2 Structure and functions in living organisms
- Syllabus
- 2024
- Section
- 2
- Level
- —
Organisation in a multicellular organism forms a hierarchy: specialised parts combine into progressively larger units that coordinate a shared function.
| Level | Meaning | Example in one animal hierarchy |
|---|---|---|
| organelle | a structure within a cell that performs a particular function | a mitochondrion in a muscle cell |
| cell | the living unit that contains organelles | a cardiac muscle cell |
| tissue | a group of similar cells working together for a function | cardiac muscle tissue |
| organ | different tissues working together for a particular function | the heart |
| organ system | several organs working together for a major body function | the circulatory system |
The direction is: organelle ightarrow cell ightarrow tissue ightarrow organ ightarrow organ system. At each step, the smaller level becomes a component of the next; the heart, for example, contains muscle tissue but also other tissues that let the organ work as a whole.
A tissue is not simply any collection of cells: its similar cells cooperate in a function. An organ contains more than one tissue type, whereas an organ system contains multiple organs. Do not include the whole organism as one of the five levels required by this objective.
A cell contains distinct structures that can be described by their position, boundary and appearance before their functions are considered.
| Structure | Description |
|---|---|
| nucleus | a compartment in the cytoplasm that contains chromosomes |
| cytoplasm | the material filling the inside of the cell |
| cell membrane | a thin boundary enclosing the cytoplasm |
| cell wall | a rigid layer outside the cell membrane in plant cells |
| mitochondria | small structures distributed through the cytoplasm |
| chloroplasts | chlorophyll-containing structures in photosynthetic plant cells |
| ribosomes | very small structures in the cytoplasm |
| vacuole | a fluid-filled space; mature plant cells usually have a large central vacuole containing cell sap |
The cell wall and cell membrane are separate layers: the wall lies outside the membrane. Ribosomes are much smaller than nuclei, chloroplasts and mitochondria, so a simple light-microscope drawing may not show every structure.
Do not infer that every plant cell contains chloroplasts: only photosynthetic plant cells require them. A vacuole is a space within the cell, whereas cytoplasm surrounds the cell structures.
Each cell structure has a specific job, and the abundance of a structure reflects how strongly the cell depends on that job.
| Structure | Function |
|---|---|
| nucleus | contains genetic material and controls cell activities |
| cytoplasm | site of many metabolic reactions |
| cell membrane | controls movement of substances into and out of the cell |
| cell wall | supports the cell and helps maintain its shape |
| mitochondria | site of aerobic respiration, which releases energy for cell activities |
| chloroplasts | absorb light using chlorophyll and carry out photosynthesis |
| ribosomes | site of protein synthesis |
| vacuole | contains cell sap and helps support a plant cell when full |
A cell with a high energy demand often contains many mitochondria. A palisade cell exposed to light contains many chloroplasts, while a root cell underground usually contains none because it does not photosynthesise.
Mitochondria release energy by respiration; they do not create energy. Ribosomes are the site of protein synthesis, while the nucleus supplies genetic instructions rather than assembling proteins itself.
Plant and animal cells share the core structures needed for cellular control and metabolism, while plant cells have additional structures for support and photosynthesis.
| Structure | Plant cell | Animal cell |
|---|---|---|
| nucleus | present | present |
| cytoplasm | present | present |
| cell membrane | present | present |
| mitochondria | present | present |
| ribosomes | present | present |
| cellulose cell wall | present | absent |
| chloroplasts | present in photosynthetic cells | absent |
| large permanent vacuole containing cell sap | usually present | absent |
The rigid wall and large vacuole often give a plant cell a more regular outline. An animal cell has only a membrane at its outer boundary, so its outline can be less regular.
Cell shape alone is not enough for identification. Use the combination of wall, chloroplasts and large permanent vacuole, and remember that a non-photosynthetic plant cell may lack chloroplasts but still has a cellulose wall.
Differentiation is the process by which an unspecialised cell develops the structures and abilities needed for a particular function.
An unspecialised cell divides, then daughter cells can differentiate into specialised types. Their structures become suited to different jobs; groups of specialised cells can therefore form tissues and organs with a division of labour.
| Without differentiation | With differentiation |
|---|---|
| cells remain similar and cannot perform the full range of body functions efficiently | different cell types perform particular jobs efficiently |
| complex tissues and organs cannot develop normally | specialised cells combine into working tissues and organs |
A stem cell is unspecialised and can continue to divide. If it differentiates into a red blood cell, it develops a specialised role in oxygen transport; if it differentiates into a muscle cell, it develops the ability to contract.
Differentiation is not ordinary growth: a cell changes what it is specialised to do, rather than merely becoming larger. Most specialised animal cells have a more limited range of possible future cell types than stem cells.
Stem cells can divide repeatedly and differentiate, so medicine can use them to replace damaged or missing specialised cells.
| Potential advantage | Corresponding disadvantage or condition |
|---|---|
| can produce specialised cells to repair damaged tissue | differentiation must be controlled so the required cell type forms |
| repeated division can supply many replacement cells | uncontrolled division may form a tumour |
| a patient's own cells are genetically matched, reducing immune rejection | donor cells may be rejected and may require immunosuppressant treatment |
| donor or embryonic cells may provide options when a patient's cells are unsuitable | transplanted material can carry infection; using embryonic cells raises ethical objections for some people |
For a damaged heart, stem cells may divide and differentiate into replacement muscle cells. Bone-marrow stem cells can form blood-cell types and may therefore help treat some blood conditions.
A justified medical decision weighs likely benefit against tumour, rejection, infection and ethical risks for the particular cell source. A possible treatment is not automatically safe or effective simply because stem cells can differentiate.
Carbohydrates, proteins and lipids are carbon-based biological molecules, but their usual elemental compositions are not identical.
| Molecule group | Elements present | Symbols |
|---|---|---|
| carbohydrate | carbon, hydrogen and oxygen | C, H, O |
| lipid (fat or oil) | carbon, hydrogen and oxygen | C, H, O |
| protein | carbon, hydrogen, oxygen and nitrogen | C, H, O, N |
Carbon, hydrogen and oxygen occur in all three groups. Nitrogen is the distinguishing element in the syllabus comparison because proteins are built from amino acids.
Do not infer the molecule group from carbon alone. Carbohydrates and lipids contain the same three named elements, so their structure—not a different element list—distinguishes them.
Large biological molecules are assembled from smaller basic units; the type and arrangement of those units determine the molecule group.
| Large molecule | Smaller basic unit or units |
|---|---|
| starch | many simple sugar units |
| glycogen | many simple sugar units |
| protein | amino acids |
| lipid | fatty acids and glycerol |
Starch and glycogen are both large carbohydrate molecules made from simple sugars, but they are different storage molecules. A protein uses amino acids rather than sugars; a lipid combines glycerol with fatty acids.
A lipid is not described here as a chain of only one repeating unit: it requires both glycerol and fatty acids. Do not confuse a molecule's building units with the chemical elements inside those units.
A food test is valid only when the reagent, treatment and positive colour change are matched to the molecule being detected.
| Molecule | Method | Positive result |
|---|---|---|
| glucose | add Benedict's solution and heat in a hot-water bath | blue changes through green, yellow or orange to brick-red |
| starch | add iodine solution | orange-brown changes to blue-black |
| protein | add Biuret reagent | blue changes to lilac or purple |
| lipid (fat) | shake with ethanol, then add water | a cloudy white emulsion forms |
Crush a solid sample and mix it with water when an extract is needed. Use comparable sample and reagent volumes when comparing foods, and include known positive and negative samples if the test must be checked.
Wear eye protection. Heat Benedict's tubes in a water bath rather than directly in a flame; ethanol is flammable, so keep it away from ignition sources. A negative result means the test did not detect the molecule, not that the food contains nothing else.
An enzyme is a biological catalyst: it increases the rate of a metabolic reaction without being used up by that reaction.
A substrate with a complementary shape binds to the enzyme's active site, forming an enzyme–substrate complex. The reaction occurs, products leave, and the unchanged enzyme can catalyse another reaction.
ext{enzyme}+ ext{substrate}
ightarrow ext{enzyme–substrate complex}
ightarrow ext{enzyme}+ ext{products}
Metabolism means the chemical reactions occurring in cells or organisms. Enzymes make these reactions fast enough under cellular conditions, and active-site shape gives each enzyme specificity for particular substrate shapes.
An enzyme changes reaction rate, not the final products, and it is not consumed as a reactant. A substrate must fit the active site; merely colliding with any enzyme is insufficient.
