Mass transport in animals
Haemoglobin is a globular protein with quaternary structure: four polypeptide chains, two alpha and two beta in adult humans, each folded into its own tertiary structure and each holding one haem group containing an iron ion. Quaternary structure means more than one polypeptide chain, held together by interactions between the chains such as hydrogen bonds, ionic bonds and hydrophobic interactions. Because each haem group binds one oxygen molecule, one haemoglobin molecule carries four oxygen molecules, and the product is called oxyhaemoglobin. The plural in the haemoglobins matters: the same basic architecture appears across many organisms and at different life stages, but the primary structure of the globin chains differs. A different amino acid sequence gives a different tertiary and quaternary structure, and so a different affinity for oxygen.
Subtopics in this area
Mass transport in animals Revision Guide
Learning Objectives
What you need to know and understand
- State what makes a protein quaternary and name the bonds holding the four chains of haemoglobin together.
- Explain how a change in the amino acid sequence of a globin chain can alter the molecule's affinity for oxygen.
- Deduce the maximum number of oxygen molecules that a stated number of haemoglobin molecules can carry.
- Explain two features of a mature mammalian red blood cell that increase the rate at which it takes up oxygen.
- Suggest which molecule a red blood cell stain binds to, and explain why a DNA stain fails to show mammalian red blood cells.
- Describe where oxygen is loaded and where it is unloaded, naming the partial pressure of oxygen conditions in each place.
- Read percentage saturation at a stated partial pressure of oxygen, then calculate both the fall in percentage saturation between lungs and tissues and what fraction of the oxygen carried that fall represents.
- Explain why the steep region of the curve is the one that matters most to a respiring tissue.
- Describe how oxygen is transported bound to haemoglobin in the blood.
- Sketch a curve of higher or lower affinity relative to a given curve, keeping its start and maximum unchanged.
- Explain the shallow, steep and plateau regions of the dissociation curve in terms of cooperative binding and saturation.
- Describe how binding of the first oxygen molecule changes the tertiary and quaternary structure of haemoglobin and increases affinity for subsequent binding events.
- Apply cooperative binding to explain why unloading in a respiring tissue is rapid once it has started.
- Explain how a rise in carbon dioxide concentration lowers the affinity of haemoglobin for oxygen.
- Identify a Bohr-shifted curve on a graph, state the direction of the shift and say what it means for unloading.
- Use the Bohr effect to explain why exercising muscle receives more oxygen than resting muscle at the same partial pressure of oxygen.
- Deduce, from two curves drawn on the same axes, which haemoglobin has the higher affinity for oxygen.
- Suggest the environment or activity level of an unfamiliar organism from the position of its dissociation curve.
- Explain why fetal haemoglobin must have a higher affinity for oxygen than adult haemoglobin.
- Trace a red blood cell through both circuits of a mammal, naming the chambers and vessels in order.
- Explain the advantage of a double circulation to an organism with a high metabolic rate.
- Describe the general pattern of blood circulation in a mammal, including the route taken and the separation of oxygenated and deoxygenated blood.
- Label the vena cava, pulmonary artery, pulmonary vein and aorta on a heart diagram and state which carry oxygenated blood.
- Name the vessels entering and leaving a kidney and give the direction of flow in each.
- Explain how blockage of a coronary artery affects respiration in cardiac muscle.
- Label the chambers, valves, vena cava, pulmonary vein, aorta and pulmonary artery on a diagram of the heart.
- Explain why the wall of the left ventricle is thicker than that of the right in terms of the pressure each generates.
- Describe the position and function of the atrioventricular and semilunar valves.
- Identify from a pressure against time graph when each valve opens and closes, giving the pressure reason in each case.
- Describe the three stages of the cardiac cycle in terms of chamber contraction, pressure and volume.
- Calculate heart rate in beats per minute from the duration of one cardiac cycle read from a graph.
- Explain how elastic tissue in an artery wall maintains blood pressure between heartbeats.
- Compare an artery with a vein, linking each structural difference to the pressure of the blood it carries.
- Explain how contraction of smooth muscle in arterioles changes the distribution of blood between organs.
