3.2- Transport in Animals (copy)

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62 Terms

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the need for transport systems in multicellular animals

larger organisms require mass transport systems due to:

  • large transport distances between exchange sites→ diffusion not fast enough to meet metabolic requirements of cells

  • SA:V ratio decreases as size of organism increases→ less SA for absorption and excretion, greater volume= longer diffusion distance

  • high metabolic rate→ higher demand for oxygen and nutrients, more waste produced

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what is mass flow

the bulk movement of materials between exchange sites

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what is the purpose of mass transport systems

  • move substances quickly between exchange site to another

  • maintain diffusion gradient at exchange sites and between cells and extracellular fluid

  • ensure effective cell activity by keeping immediate fluid environment within suitable metabolic range

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single circulatory system

blood passes through heart once during one complete circuit of the body

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single circulatory system in fish

  • deoxygenated blood pumped from heart to gills

  • oxygen and carbon dioxide exchanged at gills

  • oxygenated blood flows from gills to rest of body→ travels through capillaries in organs delivering oxygen and nutrients

  • blood returns to heart→ 1 atrium, 1 ventricle

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double circulatory system

blood passes through heart twice during one complete circuit of the body

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double circulatory system in mammals

  • heart has left and right side separated by septum:

    • left side→ oxygenated blood

    • right side→ deoxygenated blood

  • blood in right side leaves and travels to lungs

  • returns to left side and is pumped around the rest of the body

  • once body has passed through organs, it returns to right side of the heart again

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advantages of double circulation

  • higher blood pressure and avg speed of flow→ blood only passes through one capillary network before returning to the heart

  • increased pressure and speed= steeper concentration gradient

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open circulatory system

  • blood not contained in blood vessels→ pumped directly into body cavities

  • arthropods and molluscs have open circulatory systems

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closed circulatory system

  • blood pumped around body and is always contained in a network of blood vessel

  • all vertebrates and invertebrates have closed circulatory systems

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path of blood around the body

heart → arteries → arterioles → capillaries → venules → veins

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insect circulatory systems

  • have one main blood vessel→ dorsal vessel

  • tubular heart in abdomen pumps haemolymph (insect blood) into dorsal vessel

  • haemolymph delivered into haemocoel (body cavity)→ surrounds organs and re-enters the heart via ostia (one way valves)

  • oxygen not transported in haemolymph→ tracheal system

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arteries

transport blood away from heart

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veins

transport blood to the heart

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arterioles

narrower blood vessels that transport blood from arteries to capillaries

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venules

narrower blood vessels that transport blood from capillaries to veins

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structure of arteries

  • consist of three layers:

    • tunica externa, tunica media, tunica intima

    • tunica externa→ made of collagen to provide rigidity and overprotection

    • tunica media→ layer of muscle cells strengthening arteries so they can withstand high pressure. elastic tissue maintains blood pressure

    • tunica intima→ endothelial layer- one cell thick

<ul><li><p>consist of three layers:</p><ul><li><p>tunica externa, tunica media, tunica intima</p></li><li><p>tunica externa→ made of collagen to provide rigidity and overprotection</p></li><li><p>tunica media→ layer of muscle cells strengthening arteries so they can withstand high pressure. elastic tissue maintains blood pressure</p></li><li><p>tunica intima→ endothelial layer- one cell thick</p></li></ul></li></ul>
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structure of arterioles

  • have muscular layer→ can contract to partially cut off blood flow to specific organs

  • lower proportion of elastic fibres and large number of muscle cells

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structure of veins

  • thinner tunica media due to lower blood pressure

  • larger lumen than in artery→ ensures blood returns to heart at adequate speed

  • have valves→ prevent backflow

<ul><li><p>thinner tunica media due to lower blood pressure</p></li><li><p>larger lumen than in artery→ ensures blood returns to heart at adequate speed</p></li><li><p>have valves→ prevent backflow</p></li></ul>
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structure of venules