Enzyme activity usually rises with temperature to an optimum, then falls sharply when higher temperature changes the active site.
| Temperature region | Molecular explanation | Effect on rate |
|---|---|---|
| below optimum | enzyme and substrate have less kinetic energy, so successful collisions and complexes form less often | rate is lower but rises as temperature increases |
| at optimum | active sites retain their shape and successful complex formation is most frequent | maximum rate |
| above optimum | bonds maintaining enzyme shape are disrupted; the active site changes shape | substrate fits less well or not at all, so rate falls |
When the active site changes permanently enough that the substrate is no longer complementary, the enzyme is denatured. The reaction may stop even though substrate remains.
Low temperature does not usually denature an enzyme; it slows molecular movement and is often reversible on warming. Do not say the enzyme itself is killed—enzymes are molecules, not living organisms.
To test temperature fairly, change only temperature and measure enzyme activity with a repeatable endpoint or rate.
| Step | Action |
|---|---|
| 1 | prepare water baths across a suitable temperature range |
| 2 | keep enzyme and substrate volumes and concentrations, pH and total volume constant |
| 3 | equilibrate enzyme and substrate separately at each temperature, then mix and start timing |
| 4 | for amylase and starch, sample at fixed intervals onto iodine until iodine remains orange-brown |
| 5 | repeat each temperature, calculate a mean time and compare rate using 1/exttime |
Use smaller temperature intervals around the fastest result to estimate the optimum more accurately. A shorter endpoint time means a faster reaction, so time itself is inversely related to rate.
Use water baths and eye protection. Equilibrating before mixing prevents the reaction starting at an unintended temperature; a single reading cannot reveal random variation, so repeats are required.
Each enzyme has an optimum pH at which its active site has the most effective shape for binding its substrate.
Changing pH changes the chemical conditions around the enzyme. Away from the optimum, bonds maintaining its three-dimensional shape can be disrupted, altering the active site so fewer enzyme–substrate complexes form.
| Condition | Active site and rate |
|---|---|
| optimum pH | substrate is complementary; complex formation and rate are greatest |
| moderately away from optimum | fewer successful complexes form; rate decreases |
| sufficiently extreme pH | active site may change so much that the enzyme is denatured |
Optimum pH is enzyme-specific; it is not always neutral. pH changes enzyme activity by altering the active site, not by changing the amount of substrate present.
A pH investigation uses buffer solutions to set different pH values while every other factor affecting enzyme rate is controlled.
| Step | Action |
|---|---|
| 1 | prepare labelled tubes containing buffers across a suitable pH range |
| 2 | add equal volumes and concentrations of amylase and starch; keep temperature constant in a water bath |
| 3 | mix one pH treatment, start timing and sample at fixed intervals onto iodine |
| 4 | record the time when iodine stays orange-brown, showing no starch is detected |
| 5 | repeat each pH, calculate mean time and compare rate using 1/exttime |
Independent variable: buffer pH. Dependent variable: time to the starch endpoint or calculated rate. Controls include temperature, enzyme and substrate concentration and volume, total volume, sampling interval and iodine volume.
Use a buffer rather than an unmeasured amount of acid or alkali so pH is known and stable. Test smaller pH intervals around the fastest result before claiming an optimum, and wear eye protection when handling reagents.
Cells exchange substances with their surroundings by diffusion, osmosis and active transport. The three processes differ in what moves, its direction and whether cellular energy is required.
| Process | What moves | Direction | Membrane and energy |
|---|---|---|---|
| diffusion | particles of a substance | net movement from higher to lower concentration | no energy from respiration; a membrane is not essential |
| osmosis | water molecules only | from higher water potential (more dilute) to lower water potential (more concentrated) | through a partially permeable membrane; no energy from respiration |
| active transport | dissolved ions or other solutes | from lower to higher concentration, against the concentration gradient | across a living cell membrane using carrier proteins and energy from respiration |
Mineral ions can enter root hair cells by active transport when their concentration is lower in the soil than in the cell. Water can then move across partially permeable membranes by osmosis, while gases such as oxygen and carbon dioxide commonly move down concentration gradients by diffusion.
Osmosis is the movement of water, not solute. Active transport can move a substance against its gradient because it uses energy; diffusion and osmosis are passive. At equilibrium particles still move randomly, but there is no net movement in either direction.
The rate of movement into or out of cells depends on how much exchange surface is available and how quickly particles can cross it.
| Change | Effect on rate | Explanation |
|---|---|---|
| larger surface-area-to-volume ratio | faster | more membrane area is available for exchange for each unit of cell volume |
| shorter diffusion distance or thinner exchange surface | faster | particles have a shorter path to travel |
| higher temperature | faster, within a suitable range | particles have more kinetic energy and move more rapidly |
| steeper concentration gradient | faster net movement | the difference in concentration across the surface is greater |
Small cells have a larger surface-area-to-volume ratio than equally shaped large cells. Exchange surfaces can therefore be adapted by being folded to increase area and thin to reduce distance, while circulation or ventilation can maintain a steep concentration gradient.
These factors change rate, not the direction set by the gradient. Surface area alone is not the same as surface-area-to-volume ratio, and active transport additionally depends on carrier proteins and a supply of energy from respiration.
Diffusion and osmosis can be investigated in living tissue and in a non-living model. A valid investigation changes one factor, measures movement quantitatively and controls the other rate factors.
| System | Example method | Quantitative evidence |
|---|---|---|
| living | equal potato cylinders placed in a range of sucrose or salt concentrations | change in mass or percentage change in mass |
| non-living | partially permeable Visking or dialysis tubing containing solution, immersed in another solution | change in mass, volume or liquid-column height |
| Step | Action |
|---|---|
| 1 | cut equal potato cylinders, blot them in the same way and record each initial mass |
| 2 | place them in equal volumes of a suitable range of solution concentrations |
| 3 | keep time, temperature, cylinder dimensions and potato source constant |
| 4 | remove after the same time, blot consistently and record final mass |
| 5 | calculate percentage mass change; repeat each concentration and calculate a mean |
% ext{ change in mass}=rac{ ext{final mass}- ext{initial mass}}{ ext{initial mass}} imes100
A positive value means net water entry; a negative value means net water loss. The concentration giving approximately zero change has a similar water potential to the tissue. In the tubing model, a mass or height increase shows net water movement into the partially permeable bag without requiring living cells.
Blotting removes surface liquid that would otherwise distort mass, while percentage change allows samples with different starting masses to be compared. Use repeats to reveal variation, handle cutting tools safely, and use a water bath rather than direct heating when temperature is investigated.
Photosynthesis transfers light energy into chemical energy stored in glucose. It occurs mainly in chloroplasts, where chlorophyll absorbs light.
The absorbed energy drives the conversion of carbon dioxide and water into glucose; oxygen is released. The glucose can be respired, stored as starch, transported as sucrose, or used to make substances such as cellulose that support growth.
This conversion supplies plant biomass and stores energy in chemical bonds. That chemical energy can pass to consumers through food chains and can be released during respiration.
Photosynthesis does not create energy: it converts and stores it. Chlorophyll absorbs light energy; glucose is the energy-containing chemical product.
Photosynthesis uses carbon dioxide and water to make glucose and oxygen. Light supplies energy and chlorophyll absorbs it; neither is a reactant consumed in the equation.
ext{carbon dioxide}+ ext{water}\longrightarrow ext{glucose}+ ext{oxygen}
6\mathrm{CO}{2}+6\mathrm{H}{2}\mathrm{O}\longrightarrow\mathrm{C}{6}\mathrm{H}{12}\mathrm{O}{6}+6\mathrm{O}{2}
The coefficients balance six carbon atoms, twelve hydrogen atoms and eighteen oxygen atoms on each side. Changing a subscript would change the substance, so balance an equation only by changing coefficients.
The rate of photosynthesis is controlled by the factor in shortest effective supply: the limiting factor. Increasing that factor raises the rate until a different factor becomes limiting.
| Factor increased | Why rate can rise | Why the rise stops or reverses |
|---|---|---|
| light intensity | more light energy is absorbed by chlorophyll | another factor, such as carbon dioxide or temperature, becomes limiting |
| carbon dioxide concentration | more reactant is available for carbon fixation | light or temperature becomes limiting |
| temperature | enzyme-controlled reactions proceed faster as particles have more kinetic energy and successful collisions increase | above the optimum, enzymes denature and the rate falls |
A plateau does not mean photosynthesis has stopped; it means changing the plotted factor no longer changes the rate under those conditions. Two curves can plateau at different rates because their other conditions differ.
State which factor is limiting from the evidence. More light or carbon dioxide cannot keep increasing the rate indefinitely, and high temperature can reduce rather than increase the rate.
