systole.

A

The atria contract, pushing any remaining blood into the ventricles. 70% has already passively flowed down. Atrioventricular valves open due to pressure against them.

21
Q

Describe what happens during ventricular systole.

A

The ventricles contract. The pressure increases, closing the atrioventricular valves to prevent back flow (LUB), and opening the semilunar valves. Blood flows into the arteries (aorta from left ventricle, pul.artery from right ventricle).

22
Q

How do you calculate cardiac output?

A

Heart rate x stroke volume.

23
Q

What does myogenic mean?

A

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

24
Q

Explain how the heart contracts.

A
  • SAN initiates and spreads impulse across 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, sending the impulse from the apex of the heart (bottom) upwards.
25
Q

What is an electrocardiogram ((ECG)?

A

A graph showing the amount of electrical activity in the heart during the cardiac cycle.

26
Q

Describe types of abnormal activity that may be seen on an ECG.

A
  • Tachycardia = fast heartbeat (over 100bpm)
  • Bradycardia = slow heartbeat (under 60bpm)
  • Atrial fibrillation = fast, irregular heartbeat caused by quivering atrial muscles.
  • Ectopic = early or extra heartbeats.
27
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, they dissociate when needed in respiring tissues. The first and last oxygen molecules are more difficult to bind than the second and third.

28
Q

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

A
  • Low ppO2, fewer Hb molecules have 02 molecules bound. Low affinity for oxygen, will readily dissociate at respiring tissues.
  • High ppO2, more haem groups bound to oxygen, making it easier for more O2 to be picked up. Will readily associate.
29
Q

Why is it advantageous for Hb to have a higher affinity for oxygen at high oxygen partial pressures and vice versa?

A

Will readily associate with oxygen at the lungs (high ppO2), will readily dissociate at respiring tissues (low ppO2).

30
Q

Describe the Bohr effect.

A

As partial pressure of carbon dioxide increases, the conditions becomes acidic causing haemoglobin to change shape. The affinity of haemoglobin for oxygen therefore decreases, so oxygen is therefore released from Hb more readily. The O2 dissociation curve shifts to the right.

31
Q

Why is the Bohr effect advantageous?

A

At tissues with high ppCO2, oxygen will more readily dissociate.

32
Q

Explain the role of carbonic anhydrase in the Bohr effect.

A
  • C.A is present in RBCs.
  • Converts CO2 to carbonic acid, which dissociates to produce H+ ions.
    These combine with the Hb to form haemoglobinic acid.
  • Encourages oxygen to dissociate from Hb.
33
Q

Explain the role of HCO3- ions in gas exchange.

A

Produced by dissociation of carbonic acid. 70% of CO2 is carried in this form. In the lungs, HCO3- ions are converted back into CO2 which we breathe out.

34
Q

Describe the chloride shift.

A

The intake of chloride ions across a RBC membrane. This repolarises the cell after HCO3- ions have diffused out, balancing the H+ ions.

35
Q

How does foetal Hb differ from adult Hb.

A

The ppO2 of oxygen is low by the time it reaches the foetus, therefore foetal haemoglobin must have a higher affinity from oxygen so that foetal blood can be transferred oxygen from the mother’s blood at the placenta. Allows for both the mother’s and child’s oxygen needs to be met.

36
Q

What are the properties and functions of myoglobin?

A
  • Myoglobin will only release its O2 at very low ppO2.
  • Oxymyoglobin will only dissociate when O2 levels are low.
  • Found in muscles cells, acts as a reserve for oxygen.
37
Q

Why is the cardiac muscle described as ‘myogenic’?

A
  • It can initiate its own contractions without the need for nervous stimulation. Impulse originates from within the heart.
38
Q

What is the role of the SAN?

A
  • Muscle cells (myocytes) in the heart have a slight electrical charge across their membranes (polarised). When they become depolarised (charge reversed) they contract. A wave of depolarisation/excitation is initiated in the SAN where there are specialised fibres collectively known as the ‘pacemaker of the heart’.
39
Q

What happens after the SAN initiates the wave of excitation?

A
  • Depolarisation spreads through the atria, where they contract. The electrical wave cannot speed directly to the ventricles due to the region of nonconductive tissue, known as annulus fibrosis, at the base of the atria. This channels the wave of excitation down the septum.
40
Q

What happens after the atria contract?

A
  • The AVN is stimulated by the wave of excitation. Causes a slight delay in the waves transmission, then passes the wave of excitation down to the bundle of His which consists of Purkinje fibres which are conductive. There is only one pathway for the wave of the SAN.
41
Q

What happens after the wave of excitation is passed into the AVN and the bundle of His?

A
  • The bundle of His splits into two branches of Purkinje fibres, based in the apex, which carry the wave to the apex and upwards to the ventricles. This delay enables the ventricles to fill with a sufficient amount of blood before contracting.