AQA
    Level 3
    QN: 601/4625/4
    Curriculum Active

    AQA Level 3 Advanced GCE in Biology

    Official qualification regulated by Ofqual, awarded by AQA. Classified as a GCE A Level.

    Qualification Level
    Level 3
    Awarding Body
    AQA
    Syllabus Units
    3 Units
    Guided Hours
    Flexible
    Instant access to interactive lessons, quizzes, and spaced revision.

    Course Syllabus & Study Modules

    Complete breakdown of verified curriculum topics and learning objectives.

    1

    All cells arise from other cells

    Being non-living, viruses do not undergo cell division. Following injection of their nucleic acid, the infected host cell replicates the virus particles.

    Verified
    Key Learning Objectives:
    • Describe viral replication in sequence, from attachment through to release of new virus particles.
    • Explain why viral replication is not cell division and cannot happen outside a host cell.
    • Explain why a virus can infect only certain cell types, referring to attachment proteins and receptors.
    • Suggest why a drug that inhibits reverse transcriptase reduces the replication of a retrovirus.
    2

    All cells arise from other cells

    Binary fission in prokaryotic cells involves: replication of the circular DNA and of plasmids division of the cytoplasm to produce two daughter cells, each with a single copy of the circular DNA and a variable number of copies of plasmids.

    Verified
    Key Learning Objectives:
    • Describe binary fission in the order the specification gives, from replication of the circular DNA to division of the cytoplasm.
    • Explain why the two daughter cells may contain different numbers of plasmids but the same circular DNA.
    • Complete a table distinguishing binary fission from a cell cycle involving mitosis.
    • Explain why bacterial numbers can rise exponentially under favourable conditions.
    3

    All cells arise from other cells

    Division of the cytoplasm (cytokinesis) usually occurs, producing two new cells.

    Verified
    Key Learning Objectives:
    • Describe how the cytoplasm divides in an animal cell and in a plant cell, and explain the difference.
    • Suggest what a cell would look like if mitosis occurred but cytokinesis was prevented.
    • Explain why cytokinesis is described as usually occurring rather than always occurring.
    • Interpret data from a drug that inhibits cytokinesis and state what happens to cell number and nuclei.
    4

    All cells arise from other cells

    DNA replication occurs during the interphase of the cell cycle.

    Verified
    Key Learning Objectives:
    • State when in the cell cycle DNA is replicated.
    • Explain the difference between DNA mass and chromosome number during interphase.
    • Describe the structure of a chromosome after S phase.
    • Explain the importance of DNA replication occurring before mitosis.
    5

    All cells arise from other cells

    Eukaryotic cells that do retain the ability to divide show a cell cycle.

    Verified
    Key Learning Objectives:
    • Name the stages of the cell cycle in order and state what happens to the DNA in each.
    • Explain why interphase is the longest stage and why calling it a resting stage is wrong.
    • Complete a table distinguishing a cell cycle involving mitosis from binary fission, using DNA shape, cell type and number of daughter cells.
    • Predict how the proportion of cells seen in each stage on a slide relates to the length of that stage.
    6

    All cells arise from other cells

    Many cancer treatments are directed at controlling the rate of cell division.

    Verified
    Key Learning Objectives:
    • Explain how a drug that prevents DNA replication stops a cancer cell completing the cell cycle.
    • Explain how a spindle inhibitor blocks mitosis and state at which stage division halts.
    • Suggest why hair loss and reduced immunity are common side effects of chemotherapy.
    • Evaluate data showing the effect of increasing drug concentration on the number of cells in a culture.
    7

    All cells arise from other cells

    Meiosis is covered in section 3.4.3 Students should be able to: recognise the stages of the cell cycle: interphase, prophase, metaphase, anaphase and telophase (including cytokinesis) explain the appearance of cells in each stage of mitosis.

    Verified
    Key Learning Objectives:
    • Name the stage of mitosis shown in a micrograph and explain the appearance from the event taking place.
    • Distinguish metaphase from anaphase in an image by the position and movement of the chromatids.
    • Explain what a cell containing two nuclei and one cytoplasm shows about which stage was blocked.
    • Recognise interphase cells on a slide and explain why they are the most numerous.
    8

    All cells arise from other cells

    Mitosis is a controlled process.

    Verified
    Key Learning Objectives:
    • Describe two checkpoints in the cell cycle and state what each one verifies before division continues.
    • Explain how genes control whether the cell cycle continues or is halted.
    • Explain how apoptosis prevents a cell with damaged DNA from producing damaged daughter cells.
    • Predict the effect on a tissue of losing the function of a gene that normally halts the cell cycle.
    9

    All cells arise from other cells

    Mitosis is the part of the cell cycle in which a eukaryotic cell divides to produce two daughter cells, each with the identical copies of DNA produced by the parent cell during DNA replication.

    Verified
    Key Learning Objectives:
    • Explain why the two cells produced by mitosis are genetically identical, referring to replication in interphase.
    • State three roles of mitosis in a multicellular organism.
    • Contrast mitosis with meiosis in terms of number of divisions, number of daughter cells and genetic variation.
    • Complete a comparison of mitosis and binary fission using DNA shape, cell type and number of daughter cells.
    10

    All cells arise from other cells

    Required practical 2: Preparation of stained squashes of cells from plant root tips; set-up and use of an optical microscope to identify the stages of mitosis in these stained squashes and calculation of a mitotic index.

    Verified
    Key Learning Objectives:
    • Describe how to prepare a stained root tip squash and explain the purpose of the acid, the stain and the squash.
    • Describe how to set up and use an optical microscope to identify stages of mitosis.
    • Calculate a mitotic index from counts of cells in mitosis and total cells, and express it as a percentage.
    • Suggest two reasons other than counting errors why students obtain different mitotic indices from the same method.
    11

    All cells arise from other cells

    The behaviour of chromosomes during interphase, prophase, metaphase, anaphase and telophase of mitosis.

    Verified
    Key Learning Objectives:
    • Describe what happens to the chromosomes in each named stage of mitosis, in order.
    • Identify the stage of mitosis shown in a micrograph and justify the answer from what is visible.
    • Explain why chromatids appear V shaped as they move towards the poles in anaphase.
    • Explain why most cells on a stained root tip slide are in interphase rather than in a mitotic stage.
    12

    All cells arise from other cells

    The role of spindle fibres attached to centromeres in the separation of chromatids.

    Verified
    Key Learning Objectives:
    • Describe where spindle fibres attach to a chromosome and why attachment from both poles is needed.
    • Explain how shortening spindle fibres separates sister chromatids in anaphase.
    • Suggest the effect on the daughter cells of a drug that prevents spindle fibres forming.
    • Explain why a cell whose mitochondria are inhibited cannot complete anaphase.
    13

    All cells arise from other cells

    Uncontrolled cell division can lead to the formation of tumours and of cancers.

    Verified
    Key Learning Objectives:
    • Explain how a single base change in DNA can lead to uncontrolled cell division, working through the protein produced.
    • Distinguish a benign tumour from a malignant tumour using rate of growth, encapsulation and spread.
    • Explain why the immune system can identify tumour cells as abnormal body cells.
    • Suggest why a blood test may detect a cancer before a tumour can be seen or felt.
    14

    All cells arise from other cells

    Within multicellular organisms, not all cells retain the ability to divide.

    Verified
    Key Learning Objectives:
    • Name two specialised cells that cannot divide and give the structural reason in each case.
    • Explain why a root tip is chosen over other plant tissue when preparing a slide to observe mitosis.
    • Suggest why damage to cardiac muscle after a heart attack is not repaired in the way a skin wound is.
    • Identify, from a description of a tissue, whether it is likely to contain cells that are still in the cell cycle.
    15

    Alteration of the sequence of bases in DNA can alter the

    Due to the degenerate nature of the genetic code, not all such mutations result in a change to the encoded amino acid.

    Verified
    Key Learning Objectives:
    • Explain, using the number of triplets and the number of amino acids, why the genetic code must be degenerate.
    • Explain why a base substitution may produce no change at all in the encoded polypeptide.
    • Select the correct property of the genetic code, degenerate, non-overlapping or universal, for a given exam context.
    16

    Alteration of the sequence of bases in DNA can alter the

    Gene mutations might arise during DNA replication. They include addition, deletion, substitution, inversion, duplication and translocation of bases.

    Verified
    Key Learning Objectives:
    • Name six types of gene mutation and describe what each does to the base sequence.
    • Explain why a mutation arising during DNA replication is passed on to daughter cells.
    • Predict the effect of a given mutation on the encoded polypeptide, using the terms triplet, codon and amino acid sequence.
    17

    Alteration of the sequence of bases in DNA can alter the

    Gene mutations occur spontaneously.

    Verified
    Key Learning Objectives:
    • State what is meant by a spontaneous mutation and give its main cause in a dividing cell.
    • Explain why a resistance allele must already exist in a population before the selection pressure is applied.
    • Write a natural selection explanation in the correct order, using allele rather than gene and frequency rather than number.
    18

    Alteration of the sequence of bases in DNA can alter the

    Mutations can result in a different amino acid sequence in the encoded polypeptide.

    Verified
    Key Learning Objectives:
    • Explain how a change to one DNA triplet alters the amino acid sequence of the polypeptide produced.
    • Explain how a changed amino acid alters the tertiary structure of a protein, referring to R group interactions.
    • Predict the effect on enzyme activity of a substitution affecting the active site, using complementary shape and enzyme-substrate complexes.
    19

    Alteration of the sequence of bases in DNA can alter the

    Some gene mutations change only one triplet code.

    Verified
    Key Learning Objectives:
    • Explain why a base substitution changes only one triplet, referring to the non-overlapping triplet code.
    • Predict, from the new triplet a substitution creates, whether the polypeptide has one amino acid changed, no change at all, or is shortened at a premature stop triplet.
    • Explain why a mutation affecting one triplet can have effects ranging from none to a completely non-functional protein.
    20

    Alteration of the sequence of bases in DNA can alter the

    Some gene mutations change the nature of all base triplets downstream from the mutation, ie result in a frame shift.

    Verified
    Key Learning Objectives:
    • Explain why the addition or deletion of one base causes a frame shift while a substitution does not.
    • Rewrite a given base sequence in codons after an insertion to show which codons change.
    • Explain why a frame shift near the start of a gene usually has a greater effect than one near the end.
    21

    Alteration of the sequence of bases in DNA can alter the

    Students should be able to relate the nature of a gene mutation to its effect on the encoded polypeptide.

    Verified
    Key Learning Objectives:
    • Identify the type of mutation from two given DNA sequences and state how many triplets are affected.
    • Predict the effect of a given mutation on the length and the amino acid sequence of the polypeptide.
    • Justify why two different mutations in the same gene can have very different effects on the protein.
    22

    Alteration of the sequence of bases in DNA can alter the

    The mutation rate is increased by mutagenic agents.

    Verified
    Key Learning Objectives:
    • Name three mutagenic agents and describe the mechanism by which each raises the mutation rate.
    • Explain why a mutagen increases the number of mutations without determining which gene mutates.
    • Distinguish the consequences of a mutagen-induced mutation in a somatic cell from one in a cell that forms gametes.
    23

    ATP

    A single molecule of adenosine triphosphate (ATP) is a nucleotide derivative and is formed from a molecule of ribose, a molecule of adenine and three phosphate groups.

    Verified
    Key Learning Objectives:
    • Name the three components of an ATP molecule and identify which one is removed during hydrolysis.
    • Write the equation for the hydrolysis of ATP and name the enzyme that catalyses it and the enzyme that reverses it.
    • Explain two properties of ATP that make it a suitable immediate source of energy rather than a long-term store.
    24

    ATP

    The hydrolysis of ATP can be coupled to energy-requiring reactions within cells.

    Verified
    Key Learning Objectives:
    • Describe the role of ATP hydrolysis in the movement of a myosin head during muscle contraction.
    • Explain how the energy released from ATP is coupled to a named energy-requiring process rather than lost as heat.
    • Suggest, for an organism that no longer needs to carry out one ATP-consuming process, two other processes the saved ATP could be used for.
    25

    ATP

    The inorganic phosphate released during the hydrolysis of ATP can be used to phosphorylate other compounds, often making them more reactive.

    Verified
    Key Learning Objectives:
    • Explain how the phosphate released from ATP makes another molecule more reactive, using glucose in glycolysis as the example.
    • Give two properties of ATP, other than the amount of energy released, that make it suitable as an immediate energy source.
    • Distinguish phosphorylation of a substrate from the condensation reaction that forms ATP from ADP.
    26

    Biodiversity within a community

    An index of diversity describes the relationship between the number of species in a community and the number of individuals in each species.

    Verified
    Key Learning Objectives:
    • Calculate an index of diversity from a table of species counts, showing the n(n - 1) values you summed.
    • Explain why two communities with the same species richness can have different indices of diversity.
    • Interpret calculated index values to compare the stability or harshness of different environments.
    27

    Biodiversity within a community

    Biodiversity can relate to a range of habitats, from a small local habitat to the Earth.

    Verified
    Key Learning Objectives:
    • State the scale of habitat to which a given biodiversity measurement applies, and explain why it cannot be generalised beyond it.
    • Criticise a conclusion drawn from biodiversity data collected at a single site or at a single time of year.
    • Distinguish species richness from genetic diversity when interpreting a biodiversity figure.
    28

    Biodiversity within a community

    Farming techniques reduce biodiversity. The balance between conservation and farming.

    Verified
    Key Learning Objectives:
    • Explain how a named farming practice lowers biodiversity by removing habitats, niches or food sources.
    • Describe two conservation measures that raise biodiversity on farmland without stopping production.
    • Evaluate the conflict between maximising crop yield and conserving biodiversity, including the cost of conservation.
    29

    Biodiversity within a community

    Species richness is a measure of the number of different species in a community.

    Verified
    Key Learning Objectives:
    • Define species richness and state what it does not take into account.
    • Compare the species richness of two communities from a figure and state the limitation of that comparison.
    • Describe how random sampling and repeat samples make a species richness estimate representative of a habitat.
    30

    Carbohydrates

    A condensation reaction between two monosaccharides forms a glycosidic bond.

    Verified
    Key Learning Objectives:
    • Describe the formation of a glycosidic bond between two monosaccharides, naming the reaction and the molecule released.
    • Identify from a diagram whether the glycosidic bonds shown are 1,4 or 1,6, and say what that means for the shape of the chain.
    • Explain why a glycosidic bond between two beta-glucose molecules requires one of them to be rotated through 180 degrees.
    31

    Carbohydrates

    Biochemical tests using Benedict's solution for reducing sugars and non-reducing sugars and iodine/potassium iodide for starch.

    Verified
    Key Learning Objectives:
    • Describe the method for testing a solution for reducing sugars, including the reagent, heating, and the positive result.
    • Describe how to test for a non-reducing sugar, explicitly including boiling with dilute acid, neutralisation, and retesting.
    • Explain how the Benedict's test can be made quantitative using a colorimeter and a calibration curve.
    32

    Carbohydrates

    Disaccharides are formed by the condensation of two monosaccharides: maltose is a disaccharide formed by condensation of two glucose molecules sucrose is a disaccharide formed by condensation of a glucose molecule and a fructose molecule lactose is a disaccharide formed by condensation of a glucose molecule and a galactose molecule.

    Verified
    Key Learning Objectives:
    • State which two monosaccharides condense to form maltose, sucrose and lactose.
    • Describe how a disaccharide is formed and broken down, naming the bond, the reaction and the enzyme involved.
    • Suggest why an organism supplied with a disaccharide shows a delay before its respiration rate rises.
    33

    Carbohydrates

    Glucose has two isomers, α-glucose and β-glucose, with structures: Polysaccharides are formed by the condensation of many glucose units.

    Verified
    Key Learning Objectives:
    • Explain the structural difference between alpha-glucose and beta-glucose, naming the carbon atom involved.
    • Draw or label a diagram to show the inverted hydrogen and hydroxyl groups on carbon 1 of beta-glucose.
    • Explain how the isomer used determines whether the resulting polysaccharide chain is coiled, branched or straight.
    34

    Carbohydrates

    Glycogen and starch are formed by the condensation of α- glucose. Cellulose is formed by the condensation of β-glucose.

    Verified
    Key Learning Objectives:
    • State which glucose isomer forms starch, glycogen and cellulose, and give the bond type in each.
    • Compare and contrast starch and cellulose in linked sentences covering monomer, bond, branching and chain shape.
    • Explain why glycogen has more 1,6 branch points than amylopectin and what that means for its chain structure.
    35

    Carbohydrates

    Monosaccharides are the monomers from which larger carbohydrates are made. Glucose, galactose and fructose are common monosaccharides.

    Verified
    Key Learning Objectives:
    • Define monosaccharides as the monomers of larger carbohydrates.
    • Name glucose, galactose and fructose as common monosaccharides.
    • Explain how monosaccharide monomers relate to the formation of larger carbohydrates.
    36

    Carbohydrates

    The basic structure and functions of glycogen, starch and cellulose.

    Verified
    Key Learning Objectives:
    • Describe the basic structure of glycogen, starch and cellulose in terms of monomer, bond type and branching.
    • State where each of the three polysaccharides is found and what job it does there.
    • Explain why cellulose is described as a structural polysaccharide while starch and glycogen are stores of glucose.
    37

    Carbohydrates

    The relationship of structure to function of these substances in animal cells and plant cells.

    Verified
    Key Learning Objectives:
    • Explain why an insoluble polysaccharide is a better store of glucose in a cell than the equivalent mass of soluble glucose.
    • Explain how branching in glycogen allows glucose to be released more rapidly than from amylose.
    • Explain how hydrogen bonding between cellulose chains produces microfibrils and gives the plant cell wall tensile strength.
    38

    Cell recognition and the immune system

    Antibody structure.

    Verified
    Key Learning Objectives:
    • Draw and label an antibody, marking the variable regions, constant region, hinge region and disulfide bridges.
    • Explain how the variable region gives an antibody its specificity, referring to amino acid sequence and tertiary structure.
    • Explain how having two binding sites and a flexible hinge makes agglutination possible.
    39

    Cell recognition and the immune system

    Definition of antibody.

    Verified
    Key Learning Objectives:
    • State the definition of an antibody in one sentence containing all four creditworthy elements.
    • Explain why a given antibody binds only one antigen, referring to tertiary structure and complementary shape.
    • Identify and correct an answer that describes antibody binding using enzyme vocabulary such as active site or induced fit.
    40

    Cell recognition and the immune system

    Definition of antigen. The effect of antigen variability on disease and disease prevention.

    Verified
    Key Learning Objectives:
    • State in one sentence what an antigen is, naming the type of molecule, where it is found and what it does.
    • Explain, as an unbroken chain from mutation to symptoms, why a person can catch influenza repeatedly.
    • Suggest why a vaccine effective against one strain of a pathogen may give no protection against another strain of the same species.
    41

    Cell recognition and the immune system

    Each type of cell has specific molecules on its surface that identify it. These molecules include proteins and enable the immune system to identify: pathogens cells from other organisms of the same species abnormal body cells toxins.

    Verified
    Key Learning Objectives:
    • Name the four categories of material the immune system identifies as foreign.
    • Explain how the tertiary structure of a surface protein allows a lymphocyte to distinguish a self cell from a non-self cell.
    • Suggest why tissue transplanted from another person is attacked while the patient's own tissue is not.
    42

    Cell recognition and the immune system

    Ethical issues associated with the use of vaccines and monoclonal antibodies.

    Verified
    Key Learning Objectives:
    • Identify three distinct ethical issues raised by the use of vaccines and three raised by the use of monoclonal antibodies.
    • Explain why a control group in a cancer drug trial is given an existing treatment rather than a placebo.
    • Construct a balanced argument, for and against, about a named use of a vaccine or monoclonal antibody, and justify a conclusion.
    43

    Cell recognition and the immune system

    How HIV causes the symptoms of AIDS. Why antibiotics are ineffective against viruses.

    Verified
    Key Learning Objectives:
    • Explain the chain of events from the loss of helper T cells to the appearance of AIDS symptoms.
    • State two pieces of evidence a doctor needs before diagnosing AIDS, and explain why an antibody test alone is insufficient.
    • Give a named bacterial structure or process targeted by antibiotics and explain why its absence makes viruses unaffected.
    44

    Cell recognition and the immune system

    Phagocytosis of pathogens. The subsequent destruction of ingested pathogens by lysozymes.

    Verified
    Key Learning Objectives:
    • Describe phagocytosis as a sequence of distinct stages, naming the vesicle and the organelle involved.
    • Explain what happens to the products of hydrolysis inside a phagocyte.
    • Distinguish the non-specific action of a phagocyte from the specific response of a lymphocyte.
    45

    Cell recognition and the immune system

    Structure of the human immunodeficiency virus (HIV) and its replication in helper T cells.