A leaf is broad and thin, giving a large surface for light absorption and a short diffusion distance for gases.
| Structure | Adaptation for photosynthesis |
|---|---|
| transparent cuticle and upper epidermis | allow light to reach mesophyll cells while the waxy cuticle limits water loss |
| palisade mesophyll near the upper surface | tightly packed cells contain many chloroplasts to absorb light |
| spongy mesophyll | large air spaces create internal surfaces and allow carbon dioxide and oxygen to diffuse |
| stomata and guard cells | pores allow gas exchange; guard cells control opening |
| xylem in veins | supplies water and mineral ions |
| phloem in veins | carries products such as sucrose away from the leaf |
Palisade cells contain more chloroplasts than spongy cells, not all the leaf's chloroplasts. Air spaces aid gas movement; they are not empty because the leaf is poorly packed.
Plants need mineral ions because carbohydrates made by photosynthesis do not supply every element required to build new cells.
| Mineral ion | Required to make | Likely effect of deficiency |
|---|---|---|
| nitrate | amino acids, then proteins needed for growth and enzymes | stunted growth |
| magnesium | chlorophyll needed to absorb light for photosynthesis | yellow leaves (chlorosis) and reduced photosynthesis |
A valid mineral-deficiency comparison uses a complete mineral solution as the control and a solution lacking only one ion as the treatment. Any growth difference can then be linked to that missing ion if other conditions are controlled.
Mineral ions do not provide energy. Nitrate supplies nitrogen for amino acids, while magnesium is a component needed for chlorophyll; their functions are not interchangeable.
Photosynthesis can be demonstrated by measuring oxygen production and by showing that starch forms only where light, carbon dioxide and chlorophyll are available.
| Claim tested | Method and comparison | Positive evidence |
|---|---|---|
| oxygen evolves from a water plant | illuminate equal lengths of pondweed; collect gas by displacement or measure its volume over time | gas volume rises; collected oxygen relights a glowing splint |
| light is required | destarch a plant, cover part of a leaf, then expose it to light | only the uncovered region tests blue-black for starch |
| carbon dioxide is required | enclose a destarched leaf with potassium hydroxide or soda lime; compare with a control containing water | control leaf forms starch; carbon-dioxide-free leaf does not |
| chlorophyll is required | expose a destarched variegated leaf to light | green regions form starch; non-green regions do not |
For a starch test, boil the leaf in water, heat it in ethanol using a water bath to remove chlorophyll, rinse it, then add iodine solution. Blue-black shows starch; orange-brown shows no starch.
Destarching in darkness makes any later starch attributable to the experiment. Keep temperature, exposure time and plant material comparable, use repeats, and never heat flammable ethanol directly over a flame.
A balanced diet supplies carbohydrate, protein, lipid, vitamins, minerals, water and dietary fibre in proportions that meet the body's needs without persistent excess or deficiency.
| Component group | Main contribution to balance |
|---|---|
| carbohydrate and lipid | energy supply; lipid also provides longer-term energy storage |
| protein | material for growth and repair |
| vitamins and mineral ions | required in small amounts for specific body functions |
| water | medium for transport and chemical reactions |
| dietary fibre | supports movement of material through the gut |
Appropriate proportions are not identical for everyone. Energy and nutrient needs vary with factors such as activity, age and pregnancy, while the overall diet must still include all required component groups.
Balanced does not mean equal amounts of every component or a single 'healthy' food. A food rich in one useful nutrient cannot by itself supply the full diet.
Each dietary component has characteristic sources and functions, so a varied diet reduces the risk that one essential function is left unsupported.
| Component | Example sources | Main functions |
|---|---|---|
| carbohydrate | bread, rice, pasta, potatoes | energy released in respiration |
| protein | meat, fish, eggs, beans, pulses | growth and tissue repair; making enzymes |
| lipid | oils, butter, nuts, seeds | energy store, insulation and organ protection |
| vitamin A | liver, eggs, dairy, orange or dark-green vegetables | normal vision |
| vitamin C | citrus fruits and vegetables | healthy connective tissue; prevents scurvy |
| vitamin D | oily fish, eggs, fortified foods; made in skin in sunlight | helps calcium absorption and healthy bones |
| calcium ions | milk and dairy foods, leafy vegetables | bones and teeth |
| iron ions | red meat, liver, beans, leafy vegetables | haemoglobin in red blood cells |
| water | drinks and water-rich foods | solvent, transport medium and reaction medium |
| dietary fibre | wholegrains, fruit and vegetables | adds bulk and supports peristalsis, reducing constipation |
Fibre is not digested for energy, but it still has an important gut function. Vitamins and mineral ions have specific roles and cannot replace energy-providing carbohydrate or lipid.
Energy requirements change when the amount of energy used for movement, growth or reproduction changes.
| Factor | Effect on requirement | Why |
|---|---|---|
| greater activity level | increases | contracting muscles need more ATP, so respiration releases more energy |
| age | varies | children and adolescents require energy for growth; requirements often fall when growth ends or activity decreases |
| pregnancy | increases | energy supports growth of the fetus and changes in maternal tissues |
If energy intake persistently exceeds energy use, surplus energy is stored, mainly as fat, and body mass can increase. If intake is lower than use, stored fat and glycogen are respired and body mass can decrease.
These factors change requirements, not a fixed amount for every person. Age alone does not determine need: body size, activity and physiological state also matter.
The alimentary canal is a continuous tube that ingests food, digests large molecules, absorbs useful products and egests undigested material.
| Part | Main function |
|---|---|
| mouth | ingestion, chewing, mixing with saliva and starting starch digestion |
| oesophagus | carries the bolus to the stomach by peristalsis |
| stomach | churns food; acid kills many pathogens and provides conditions for protease |
| duodenum | receives pancreatic enzymes and bile; much chemical digestion occurs |
| ileum | completes digestion and absorbs soluble products through villi |
| colon | absorbs water and compacts undigested material |
| rectum | stores faeces before egestion |
| pancreas | produces digestive enzymes released into the duodenum |
The pancreas is an associated digestive organ, not part of the tube food passes through. Digestion breaks molecules down; absorption moves soluble products into blood or lymph.
Peristalsis is a coordinated wave of muscle contraction that pushes food along the gut.
Circular muscle contracts behind a bolus and relaxes ahead of it, narrowing the gut behind the food. Coordinated contractions of the gut wall then move the bolus forward through the oesophagus and intestines.
Because the movement is produced by muscle, food can travel through the digestive system even when gravity is not acting in the direction of movement. Dietary fibre adds bulk that helps the gut contents stimulate this process.
Peristalsis moves food; it does not chemically digest it. The wave is coordinated contraction and relaxation, not the food sliding down only because of gravity.
Digestive enzymes hydrolyse large, insoluble food molecules into smaller soluble molecules that can be absorbed.
| Substrate | Enzyme | Product |
|---|---|---|
| starch | amylase | maltose |
| maltose | maltase | glucose |
| protein | proteases | amino acids |
| lipid | lipases | fatty acids and glycerol |
Carbohydrate digestion therefore uses two named steps: amylase changes starch to maltose, then maltase changes maltose to glucose. Each enzyme is specific to its substrate because its active site has a complementary shape.
Amylase does not convert starch directly to glucose in the named syllabus pathway, and bile is not an enzyme. Mechanical breakdown increases surface area but does not replace chemical digestion.
Bile is produced continuously by the liver and stored in the gall bladder until it is needed.
After food enters the duodenum, bile is released from the gall bladder through the bile duct into the small intestine. Storage allows a supply to be released when lipid-containing food arrives.
The gall bladder stores and releases bile; it does not make it. The pancreas produces digestive enzymes, not bile.
Bile helps digestion in the duodenum by neutralising acid and emulsifying lipids.
| Role | Mechanism and benefit |
|---|---|
| neutralisation | bile neutralises acidic chyme from the stomach, providing a more suitable pH for enzymes in the small intestine |
| emulsification | bile separates large lipid globules into many small droplets, increasing surface area for lipase action |
Emulsification is physical subdivision, not chemical digestion. Bile contains no digestive enzyme and does not convert lipid into fatty acids and glycerol; lipase does that.
The ileum absorbs digested nutrients rapidly because its inner surface is folded into villi, and each villus has structures that shorten transport paths and maintain gradients.
| Feature | How it improves absorption |
|---|---|
| many villi and microvilli | provide a very large surface area |
| epithelium one cell thick | gives a short diffusion distance |
| dense capillary network | quickly carries away glucose and amino acids, maintaining concentration gradients |
| lacteal | absorbs and transports products of lipid digestion |
| many mitochondria in epithelial cells | supply ATP for active transport when needed |
Small soluble products cross the epithelium by diffusion or active transport. Blood capillaries carry water-soluble nutrients away, while lipid products enter lacteals and are transported in lymph.
Villi absorb products after digestion; they do not produce the digestive enzymes listed in the previous step. A large surface area is effective only because it is paired with a thin barrier and rapid transport away.
