Alberta · Grade 12
Biology 30
- SCN3230
Alberta’s Grade 12 science course, from Nervous & Endocrine Systems to Population & Community Dynamics.
- Units
- 4
- Lessons
- 16
- Skills
- 55
- Provincial exam
- 30% of the final mark
- Official curriculum
- Alberta Education
Unit by unit
Every skill in the course, with its official code.
Unit 1 · 12 skills
Nervous & Endocrine Systems
The Neuron & Nervous System
Neurons and the action potential
I can describe a neuron and explain how an action potential forms, travels, and crosses a synapse.
Official code: 30-A1.1k
Central & peripheral nervous systems
I can identify the structures of the central and peripheral nervous systems and explain how they regulate voluntary and involuntary actions.
Official code: 30-A1.2k
Nerves and reflex arcs
I can describe how neurons organize into nerves and how a reflex arc works, using an example.
Official code: 30-A1.3k
Sensing the Environment
Structure and function of the eye
I can describe the structure and function of the parts of the human eye.
Official code: 30-A1.4k
Structure and function of the ear
I can describe the structure and function of the parts of the human ear.
Official code: 30-A1.5k
Other human senses
I can explain other ways humans sense their environment and their spatial orientation.
Official code: 30-A1.6k
Endocrine Glands & Hormones
The principal endocrine glands
I can identify the principal endocrine glands of humans.
Official code: 30-A2.1k
Hormones and feedback
I can describe the functions of the principal hormones and how feedback maintains homeostasis.
Official code: 30-A2.2k
Metabolic roles of hormones
I can explain the metabolic roles hormones play in homeostasis.
Official code: 30-A2.3k
Endocrine Control & Imbalance
Sensing the internal environment
I can explain how the endocrine system senses the internal environment and responds appropriately.
Official code: 30-A2.4k
Comparing endocrine and nervous control
I can compare the endocrine and nervous control systems and explain how they work together.
Official code: 30-A2.5k
Consequences of hormone imbalance
I can describe, using an example, the physiological consequences of hormone imbalances.
Official code: 30-A2.6k
The official wording · 12 outcomes
- 30-A1.1k
- describe the general structure and function of a neuron and myelin sheath, explaining the formation and transmission of an action potential, including all-or-none response and intensity of response
- 30-A1.2k
- identify the principal structures of the central and peripheral nervous systems and explain their functions in regulating the voluntary (somatic) and involuntary (autonomic) systems of the human organism
- 30-A1.3k
- describe, using an example, the organization of neurons into nerves and the composition and function of reflex arcs
- 30-A1.4k
- describe the structure and function of the parts of the human eye
- 30-A1.5k
- describe the structure and function of the parts of the human ear
- 30-A1.6k
- explain other ways that humans sense their environment and their spatial orientation in it
- 30-A2.1k
- identify the principal endocrine glands of humans
- 30-A2.2k
- describe the function of the hormones of the principal endocrine glands
- 30-A2.3k
- explain the metabolic roles hormones may play in homeostasis
- 30-A2.4k
- explain how the endocrine system allows humans to sense their internal environment and respond appropriately
- 30-A2.5k
- compare the endocrine and nervous control systems and explain how they act together
- 30-A2.6k
- describe, using an example, the physiological consequences of hormone imbalances
Key ideas
A neuron has dendrites, a cell body and an axon; the myelin sheath speeds transmission by letting the impulse jump between gaps.
Light passes through the cornea and lens, which focus it onto the retina; the iris adjusts the pupil to control how much light enters.
The principal endocrine glands are the hypothalamus/pituitary complex, thyroid, parathyroid, adrenal glands, and the islet cells of the pancreas.
Endocrine glands detect internal conditions (blood calcium, osmotic pressure, blood sugar) and release hormones to correct them.
An action potential is an all-or-none wave of ion movement ( in, then out); a stronger stimulus means MORE impulses, not a bigger one. At the synapse, neurotransmitters (e.g. acetylcholine) carry the signal chemically and cholinesterase clears it.
Watch out for
- Thinking a nerve impulse is electric current flowing like electricity through a wire — it is a self-propagating wave of ion movement across the membrane, far slower than a wire and requiring living cells.