  • connect capillaries to veins

  • few/ no elastic fibres and a large lumen

  • no need for muscular layer→ blood is at low pressure

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structure of capillaries

  • very small lumen→ blood travels slower so more diffusion can occur

  • large number of capillaries→ short diffusion distance

  • wall of capillary is one cell thick→ reduced diffusion distance

  • cells of walls have gaps→ allow blood plasma to leak out and form tissue fluid

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what is tissue fluid

  • a liquid that has substances dissolved in it→ similar to plasma but with fewer proteins

  • exchange of substances between cells and blood occurs via tissue fluid→ surrounds all cells of the body not in circulatory system

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hydrostatic pressure

  • pressure exerted by a fluid e.g. blood

  • e.g. blood pressure

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oncotic pressure

  • osmotic pressure exerted by plasma proteins within a blood vessel

  • lower WP within blood vessel→ water moves into vessel by osmosis

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tissue fluid formation

  • at arterial end of capillary:

    • hydrostatic pressure forces fluid out of capillary

    • proteins remain in blood→ too large

    • WP gradient created due to increased protein content

    • hydrostatic pressure>oncotic pressure→ water moves out of capillaries into tissue fluid

  • at venous end:

    • hydrostatic pressure reduced due to greater distance from heart

    • WP gradient stays same as at arterial end

    • osmotic pressure>HS pressure→ water flows back into capillary from tissue fluid

<ul><li><p>at arterial end of capillary:</p><ul><li><p>hydrostatic pressure forces fluid out of capillary</p></li><li><p>proteins remain in blood→ too large</p></li><li><p>WP gradient created due to increased protein content</p></li><li><p>hydrostatic pressure&gt;oncotic pressure→ water moves out of capillaries into tissue fluid</p></li></ul></li><li><p>at venous end:</p><ul><li><p>hydrostatic pressure reduced due to greater distance from heart</p></li><li><p>WP gradient stays same as at arterial end</p></li><li><p>osmotic pressure&gt;HS pressure→ water flows back into capillary from tissue fluid</p></li></ul></li></ul>
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formation of lymph

  • not all tissue fluid re-enters capillaries→ enters lymph vessels

  • vessels separate to circulatory system

  • larger molecules that can’t pass through capillary wall enter lymphatic system as lymph

  • liquid moves along larger vessels in system by compression caused by body movement→ backflow prevented by valves

  • lymph re-enters bloodstream through veins located close to the heart→ plasma proteins are returned to blood via lymph capillaries to maintain WP gradient

  • lipids transported from intestines to bloodstream by lymph system

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structure of the heart

  • divided into 4 chambers

  • left and right sides of the heart separated by septum

  • atria and ventricles separated by valves

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When are valves open/ closed?

What valves are found in the heart

  • open when BP behind is greater than BP in front of them

  • closed when BP in front of them is greater than BP behind them

  • RA and RV separated by tricuspid valve

  • RV and PA separated pulmonary valve

  • LA and LV separated by bicuspid valve

  • LV and aorta separated by aortic valve

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blood vessels going into and coming from heart

  • Pulmonary artery:

    • heart→ lungs

    • from right ventricle

  • Pulmonary vein:

    • lungs→ heart

    • into left atrium

  • Vena Cava:

    • body→ heart

    • to right atrium

  • Aorta:

    • heart→ body

    • from left ventricle

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coronary arteries

Arteries that provide blood to the heart for its own aerobic respiration for muscle contraction

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stages of the cardiac cycle

  • atrial systole

  • ventricular systole

  • diastole

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atrial systole

  1. atrial walls contract:

    • volume in atrium decreases, pressure increases

  2. atrial pressure rises→ AV valves open

  3. blood forced into ventricles

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ventricular systole

  1. walls of ventricles contract:

    • volume decreases, pressure increases

  2. pressure in ventricles rises above atrial pressure:

    • AV valves forced close

  3. pressure in ventricles rises above that in aorta and PA:

    • semilunar valves forces open→ blood forced into arteries

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diastole

  • atria and ventricles both relaxed

  • pressure in ventricles drop below that in arteries→ SL valves forced close

  • atria continue to fill with blood

  • pressure in atria rises above that in ventricles→ AV valves forced open

  • blood passively flows into ventricles

  • cycle begins again

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cardiac output

the volume of blood pumped by the heart per unit time

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factors affecting cardiac output

