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TCE Biology past exams 2024–2025, by year and topic
The official TASC exams, marking guides and examiner reports we index, organised by topic and subtopic and labelled with the study design it was written under. Open the official paper, work the question in your own workspace, or bring a tutor into it live.
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ATARMAxxing indexes 2 official TASC Biology papers from 2024 to 2025, across 20 topics. Every paper opens on the TASC website.
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Preview the worked question →TCE Biology exams by year: official papers & marking guidance
Past exams indexed: 2025, 2024. Open the official TASC papers, with marking guidance where available.
| Year | Study design | Official paper(s) | Marking guidance |
|---|---|---|---|
| 2025 TCE Biology exam | BIO315124 | 2025 official paper ↗ | Marking guidance ↗ |
| 2024 TCE Biology exam | BIO315124 | 2024 official paper ↗ | Marking guidance ↗ |
2 official papers across 2 years (2024–2025), 2 with marking guidance, published by TASC.
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The rest of the syllabus
Question-level mapping for these areas is still being verified. Every official paper covering them is in the year table above.
- Experimental questions, variables and directional hypotheses — Turn a biological observation into a testable question · Identify the variable and its operational measurement · Write a directional, mechanistically justified hypothesis · Control competing explanations with specific decisions · Choose replication and sampling that match the comparison · Build a reproducible method and an honest conclusion
- Evidence quality, data representation and inquiry ethics — Distinguish validity, reliability and measurement accuracy · Summarise a dataset without concealing its variation · Select graphs that preserve the biological relationship · Reason from evidence to a bounded causal conclusion · Apply ethical reasoning to the actual investigation · Evaluate sources and communicate uncertainty transparently
- Science as a human endeavour and internal inquiry folios — Connect biological knowledge with how it was developed · Analyse a discovery through a concrete case framework · Plan the current practical skills and inquiry folios · Develop the human-endeavour folio with traceable sources · Use ethical attribution and distinguish evidence from advocacy · Reconcile internal preparation with the external examination
- Enzyme mechanisms and rate investigations — Explain catalysis through structure and successful interaction · Interpret temperature and pH effects without overgeneralising · Distinguish substrate saturation from enzyme limitation · Compare inhibition with support from cofactors and coenzymes · Design an initial-rate enzyme experiment · Construct complete explanations from unfamiliar enzyme data
- Photosynthesis and cellular respiration — Track matter and energy with balanced net equations · Relate chloroplast structure to the stages of photosynthesis · Follow glucose through aerobic respiration at course depth · Compare aerobic and anaerobic pathways by outcomes · Interpret limiting factors and net gas exchange · Evaluate investigations of photosynthesis and respiration
- DNA structure, replication and manipulation — Relate nucleotide structure to genetic information · Use complementarity to explain accurate copying · Assign the required replication enzymes distinct roles · Explain the evidence logic of semi-conservative replication · Distinguish DNA manipulation from copying an organism · Interpret sequencing and fragment evidence cautiously
- Protein synthesis and codon interpretation — Connect gene information to a functional protein · Explain transcription as RNA construction from a template · Distinguish RNA processing from changing DNA · Explain translation through codons and matching transfer RNA · Work a codon-chart question with explicit checking · Evaluate the consequences of a changed sequence
- Gene expression, lac operon and mutation — Explain why cells regulate gene expression · Model the lac operon with lactose absent and present · Apply the current Lac Z and Lac Y requirement · Classify mutations by the molecular change · Separate expression changes from inherited sequence variation · Evaluate a gene-to-phenotype argument using linked evidence
- Neurons and synaptic transmission — Relate neuron structures to information transfer · Explain resting potential through ions and permeability · Describe threshold and the phases of an action potential · Explain propagation without moving one spike as an object · Trace chemical transmission across a synapse · Connect neural signalling to homeostatic responses
- Negative feedback and blood glucose — Build a complete negative-feedback explanation · Trace the response to rising blood glucose · Trace the response to falling blood glucose · Compare endocrine targeting with neural communication · Interpret glucose and hormone time-series data · Evaluate a glucose-regulation model and its limitations
- Thermoregulation — Define the regulated condition and the heat balance · Trace detection and control through negative feedback · Explain vasodilation and vasoconstriction by blood distribution · Distinguish sweating from successful evaporative cooling · Compare shivering, insulation and behaviour in cold conditions · Interpret thermoregulation evidence and model boundaries
- Animal and plant water balance — Explain why water balance depends on solutes and movement · Trace ADH feedback from detection to urine change · Distinguish filtration from selective reabsorption in the nephron · Explain the transpiration stream from roots to leaves · Interpret environmental effects on transpiration · Compare arid adaptations and integrate competing demands
- Pathogen types and transmission — Distinguish pathogen categories without treating all as cells · Separate exposure, infection, disease and transmission · Compare direct, fluid, food, water and airborne routes · Explain vectors and pathogen adaptations functionally · Interpret population disease data with denominators · Evaluate control strategies by their place in the chain
- Innate immunity and inflammation — Organise defence without turning it into a rigid timetable · Compare structural, chemical and biological barriers · Trace inflammation through mediators and vascular changes · Explain phagocytosis as a membrane-mediated process · Connect antigen presentation with adaptive activation · Evaluate innate-response data without assuming more is always better
- Adaptive immunity — Explain specificity and clonal expansion · Trace the B-cell response to plasma cells and antibodies · Explain antibody action without making antibodies into cells · Distinguish helper, cytotoxic, regulatory and memory T cells · Interpret primary and secondary responses through memory · Integrate humoral and cellular evidence in one explanation
- Vaccination, immunity types and population protection — Classify immunity using source and mechanism separately · Explain vaccination through antigen exposure and memory · Compare passive protection with active memory formation · Explain population protection through transmission opportunities · Calculate comparative outcomes without overstating them · Evaluate a transmission model and communicate its limits
- Cell cycle, mitosis and meiosis — Locate DNA replication within the cell cycle · Trace mitosis through chromosome movement and cytokinesis · Explain meiosis I through homologous chromosome separation · Explain meiosis II and the relationship to fertilisation · Connect independent assortment with genetic variation · Interpret division diagrams and evaluate errors carefully
- Monohybrid inheritance and ABO blood groups — Define alleles, genotype and phenotype before calculating · Construct a Punnett square from gamete probabilities · Use test-cross logic while respecting finite evidence · Distinguish incomplete dominance from codominance · Work ABO crosses using multiple alleles and codominance · Check probabilities and distinguish expected from observed
- X-linked inheritance and pedigree analysis — Set the sex-linked model and notation explicitly · Calculate an X-linked recessive cross carefully · Use X-linked dominant transmission as a discriminating pattern · Eliminate autosomal models through informative relationships · Represent genotype uncertainty instead of guessing · Write a pedigree argument that addresses alternatives
- Evolution and speciation — Distinguish genetic variation from changes in its frequency · Explain natural selection through differential reproduction · Separate genetic drift, founder effects and bottlenecks · Explain gene flow and interactions among mechanisms · Trace geographical isolation towards speciation · Evaluate diversity, extinction risk and evolutionary evidence
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