- Thinking the eye "sees" — the eye only detects and focuses light; the BRAIN interprets the image (which arrives upside-down).
- Thinking all glands are endocrine — sweat and salivary glands are exocrine (use ducts), not endocrine.
Every skill’s key ideas, worked examples and checks are in MapleMind.Practise this unit
Unit 2 · 13 skills
Reproduction & Development
Reproductive Anatomy
The female reproductive system
I can identify the structures of the female reproductive system and describe their functions.
Official code: 30-B1.1k
The male reproductive system
I can identify the structures of the male reproductive system and describe their functions.
Official code: 30-B1.2k
Gametes and supporting structures
I can distinguish sperm and eggs from the structures that support them.
Official code: 30-B1.3k
Sex Determination & Reproductive Health
Chromosomes, hormones and sex determination
I can describe how chromosomes and hormones determine the formation of reproductive organs.
Official code: 30-B1.4k
STIs and fertility
I can explain how sexually transmitted infections can interfere with fertility and reproduction.
Official code: 30-B1.5k
Reproductive Hormones & the Menstrual Cycle
Hormones and sex characteristics
I can describe how reproductive hormones regulate primary and secondary sex characteristics.
Official code: 30-B2.1k
Hormones of the menstrual cycle
I can explain how estrogen, progesterone, FSH and LH interact to maintain the menstrual cycle.
Official code: 30-B2.2k
Male reproductive hormones
I can identify the male reproductive hormones and explain their interactions.
Official code: 30-B2.3k
Fertilization & Development
Fertilization, pregnancy and birth
I can trace the events from fertilization to birth and lactation and the hormones that control them.
Official code: 30-B3.1k
Stages of development
I can describe development from fertilization to birth through its main stages.
Official code: 30-B3.2k
Germ layers and tissue differentiation
I can identify the tissues and organs that arise from the three germ layers.
Official code: 30-B3.3k
Environmental factors in development
I can describe how environmental factors influence embryonic and fetal development.
Official code: 30-B3.4k
Reproductive technologies
I can describe the physiological or mechanical basis of different reproductive technologies.
Official code: 30-B3.5k
The official wording · 13 outcomes
- 30-B1.1k
- identify the structures in the human female reproductive system and describe their functions
- 30-B1.2k
- identify the structures in the human male reproductive system and describe their functions
- 30-B1.3k
- distinguish sperm and egg from their supporting structures
- 30-B1.4k
- describe the chromosomal factors and hormonal influence on the formation of the gonads and reproductive organs in the female and male embryo and fetus
- 30-B1.5k
- explain how sexually transmitted infections (STIs) can interfere with fertility and reproduction
- 30-B2.1k
- describe the role of hormones
- 30-B2.2k
- identify the principal reproductive hormones in the female and explain their interactions in the maintenance of the menstrual cycle
- 30-B2.3k
- identify the principal reproductive hormones in the male and explain their interactions in the maintenance and functioning of the male reproductive system
- 30-B3.1k
- trace the processes of fertilization, implantation and extra-embryonic membrane formation
- 30-B3.2k
- describe development from fertilization to parturition in the context of the main physiological events that occur in the development of organ systems during each major stage
- 30-B3.3k
- identify major tissues and organs that arise from differentiation and morphological development of the ectoderm, mesoderm and endoderm in the embryo
- 30-B3.4k
- describe the influence of environmental factors on embryonic and fetal development
- 30-B3.5k
- describe the physiological or mechanical basis of different reproductive technologies
Key ideas
The ovaries produce eggs and hormones; the Fallopian tubes carry the egg (and are where fertilization usually occurs); the uterus (lined by the endometrium) holds a developing fetus.
The Y chromosome carries a gene that triggers testis development; without it, the embryo develops ovaries — the default pathway is female.
GnRH from the hypothalamus triggers FSH and LH from the pituitary, which drive the gonads to release estrogen, progesterone (female) or testosterone (male).
Fertilization forms a zygote that implants in the endometrium; extra-embryonic membranes (placenta, amnion, chorion, allantois) support the embryo, exchanging materials with the mother.
The cervix and vagina form the lower passage; each structure has a distinct role in producing, transporting or supporting reproduction.