    Verified
    Key Learning Objectives:
    • Label the structure of HIV from the RNA core outwards, naming the enzyme it carries.
    • Describe HIV replication in a helper T cell as a series of ordered steps.
    • Explain why a drug that inhibits reverse transcriptase would slow HIV replication but not affect the host cell's own transcription.
    46

    Cell recognition and the immune system

    Students should be able to: discuss ethical issues associated with the use of vaccines and monoclonal antibodies evaluate methodology, evidence and data relating to the use of vaccines and monoclonal antibodies.

    Verified
    Key Learning Objectives:
    • Discuss the ethical issues surrounding the development and use of vaccines and monoclonal antibodies, including animal testing and clinical trial risks.
    • Evaluate methodology and data from vaccine and mAb studies by identifying limitations such as sample size, study duration, and lack of controls.
    • Interpret standard deviations and error bars correctly, understanding their relationship to statistical significance without overgeneralising.
    47

    Cell recognition and the immune system

    The differences between active and passive immunity.

    Verified
    Key Learning Objectives:
    • Contrast active and passive immunity in paired statements covering antigen exposure, memory cells, speed and duration.
    • Classify examples such as vaccination, infection, breast milk and antivenom as active or passive, natural or artificial.
    • Explain why passive immunity gives immediate but temporary protection.
    48

    Cell recognition and the immune system

    The formation of an antigen-antibody complex, leading to the destruction of the antigen, limited to agglutination and phagocytosis of bacterial cells.

    Verified
    Key Learning Objectives:
    • Describe how an antigen-antibody complex forms and explain why binding is specific.
    • Explain how agglutination increases the rate at which bacteria are destroyed by phagocytes.
    • Describe the destruction of bacterial cells by agglutination and phagocytosis, as limited by the specification.
    49

    Cell recognition and the immune system

    The response of B lymphocytes to a foreign antigen, clonal selection and the release of monoclonal antibodies (the humoral response).

    Verified
    Key Learning Objectives:
    • Describe the humoral response from antigen binding to antibody secretion, using the terms clonal selection and clonal expansion correctly.
    • Explain why the antibodies released by one clone of plasma cells are all identical.
    • Explain the role of the helper T cell in activating a B cell, and predict what would happen to antibody production if helper T cells were destroyed.
    50

    Cell recognition and the immune system

    The response of T lymphocytes to a foreign antigen (the cellular response).

    Verified
    Key Learning Objectives:
    • Describe the cellular response as a sequence from antigen presentation to the differentiation of the clone.
    • Explain how a cytotoxic T cell destroys a virus-infected cell, naming perforin and its effect on the cell-surface membrane.
    • Suggest why cells carrying a mutated membrane protein, such as those in a tumour, can be destroyed by the immune system.
    51

    Cell recognition and the immune system

    The role of antigen-presenting cells in the cellular response.

    Verified
    Key Learning Objectives:
    • Identify three different cells that can act as antigen-presenting cells and state how each acquires the antigen it displays.
    • Explain why antigen presentation speeds up the cellular response, using the idea of one specific receptor per T cell.
    • Describe what happens to a helper T cell immediately after it binds to a presented antigen.
    52

    Cell recognition and the immune system

    The roles of plasma cells and of memory cells in producing primary and secondary immune responses.

    Verified
    Key Learning Objectives:
    • Describe three measurable differences between a primary and a secondary response using an antibody concentration graph.
    • Explain why the primary response has a lag of several days before antibody appears.
    • Explain the different roles of plasma cells and memory cells, stating the lifespan of each.
    53

    Cell recognition and the immune system

    The use of antibodies in the ELISA test.

    Verified
    Key Learning Objectives:
    • Describe the ELISA procedure in order, naming what binds at each stage and stating the purpose of every washing step.
    • Explain why a positive ELISA result in a baby born to an HIV-positive mother is not proof of infection.
    • Evaluate an antibody-based diagnostic test against alternatives using data on detection rate and time after the onset of symptoms.
    54

    Cell recognition and the immune system

    The use of monoclonal antibodies in: targeting medication to specific cell types by attaching a therapeutic drug to an antibody medical diagnosis.

    Verified
    Key Learning Objectives:
    • Explain how attaching a drug to a monoclonal antibody reduces the dose needed and the side effects experienced.
    • Describe how a labelled monoclonal antibody is used to detect the presence of a specific antigen.
    • Suggest a reason why a targeted antibody therapy might still damage some healthy cells.
    55

    Cell recognition and the immune system

    The use of vaccines to provide protection for individuals and populations against disease. The concept of herd immunity.

    Verified
    Key Learning Objectives:
    • Explain how a vaccine produces long-term protection without the person developing the disease.
    • Explain herd immunity in terms of transmission, and identify who it protects.
    • Suggest what happens to the incidence of a disease in a population when vaccination coverage falls below the threshold.
    56

    Control of blood glucose concentration (A-level only)

    Required practical 11: Production of a dilution series of a glucose solution and use of colorimetric techniques to produce a calibration curve with which to identify the concentration of glucose in an unknown ‘urine’ sample.

    Verified
    Key Learning Objectives:
    • Describe how to produce a dilution series of a glucose solution, stating the volumes used at each step.
    • Explain why the Benedict's solution must be in excess and why every tube must be heated for the same time.
    • Use a calibration curve to determine the glucose concentration of an unknown sample and state the limits of that reading.
    57

    Control of blood glucose concentration (A-level only)

    Students should be able to evaluate the positions of health advisers and the food industry in relation to the increased incidence of type II diabetes.

    Verified
    Key Learning Objectives:
    • Construct an argument for and an argument against a food industry position using data supplied.
    • Explain why a correlation between sugar consumption and type II diabetes does not establish cause.
    • Identify two limitations of an animal study used as evidence about human diabetes.
    58

    Control of blood glucose concentration (A-level only)

    The action of glucagon by: attaching to receptors on the surfaces of target cells activating enzymes involved in the conversion of glycogen to glucose activating enzymes involved in the conversion of glycerol and amino acids into glucose.

    Verified
    Key Learning Objectives:
    • Describe how glucagon raises blood glucose concentration, naming the cells that secrete it and its target cells.
    • Explain why glucagon must act through a membrane receptor rather than entering liver cells.
    • Compare the actions of insulin and glucagon on liver cells.
    59

    Control of blood glucose concentration (A-level only)

    The action of insulin by: attaching to receptors on the surfaces of target cells controlling the uptake of glucose by regulating the inclusion of channel proteins in the surface membranes of target cells activating enzymes involved in the conversion of glucose to glycogen.

    Verified
    Key Learning Objectives:
    • Describe the ways insulin lowers blood glucose concentration after a meal.
    • Explain why a cell whose receptors are faulty takes up glucose slowly even when the insulin concentration is high.
    • Explain how the fall in blood glucose that insulin causes switches off its own secretion.
    60

    Control of blood glucose concentration (A-level only)

    The causes of types I and II diabetes and their control by insulin and/or manipulation of the diet.

    Verified
    Key Learning Objectives:
    • Explain the difference in cause between type I and type II diabetes in terms of insulin production and receptor sensitivity.
    • Explain why insulin must be injected rather than taken by mouth.
    • Evaluate data from a study as evidence that a high-fat diet is a risk factor for type II diabetes, commenting on species and duration.
    61

    Control of blood glucose concentration (A-level only)

    The factors that influence blood glucose concentration.

    Verified
    Key Learning Objectives:
    • List factors that raise and lower blood glucose concentration.
    • Explain how blood glucose concentration changes during exercise.
    • Distinguish the roles of insulin, glucagon and adrenaline in blood glucose regulation.
    62

    Control of blood glucose concentration (A-level only)

    The role of adrenaline by: attaching to receptors on the surfaces of target cells activating enzymes involved in the conversion of glycogen to glucose.

    Verified
    Key Learning Objectives:
    • Describe how adrenaline raises blood glucose concentration via cell-surface receptors.
    • Explain the difference in glycogenolysis outcomes between liver and muscle cells.
    • Understand the mechanism of enzyme activation involved in the conversion of glycogen to glucose.
    63

    Control of blood glucose concentration (A-level only)

    The role of the liver in glycogenesis, glycogenolysis and gluconeogenesis.

    Verified
    Key Learning Objectives:
    • Define glycogenesis, glycogenolysis and gluconeogenesis and state the effect of each on blood glucose concentration.
    • Explain what happens in the liver during prolonged fasting as glycogen stores fall.
    • Explain why liver glycogen, but not muscle glycogen, can raise blood glucose concentration.
    64

    Control of blood glucose concentration (A-level only)

    The second messenger model of adrenaline and glucagon action, involving adenylate cyclase, cyclic AMP (cAMP) and protein kinase.

    Verified
    Key Learning Objectives:
    • Sequence the second messenger model from hormone binding through to the release of glucose from glycogen.
    • Explain why a hydrophilic hormone needs a second messenger rather than acting inside the cell directly.
    • Explain how the cascade amplifies the effect of a very low hormone concentration.
    65

    Control of blood water potential (A-level only)

    Osmoregulation as control of the water potential of the blood.

    Verified
    Key Learning Objectives:
    • Explain why the water potential of blood plasma must be held within narrow limits, using osmosis into and out of body cells.
    • Describe how osmoreceptors in the hypothalamus detect a fall in blood water potential, and trace the response through to the urine produced.
    • Predict the change in urine volume and concentration after a salty meal, heavy sweating or drinking a litre of water, and justify each prediction.
    66

    Control of blood water potential (A-level only)

    The roles of the hypothalamus, posterior pituitary and antidiuretic hormone (ADH) in osmoregulation.

    Verified
    Key Learning Objectives:
    • Describe how osmoreceptors in the hypothalamus detect changes in blood water potential by shrinking or swelling.
    • Trace the pathway of ADH from its production in the hypothalamus to its secretion by the posterior pituitary.
    • Explain how ADH increases the permeability of the distal convoluted tubule and collecting duct to water, resulting in concentrated urine and restored water potential.
    67

    Control of blood water potential (A-level only)

    The structure of the nephron and its role in: the formation of glomerular filtrate reabsorption of glucose and water by the proximal convoluted tubule maintaining a gradient of sodium ions in the medulla by the loop of Henle reabsorption of water by the distal convoluted tubule and collecting ducts.

    Verified
    Key Learning Objectives:
    • Name the two regions of the nephron that respond to ADH and describe what happens to their permeability to water when ADH binds.
    • Explain how the difference in diameter between the afferent and efferent arterioles produces the pressure needed for ultrafiltration.
    • Describe how the loop of Henle acts as a counter-current multiplier to build a sodium ion gradient in the medulla, and use it to explain why an animal with a longer loop produces more concentrated urine.
    68

    Control of heart rate (A-level only)

    Myogenic stimulation of the heart and transmission of a subsequent wave of electrical activity.

    Verified
    Key Learning Objectives:
    • Define myogenic and use it to explain why a heart removed from the body, or a transplanted heart, continues to beat.
    • Trace the wave of depolarisation from the SAN across both atria and explain why the atria contract before the ventricles.
    • Explain why a band of non-conducting tissue between the atria and the ventricles is essential for efficient pumping.
    69

    Control of heart rate (A-level only)

    The roles and locations of chemoreceptors and pressure receptors and the roles of the autonomic nervous system and effectors in controlling heart rate.

    Verified
    Key Learning Objectives:
    • Trace the full pathway from chemoreceptor to SAN for a rise in blood carbon dioxide, naming the division of the autonomic nervous system used.
    • Predict how sympathetic and parasympathetic impulse frequency change when blood pressure rises, and justify the prediction.
    • Explain why exercise raises heart rate through carbon dioxide detection rather than through oxygen detection.
    70

    Control of heart rate (A-level only)

    The roles of the sinoatrial node (SAN), atrioventricular node (AVN) and Purkyne tissue in the bundle of His.

    Verified
    Key Learning Objectives:
    • Sequence the route of the wave of depolarisation from SAN to AVN to bundle of His to Purkyne tissue, stating what each structure does.
    • Explain why the delay at the AVN is essential, referring to ventricular filling and atrial emptying.
    • Explain why losing Purkyne tissue, or the gap junction proteins between cardiac muscle cells, would weaken ventricular emptying.
    71

    Differences in DNA between individuals of the same species can be exploited

    Students should be able to evaluate information relating to screening individuals for genetically determined conditions and drug responses.

    Verified
    Key Learning Objectives:
    • Evaluate a screening programme for genetically determined conditions by giving benefits, limitations and a justified conclusion.
    • Evaluate the use of screening for drug responses to improve treatment efficacy and reduce adverse reactions.
    • Explain why a positive screening result may be a false positive and why a negative result does not guarantee absence of risk.
    • Suggest an ethical consequence of genetic screening and state who is affected by it.
    72

    Differences in DNA between individuals of the same species can be exploited

    The use of labelled DNA probes and DNA hybridisation to locate specific alleles of genes.

    Verified
    Key Learning Objectives:
    • Describe, in order, how a labelled DNA probe is used to locate a specific allele in a sample of DNA.
    • Explain why the sample DNA must be amplified and made single-stranded before hybridisation.
    • Describe how a bound probe is detected, naming a suitable label and the method used to see it.
    73

    Differences in DNA between individuals of the same species can be exploited

    The use of labelled DNA probes that can be used to screen patients for heritable conditions, drug responses or health risks.

    Verified
    Key Learning Objectives:
    • Describe how labelled DNA probes are used to screen a patient's fixed DNA for specific alleles.
    • Explain why a separate complementary probe is needed for each allele, and what a negative result therefore does and does not prove.
    • Describe one use of screening for each of a heritable condition, a drug response and a health risk, naming a specific example for each.
    74

    Differences in DNA between individuals of the same species can be exploited

    The use of this information in genetic counselling and personalised medicine.

    Verified
    Key Learning Objectives:
    • Explain what a genetic counsellor provides to a couple who both carry a recessive allele, including how risk is calculated.
    • Describe how knowing a patient's alleles changes the choice of drug or dose prescribed.
    • Distinguish personalised medicine from gene therapy by stating what each one changes.
    75

    Digestion and absorption

    Digestion in mammals of: carbohydrates by amylases and membrane-bound disaccharidases lipids by lipase, including the action of bile salts proteins by endopeptidases, exopeptidases and membrane- bound dipeptidases.

    Verified
    Key Learning Objectives:
    • Describe the complete digestion of starch, naming amylase, maltose and a membrane-bound disaccharidase.
    • Explain how bile salts increase the rate of lipid digestion without hydrolysing any bonds themselves.
    • Sequence endopeptidases, exopeptidases and dipeptidases, stating which bond each hydrolyses and why acting in that order speeds digestion up.
    76

    Digestion and absorption

    During digestion, large biological molecules are hydrolysed to smaller molecules that can be absorbed across cell membranes.

    Verified
    Key Learning Objectives:
    • Name the bond hydrolysed and the products formed when starch, a triglyceride and a protein are each digested.
    • Explain, using size and solubility, why a polymer must be hydrolysed before it can cross the cell-surface membrane of an ileum epithelial cell.
    • Contrast hydrolysis with the condensation reaction that formed the bond, stating what happens to the water molecule in each case.
    77

    Digestion and absorption

    Mechanisms for the absorption of the products of digestion by cells lining the ileum of mammals, to include: co-transport mechanisms for the absorption of amino acids and of monosaccharides the role of micelles in the absorption of lipids.

    Verified
    Key Learning Objectives:
    • Describe the sequence by which glucose is absorbed into an ileum epithelial cell, beginning with the sodium-potassium pump.
    • Explain why micelles are needed for fatty acid absorption even though fatty acids can cross the bilayer unaided.
    • Predict the effect of damaged microvilli on absorption, on the water potential of the lumen and so on the volume of water lost.
    78

    DNA and protein synthesis

    In eukaryotes, transcription results in the production of pre- mRNA; this is then spliced to form mRNA.

    Verified
    Key Learning Objectives:
    • Describe how pre-mRNA is converted into mature mRNA, naming introns, exons and splicing.
    • Explain why a polypeptide translated from unspliced pre-mRNA would have the wrong amino acid sequence.
    • Explain how alternative combinations of exons allow one gene to code for more than one polypeptide.
    79

    DNA and protein synthesis

    In prokaryotes, transcription results directly in the production of mRNA from DNA.

    Verified
    Key Learning Objectives:
    • Explain why a bacterium produces functional mRNA directly, referring to the absence of introns.
    • Suggest why a bacterium given an unmodified human gene may fail to produce a functional protein.
    • Distinguish 'the genetic code is universal' from 'the genetic code is degenerate' and state which explains bacterial expression of human genes.
    • Recognise that while the genetic code is universal, the mechanisms of transcription and translation differ between prokaryotes and eukaryotes.
    80

    DNA and protein synthesis

    Students should be able to: relate the base sequence of nucleic acids to the amino acid sequence of polypeptides, when provided with suitable data about the genetic code interpret data from experimental work investigating the role of nucleic acids.

    Verified
    Key Learning Objectives:
    • Convert a given DNA template sequence into mRNA codons and then into an amino acid sequence using a supplied table.
    • Deduce the tRNA anticodons required to translate a given mRNA sequence.
    • Interpret data from a labelling or cell-free experiment to state which nucleic acid carries out a stated role.
    81

    DNA and protein synthesis

    The concept of the genome as the complete set of genes in a cell and of the proteome as the full range of proteins that a cell is able to produce.

    Verified
    Key Learning Objectives:
    • Define genome and proteome, naming the cell or organism as the unit in both.
    • Explain why two cells from the same organism share a genome but have different proteomes.
    • Explain why a eukaryotic cell can produce more different proteins than it has genes, using splicing of pre-mRNA.
    82

    DNA and protein synthesis

    The structure of molecules of messenger RNA (mRNA) and of transfer RNA (tRNA).

    Verified
    Key Learning Objectives:
    • Draw and label a tRNA molecule, marking the anticodon and the amino acid binding site.
    • Give three differences between a DNA molecule and a tRNA molecule, writing both sides of each difference.
    • Explain how the structure of tRNA allows a specific amino acid to be delivered to a specific mRNA codon.
    83

    DNA and protein synthesis

    Transcription as the production of mRNA from DNA. The role of RNA polymerase in joining mRNA nucleotides.

    Verified
    Key Learning Objectives:
    • Describe transcription as an ordered sequence of steps.
    • Write the mRNA base sequence produced from a given DNA template strand.
    • Explain the role of RNA polymerase in joining mRNA nucleotides.
    84

    DNA and protein synthesis

    Translation as the production of polypeptides from the sequence of codons carried by mRNA. The roles of ribosomes, tRNA and ATP.

    Verified
    Key Learning Objectives:
    • Describe translation in sequence from mRNA binding to release of the completed polypeptide.
    • Explain the specific role of the ribosome, of tRNA and of ATP in forming a polypeptide.
    • Explain how a change to a tRNA anticodon alters the protein produced and its function.
    85

    DNA replication

    Students should be able to evaluate the work of scientists in validating the Watson–Crick model of DNA replication.

    Verified
    Key Learning Objectives:
    • Predict the banding pattern expected after one and two replications for each of the conservative, dispersive and semi-conservative models.
    • Interpret a density gradient result to say which model it eliminates and why.
    • Evaluate the strength of the evidence for semi-conservative replication, referring to repetition and peer review.
    86

    DNA replication

    The process of semi-conservative replication of DNA in terms of: unwinding of the double helix breakage of hydrogen bonds between complementary bases in the polynucleotide strands the role of DNA helicase in unwinding DNA and breaking its hydrogen bonds attraction of new DNA nucleotides to exposed bases on template strands and base pairing the role of DNA polymerase in the condensation reaction that joins adjacent nucleotides.

    Verified
    Key Learning Objectives:
    • Describe semi-conservative replication in sequence, naming both enzymes and the bonds each one breaks or makes.
    • Explain why new nucleotides can be added in only one direction, referring to the specificity of DNA polymerase.
    • Distinguish replication from transcription by naming three differences in enzymes, nucleotides and templates used.
    87

    DNA replication

    The semi-conservative replication of DNA ensures genetic continuity between generations of cells.

    Verified
    Key Learning Objectives:
    • Explain how semi-conservative replication produces two identical DNA molecules (sister chromatids) with identical base sequences.
    • State where in the cell cycle DNA replication occurs and describe the state of a chromosome immediately afterwards.
    • Define genetic continuity and explain how DNA replication ensures it between generations of cells.
    88

    DNA, genes and chromosomes

    A gene is a base sequence of DNA that codes for: the amino acid sequence of a polypeptide a functional RNA (including ribosomal RNA and tRNAs).

    Verified
    Key Learning Objectives:
    • Define a gene in a way that covers both polypeptide-coding genes and functional RNA genes.
    • Explain how a change in the base sequence of a gene can change the tertiary structure of the polypeptide it codes for.
    • Distinguish between a gene and an allele using the idea of base sequence at a locus.
    89

    DNA, genes and chromosomes

    A gene occupies a fixed position, called a locus, on a particular DNA molecule.

    Verified
    Key Learning Objectives:
    • State what is meant by the locus of a gene and relate it to homologous chromosomes.
    • Explain why crossing over between homologous chromosomes neither adds nor removes genes.
    • Explain why two genes at different loci on the same chromosome may fail to assort independently.
    90

    DNA, genes and chromosomes

    A sequence of three DNA bases, called a triplet, codes for a specific amino acid. The genetic code is universal, non-overlapping and degenerate.

