Edexcel A Level Biology Topic 7 Exam Questions

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25 Terms

1
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Explain why it is necessary for the cardiac output of marathon runners to increase during a race. (3)

  • M1: Increase supply of oxygenated blood to muscles

  • M2: To allow aerobic respiration

  • M3: To provide more energy (to meet the increased demands)

2
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Adrenaline acts on the heart to cause changes in heart rate. Deduce how adrenaline can cause a change in heart rate. (4)

  • M1: Adrenaline carried in the blood

  • M2: Acts on the sinoatrial node

  • M3: Increasing the frequency of impulses {produced by SAN/ that spread across the heart}

  • M4: Increasing the rate at which heart contracts

3
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At the start of exercise, breathing rate increases.

Explain how starting to exercise causes an increase in breathing rate. (3)

  • M1: Exercise initiates impulses from the {motor cortex/ stretch receptors in muscles/ proprioceptors}

  • M2: Impulses sent from the {ventilation centre/ respiratory control centre/ medulla oblongata}

  • M3: Leading to increased impulses to {intercostal muscles/ diaphragm}

4
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The demand for oxygen changes during exercise.

The change in demand affects the breathing rate.

Explain the effect of exercise on the changes in oxygen consumption. (4)

  • M1: Exercise will increase oxygen consumption

  • M2: Because there is increased aerobic respiration

  • M3: Because more {energy/ ATP} is needed by muscles

  • M4: Oxygen required to convert {lactate/ lactic acid} into {glucose/ pyruvate}

  • M5: Oxygen consumption begins to decrease after exercise

5
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Describe how a spirometer trace can be used to calculate the respiratory minute ventilation and the oxygen consumption per minute. (4)

Respiratory Minute Ventilation

  • M1: Find the difference in peak to trough volume (to give the tidal volume)

  • M2: Find Ventilation rate (count the no. of peaks in a stated time)

  • M3: Multiply the tidal volume by ventilation rate

Oxygen Consumption

  • M1: Difference in volume of one {peak/ trough} compared to a subsequent one

  • M2: Divide by time between the two peaks/ trough and multiply by 60

6
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Describe how the sinoatrial node (SAN) is involved in bringing about a change in heart rate as the level of activity increases. (2)

  • M1: More {stimulation/ depolarisation} of the SAN from the sympatric nervous system/ more impulses to the SAN

  • M2: Causing more frequent waves of depolarisation from the SAN to the atria

  • M3: Leading to more frequent {contraction of atria/ stimulation of AVN}

7
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Heat stress occurs when the core body temperature rises above 40 °C. Describe how thermoregulatory mechanisms are controlled to help marathon runners avoid heat stress. (4)

  • M1: Thermoreceptors in the hypothalamus/ skin detect increase in temperature

  • M2: {heat loss/ thermoregulatory} centre in the hypothalamus stimulated

  • M3: Hypothalamus sends impulses to sweat glands

  • M4: Increased blood flow to the surface of the skin by {vasodilation/ constriction of shunt vessels}

  • M5: Decreased metabolic rate

8
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Explain the role of the brain in reducing the student's heart rate after the exercise. (2)

  • M1: Chemoreceptors detect change in {carbon dioxide/ pH}

  • M2: The cardiovascular control centre receives impulses from the {chemoreceptors/ sends impulses to the heart}

  • M3: Therefore, impulses are transmitted along the parasympathetic {nerve/ nervous system/ nerve pathway} to the SAN reducing heart rate

9
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Describe how the brain reduces the activity of the sweat glands after the exercise. (2)

  • M1: Thermoreceptors detect a decrease in temperature

  • M2: {hypothalamus/ thermoregulatory centre} sends fewer impulses to sweat glands

10
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Explain why too much exercise could be harmful to the human body. (3)

  • M1: increased exercise results in wear and tear of {joints/ cartilage/ tendons/ ligaments}

  • M2: Therefore leading to joint damage

  • M3: Suppression of immune system

  • M4: Therefore leading to increased risk of infection

11
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Explain how transcription factors could activate insulin gene expression in beta cells. (3)

  • M1: Interaction between transcription factor and promoter region on gene

  • M2: RNA polymerase binds to promoter region

  • M3: {transcription/ mRNA} produced for insulin gene

12
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Extracellular enzymes are produced by specialised cells. Explain how groups of cells can produce the same enzyme. (3)

  • M1: Genes can be activated or deactivated

  • M2: These cells receive the same stimulus

  • M3: All of these cells have the gene for the enzyme {activated/ switched on}

  • M4: Resulting in production of mRNA for the enzyme

13
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Describe the changes caused when calcium ions bind to the molecules shown in the diagram (troponin, tropomyosin). (2)