Watch out for
- Thinking fertilization happens in the uterus — it usually occurs in the Fallopian tube.
- Thinking the X chromosome "makes" female and the Y "makes" male directly — the Y triggers testes, and hormones then guide development.
- Thinking sex hormones are made "on their own" — they are controlled by a hypothalamus-pituitary chain.
Every skill’s key ideas, worked examples and checks are in MapleMind.Practise this unit
Unit 3 · 19 skills
Cell Division, Genetics & Molecular Biology
Chromosomes & Cell Division
Chromosome number
I can define and explain the significance of chromosome number in somatic and sex cells.
Official code: 30-C1.1k
The cell cycle and mitosis
I can explain, in general terms, the events of the cell cycle.
Official code: 30-C1.2k
Meiosis
I can describe meiosis and why chromosome number must be reduced.
Official code: 30-C1.3k
Comparing mitosis and meiosis
I can compare the processes of mitosis and meiosis.
Official code: 30-C1.4k
Crossing Over & Reproductive Strategies
Crossing over and nondisjunction
I can describe crossing over and nondisjunction and evaluate their significance.
Official code: 30-C1.5k
Fraternal and identical offspring
I can compare the formation of fraternal and identical offspring in a single birth.
Official code: 30-C1.6k
Diversity of reproductive strategies
I can describe the diversity of reproductive strategies across organisms.
Official code: 30-C1.7k
Mendelian Genetics
Mendel's evidence and laws
I can describe Mendel's evidence for dominance, segregation and independent assortment.
Official code: 30-C2.1k
Genotype and phenotype ratios
I can compare ratios and probabilities of genotypes and phenotypes for different allele types.
Official code: 30-C2.2k
Gene linkage and crossing over
I can explain how gene linkage and crossing over affect variability.
Official code: 30-C2.3k
Number of genes and variability
I can explain how the number of genes controlling a trait affects its variability.
Official code: 30-C2.4k
Sex-linked inheritance
I can compare inheritance of genes on the sex chromosomes with genes on autosomes.
Official code: 30-C2.5k
DNA: Structure & Expression
Discovery of DNA structure
I can summarize the historical events that led to the discovery of DNA's structure.
Official code: 30-C3.1k
DNA information and replication
I can describe how information is stored in DNA bases and how DNA replicates.
Official code: 30-C3.2k
Transcription and translation
I can describe, in general, how DNA is transcribed to RNA and translated to protein.
Official code: 30-C3.3k
Genetic Engineering & Mutation
Restriction enzymes and ligases
I can explain how restriction enzymes cut DNA and how ligases reassemble it.
Official code: 30-C3.4k
Cell transformation
I can explain how cells may be transformed by inserting new DNA into their genomes.
Official code: 30-C3.5k
Mutation and genetic variability
I can explain how a mutation causes abnormalities or provides genetic variability.
Official code: 30-C3.6k
DNA evidence for relationships
I can explain how base sequences give evidence for relationships among species.
Official code: 30-C3.7k
The official wording · 19 outcomes
- 30-C1.1k
- define and explain the significance of chromosome number in somatic and sex cells
- 30-C1.2k
- explain, in general terms, the events of the cell cycle
- 30-C1.3k
- describe the process of meiosis (spermatogenesis and oogenesis) and the necessity for the reduction of chromosome number
- 30-C1.4k
- compare the processes of mitosis and meiosis
- 30-C1.5k
- describe the processes of crossing over and nondisjunction and evaluate their significance to organism inheritance and development
- 30-C1.6k
- compare the formation of fraternal and identical offspring in a single birthing event
- 30-C1.7k
- describe the diversity of reproductive strategies by comparing the alternation of generations in a range of organisms
- 30-C2.1k
- describe the evidence for dominance, segregation and the independent assortment of genes on different chromosomes, as investigated by Mendel
- 30-C2.2k
- compare ratios and probabilities of genotypes and phenotypes for dominant and recessive, multiple, incompletely dominant, and codominant alleles
- 30-C2.3k
- explain the influence of gene linkage and crossing over on variability
- 30-C2.4k
- explain the relationship between variability and the number of genes controlling a trait
- 30-C2.5k
- compare the pattern of inheritance produced by genes on the sex chromosomes to that produced by genes on autosomes
- 30-C3.1k
- summarize the historical events that led to the discovery of the structure of the DNA molecule
- 30-C3.2k
- describe, in general, how genetic information is contained in the sequence of bases in DNA molecules in chromosomes and how the DNA molecules replicate themselves
- 30-C3.3k
- describe, in general, how genetic information is transcribed into sequences of bases in RNA molecules and is finally translated into sequences of amino acids in proteins
- 30-C3.4k
- explain, in general, how restriction enzymes cut DNA molecules into smaller fragments and how ligases reassemble them
- 30-C3.5k
- explain, in general, how cells may be transformed by inserting new DNA sequences into their genomes
- 30-C3.6k
- explain how a random change (mutation) in the sequence of bases results in abnormalities or provides a source of genetic variability
- 30-C3.7k
- explain how base sequences in nucleic acids contained in the nucleus, mitochondrion and chloroplast give evidence for the relationships among organisms of different species
Key ideas
Somatic (body) cells are diploid (2n) — two sets of chromosomes; sex cells (gametes) are haploid (n) — one set; polyploidy is having extra full sets.
