Specification points
OCR AS Level Biology B (Advancing Biology) H022
259 points in 5 topics, with OCR's codes and titles.
Codes and titles are read by a script from OCR's published specification and have not been checked by a person. What each point covers is in the specification itself: OCR’s specification.
1 Development of practical skills in biology
- 1.1 Practical skills assessed in a written examination
- 1.1.1 Planning
- 1.1.1(a) Designing experiments to solve practical problems
- 1.1.1(b) Identifying variables to control
- 1.1.1(c) Judging whether a method suits the aims
- 1.1.2 Implementing
- 1.1.2(a) Using practical apparatus and techniques correctly
- 1.1.2(b) Units for measurements
- 1.1.2(c) Presenting observations and data
- 1.1.3 Analysis
- 1.1.3(a) Processing and interpreting experimental results
- 1.1.3(b) Maths skills for analysing quantitative data
- 1.1.3(c) Significant figures
- 1.1.3(d) Plotting and interpreting graphs of results
- 1.1.3(d)(i) Choosing and labelling graph axes
- 1.1.3(d)(ii) Gradients and intercepts from graphs
- 1.1.4 Evaluation
- 1.1.4(a) Evaluating results and drawing conclusions
- 1.1.4(b) Spotting anomalies in measurements
- 1.1.4(c) Limitations of experimental procedures
- 1.1.4(d) Precision, accuracy, errors and uncertainties
- 1.1.4(e) Improving experimental procedures and apparatus
2 Cells, chemicals for life, transport and gas exchange
- 2.1 Cells and chemicals for life
- 2.1.1 Cells and microscopy
- 2.1.1(a) Microscopy, cell theory and blood smears
- 2.1.1(a)(i) Microscopy and the cell theory
- 2.1.1(a)(ii) Preparing blood smears
- 2.1.1(b) Differential staining
- 2.1.1(c) Animal cells seen in blood smears
- 2.1.1(c)(i) Blood cells under the light microscope
- 2.1.1(c)(ii) Drawing cells in a blood smear
- 2.1.1(d) Cell dimensions and the magnification formula
- 2.1.1(e) Practical: haemocytometer cell counts
- 2.1.1(f) Flow cytometry in blood analysis
- 2.1.1(g) Ultrastructure of an animal cell
- 2.1.1(h) Plant and prokaryotic cell ultrastructure compared
- 2.1.1(h)(i) Ultrastructure of plant and prokaryotic cells
- 2.1.1(h)(ii) Plant, animal and prokaryotic cells compared
- 2.1.1(i) Practical: measuring cells with a graticule
- 2.1.1(j) Lipids in the plasma membrane
- 2.1.1(k) The fluid mosaic model
- 2.1.1(l) Movement of molecules across membranes
- 2.1.1(m) Practical: diffusion rates in cells
- 2.1.1(n) Roles of membranes
- 2.1.1(o) Organelles in protein production and secretion
- 2.1.2 Water and its importance in plants and animals
- 2.1.2(a) Properties of water
- 2.1.2(b) Water in cells, fluids and transport
- 2.1.2(b)(i) Importance of water in living organisms
- 2.1.2(b)(ii) Secondary data on water as a solvent
- 2.1.2(c) Detecting and measuring sugars and proteins
- 2.1.2(c)(i) Detecting sugars and proteins in fluids
- 2.1.2(c)(ii) Biuret, Benedict's tests and colorimetry
- 2.1.2(d) Hydrolysis and condensation in metabolism
- 2.1.2(e) Alpha-glucose and lactose structure
- 2.1.2(f) Polysaccharides and the starch test
- 2.1.2(f)(i) Polysaccharide formation by condensation
- 2.1.2(f)(ii) Testing for starch
- 2.1.2(g) Osmosis and water potential gradients
- 2.1.2(h) Practical: factors affecting osmosis
- 2.1.3 Proteins and enzymes
- 2.1.3(a) Amino acids, peptide bonds and chromatography
- 2.1.3(a)(i) Amino acid structure and peptide bonds
- 2.1.3(a)(ii) Chromatography of amino acids
- 2.1.3(b) Structure of globular proteins
- 2.1.3(c) Globular protein structure and enzyme specificity
- 2.1.3(d) Rate of enzyme-catalysed reactions
- 2.1.3(d)(i) Factors affecting enzyme reaction rates
- 2.1.3(d)(ii) Practical: enzyme reaction rates
- 2.1.3(e) Blood clotting and first aid
- 2.1.3(e)(i) Proteins in blood clotting
- 2.1.3(e)(ii) First aid for bleeding
- 2.1.3(f) Enzymes and inhibitors in medicine
- 2.1.3(g) Blood donation and blood products
- 2.1.4 Nucleic acids
- 2.1.4(a) Nucleotide structure
- 2.1.4(b) ADP and ATP structure
- 2.1.4(c) DNA structure and purification