- Describe how tissue fluid is formed at the arteriole end of a capillary and how most of it returns at the venule end.
- Explain, in terms of water potential, why a low plasma protein concentration causes tissues to swell.
- Explain two features of a capillary bed that increase the rate of exchange between blood and cells.
- Interpret pressure and volume changes during the cardiac cycle to identify valve movements and calculate heart rate.
- Analyse data on cardiovascular disease incidence to distinguish between correlation and causation.
- Evaluate conflicting evidence regarding risk factors by comparing study methodologies and standard deviations.
- Describe a safe method for dissecting a named gas exchange or mass transport organ, justifying precautions.
- Produce a labelled biological drawing following conventions of continuous lines and proportion.
- Calculate the actual size of a structure from a measured image size and a stated magnification.
Marking Points
Key points examiners look for in your answers
- Quaternary structure means more than one polypeptide chain, held together by bonds or interactions between the chains, such as hydrogen bonds, ionic bonds and hydrophobic interactions.
- Four polypeptide chains, each carrying a haem group containing an iron ion, so one haemoglobin molecule binds four oxygen molecules.
- Name the product formed when oxygen binds as oxyhaemoglobin.
- State that a different amino acid sequence gives a different tertiary and quaternary structure.
- Link that structural difference to a different affinity for oxygen, e.g. in organisms living at different oxygen concentrations.
- Deduce the number of oxygen molecules carried from a stated number of haemoglobin molecules, using four oxygen molecules per haemoglobin.
- A mature mammalian red blood cell has no nucleus and no other organelles, leaving more space for haemoglobin; a DNA-binding stain therefore fails to show it, whereas a stain binding haemoglobin does.
- The biconcave shape gives a large surface area to volume ratio, so oxygen diffuses in and out rapidly; the small, flexible cell also passes through capillaries in single file, keeping the diffusion distance short.
- In the lungs the partial pressure of oxygen is high, so haemoglobin associates with, or loads, oxygen to form oxyhaemoglobin.
- In respiring tissues the partial pressure of oxygen is low, so oxyhaemoglobin dissociates and unloads its oxygen.
- Answers should link each structural feature to the rate of oxygen uptake or release, rather than merely listing features; for example, no nucleus means more haemoglobin per cell, so more oxygen can be carried per cell.
- Credit depends on the wording of the actual question; the points above are teaching guidance, not an official question-specific mark scheme.
- Reading the correct percentage saturation from the graph at a stated partial pressure of oxygen.
- Stating that haemoglobin has a high affinity for oxygen at the high partial pressure found in the lungs, so it loads oxygen there.
- Stating that oxygen is transported bound to haemoglobin in the blood from the lungs to respiring tissues.
- Explaining that the low partial pressure of oxygen in respiring tissues causes dissociation and unloading.
- Sketching a shifted curve that maintains the sigmoid shape, starts at the origin, and finishes at the same maximum percentage saturation if only affinity has changed.
- Quoting figures from the graph with the correct unit when comparing loading and unloading.
- Stating that the first oxygen molecule binding causes a change in the tertiary or quaternary structure of haemoglobin.
- Explaining that this conformational change increases the affinity of the remaining haem groups, making further oxygen bind more easily.
- Linking this increased affinity to the steep middle section of the dissociation curve.
- Explaining the plateau at high partial pressures as the point where most binding sites are occupied and haemoglobin approaches full saturation.
- Applying the cooperative principle in reverse to explain rapid unloading of oxygen in respiring tissues.
- one mark for a higher concentration or partial pressure of carbon dioxide in respiring tissues
- one mark for carbon dioxide leading to the formation of carbonic acid, which releases hydrogen ions and lowers the pH inside the red blood cell
- one mark for the hydrogen ions changing the shape of haemoglobin and so reducing its affinity for oxygen
- one mark for the dissociation curve shifting to the right, so haemoglobin is less saturated at the same partial pressure of oxygen
- one mark for linking the increased unloading to a greater supply of oxygen for aerobic respiration in an active tissue
- one mark for reading from the graph that one haemoglobin is more saturated than another at the same partial pressure of oxygen
- one mark for stating that the curve further to the left shows the higher affinity for oxygen
- one mark for linking a high affinity to loading oxygen where the partial pressure of oxygen is low
- one mark for linking a low affinity, or a right-shifted curve, to readier unloading in tissues with a high rate of respiration
- one mark for relating the difference between the two haemoglobins to a different amino acid sequence and so a different tertiary or quaternary structure
- A mammal has four chambers: two atria and two ventricles.