Crossing over swaps segments between paired chromosomes during meiosis, producing new gene combinations and increasing variation.
Mendel found that traits are controlled by discrete factors (genes): one allele can be dominant over a recessive one; alleles segregate into separate gametes.
Rosalind Franklin's X-ray images revealed DNA was a helix; Watson and Crick used that evidence to build the double-helix model.
Restriction enzymes recognize specific base sequences and cut DNA there, producing fragments (often with "sticky ends").
Watch out for
- Thinking gametes are diploid like body cells — they are haploid.
- Thinking crossing over damages chromosomes — it recombines them, increasing healthy variation.
- Thinking traits BLEND in offspring (tall × short → medium) — Mendel showed traits are discrete units that reappear unchanged.
Every skill’s key ideas, worked examples and checks are in MapleMind.Practise this unit
Unit 4 · 11 skills
Population & Community Dynamics
Gene Pools & Change
The Hardy-Weinberg principle
I can describe the Hardy-Weinberg principle and its significance.
Official code: 30-D1.1k
Factors that change the gene pool
I can describe the factors that cause a gene pool to change.
Official code: 30-D1.2k
Applying Hardy-Weinberg
I can apply the Hardy-Weinberg equations to find allele and genotype frequencies.
Official code: 30-D1.3k
Molecular basis of gene-pool change
I can describe the molecular basis of gene-pool change and its significance over time.
Official code: 30-D1.4k
Species Interactions & Succession
Species interactions and symbiosis
I can describe species interactions and symbiotic relationships and their effect on populations.
Official code: 30-D2.1k
Defence mechanisms
I can explain the role of defence mechanisms in predation and competition.
Official code: 30-D2.2k
Ecological succession
I can explain how communities change over time or remain a climax community.
Official code: 30-D2.3k
Population Growth
Factors in population growth
I can describe and calculate the factors that influence population growth.
Official code: 30-D3.1k
Carrying capacity and growth math
I can describe population growth in terms of carrying capacity, biotic potential and environmental resistance.
Official code: 30-D3.2k
Population growth patterns
I can explain the different population growth patterns.
Official code: 30-D3.3k
r-selected and K-selected organisms
I can describe the characteristics and strategies of r-selected and K-selected organisms.
Official code: 30-D3.4k
The official wording · 11 outcomes
- 30-D1.1k
- describe the Hardy-Weinberg principle and explain its significance in population gene-pool stability and nonequilibrium values
- 30-D1.2k
- describe the factors that cause the diversity in the gene pool to change
- 30-D1.3k
- apply, quantitatively, the Hardy-Weinberg principle to observed and published data to determine allele and genotype frequencies
- 30-D1.4k
- describe the molecular basis of gene-pool change and the significance of these changes over time
- 30-D2.1k
- describe the basis of species interactions and symbiotic relationships and describe the influence of these interactions on population changes
- 30-D2.2k
- explain the role of defence mechanisms in predation and competition
- 30-D2.3k
- explain how mixtures of populations that define communities may change over time or remain as a climax community
- 30-D3.1k
- describe and explain, quantitatively, factors that influence population growth
- 30-D3.2k
- describe the growth of populations in terms of the mathematical relationship among carrying capacity, biotic potential, environmental resistance and the number of individuals in the population
- 30-D3.3k
- explain the different population growth patterns
- 30-D3.4k
- describe the characteristics and reproductive strategies of r -selected and K -selected organisms
Key ideas
The Hardy-Weinberg principle describes a non-evolving population: allele and genotype frequencies stay constant if no evolutionary forces act (no selection, drift, migration, mutation, or nonrandom mating).