- 2.1.4(c)(i) DNA structure and Chargaff's rules
- 2.1.4(c)(ii) Practical: purifying DNA by precipitation
- 2.1.4(d) Semi-conservative DNA replication
- 2.1.4(e) The genetic code
- 2.1.4(f) RNA structure compared with DNA
- 2.1.4(g) Transcription and translation
- 2.2 Transport and gas exchange systems
- 2.2.1 The heart and monitoring heart function
- 2.2.1(a) Why mammals need mass transport
- 2.2.1(b) Structure and dissection of the heart
- 2.2.1(b)(i) Structure of the mammalian heart
- 2.2.1(b)(ii) Dissecting and drawing the heart
- 2.2.1(c) The cardiac cycle
- 2.2.1(d) Initiation and coordination of heart action
- 2.2.1(e) Practical: factors affecting heart rate
- 2.2.1(f) Heart rate and cardiac output
- 2.2.1(g) Measuring and interpreting pulse rate
- 2.2.1(h) Electrocardiograms (ECG)
- 2.2.1(i) Emergency treatment for heart attack or cardiac arrest
- 2.2.2 Transport systems in mammals
- 2.2.2(a) The closed double circulatory system
- 2.2.2(b) Blood vessels and their sections
- 2.2.2(b)(i) Blood vessel structure and function
- 2.2.2(b)(ii) Microscope sections of blood vessels
- 2.2.2(c) Tissue fluid
- 2.2.2(d) Measuring and comparing blood pressure
- 2.2.2(d)(i) Measuring blood pressure with a sphygmomanometer
- 2.2.2(d)(ii) Comparing blood pressure readings
- 2.2.2(e) Interpreting blood pressure measurements
- 2.2.3 Gas exchange in mammals and plants
- 2.2.3(a) Gas exchange system tissues and microscopy
- 2.2.3(a)(i) Cells, tissues and organs of gas exchange
- 2.2.3(a)(ii) Microscopy of gas exchange tissues
- 2.2.3(b) Gas exchange in the alveoli
- 2.2.3(c) Factors affecting pulmonary ventilation
- 2.2.3(d) Expired air resuscitation
- 2.2.3(e) Gas exchange in plants
- 2.2.3(f) Stomata: structure and appearance
- 2.2.3(f)(i) Stomatal structure, opening and closing
- 2.2.3(f)(ii) Stomata under the microscope
- 2.2.4 Transport systems in plants
- 2.2.4(a) Why multicellular plants need transport systems
- 2.2.4(b) Vascular tissue in roots, stems and leaves
- 2.2.4(c) Plant tissue sections and dissection
- 2.2.4(c)(i) Drawing stained plant tissue sections
- 2.2.4(c)(ii) Dissecting plant organs to show vascular tissue
- 2.2.4(d) Water uptake and transport in plants
- 2.2.4(e) Transpiration and its rate
- 2.2.4(e)(i) Transpiration and factors affecting its rate
- 2.2.4(e)(ii) Practical: estimating transpiration rates
- 2.2.4(f) Translocation
3 Cell division, development and disease control
- 3.1 Cell division and development
- 3.1.1 The developing cell: cell division and cell differentiation
- 3.1.1(a) The cell cycle
- 3.1.1(b) Mitosis in plant and animal cells
- 3.1.1(b)(i) Nuclear and cell changes during mitosis
- 3.1.1(b)(ii) Cells undergoing mitosis under the microscope
- 3.1.1(c) Stages and features of apoptosis
- 3.1.1(d) Apoptosis and mitosis in growth and repair
- 3.1.1(e) Stem cells: differentiation and uses
- 3.1.1(e)(i) Differentiation of stem cells
- 3.1.1(e)(ii) Applications of stem cells
- 3.1.2 The developing individual: meiosis, growth and development
- 3.1.2(a) Meiosis, sexual reproduction and gametes
- 3.1.2(b) Stages of meiosis
- 3.1.2(c) Genetic variation from meiosis
- 3.1.2(d) Antenatal care in the UK
- 3.1.2(e) Diet in pregnancy
- 3.1.2(f) Alcohol, smoking and fetal development
- 3.1.2(g) Measuring fetal growth
- 3.1.2(g)(i) Ultrasound to measure fetal growth
- 3.1.2(g)(ii) Fetal growth chart data
- 3.1.2(h) Techniques for assessing fetal development
- 3.1.2(i) Karyotypes
- 3.1.3 The development of species: evolution and classification
- 3.1.3(a) Classification and the species concept
- 3.1.3(b) Evidence for classification and changing theories
- 3.1.3(c) DNA barcoding in classification
- 3.1.3(d) Phylogenetic trees and genetic relatedness
- 3.1.3(e) Adaptations to the environment, with practical work
- 3.1.3(e)(i) Types of adaptation: behavioural, physiological, anatomical
- 3.1.3(e)(ii) Practical: plant adaptations to environment
- 3.1.3(f) Evolution of language: competing theories