- Blood passes through the heart twice for every complete circuit of the body, defining the double circulation.
- Blood returns to the heart after being oxygenated, restoring its pressure before it is pumped to the systemic circuit.
- The right side of the heart pumps deoxygenated blood to the lungs via the pulmonary artery, while the left side pumps oxygenated blood to the body via the aorta.
- Oxygenated and deoxygenated blood are kept separate by the septum.
- Name the major vessels in sequence: vena cava → right atrium → right ventricle → pulmonary artery → lungs → pulmonary vein → left atrium → left ventricle → aorta → body.
- one mark for each vessel named on a labelled diagram: vena cava into the right atrium, aorta out of the left ventricle, renal artery into the kidney and renal vein out of it
- one mark for stating that the pulmonary artery carries deoxygenated blood and the pulmonary vein carries oxygenated blood
- one mark for naming the coronary arteries as the vessels supplying the heart muscle itself
- one mark for describing the consequence of a blocked coronary artery in terms of oxygen supply to cardiac muscle
- one mark for applying the direction rule, arteries away from the heart and veins towards it
- Identifies the vena cava and pulmonary vein as the major vessels returning blood to the right and left atria respectively.
- Explains that the left ventricle has a thicker muscular wall than the right ventricle to generate higher pressure for systemic circulation.
- States that the septum prevents oxygenated and deoxygenated blood from mixing.
- Describes the position of atrioventricular valves (between atria and ventricles) and semilunar valves (at the base of the aorta and pulmonary artery), and states their function in preventing backflow.
- Identifies coronary arteries as the vessels supplying oxygenated blood to cardiac muscle tissue.
- one mark for stating that a valve opens when the pressure behind it is greater than the pressure in front of it
- one mark for identifying the point where two pressure curves cross as a named valve opening or closing
- one mark for linking contraction of a chamber to a decrease in its volume and an increase in its pressure
- one mark for explaining that the closed atrioventricular valves during ventricular systole prevent backflow into the atria
- one mark for calculating heart rate in beats per minute from the duration of one cycle read from the graph
- one mark for a thick artery wall containing elastic tissue enabling the vessel to withstand and maintain high pressure
- one mark for elastic recoil of the artery wall smoothing out the pulse and maintaining flow during diastole
- one mark for smooth muscle in arterioles contracting to narrow the lumen and redirect blood flow
- one mark for a vein having a wide lumen and valves to prevent backflow of low pressure blood
- one mark for a vein having a thin wall with little elastic tissue because the blood it carries is at low pressure
- one mark for high hydrostatic pressure at the arteriole end forcing water and small solutes out of the capillary
- one mark for plasma proteins remaining in the capillary, so the water potential of the blood is lower than that of the tissue fluid
- one mark for water returning at the venule end by osmosis down a water potential gradient
- one mark for excess tissue fluid draining into the lymphatic system and returning to the blood
- one mark for explaining that a fall in plasma protein raises the water potential of the blood, so less water returns by osmosis and tissue fluid accumulates
- Quote figures with units from the data to support statements about pressure, volume, or CVD incidence.
- State that non-overlapping standard deviation bars suggest a difference is unlikely to be due to chance, but note that a statistical test is needed to confirm significance.
- Identify a named variable as a risk factor rather than a definitive cause when only a correlation is shown.
- Evaluate conflicting evidence by identifying limitations, such as small sample sizes, lack of control groups, or differing methodologies between studies.
- Calculate heart rate using the duration of one cardiac cycle from a pressure or volume trace (e.g., 60 / cycle duration in seconds).
- State a named safety or hygiene precaution with a valid reason, such as cutting away from the body to prevent injury.