Interactions include predator-prey, producer-consumer, and competition (between species and within a species); symbiosis includes mutualism (both benefit), commensalism (one benefits, other unaffected), and parasitism (one benefits, host harmed).
A population changes through four processes: births (natality) and immigration ADD individuals; deaths (mortality) and emigration REMOVE them.
It is a null model — a baseline; when real frequencies DIFFER from Hardy-Weinberg predictions, it signals that evolution is occurring.
These relationships regulate population sizes — e.g. predator and prey numbers rise and fall in linked cycles.
Watch out for
- Thinking Hardy-Weinberg describes how populations usually behave — it describes an idealized, non-evolving baseline that real populations rarely meet.
- Thinking symbiosis always means "helpful to both" — parasitism is symbiosis where one partner is harmed.
- Thinking only births and deaths change a population — immigration and emigration matter too.
Every skill’s key ideas, worked examples and checks are in MapleMind.Practise this unit
Plan the term
Pick your term and the days you study. Each unit gets its share of the weeks and comes back a week later for a review. The last two weeks go over the whole course.
The mark you need
Your class mark counts for 70% of the final mark, the exam for 30%.
You need
59% on the exam
With 75% in class, your final mark lands between 52.5% (0 on the exam) and 82.5% (100% on it).
Which course?
Alberta has 4 science courses for Grade 12. Here they are side by side.
- Biology 30This courseSCN32304 units · 55 skillsBiology 30 Diploma ExamWhat it coversNervous & Endocrine Systems · Reproduction & Development · Cell Division, Genetics & Molecular Biology · Population & Community Dynamics
- Chemistry 30SCN37964 units · 52 skillsChemistry 30 Diploma ExamWhat it coversThermochemical Changes · Electrochemical Changes · Chemical Changes of Organic Compounds · Chemical Equilibrium Focusing on Acid–Base Systems
- Physics 30SCN37974 units · 72 skillsPhysics 30 Diploma ExamWhat it coversMomentum & Impulse · Forces & Fields · Electromagnetic Radiation · Atomic & Nuclear (Modern) Physics
- Science 30SCN32704 units · 79 skillsScience 30 Diploma ExamWhat it coversLiving Systems Respond to Change · Chemistry & the Environment · Electromagnetic Energy · Energy & the Environment
What a university, college or program asks for is theirs to say: check its admission page, and your school’s course guide.
The official curriculum
This page follows Alberta’s own curriculum for Biology 30.
Study it in MapleMind
MapleMind teaches Biology 30 one skill at a time. Each skill gets a short lesson, practice as you go and a check worth up to three stars. It remembers where you stopped.


Course Companion
Your year in one workbook
A fun way to keep Biology 30 organized, get to know your child better and see early when they need a hand. Fill it in on a screen, or print it.
- Pages
- 33
- Fillable fields
- 1,800
- Price
- $4.99
Questions about Biology 30
What is Biology 30?
Alberta’s Grade 12 science course: 4 units and 55 skills, from Nervous & Endocrine Systems to Population & Community Dynamics.
What units are in Biology 30?
1. Nervous & Endocrine Systems, 2. Reproduction & Development, 3. Cell Division, Genetics & Molecular Biology and 4. Population & Community Dynamics.
Is there a provincial exam for Biology 30?
Yes. The Biology 30 Diploma Exam counts for 30% of the final mark. Next sitting: January 25, 2027.
Can MapleMind help with Biology 30?
Yes. MapleMind teaches every skill of Biology 30, step by step, with practice and checks, and its tutor answers questions about any of them. It’s free with daily limits, on iPhone, Android and the web.