  • M1: Tropomyosin is moved by troponin

  • M2: Myosin binding sites on actin are exposed

14
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Explain how changes to troponin/tropomyosin cause muscles to contract. (4)

  • M1: Myosin heads can bind to binding sites

  • M2: Bound myosin changes shape

  • M3: Actin filaments {slide/ pull} over the myosin

  • M4: Therefore {muscle fibres/ myofibril sarcomeres} shorten

  • M5: ATP hydrolysed/ ADP and {inorganic phosphate} released

15
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Describe how the concentration of calcium ions around the myofibrils is controlled. (3))

  • M1: Calcium ions released from sarcoplasmic reticulum

  • M2: In response to {nerve impulse/ action potential/ depolarisaiton} at neuromuscular junction

  • M3: Calcium channels open to allow calcium ions to cross the membrane/ enter the sarcoplasm

  • M4: Calcium ions taken back up into the sarcoplasmic reticulum by active transport

16
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Calcium ions are required for muscle contraction. Describe the role of calcium ions in the contraction of muscle fibres. (3)

  • M1: Calcium ions {bind/ attach} to the troponin

  • M2: Causing tropomyosin to be {displaced/ shape altered}

  • M3: Exposing myosin binding sites on actin

17
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Describe two structural differences between fast twitch muscle fibres and slow twitch muscle fibres. (2)

  • M1: Fast twitch fibres have {no/ few} mitochondria present/ slow twitch fibres have many mitochondria

  • M2: Fast twitch fibres have {no/ few} capillaries present/ slow twitch fibres have many capillaries present

18
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A muscle fibre is a specialised body cell. Explain how the structure of a muscle fibre is related to its specialised function. (3)

  • M1: {cell surface membrane/ sarcolemma} contain voltage gated channels to allow depolarisation of muscle fibres

  • M2: Many mitochondria for {aerobic respiration/ to supply ATP}

  • M3: Presence of {myofibrils/ actin and myosin}

  • M4: Myofibrils allow contraction of muscles

19
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The outer mitochondrial membrane is not permeable to hydrogen ions (H+ ). Explain the importance of this feature of the membrane. (4)

  • M1: To stop H+ diffusing out of mitochondrion/ into cytoplasm

  • M2: Therefore maintaining high concentration of H+ in the intermembrane space

  • M3: So {H+/ protons} can move down {concentration/ electrochemical gradient}

  • M4: By chemiosmosis

  • M5: to sythesise ATP

20
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Explain why some ATP is broken down during glycolysis. (2)

  • M1: because breakdown of ATP {donates phosphate to/ phosphorylates} glucose

  • M2: ATP supplies energy to break down the glucose

  • M3: To produce phosphorylated 3-carbon compounds

21
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The electron transport chain occurs in the cristae of mitochondria.

The electron transport chain involves a number of carrier molecules. Explain the role of these carrier molecules in the electron transport chain. (3)

  • M1: Receives hydrogen from reduced {NAD/ FAD}/ to allow reduced {NAD/ FAD} to be oxidised

  • M2: Break down into {protons/ hydrogen ions} and electrons

  • M3: Electrons transferred by a series of redox reactions

  • M4: Energy released is used to pump {hydrogen ions/ protons} into intermembranal space

22
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Explain the need for reduced NAD to be oxidised in a mitochondrion.

  • M1: So that hydrogen can be delivered to electron transport chain (allow: supply of {hydrogen ions/ protons})

  • M2: To allow {ATP synthesis/ chemiosmosis}

  • M3: To regenerate NAD

23
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Devise a valid investigation, using a spirometer, to compare the breathing rate and tidal volume of people with larger thorax vs smaller thorax. (4)

  • M1: Select people with different thorax sizes/ large thorax and small thorax

  • M2: Select people who are similar in other respects (e.g. same age, same fitness level, same sex)

  • M3: One relevant variable controlled (e.g. temperature, same level of previous activity, data collected when subjects were at rest)

  • M4: Measurement of tidal volume from spirometer trace (difference in peak to trough volume gives tidal volume)

  • M5: Measure breathing rate as number of {peaks / troughs} in a set time

24
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Explain why there is a greater ratio of wound infections in open surgery compared with keyhole surgery. (2)

  • M1: Larger opening / slower recovery time

  • M2: Access for (more) {pathogens / bacteria} / (therefore) more time for { pathogen entry / bacteria entry / infection }

25
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Explain how the production of sweat is controlled during exercise in humans. (4)

  • M1: By {homeostasis / a negative feedback response}

  • M2: Thermoreceptors {in the skin / hypothalamus} detect a rise in temperature

  • M3: Send impulses to the {heat loss centre / thermoregulatory centre / hypothalamus}

  • M4: {heat loss centre / thermoregulatory centre / hypothalamus} sends impulses to the sweat glands

  • M5: to increase sweat production