    Verified
    Key Learning Objectives:
    • Explain why a bacterium given a human gene can produce the human protein, noting the need to remove introns or use cDNA.
    • Explain how the code being non-overlapping causes an insertion to have a greater effect than a substitution.
    • Use the degeneracy of the code to explain why a substitution mutation may leave the polypeptide unchanged.
    91

    DNA, genes and chromosomes

    Even within a gene only some sequences, called exons, code for amino acid sequences.

    Verified
    Key Learning Objectives:
    • Describe what happens to a pre-messenger RNA molecule before it leaves the nucleus.
    • Explain how a single gene can code for more than one polypeptide.
    • Explain why a gene taken directly from a human chromosome may not be expressed correctly in a bacterium.
    92

    DNA, genes and chromosomes

    In eukaryotes, much of the nuclear DNA does not code for polypeptides.

    Verified
    Key Learning Objectives:
    • State that much of eukaryotic nuclear DNA does not code for polypeptides.
    • Describe the location and nature of non-coding multiple repeats and introns.
    • Explain the difference between eukaryotic and prokaryotic DNA regarding non-coding sequences within genes.
    93

    DNA, genes and chromosomes

    In prokaryotic cells, DNA molecules are short, circular and not associated with proteins.

    Verified
    Key Learning Objectives:
    • Give three features of the DNA of all prokaryotic cells that distinguish it from eukaryotic nuclear DNA.
    • Explain why a plasmid is not the cell's main DNA molecule when describing where prokaryotic DNA is found.
    • Compare the structure of prokaryotic DNA with eukaryotic DNA in terms of length, shape, and protein association.
    94

    DNA, genes and chromosomes

    In the nucleus of eukaryotic cells, DNA molecules are very long, linear and associated with proteins, called histones.

    Verified
    Key Learning Objectives:
    • Describe how a very long DNA molecule is packaged with histones to fit inside a nucleus.
    • Compare the DNA in a eukaryotic nucleus with prokaryotic DNA in terms of length, shape and associated proteins.
    • Explain why the degree of coiling of DNA around histones affects whether a gene can be transcribed.
    95

    DNA, genes and chromosomes

    The mitochondria and chloroplasts of eukaryotic cells also contain DNA which, like the DNA of prokaryotes, is short, circular and not associated with protein.

    Verified
    Key Learning Objectives:
    • Compare the DNA of a mitochondrion with the DNA in the nucleus of the same cell.
    • Explain how the features of mitochondrial DNA support the idea that mitochondria evolved from prokaryotes.
    • Deduce from family data whether a condition is caused by a mitochondrial or a nuclear mutation.
    96

    DNA, genes and chromosomes

    There are, for example, non-coding multiple repeats of base sequences between genes.

    Verified
    Key Learning Objectives:
    • Explain why variation in the number of repeats between individuals is often tolerated, in terms of the repeats being non-coding.
    • Give features of DNA fragments that allow them to be separated by gel electrophoresis.
    • Describe how restriction endonucleases are used to cut DNA at specific recognition sequences.
    97

    DNA, genes and chromosomes

    Together a DNA molecule and its associated proteins form a chromosome.

    Verified
    Key Learning Objectives:
    • Given a diagram or a stated stage of the cell cycle, say whether each chromosome is one chromatid or two, justifying the count by whether DNA replication has already happened.
    • Distinguish between a chromosome, a chromatid and a homologous pair using a labelled diagram.
    • Explain why a chromosome is only visible under a light microscope during cell division.
    98

    DNA, genes and chromosomes

    Within the gene, these exons are separated by one or more non-coding sequences, called introns.

    Verified
    Key Learning Objectives:
    • Describe the position and the fate of introns from transcription through to translation.
    • Calculate the number of amino acids in a polypeptide from the number of bases in the exons of its gene.
    • Explain why complementary DNA produced from mature messenger RNA is shorter than a gene containing introns.
    99

    Energy and ecosystems (A-level only)

    Biomass can be measured in terms of mass of carbon or dry mass of tissue per given area.

    Verified
    Key Learning Objectives:
    • State two units in which biomass can be expressed and give a correct unit for each.
    • Calculate the biomass per square metre of an area from the dry mass of a sampled quadrat.
    • Explain why mass of carbon is a valid measure of the organic material an organism contains.
    • Evaluate the reliability of a biomass estimate made from a small number of samples.
    100

    Energy and ecosystems (A-level only)

    Gross primary production ( GPP) is the chemical energy store in plant biomass, in a given area or volume.

    Verified
    Key Learning Objectives:
    • Define gross primary production as a chemical energy store in plant biomass.
    • Explain why only a small percentage of the light energy reaching a leaf appears as gross primary production.
    • Identify from units alone whether a printed figure represents an energy store or a rate.
    • List reasons why incident light is not converted into chemical energy by producers.
    101

    Energy and ecosystems (A-level only)

    In any ecosystem, plants synthesise organic compounds from atmospheric, or aquatic, carbon dioxide.

    Verified
    Key Learning Objectives:
    • Identify the carbon source for terrestrial and aquatic producers.
    • Explain how the synthesis of organic compounds contributes to producer biomass.
    • Describe the relationship between producer biomass and the energy available to consumers.
    102

    Energy and ecosystems (A-level only)

    It is also available to other trophic levels in the ecosystem, such as herbivores and decomposers.

    Verified
    Key Learning Objectives:
    • Explain three distinct reasons why energy transfer between trophic levels is inefficient.
    • Calculate the percentage efficiency of energy transfer between two trophic levels from given data.
    • Describe how the energy in dead material, faeces and urine becomes available to saprobionts.
    • Rewrite a sentence containing 'energy used in respiration' so that it accurately describes energy loss.
    103

    Energy and ecosystems (A-level only)

    Most of the sugars synthesised by plants are used by the plant as respiratory substrates.

    Verified
    Key Learning Objectives:
    • Explain how a plant uses glucose as a respiratory substrate, naming glycolysis, the link reaction, the Krebs cycle and oxidative phosphorylation.
    • Link a faster rate of photosynthesis to faster growth through sugar supply, ATP and synthesis of organic materials.
    • Justify why respiratory loss makes net primary production smaller than gross primary production.
    • Rewrite a statement containing 'energy used in respiration' so that it would gain the mark.
    104

    Energy and ecosystems (A-level only)

    Primary and secondary productivity is the rate of primary or secondary production, respectively.

    Verified
    Key Learning Objectives:
    • Distinguish production from productivity using their units.
    • Convert a production figure into a productivity by dividing by the time period, and quote the unit.
    • Classify a given value as gross primary, net primary or secondary productivity from its context.
    • Explain why secondary productivity is much lower than net primary productivity in the same ecosystem.
    105

    Energy and ecosystems (A-level only)

    The chemical energy store in dry biomass can be estimated using calorimetry.

    Verified
    Key Learning Objectives:
    • Describe how a calorimeter is used to estimate the chemical energy store in a dried sample of biomass.
    • Calculate an energy value in kJ g-1 from the mass of water, its temperature rise and the dry mass burnt.
    • Explain why the sample must be dried and burnt in excess oxygen before measurement.
    • Identify two sources of error in a calorimetry experiment and state the effect of each on the result.
    106

    Energy and ecosystems (A-level only)

    The net production of consumers ( N), such as animals, can be calculated as: N = I – (F + R) where I represents the chemical energy store in ingested food, F represents the chemical energy lost to the environment in faeces and urine and R represents the respiratory losses to the environment.

    Verified
    Key Learning Objectives:
    • Calculate the net production of a consumer from given values of I, F and R, and state the unit.
    • Explain what each of I, F and R represents in terms of where the energy goes.
    • Give three distinct reasons for the low efficiency of energy transfer from one consumer to the next.
    • Compare the net production of an endotherm and an ectotherm with the same energy intake, and justify the difference.
    107

    Energy and ecosystems (A-level only)

    The rest are used to make other groups of biological molecules.

    Verified
    Key Learning Objectives:
    • Name the groups of biological molecules made from photosynthetic sugars, including nucleic acids.
    • Explain why a plant needs nitrate and phosphate ions to convert sugars into proteins and nucleic acids.
    • Describe how condensation reactions are used to build polymers like starch and cellulose.
    108

    Energy and ecosystems (A-level only)

    These biological molecules form the biomass of the plants.

    Verified
    Key Learning Objectives:
    • Describe the fate of sugars synthesised during photosynthesis.
    • Identify the biological molecules that constitute plant biomass.
    • Explain that the biological molecules forming biomass represent the chemical energy store of an organism.
    109

    Energy and ecosystems (A-level only)

    This net primary production is available for plant growth and reproduction.

    Verified
    Key Learning Objectives:
    • Explain how net primary production becomes new plant tissue, naming at least two organic molecules that store it.
    • Calculate net primary production from gross primary production and respiratory loss, using correct rate units.
    • Explain why a higher gross primary production does not necessarily give a higher net primary production.
    • Distinguish net primary production from the energy a herbivore assimilates from the same plant.
    110

    Evolution may lead to speciation (A-level only)

    Allopatric and sympatric speciation.

    Verified
    Key Learning Objectives:
    • Distinguish allopatric from sympatric speciation by the type of isolation involved in each.
    • Use a distribution map or altitude data to justify allopatric or sympatric speciation for a named pair of species.
    • Explain how polyploidy can produce a new plant species in one generation without any geographical separation.
    111

    Evolution may lead to speciation (A-level only)

    Evolution as a change in the allele frequencies in a population.

    Verified
    Key Learning Objectives:
    • Define evolution in terms of allele frequency and explain why the definition applies to populations rather than individuals.
    • Use two sets of allele frequencies to decide whether a population has evolved.
    • Distinguish evolution from speciation and state the relationship between them.
    112

    Evolution may lead to speciation (A-level only)

    In this way, new species arise from existing species.

    Verified
    Key Learning Objectives:
    • Set out the full sequence from variation within one population to the existence of two species.
    • Use a phylogenetic tree to state which species share the most recent common ancestor.
    • Explain why populations that interbreed only with difficulty are expected during speciation.
    113

    Evolution may lead to speciation (A-level only)

    Individuals within a population of a species may show a wide range of variation in phenotype.

    Verified
    Key Learning Objectives:
    • Distinguish continuous from discontinuous variation and give an example of each in a named species.
    • Use means and standard deviations from a figure to decide whether two groups genuinely differ.
    • Explain why a population must show phenotypic variation before natural selection can act on it.
    114

    Evolution may lead to speciation (A-level only)

    Meiosis and the random fertilisation of gametes during sexual reproduction produce further genetic variation.

    Verified
    Key Learning Objectives:
    • Describe the three processes in sexual reproduction that increase genetic variation and state what each one produces.
    • Explain why the independent segregation of 23 homologous pairs generates over eight million chromosome combinations in a gamete.
    • Distinguish the variation produced by meiosis and fertilisation from the variation produced by mutation.
    115

    Evolution may lead to speciation (A-level only)

    New species arise when these genetic differences lead to an inability of members of the populations to interbreed and produce fertile offspring.

    Verified
    Key Learning Objectives:
    • State the test for whether two populations have become separate species, using the idea of fertile offspring.
    • Explain why a sterile hybrid such as a mule shows that two species remain distinct.
    • Explain how accumulated genetic differences prevent successful interbreeding between two populations.
    116

    Evolution may lead to speciation (A-level only)

    Predation, disease and competition for the means of survival result in differential survival and reproduction, ie natural selection.

    Verified
    Key Learning Objectives:
    • Identify the selection pressure acting in an unfamiliar context and state which phenotype it favours.
    • Explain how predation, disease and competition each produce differential survival and reproduction.
    • Write a full natural selection explanation in the order variation, selection pressure, survival, reproduction, allele frequency.
    117

    Evolution may lead to speciation (A-level only)

    Reproductive separation of two populations can result in the accumulation of difference in their gene pools.

    Verified
    Key Learning Objectives:
    • Explain how reproductive separation allows two gene pools to change independently of one another.
    • Describe, in the correct order, how genetic differences accumulate between two separated populations.
    • Identify from data the feature that has stopped gene flow between two populations.
    118

    Evolution may lead to speciation (A-level only)

    The effect of this differential reproductive success on the allele frequencies within a gene pool.

    Verified
    Key Learning Objectives:
    • Explain how differential reproductive success changes the allele frequencies of a gene pool over successive generations.
    • Explain why a recessive allele falls in frequency only slowly even under strong selection.
    • Predict how the allele frequencies of two separated populations diverge when they face different selection pressures.
    119

    Evolution may lead to speciation (A-level only)

    The effects of stabilising, directional and disruptive selection.

    Verified
    Key Learning Objectives:
    • Identify stabilising, directional or disruptive selection from distribution curves drawn before and after an environmental change.
    • Explain how a change in environment can switch a population from stabilising to directional selection.
    • Explain why disruptive selection increases variation and can lead to sympatric speciation.
    120

    Evolution may lead to speciation (A-level only)

    The importance of genetic drift in causing changes in allele frequency in small populations.

    Verified
    Key Learning Objectives:
    • Explain why chance changes in allele frequency have a greater effect in small populations than in large ones.
    • Distinguish the founder effect from a genetic bottleneck, giving an example of each.
    • Explain why a population with low genetic diversity is more vulnerable to a new disease or a change in its environment.
    121

    Evolution may lead to speciation (A-level only)

    The primary source of genetic variation is mutation.

    Verified
    Key Learning Objectives:
    • Describe how a change in the base sequence of a gene can produce a non-functional protein, naming each step in the chain.
    • Explain why the use of antibiotics does not create resistance alleles but does increase their frequency.
    • Explain why only mutations occurring in gametes contribute to genetic variation in the next generation.
    122

    Evolution may lead to speciation (A-level only)

    This is due to genetic and environmental factors.

    Verified
    Key Learning Objectives:
    • Explain, for a named characteristic, how genetic and environmental factors each contribute to the variation observed.
    • Name a specific abiotic factor rather than a location when accounting for differences between two populations.
    • Design a comparison that separates genetic from environmental causes of a difference between two groups of organisms.
    123

    Evolution may lead to speciation (A-level only)

    Those organisms with phenotypes providing selective advantages are likely to produce more offspring and pass on their favourable alleles to the next generation.

    Verified
    Key Learning Objectives:
    • Explain in linked steps why a resistance allele becomes common in a population exposed to a pathogen.
    • Explain why a selective advantage in one environment can be a disadvantage in another.
    • Rewrite a statement such as 'the organism developed resistance' into correct natural selection language.
    124

    Gas exchange

    Adaptations of gas exchange surfaces, shown by gas exchange: across the body surface of a single-celled organism in the tracheal system of an insect (tracheae, tracheoles and spiracles) across the gills of fish (gill lamellae and filaments including the counter-current principle) by the leaves of dicotyledonous plants (mesophyll and stomata).

    Verified
    Key Learning Objectives:
    • Explain the importance of one named adaptation of the insect tracheal system, pairing the structure with its effect on diffusion.
    • Describe counter-current flow in a fish gill and explain why it allows oxygen to diffuse into the blood along the whole lamella.
    • Identify the features common to gas exchange surfaces and find each one in a single-celled organism, an insect, a fish and a leaf.
    125

    Gas exchange

    Structural and functional compromises between the opposing needs for efficient gas exchange and the limitation of water loss shown by terrestrial insects and xerophytic plants.

    Verified
    Key Learning Objectives:
    • Explain how named xerophytic adaptations reduce water loss, distinguishing between physical barriers and water potential gradient reduction.
    • Explain why an adaptation that reduces water loss in a terrestrial insect also reduces the rate of gas exchange.
    • Evaluate the structural and functional compromises made by terrestrial organisms to balance gas exchange and water conservation.
    126

    Gas exchange

    Students should be able to: interpret information relating to the effects of lung disease on gas exchange and/or ventilation interpret data relating to the effects of pollution and smoking on the incidence of lung disease analyse and interpret data associated with specific risk factors and the incidence of lung disease evaluate the way in which experimental data led to statutory restrictions on the sources of risk factors recognise correlations and causal relationships.

    Verified
    Key Learning Objectives:
    • Explain how named lung diseases change gas exchange or ventilation, starting from the structural changes they cause.
    • Interpret spirometer data on forced expiratory volume and forced vital capacity, linking patterns to specific diseases.
    • Analyse data on smoking and pollution to distinguish correlation from causation, and evaluate how this evidence supports statutory restrictions on risk factors.
    127

    Gas exchange

    The essential features of the alveolar epithelium as a surface over which gas exchange takes place.

    Verified
    Key Learning Objectives:
    • Explain four features of the alveolar epithelium, pairing each with its effect on the rate of diffusion.
    • Explain how a thickened alveolar wall reduces the rate of gas exchange, using the idea of diffusion pathway length.
    • Describe how the structure of the surrounding capillaries increases the rate of gas exchange.
    128

    Gas exchange

    The gross structure of the human gas exchange system limited to the alveoli, bronchioles, bronchi, trachea and lungs.

    Verified
    Key Learning Objectives:
    • Describe the macroscopic path taken by air from the trachea to the alveoli in the correct order.
    • Identify the gross structural features of the trachea, bronchi, bronchioles and alveoli.
    • Label a diagram of the human gas exchange system with the specified macroscopic structures.
    129

    Gas exchange

    The mechanism of breathing to include the role of the diaphragm and the antagonistic interaction between the external and internal intercostal muscles in bringing about pressure changes in the thoracic cavity.

    Verified
    Key Learning Objectives:
    • Describe inspiration as a sequence of muscle contraction, volume change, pressure change and air movement.
    • Explain what antagonistic means using the external and internal intercostal muscles as the example.
    • Explain why expiration at rest requires little energy whereas inspiration always requires ATP.
    130

    Gas exchange

    Ventilation and the exchange of gases in the lungs.

    Verified
    Key Learning Objectives:
    • Explain how ventilation maintains the concentration gradients for both oxygen and carbon dioxide at the alveolus.
    • Describe the direction of diffusion of each gas and the layers it crosses between alveolar air and blood.
    • Predict what happens to the rate of gas exchange if ventilation stops, and justify the prediction using equilibrium.
    131

    Gene expression and cancer (A-level only)

    The main characteristics of benign and malignant tumours.

    Verified
    Key Learning Objectives:
    • Compare benign and malignant tumours using growth rate, capsule, differentiation and ability to spread.
    • Explain why metastasis makes a malignant tumour far harder to treat than a benign one of the same size.
    • Identify, from a description or micrograph, whether a tumour is likely to be benign or malignant and justify the choice.
    132

    Gene expression and cancer (A-level only)

    The role of the following in the development of tumours: tumour suppressor genes and oncogenes abnormal methylation of tumour suppressor genes and oncogenes increased oestrogen concentrations in the development of some breast cancers.

    Verified
    Key Learning Objectives:
    • Explain how a single mutation in a proto-oncogene produces a protein that drives division without a growth factor.
    • Describe two different ways, one genetic and one epigenetic, in which a tumour suppressor gene can stop producing its protein.
    • Suggest how a raised oestrogen concentration increases the rate of mitosis in breast tissue, referring to transcriptional factors.
    133

    General properties of proteins

    A condensation reaction between two amino acids forms a peptide bond.

    Verified
    Key Learning Objectives:
    • Describe how a peptide bond is formed, naming the two functional groups involved and the molecule released.
    • Explain why a peptide bond involves the backbone of an amino acid rather than its R group.
    • Describe how peptide bonds are hydrolysed, naming the molecule required to break the bond.
    134

    General properties of proteins

    A functional protein may contain one or more polypeptides.

    Verified
    Key Learning Objectives:
    • State what quaternary structure means and name a protein that has it and one that does not.
    • Describe the interactions that hold two or more polypeptides together in a functional protein.
    • Explain why haemoglobin needs four polypeptide chains to show cooperative binding of oxygen.
    135

    General properties of proteins

    Amino acids are the monomers from which proteins are made. The general structure of an amino acid as: where NH represents an amine group, COOH represents a carboxyl group and R represents a side chain. The twenty amino acids that are common in all organisms differ only in their side group.

    Verified
    Key Learning Objectives:
    • Draw and label the general structure of an amino acid, naming the amine group, the carboxyl group and the R group.
    • State what is the same and what differs between the twenty amino acids common to all organisms.
    • Explain how variation in R groups leads to variation in the bonds that can form within a folded protein.
    136

    General properties of proteins

    Dipeptides are formed by the condensation of two amino acids. Polypeptides are formed by the condensation of many amino acids.

    Verified
    Key Learning Objectives:
    • Calculate the number of peptide bonds formed and water molecules released when a stated number of amino acids condenses.
    • Describe the formation of a dipeptide and a polypeptide by condensation.
    • Explain how hydrolysis reverses condensation and breaks peptide bonds.
    137

    General properties of proteins

    Proteins have a variety of functions within all living organisms.

