3.2 Transport in Animals

Cards (27)

  • Why do multicellular organisms transport systems?
    • Large size ( small surface area to volume ratio), subsequently high metabolic rates.
    • Demand for oxygen is high, so need a specialised system to ensure a strong supply to all respiring tissues.
  • What are the different types of circulatory system:
    • Open = blood can diffused out of vessels e.g. inspects
    • Closed = blood confined to vessels e.g. fish, mammals:
    — single = blood passes through pump once per circuit of the body
    — double = blood passes through heart twice per circuit of the body
  • Explain how the structure of arteries relate to their function:
    • Thick muscular walls - handle high pressure without tearing.
    • Elastic tissue - allows recoil to prevent pressure surges.
    • Narrow lumen - maintain pressure
  • Explain how the structure of veins relate to their function:
    • Thin walls - due to low pressure.
    • Valves - ensure blood doesn’t flow backwards.
    • Less muscular & elastic tissue - b/c they dont have to control blood flow.
  • Explain how the structure of veins relate to their function:
    • One cell thick wall - short diffusion pathway.
    • Very narrow - so can permeate tissues & red blood cells can lie flat against the wall, effectively delivering oxygen to tissues.
    • Numerous & highly branched - provides large surface area.
  • Explain the role of arterioles & venules:
    • Branch off arteries & 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.
  • What is tissue fluid?
    • A watery substance containing glucose, amino acids , oxygen and other nutrients. It supplies these to the cells, while also removing any waste materials.
  • What type of pressure influence formation of tissue fluid?
    • Hydrostatic pressure : higher at arterial end of capillary than venous end.
    • Oncotic pressure : changing water potential of the capillaries as water moves out, induced by proteins in the plasma.
  • How is tissue fluid formed?
    • as blood is pumped through increasingly small vessels, hydrostatic pressure is greater than oncotic pressure, so fluid moves out of the capillaries. It then exchanges substances with the cells.
  • How does tissue fluid differ from blood & lymph?
    • Tissue fluid is formed from blood, but does not contain red blood cells, platelets & various other solutes usually present in blood.
    • After tissue fluid has bathed cells it becomes lymph, therefore this contains less oxygen & nutrients & more waste products.
  • Diagram of the human heart
  • Describe what happens during cardiac diastole:
    • Heart is relaxed.
    • Blood enters the atria, increasing the pressure & pushing open the atrioventricular valves.
    • this allows blood to flow into the ventricles.
    • Pressure in the heart is lower than in the arterioles, so semilunar valves remain closed.
  • Describe what happens during atrial systole:
    • the atria contract, pushing any remaining blood into the ventricles.
  • Describe what happens during ventricular systole:
    • the ventricle contract
    • pressure increases, closing the atrioventricular valves to prevent back flow, & opening the semilunar valves.
    • Blood flows into the arteries
  • Describe the role of haemoglobin:
    • present in RBCs
    • oxygen binds to the harem groups & are carried around the body, then released when needed in respiring tissues
  • How does partial pressure of oxygen affect oxygen-haemoglobin binding?
    • As partial pressure of oxygen increase, the affinity of haemoglobin for O2 also increases, so oxygen binds tightly to haemoglobin
    • when partial pressure is low, oxygen is released from haemoglobin
  • What do oxyhemoglobin disassociation curves show?
    • saturation of haemoglobin with oxygen (in %), plotted against partial pressure of oxygen in oxygen (in kPa).
    • Curved further to the left show the haemoglobin has a higher affinity for oxygen.
  • Describe the Bohr effect:
    • as partial pressure of carbon dioxide increase, the conditions become acidic causing haemoglobin to change shape
    • the affinity of haemoglibn for oxygen therefore decreases, so oxygen is released from haemoglobin
  • Explain the role of carbonic anhydrase in the Bohr effect:
    • Carbonic anhydrase is present in RBCs
    • Converts carbon dioxide to carbonic acid, which dissociates to produce H+ ions
    • there combine with haemoglobin to form haemoglobinic acid
    • encourages oxygen to dissociate from haemoglobin
  • Explain the role of hydrogen carbonate ions (CO3-) in gas exchange:
    • produced alongside carbonic acid.
    • 70% of carbon dioxide is carried in this form
    • in the lungs bicarbonate ions are converted back into carbon dioxide which we breathe out
  • How does foetal haemoglobin differ from adult haemoglobin?
    • the partial pressure of oxygen is low by the time it reaches the foetus
    • thus, foetal haemoglobin has a higher affinity for oxygen than adult
    • allows both mother’s & child’s oxygen needs to be met
  • How do you calculate cardiac output?
    Cardiac output = heart rate x stroke volume
  • Myogenic - heart’s contraction is initiated from within the muscle itself, rather than by nerve impulses
  • Explain how the heart contracts:
    • SAN initiate & spreads impulse across atria, so they contract
    • AVN receives delays, then conveys the impulse down the bundle of His
    • Impulse travels into the Purkyne fibres which branch across the ventricles, so they contract from the bottom up
  • What is an electrocardiogram (ECG)?
    • A graph showing the amount of electrical activity in the heart during the cardiac cycle
  • Describe the types of abnormal activity that may be seen on an ECG:
    • Tachycardia = fast heartbeat (over 100bpm)
    • Bradycardia = slow heartbeat (under 60 bpm)
    • Fibrillation = irregular, fast heartbeat
    • Ectopic = early or extra heartbeats
  • Describe the chloride shift:
    • the intake of chloride ions across a red blood cell membrane.
    • This repolarises the cell after bicarbonate ions have diffused out.