Food energy can be estimated by burning a measured mass of food and measuring the temperature rise of a known mass of water.
| Step | Action |
|---|---|
| 1 | record the mass of food and the mass or volume of water |
| 2 | record the initial water temperature, ignite the food and heat the water |
| 3 | stir the water and record its highest temperature |
| 4 | reweigh the remaining food to find the mass actually burned |
| 5 | repeat, calculate a mean and compare energy transferred per gram |
E=mc\Delta T
For water, use c=4.2Jg−1∘C−1. Divide E by the mass of food burned to obtain joules per gram. Keep water mass, flame-to-container distance and apparatus the same when comparing foods.
The estimate is usually lower than the food's true energy value because combustion may be incomplete and heat is lost to the air and apparatus. Insulation, a lid, stirring and an oxygen supply improve accuracy; wear eye protection and secure hair around flames.
Respiration is a series of enzyme-controlled reactions that transfers chemical energy from glucose into ATP in living cells.
Breaking down glucose releases energy in controlled steps. Cells capture part of this energy by making ATP rather than releasing it all at once as heat. Aerobic respiration uses oxygen and transfers more energy to ATP than anaerobic respiration.
A cell's respiration rate rises when its ATP demand rises. For example, active muscle cells need more ATP, so they consume glucose and—during aerobic respiration—oxygen more rapidly.
Respiration is not the same as breathing: breathing moves air, whereas respiration is a chemical process in cells. ATP is the immediate energy carrier made using energy transferred from glucose.
ATP provides cells with small, immediately usable transfers of energy for energy-requiring processes.
| Cellular process | Why ATP is needed |
|---|---|
| active transport | moves substances across membranes against a concentration gradient |
| synthesis of large molecules | joins smaller units to support growth and repair |
| muscle contraction | powers movement of contractile proteins |
| cell division and movement | powers chromosome movement and other cellular work |
When ATP releases energy it is converted to ADP and phosphate. Energy transferred during respiration is then used to regenerate ATP, linking glucose breakdown to the cell's changing energy demands.
ATP is not a long-term energy store like glycogen or lipid. It is continually used and regenerated, so reduced respiration can quickly limit active transport, synthesis and movement.
Aerobic and anaerobic respiration both transfer energy from glucose to ATP, but they differ in oxygen use, completeness of breakdown, energy yield and products.
| Feature | Aerobic respiration | Anaerobic respiration |
|---|---|---|
| oxygen | required | not required |
| glucose breakdown | complete | incomplete |
| ATP yield per glucose | greater | smaller |
| products in animals | carbon dioxide and water | lactic acid |
| products in plants and yeast | carbon dioxide and water | ethanol and carbon dioxide |
During vigorous exercise, oxygen delivery may not meet muscle demand, so anaerobic respiration supplies some ATP and lactic acid accumulates. Afterwards, breathing remains elevated while the body deals with the lactic acid and repays the oxygen debt.
Anaerobic does not mean no energy is transferred; it means less ATP is obtained from each glucose molecule because breakdown is incomplete.
Aerobic respiration uses glucose and oxygen and produces carbon dioxide and water while transferring energy to ATP.
ext{glucose}+ ext{oxygen}\longrightarrow ext{carbon dioxide}+ ext{water}
\mathrm{C}{6}\mathrm{H}{12}\mathrm{O}{6}+6\mathrm{O}{2}\longrightarrow6\mathrm{CO}{2}+6\mathrm{H}{2}\mathrm{O}
The balanced equation has six carbon, twelve hydrogen and eighteen oxygen atoms on each side. Energy transferred to ATP is a consequence of the reaction, not a chemical atom that is balanced into the symbol equation.
Without sufficient oxygen, cells can transfer some energy from glucose by anaerobic respiration, but animals and plants form different products.
| Organisms | Word equation |
|---|---|
| animals | glucose ⟶ lactic acid |
| plants and yeast | glucose ⟶ ethanol + carbon dioxide |
The products still contain chemical energy because glucose is only partly broken down. This explains why anaerobic respiration transfers less energy to ATP than aerobic respiration.
Animals do not produce ethanol and carbon dioxide in this pathway, and plant/yeast anaerobic respiration does not produce lactic acid in the syllabus equations. Oxygen is absent from both reactant sides.
Respiring seeds provide measurable evidence that respiration releases carbon dioxide and transfers some energy as heat.
| Product | Experimental comparison | Evidence |
|---|---|---|
| carbon dioxide | place equal masses of germinating seeds and boiled or dry control seeds in separate sealed apparatus; keep temperature and time equal | a carbon-dioxide sensor rises, or gas from germinating seeds turns limewater cloudy |
| heat | place equal masses of germinating and boiled control seeds in insulated flasks with thermometers; use the same starting temperature | a larger temperature rise in the germinating-seed flask shows heat release |
Use the same seed species, age or stage, mass, moisture, oxygen supply and measurement time. Repeat each condition and compare mean changes. A control separates respiration from temperature drift or other environmental change.
Disinfect seeds to reduce microbial respiration, but do not kill the experimental seeds. Carbon dioxide production alone does not distinguish aerobic from anaerobic respiration, so ensure oxygen is available when claiming aerobic respiration.
Gas exchange occurs by diffusion: the net movement of gas particles from a region of higher concentration to a region of lower concentration.
Oxygen diffuses across an exchange surface when its concentration is higher on one side, while carbon dioxide diffuses in the opposite direction when its gradient is reversed. Thin, permeable surfaces shorten the diffusion path; a large area allows more particles to cross at once.
Ventilation replaces air and circulation carries gases away or supplies them, maintaining steep concentration gradients. A steeper gradient produces faster net diffusion.
Diffusion is passive and does not pump gases against a gradient. Gas particles move in both directions, but net movement is toward the lower concentration.
Leaf cells respire continuously, while photosynthesis occurs only when light is available; both processes affect oxygen and carbon dioxide exchange.
| Process | Gas used | Gas produced | When it occurs |
|---|---|---|---|
| respiration | oxygen | carbon dioxide | day and night |
| photosynthesis | carbon dioxide | oxygen | when sufficient light is available |
The gases measured outside a leaf show the net result of both processes. In strong light, photosynthesis can exceed respiration, so carbon dioxide enters and oxygen leaves overall. In darkness, only respiration affects net exchange, so oxygen enters and carbon dioxide leaves.
Plants do not stop respiring in daylight. Oxygen released by photosynthesis and carbon dioxide released by respiration can be reused inside the leaf, so net exchange is the difference between the two rates.
A leaf is adapted to move carbon dioxide and oxygen rapidly between the atmosphere and photosynthesising or respiring cells.
| Feature | Gas-exchange advantage |
|---|---|
| broad, thin blade | large external area and short diffusion distance |
| many stomata, mainly in the lower epidermis | pores connect outside air to internal spaces while limiting exposure to direct sunlight |
| loosely packed spongy mesophyll | large air spaces let gases spread through the leaf |
| moist mesophyll cell surfaces | gases dissolve before diffusing across cell membranes |
| thin mesophyll cell walls | short path between air spaces and cells |
Internal air spaces are not themselves photosynthetic cells; they create routes and surfaces for diffusion. Floating leaves may place stomata on the upper surface because the lower surface is under water.
A stoma is a pore in the epidermis controlled by two guard cells; changing the pore width regulates gas exchange.
| Stoma state | Gas and water movement |
|---|---|
| open | carbon dioxide diffuses in; oxygen and water vapour can diffuse out |
| partly closed or closed | carbon dioxide entry and oxygen exit fall, but water loss by transpiration is reduced |
Opening supports photosynthesis by maintaining carbon dioxide supply. Closing conserves water during dry conditions but can limit photosynthesis, so stomatal control is a compromise between gas exchange and water loss.
Stomata do not actively pull gases into the leaf; they change the resistance of the diffusion pathway. Guard cells control the pore, while gradients determine net gas direction.
Respiration continues at every light intensity, but increasing light raises photosynthesis until another factor limits it; net gas exchange depends on which rate is greater.
| Light condition | Relative rates | Net exchange |
|---|---|---|
| darkness or very low light | respiration exceeds photosynthesis | oxygen enters; carbon dioxide leaves |
| compensation point | photosynthesis equals respiration | no net oxygen or carbon dioxide exchange |
| bright light | photosynthesis exceeds respiration | carbon dioxide enters; oxygen leaves |
No net exchange at the compensation point does not mean both processes have stopped. Their opposite gas movements are equal, so they cancel at the whole-leaf boundary.
