Magnification Relationship
Ensure consistent units (e.g., convert µm to mm) before calculating.
Magnification = Image size / Actual size Actual size = Image size / Magnification Cambridge International A Level 9700
Quantitative relationships for microscopy, transport, genetics, ecology and statistics — organised for Cambridge 9700 papers.
Although Biology is concept-based, Cambridge exams expect precise quantitative work. Use this formula sheet to keep magnification calculations, water potential, genetic ratios and statistical tests at your fingertips.
Microscopy & cell measurement calculations
Water potential and gas exchange relationships
Population genetics and inheritance maths
Ecological diversity and productivity formulas
Ensure consistent units (e.g., convert µm to mm) before calculating.
Magnification = Image size / Actual size Actual size = Image size / Magnification Magnification = Measured scale bar length (on image) / Actual scale bar value (given).
Calibrate using stage micrometer: 1 graticule unit = Stage micrometer length / Number of graticule divisions.
Express in simplest ratio form to compare different organisms or sizes.
SA:V = Surface area / Volume Ψ total water potential, Ψs solute potential, Ψp pressure potential. C concentration (mol dm⁻³), R 8.31 J mol⁻¹ K⁻¹, T temperature (K). Ψp is positive in turgid cells.
Ψ = Ψs + Ψp Ψs = −CRT Volume in cm³ (or cm³ converted from distance × area); time in minutes or seconds to give rate units.
Rate = Volume of water lost / Time Stroke volume (SV) in cm³ per beat, heart rate (HR) in beats per minute; cardiac output reported in dm³ min⁻¹.
Cardiac output = Stroke volume × Heart rate Tidal volume (TV) in dm³ per breath, breathing rate (f) in breaths per minute.
Ventilation rate = Tidal volume × Breathing rate Greater surface area (A) and concentration gradient (ΔC) increase rate; greater thickness (d) reduces rate.
Rate ∝ (Surface area × Difference in concentration) / Thickness Use Punnett squares to show genotype combinations. Expected phenotypic ratios: Monohybrid (3:1), Dihybrid (9:3:3:1) for heterozygous crosses.
O observed counts, E expected counts. Compare χ² with critical value at degrees of freedom = categories − 1.
χ² = Σ [(O − E)² / E] p = dominant allele frequency, q = recessive allele frequency. Conditions: large population, random mating, no selection/migration/mutation.
p + q = 1 p² + 2pq + q² = 1 Rate = Number of mutations / Total number of genes examined × Time. Use data to compare relative rates.
Recombinants are offspring with new allele combinations; frequency < 50% indicates linkage.
Recombination frequency (%) = (Number of recombinants / Total offspring) × 100 Area in m² (terrestrial) or volume in m³ (aquatic) for consistent units.
Density = Number of organisms / Area (or volume) sampled Assumptions: even mixing, no immigration/emigration, marks remain.
Estimated population size = (Number marked in first sample × Number in second sample) / Number of marked recaptured n = number of individuals in each species, N = total individuals.
D = 1 − Σ [n(n − 1) / N(N − 1)] GPP = Gross Primary Productivity, R = Respiratory losses.
NPP = GPP − R Energy measured in kJ; compare trophic levels to discuss losses.
Efficiency (%) = (Energy transferred to next level / Energy available at previous level) × 100 Use classification ranges: <18.5 underweight, 18.5–24.9 healthy, etc.
BMI = Mass (kg) / Height² (m²) Thresholds: >0.85 (women) or >0.90 (men) linked to higher cardiovascular risk.
WHR = Waist circumference / Hip circumference Specific heat capacity of water = 4.18 kJ kg⁻¹ K⁻¹ (or 4.18 J g⁻¹ K⁻¹).
Energy (kJ) = (Mass of water × Specific heat capacity × Temperature rise) / Mass of food burned Compare solution Ψ to cell Ψ to predict red blood cell swelling/lysis or plant cell plasmolysis.
Mean = Σx / n; median is middle value; mode is most frequent. Choose appropriate measure for data set.
x individual value, x̄ sample mean, n number of samples. Use sample standard deviation for Cambridge practical papers.
s = √[Σ (x − x̄)² / (n − 1)] s sample standard deviation, n number of replicates, x̄ sample mean. Mention overlap of confidence intervals when comparing treatments.
Standard error (SE) = s / √n 95% CI ≈ x̄ ± 1.96 × SE Absolute error usually half the instrument resolution; report result to same precision.
Percentage error = (Absolute error / Measured value) × 100% Plot absorbance vs concentration, draw line of best fit, use measured absorbance to read unknown concentration.
Boost your Cambridge exam confidence with these proven study strategies from our tutoring experts.
Write the relevant formula before substitution and track units carefully — especially for water potential and gas calculations.
When presenting practical conclusions, use calculated means, standard deviations and χ² to justify claims.
Sense-check your final values against typical biological ranges (e.g., realistic cell sizes, population counts).
After calculations, explain the biological mechanism behind the result to collect explanation marks.
Practise Cambridge-style data analysis, planning and evaluation with specialist tutors who guide you through the calculations and the biology behind them.
Matches the quantitative requirements of Cambridge International AS & A Level Biology (9700), including practical assessment expectations.
Always specify significant figures based on instrument precision and indicate biological context in written answers.