Micrographs, drawing and annotation

Cells (Unity and diversity) · Cell structure · note 7 of 7

Micrographs, drawing and annotationSpec A2.2.10, A2.2.11

In short

In light and electron micrographs, cells are identified as prokaryote, plant or animal from features such as the nucleus, cell wall, vacuole and chloroplasts. In electron micrographs you should recognise structures including the mitochondrion, Golgi apparatus and rough and smooth endoplasmic reticulum. Drawings use clear pencil lines and ruled labels, and annotations state each structure's function.

Identifying the cell type

Clues to cell type in micrographs
Cell typeLook for
ProkaryoteSmall (about 0.5–5 µm); nucleoid region with no nuclear membrane; cell wall; no membrane-bound organelles
PlantCell wall; large sap vacuole; chloroplasts in green tissue; often a regular, angular shape
AnimalNo cell wall; no large vacuole; may have microvilli; often an irregular shape

Structures in electron micrographs

Appearance and function of structures in electron micrographs
StructureAppearanceFunction (for annotations)
Nucleoid regionPaler area of fine fibres in a prokaryote, with no membrane around itContains the loop of DNA
Prokaryotic cell wallDense layer just outside the plasma membraneProtects the cell and prevents bursting
NucleusLarge and round; double membrane with pores; dark patches of chromatinContains the chromosomes; controls the cell through gene expression
ChromosomesDark, condensed bodies, visible in dividing cellsCarry the genes; condensed so they can be separated in division
MitochondrionOval; double membrane, with the inner membrane folded into cristaeSite of aerobic respiration, producing ATP
ChloroplastDouble membrane; stacks of thylakoids (grana); may contain starch grainsSite of photosynthesis
Sap vacuoleLarge, pale area bounded by a single membraneStores cell sap; maintains turgor
Golgi apparatusStack of curved, flattened membrane sacs with vesicles at the edgesProcesses proteins and packages them into vesicles
Rough endoplasmic reticulumFlattened membrane sacs studded with ribosomesSynthesises proteins for secretion or for membranes
Smooth endoplasmic reticulumBranching tubular membranes without ribosomesSynthesises lipids, including steroids
RibosomesTiny dark granules, free in the cytoplasm or on rough ERProtein synthesis
Cell wall (plant)Thick layer outside the plasma membraneSupports the cell and resists turgor pressure
Plasma membraneThin dark line at the edge of the cytoplasmControls the entry and exit of substances
Secretory vesiclesSmall membrane-bound spheres near the Golgi apparatus or plasma membraneCarry proteins to the plasma membrane for secretion by exocytosis
MicrovilliFinger-like projections of the plasma membraneIncrease the surface area for absorption

Drawing and annotating from an electron micrograph

  • Use a sharp pencil and clear, continuous lines, with no shading or colouring.
  • Draw only what is visible, with structures in the correct proportions and positions.
  • Label with straight, ruled lines that do not cross and that end exactly on the structure.
  • Annotate each labelled structure with its function; this is required, not optional.
  • Add a title and a scale bar or magnification.
Exam tip:

An annotation is more than a label. 'Mitochondrion: site of aerobic respiration, producing ATP' is an annotation; 'mitochondrion' alone is only a label.

Annotated drawing of a secretory animal cell from an electron micrograph: microvilli, secretory vesicles, Golgi apparatus, smooth ER, nuclear pore, chromatin, plasma membrane, mitochondrion, free 80S ribosomes, rough ER and nucleus, each with its function, and a 5 µm scale bar. (opens full size in a new tab)
A secretory cell: proteins are made on rough ER, processed in the Golgi apparatus and secreted by exocytosis.

Quick check

  1. State the three parts of cell theory.

    Show answer

    All organisms consist of one or more cells; cells are the basic structural unit of life; cells only arise from pre-existing cells.

  2. Why must an eyepiece graticule be calibrated for each objective lens?

    Show answer

    The length of specimen covered by one eyepiece unit changes with magnification.

  3. What size of ribosome do prokaryotes have?

    Show answer

    70S.

  4. Which substance makes up fungal cell walls?

    Show answer

    Chitin.

Written and checked against the IB Biology SL specification · Updated October 2026

Frequently asked questions

What is the difference between prokaryotic and eukaryotic cells?

Prokaryotic cells have no nucleus: their DNA is a naked loop in the cytoplasm, and they have 70S ribosomes and no membrane-bound organelles. Eukaryotic cells have a nucleus with a double membrane and pores, chromosomes of DNA bound to histones, 80S ribosomes, membrane-bound organelles and a cytoskeleton.

How do you calculate magnification in biology?

Magnification equals the size of the image divided by the actual size of the specimen. Measure the image with a ruler, convert both values to the same unit, usually micrometres (1 mm = 1000 µm), then divide. Rearranged, actual size equals image size divided by magnification, which is how cell sizes are found from micrographs.

How do you calculate magnification using a scale bar?

Measure the length of the scale bar on the image with a ruler, convert it to the same unit as the value written on the bar, then divide the measured length by that value. For example, a 20 mm bar labelled 0.5 µm gives 20 000 µm divided by 0.5 µm, a magnification of ×40 000.

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