    Verified
    Key Learning Objectives:
    • Name four different functions of proteins and give a named protein for each.
    • Explain why proteins can perform such a wide range of roles, referring to the three-dimensional shape of each molecule.
    • Describe the role of specific proteins in transport, structural support, and regulation.
    138

    General properties of proteins

    Students should be able to relate the structure of proteins to properties of proteins named throughout the specification.

    Verified
    Key Learning Objectives:
    • Relate a named protein's property, such as the cooperative binding of haemoglobin, to a specific feature of its structure.
    • Explain how the tertiary structure of an enzyme, antibody or carrier protein produces its specificity.
    • Explain how denaturation changes a protein's tertiary structure and so removes its function.
    139

    General properties of proteins

    The biuret test for proteins.

    Verified
    Key Learning Objectives:
    • Describe the biuret test, naming both reagents and stating the positive and negative results.
    • Explain why a solution of free amino acids gives a negative biuret result while a protein gives a positive one, referring to peptide bonds.
    • Describe how the biuret test can be used to compare the protein concentrations of two solutions.
    140

    General properties of proteins

    The relationship between primary, secondary, tertiary and quaternary structure, and protein function.

    Verified
    Key Learning Objectives:
    • Describe each of the four levels of protein structure and name the bonds responsible for each.
    • Explain how the primary structure of a polypeptide determines its tertiary structure and therefore its function.
    • Explain how quaternary structure, including multiple polypeptides and prosthetic groups, contributes to protein function.
    141

    General properties of proteins

    The role of hydrogen bonds, ionic bonds and disulfide bridges in the structure of proteins.

    Verified
    Key Learning Objectives:
    • Name the bonds and interactions that hold secondary, tertiary and quaternary structure together, and say where each forms.
    • Explain why a change in pH breaks ionic bonds within a protein and what this does to its tertiary structure.
    • Suggest why a protein containing many disulfide bridges is more resistant to high temperatures than one with none.
    142

    Genetic diversity and adaptation

    As a result, over many generations, the new allele increases in frequency in the population.

    Verified
    Key Learning Objectives:
    • Explain in terms of allele frequency how a population changes over many generations of selection.
    • Describe data from a graph showing the change in frequency of an allele, quoting figures and units.
    • Explain why a bacterial population changes far faster than a human population under an equivalent selection pressure.
    143

    Genetic diversity and adaptation

    Directional selection, exemplified by antibiotic resistance in bacteria, and stabilising selection, exemplified by human birth weights.

    Verified
    Key Learning Objectives:
    • Distinguish directional from stabilising selection using labelled distribution curves before and after selection.
    • Explain how the use of antibiotics produces directional selection in a population of bacteria.
    • Explain why human birth mass is an example of stabilising selection, naming the disadvantage at each extreme.
    144

    Genetic diversity and adaptation

    Genetic diversity as the number of different alleles of genes in a population.

    Verified
    Key Learning Objectives:
    • Define genetic diversity accurately.
    • Distinguish genetic diversity from species diversity and population size.
    • Explain the relationship between genetic diversity and the potential for natural selection.
    145

    Genetic diversity and adaptation

    Genetic diversity is a factor enabling natural selection to occur.

    Verified
    Key Learning Objectives:
    • Explain why natural selection cannot occur in a population with no genetic diversity.
    • Describe how different alleles lead to differential survival and reproductive success under a selection pressure.
    • Suggest the consequences for a species of low genetic diversity when a new disease appears.
    146

    Genetic diversity and adaptation

    Many mutations are harmful but, in certain environments, the new allele of a gene might benefit its possessor, leading to increased reproductive success.

    Verified
    Key Learning Objectives:
    • Explain why most mutations that alter a protein are harmful, using the link between primary and tertiary structure.
    • Use data on a resistant population to explain how a new allele leads to increased reproductive success.
    • Explain why an allele that is advantageous in one environment may be disadvantageous in another.
    147

    Genetic diversity and adaptation

    Natural selection results in species that are better adapted to their environment. These adaptations may be anatomical, physiological or behavioural.

    Verified
    Key Learning Objectives:
    • Classify a given adaptation as anatomical, physiological or behavioural and justify the classification.
    • Explain how a named adaptation increases an organism's chance of survival and reproduction in a stated environment.
    • Explain how an adaptation coded for by alleles becomes more common in a population through natural selection.
    148

    Genetic diversity and adaptation

    Random mutation can result in new alleles of a gene.

    Verified
    Key Learning Objectives:
    • Explain how a random mutation produces a new allele of a gene.
    • Distinguish between processes that produce new alleles and processes that produce new combinations of existing alleles.
    • Explain why a mutation in a body cell does not contribute to the genetic diversity of the next generation.
    149

    Genetic diversity and adaptation

    Required practical 6: Use of aseptic techniques to investigate the effect of antimicrobial substances on microbial growth.

    Verified
    Key Learning Objectives:
    • Describe three aseptic techniques used when culturing bacteria and explain the purpose of each.
    • Calculate and compare the area of the zones of inhibition produced by different antimicrobial substances.
    • Explain why a control disc and a stated maximum incubation temperature are needed in this investigation.
    150

    Genetic diversity and adaptation

    Students should be able to: use unfamiliar information to explain how selection produces changes within a population of a species interpret data relating to the effect of selection in producing change within populations show understanding that adaptation and selection are major factors in evolution and contribute to the diversity of living organisms.

    Verified
    Key Learning Objectives:
    • Use unfamiliar information to explain how natural selection produces changes within a population.
    • Interpret data relating to the effect of selection in producing change within populations, evaluating its validity.
    • Explain how adaptation and selection act as major factors in evolution and contribute to the diversity of living organisms.
    151

    Genetic diversity and adaptation

    The advantageous allele is inherited by members of the next generation.

    Verified
    Key Learning Objectives:
    • Explain why survival alone does not change the allele frequency of a population.
    • Describe how an advantageous allele passes from parent to offspring.
    • Use a named example to explain why individuals carrying a protective allele leave more offspring than those without it.
    152

    Genetic diversity and adaptation

    The principles of natural selection in the evolution of populations.

    Verified
    Key Learning Objectives:
    • Explain how a named selection pressure changes the frequency of an allele in a population over several generations.
    • Explain why antibiotic resistance spreads faster among bacteria in a hospital than elsewhere.
    • Identify and correct a statement that implies an organism mutates in response to its environment.
    153

    Genetic diversity can arise as a result of mutation or during

    Due to the degenerate nature of the genetic code, not all base substitutions cause a change in the sequence of encoded amino acids.

    Verified
    Key Learning Objectives:
    • Explain, using the degenerate nature of the code, why some base substitutions do not change the polypeptide produced.
    • Use a codon table to decide whether a stated base substitution is silent.
    • Distinguish the degenerate and universal properties of the genetic code and state which applies in a given context.
    154

    Genetic diversity can arise as a result of mutation or during

    Gene mutations involve a change in the base sequence of chromosomes.

    Verified
    Key Learning Objectives:
    • Define a gene mutation as a change in the base sequence of DNA within a chromosome.
    • Explain how a change in the base sequence of a gene leads to a change in the tertiary structure of the protein it codes for.
    • Explain why some changes to the base sequence of a gene have no effect on the polypeptide produced.
    155

    Genetic diversity can arise as a result of mutation or during

    Meiosis produces daughter cells that are genetically different from each other.

    Verified
    Key Learning Objectives:
    • Describe two events within meiosis that make the daughter cells genetically different from each other.
    • Explain how crossing over produces new combinations of alleles on one chromosome.
    • Calculate the number of different chromosome combinations possible in the gametes of an organism using $2^n$.
    156

    Genetic diversity can arise as a result of mutation or during

    Mutagenic agents can increase the rate of gene mutation.

    Verified
    Key Learning Objectives:
    • Name two mutagenic agents and describe how each increases the rate of gene mutation.
    • Explain why a mutagen increases the frequency of mutation but does not determine which mutation occurs.
    • Explain why exposure to an antibiotic cannot create an allele for antibiotic resistance.
    157

    Genetic diversity can arise as a result of mutation or during

    Mutations in the number of chromosomes can arise spontaneously by chromosome non-disjunction during meiosis.

    Verified
    Key Learning Objectives:
    • Explain how non-disjunction in meiosis I and in meiosis II produce gametes with abnormal chromosome numbers.
    • Complete a diagram showing the chromosome content of the gametes when non-disjunction occurs at a stated division.
    • Explain why a zygote formed from a gamete carrying an extra chromosome has forty-seven chromosomes.
    158

    Genetic diversity can arise as a result of mutation or during

    Students should be able to: complete diagrams showing the chromosome content of cells after the first and second meiotic division, when given the chromosome content of the parent cell explain the different outcome of mitosis and meiosis recognise where meiosis occurs when given information about an unfamiliar life cycle explain how random fertilisation of haploid gametes further increases genetic variation within a species.

    Verified
    Key Learning Objectives:
    • Complete diagrams of the chromosome content of cells after the first and second meiotic divisions from a given parent cell.
    • Explain the different outcomes of mitosis and meiosis in terms of cell number, chromosome number and genetic variation.
    • Identify where meiosis occurs in an unfamiliar life cycle and justify the choice using chromosome number.
    • Explain how random fertilisation of haploid gametes further increases genetic variation.
    159

    Genetic diversity can arise as a result of mutation or during

    The process of meiosis only in sufficient detail to show how: two nuclear divisions result usually in the formation of four haploid daughter cells from a single diploid parent cell genetically different daughter cells result from the independent segregation of homologous chromosomes crossing over between homologous chromosomes results in further genetic variation among daughter cells.

    Verified
    Key Learning Objectives:
    • Describe the outcome of each meiotic division in terms of chromosome number and chromatid content.
    • Explain how independent segregation and crossing over together produce genetically different gametes.
    • Explain why the chromosome number must be halved during gamete formation in a sexually reproducing species.
    160

    Genetic diversity can arise as a result of mutation or during

    They can arise spontaneously during DNA replication and include base deletion and base substitution.

    Verified
    Key Learning Objectives:
    • Describe how base substitutions and base deletions change the base sequence of a gene.
    • Explain why a base deletion usually has a greater effect on the polypeptide than a base substitution.
    • Predict the amino acid sequence produced after a stated substitution or deletion, using a supplied codon table.
    161

    Genetic fingerprinting (A-level only)

    An organism’s genome contains many variable number tandem repeats (VNTRs). The probability of two individuals having the same VNTRs is very low.

    Verified
    Key Learning Objectives:
    • Describe a VNTR as a short base sequence repeated in tandem, stating that individuals differ in the number of repeats.
    • Explain why many different repeat numbers exist, linking this to many VNTRs being non-coding and therefore often not selected against.
    • Calculate the probability of a chance match across several VNTR loci by multiplying the individual probabilities.
    • Explain why genetic fingerprinting cannot distinguish two monozygotic twins.
    162

    Genetic fingerprinting (A-level only)

    Students should be able to: explain the biological principles that underpin genetic fingerprinting techniques interpret data showing the results of gel electrophoresis to separate DNA fragments explain why scientists might use genetic fingerprinting in the fields of forensic science, medical diagnosis, animal and plant breeding.

    Verified
    Key Learning Objectives:
    • Explain the biological principles of genetic fingerprinting, including the roles of VNTRs, restriction endonucleases or PCR, gel electrophoresis, Southern blotting and DNA probes.
    • Interpret gel electrophoresis data by comparing fragment distances against a lane of known standards.
    • Explain why scientists use genetic fingerprinting in forensics, medical diagnosis, and breeding to assess genetic relationships.
    163

    Genetic fingerprinting (A-level only)

    The technique of genetic fingerprinting in analysing DNA fragments that have been cloned by PCR, and its use in determining genetic relationships and in determining the genetic variability within a population.

    Verified
    Key Learning Objectives:
    • Describe the genetic fingerprinting sequence, from PCR amplification through electrophoresis and probe hybridisation to visualisation.
    • Explain why shorter DNA fragments travel further through the gel during electrophoresis.
    • Use the number of shared bands between two individuals to judge how closely related they are.
    • Use the number of different band positions across sampled individuals to determine genetic variability within a population.
    164

    Genetic fingerprinting (A-level only)

    The use of genetic fingerprinting in the fields of forensic science, medical diagnosis, animal and plant breeding.

    Verified
    Key Learning Objectives:
    • Explain how forensic scientists use VNTR band patterns to reach conclusions about crime scene samples.
    • Determine paternity from a set of band patterns by tracing each of the child's bands to a parent.
    • Suggest why breeders use genetic fingerprinting to measure genetic diversity and prevent inbreeding.
    • Describe a medical application of fingerprinting, such as identifying pathogen strains or diagnosing repeat expansion disorders.
    165

    Inheritance (A-level only)

    Alleles may be dominant, recessive or codominant.

    Verified
    Key Learning Objectives:
    • Explain how a family tree shows that an allele is dominant rather than recessive, quoting the individuals involved and excluding codominance.
    • Predict the phenotypes of all three genotypes for a pair of codominant alleles.
    • Write correct allele symbols for dominant, recessive and codominant alleles within a genetic diagram.
    166

    Inheritance (A-level only)

    In a diploid organism, the alleles at a specific locus may be either homozygous or heterozygous.

    Verified
    Key Learning Objectives:
    • Explain why unaffected parents can have a child with a recessive condition, giving the parental genotypes.
    • Calculate the probability that the next child of two heterozygous parents is homozygous recessive, and express it as a fraction or a percentage.
    • Explain why males cannot be described as homozygous or heterozygous for most X-linked genes.
    167

    Inheritance (A-level only)

    The genotype is the genetic constitution of an organism.

    Verified
    Key Learning Objectives:
    • Define genotype in a way that makes clear it describes one organism and the alleles it carries.
    • Distinguish genotype, genome and gene pool by saying which level of organisation each one describes.
    • Write the genotype of an organism using the allele symbols given in a question, for one gene and for two genes.
    168

    Inheritance (A-level only)

    The phenotype is the expression of this genetic constitution and its interaction with the environment.

    Verified
    Key Learning Objectives:
    • Define phenotype as the expression of the genetic constitution and its interaction with the environment.
    • Explain why two organisms with the same genotype can show different phenotypes, naming an environmental factor responsible.
    • Explain why two organisms with the same phenotype can have different genotypes, using a dominant characteristic as an example.
    169

    Inheritance (A-level only)

    The use of fully labelled genetic diagrams to interpret, or predict, the results of: monohybrid and dihybrid crosses involving dominant, recessive and codominant alleles crosses involving sex-linkage, autosomal linkage, multiple alleles and epistasis.

    Verified
    Key Learning Objectives:
    • Complete a fully labelled genetic diagram for a dihybrid cross, including gametes, offspring genotypes, phenotypes and the expected ratio.
    • Write sex-linked genotypes using X and Y chromosome symbols, and explain why a male cannot be a carrier for a sex-linked gene.
    • Explain why a cross involving two linked genes produces fewer recombinant offspring than a 9:3:3:1 ratio predicts.
    170

    Inheritance (A-level only)

    There may be many alleles of a single gene.

    Verified
    Key Learning Objectives:
    • State what is meant by genetic diversity in terms of alleles, and explain how a gene with many alleles increases it.
    • List all the genotypes possible for a gene with three alleles and give the phenotype produced by each.
    • Explain how mutation increases the number of alleles of a gene in a population over time.
    171

    Inheritance (A-level only)

    Use of the chi-squared ( Χ ) test to compare the goodness of fit of observed phenotypic ratios with expected ratios.

    Verified
    Key Learning Objectives:
    • Calculate the expected numbers of each phenotype from a predicted ratio and a total number of offspring.
    • Calculate a chi-squared value from observed and expected counts, showing the working in a table.
    • Compare a calculated chi-squared value with the critical value at p = 0.05 and write a conclusion that refers back to the null hypothesis.
    172

    Inorganic ions

    Each type of ion has a specific role, depending on its properties.

    Verified
    Key Learning Objectives:
    • Explain, for a named ion, how one of its chemical properties allows it to carry out its biological role.
    • Predict the effect on an organism of a shortage of a named ion, referring to the process that ion is needed for.
    • Compare the roles of two named ions that occur at very different concentrations in the same fluid.
    173

    Inorganic ions

    Inorganic ions occur in solution in the cytoplasm and body fluids of organisms, some in high concentrations and others in very low concentrations.

    Verified
    Key Learning Objectives:
    • Name one ion found in high concentration and one found in very low concentration in a named body fluid, and give the role of each.
    • Explain why an ion present at very low concentration can still be essential to an organism.
    • Explain why inorganic ions require transport proteins to cross a cell-surface membrane.
    174

    Inorganic ions

    Students should be able to recognise the role of ions in the following topics: hydrogen ions and pH; iron ions as a component of haemoglobin; sodium ions in the co-transport of glucose and amino acids; and phosphate ions as components of DNA and of ATP.

    Verified
    Key Learning Objectives:
    • Explain how a fall in pH affects the rate of an enzyme-controlled reaction, referring to hydrogen ions and to bonds in the tertiary structure.
    • Describe the role of iron ions in the transport of oxygen and state how many oxygen molecules one haemoglobin molecule carries.
    • Explain how a sodium ion gradient allows glucose to be absorbed against its concentration gradient in the ileum.
    175

    Investigating diversity

    Genetic diversity within, or between species, can be made by comparing: the frequency of measurable or observable characteristics the base sequence of DNA the base sequence of mRNA the amino acid sequence of the proteins encoded by DNA and mRNA.

    Verified
    Key Learning Objectives:
    • Compare two DNA or amino acid sequences and state what the number of differences shows about genetic diversity.
    • Explain why mRNA base sequences and amino acid sequences can stand in for DNA sequences in such comparisons.
    • Justify why comparing observable characteristics is a less reliable measure of genetic diversity than molecular sequencing.
    176

    Investigating diversity

    Quantitative investigations of variation within a species involve: collecting data from random samples calculating a mean value of the collected data and the standard deviation of that mean interpreting mean values and their standard deviations.

    Verified
    Key Learning Objectives:
    • Describe how to collect a random sample of individuals from a population and explain why it avoids bias.
    • Interpret means and standard deviations, recognising that overlapping SDs indicate a difference is likely not significant.
    • Evaluate investigations by identifying when a statistical test is required to confirm whether a difference is significant.
    177

    Investigating diversity

    Students should be able to: interpret data relating to similarities and differences in the base sequences of DNA and in the amino acid sequences of proteins to suggest relationships between different organisms within a species and between species appreciate that gene technology has caused a change in the methods of investigating genetic diversity; inferring DNA differences from measurable or observable characteristics has been replaced by direct investigation of DNA sequences. Knowledge of gene technologies will not be tested.

    Verified
    Key Learning Objectives:
    • Rank organisms by relatedness from a table of sequence differences and justify the ranking.
    • Explain why direct DNA sequencing replaced inference from observable characteristics when investigating genetic diversity.
    • State one limitation of drawing conclusions about a whole species from a single gene or a small sample.
    178

    Lipids

    A condensation reaction between glycerol and a fatty acid (RCOOH) forms an ester bond.

    Verified
    Key Learning Objectives:
    • Name the bond formed between glycerol and a fatty acid and identify the two functional groups that react.
    • Describe how an ester bond is formed and broken, stating what happens to a water molecule in each case.
    • Explain why the R group of a fatty acid is not involved in the ester bond, and what it determines instead.
    179

    Lipids

    In phospholipids, one of the fatty acids of a triglyceride is substituted by a phosphate-containing group.

    Verified
    Key Learning Objectives:
    • Describe how the structure of a phospholipid differs from that of a triglyceride.
    • Explain why phospholipids arrange themselves into a bilayer when placed in water.
    • Suggest how the hydrophobic and hydrophilic regions of a protein determine its position in a phospholipid bilayer.
    180

    Lipids

    Students should be able to: recognise, from diagrams, saturated and unsaturated fatty acids explain the different properties of triglycerides and phospholipids.

    Verified
    Key Learning Objectives:
    • Identify from a diagram whether a fatty acid is saturated or unsaturated and justify the choice.
    • Explain the properties of a triglyceride and a phospholipid by reference to their different structures.
    • Suggest how the hydrophobic and hydrophilic parts of a phospholipid determine its arrangement in a bilayer.
    181

    Lipids

    The different properties of triglycerides and phospholipids related to their different structures.

    Verified
    Key Learning Objectives:
    • Explain how the three hydrophobic tails of a triglyceride make it suitable as an energy store in a cell.
    • Explain why a phospholipid, but not a triglyceride, can form a bilayer in an aqueous environment.
    • Compare and contrast triglycerides and phospholipids in terms of structure and the role each plays in a cell.
    182

    Lipids

    The emulsion test for lipids.

    Verified
    Key Learning Objectives:
    • Describe the emulsion test for lipids, giving the reagents in the correct order and the positive result.
    • Explain why a cloudy white emulsion forms when the ethanol solution is added to water.
    • Suggest a suitable control for the emulsion test and explain why the apparatus must be clean and dry.
    183

    Lipids

    The R-group of a fatty acid may be saturated or unsaturated.