Hydrogen-carbonate indicator reveals changes in carbon dioxide concentration around a leaf: yellow means carbon dioxide increased, orange-red means little or no change, and dark red or purple means it decreased.
| Step | Action |
|---|---|
| 1 | place equal leaf areas in sealed tubes containing equal volumes of indicator; include a tube with indicator but no leaf |
| 2 | expose tubes to a measured range of light intensities using lamp distance, neutral filters or darkness |
| 3 | keep leaf species, temperature and exposure time constant |
| 4 | record final colour or use a colorimeter; repeat each intensity and compare means |
Yellow shows net respiration and carbon dioxide release. Purple or dark red shows net photosynthesis and carbon dioxide uptake. Orange-red suggests the compensation point or no biological change in the empty control.
Keep tubes sealed and prevent lamp heating from becoming a second variable. The indicator measures net carbon dioxide change, not photosynthesis alone.
The thorax contains the lungs and the structures that conduct air, exchange gases and change chest volume during ventilation.
| Structure | Position or role |
|---|---|
| trachea | main airway supported by cartilage; divides into two bronchi |
| bronchi | one enters each lung and branches into bronchioles |
| bronchioles | narrow branching airways ending at alveoli |
| alveoli | microscopic air sacs where gases diffuse between air and blood |
| ribs | protect the lungs and move to change thoracic volume |
| intercostal muscles | lie between ribs and move the rib cage |
| diaphragm | muscular sheet below the lungs that changes thoracic volume |
| pleural membranes | surround the lungs with a thin fluid layer that reduces friction during movement |
During inhalation, air follows trachea ightarrow bronchus ightarrow bronchioles ightarrow alveoli. The oesophagus is part of the digestive system, not this airway.
Ventilation moves air because the diaphragm and intercostal muscles change thoracic volume, which changes pressure inside the lungs.
| Event | Inhalation | Exhalation at rest |
|---|---|---|
| diaphragm | contracts and flattens | relaxes and becomes dome-shaped |
| external intercostal muscles | contract | relax |
| ribs | move up and out | move down and in |
| thoracic volume | increases | decreases |
| pressure in lungs | falls below atmospheric pressure | rises above atmospheric pressure |
| air movement | into lungs | out of lungs |
The lungs do not contain muscles that pull themselves open. Air flows down a pressure gradient created by changing thoracic volume; inhalation does not occur because the lungs actively suck air in.
Millions of alveoli form an exchange surface that lets oxygen diffuse into blood and carbon dioxide diffuse from blood into air rapidly.
| Adaptation | Effect on diffusion |
|---|---|
| many tiny alveoli | very large total surface area |
| alveolar and capillary walls one cell thick | very short diffusion distance |
| moist lining | oxygen and carbon dioxide dissolve before crossing membranes |
| dense capillary network and continuous blood flow | carries oxygen away and brings carbon dioxide, maintaining gradients |
| ventilation | renews alveolar air, maintaining steep oxygen and carbon dioxide gradients |
Oxygen concentration is higher in alveolar air than in deoxygenated blood, so oxygen diffuses into capillaries. Carbon dioxide concentration is higher in the blood, so it diffuses into alveoli.
A large surface area alone is insufficient: thin walls and maintained concentration gradients are also required. Diffusion crosses both the alveolar wall and capillary wall.
Cigarette smoke damages both the lungs and circulatory system, reducing oxygen delivery and increasing disease risk.
| Smoke component or damage | Biological consequence |
|---|---|
| tar damages cilia | mucus and pathogens accumulate, increasing bronchitis and infection risk |
| carcinogens in tar | mutations increase lung-cancer risk |
| alveolar walls break down in emphysema | surface area and elasticity fall, causing breathlessness and reduced diffusion |
| carbon monoxide binds strongly to haemoglobin | less oxygen is transported to tissues |
| nicotine and damage to artery linings | heart workload and risk of narrowed or blocked coronary arteries increase |
Coronary heart disease restricts blood flow through coronary arteries, reducing oxygen supply to heart muscle. Combined lung and blood-vessel damage therefore limits aerobic respiration in tissues.
Smoking raises risk; it does not guarantee one outcome. Explaining a consequence requires the causal link—for example, damaged alveoli reduce surface area, which reduces oxygen diffusion.
Breathing investigations can show that exhaled air contains more carbon dioxide and that exercise increases ventilation to meet greater respiratory demand.
| Question | Method and evidence |
|---|---|
| is more carbon dioxide exhaled? | bubble equal volumes of inhaled and exhaled air through separate limewater samples using one-way tubing; exhaled air turns limewater cloudy faster |
| how does exercise affect breathing? | count breaths per minute at rest, immediately after a fixed exercise, and at regular recovery intervals; increased rate and slower return indicate greater ventilatory demand |
| how does exercise affect carbon dioxide release? | compare the time for equal volumes of exhaled air before and after exercise to change equal indicator or limewater samples |
Standardise exercise type, duration and intensity; use the same participant for paired readings where possible; keep solution volume and temperature constant. Repeat trials or participants and calculate means.
Breathing rate counts breaths, while ventilation rate also depends on volume per breath. Exercise can increase both, so breathing rate alone is not a complete measure of ventilation.
A unicellular organism exchanges substances directly with its surroundings by diffusion because its single cell is always next to the environment.
Its small size gives a large surface-area-to-volume ratio and a short diffusion distance. Oxygen and dissolved food can enter, while carbon dioxide and other wastes can leave, fast enough for the cell's relatively low demand.
A unicellular organism does not need a specialised transport system. Diffusion is sufficient because distances and demand are small—not because diffusion becomes faster inside a single cell.
Large multicellular organisms need specialised transport systems because diffusion across the outer surface alone cannot supply every cell fast enough.
| Feature of a large organism | Consequence |
|---|---|
| small surface-area-to-volume ratio | too little exchange surface for the volume of living tissue |
| many internal cells | some cells are far from the external environment |
| long diffusion distances | substances take too long to reach cells or leave them |
| high metabolic demand | oxygen and nutrients are used, and wastes produced, faster |
A transport system moves materials rapidly between exchange surfaces and cells. Continuous delivery and removal also maintain steep concentration gradients for diffusion at both ends.
Transport does not replace diffusion: bulk flow covers long distances, while diffusion still moves substances across exchange surfaces and cell membranes.
Phloem translocates dissolved sucrose and amino acids between leaves and other parts of a plant.
| Source or sink | Typical role |
|---|---|
| photosynthesising leaf | source: loads sucrose made from photosynthetic products |
| growing root, bud, flower or fruit | sink: uses sucrose and amino acids for respiration, growth and synthesis |
| storage organ | can be a sink while storing and a source when reserves are mobilised |
Translocation can occur up or down the plant because the source–sink relationship changes. Phloem is living tissue; movement is not restricted to the root-to-leaf direction.
Phloem transports sucrose and amino acids, not starch molecules. Do not confuse it with xylem, which carries water and mineral ions mainly upward.
Xylem carries water and dissolved mineral ions from roots through stems to leaves and the rest of the plant.
| Feature | Transport advantage |
|---|---|
| dead cells joined end to end | forms a continuous hollow pathway |
| no end walls or cytoplasm | reduces resistance to water flow |
| lignified walls | resist collapse under tension and support the plant |
Water loss from leaves creates transpiration pull, drawing a continuous column of water upward through xylem. Mineral ions dissolved in that water travel with the transpiration stream.
Xylem flow is mainly one-way from roots upward. It is not the tissue that translocates sucrose and amino acids between sources and sinks.
Water enters root hair cells by osmosis, from soil with higher water potential to cell contents with lower water potential through a partially permeable cell membrane.
| Adaptation | Effect |
|---|---|
| long hair-like extension | large contact area with water between soil particles |
| thin wall and membrane | short pathway into the cell |
| concentrated cell sap | helps maintain a lower water potential than the soil solution |
Water then moves across the root into xylem. Mineral ions may be absorbed by active transport and can help lower cell water potential, but the water itself enters by osmosis.
Osmosis describes water movement only. Do not say water is actively transported into the root hair cell or that mineral ions enter by osmosis.
Transpiration is the loss of water vapour from a plant's surface, mainly through stomata in the leaves.
| Stage | Event |
|---|---|
| 1 | water evaporates from moist mesophyll cell surfaces into leaf air spaces |
| 2 | water vapour diffuses through open stomata down its concentration gradient |
| 3 | water leaving mesophyll is replaced from leaf xylem |
| 4 | tension pulls a continuous water column upward through xylem from the roots |
The transpiration stream supplies water for photosynthesis and turgor, carries mineral ions and can cool leaves by evaporation.
Evaporation occurs inside the leaf before water vapour diffuses out. Transpiration is the overall water loss, not a pump located in the stomata.
