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

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

  1. A neuron has dendrites, a cell body and an axon; the myelin sheath speeds transmission by letting the impulse jump between gaps.

  2. Light passes through the cornea and lens, which focus it onto the retina; the iris adjusts the pupil to control how much light enters.

  3. The principal endocrine glands are the hypothalamus/pituitary complex, thyroid, parathyroid, adrenal glands, and the islet cells of the pancreas.

  4. Endocrine glands detect internal conditions (blood calcium, osmotic pressure, blood sugar) and release hormones to correct them.

  5. An action potential is an all-or-none wave of ion movement (Na+\text{Na}^+ in, then K+\text{K}^+ 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

  1. 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.

  2. The Y chromosome carries a gene that triggers testis development; without it, the embryo develops ovaries — the default pathway is female.

  3. GnRH from the hypothalamus triggers FSH and LH from the pituitary, which drive the gonads to release estrogen, progesterone (female) or testosterone (male).

  4. Fertilization forms a zygote that implants in the endometrium; extra-embryonic membranes (placenta, amnion, chorion, allantois) support the embryo, exchanging materials with the mother.

  5. 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

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

  1. Somatic (body) cells are diploid (2n) — two sets of chromosomes; sex cells (gametes) are haploid (n) — one set; polyploidy is having extra full sets.

  2. Crossing over swaps segments between paired chromosomes during meiosis, producing new gene combinations and increasing variation.

  3. Mendel found that traits are controlled by discrete factors (genes): one allele can be dominant over a recessive one; alleles segregate into separate gametes.

  4. Rosalind Franklin's X-ray images revealed DNA was a helix; Watson and Crick used that evidence to build the double-helix model.

  5. 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

  1. 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).

  2. 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).

  3. A population changes through four processes: births (natality) and immigration ADD individuals; deaths (mortality) and emigration REMOVE them.

  4. It is a null model — a baseline; when real frequencies DIFFER from Hardy-Weinberg predictions, it signals that evolution is occurring.

  5. 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

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).

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.

Mathematics 31 in the MapleMind app on a tablet: its units, Unit 1 open, and the skills done so far with their starsMathematics 31 in the MapleMind app on a phone: its units, Unit 1 open, and the skills done so far with their stars
Pictured: Mathematics 31, another Alberta course, partway through Unit 1.

Practise it

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
See the Course Companion

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.

Get ready for Biology 30

Practise every skill of Biology 30 in MapleMind, free with daily limits.