  • fitness→ fitter=higher cardiac output due to thicker ventricular muscles in the heart

  • exercise→ cardiac output increases during exercise

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heart rate

number of times a heart beats per minute

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stroke volume

volume of blood pumped out of left ventricle in one cardiac cycle

<p>volume of blood pumped out of left ventricle in one cardiac cycle</p>
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calculating cardiac output

cardiac output= heart rate*stroke volume

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myogenic

heart beats without external stimulus

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sinoatrial node

  • group of cells in right atrial wall

  • initiates wave of depolarisation→ causes atrial contraction

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myogenic contraction

  1. SAN creates wave of depolarisation→ causes atrial contraction

  2. Annulus Fibrosus→ non-conducting so prevents depolarisation spreading straight to ventricles

  3. depolarisation carried to atrioventricular node (AVN)→ conducting tissue between atria and ventricles

  4. After delay, AVN is stimulated→ stimulation passed along bundle of His (in septum):

    • delay= ventricles contract after atria

  5. bundle of His divides into two conducting fibres→ Purkyne tissue- carries wave of excitation along them

  6. Purkyne fibres spread around ventricles and initiate depolarisation of ventricles from bottom of heart→ causes ventricular contraction

<ol><li><p>SAN creates wave of depolarisation→ causes atrial contraction</p></li><li><p>Annulus Fibrosus→ non-conducting so prevents depolarisation spreading straight to ventricles</p></li><li><p>depolarisation carried to atrioventricular node (AVN)→ conducting tissue between atria and ventricles</p></li><li><p>After delay, AVN is stimulated→ stimulation passed along bundle of His (in septum):</p><ul><li><p>delay= ventricles contract after atria</p></li></ul></li><li><p>bundle of His divides into two conducting fibres→ Purkyne tissue- carries wave of excitation along them</p></li><li><p>Purkyne fibres spread around ventricles and initiate depolarisation of ventricles from bottom of heart→ causes ventricular contraction</p></li></ol>
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ECG

  • electrocardiogram

  • electrodes that detect electrical signals are placed on skin→ produce electrocardiogram

  • shows distinctive electrical waves produced by activity of heart

  • used to detect heart problems

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reading ECG traces

  • P wave:

    • depolarisation of atria, resulting in atrial systole

  • QRS complex:

    • depolarisation of ventricles, resulting in ventricular systole

    • largest→ ventricles have largest muscle mass

  • T wave:

    • repolarisation of ventricles→ ventricular diastole

  • U wave:

    • uncertainty→ repolarisation of Purkyne fibres?

<ul><li><p>P wave:</p><ul><li><p>depolarisation of atria, resulting in atrial systole</p></li></ul></li><li><p>QRS complex:</p><ul><li><p>depolarisation of ventricles, resulting in ventricular systole</p></li><li><p>largest→ ventricles have largest muscle mass</p></li></ul></li><li><p>T wave:</p><ul><li><p>repolarisation of ventricles→ ventricular diastole</p></li></ul></li><li><p>U wave:</p><ul><li><p>uncertainty→ repolarisation of Purkyne fibres?</p></li></ul></li></ul>
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tachycardia

  • heart beat too fast

  • peaks of ECG too close together

<ul><li><p>heart beat too fast</p></li><li><p>peaks of ECG too close together</p></li></ul>
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bradycardia

  • heart beat too slow

  • peaks of ECG too far apart

<ul><li><p>heart beat too slow</p></li><li><p>peaks of ECG too far apart</p></li></ul>
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ectopic heartbeat

  • early heartbeat followed by a pause

<ul><li><p>early heartbeat followed by a pause</p></li></ul>
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fibrillation

  • irregular heartbeat→ rhythm is lost

<ul><li><p>irregular heartbeat→ rhythm is lost</p></li></ul>
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role of haemoglobin

  • allows for transport of oxygen around body

  • each haemoglobin molecule contains 4 haem groups- each able to bond to one O2 molecule

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equation of fomation of oxyhaemoglobin

