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BioMedical Admissions Test (BMAT) Section 2: Scientific Knowledge and Applications — Biology Flashcards

52 question-and-answer cards covering Section 2: Scientific Knowledge and Applications — Biology as it is examined in BioMedical Admissions Test (BMAT). 24 of them are printed below, taken from across the deck — no signup, no paywall on the preview.

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24 sample cards from the Section 2: Scientific Knowledge and Applications — Biology deck

Sampled from the end of the deck, so these are different cards from the ones shown on the syllabus page.

  1. What is codominance? Give an example.

    Codominance is when both alleles in a heterozygote are fully expressed in the phenotype. Example: human ABO blood group, where alleles $I^A$ and $I^B$ are codominant, so genotype $I^A I^B$ gives blood group AB.

  2. How are sex-linked characteristics inherited, and why are males more often affected by X-linked recessive conditions?

    Sex-linked genes are carried on the sex chromosomes (usually X). Males (XY) have only one X, so a single recessive allele (e.g. for haemophilia or red-green colour blindness) is always expressed; females (XX) need two copies to be affected and can be carriers.

  3. Distinguish between continuous and discontinuous variation, giving an example of each.

    Continuous variation shows a range of values controlled by many genes and influenced by environment (e.g. height, mass). Discontinuous variation shows distinct categories with no intermediates, usually controlled by one or few genes (e.g. blood group, sex).

  4. Outline the process of natural selection.

    Variation exists within a population (from mutation). There is competition for limited resources. Individuals with advantageous alleles are better adapted and more likely to survive and reproduce (survival of the fittest). They pass on these favourable alleles, so over generations the allele frequency increases in the population.

  5. What is the difference between a mutation and the role it plays in variation?

    A mutation is a random change in the base sequence of DNA (or chromosome structure/number). Mutations are the original source of new alleles and therefore of genetic variation, providing the raw material on which natural selection acts.

  6. Describe the double circulatory system of mammals.

    Blood passes through the heart twice for each complete circuit. The pulmonary circuit carries deoxygenated blood from the heart to the lungs and back. The systemic circuit carries oxygenated blood from the heart to the body and back, maintaining high pressure for efficient delivery.

  7. Compare the structure and function of arteries, veins, and capillaries.

    Arteries: thick muscular/elastic walls, narrow lumen, carry blood at high pressure away from the heart. Veins: thinner walls, wide lumen, valves to prevent backflow, carry blood at low pressure to the heart. Capillaries: one-cell-thick walls for short diffusion distance, site of exchange between blood and tissues.

  8. Trace the path of blood through the heart starting from the vena cava.

    Vena cava → right atrium → tricuspid valve → right ventricle → pulmonary artery → lungs → pulmonary vein → left atrium → bicuspid (mitral) valve → left ventricle → aorta → body.

  9. Why is the wall of the left ventricle thicker than the right ventricle?

    The left ventricle pumps oxygenated blood around the whole body (systemic circulation) at high pressure, so it needs a thicker, more muscular wall. The right ventricle only pumps blood the short distance to the lungs at lower pressure.

  10. Write the balanced equation for aerobic respiration.

    $$\ce{C6H12O6 + 6O2 -> 6CO2 + 6H2O}$$ This releases energy (ATP). In words: glucose + oxygen → carbon dioxide + water.

  11. Compare aerobic and anaerobic respiration in terms of oxygen, products, and energy yield.

    Aerobic respiration uses oxygen, fully oxidises glucose to $\ce{CO2}$ and water, and releases a large amount of energy (~38 ATP). Anaerobic respiration occurs without oxygen, gives a small energy yield (~2 ATP), and produces lactate in animals or ethanol and $\ce{CO2}$ in yeast/plants.

  12. List the adaptations of the alveoli for efficient gas exchange.

    Large surface area (many alveoli), thin walls (one cell thick) giving a short diffusion distance, moist surface for gases to dissolve, and a dense capillary network with continuous blood flow to maintain a steep concentration gradient.

  13. Describe the changes during inhalation (breathing in).

    The diaphragm contracts and flattens, and the external intercostal muscles contract, raising the ribs up and out. This increases thoracic volume, decreases pressure below atmospheric, so air is drawn into the lungs.

  14. Describe the structure and function of a motor neurone.

    A motor neurone has a cell body with dendrites, a long myelinated axon, and motor end plates. It carries electrical impulses from the central nervous system to effectors (muscles or glands). Myelin (Schwann cells) insulates the axon and speeds up impulse transmission.