    Verified
    Key Learning Objectives:
    • State the difference between a saturated and an unsaturated fatty acid in terms of carbon-carbon double bonds.
    • Explain why a triglyceride containing unsaturated fatty acids is liquid at room temperature while a saturated one is solid.
    • Suggest how the proportion of unsaturated fatty acid tails affects the fluidity of a cell-surface membrane.
    184

    Lipids

    Triglycerides and phospholipids are two groups of lipid.

    Verified
    Key Learning Objectives:
    • Name the two groups of lipid in the specification and state the components of each.
    • Explain why lipids are not classified as polymers even though they are large organic molecules.
    • State the roles of triglycerides and phospholipids in a cell and link each role to where the molecule is found.
    185

    Lipids

    Triglycerides are formed by the condensation of one molecule of glycerol and three molecules of fatty acid.

    Verified
    Key Learning Objectives:
    • Describe the formation of a triglyceride, stating the number of condensation reactions, ester bonds and water molecules involved.
    • Draw or label a triglyceride to show glycerol, the three fatty acids and the position of the ester bonds.
    • Explain how a triglyceride is broken down again, naming the enzyme, the reaction and the products.
    186

    Many proteins are enzymes

    Each enzyme lowers the activation energy of the reaction it catalyses.

    Verified
    Key Learning Objectives:
    • Explain, using an energy level diagram, why a catalysed reaction proceeds quickly at 37 degrees Celsius when the uncatalysed reaction needs far more heat.
    • Describe how binding of the substrate in the active site strains its bonds so that less energy is needed to reach the transition state.
    • State two quantities an enzyme does not change, the overall energy change of the reaction and the final amount of product, and justify each.
    187

    Many proteins are enzymes

    Required practical 1: Investigation into the effect of a named variable on the rate of an enzyme-controlled reaction.

    Verified
    Key Learning Objectives:
    • Plan an investigation into one named variable affecting enzyme activity, stating the range of values, the measure of rate and three controlled variables.
    • Calculate an initial rate of reaction from a product against time curve by drawing a tangent at the origin.
    • Evaluate a given enzyme method, identifying one variable that has not been controlled and explaining how it would affect the results.
    188

    Many proteins are enzymes

    Students should be able to: appreciate how models of enzyme action have changed over time appreciate that enzymes catalyse a wide range of intracellular and extracellular reactions that determine structures and functions from cellular to whole-organism level.

    Verified
    Key Learning Objectives:
    • Explain how the induced fit model developed from the lock-and-key model due to new evidence.
    • Distinguish between intracellular and extracellular enzyme reactions with named examples.
    • Describe how enzymes determine both structures and functions from the cellular to the whole-organism level.
    189

    Many proteins are enzymes

    The induced-fit model of enzyme action.

    Verified
    Key Learning Objectives:
    • Describe what happens to the active site as a substrate enters, and name the change as a change in tertiary structure.
    • Compare the induced-fit and lock-and-key models, giving one observation that induced fit explains and lock and key does not.
    • Explain why an enzyme can catalyse many reactions one after another, referring to the active site returning to its original shape.
    190

    Many proteins are enzymes

    The properties of an enzyme relate to the tertiary structure of its active site and its ability to combine with complementary substrate(s) to form an enzyme-substrate complex.

    Verified
    Key Learning Objectives:
    • Explain how two enzymes with different amino acid sequences can catalyse the same reaction, referring to the tertiary structure of their active sites.
    • Describe the formation of an enzyme-substrate complex, naming the property of the substrate that allows it to bind.
    • Predict the effect on the rate of reaction of a mutation that changes one amino acid within the active site, and justify the prediction.
    191

    Many proteins are enzymes

    The specificity of enzymes The effects of the following factors on the rate of enzyme- controlled reactions – enzyme concentration, substrate concentration, concentration of competitive and of non- competitive inhibitors, pH and temperature.

    Verified
    Key Learning Objectives:
    • Explain the shape of a rate against substrate concentration curve by naming the limiting factor for each region of the graph.
    • Distinguish competitive from non-competitive inhibition from data showing what happens when substrate concentration is raised.
    • Describe, in terms of bonds and tertiary structure, why activity falls either side of the optimum pH and above the optimum temperature.
    192

    Mass transport in animals

    Many animals are adapted to their environment by possessing different types of haemoglobin with different oxygen transport properties.

    Verified
    Key Learning Objectives:
    • Deduce, from two curves drawn on the same axes, which haemoglobin has the higher affinity for oxygen.
    • Suggest the environment or activity level of an unfamiliar organism from the position of its dissociation curve.
    • Explain why fetal haemoglobin must have a higher affinity for oxygen than adult haemoglobin.
    193

    Mass transport in animals

    Names are required only of the coronary arteries and of the blood vessels entering and leaving the heart, lungs and kidneys.

    Verified
    Key Learning Objectives:
    • Label the vena cava, pulmonary artery, pulmonary vein and aorta on a heart diagram and state which carry oxygenated blood.
    • Name the vessels entering and leaving a kidney and give the direction of flow in each.
    • Explain how blockage of a coronary artery affects respiration in cardiac muscle.
    194

    Mass transport in animals

    Pressure and volume changes and associated valve movements during the cardiac cycle that maintain a unidirectional flow of blood.

    Verified
    Key Learning Objectives:
    • Identify from a pressure against time graph when each valve opens and closes, giving the pressure reason in each case.
    • Describe the three stages of the cardiac cycle in terms of chamber contraction, pressure and volume.
    • Calculate heart rate in beats per minute from the duration of one cardiac cycle read from a graph.
    195

    Mass transport in animals

    Required practical 5: Dissection of animal or plant gas exchange system or mass transport system or of organ within such a system.

    Verified
    Key Learning Objectives:
    • Describe a safe method for dissecting a named gas exchange or mass transport organ, justifying precautions.
    • Produce a labelled biological drawing following conventions of continuous lines and proportion.
    • Calculate the actual size of a structure from a measured image size and a stated magnification.
    196

    Mass transport in animals

    Students should be able to: analyse and interpret data relating to pressure and volume changes during the cardiac cycle analyse and interpret data associated with specific risk factors and the incidence of cardiovascular disease evaluate conflicting evidence associated with risk factors affecting cardiovascular disease recognise correlations and causal relationships.

    Verified
    Key Learning Objectives:
    • Interpret pressure and volume changes during the cardiac cycle to identify valve movements and calculate heart rate.
    • Analyse data on cardiovascular disease incidence to distinguish between correlation and causation.
    • Evaluate conflicting evidence regarding risk factors by comparing study methodologies and standard deviations.
    197

    Mass transport in animals

    The cooperative nature of oxygen binding to show that the change in shape of haemoglobin caused by binding of the first oxygens makes the binding of further oxygens easier.

    Verified
    Key Learning Objectives:
    • Explain the shallow, steep and plateau regions of the dissociation curve in terms of cooperative binding and saturation.
    • Describe how binding of the first oxygen molecule changes the tertiary and quaternary structure of haemoglobin and increases affinity for subsequent binding events.
    • Apply cooperative binding to explain why unloading in a respiring tissue is rapid once it has started.
    198

    Mass transport in animals

    The effects of carbon dioxide concentration on the dissociation of oxyhaemoglobin (the Bohr effect).

    Verified
    Key Learning Objectives:
    • Explain how a rise in carbon dioxide concentration lowers the affinity of haemoglobin for oxygen.
    • Identify a Bohr-shifted curve on a graph, state the direction of the shift and say what it means for unloading.
    • Use the Bohr effect to explain why exercising muscle receives more oxygen than resting muscle at the same partial pressure of oxygen.
    199

    Mass transport in animals

    The general pattern of blood circulation in a mammal.

    Verified
    Key Learning Objectives:
    • Trace a red blood cell through both circuits of a mammal, naming the chambers and vessels in order.
    • Explain the advantage of a double circulation to an organism with a high metabolic rate.
    • Describe the general pattern of blood circulation in a mammal, including the route taken and the separation of oxygenated and deoxygenated blood.
    200

    Mass transport in animals

    The gross structure of the human heart.

    Verified
    Key Learning Objectives:
    • Label the chambers, valves, vena cava, pulmonary vein, aorta and pulmonary artery on a diagram of the heart.
    • Explain why the wall of the left ventricle is thicker than that of the right in terms of the pressure each generates.
    • Describe the position and function of the atrioventricular and semilunar valves.
    201

    Mass transport in animals

    The haemoglobins are a group of chemically similar molecules found in many different organisms. Haemoglobin is a protein with a quaternary structure.

    Verified
    Key Learning Objectives:
    • State what makes a protein quaternary and name the bonds holding the four chains of haemoglobin together.
    • Explain how a change in the amino acid sequence of a globin chain can alter the molecule's affinity for oxygen.
    • Deduce the maximum number of oxygen molecules that a stated number of haemoglobin molecules can carry.
    202

    Mass transport in animals

    The loading, transport and unloading of oxygen in relation to the oxyhaemoglobin dissociation curve.

    Verified
    Key Learning Objectives:
    • Read percentage saturation at a stated partial pressure of oxygen, then calculate both the fall in percentage saturation between lungs and tissues and what fraction of the oxygen carried that fall represents.
    • Explain why the steep region of the curve is the one that matters most to a respiring tissue.
    • Describe how oxygen is transported bound to haemoglobin in the blood.
    • Sketch a curve of higher or lower affinity relative to a given curve, keeping its start and maximum unchanged.
    203

    Mass transport in animals

    The role of haemoglobin and red blood cells in the transport of oxygen.

    Verified
    Key Learning Objectives:
    • Explain two features of a mature mammalian red blood cell that increase the rate at which it takes up oxygen.
    • Suggest which molecule a red blood cell stain binds to, and explain why a DNA stain fails to show mammalian red blood cells.
    • Describe where oxygen is loaded and where it is unloaded, naming the partial pressure of oxygen conditions in each place.
    204

    Mass transport in animals

    The structure of arteries, arterioles and veins in relation to their function.

    Verified
    Key Learning Objectives:
    • Explain how elastic tissue in an artery wall maintains blood pressure between heartbeats.
    • Compare an artery with a vein, linking each structural difference to the pressure of the blood it carries.
    • Explain how contraction of smooth muscle in arterioles changes the distribution of blood between organs.
    205

    Mass transport in animals

    The structure of capillaries and the importance of capillary beds as exchange surfaces. The formation of tissue fluid and its return to the circulatory system.

    Verified
    Key Learning Objectives:
    • Describe how tissue fluid is formed at the arteriole end of a capillary and how most of it returns at the venule end.
    • Explain, in terms of water potential, why a low plasma protein concentration causes tissues to swell.
    • Explain two features of a capillary bed that increase the rate of exchange between blood and cells.
    206

    Mass transport in plants

    Phloem as the tissue that transports organic substances in plants.

    Verified
    Key Learning Objectives:
    • Describe how sucrose is loaded into a sieve tube element, naming the role of the companion cell and of ATP.
    • Compare the structure of phloem with that of xylem and relate each difference to what the tissue transports.
    • Identify sources and sinks in a given plant and state the direction of transport between them.
    207

    Mass transport in plants

    Students should be able to: recognise correlations and causal relationships interpret evidence from tracer and ringing experiments and to evaluate the evidence for and against the mass flow hypothesis.

    Verified
    Key Learning Objectives:
    • Evaluate a set of results as evidence for and against the mass flow hypothesis, quoting data on both sides.
    • Explain why a correlation between two variables in a transport experiment does not establish cause.
    • Identify a limitation of a ringing or tracer experiment and state what further evidence would strengthen the conclusion.
    208

    Mass transport in plants

    The mass flow hypothesis for the mechanism of translocation in plants. The use of tracers and ringing experiments to investigate transport in plants.

    Verified
    Key Learning Objectives:
    • Explain how loading sucrose at a source generates the hydrostatic pressure that drives mass flow.
    • Predict and explain the appearance of a ringed stem above and below the ring.
    • Describe how radioactive tracers and autoradiography are used to investigate transport in plants.
    209

    Mass transport in plants

    Xylem as the tissue that transports water in the stem and leaves of plants. The cohesion-tension theory of water transport in the xylem.

    Verified
    Key Learning Objectives:
    • Explain how evaporation from a leaf creates the tension that pulls water up a xylem vessel.
    • Explain the importance of hydrogen bonding between water molecules to cohesion-tension.
    • Predict the effect on water transport of an air bubble in a xylem vessel or of a vessel that has lost its lignin.
    210

    Methods of studying cells

    Measuring the size of an object viewed with an optical microscope.

    Verified
    Key Learning Objectives:
    • Calibrate an eyepiece graticule against a stage micrometer and state the value of one division for a given objective lens.
    • Calculate the magnification of a printed image from a measured image length and a stated real size, showing the conversion to a common unit.
    • Rearrange the magnification equation to find the real size of a structure from an image and a stated magnification.
    • Convert confidently between millimetres, micrometres and nanometres inside a microscopy calculation.
    211

    Methods of studying cells

    Students should be able to appreciate that there was a considerable period of time during which the scientific community distinguished between artefacts and cell organelles.

    Verified
    Key Learning Objectives:
    • Define an artefact and give two preparation steps that can create one.
    • Explain how scientists established that a newly seen structure was a genuine organelle rather than an artefact.
    • Suggest, for a structure seen in only one electron micrograph, why other scientists would not accept it immediately.
    • Evaluate a claim about cell structure by judging whether it has been repeated with different preparation methods.
    212

    Methods of studying cells

    The difference between magnification and resolution.

    Verified
    Key Learning Objectives:
    • Distinguish magnification from resolution by naming the quantity each measures and the units each carries.
    • Explain why two structures 0.1 micrometres apart cannot be separated by an optical microscope at any magnification.
    • Suggest why a discovery about cell structure had to wait for the electron microscope, referring to resolution rather than magnification.
    • Correct an answer that uses the word magnification where resolution is required.
    213

    Methods of studying cells

    The principles and limitations of optical microscopes, transmission electron microscopes and scanning electron microscopes.

    Verified
    Key Learning Objectives:
    • Explain why the resolution of an optical microscope cannot be improved beyond about 0.2 micrometres however much the image is magnified.
    • Choose the appropriate microscope for a stated purpose and justify the choice from resolution and the type of image produced.
    • Describe two limitations of electron microscopy that arise from specimen preparation rather than from the instrument.
    • Suggest why a cell structure first reported in the 1950s could not have been seen with a light microscope.
    214

    Monomers and polymers

    A condensation reaction joins two molecules together with the formation of a chemical bond and involves the elimination of a molecule of water.

    Verified
    Key Learning Objectives:
    • Describe a condensation reaction in terms of the two molecules joined, the bond formed and the water molecule eliminated.
    • Calculate the number of bonds formed and water molecules released when a stated number of monomers is joined into one polymer.
    • Name the bond formed by condensation for each of monosaccharides, amino acids, nucleotides and glycerol with fatty acids.
    215

    Monomers and polymers

    A hydrolysis reaction breaks a chemical bond between two molecules and involves the use of a water molecule.

    Verified
    Key Learning Objectives:
    • Describe hydrolysis in terms of the bond broken, the water molecule used and the products formed.
    • Explain why yeast supplied with maltose releases carbon dioxide more slowly than yeast supplied with glucose.
    • Distinguish between the action of endopeptidases, exopeptidases and dipeptidases on a polypeptide chain.
    216

    Monomers and polymers

    Monomers are the smaller units from which larger molecules are made.

    Verified
    Key Learning Objectives:
    • Define a monomer in one sentence that names both the small unit and the larger molecule it builds.
    • Identify the repeating monomer and the bond between monomers from a diagram of an unfamiliar polymer such as chitin.
    • Explain why glycerol and fatty acids are not monomers even though a triglyceride is a large molecule.
    217

    Monomers and polymers

    Monosaccharides, amino acids and nucleotides are examples of monomers.

    Verified
    Key Learning Objectives:
    • Name the three monomers in the specification and state the polymer and the bond associated with each.
    • Describe the three components of a DNA nucleotide and say how this differs from an RNA nucleotide.
    • Explain why a triglyceride is not described as a polymer, using the meaning of monomer in your answer.
    218

    Monomers and polymers

    Polymers are molecules made from a large number of monomers joined together.

    Verified
    Key Learning Objectives:
    • Describe how a polymer is built from monomers, naming the reaction, the bond formed and the molecule released.
    • Use a diagram of an unfamiliar polymer to describe three structural features, referring to the monomer, the bond and the shape of the chain.
    • Explain why alternate beta-glucose molecules must be rotated through 180 degrees before a glycosidic bond can form.
    219

    Monomers and polymers

    The variety of life, both past and present, is extensive, but the biochemical basis of life is similar for all living things.

    Verified
    Key Learning Objectives:
    • Name the four groups of organic molecule found in all living organisms, and give the monomer from which carbohydrates, proteins and nucleic acids are built.
    • Explain why carbon is the element at the centre of biological molecules, referring to its ability to form four covalent bonds and long chains.
    • Suggest why comparing DNA base sequences or amino acid sequences between two species gives better evidence of relatedness than comparing their appearance.
    220

    Most of a cell’s DNA is not translated (A-level only)

    During development, totipotent cells translate only part of their DNA, resulting in cell specialisation.

    Verified
    Key Learning Objectives:
    • Explain how two cells with identical DNA can have different structures and functions.
    • Describe the sequence from a gene being switched on to a protein determining a cell's specialisation.
    • Explain why a cell's potency decreases as development proceeds due to gene silencing.
    221

    Most of a cell’s DNA is not translated (A-level only)

    Induced pluripotent stem cells (iPS cells) can be produced from adult somatic cells using appropriate protein transcription factors.

    Verified
    Key Learning Objectives:
    • Describe how an adult somatic cell is converted into an induced pluripotent stem cell.
    • Explain how a protein transcription factor switches a gene on, referring to the promoter region and RNA polymerase.
    • Give two advantages of using iPS cells rather than embryonic stem cells in treatment.
    222

    Most of a cell’s DNA is not translated (A-level only)

    Pluripotent cells are found in embryos; multipotent and unipotent cells are found in mature mammals and can divide to form a limited number of different cell types.

    Verified
    Key Learning Objectives:
    • Define pluripotent, multipotent and unipotent cells and identify where they are found.
    • Explain how multipotent and unipotent cells differ in the number of cell types they can form.
    • Describe how the restriction of cell potency relates to gene expression and epigenetic silencing.
    223

    Most of a cell’s DNA is not translated (A-level only)

    Pluripotent stem cells can divide in unlimited numbers and can be used in treating human disorders.

    Verified
    Key Learning Objectives:
    • State the two properties of pluripotent stem cells that make them useful in treatment.
    • Explain how supplying stem cells to damaged cardiac muscle could raise ventricular pressure.
    • Interpret data from a stem cell treatment experiment, using the control to justify a conclusion about differentiation.
    224

    Most of a cell’s DNA is not translated (A-level only)

    Students should be able to evaluate the use of stem cells in treating human disorders.

    Verified
    Key Learning Objectives:
    • Evaluate the use of stem cells for a named disorder, giving at least two points for and two against.
    • Explain why using a patient's own adult stem cells or iPS cells reduces the risk of rejection, referring to antigens.
    • Identify two limitations of evidence from an animal stem cell trial when it is applied to human patients.
    225

    Most of a cell’s DNA is not translated (A-level only)

    Totipotent cells can divide and produce any type of body cell.

    Verified
    Key Learning Objectives:
    • Define a totipotent cell and state what it can produce that a pluripotent cell cannot.
    • Explain why all the body cells of one organism contain the same DNA yet have different structures.
    • Give one example of a totipotent cell in a mammal, and explain why being able to divide, as well as to differentiate, is part of the definition.
    226

    Most of a cell’s DNA is not translated (A-level only)

    Totipotent cells occur only for a limited time in early mammalian embryos.

    Verified
    Key Learning Objectives:
    • State at which stages of mammalian development totipotent cells are present.
    • Explain why the cells of a blastocyst's inner cell mass are pluripotent rather than totipotent.
    • Explain, in terms of gene expression, why potency decreases as an embryo develops.
    227

    Most of a cell’s DNA is not translated (A-level only)

    Unipotent cells, exemplified by the formation of cardiomyocytes.

    Verified
    Key Learning Objectives:
    • Define unipotent cells and describe their restricted differentiation potential.
    • State that the formation of cardiomyocytes is an example of unipotent cell activity.
    • Compare unipotent cells with other types of stem cells based on their potency.
    228

    Nerve impulses (A-level only)

    Changes in membrane permeability lead to depolarisation and the generation of an action potential. The all-or-nothing principle.

    Verified
    Key Learning Objectives:
    • Annotate a trace of an action potential with the ion movements responsible for each phase.
    • Explain, using threshold, why a stimulus below threshold produces no action potential at all.
    • Explain how the nervous system codes a stronger stimulus when every action potential is the same size.
    229

    Nerve impulses (A-level only)

    Factors affecting the speed of conductance: myelination and saltatory conduction; axon diameter; temperature.