Environmental conditions alter transpiration by changing evaporation, the water-vapour gradient or stomatal opening.
| Change | Effect on rate | Mechanism |
|---|---|---|
| lower humidity | increases | steepens the water-vapour gradient from leaf to air |
| greater wind speed | increases | removes the moist boundary layer around the leaf |
| higher temperature | increases | gives water molecules more kinetic energy, increasing evaporation and diffusion |
| brighter light | usually increases | opens stomata for carbon dioxide entry, reducing resistance to water loss |
The converse changes usually reduce the rate. Once stomata are fully open or another factor becomes limiting, further change may have little additional effect.
State the mechanism, not only the direction. Light acts mainly through stomata; wind does not heat the leaf in the standard explanation, and high humidity slows loss by reducing the gradient.
A bubble potometer measures water uptake by a cut leafy shoot. Water uptake is used as a proxy for transpiration because most absorbed water is lost from leaves.
| Step | Action |
|---|---|
| 1 | cut the shoot under water and connect it to water-filled apparatus |
| 2 | seal every joint, dry the leaves and check that the apparatus is airtight |
| 3 | introduce one air bubble and record its starting position |
| 4 | expose the shoot to one measured condition for a fixed time |
| 5 | measure bubble distance; calculate volume as capillary cross-sectional area × distance, then divide by time |
| 6 | reset the bubble, repeat and calculate a mean |
Change one factor such as wind speed, light intensity, humidity or temperature. Control the other environmental factors, shoot species, leaf area and time; allow the shoot to acclimatise before readings.
A potometer does not measure transpiration directly: some absorbed water is used in photosynthesis, growth or turgor. Avoid air entering the xylem by cutting under water, and keep water away from electrical equipment.
Blood is a tissue made of red blood cells, white blood cells and platelets suspended in liquid plasma.
| Component | Main function |
|---|---|
| red blood cells | transport oxygen using haemoglobin |
| phagocytes and lymphocytes (white blood cells) | defend against pathogens |
| platelets | trigger clotting at damaged vessels |
| plasma | transports cells and dissolved substances, and distributes heat |
Platelets are cell fragments, not white blood cells. Plasma is the liquid carrier; it is not the same as the whole blood or the clear fluid inside every cell.
Plasma is the liquid part of blood that carries dissolved substances between the organs that produce, absorb, use or remove them.
| Cargo | Main route |
|---|---|
| carbon dioxide | respiring tissues → lungs |
| digested food such as glucose and amino acids | small intestine → liver and body cells |
| urea | liver → kidneys |
| hormones | endocrine glands → target organs |
| heat | redistributed from active organs such as muscles and liver to the rest of the body |
Oxygen is transported mainly bound to haemoglobin inside red blood cells, whereas these listed substances travel in plasma. Always name both the substance and a biologically correct source or destination.
A red blood cell is specialised to load oxygen in the lungs and release it to respiring tissues.
| Adaptation | Oxygen-transport advantage |
|---|---|
| biconcave disc | large surface-area-to-volume ratio and short diffusion path |
| no nucleus when mature | leaves more internal space for haemoglobin |
| packed with haemoglobin | haemoglobin binds oxygen reversibly |
| small and flexible | squeezes through narrow capillaries close to cells |
Red blood cells contain cytoplasm and haemoglobin but no nucleus. Iron is part of haemoglobin; the cell does not carry oxygen because it is hollow.
White blood cells defend the body in two distinct ways: phagocytes ingest pathogens, while lymphocytes make specific antibodies.
| Cell | Recognition and action |
|---|---|
| phagocyte | surrounds and engulfs a pathogen, then digests it with enzymes |
| lymphocyte | recognises a particular antigen and produces antibodies with complementary binding sites |
Antibodies bind specifically to their matching antigens and can clump pathogens or mark them for destruction. Some activated lymphocytes form memory cells.
Phagocytes do not produce antibodies, and lymphocytes do not normally engulf pathogens. Antibody specificity depends on complementary antigen-binding shape.
Vaccination exposes the immune system to harmless pathogen antigens so that protection develops without the full disease.
| Stage | Immune event |
|---|---|
| 1 | dead, weakened, inactive or antigen-containing material is introduced |
| 2 | specific lymphocytes recognise the antigen and produce antibodies |
| 3 | some lymphocytes remain as memory cells |
| 4 | later exposure to the same antigen triggers a secondary response |
| 5 | antibodies are produced sooner, faster and in greater quantity, often removing the pathogen before symptoms develop |
A vaccine does not kill every future pathogen directly and does not cause antibiotics to be made. Memory is antigen-specific, so protection against one pathogen may not protect against another.
Blood clotting rapidly seals a damaged vessel, limiting blood loss and blocking microorganisms from entering the body.
| Stage | Event |
|---|---|
| 1 | a vessel is damaged and platelets collect at the site |
| 2 | clotting reactions produce strands of fibrin |
| 3 | the fibrin mesh traps blood cells and forms a clot |
| 4 | the clot dries into a scab while repair occurs underneath |
Platelets help start clotting but are not antibodies or phagocytes. A clot prevents both excessive bleeding and pathogen entry; these are separate benefits.
The heart is a muscular double pump: its right side sends deoxygenated blood to the lungs, and its left side sends oxygenated blood around the body.
| Flow step | Structure |
|---|---|
| 1 | vena cava → right atrium |
| 2 | right atrium → valve → right ventricle |
| 3 | right ventricle → pulmonary artery → lungs |
| 4 | lungs → pulmonary vein → left atrium |
| 5 | left atrium → valve → left ventricle |
| 6 | left ventricle → aorta → body |
| Feature | Function |
|---|---|
| valves | prevent backflow |
| septum | prevents oxygenated and deoxygenated blood mixing |
| thick left-ventricle wall | generates high pressure for the whole body |
| thinner right-ventricle wall | pumps only to nearby lungs |
| coronary arteries | supply heart muscle with oxygen and glucose |
Arteries carry blood away from the heart and veins return it; oxygen content does not define the vessel. The pulmonary artery is deoxygenated and the pulmonary vein oxygenated.
Heart rate rises when muscles need faster delivery of oxygen and glucose and faster removal of carbon dioxide during exercise.
More muscular contraction increases respiration and ATP demand. Increasing heart rate raises blood flow, supporting aerobic respiration and helping transport heat and respiratory products away.
Adrenal glands release the hormone adrenaline into the blood during stress or excitement. Adrenaline acts on the heart's pacemaker to increase heart rate as part of the fight-or-flight response.
Adrenaline is a hormone carried in plasma; it is not produced by the heart. A higher heart rate supports increased respiration—it is not itself cellular respiration.
Coronary heart disease occurs when coronary arteries become narrowed or blocked, reducing blood and oxygen supply to heart muscle.
| Risk factor | How risk can increase |
|---|---|
| smoking | damages artery lining, raises clot risk and blood pressure |
| high saturated-fat or cholesterol diet | promotes fatty deposits that narrow coronary arteries |
| inactivity and obesity | increase strain on the circulatory system and often raise blood pressure |
| persistent high blood pressure or stress | damages vessels and increases heart workload |
| diabetes, inherited alleles and increasing age | can increase susceptibility independently or with lifestyle factors |
A narrowed lumen limits oxygen and glucose delivery. Complete blockage can stop aerobic respiration in part of the heart muscle, causing tissue death and a heart attack.
A risk factor changes probability; it does not prove that one individual will develop CHD. Correlation in population data also does not isolate cause unless other variables are controlled.
Arteries, veins and capillaries have structures matched to the pressure, direction and exchange role of the blood they carry.
| Vessel | Structure | Structure–function link |
|---|---|---|
| artery | thick muscular, elastic wall; relatively narrow lumen; no valves along most of its length | withstands high pressure; elastic recoil smooths flow away from heart |
| vein | thinner wall with less muscle and elastic tissue; wide lumen; valves | low-resistance return at low pressure; valves prevent backflow |
| capillary | wall one cell thick; extremely narrow lumen; branching network | short diffusion distance, slow close flow and large total exchange area |
Vessel type is defined by direction relative to the heart, not oxygen content. Capillaries are not simply tiny veins: their one-cell-thick walls are specialised for exchange.
Humans have double circulation: blood passes through the heart once in the pulmonary circuit and again in the systemic circuit during one complete journey.
| Organ route | Named vessels and direction |
|---|---|
| lungs | heart → pulmonary artery → lungs → pulmonary vein → heart |
| body tissues | heart → aorta → organ arteries → capillaries → organ veins → vena cava → heart |
| liver | hepatic artery brings oxygenated blood; hepatic portal vein brings nutrient-rich blood from the gut; hepatic vein drains to vena cava |
| kidneys | renal arteries bring blood from aorta; renal veins return blood to vena cava |
The pulmonary circuit oxygenates blood. The systemic circuit distributes oxygen and nutrients and returns carbon dioxide and other wastes. Separate pumps allow high systemic pressure without exposing lung capillaries to the same pressure.