  15. Outline the sequence of a reflex arc.

    Stimulus → receptor → sensory neurone → relay (intermediate) neurone in the spinal cord/CNS → motor neurone → effector → response. It is rapid and automatic, bypassing conscious brain processing for protection.

  16. How is an impulse transmitted across a synapse?

    An impulse arrives at the presynaptic terminal, triggering vesicles to release neurotransmitter into the synaptic cleft. The neurotransmitter diffuses across and binds to receptors on the postsynaptic membrane, generating a new impulse. It is then broken down/reabsorbed.

  17. Compare nervous and hormonal (endocrine) control.

    Nervous control uses electrical impulses along neurones, is very fast, short-lived, and targets specific cells. Hormonal control uses chemical hormones transported in the blood, is slower, longer-lasting, and may affect many target organs.

  18. Define homeostasis and give two examples of conditions it regulates.

    Homeostasis is the maintenance of a constant internal environment within narrow limits despite external changes. Examples include regulation of blood glucose concentration, body temperature, blood pH, and water/osmotic balance.

  19. Explain how insulin and glucagon control blood glucose concentration (negative feedback).

    When blood glucose is high, the pancreas releases insulin, which stimulates cells to take up glucose and the liver to convert glucose to glycogen, lowering it. When glucose is low, glucagon is released, stimulating the liver to break glycogen down to glucose, raising it. This is negative feedback.

  20. What is a food chain, and what do the arrows represent?

    A food chain shows the feeding relationships and transfer of energy/biomass between organisms, starting with a producer. The arrows point in the direction of energy flow, i.e. from the organism being eaten to the organism that eats it.

  21. Why is energy lost between trophic levels, and roughly how much is transferred?

    Energy is lost as heat from respiration, in movement, and in undigested material (faeces) and excretion (urine). Only about 10% of energy is transferred to the next trophic level, which limits food chains to about 4–5 links.

  22. Distinguish between pathogens and the main types of pathogen.

    A pathogen is a microorganism that causes disease. Main types: bacteria (e.g. tuberculosis), viruses (e.g. influenza, HIV), fungi (e.g. athlete's foot), and protists/protozoa (e.g. malaria, caused by Plasmodium).

  23. Distinguish between the body's non-specific defences and the specific immune response.

    Non-specific (innate) defences act the same against all pathogens: skin, mucus, stomach acid, and phagocytosis. The specific (adaptive) response is targeted: lymphocytes recognise particular antigens, with B-cells producing specific antibodies and T-cells destroying infected cells, and it creates immunological memory.

  24. Explain how vaccination produces immunity.

    A vaccine introduces a dead, weakened, or antigenic part of a pathogen. The antigens stimulate B-lymphocytes to produce specific antibodies and memory cells. On later infection by the real pathogen, memory cells trigger a faster, larger secondary response, destroying it before symptoms develop (active immunity).

What this deck covers

The Section 2: Scientific Knowledge and Applications — Biology deck follows the BioMedical Admissions Test (BMAT) Section 2: Scientific Knowledge and Applications — Biology syllabus — 4 chapters and 15 topics — so questions land on material that is genuinely examinable rather than trivia around it. That works out to roughly 13.0 cards per chapter.

Answers are written to be recallable, not just readable — averaging about 249 characters, which is long enough to carry the reasoning and short enough to say out loud.

A deck like this earns its keep on the second and third pass. Read the syllabus first so you know the shape of the subject, then use the cards to find the specific facts that have not stuck.

Section 2: Scientific Knowledge and Applications — Biology flashcards FAQ

How many Section 2: Scientific Knowledge and Applications — Biology flashcards are in this BioMedical Admissions Test (BMAT) deck?

52 cards. This page previews 24 of them, sampled evenly across the deck so you can judge the difficulty before installing anything.

Are these BioMedical Admissions Test (BMAT) flashcards free?

Yes. The preview here is free to read with no signup, and the full 52-card deck is free inside the Examius app.

What do the Section 2: Scientific Knowledge and Applications — Biology cards cover?

They follow the BioMedical Admissions Test (BMAT) Section 2: Scientific Knowledge and Applications — Biology syllabus — 4 chapters and 15 topics — so the questions track what is actually examinable.

How should I use these flashcards?

Read the syllabus first so you know the shape of the subject, then drill the deck. Examius schedules each card with spaced repetition, so cards you keep missing come back sooner and ones you know drift further apart.