Why transport systems are needed, the double circulatory system, heart structure, blood vessels, blood components, and immunity and vaccination.
As organisms grow larger, diffusion alone cannot deliver substances fast enough — the distance from the surface to the innermost cells becomes too great. Multicellular organisms therefore develop specialised transport systems to move materials quickly over long distances.
A small organism has a high surface area to volume ratio, so diffusion supplies every cell adequately. In a large organism the ratio is much lower, and cells deep inside would starve of oxygen or accumulate waste. Transport systems solve this by:
Humans have a closed, double circulatory system:
Pulmonary circulation: right ventricle → lungs → left atrium. Blood picks up oxygen and loses CO₂.
Systemic circulation: left ventricle → body → right atrium. Blood delivers oxygen and nutrients; returns with CO₂ and waste.
The heart is a muscular pump with four chambers: two atria (receive blood) and two ventricles (pump blood out). Valves prevent backflow.

| Vessel | Wall structure | Lumen | Valves | Direction | Function |
|---|---|---|---|---|---|
| Artery | thick, muscular, elastic | narrow | no | away from heart | carries blood at high pressure |
| Vein | thin, less muscular | wide | yes | toward heart | returns blood at low pressure |
| Capillary | one cell thick | very narrow | no | connects arteries to veins | site of exchange between blood and tissues |
Capillaries are so thin that red blood cells must squeeze through in single file. Their walls allow plasma to leak out, forming tissue fluid that bathes cells.
Blood is a liquid connective tissue. It has four main components:
Plasma is the pale yellow liquid portion of blood (about 55%). It transports:
Red blood cells carry oxygen using haemoglobin, an iron-containing protein that combines reversibly with oxygen:
haemoglobin + oxygen ⇌ oxyhaemoglobin
In the lungs (high O₂): oxyhaemoglobin forms. In the tissues (low O₂): oxygen is released.
Adaptations of red blood cells:
White blood cells defend the body. Two main types:
Phagocytes — engulf and destroy pathogens by phagocytosis (the phagocyte surrounds the pathogen, encloses it in a vacuole, and enzymes from lysosomes digest it).
Lymphocytes — produce antibodies. B-lymphocytes differentiate into:
T-lymphocytes coordinate the immune response and attack infected or abnormal cells.
Platelets are cell fragments that trigger blood clotting when a vessel is damaged:
damaged tissue → platelets release thromboplastin → prothrombin → thrombin → fibrinogen → fibrin mesh → clot forms
Clotting prevents excessive blood loss and blocks entry of pathogens.
Antigens are foreign molecules (usually on pathogen surfaces) that trigger an immune response.
Antibodies are proteins produced by B-lymphocytes that are specific to one antigen. They may neutralise toxins, cause pathogens to clump (agglutination), or mark them for destruction.
| Type of immunity | How acquired | Duration |
|---|---|---|
| Active natural | body produces own antibodies after infection | long-lasting |
| Active artificial | body produces own antibodies after vaccination | long-lasting |
| Passive natural | antibodies passed from mother to baby via placenta or breast milk | temporary |
| Passive artificial | ready-made antibodies injected | temporary |
Vaccination works by introducing weakened or dead pathogens, or their antigens, so the immune system produces antibodies and memory cells without the person suffering the disease. If the pathogen is later encountered, the memory cells allow a rapid secondary immune response.
Active immunity lasts because memory cells are produced. Passive immunity is immediate but short-lived because no memory cells are made — the antibodies eventually break down.