- Identify the left side of a mammalian heart by locating the thicker muscular wall of the left ventricle.
- Produce a biological drawing using continuous, unshaded lines with structures drawn in correct proportion.
- Draw straight, non-crossing label lines without arrowheads.
- Calculate actual size using the formula: actual size = image size / magnification, providing appropriate units.
Examiner Tips
Expert advice for maximising your marks
- 💡Define quaternary structure as more than one polypeptide chain, and name a type of bond or interaction holding the chains together.
- 💡Write haemoglobin and oxyhaemoglobin in full rather than relying on the abbreviation Hb.
- 💡For questions about chemically similar haemoglobins, compare primary structures first, then explain the consequence for oxygen affinity.
- 💡Use loads or associates and unloads or dissociates; these are the terms generally credited.
- 💡Tie every statement to the partial pressure of oxygen rather than to how much oxygen there is.
- 💡In a comparison with fish blood, the presence of a nucleus is a feature examiners commonly look for, but check what the question actually asks.
- 💡Quote two figures with units from the graph; a described trend rarely earns full marks on a data question.
- 💡Use 'affinity for oxygen' when discussing the position of the curve and 'percentage saturation' for values on the y-axis.
- 💡When asked to sketch a shifted curve for a change in affinity, keep the origin the same, move the middle section, and maintain the original maximum saturation.
- 💡The key phrase examiners look for is that the change in shape of haemoglobin makes the binding of further oxygen easier.
- 💡Match each part of your explanation to a specific region of the curve: shallow start, steep middle, and the saturation plateau.
- 💡While you can name 'positive cooperativity', you must explicitly describe the change in tertiary or quaternary structure to secure the marks.
- 💡Answer in a fixed order: carbon dioxide, hydrogen ions, shape, affinity, curve to the right, more unloading.
- 💡If asked to compare exercising and resting muscle, quote saturations from both curves at the same partial pressure of oxygen.
- 💡The AQA specification does not require the names carbonic anhydrase or carbonic acid, so do not rely on naming the enzyme to gain credit; describe the reaction and the hydrogen ions instead.
- 💡Decide first whether the organism has a loading problem or an unloading problem; the direction of the shift follows from that.
- 💡Support the statement with a pair of saturations read at one partial pressure of oxygen.
- 💡In suggest questions any sensible argument consistent with the curve you were given is credited, so commit to one.
- 💡In a comparison table, every row must state both sides of the same difference; unlinked statements score nothing.
- 💡The pressure mark is about blood reaching the body capillaries, so explicitly state that pressure is restored at the heart before entering the systemic circuit.
- 💡When asked to trace the circulation, name the chambers and major vessels in order: vena cava → right atrium → right ventricle → pulmonary artery → lungs → pulmonary vein → left atrium → left ventricle → aorta → body.
- 💡Learn the four heart vessels as two in and two out, then add the renal and coronary vessels.
- 💡On an unlabelled heart, find the thick-walled left ventricle first and work outwards from there.
- 💡Spell vessel names accurately; a vague answer is ignored but a named wrong vessel loses the mark outright.
- 💡When explaining ventricle wall thickness, always explicitly use the word 'pressure' rather than just saying it pumps blood 'further'.
- 💡Note that the right ventricle pumps at a lower pressure to protect the delicate pulmonary capillaries, not to slow blood flow for gas exchange.
- 💡Label the three curves on a cardiac cycle graph before answering anything: atrium, ventricle, aorta.
- 💡Every valve answer needs the words pressure greater than; the valve shuts to stop backflow is only half an answer.
- 💡To find heart rate, read the length of one full cycle in seconds and work out sixty divided by that value.
- 💡Write every point as structure, then because, then function, in one sentence.
- 💡Use the word lumen, and say relative to the wall thickness when you compare vessels.
- 💡Remember it is the arterioles, not the arteries, that control the distribution of blood between organs.
- 💡Answer in a fixed order: hydrostatic pressure out, water potential and osmosis in, lymph for the remainder.
- 💡When explaining osmosis, state the direction of the water potential gradient explicitly; equivalent wording is normally accepted unless a question-specific scheme says otherwise.