The hepatic portal vein is unusual because it connects gut capillaries to liver capillaries before blood returns to the heart. The renal vein carries blood away from the kidney, even though all veins carry blood toward the heart overall.
Leaf metabolism can produce carbon dioxide and oxygen faster than the plant uses them; the excess gases diffuse out through stomata.
| Metabolic process | Gas produced | When it becomes a waste product |
|---|---|---|
| respiration | carbon dioxide | production exceeds its use in photosynthesis, especially in darkness |
| photosynthesis | oxygen | production exceeds its use in respiration, commonly in sufficient light |
Each gas moves from a higher concentration in the leaf air spaces to a lower concentration outside. Stomata provide the pore through which this diffusion occurs.
Plants respire in both light and darkness. Calling oxygen or carbon dioxide a waste product depends on net production at that time; neither gas is always waste to the plant.
Excretion removes waste products of metabolism and substances present in excess; the lungs, kidneys and skin remove different mixtures.
| Organ | Excretory products | Route out |
|---|---|---|
| lungs | carbon dioxide and water vapour | exhaled air |
| kidneys | urea, excess water and excess mineral ions | urine |
| skin | water, mineral ions and a small amount of urea | sweat |
Excretion is not egestion: faeces contain mainly unabsorbed food leaving the gut, whereas excretory products were made by metabolism or are excess internal substances.
Kidneys clean the blood by excreting urea and regulate blood water and ion content by adjusting what the nephrons return to the blood.
| Nephron process | Contribution |
|---|---|
| ultrafiltration | forces water and small dissolved substances out of glomerular blood |
| selective reabsorption | returns all useful glucose and required ions from filtrate to blood |
| variable water reabsorption | returns more or less water according to the body's water balance |
| urine formation | leaves urea plus excess water and ions for removal |
Osmoregulation maintains a suitable blood water concentration. Dehydration causes more water reabsorption and a smaller volume of concentrated urine; excess body water causes less reabsorption and a larger volume of dilute urine.
Excretion removes metabolic waste such as urea; osmoregulation controls water and ion balance. They occur in the same organ but are not identical functions.
The urinary system makes urine in two kidneys, carries it through two ureters, stores it in the bladder and releases it through the urethra.
| Structure | Direction and function |
|---|---|
| renal artery | brings unfiltered blood to each kidney |
| kidney | filters blood and forms urine in nephrons |
| renal vein | returns adjusted blood from each kidney |
| ureter | carries urine from one kidney to the bladder |
| bladder | stores urine temporarily |
| urethra | carries urine from the bladder out of the body |
A ureter connects a kidney to the bladder; the urethra leaves the bladder. Blood enters by the renal artery, but urine never travels through a blood vessel.
A nephron is the kidney's microscopic processing unit; its connected regions filter blood, recover useful substances and form urine.
| Route through nephron | Main structural relationship |
|---|---|
| 1. glomerulus inside Bowman's capsule | capillary knot where filtrate is forced into the capsule |
| 2. proximal convoluted tubule | first coiled region leaving the capsule |
| 3. loop of Henle | long U-shaped section extending into the kidney medulla |
| 4. distal convoluted tubule | second coiled region returning toward the cortex |
| 5. collecting duct | receives fluid from nephrons and carries it toward the renal pelvis and ureter |
The glomerulus is a blood-capillary network; Bowman's capsule surrounds it and receives filtrate. The collecting duct is downstream of the convoluted tubules and loop, not part of the blood supply.
Ultrafiltration occurs when high pressure in the glomerulus forces water and small dissolved substances through the filtration barrier into Bowman's capsule.
| Substance in blood | Enters glomerular filtrate? | Reason |
|---|---|---|
| water, glucose, urea and mineral ions | yes | small enough to pass the filtration barrier |
| blood cells and large plasma proteins | no | too large to cross and remain in the blood |
The glomerulus has high hydrostatic pressure, helped by blood entering through a wider arteriole than the one leaving. The filtrate collected in Bowman's capsule then enters the proximal convoluted tubule.
Ultrafiltration is non-selective among small molecules: useful glucose enters the filtrate alongside urea. Selective recovery happens later, so filtrate and urine do not have the same composition.
Water moves from fluid in the collecting duct into the surrounding kidney tissue and then the blood by osmosis.
The medulla around the collecting duct has a lower water potential because it contains a high concentration of dissolved ions. When the duct wall is permeable, water moves down this water-potential gradient and is carried away by capillaries.
| Water reabsorbed | Urine outcome |
|---|---|
| more | smaller volume and higher concentration |
| less | larger volume and lower concentration |
Water is reabsorbed by osmosis, not active transport. The amount depends on collecting-duct permeability, which ADH regulates in the next control step.
Glucose enters glomerular filtrate because it is small, but a healthy kidney selectively reabsorbs it from the proximal convoluted tubule into the blood.
Glucose is a useful respiratory substrate, so losing it in urine would waste chemical energy. Proximal-tubule cells use active transport, requiring energy from ATP, to move glucose from filtrate even against its concentration gradient; it then returns to nearby capillaries.
Selective reabsorption is different from ultrafiltration: filtration lets small molecules leave blood without deciding whether they are useful, while reabsorption retrieves specific useful substances. Normally, no glucose remains in urine.
ADH regulates blood water content by changing the permeability of collecting ducts and therefore how much water is reabsorbed.
| Blood state | Control response | Kidney effect | Urine |
|---|---|---|---|
| too little water; blood too concentrated | hypothalamic osmoreceptors stimulate more ADH release from the pituitary | collecting ducts become more permeable; more water returns to blood | small volume, concentrated |
| too much water; blood too dilute | less ADH is released | collecting ducts become less permeable; less water returns | large volume, dilute |
As blood concentration returns toward normal, the original stimulus falls and ADH release adjusts. This negative feedback prevents uncontrolled correction.
ADH is released from the pituitary and acts on collecting ducts; it does not add water to urine or filter urea. More ADH produces less urine, not more.
Urine contains water, urea and mineral ions that remain after filtration and selective reabsorption.
| Component | Why it remains |
|---|---|
| water | the amount not required to maintain blood water balance |
| urea | nitrogen-containing metabolic waste made in the liver and excreted by kidneys |
| mineral ions | quantities present in excess of the body's needs |
Urine volume and concentration vary with water balance: reabsorbing more water concentrates the urea and ions left in the tubule.
Healthy urine normally lacks blood cells, large proteins and glucose. Urine is not simply filtered blood: useful substances and much water have been reabsorbed before it reaches the bladder.
An organism responds when it detects a change in its internal or external environment and produces an action that can improve survival.
| Stage | Role | Example |
|---|---|---|
| stimulus | detectable environmental change | increasing light, heat, sound or touch |
| detection and coordination | receptors detect the change and information is processed | sensory cells and a coordination system |
| response | an effector changes activity | muscle contracts, gland secretes or a plant changes growth direction |
Responses can move an organism toward useful conditions or away from harm. Repeated harmless stimulation can sometimes reduce a response, preventing unnecessary energy use.
A stimulus is the change, not the action it causes. A response need not involve conscious choice: plants, microorganisms and reflex pathways all respond without deliberate decision-making.
Homeostasis is the maintenance of a constant internal environment within narrow limits despite internal or external change.
| Regulated condition | Why control matters | Corrective examples |
|---|---|---|
| body temperature | enzyme-controlled reactions work best in a suitable range | sweating and vasodilation when hot; reduced sweating and vasoconstriction when cold |
| body water content | cells need a suitable water balance | ADH changes kidney water reabsorption and urine concentration |
A deviation is detected, a coordination system activates effectors, and the response opposes the deviation. As the condition returns toward its set range, the corrective response is reduced: this is negative feedback.
Homeostasis does not keep every value perfectly fixed; it holds conditions within a tolerable range. It concerns the internal environment, not simply keeping the external environment unchanged.
A coordinated response links a stimulus to a receptor and then to an effector whose action produces the response.
| Component | What it does |
|---|---|
| stimulus | changes a condition, such as light intensity or temperature |
| receptor | detects the stimulus and converts it into information for the coordination system |
| coordinator | processes information and sends instructions |
| effector | carries out the response; usually a muscle or gland in animals |
Touching a hot object is the stimulus; temperature or pain receptors in skin detect it; the nervous system coordinates; arm muscles contract as effectors, withdrawing the hand.
A receptor detects; an effector acts. The organ that senses a change should not be named as the effector unless it also performs the response.