    Verified
    Key Learning Objectives:
    • Explain why destroying myelin, as happens in multiple sclerosis, produces slower responses to a stimulus.
    • Predict and justify the effect of increasing axon diameter on the speed of conduction.
    • Explain how temperature affects conduction speed through the kinetic energy of ions and protein denaturation.
    230

    Nerve impulses (A-level only)

    The establishment of a resting potential in terms of differential membrane permeability, electrochemical gradients and the movement of sodium ions and potassium ions.

    Verified
    Key Learning Objectives:
    • Explain how moving three sodium ions out for every two potassium ions in contributes to a negative interior.
    • Describe the differential permeability of the axon membrane at rest and predict what happens if potassium ion channels are blocked.
    • Explain why a respiratory inhibitor such as cyanide causes the resting potential to decay.
    231

    Nerve impulses (A-level only)

    The nature and importance of the refractory period in producing discrete impulses and in limiting the frequency of impulse transmission.

    Verified
    Key Learning Objectives:
    • Explain why an action potential cannot travel backwards along the stretch of axon it has just passed along.
    • Calculate the maximum frequency of impulses from a given refractory period and say what that means for coding stimulus intensity.
    • Distinguish the absolute from the relative refractory period in terms of the state of the sodium ion channels and the membrane potential.
    232

    Nerve impulses (A-level only)

    The passage of an action potential along non-myelinated and myelinated axons, resulting in nerve impulses.

    Verified
    Key Learning Objectives:
    • Explain how local currents depolarise the next region of membrane to threshold in a non-myelinated axon.
    • Compare conduction in myelinated and non-myelinated axons in terms of how much membrane depolarises.
    • Explain why the refractory period, rather than the myelin sheath, makes propagation one-way.
    233

    Nerve impulses (A-level only)

    The structure of a myelinated motor neurone.

    Verified
    Key Learning Objectives:
    • Label the axon, Schwann cell, myelin sheath, node of Ranvier and cell body on a diagram of a myelinated motor neurone.
    • Explain how the layered membranes of a Schwann cell insulate the axon and restrict depolarisation to the nodes.
    • Distinguish a motor neurone from a sensory neurone by the position of the cell body and the direction of conduction.
    234

    Nutrient cycles (A-level only)

    Microorganisms play a vital role in recycling chemical elements such as phosphorus and nitrogen.

    Verified
    Key Learning Objectives:
    • Name four groups of soil microorganism and state the conversion each one carries out.
    • Explain why sterilising the soil is a valid control in an experiment on a single soil organism.
    • Describe how extracellular digestion by saprobionts releases ammonium and phosphate ions.
    • Predict the effect on plant growth of soil that has been sterilised and not re-inoculated.
    235

    Nutrient cycles (A-level only)

    Nutrients are recycled within natural ecosystems, exemplified by the nitrogen cycle and the phosphorus cycle.

    Verified
    Key Learning Objectives:
    • Contrast the one-way flow of energy with the recycling of nitrogen and phosphorus in an ecosystem.
    • Name the inorganic ion by which plants take up each of nitrogen and phosphorus, and the transport mechanism used.
    • Describe two named organic molecules that require nitrogen and two that require phosphorus.
    • Predict what happens to nutrient availability in an ecosystem from which decomposers are removed.
    236

    Nutrient cycles (A-level only)

    The environmental issues arising from the use of fertilisers including leaching and eutrophication.

    Verified
    Key Learning Objectives:
    • Describe the sequence of eutrophication from fertiliser application to the death of fish, in the correct causal order.
    • Explain why nitrate leaches more readily than phosphate from agricultural soil, referring to the solubility of nitrate and to the adsorption of phosphate.
    • Identify which organisms consume the dissolved oxygen during eutrophication, and why.
    • Suggest two farming practices that reduce leaching, and justify each one.
    237

    Nutrient cycles (A-level only)

    The role of bacteria in the nitrogen cycle in sufficient detail to illustrate the processes of saprobiotic nutrition, ammonification, nitrification, nitrogen fixation and denitrification.

    Verified
    Key Learning Objectives:
    • Sequence the nitrogen cycle from dead organic matter through to nitrate, naming the bacteria responsible for each step.
    • Explain why nitrification requires an aerated soil and denitrification an anaerobic one.
    • Describe nitrogen fixation in terms of nitrogenase, the reduction of nitrogen gas and the ATP cost.
    • Predict the effect of ploughing or draining a field on the nitrate content of its soil, and justify it.
    238

    Nutrient cycles (A-level only)

    The role of mycorrhizae in facilitating the uptake of water and inorganic ions by plants.

    Verified
    Key Learning Objectives:
    • Explain how fungal hyphae increase the uptake of water and inorganic ions by a plant root.
    • Describe what each partner gains in a mycorrhizal association.
    • Use overlapping or non-overlapping standard deviations to decide whether a difference in yield is significant.
    • Evaluate a mycorrhizae experiment by identifying limitations such as a single species, sterile soil or greenhouse conditions.
    239

    Nutrient cycles (A-level only)

    The role of saprobionts in decomposition.

    Verified
    Key Learning Objectives:
    • Describe saprobiotic nutrition as a sequence of secretion of enzymes, hydrolysis and absorption of products.
    • Name two hydrolytic enzymes a saprobiont secretes and the polymer each one acts on.
    • Explain how saprobiont activity returns ammonium and phosphate ions to the soil.
    • Predict the effect of waterlogging or low temperature on the rate of decomposition, and justify it.
    240

    Nutrient cycles (A-level only)

    The use of natural and artificial fertilisers to replace the nitrates and phosphates lost by harvesting plants and removing livestock.

    Verified
    Key Learning Objectives:
    • Explain why harvesting a crop depletes soil nitrate and phosphate whereas a natural ecosystem does not.
    • Compare natural and artificial fertilisers in terms of how quickly their ions become available.
    • Name a molecule requiring nitrogen and one requiring phosphorus, and link each to growth.
    • Justify keeping fertiliser application constant as a controlled variable in a plant growth investigation.
    241

    Photosynthesis (A-level only)

    Required practical 7: Use of chromatography to investigate the pigments isolated from leaves of different plants, eg, leaves from shade-tolerant and shade-intolerant plants or leaves of different colours.

    Verified
    Key Learning Objectives:
    • Describe how to separate leaf pigments using paper or thin-layer chromatography, detailing the correct setup.
    • Calculate Rf values to identify and compare pigments isolated from leaves of different plants.
    • Explain differences in pigment composition between shade-tolerant and shade-intolerant plants as adaptations to light availability.
    242

    Photosynthesis (A-level only)

    Required practical 8: Investigation into the effect of a named factor on the rate of dehydrogenase activity in extracts of chloroplasts.

    Verified
    Key Learning Objectives:
    • Explain why the chloroplast extraction medium must be ice-cold, buffered and isotonic.
    • Describe how the reduction of DCPIP is used to measure the rate of the light-dependent reaction.
    • Design a valid investigation into one named factor affecting dehydrogenase activity, naming the control and the controlled variables.
    243

    Photosynthesis (A-level only)

    Students should be able to: identify environmental factors that limit the rate of photosynthesis evaluate data relating to common agricultural practices used to overcome the effect of these limiting factors.

    Verified
    Key Learning Objectives:
    • Identify the limiting factor in each region of a photosynthesis rate graph and justify your choice.
    • Explain how low light, low carbon dioxide and low temperature each reduce the rate, in terms of named molecules.
    • Evaluate an agricultural practice such as carbon dioxide enrichment, weighing yield against cost and the design of the trial.
    244

    Photosynthesis (A-level only)

    The hydrolysis of ATP, also from the light-dependent reaction, provides the additional energy for this reaction.

    Verified
    Key Learning Objectives:
    • Explain how the hydrolysis of ATP supplies the energy for the reduction of glycerate 3-phosphate.
    • Identify the two steps of the Calvin cycle that require ATP and say what each one achieves.
    • Predict the effect on GP, triose phosphate and RuBP of a fall in the supply of ATP from the light-dependent reaction.
    245

    Photosynthesis (A-level only)

    The light-dependent reaction in such detail as to show that: chlorophyll absorbs light, leading to photoionisation of chlorophyll some of the energy from electrons released during photoionisation is conserved in the production of ATP and reduced NADP the production of ATP involves electron transfer associated with the transfer of electrons down the electron transfer chain and passage of protons across chloroplast membranes and is catalysed by ATP synthase embedded in these membranes (chemiosomotic theory) photolysis of water produces protons, electrons and oxygen.

    Verified
    Key Learning Objectives:
    • Describe the path of an electron from chlorophyll to reduced NADP, naming photoionisation and the electron transfer chain.
    • Explain how a proton gradient across the thylakoid membrane leads to ATP synthesis by ATP synthase.
    • State the three products of photolysis and say what happens to each of them, including how the electrons replace those lost from chlorophyll.
    • Use the rate of oxygen production as a measure of the rate of the light-dependent reaction.
    246

    Photosynthesis (A-level only)

    The light-independent reaction in such detail as to show that: carbon dioxide reacts with ribulose bisphosphate (RuBP) to form two molecules of glycerate 3-phosphate (GP). This reaction is catalysed by the enzyme rubisco ATP and reduced NADP from the light-dependent reaction are used to reduce GP to triose phosphate some of the triose phosphate is used to regenerate RuBP in the Calvin cycle some of the triose phosphate is converted to useful organic substances.

    Verified
    Key Learning Objectives:
    • Describe one turn of the Calvin cycle, naming RuBP, GP, triose phosphate and rubisco in the correct order.
    • Explain the separate roles of reduced NADP and of ATP in the reduction of GP.
    • Account for the fate of triose phosphate, distinguishing the fraction that regenerates RuBP from the fraction that leaves the cycle.
    • Predict how the concentrations of RuBP and GP change when the carbon dioxide supply is cut off.
    247

    Photosynthesis (A-level only)

    The light-independent reaction uses reduced NADP from the light- dependent reaction to form a simple sugar.

    Verified
    Key Learning Objectives:
    • Explain the role of reduced NADP in converting glycerate 3-phosphate to triose phosphate.
    • Predict the effect of a reduced supply of reduced NADP on the amounts of GP, triose phosphate and sugar.
    • State where in the chloroplast the light-independent reaction occurs and why it depends on the light-dependent reaction.
    248

    Populations (A-level only)

    A population as a group of organisms of the same species occupying a particular space at a particular time that can potentially interbreed.

    Verified
    Key Learning Objectives:
    • Define a population in a single sentence containing all four required elements.
    • Explain why the definition says organisms can potentially interbreed rather than do interbreed.
    • Decide from information about two groups of organisms whether they form one population or two, and justify the decision.
    249

    Populations (A-level only)

    Species exist as one or more populations.

    Verified
    Key Learning Objectives:
    • Explain how several populations can belong to one species, using the idea of gene flow.
    • Interpret a distribution map to identify separate populations and describe what is preventing gene flow between them.
    • State what must happen to two populations of one species before they count as two species.
    250

    Populations (A-level only)

    The concepts of gene pool and allele frequency.

    Verified
    Key Learning Objectives:
    • Define gene pool and allele frequency, and explain why a frequency is a proportion rather than a count.
    • Explain how the use of antibiotics raises the frequency of a resistance allele in a bacterial population.
    • Describe what happens to the gene pools of two populations of one species when gene flow between them stops.
    251

    Populations (A-level only)

    The conditions under which the principle applies.

    Verified
    Key Learning Objectives:
    • List the five conditions under which the Hardy-Weinberg principle predicts constant allele frequencies.
    • Explain how breaking each condition would change allele frequencies, giving the direction of change.
    • Suggest, from data showing changed allele frequencies, which of the conditions the population has broken.
    252

    Populations (A-level only)

    The Hardy–Weinberg principle provides a mathematical model, which predicts that allele frequencies will not change from generation to generation.

    Verified
    Key Learning Objectives:
    • Calculate allele and genotype frequencies from the proportion of a population showing a recessive characteristic.
    • Calculate the percentage of heterozygous carriers in a population using 2pq.
    • Decide whether the Hardy-Weinberg principle would hold for a described population and justify the decision by reference to the conditions of the model.
    253

    Populations in ecosystems (A-level only)

    A community and the non-living components of its environment together form an ecosystem.

    Verified
    Key Learning Objectives:
    • State the two components of an ecosystem and give a named example of each for one named ecosystem.
    • Classify factors such as light intensity, predation, soil pH and interspecific competition as abiotic or biotic.
    • Explain how energy flow and nutrient cycling link the living and non-living parts of one named ecosystem.
    254

    Populations in ecosystems (A-level only)

    An ecosystem supports a certain size of population of a species, called the carrying capacity. This population size can vary as a result of: the effect of abiotic factors interactions between organisms: interspecific and intraspecific competition and predation.

    Verified
    Key Learning Objectives:
    • Define carrying capacity and explain why a population fluctuates around it rather than settling on it.
    • Explain how one named abiotic factor changes the carrying capacity of a named ecosystem, linking the factor to survival and reproduction.
    • Distinguish intraspecific from interspecific competition in a given example and predict the effect of each on population size.
    • Interpret a predator-prey graph, describing the lag between the prey peak and the predator peak.
    255

    Populations in ecosystems (A-level only)

    At each stage in succession, certain species may be recognised which change the environment so that it becomes more suitable for other species with different adaptations.

    Verified
    Key Learning Objectives:
    • Explain how one named species at one seral stage changes a named abiotic factor.
    • Predict the adaptations of the next colonising species, given the abiotic change described.
    • Explain why species diversity usually increases during succession, in terms of the number of niches available.
    256

    Populations in ecosystems (A-level only)

    Changes that organisms produce in their abiotic environment can result in a less hostile environment and change biodiversity.

    Verified
    Key Learning Objectives:
    • Explain how colonising organisms change two named abiotic factors during succession.
    • Interpret species richness and index of diversity data across seral stages and describe the trend.
    • Suggest why biodiversity may fall between a mid-successional stage and the climax community.
    257

    Populations in ecosystems (A-level only)

    Conservation of habitats frequently involves management of succession.

    Verified
    Key Learning Objectives:
    • Explain why a named early-successional habitat disappears if it is not managed.
    • Describe two management methods used to arrest succession and state what each removes.
    • Give two distinct reasons for conserving a named habitat, going beyond protecting wildlife.
    258

    Populations in ecosystems (A-level only)

    Ecosystems are dynamic systems.

    Verified
    Key Learning Objectives:
    • Explain what is meant by a dynamic equilibrium in an ecosystem, using a named fluctuating population.
    • Describe one short-term and one long-term process that changes the composition of an ecosystem.
    • Predict the effects on at least two other populations of removing one named species from a given food web.
    259

    Populations in ecosystems (A-level only)

    Ecosystems can range in size from the very small to the very large.

    Verified
    Key Learning Objectives:
    • Give one small-scale and one large-scale example of an ecosystem and identify the community and abiotic components of each.
    • Explain why the boundary of an ecosystem is chosen by the investigator rather than fixed in nature.
    • Suggest how the size of an ecosystem affects the sampling method and the number of samples needed.
    260

    Populations in ecosystems (A-level only)

    Populations of different species form a community.

    Verified
    Key Learning Objectives:
    • Distinguish a population from a community by stating what each includes, using the same named habitat for both.
    • Name two interactions between populations in a named community and state which population is affected in each.
    • Explain why a conclusion drawn from one sampled community cannot be applied to all communities of that type.
    261

    Populations in ecosystems (A-level only)

    Primary succession, from colonisation by pioneer species to climax community.

    Verified
    Key Learning Objectives:
    • Describe the sequence of primary succession from bare rock to a climax community, naming the organisms at three stages.
    • Explain how pioneer species make the abiotic environment less hostile, referring to soil formation.
    • Distinguish primary from secondary succession given an unfamiliar description of a site.
    262

    Populations in ecosystems (A-level only)

    Required practical 12: Investigation into the effect of a named environmental factor on the distribution of a given species.

    Verified
    Key Learning Objectives:
    • Design an investigation into the effect of one named environmental factor on the distribution of a named species, stating the sampling method and the measure of abundance.
    • Justify the use of a belt transect rather than random quadrats where an environmental gradient is present.
    • State three conclusions about distribution from a given map or figure without going beyond the data.
    • Explain why a correlation between an abiotic factor and abundance does not prove a causal relationship.
    263

    Populations in ecosystems (A-level only)

    Students should be able to: show understanding of the need to manage the conflict between human needs and conservation in order to maintain the sustainability of natural resources evaluate evidence and data concerning issues relating to the conservation of species and habitats and consider conflicting evidence use given data to calculate the size of a population estimated using the mark-release-recapture method.

    Verified
    Key Learning Objectives:
    • Evaluate a claim about conservation from given data by writing at least one point for and one against, each supported by a figure.
    • Identify three specific limitations of an investigation, such as sample size, absence of a control or absence of a statistical test.
    • Calculate a population size from mark-release-recapture data and state one assumption that may make the estimate unreliable.
    • Explain how one named sustainable practice reduces the conflict between a human need and conservation.
    264

    Populations in ecosystems (A-level only)

    The new species may change the environment in such a way that it becomes less suitable for the previous species.

    Verified
    Key Learning Objectives:
    • Explain how a later seral stage makes a habitat unsuitable for an earlier species, naming the resource competed for.
    • Describe what happens to a pioneer population once shrubs and trees establish, and state where that species persists.
    • Use data on the species present at different seral stages to identify which species have been excluded.
    265

    Populations in ecosystems (A-level only)

    The size of a population can be estimated using: randomly placed quadrats, or quadrats along a belt transect, for slow-moving or non-motile organisms the mark-release-recapture method for motile organisms. The assumptions made when using the mark-release-recapture method.

    Verified
    Key Learning Objectives:
    • Describe how to place quadrats randomly in a uniform habitat and how to scale a mean quadrat count up to a population estimate.
    • Calculate a population size from mark-release-recapture data, writing the formula before substituting values.
    • Explain how breaking each of two named mark-release-recapture assumptions would make the estimate too high or too low.
    • Justify the use of a belt transect rather than random quadrats where an environmental gradient is present.
    266

    Populations in ecosystems (A-level only)

    Within a habitat, a species occupies a niche governed by adaptation to both abiotic and biotic conditions.

    Verified
    Key Learning Objectives:
    • Define niche and contrast it with habitat using one named species.
    • Describe the niche of a named species by listing at least two abiotic and two biotic conditions it is adapted to.
    • Explain, in terms of competition, why two species cannot occupy the same niche in the same habitat.
    267

    Principles of homeostasis and negative feedback (A-level only)

    Homeostasis in mammals involves physiological control systems that maintain the internal environment within restricted limits.

    Verified
    Key Learning Objectives:
    • Define homeostasis and explain what is meant by the internal environment.
    • Identify the receptor, coordinator and effector in an unfamiliar physiological control system.
    • Explain why a homeostatically controlled variable fluctuates around a set point rather than staying fixed.
    268

    Principles of homeostasis and negative feedback (A-level only)

    Negative feedback restores systems to their original level.

    Verified
    Key Learning Objectives:
    • Explain how negative feedback returns a variable to its set point, naming every stage of the loop.
    • Explain why a negative feedback system must switch off its own corrective response.
    • Distinguish negative from positive feedback using a named physiological example of each.
    269

    Principles of homeostasis and negative feedback (A-level only)

    Students should be able to interpret information relating to examples of negative and positive feedback.

    Verified
    Key Learning Objectives:
    • Decide from an unfamiliar trace whether a system shows negative or positive feedback, and justify the decision with data.
    • Identify the receptor and the effector in a control system described only in an exam passage.
    • Explain why the response in a positive feedback system must be ended by some separate event.
    270

    Principles of homeostasis and negative feedback (A-level only)

    The importance of maintaining a stable blood glucose concentration in terms of availability of respiratory substrate and of the water potential of blood.

    Verified
    Key Learning Objectives:
    • Explain why brain cells are the first to be affected by a fall in blood glucose concentration.
    • Predict the direction of water movement between blood and cells when blood glucose rises sharply, using water potential.
    • Explain why the appearance of glucose in urine leads to dehydration.
    271

    Principles of homeostasis and negative feedback (A-level only)

    The importance of maintaining a stable core temperature and stable blood pH in relation to enzyme activity.

    Verified
    Key Learning Objectives:
    • Explain why enzymes are denatured above their optimum temperature.
    • Explain why a change from blood pH 7.4 reduces the rate of a metabolic reaction.
    • Interpret a graph of reaction rate against temperature.
    272

    Principles of homeostasis and negative feedback (A-level only)

    The possession of separate mechanisms involving negative feedback controls departures in different directions from the original state, giving a greater degree of control.

    Verified
    Key Learning Objectives:
    • Explain why two opposing mechanisms give closer control than a single corrective mechanism.
    • Name a pair of mechanisms that correct departures in opposite directions for a named variable.
    • Predict the consequence for control if one of a pair of opposing mechanisms fails.
    273

    Receptors (A-level only)

    Deformation of stretch-mediated sodium ion channels in a Pacinian corpuscle leads to the establishment of a generator potential.