  • Oxygen + Haemoglobin Oxyhaemoglobin

  • 4O2 + Hb ⇌ Hb4O2

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cooperative binding

binding of first oxygen molecule results in conformational change in structure of haemoglobin molecule→ easier for each successive oxygen molecule to bind

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How is carbon dioxide transported around the body

  • dissolves directly in blood plasma

  • binds to haemoglobin→ forms carbaminohaemoglobin

  • most transported as hydrogen carbonate (HCO3-)

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formation of HCO3- ions

  1. CO2 diffuses into RBC from plasma

  2. In RBC, carbon dioxide combines with water to make carbonic acid:

    • CO2 + H2O  ⇌  H2CO3

    • carbonic anhydrase catalyses reaction

  3. Carbonic acid readily dissociates into H+ and HCO3- ions:

    • H2CO3⇌  HCO3 + H+

  4. H+ ions combine with haemoglobin→ forms haemoglobinic acid:

    • acts as a pH buffer

  5. Hydrogen carbonate ions diffuse out of RBC into plasma

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The chloride shift

  • movement of chloride ions into RBC→ occurs when hydrogencarbonate ions are formed

  • negatively charged hydrogencarbonate ions transported out of red blood cells

  • negatively charged chloride ions transported into RBC via transport proteins→ prevents electrical imbalance

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oxygen dissociation curves

shows rate at which oxygen associates and dissociates with haemoglobin at different partial pressures of oxygen

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partial pressure of oxygen

  • pressure exerted by oxygen within mixture of gases→ measure of oxygen concentration

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affinity for oxygen

  • ease with which haemoglobin binds and dissociates with oxygen

  • high affinity→ binds easily and dissociates slowly

  • low affinity→ binds slowly and dissociates easily

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explanation of oxygen dissociation curve

  • shallow gradient at start→ difficult for 1st oxygen molecule to bind

  • after first O2 molecule binds, protein changes shape→ easier for next oxygen molecule to bind ∴ steeper gradient in middle

  • levels off at end→ less remaining binding sites so longer for 4th oxygen molecule to bind

<ul><li><p>shallow gradient at start→ difficult for 1st oxygen molecule to bind</p></li><li><p>after first O<sub>2</sub> molecule binds, protein changes shape→ easier for next oxygen molecule to bind <span>∴ steeper gradient in middle</span></p></li><li><p>levels off at end→ less remaining binding sites so longer for 4th oxygen molecule to bind</p></li></ul>
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interpretation of oxygen dissociation curves

  • low pO2:

    • oxygen binds slowly to haemoglobin

    • low affinity for oxygen at low pO2

  • medium pO2:

    • oxygen binds more easily to haemoglobin

    • saturation increases quickly

    • small increase in pO2=large increase in haemoglobin saturation

  • high pO2

    • oxygen binds easily to haemoglobin→ can pick up oxygen and become saturated as blood passes through lungs

    • high affinity for O2 at high pO2

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foetal haemoglobin

  • higher affinity for oxygen than adult haemoglobin

  • allows foetus to obtain oxygen from mother’s blood:

    • foetal haemoglobin can bind at low pO2

    • at low pO2, mother’s haemoglobin is dissociating with oxygen

  • after birth, baby produces adult haemoglobin→ gradually replaces foetal haemoglobin:

    • important for release of oxygen in respiring tissue

<ul><li><p>higher affinity for oxygen than adult haemoglobin</p></li><li><p>allows foetus to obtain oxygen from mother’s blood:</p><ul><li><p>foetal haemoglobin can bind at low pO<sub>2</sub></p></li><li><p>at low pO<sub>2</sub>, mother’s haemoglobin is dissociating with oxygen</p></li></ul></li><li><p>after birth, baby produces adult haemoglobin→ gradually replaces foetal haemoglobin:</p><ul><li><p>important for release of oxygen in respiring tissue</p></li></ul></li></ul>
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types of haemoglobin

  • haem groups same

  • globin chains can differ between species→ determine precise properties of haemoglobin

  • can bind to oxygen in different conditions→ adaptations

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effects of altitude on haemoglobin

  • pO2 is lower at higher altitudes

  • haemoglobin adapted to conditions→ binds more readily