- 💡For swelling of tissues, state the direction of the change in water potential before the direction of water movement.
- 💡Answer evaluation questions systematically: state what the data show using figures, what they do not show, and what further information (like a statistical test) is needed.
- 💡When identifying valve events on a graph, look for the exact points where pressure curves cross; this is where valves open or close, triggering volume changes.
- 💡Always link a safety precaution to its specific reason when describing dissection methods.
- 💡Practise rearranging the magnification equation and ensure you state the units clearly in your final answer.
Common Mistakes
Pitfalls to avoid in your exam answers
- Describing quaternary structure as the three-dimensional shape. Correction: that is tertiary structure; quaternary means more than one polypeptide chain.
- Writing that haemoglobin carries four oxygen atoms. Correction: it carries four oxygen molecules, one per haem group.
- Saying oxygen binds to the polypeptide chain. Correction: oxygen binds to the haem group and its iron ion.
- Calling oxygen binding a permanent chemical change. Correction: it is reversible binding, forming oxyhaemoglobin.
- Listing disulfide bridges as the main interactions holding haemoglobin subunits together. Correction: the subunits are held mainly by hydrophobic interactions, hydrogen bonds and ionic bonds.
- Saying red blood cells have no organelles at all and then referring to their mitochondria; mature mammalian red blood cells lack mitochondria and respire anaerobically.
- Assuming every red blood cell lacks a nucleus; fish and other non-mammalian red blood cells have one.
- Saying haemoglobin carries oxygen to cells and gives them energy; haemoglobin transports oxygen, and cells release energy by respiration.
- Confusing loading with unloading, so dissociation is described as happening in the lungs; loading occurs in the lungs and unloading in respiring tissues.
- Writing Hb without first giving the full name, which risks the abbreviation not being credited.
- Reading the y-axis as oxygen concentration rather than percentage saturation of haemoglobin.
- Treating the x-axis as oxygen concentration instead of partial pressure (pO₂), often omitting the kPa unit.
- Drawing a shifted curve that finishes below the original maximum saturation when only affinity has changed; the maximum should remain the same.
- Stating that haemoglobin loads more oxygen at low partial pressures; it actually has a lower affinity and unloads oxygen.
- Stating that affinity rises simply because there is more oxygen present, failing to mention the conformational shape change of the protein.
- Claiming all four oxygen molecules bind simultaneously rather than sequentially.
- Describing the haem group itself changing shape rather than the tertiary and quaternary structure of the whole protein.
- Explaining the plateau by stating the lungs run out of oxygen or that the final binding site is 'hard to find', rather than the sites simply becoming saturated.
- Using cooperative binding to explain the Bohr shift, which is a different mechanism.
- saying carbon dioxide takes the place of oxygen on the haem group; carbon dioxide lowers affinity indirectly through hydrogen ions, it does not compete for the haem group
- shifting the curve to the left instead of the right, or moving the axes instead of the curve; a right shift means less saturation at the same partial pressure of oxygen
- writing that the Bohr effect changes how much oxygen the blood contains rather than how readily haemoglobin releases it; it changes the affinity and so the unloading, not the total oxygen carried
- leaving pH out entirely and saying carbon dioxide changes affinity directly; the hydrogen ions and the pH change are the link
- claiming the Bohr effect operates in the lungs rather than in respiring tissues; in the lungs carbon dioxide is lost and affinity rises again
- saying an organism in low oxygen needs haemoglobin that carries more oxygen, rather than one with a higher affinity
- reversing left and right when describing affinity
- describing fetal haemoglobin as stronger instead of as having a higher affinity than maternal haemoglobin
- arguing entirely from the organism's habitat without quoting a value from the graph
- saying different species have different haem groups, when it is the globin chains that differ
- Writing double circulation without saying that blood passes through the heart twice per circuit. Correction: the definition needs the twice-per-circuit idea.
- Confusing the simultaneous contraction of the ventricles with the overall flow of blood. Correction: blood flows through the pulmonary and systemic circuits in series (one after the other), even though the two ventricles pump simultaneously.