    Verified
    Key Learning Objectives:
    • Describe, in five steps, how pressure on a Pacinian corpuscle produces a generator potential.
    • Explain why the channels involved are described as stretch-mediated rather than voltage-gated.
    • Predict the effect of a greater pressure on the size of the generator potential and on the frequency of action potentials.
    • Interpret a trace of membrane potential against time for two different pressures applied to a corpuscle.
    274

    Receptors (A-level only)

    The basic structure of a Pacinian corpuscle.

    Verified
    Key Learning Objectives:
    • Describe the structure of a Pacinian corpuscle, naming the lamellae and the sensory neurone ending.
    • Locate the stretch-mediated sodium ion channels within the corpuscle.
    • Explain how the layered structure transmits an external pressure to the neurone membrane.
    • Link each named structure of the corpuscle to its role in producing a generator potential.
    275

    Receptors (A-level only)

    The human retina in sufficient detail to show how differences in sensitivity to light, sensitivity to colour and visual acuity are explained by differences in the optical pigments of rods and cones and the connections rods and cones make in the optic nerve.

    Verified
    Key Learning Objectives:
    • Explain why rods give high sensitivity but low visual acuity, using their pigment and their connections.
    • Use an absorption spectrum for the three cone types to explain how a given colour is perceived.
    • Contrast the connection of rods and cones to bipolar neurones and link each to visual acuity.
    • Predict how vision changes in dim light, justifying the prediction using rhodopsin and iodopsin.
    276

    Receptors (A-level only)

    The Pacinian corpuscle should be used as an example of a receptor to illustrate that: receptors respond only to specific stimuli stimulation of a receptor leads to the establishment of a generator potential.

    Verified
    Key Learning Objectives:
    • Explain why a Pacinian corpuscle responds to pressure but not to light, in terms of its channel proteins.
    • Describe how stimulation of a receptor produces a generator potential.
    • Distinguish a generator potential from an action potential in terms of size, grading and threshold.
    • Suggest why a measured reaction time is longer than the time predicted from nerve conduction speed alone.
    277

    Recombinant DNA technology (A-level only)

    Fragments of DNA can be amplified by in vitro and in vivo techniques.

    Verified
    Key Learning Objectives:
    • Distinguish in vitro from in vivo amplification and name the method used in each case.
    • Explain why culturing transformed host cells increases the number of copies of an inserted fragment.
    • Compare PCR and in vivo amplification on speed, quantity, accuracy and whether protein is produced.
    278

    Recombinant DNA technology (A-level only)

    Fragments of DNA can be produced by several methods, including: conversion of mRNA to complementary DNA (cDNA), using reverse transcriptase using restriction enzymes to cut a fragment containing the desired gene from DNA creating the gene in a ‘gene machine’.

    Verified
    Key Learning Objectives:
    • Describe how reverse transcriptase is used to produce a DNA fragment from mRNA, naming the substrates needed.
    • Explain why a gene made as cDNA or in a gene machine can be expressed by a bacterium when a chromosomal copy cannot.
    • Describe how a restriction endonuclease produces sticky ends, naming the site it recognises and the bond it hydrolyses.
    279

    Recombinant DNA technology (A-level only)

    Recombinant DNA technology involves the transfer of fragments of DNA from one organism, or species, to another.

    Verified
    Key Learning Objectives:
    • Outline the full sequence by which a gene from one species ends up being expressed in another.
    • Distinguish between a vector, a host cell and a transgenic organism, using each term correctly.
    • Explain why promoter and terminator regions are added to the fragment before it is placed in a vector.
    280

    Recombinant DNA technology (A-level only)

    Since the genetic code is universal, as are transcription and translation mechanisms, the transferred DNA can be translated within cells of the recipient (transgenic) organism.

    Verified
    Key Learning Objectives:
    • State two distinct reasons, code and mechanism, why a bacterium can express a human gene.
    • Explain why cDNA rather than chromosomal DNA is transferred when a eukaryotic gene is to be expressed in a bacterium.
    • Suggest, naming a specific organelle or mechanism that bacteria lack, why some human proteins cannot be produced in bacteria.
    281

    Recombinant DNA technology (A-level only)

    The addition of promoter and terminator regions to the fragments of DNA.

    Verified
    Key Learning Objectives:
    • Name the regions added to either end of a DNA fragment and state what each does during transcription.
    • Explain why a gene transferred without a promoter produces no protein in the host cell.
    • Suggest how choosing a particular promoter controls which tissue of a transgenic organism expresses the gene.
    282

    Recombinant DNA technology (A-level only)

    The culture of transformed host cells as an in vivo method to amplify DNA fragments.

    Verified
    Key Learning Objectives:
    • Describe how transformed cells are identified using marker genes and insertional inactivation.
    • Explain why the number of copies of a plasmid increases as a bacterial population grows.
    • Compare in vivo amplification with PCR in terms of quantity of product, accuracy and whether protein is obtained.
    283

    Recombinant DNA technology (A-level only)

    The principles of the polymerase chain reaction (PCR) as an in vitro method to amplify DNA fragments.

    Verified
    Key Learning Objectives:
    • Describe the three temperature stages of one PCR cycle and state what happens to the DNA at each.
    • Explain why a thermostable polymerase and short primers are both essential to the reaction.
    • Calculate the number of DNA molecules present after a stated number of cycles, starting from a given number.
    284

    Recombinant DNA technology (A-level only)

    The use of marker genes to detect genetically modified (GM) cells or organisms.

    Verified
    Key Learning Objectives:
    • Explain the purpose of a marker gene in terms of which cells can be identified after transformation.
    • Describe how an antibiotic resistance marker is used to separate transformed from untransformed cells.
    • Suggest why fluorescent or enzyme markers are now preferred to antibiotic resistance genes.
    285

    Recombinant DNA technology (A-level only)

    The use of restriction endonucleases and ligases to insert fragments of DNA into vectors.

    Verified
    Key Learning Objectives:
    • Explain why the same restriction enzyme must be used on both the fragment and the vector.
    • Describe the two kinds of bond involved in inserting a fragment into a plasmid and state which enzyme, if any, forms each.
    • Explain why using a single restriction enzyme allows a fragment to be inserted in either orientation.
    286

    Recombinant DNA technology (A-level only)

    Transformation of host cells using these vectors.

    Verified
    Key Learning Objectives:
    • Describe how bacterial cells are treated so they will take up a recombinant plasmid, and explain why the treatment works.
    • Name a suitable vector and transformation method for a plant cell and for an animal cell.
    • Explain why a selection step is always required after transformation.
    287

    Regulation of transcription and translation (A-level only)

    Epigenetic control of gene expression in eukaryotes.

    Verified
    Key Learning Objectives:
    • Explain how the charge on a histone changes when acetyl groups are added or removed, and what this does to the accessibility of the DNA.
    • Describe where methyl groups are added and why their presence stops transcription factors binding.
    • Distinguish an epigenetic change from a mutation by stating precisely what is and is not altered in the DNA.
    288

    Regulation of transcription and translation (A-level only)

    Epigenetics involves heritable changes in gene function, without changes to the base sequence of DNA. These changes are caused by changes in the environment that inhibit transcription by: increased methylation of the DNA or decreased acetylation of associated histones.

    Verified
    Key Learning Objectives:
    • State the definition of epigenetics in a form that makes clear the base sequence is unaltered.
    • Explain why increasing methylation of a promoter and decreasing acetylation of histones both have the same effect on transcription.
    • Describe how an environmental factor can change the expression of a gene in an individual and in that individual's daughter cells.
    289

    Regulation of transcription and translation (A-level only)

    In eukaryotes and some prokaryotes, translation of the mRNA produced from target genes can be inhibited by RNA interference (RNAi).

    Verified
    Key Learning Objectives:
    • Describe how siRNA is produced from double-stranded RNA and what it combines with in the cytoplasm.
    • Explain why an mRNA molecule targeted by siRNA yields no polypeptide, naming the stage of protein synthesis that is blocked.
    • Distinguish RNA interference from control by transcriptional factors by stating where in the pathway each one acts.
    290

    Regulation of transcription and translation (A-level only)

    In eukaryotes, transcription of target genes can be stimulated or inhibited when specific transcriptional factors move from the cytoplasm into the nucleus.

    Verified
    Key Learning Objectives:
    • Describe the route an activated transcriptional factor takes from the cytoplasm to the promoter region, naming the nuclear pore and the base sequence it binds.
    • Explain how the presence or absence of a transcriptional factor at the promoter changes the quantity of mRNA and therefore of polypeptide made.
    • Suggest why a bacterium given a human gene may produce no protein, referring to the transcriptional factors it lacks.
    291

    Regulation of transcription and translation (A-level only)

    Students should be able to: interpret data provided from investigations into gene expression evaluate appropriate data for the relative influences of genetic and environmental factors on phenotype.

    Verified
    Key Learning Objectives:
    • Describe a trend in gene expression data by quoting figures with units and comparing the relevant groups.
    • Decide, from error bars or standard deviations, whether a difference in expression is significant, and say why.
    • Explain how a study using monozygotic twins separates the contribution of alleles from that of the environment and other factors.
    292

    Regulation of transcription and translation (A-level only)

    The relevance of epigenetics on the development and treatment of disease, especially cancer.

    Verified
    Key Learning Objectives:
    • Explain how hypermethylation of a tumour suppressor gene leads to uncontrolled cell division without any mutation occurring.
    • Suggest, in the correct direction, how a drug altering methylation or acetylation could treat a tumour.
    • Justify why epigenetic changes can be promising drug targets, referring to what is and is not altered in the DNA.
    293

    Regulation of transcription and translation (A-level only)

    The role of the steroid hormone, oestrogen, in initiating transcription.

    Verified
    Key Learning Objectives:
    • Describe how a lipid-soluble hormone reaches its receptor inside a cell and what the change in tertiary structure does to the receptor.
    • Explain, step by step, how an oestrogen-receptor complex increases transcription of a target gene in the nucleus.
    • Suggest how a drug shaped like oestrogen reduces transcription in an ER-positive tumour, linking receptor binding to the amount of mRNA produced.
    294

    Respiration (A-level only)

    Aerobic respiration in such detail as to show that: pyruvate is oxidised to acetate, producing reduced NAD in the process acetate combines with coenzyme A in the link reaction to produce acetylcoenzyme A acetylcoenzyme A reacts with a four-carbon molecule, releasing coenzyme A and producing a six-carbon molecule that enters the Krebs cycle in a series of oxidation-reduction reactions, the Krebs cycle generates reduced coenzymes and ATP by substrate-level phosphorylation, and carbon dioxide is lost synthesis of ATP by oxidative phosphorylation is associated with the transfer of electrons down the electron transfer chain and passage of protons across inner mitochondrial membranes and is catalysed by ATP synthase embedded in these membranes (chemiosomotic theory) other respiratory substrates include the breakdown products of lipids and amino acids, which enter the Krebs cycle.

    Verified
    Key Learning Objectives:
    • Complete a diagram of the link reaction showing pyruvate, carbon dioxide, reduced NAD and acetylcoenzyme A.
    • Describe one turn of the Krebs cycle in terms of carbon number, decarboxylation and the coenzymes reduced.
    • Explain how the oxidation of reduced NAD leads to ATP synthesis via chemiosmosis and the formation of water.
    • State where the breakdown products of lipids and of amino acids enter aerobic respiration.
    295

    Respiration (A-level only)

    Glycolysis involves the following stages: phosphorylation of glucose to glucose phosphate, using ATP production of triose phosphate oxidation of triose phosphate to pyruvate with a net gain of ATP and reduced NAD.

    Verified
    Key Learning Objectives:
    • Describe the stages of glycolysis in order, naming glucose phosphate, triose phosphate and pyruvate.
    • Explain why glucose must be phosphorylated before it can be broken down.
    • Calculate the net ATP yield of glycolysis from the numbers of ATP used and produced.
    296

    Respiration (A-level only)

    Glycolysis is the first stage of anaerobic and aerobic respiration. It occurs in the cytoplasm and is an anaerobic process.

    Verified
    Key Learning Objectives:
    • State where glycolysis occurs and explain why it can proceed without oxygen.
    • Explain how a cell can continue to make ATP when its oxygen supply fails, naming the stage responsible and where it happens.
    • Predict which stages of respiration continue in a cell whose mitochondria cannot function.
    297

    Respiration (A-level only)

    If respiration is aerobic, pyruvate from glycolysis enters the mitochondrial matrix by active transport.

    Verified
    Key Learning Objectives:
    • State how pyruvate crosses the inner mitochondrial membrane.
    • Explain why glucose itself does not enter the mitochondrion.
    • Suggest why cells with a high rate of respiration contain large numbers of mitochondria.
    298

    Respiration (A-level only)

    If respiration is only anaerobic, pyruvate can be converted to ethanol or lactate using reduced NAD.

    Verified
    Key Learning Objectives:
    • Describe the conversion of pyruvate to lactate and to ethanol, naming the specific hydrogen acceptor in each case.
    • Explain why anaerobic respiration yields far less ATP per glucose molecule than aerobic respiration.
    • Explain the importance of regenerating oxidised NAD for the continuation of glycolysis.
    299

    Respiration (A-level only)

    Required practical 9: Investigation into the effect of a named variable on the rate of respiration of cultures of single-celled organisms.

    Verified
    Key Learning Objectives:
    • Describe how to measure the rate of respiration in a yeast culture using gas volume or a redox indicator.
    • Explain the purpose of potassium hydroxide and of a boiled yeast control in a respirometer investigation.
    • Calculate a rate of respiration from a volume of gas collected over a measured time.
    300

    Respiration (A-level only)

    Respiration produces ATP.

    Verified
    Key Learning Objectives:
    • Describe how ATP is synthesised during glycolysis, the Krebs cycle and oxidative phosphorylation.
    • Explain why ATP is described as the immediate energy source of a cell.
    • Identify cellular processes that require the hydrolysis of ATP, including the initial stages of glycolysis.
    301

    Respiration (A-level only)

    The oxidised NAD produced in this way can be used in further glycolysis.

    Verified
    Key Learning Objectives:
    • Explain why the conversion of pyruvate to lactate or to ethanol allows glycolysis to continue.
    • Describe the fate of reduced NAD under aerobic and under anaerobic conditions.
    • Predict what happens to ATP production in a cell whose supply of oxidised NAD is blocked.
    302

    Skeletal muscles are stimulated to contract by nerves and act as

    ) The roles of ATP and phosphocreatine in muscle contraction.

    Verified
    Key Learning Objectives:
    • State the three roles of ATP in a contracting and relaxing muscle fibre.
    • Explain how phosphocreatine regenerates ATP without oxygen.
    • Distinguish between the immediate ATP store, the phosphocreatine reserve and aerobic respiration as energy sources for muscle contraction.
    303

    Skeletal muscles are stimulated to contract by nerves and act as

    Gross and microscopic structure of skeletal muscle. The ultrastructure of a myofibril.

    Verified
    Key Learning Objectives:
    • Label a sarcomere with the Z line, A band, I band and H zone and state which filaments lie in each region.
    • Describe the structure of a muscle fibre, explaining why it is multinucleate and why it contains many mitochondria.
    • Calculate the length of a sarcomere from a labelled electron micrograph and its magnification.
    304

    Skeletal muscles are stimulated to contract by nerves and act as

    Muscles act in antagonistic pairs against an incompressible skeleton.

    Verified
    Key Learning Objectives:
    • Explain why a muscle cannot return itself to its resting length and therefore needs an antagonist.
    • Name the agonist and the antagonist for flexion and for extension at a named joint.
    • Explain how an incompressible skeleton allows the force of contraction to produce movement.
    305

    Skeletal muscles are stimulated to contract by nerves and act as

    The roles of actin, myosin, calcium ions and ATP in myofibril contraction.

    Verified
    Key Learning Objectives:
    • Sequence the sliding filament mechanism from calcium ion release through to sarcomere shortening.
    • State three distinct roles for ATP in muscle contraction and relaxation.
    • Predict which regions of the sarcomere narrow during contraction and explain why the A band does not.
    306

    Skeletal muscles are stimulated to contract by nerves and act as

    The roles of calcium ions and tropomyosin in the cycle of actinomyosin bridge formation.

    Verified
    Key Learning Objectives:
    • Explain how tropomyosin prevents contraction in a resting muscle.
    • Describe the effect of calcium ions on troponin and tropomyosin, and hence on actinomyosin bridge formation.
    • Explain why a muscle relaxes when calcium ions are actively transported back into the sarcoplasmic reticulum.
    307

    Skeletal muscles are stimulated to contract by nerves and act as

    The structure, location and general properties of slow and fast skeletal muscle fibres.

    Verified
    Key Learning Objectives:
    • Compare slow and fast skeletal muscle fibres in terms of structure, type of respiration and fatigue.
    • Predict which fibre type predominates in a named muscle or athlete and justify the prediction using structural evidence.
    • Explain how high myoglobin and mitochondria content allows a slow fibre to keep contracting for long periods.
    308

    Species and taxonomy

    A phylogenetic classification system attempts to arrange species into groups based on their evolutionary origins and relationships.

    Verified
    Key Learning Objectives:
    • Explain how a phylogenetic classification differs from one based on observable similarity, using common ancestry in your answer.
    • Interpret a branching diagram of taxa to state which two groups are most closely related and why.
    • Evaluate a claim made about a set of phylogenetic data by giving evidence both for and against it.
    309

    Species and taxonomy

    Courtship behaviour as a necessary precursor to successful mating.

    Verified
    Key Learning Objectives:
    • Describe courtship as a chain of stimulus and response in which each behaviour triggers the partner's reply.
    • Explain three separate ways in which courtship raises the chance of successful mating, including synchronisation of gamete release.
    • Suggest, for an unfamiliar animal described in a question, why its courtship must be completed before mating can occur.
    310

    Species and taxonomy

    Each group is called a taxon (plural taxa).

    Verified
    Key Learning Objectives:
    • Define a taxon as any group within the classification hierarchy and give an example at two different levels.
    • Use the singular and plural forms correctly when writing about one group and several groups.
    • Write a comparison between named taxa taken from a figure, keeping the statement at the level of the group.
    311

    Species and taxonomy

    Each species is universally identified by a binomial consisting of the name of its genus and species, eg, Homo sapiens.

    Verified
    Key Learning Objectives:
    • Write the binomial of a named species as the genus name followed by the species name, using the conventional capitalisation.
    • Explain why a universal naming system is more useful to scientists than common names.
    • Deduce from two binomials whether the species share a genus, and say what that shows about their relatedness.
    312

    Species and taxonomy

    It uses a hierarchy in which smaller groups are placed within larger groups, with no overlap between groups.

    Verified
    Key Learning Objectives:
    • Describe the hierarchical arrangement of taxa using nesting and the absence of overlap between groups.
    • Decide which of two pairs of organisms is more closely related from the smallest taxon each pair shares.
    • Explain why a single organism can occupy only one group at each level of the hierarchy.
    313

    Species and taxonomy

    One hierarchy comprises the taxa: domain, kingdom, phylum, class, order, family, genus and species.

    Verified
    Key Learning Objectives:
    • Write the eight taxa in order from domain to species without prompting.
    • Complete a classification table for a named organism, keeping each column to one organism and each row to one level.
    • Identify which level of the hierarchy a given group name belongs to, and name the levels immediately above and below it.
    314

    Species and taxonomy

    Students should be able to appreciate that advances in immunology and genome sequencing help to clarify evolutionary relationships between organisms.

    Verified
    Key Learning Objectives:
    • Explain how comparing base sequences allows the evolutionary relationship between two species to be judged.
    • Describe how the binding of antibodies to proteins from another species provides evidence of relatedness.
    • Suggest why classifications based on observable features such as flagella have been revised since sequencing became available.
    315

    Species and taxonomy

    The role of courtship in species recognition.

    Verified
    Key Learning Objectives:
    • Explain why a species-specific display prevents a member of another species from completing the courtship chain.
    • Justify species recognition as an advantage by naming the cost of mating with a different species (e.g., wasted gametes).
    • Use differences in courtship to account for reproductive isolation between two closely related species that share a habitat.
    316

    Species and taxonomy

    Two organisms belong to the same species if they are able to produce fertile offspring.

    Verified
    Key Learning Objectives:
    • Decide, from a description of two organisms and the offspring they produce, whether one species or two is present.
    • Explain why the mule places the horse and the donkey in separate species, referring to the failure of chromosome pairing in meiosis.
    • Apply the definition at the end of a speciation answer to justify that two isolated populations have become separate species.
    • Distinguish between organisms that look alike and organisms that share a gene pool when deciding how many species a sample contains.
    317

    Structure of DNA and RNA

    A DNA molecule is a double helix with two polynucleotide chains held together by hydrogen bonds between specific complementary base pairs.

    Verified
    Key Learning Objectives:
    • Describe how the two strands of a DNA molecule are held together, naming the bonds and the base pairs.
    • Explain why DNA is stable enough to store information yet can still be separated for replication and transcription.
    • Calculate the percentage of each base in a sample given the percentage of one, and justify the calculation using complementary base pairing.
    318

    Structure of DNA and RNA

    An RNA molecule is a relatively short polynucleotide chain.