Plants detect environmental stimuli and alter growth or cell activity even though they have no nervous system or muscles.
| Stimulus | Plant response and value |
|---|---|
| directional light | shoots change growth direction, improving light capture |
| gravity | roots and shoots grow in opposite directions, placing organs in useful positions |
| water shortage | stomata close, reducing water loss |
| day length | flowering can occur in a season favourable for reproduction |
Plant responses are often slower than animal movements because many depend on unequal growth, but speed does not determine whether something is a response. A stimulus can also change reversible cell activity, such as stomatal opening.
A tropism is a directional growth response: positive growth is toward a stimulus and negative growth is away from it.
| Organ | Light response | Gravity response | Benefit |
|---|---|---|---|
| shoot | positive phototropism: toward light | negative geotropism: away from gravity | exposes leaves to light for photosynthesis |
| root | usually negative phototropism: away from light | positive geotropism: toward gravity | anchors the plant and grows into soil for water and ions |
Positive and negative describe direction relative to the stimulus, not whether the response is beneficial. A shoot growing upward is negatively geotropic because it grows opposite to gravity.
When light reaches a shoot from one side, auxin causes unequal cell elongation so the shoot bends toward the light.
| Stage | Event |
|---|---|
| 1 | auxin is produced near the shoot tip |
| 2 | one-sided light causes more auxin to accumulate on the shaded side |
| 3 | in shoots, auxin stimulates greater cell elongation on the shaded side |
| 4 | the shaded side grows faster, curving the tip toward the light |
Bending exposes developing leaves to stronger light, supporting a higher photosynthetic rate.
Auxin does not pull the shoot toward light and light does not make the illuminated side grow faster. In this shoot response, greater elongation occurs on the shaded side.
Nervous and hormonal systems both coordinate responses, but they carry different signals through different routes and produce different response patterns.
| Feature | Nervous communication | Hormonal communication |
|---|---|---|
| signal | electrical impulse along neurones; neurotransmitter at synapses | chemical hormone |
| route | specific nerves | blood plasma throughout the body |
| target | precise connected effector | only cells with the correct receptor respond |
| speed | usually rapid | usually slower |
| duration | often short-lived | often longer-lasting |
Hormones travel throughout the body but do not affect every cell; target cells need matching receptors. Nervous impulses travel along neurones rather than being carried in blood.
The central nervous system consists of the brain and spinal cord; nerves connect it to receptors in sense organs and to effectors.
| Direction | Route and purpose |
|---|---|
| into CNS | receptors in sense organs detect stimuli; sensory neurones carry impulses toward brain or spinal cord |
| within CNS | relay neurones connect pathways and allow information to be processed |
| out of CNS | motor neurones carry impulses to muscles or glands |
The nerves outside the brain and spinal cord belong to the peripheral nervous system, not the CNS. A sense organ contains receptors but is not itself part of the CNS.
Stimulation of receptors in a sense organ generates electrical impulses that travel along neurones into and out of the CNS to produce a rapid response.
| Stage | Information flow |
|---|---|
| 1 | a receptor detects a stimulus |
| 2 | a sensory neurone carries electrical impulses into the CNS |
| 3 | the CNS coordinates the response |
| 4 | a motor neurone carries impulses out to an effector |
| 5 | a muscle contracts or a gland secretes |
The dedicated pathway and electrical transmission along neurones allow responses to occur rapidly. Wider axons can conduct impulses faster because they offer less internal resistance to current flow.
The signal is electrical along a neurone but chemical across most synapses. Do not describe an impulse as blood-borne or say receptors themselves perform the final response.
At a synapse, a neurotransmitter carries a signal across the tiny gap from one neurone to the next cell.
| Stage | Event |
|---|---|
| 1 | an electrical impulse reaches the end of the presynaptic neurone |
| 2 | neurotransmitter is released into the synaptic cleft |
| 3 | molecules diffuse across the gap |
| 4 | neurotransmitter binds to complementary receptors on the postsynaptic membrane |
| 5 | a new electrical impulse is triggered if stimulation is sufficient |
Neurotransmitter is released on one side and receptors are concentrated on the other, making transmission one-way. Chemical diffusion also creates a small synaptic delay.
The neurotransmitter does not travel along the whole axon; the electrical impulse does. Neurotransmitter crosses only the synaptic cleft before being removed or broken down.
A withdrawal reflex is a rapid, automatic response that reduces tissue damage before conscious processing is required.
| Stage | Structure and event |
|---|---|
| 1 | heat or pain stimulates a receptor in the finger |
| 2 | a sensory neurone carries impulses to the spinal cord |
| 3 | neurotransmitters cross synapses to a relay neurone and then a motor neurone |
| 4 | the motor neurone carries impulses to an arm muscle |
| 5 | the muscle contracts as the effector and withdraws the hand |
Impulses can also travel to the brain so the person becomes aware of pain, but the protective withdrawal can begin through the spinal cord first.
A reflex is involuntary and stereotyped, not necessarily unconscious forever. The relay neurone lies inside the CNS; sensory and motor neurones connect the receptor and effector to it.
The eye is a sense organ whose structures refract light, control how much enters and convert focused light into nerve impulses.
| Structure | Function |
|---|---|
| cornea | transparent curved surface that provides most refraction |
| iris and pupil | iris muscles change pupil diameter to regulate light entry |
| lens | changes curvature to fine-focus light on the retina |
| ciliary muscles and suspensory ligaments | alter tension and therefore lens shape |
| retina | contains light-sensitive receptor cells |
| fovea | retinal region with high visual acuity |
| optic nerve | carries electrical impulses from retina to brain |
| sclera | tough outer layer that protects and supports the eye |
The pupil is a hole, not a muscle or receptor. The iris controls pupil size, while photoreceptors in the retina detect light after the cornea and lens have focused it.
The eye focuses by changing lens curvature and responds to light intensity by changing pupil diameter; these are separate control mechanisms.
| Viewing distance | Ciliary muscles | Suspensory ligaments | Lens | Refraction |
|---|---|---|---|---|
| near object | contract | loosen | thicker and more curved | bends light more |
| distant object | relax | tighten | thinner and less curved | bends light less |
| Light condition | Iris response | Pupil outcome |
|---|---|---|
| bright | circular muscles contract; radial muscles relax | constricts, reducing light entry and retinal damage |
| dim | radial muscles contract; circular muscles relax | dilates, increasing light entry |
The lens does not move forward and backward to focus. Accommodation changes lens shape; the pupil reflex changes light quantity but does not focus the image.
The skin helps regulate body temperature by changing sweat production and blood flow near the surface.
| Condition | Sweating | Skin blood vessels | Effect on heat transfer |
|---|---|---|---|
| body too hot | increases; evaporation removes thermal energy | arterioles vasodilate, increasing blood flow through surface capillaries | more heat lost by radiation and convection |
| body too cold | decreases | arterioles vasoconstrict, reducing surface-capillary blood flow | less heat transferred to the environment |
Temperature receptors and the brain coordinate these opposing responses. When temperature returns toward its normal range, the responses reduce through negative feedback.
Capillaries do not constrict or dilate because they lack muscular walls; arterioles controlling blood supply to them do. Sweat cools only when it evaporates, not merely when it is secreted.
Hormones are chemical messengers carried in blood; each is released by a source gland and acts on target tissues with matching receptors.
| Hormone | Main source | Required role or effect |
|---|---|---|
| adrenaline | adrenal glands | prepares for fight or flight: increases heart rate and blood supply to muscles and raises blood glucose availability |
| insulin | pancreas | lowers high blood glucose by promoting glucose uptake and conversion of glucose to glycogen |
| testosterone | testes | stimulates male secondary sexual characteristics and supports sperm production |
| oestrogen | ovaries | stimulates female secondary sexual characteristics and rebuilds the uterus lining |
| progesterone | ovary, especially corpus luteum | maintains the uterus lining |
A hormone's source is not necessarily its target. Insulin is made by the pancreas rather than the liver; adrenaline by adrenal glands; testosterone by testes; oestrogen and progesterone mainly by ovaries.
ADH, FSH and LH are released from the pituitary into blood, but they act on different target organs and regulate different processes.
| Hormone | Trigger or target | Main role and effect |
|---|---|---|
| ADH | released more when blood water content is low; targets kidney collecting ducts | increases duct permeability and water reabsorption, producing a smaller volume of concentrated urine |
| FSH | targets ovaries | stimulates maturation of an ovarian follicle and secretion of oestrogen |
| LH | targets ovaries | its surge triggers ovulation and supports formation of the corpus luteum |
More ADH produces a smaller volume of more concentrated urine. FSH acts earlier in the ovarian cycle to mature a follicle; LH triggers release of the egg.
At this syllabus level, the pituitary is the required release source for all three. FSH and LH are not produced by the ovaries, and ADH does not directly add water to the blood—it changes kidney permeability.