- Assuming the pulmonary artery carries oxygenated blood because arteries usually do. Correction: the pulmonary artery carries deoxygenated blood to the lungs.
- Omitting the names of major vessels when tracing the circulation. Correction: include vena cava, pulmonary artery, pulmonary vein and aorta in the correct sequence.
- generalising that all arteries carry oxygenated blood and so mislabelling the pulmonary artery
- answering simply an artery, when a named vessel is required and a named incorrect vessel is rejected outright
- confusing the renal artery with the renal vein on an unlabelled diagram
- describing the coronary arteries as the vessels carrying blood out of the heart to the body
- learning long lists of vessels this specification does not require, and still not knowing the required seven: vena cava, pulmonary artery, pulmonary vein, aorta, renal artery, renal vein and the coronary arteries
- Labelling the heart from the reader's viewpoint. Correction: label left and right from the heart's perspective, so the diagram's right is the heart's left.
- Stating the left ventricle is larger because it holds more blood. Correction: it has a thicker muscular wall to generate higher pressure, but holds approximately the same volume as the right ventricle.
- Confusing the major vessels. Correction: the vena cava and pulmonary vein bring blood into the atria, while the aorta and pulmonary artery take blood out of the ventricles.
- Stating that lower right ventricular pressure ensures blood flows slowly enough for gas exchange. Correction: lower pulmonary pressure mainly protects delicate capillaries; gas exchange depends on surface area, a thin diffusion barrier and partial-pressure gradients.
- saying valves open and close by themselves, or that muscles open them; valves are passive and respond to pressure differences
- naming the wrong valve because the atrial, ventricular and aortic curves were never identified first; label the curves before answering
- describing ventricular systole as the stage when blood flows into the ventricle; blood enters the ventricle during diastole and atrial systole, and leaves during ventricular systole
- giving heart rate in beats per second, or dividing by the wrong time value when converting; read one full cycle in seconds and use 60 divided by that value
- claiming ventricular pressure is always higher than atrial pressure; during diastole and atrial systole atrial pressure exceeds ventricular pressure, which is why the atrioventricular valves open
- writing thick muscular walls for arteries when the mark is for elastic tissue and pressure
- saying veins have valves because blood moves slowly, without mentioning backflow or low pressure
- confusing the lumen with the wall, so a vein is described as having a narrow lumen
- claiming arteries contain valves, or that arterioles contain no muscle
- listing a structure with no function attached, which scores nothing in an in relation to their function question
- reversing the mechanism, so tissue fluid is said to form by osmosis and return by hydrostatic pressure
- saying red blood cells and plasma proteins leave the capillary to form tissue fluid
- saying water potential becomes more or less without saying higher or lower, so the direction of the gradient is unclear
- leaving out the lymphatic system, so the fluid that leaves the capillary has nowhere to go
- using the abbreviation WP without defining it; write water potential in full or use the symbol
- Concluding that a risk factor causes a disease when data only show a correlation. Correction: State that the data show a correlation and suggest another variable might be responsible unless a causal mechanism is proven.
- Ignoring volume changes and focusing only on pressure during the cardiac cycle. Correction: Track both; remember that ventricular volume falls rapidly when the semilunar valves open.
- Stating a difference is significant based only on standard deviation bars. Correction: Standard deviation bars indicate spread; non-overlap suggests a difference is unlikely to be due to chance, but a statistical test is required to claim significance.
- Dismissing conflicting evidence simply because studies are different. Correction: Specify exactly why studies conflict, such as differences in sample demographics, study duration, or uncontrolled variables.
- Shading or using short sketchy strokes; Correction: always use single, continuous, unbroken lines for biological drawings.
- Assuming actual size must always be converted to micrometres; Correction: retain the unit you measured in (e.g., millimetres) unless the question specifically requests a conversion.
- Drawing label lines that cross each other or end in arrowheads; Correction: use a ruler to draw straight label lines that stop exactly at the structure without crossing or using arrows.
- Stating a safety precaution without a justification; Correction: always pair a precaution with its specific biological or safety reason (e.g., wash hands to remove pathogens).