- 3.1.3(g) Adaptation and selection in evolution
- 3.1.3(h) Defining and measuring biodiversity
- 3.1.3(i) Genetic diversity calculations
- 3.2 Pathogens, immunity and disease control
- 3.2.1 Pathogenic microorganisms
- 3.2.1(a) Pathogens and communicable disease
- 3.2.1(b) Tuberculosis and HIV/AIDS
- 3.2.1(c) Structure of HIV
- 3.2.1(d) Identifying bacteria and Gram staining
- 3.2.1(d)(i) Identifying bacteria by Gram stain and morphology
- 3.2.1(d)(ii) Culturing bacteria and Gram staining
- 3.2.1(e) Changing incidence and prevalence of disease
- 3.2.1(f) Incidence, prevalence and mortality rates
- 3.2.1(g) Using epidemiological data
- 3.2.1(h) Notifiable diseases and public health reporting
- 3.2.1(i) Controlling HIV/AIDS and TB
- 3.2.2 The immune system
- 3.2.2(a) Primary and non-specific defences
- 3.2.2(b) How phagocytes act
- 3.2.2(c) B and T lymphocytes
- 3.2.2(d) Secondary response and memory cells
- 3.2.2(e) Antibody structure and function
- 3.2.2(f) Testing for TB and HIV
- 3.2.2(g) Types of immunity: active, passive, natural, artificial
- 3.2.2(h) Allergies and hypersensitivity
- 3.2.3 Controlling communicable diseases
- 3.2.3(a) Principles of vaccination
- 3.2.3(b) Vaccination programmes and epidemics
- 3.2.3(c) Problems in developing vaccines
- 3.2.3(d) Ethics of vaccines
- 3.2.3(e) Antibiotics for communicable disease
- 3.2.3(f) Antibiotic misuse and resistant bacteria
- 3.2.3(g) Practical: antibiotics on Gram-positive and Gram-negative bacteria
- 3.3 Non-communicable diseases
- 3.3.1 The cellular basis of cancer and treatment
- 3.3.1(a) Risk factors for non-communicable diseases
- 3.3.1(b) Cellular basis of cancer
- 3.3.1(c) Proto-oncogene mutations and cancer
- 3.3.1(d) Tumour suppressor gene mutations and cancer
- 3.3.1(e) Evaluating evidence on cancer risk factors
- 3.3.1(f) Detecting cancer
- 3.3.1(g) Ethics and economics of cancer screening
- 3.3.1(h) Treating cancer
- 3.3.2 Respiratory diseases and treatment
- 3.3.2(a) Pollutants and the respiratory system
- 3.3.2(b) COPD, asthma and lung cancer
- 3.3.2(c) Acute and chronic diseases compared
- 3.3.2(d) Treating asthma
- 3.3.2(e) Plants as sources of medicines
- 3.3.2(f) Clinical trials
- 3.3.2(g) The role of NICE
5c How Science Works (HSW)
- HSW1 Theories and models to explain science
- HSW2 Posing questions and presenting scientific arguments
- HSW3 Methods, including ICT, to answer scientific questions
- HSW4 Experimental work and risk management
- HSW5 Analysing data, correlation and causation
- HSW6 Evaluating methods, evidence and data
- HSW7 How scientific knowledge develops over time
- HSW8 Communicating science with correct terminology
- HSW9 Applications, benefits and risks of science
- HSW10 Ethical issues in science
- HSW11 Scientific community and validating knowledge
- HSW12 Science in society's decision making
5d Mathematical requirements
- M0 Arithmetic and numerical computation
- M0.1 Units in calculations
- M0.2 Decimal and standard form
- M0.3 Ratios, fractions and percentages
- M0.4 Estimating results
- M1 Handling data
- M1.1 Significant figures
- M1.2 Arithmetic means
- M1.3 Frequency tables, bar charts and histograms
- M1.4 Simple probability
- M1.5 Sampling principles for scientific data
- M1.6 Mean, median and mode
- M1.7 Scatter diagrams and correlation
- M1.8 Order of magnitude calculations
- M1.9 Choosing and using statistical tests
- M1.10 Standard deviation and range
- M1.11 Uncertainties in measurements and combined data
- M2 Algebra
- M2.1 Mathematical symbols
- M2.2 Changing the subject of an equation
- M2.3 Substituting values into equations
- M2.4 Solving algebraic equations
- M3 Graphs
- M3.1 Graphical, numerical and algebraic forms
- M3.2 Plotting two variables from data
- M3.3 Linear relationships: y = mx + c
- M3.5 Rate of change from a linear graph
- M3.6 Tangents to curves as rates of change
- M4 Geometry and trigonometry
- M4.1 Circumference, surface area and volume of shapes