    Verified
    Key Learning Objectives:
    • Give three structural differences between a DNA molecule and a transfer RNA molecule, writing both sides of each comparison.
    • Describe the structure of transfer RNA and identify the two ends that carry out its function.
    • Explain why messenger RNA is used to carry the genetic code from the nucleus to the ribosome.
    319

    Structure of DNA and RNA

    Both DNA and RNA are polymers of nucleotides. Each nucleotide is formed from a pentose, a nitrogen-containing organic base and a phosphate group: The components of a DNA nucleotide are deoxyribose, a phosphate group and one of the organic bases adenine, cytosine, guanine or thymine. The components of an RNA nucleotide are ribose, a phosphate group and one of the organic bases adenine, cytosine, guanine or uracil. A condensation reaction between two nucleotides forms a phosphodiester bond.

    Verified
    Key Learning Objectives:
    • Draw and label a single nucleotide, naming the pentose and the base for both DNA and RNA.
    • Describe the condensation reaction that joins two nucleotides and name the bond and the molecule released.
    • Compare a DNA nucleotide with an RNA nucleotide, giving two differences in named components.
    320

    Structure of DNA and RNA

    Deoxyribonucleic acid (DNA) and ribonucleic acid (RNA) are important information-carrying molecules.

    Verified
    Key Learning Objectives:
    • Explain how a sequence of bases can carry information, referring to triplets and to the amino acid sequence of a polypeptide.
    • Justify why a human gene transferred into a bacterium still produces a functional human protein.
    • Distinguish the roles of DNA and of RNA in a eukaryotic cell, naming where each is found.
    321

    Structure of DNA and RNA

    In all living cells, DNA holds genetic information and RNA transfers genetic information from DNA to the ribosomes.

    Verified
    Key Learning Objectives:
    • Describe the route taken by the information in one gene from the DNA to a polypeptide at the ribosome.
    • Explain why a copy of a gene, rather than the DNA itself, is used to transfer information to the ribosome.
    • Name the types of RNA and state the role of each in producing a polypeptide.
    322

    Structure of DNA and RNA

    Ribosomes are formed from RNA and proteins.

    Verified
    Key Learning Objectives:
    • State the two components of a ribosome and name the part of the nucleus where their subunits are assembled.
    • Explain the selective toxicity of antibiotics targeting 70S ribosomes, noting the distinction between prokaryotic, chloroplast and mammalian ribosomes.
    • Distinguish the fate of proteins made on free ribosomes from those made on rough endoplasmic reticulum.
    323

    Structure of DNA and RNA

    Students should be able to appreciate that the relative simplicity of DNA led many scientists to doubt that it carried the genetic code.

    Verified
    Key Learning Objectives:
    • Explain why the small number of different bases in DNA once led scientists to doubt that it carried the genetic code.
    • Contrast the chemical complexity of proteins with the relative simplicity of DNA.
    • Describe how scientific consensus regarding the genetic code shifted in response to new experimental evidence.
    324

    Structure of eukaryotic cells

    In complex multicellular organisms, eukaryotic cells become specialised for specific functions.

    Verified
    Key Learning Objectives:
    • Explain how differential gene expression allows cells to develop into specialised types.
    • Relate specific structural features and organelle proportions of a named specialised cell to its function.
    • Deduce the specialised function of an unfamiliar cell from data regarding its organelle distribution.
    325

    Structure of eukaryotic cells

    Specialised cells are organised into tissues, tissues into organs and organs into systems.

    Verified
    Key Learning Objectives:
    • Define tissue, organ and organ system, and place a named example at each level.
    • Identify, from a description of a structure, whether it is a tissue or an organ, and justify the decision.
    • Explain why multicellular organisms of large size require organ systems rather than relying on diffusion.
    326

    Structure of eukaryotic cells

    Students should be able to apply their knowledge of these features in explaining adaptations of eukaryotic cells.

    Verified
    Key Learning Objectives:
    • Explain how three features of an epithelial cell in the proximal convoluted tubule allow rapid reabsorption of glucose.
    • Interpret an electron micrograph of an unfamiliar cell to suggest its function, citing two organelles as evidence.
    • Justify why the number of an organelle, rather than its presence, is what makes a cell adapted to its role.
    327

    Structure of eukaryotic cells

    The structure of eukaryotic cells, restricted to the structure and function of: cell-surface membrane nucleus (containing chromosomes, consisting of protein- bound, linear DNA, and one or more nucleoli) mitochondria chloroplasts (in plants and algae) Golgi apparatus and Golgi vesicles lysosomes (a membrane-bound organelle that releases hydrolytic enzymes) ribosomes rough endoplasmic reticulum and smooth endoplasmic reticulum cell wall (in plants, algae and fungi) cell vacuole (in plants).

    Verified
    Key Learning Objectives:
    • Name one structure in a micrograph or diagram of an unfamiliar cell that shows it is a eukaryote, choosing from mitochondrion, nuclear envelope, rough endoplasmic reticulum, vesicle or lysosome, and give one function of that structure.
    • Describe two functions of the Golgi apparatus and state the structures it forms.
    • Explain how one structural feature of each of the chloroplast, the cell wall, the permanent vacuole and the smooth endoplasmic reticulum lets it do its job, and state which three of the four are absent from an animal cell.
    • State that chloroplasts are found in plants and algae.
    328

    Structure of prokaryotic cells and of viruses

    In addition, many prokaryotic cells have: one or more plasmids a capsule surrounding the cell one or more flagella.

    Verified
    Key Learning Objectives:
    • Name the three structures found in many prokaryotes and state a function for each.
    • Explain why a plasmid, unlike the circular DNA molecule, cannot be quoted as a universal difference between prokaryotes and eukaryotes.
    • Suggest how the presence of a capsule makes a bacterium more likely to survive an encounter with a phagocyte.
    • Describe how plasmid transfer between bacteria spreads antibiotic resistance through a population.
    329

    Structure of prokaryotic cells and of viruses

    Prokaryotic cells are much smaller than eukaryotic cells. They also differ from eukaryotic cells in having: cytoplasm that lacks membrane-bound organelles smaller ribosomes no nucleus; instead they have a single circular DNA molecule that is free in the cytoplasm and is not associated with proteins a cell wall that contains murein, a glycoprotein.

    Verified
    Key Learning Objectives:
    • Give two features shared by every prokaryotic cell that no eukaryotic cell has, avoiding plasmids, capsules and flagella.
    • Describe how the genetic material of a bacterium differs from that of a human cell in shape, in location and in whether it is bound to protein.
    • Explain why a drug that blocks murein synthesis damages bacteria but leaves human cells and viruses unaffected.
    • Compare the ribosomes of a bacterium and a human cell and use the difference to account for the selective action of some antibiotics.
    330

    Structure of prokaryotic cells and of viruses

    Viruses are acellular and non-living. The structure of virus particles to include genetic material, capsid and attachment protein.

    Verified
    Key Learning Objectives:
    • Give the three structural features of every virus particle and state the function of each.
    • Explain separately why a virus is described as acellular and why it is described as non-living.
    • Explain why the attachment protein determines which host cells a particular virus can infect.
    • Justify why antibiotics cannot be used to treat a viral infection, using named absent structures.
    331

    Surface area to volume ratio

    Changes to body shape and the development of systems in larger organisms as adaptations that facilitate exchange as this ratio reduces.

    Verified
    Key Learning Objectives:
    • Explain why a flatworm can rely on diffusion while a mammal of the same mass cannot.
    • Describe two body shape adaptations and two systems that compensate for a low surface area to volume ratio.
    • Suggest how the body shape of a mammal living in a cold climate differs from one in a hot climate, and justify the difference in terms of the ratio.
    332

    Surface area to volume ratio

    Students should be able to appreciate the relationship between surface area to volume ratio and metabolic rate.

    Verified
    Key Learning Objectives:
    • Explain why a small mammal has a higher metabolic rate per unit mass than a large one.
    • Describe an inverse relationship between body mass and oxygen consumption per gram using figures from a graph.
    • Predict how heart rate, breathing rate and food intake differ between a shrew and an elephant, and justify each prediction.
    333

    Surface area to volume ratio

    The relationship between the size of an organism or structure and its surface area to volume ratio.

    Verified
    Key Learning Objectives:
    • Calculate the surface area to volume ratio of a cube or a named structure and express it as a ratio to 1 to the required number of significant figures.
    • Explain why the ratio falls as size increases, using the square and cube relationship.
    • Predict, for two organisms of different size, which relies on diffusion across the body surface and justify the answer using the ratio.
    334

    Survival and response (A-level only)

    In flowering plants, specific growth factors move from growing regions to other tissues, where they regulate growth in response to directional stimuli.

    Verified
    Key Learning Objectives:
    • State where IAA is produced in a flowering plant and where it exerts its effect.
    • Explain how lateral redistribution of IAA converts a directional stimulus into unequal growth.
    • Contrast coordination by plant growth factors with hormonal coordination in a mammal.
    • Predict the effect on growth of removing the tip of a shoot, and justify the prediction.
    335

    Survival and response (A-level only)

    Organisms increase their chance of survival by responding to changes in their environment.

    Verified
    Key Learning Objectives:
    • Sequence an unfamiliar animal response into stimulus, receptor, coordinator, effector and response.
    • Explain how a faster response increases an organism's chance of surviving.
    • Identify the different types of effectors in animals and plants.
    • Give one example each of a response coordinated by nerves, by hormones and by a plant growth factor.
    336

    Survival and response (A-level only)

    Required practical 10: Investigation into the effect of an environmental variable on the movement of an animal using either a choice chamber or a maze.

    Verified
    Key Learning Objectives:
    • Design a choice chamber investigation, stating the independent, dependent and controlled variables.
    • Explain why a settling period is needed before the distribution of the animals is recorded.
    • Apply a chi-squared test to choice chamber counts and state what the result shows.
    • Evaluate a choice chamber method by identifying an uncontrolled variable and its effect on the results.
    337

    Survival and response (A-level only)

    Taxes and kineses as simple responses that can maintain a mobile organism in a favourable environment.

    Verified
    Key Learning Objectives:
    • Distinguish a taxis from a kinesis by the presence or absence of direction in the response.
    • Name a taxis correctly using the stimulus and its sign for a given example.
    • Explain how a kinesis keeps an organism in a favourable environment without directed movement.
    • Interpret choice chamber data to decide whether an organism is showing a taxis or a kinesis.
    338

    Survival and response (A-level only)

    The effect of different concentrations of indoleacetic acid (IAA) on cell elongation in the roots and shoots of flowering plants as an explanation of gravitropism and phototropism in flowering plants.

    Verified
    Key Learning Objectives:
    • Explain positive phototropism in a shoot as a sequence from unilateral light to unequal elongation.
    • Explain negative phototropism in roots, detailing how IAA accumulation on the shaded side inhibits elongation.
    • Explain gravitropism in roots and shoots, detailing how high IAA concentration on the lower side affects elongation differently.
    • Contrast the effect of high IAA concentrations on root cells and on shoot cells.
    339

    Survival and response (A-level only)

    The protective effect of a simple reflex, exemplified by a three- neurone simple reflex. Details of spinal cord and dorsal and ventral roots are not required.

    Verified
    Key Learning Objectives:
    • Sequence a three-neurone reflex arc from receptor to effector, naming each neurone.
    • Explain why a reflex response is faster than a voluntary one, using the number of synapses.
    • Describe the protective outcome of a named reflex, such as withdrawing a hand from a hot object.
    • Identify which structures in a reflex pathway lie outside the specification and need not be described.
    340

    Synaptic transmission (A-level only)

    A comparison of transmission across a cholinergic synapse and across a neuromuscular junction.

    Verified
    Key Learning Objectives:
    • Give three differences between transmission at a cholinergic synapse and at a neuromuscular junction.
    • Explain why summation is normally needed at a synapse between neurones but not at a neuromuscular junction.
    • Explain why there is no inhibitory equivalent of a neuromuscular junction.
    341

    Synaptic transmission (A-level only)

    Students should be able to use information provided to predict and explain the effects of specific drugs on a synapse.

    Verified
    Key Learning Objectives:
    • Predict the effect on postsynaptic action potentials of a drug that blocks calcium ion channels, justifying each step of the chain.
    • Explain how inhibiting acetylcholinesterase can strengthen a weak muscle contraction.
    • Distinguish, from information given, between a drug that mimics a neurotransmitter and one that blocks its receptor.
    342

    Synaptic transmission (A-level only)

    The detailed structure of a synapse and of a neuromuscular junction.

    Verified
    Key Learning Objectives:
    • Label a synapse and a neuromuscular junction, identifying the knob, vesicles, cleft, receptors and sarcolemma.
    • Explain why the synaptic knob contains many mitochondria, linking this to the resynthesis of acetylcholine.
    • Explain how the arrangement of vesicles and receptors makes transmission at both junctions one-way.
    343

    Synaptic transmission (A-level only)

    The sequence of events involved in transmission across a cholinergic synapse in sufficient detail to explain: unidirectionality temporal and spatial summation inhibition by inhibitory synapses.

    Verified
    Key Learning Objectives:
    • Sequence the events at a cholinergic synapse from the arrival of an action potential to its generation in the postsynaptic neurone.
    • Explain why transmission across a cholinergic synapse is unidirectional.
    • Distinguish temporal from spatial summation and explain how each allows sub-threshold inputs to trigger an action potential.
    • Explain the mechanism of inhibition by inhibitory synapses, including the roles of chloride and potassium ions in hyperpolarisation.
    344

    Transport across cell membranes

    Cells may be adapted for rapid transport across their internal or external membranes by an increase in surface area of, or by an increase in the number of protein channels and carrier molecules in, their membranes.

    Verified
    Key Learning Objectives:
    • Explain how microvilli increase the rate at which glucose is absorbed in the ileum.
    • Name an internal membrane that is folded to increase surface area and state what the extra area carries.
    • Explain how increasing the number of carrier proteins increases the rate of active transport.
    • Suggest why damage to the epithelium of the ileum leads to water remaining in the lumen.
    345

    Transport across cell membranes

    Cholesterol may also be present in cell membranes where it restricts the movement of other molecules making up the membrane.

    Verified
    Key Learning Objectives:
    • Describe where cholesterol sits in the bilayer and explain how it restricts phospholipid movement.
    • Explain how cholesterol regulates membrane fluidity at different temperatures.
    • Assess the importance of cholesterol for the mechanical stability of animal cells.
    • Predict how the fluidity of a membrane would change if its cholesterol were removed.
    346

    Transport across cell membranes

    Movement across membranes occurs by: simple diffusion (involving limitations imposed by the nature of the phospholipid bilayer) facilitated diffusion (involving the roles of carrier proteins and channel proteins) osmosis (explained in terms of water potential) active transport (involving the role of carrier proteins and the importance of the hydrolysis of ATP) co-transport (illustrated by the absorption of sodium ions and glucose by cells lining the mammalian ileum).

    Verified
    Key Learning Objectives:
    • Explain why oxygen crosses a membrane by simple diffusion but a sodium ion cannot.
    • Describe the roles of channel proteins and carrier proteins in facilitated diffusion.
    • Describe the sequence by which glucose is absorbed from the ileum by co-transport with sodium ions.
    • Explain, in terms of water potential, the direction in which water moves between a cell and its surrounding solution.
    347

    Transport across cell membranes

    Required practical 3: Production of a dilution series of a solute to produce a calibration curve with which to identify the water potential of plant tissue.

    Verified
    Key Learning Objectives:
    • Calculate the volumes of stock solution and distilled water needed to produce each concentration in a dilution series of equal final volume.
    • Explain why percentage change in mass, rather than change in mass, must be plotted.
    • Determine the water potential of a plant tissue from the point where a calibration curve crosses zero change in mass.
    • Describe an experiment to decide whether a named plant tissue has a lower water potential than a given solution.
    348

    Transport across cell membranes

    Required practical 4: Investigation into the effect of a named variable on the permeability of cell-surface membranes.

    Verified
    Key Learning Objectives:
    • Explain why beetroot cylinders must be washed before the investigation begins.
    • Explain how increasing temperature increases membrane permeability, distinguishing the effect on phospholipids from the effect on proteins.
    • Describe how a colorimeter is set up and used to compare pigment leakage between samples.
    • Identify the controlled variables in a membrane permeability investigation and explain why each matters.
    349

    Transport across cell membranes

    Students should be able to: explain the adaptations of specialised cells in relation to the rate of transport across their internal and external membranes explain how surface area, number of channel or carrier proteins and differences in gradients of concentration or water potential affect the rate of movement across cell membranes.

    Verified
    Key Learning Objectives:
    • Explain how surface area, number of transport proteins and gradient steepness each affect the rate of movement across a membrane.
    • Describe adaptations of both internal and external membranes that increase the rate of transport.
    • Explain why the rate of facilitated diffusion levels off as the external concentration keeps rising.
    • Explain how a cell's blood supply helps maintain a steep concentration gradient for absorption.
    350

    Transport across cell membranes

    The arrangement and any movement of phospholipids, proteins, glycoproteins and glycolipids in the fluid-mosaic model of membrane structure.

    Verified
    Key Learning Objectives:
    • Explain what the words fluid and mosaic each describe in the fluid-mosaic model.
    • Describe the arrangement and movement of phospholipids, proteins, glycoproteins and glycolipids.
    • Explain how the hydrophobic and hydrophilic amino acids of a protein determine its position in the bilayer.
    • State where glycoproteins and glycolipids are found in the membrane and give their functions.
    351

    Transport across cell membranes

    The basic structure of all cell membranes, including cell-surface membranes and the membranes around the cell organelles of eukaryotes, is the same.

    Verified
    Key Learning Objectives:
    • Explain why phospholipids form a bilayer when surrounded by water, referring to the two ends of the molecule.
    • State what all cell membranes have in common and identify what makes the inner mitochondrial membrane different.
    • Name four membranes inside a eukaryotic cell that share the same basic structure.
    • Explain how the shared structure of membranes allows a vesicle to fuse with the cell-surface membrane.
    352

    Using genome projects (A-level only)

    Determining the genome of simpler organisms allows the sequences of the proteins that derive from the genetic code (the proteome) of the organism to be determined.

    Verified
    Key Learning Objectives:
    • Define the proteome in wording that survives the mark scheme's restrictions on 'number of proteins' and on species-level answers.
    • Explain why the proteome of a bacterium can be predicted from its genome but that of a mammal cannot.
    • Suggest how knowing a pathogen's proteome leads to the identification of a candidate antigen for a vaccine.
    353

    Using genome projects (A-level only)

    In more complex organisms, the presence of non-coding DNA and of regulatory genes means that knowledge of the genome cannot easily be translated into the proteome.

    Verified
    Key Learning Objectives:
    • Explain why the base sequence of a eukaryotic gene cannot be translated directly into an amino acid sequence.
    • Describe how alternative splicing lets one gene code for more than one polypeptide.
    • Suggest why two cells from the same person, with identical genomes, contain different sets of proteins.
    354

    Using genome projects (A-level only)

    Sequencing methods are continuously updated and have become automated.

    Verified
    Key Learning Objectives:
    • Describe how an automated sequencer handles a genome too long to read in one piece.
    • Explain two consequences of faster, cheaper sequencing for biology or medicine.
    • Suggest why species classified before automated sequencing have since been renamed.
    355

    Using genome projects (A-level only)

    Sequencing projects have read the genomes of a wide range of organisms, including humans.

    Verified
    Key Learning Objectives:
    • Define the genome precisely enough to avoid the species-level wording that mark schemes reject.
    • Explain how comparing base sequences between two organisms provides evidence about their evolutionary relationship.
    • Suggest why DNA sequencing has led to bacterial species being renamed when microscopy had grouped them together.
    356

    Using genome projects (A-level only)

    This may have many applications, including the identification of potential antigens for use in vaccine production.

    Verified
    Key Learning Objectives:
    • Explain how a sequenced genome leads to a shortlist of candidate antigens for a vaccine.
    • Describe the immune response that follows injection of an antigen identified in this way, naming memory cells.
    • Suggest an advantage of finding antigens from sequence data rather than from cultures of the pathogen.
    357

    Water

    Water is a major component of cells. It has several properties that are important in biology. In particular, water: is a metabolite in many metabolic reactions, including condensation and hydrolysis reactions is an important solvent in which metabolic reactions occur has a relatively high heat capacity, buffering changes in temperature has a relatively large latent heat of vaporisation, providing a cooling effect with little loss of water through evaporation has strong cohesion between water molecules; this supports columns of water in the tube-like transport cells of plants and produces surface tension where water meets air.

    Verified
    Key Learning Objectives:
    • Explain how hydrogen bonding between water molecules allows a continuous column of water to be pulled up a xylem vessel.
    • Relate the high specific heat capacity of water to the stability of enzyme activity in a cell or an aquatic habitat.
    • Give one reaction in which water is a reactant and one in which it is a product, naming each type of reaction.

    Regulatory & Verification Details

    Qualification Number (QN)
    601/4625/4
    Regulated Status
    Available to learners
    Awarding Body
    AQA
    Qualification Type
    GCE A Level
    Operational Start
    Sept 2015