A cell is the smallest membrane-bounded unit that can carry out the processes of life. A tissue is different: it is a group of cells cooperating in a shared function.
Cell theory states that:
living organisms consist of one or more cells
cells are the basic units of structure and function
new cells arise from pre-existing cells
The theory is a powerful biological model, not a claim that every cell has the same appearance. Later examples such as multinucleate fibres and mature cells without nuclei test its boundaries without removing the central idea that living organization is cellular.
Prepare and focus a specimen without losing it
1
Make a thin temporary mount, add a coverslip, and use an appropriate stain when transparent structures need contrast.
2
Start with the low-power objective. Centre the specimen while the field of view is wide.
3
Bring the image into focus with coarse adjustment, then sharpen it with fine adjustment while moving the stage away from the objective.
4
Rotate to a higher-power objective only after centring. Use fine focus only because the working distance is now small.
5
Record the specimen, stain, objective and any measurement. Preparation and staining may alter appearance, so observed features must be interpreted as evidence rather than treated as untouched reality.
Calibrate before converting divisions into micrometres
M=AIA=MII=A×M
At one objective, 10 graticule divisions correspond to 20 µm, so each division represents 2 µm. A cell spanning 18 divisions is therefore 36 µm long. If its printed image is 54 mm long, convert 54 mm to 54,000 µm before calculating: M=54,000/36=1,500×.
Calibration belongs to a particular objective lens. Changing the objective changes the real distance represented by one graticule division, so the calibration must be repeated.
Choose the microscope for the evidence you need
Magnification makes an image larger; resolution allows two close points to be seen as separate. Enlarging beyond the resolution limit only produces a larger blur.
Evidence needed
Useful method
Important limit
living cells and larger structures
compound light microscopy
about 0.2 µm resolution
location of a named molecule
fluorescence or immunofluorescence
the dye or antibody identifies only its target
internal ultrastructure in a thin section
TEM
specimen is fixed, stained and viewed in vacuum
surface form
SEM
shows surface, not a thin internal section
near-native molecular structure
cryo-EM
frozen samples and computational reconstruction are required
Preparation can introduce artefacts. Confidence increases when different preparation methods reveal a consistent structure, rather than when one impressive image is accepted alone.
Four components make every cell a workable system
All cells contain:
a plasma membrane that controls exchange with the surroundings
cytoplasm in which metabolic reactions occur
DNA that stores inherited information
ribosomes that translate information into polypeptides
None of these components alone is a cell. Together they create a bounded chemical system that can maintain itself, use information and make the proteins needed for its activities.
A prokaryote concentrates life in one small compartment
A prokaryotic cell has no nucleus and no membrane-bound organelles. Its single circular, naked chromosome occupies a nucleoid region in the cytoplasm, where 70S ribosomes make proteins. In eubacteria, a peptidoglycan wall lies outside the plasma membrane.
Plasmids, capsules, pili, flagella and specialized membrane regions occur in some bacteria, not all. E. coli, Bacillus and Staphylococcus also differ in shape and wall organization, so no optional feature should be treated as the definition of a prokaryote.
Eukaryotic compartments divide and connect cellular work
A eukaryotic cell encloses linear chromosomes in a nucleus and uses membrane-bound organelles to maintain different reaction conditions. Mitochondria transfer energy to ATP; the ER, Golgi apparatus, vesicles and lysosomes form a connected system for synthesis, transport, modification and digestion.
For a secreted protein, information and material move through a coordinated route: nuclear gene → transcription → rough-ER ribosome → ER lumen → transport vesicle → Golgi modification and sorting → secretory vesicle → plasma membrane.
The cytoskeleton gives internal organization and shape. Microtubules guide vesicles and move chromosomes; actin microfilaments resist tension and contribute to cell movement and shape change.
One cell must complete every life process
A unicellular organism cannot delegate essential work to tissues. Nutrition, metabolism, homeostasis, excretion, response, movement, growth and reproduction must all be achieved within one cell.
Life process
Amoeba or Paramecium
Chlamydomonas
E. coli
nutrition
engulfs particles into food vacuoles
photosynthesizes and absorbs ions
absorbs small molecules
water balance
contractile vacuoles expel excess water
membrane transport and vacuoles regulate contents
membrane transport maintains cytoplasm
movement or response
pseudopodia or cilia respond to local conditions
flagella and light-sensitive responses
receptors and flagella in motile strains
reproduction
cell division
cell division
binary fission
The structures differ, but the same functional problem remains: matter, information and energy must be coordinated inside one bounded cell.
Plant, fungal and animal cells modify a shared eukaryotic plan
Feature
Plant cell
Fungal cell
Animal cell
wall
cellulose
chitin
absent
plastids
chloroplasts in photosynthetic cells
absent
absent
vacuoles
often one large permanent vacuole
vacuoles present
usually small and temporary
carbohydrate store
starch
glycogen
glycogen
frequent additional structures
plasmodesmata
branching hyphae in many species
centrioles; cilia or flagella in some cells
Classification should use a combination of structures. A wall alone does not prove that a cell is plant, and the absence of a chloroplast does not exclude plant tissue because many plant cells are non-photosynthetic.
Atypical cells expose where the simple model breaks
Aseptate fungal hyphae have many nuclei in continuous cytoplasm without complete cross-walls.
Striated muscle fibres form by cell fusion and remain long and multinucleate.
Mature red blood cells lose the nucleus and most organelles, gaining space and flexibility for oxygen transport but losing the ability to divide.
Sieve-tube elements lose the nucleus and depend metabolically on adjacent companion cells.
These cases do not show that cell theory is useless. They show that specialization can redistribute cellular functions across shared cytoplasm or cooperating cells, so “one small compartment with one nucleus” is not the theory itself.
Identify a micrograph by converging clues
Build an identification from several clues:
establish the imaging method and scale
locate boundaries and decide whether they are walls or membranes
look for an internal pattern, not just a familiar outline
use tissue context and neighbouring structures
state the observation before naming the structure
Here, several parallel flattened sacs plus small vesicles at their margins support Golgi apparatus. One circular membrane profile would be weak evidence because a section can cut many organelles into circles.
Absence is weaker than presence: a thin section may miss an organelle that exists elsewhere in the cell. Identification should therefore rest on visible positive evidence whenever possible.
Translate a micrograph into an evidence-based drawing
1
Trace the main boundaries and proportions from the micrograph before naming anything.
2
Use a large drawing with single clear continuous lines. Do not shade, colour or invent structures that are not visible.
3
Add ruled, non-crossing label lines that touch the named feature. A label identifies; an annotation adds a justified structure–function statement.
4
Include magnification or a calculated scale bar, with image and actual lengths converted to the same units.
Before adding an annotation, ask whether the feature can be pointed to in the drawing and whether the claimed function follows from that observed structure. Biological knowledge may guide interpretation, but it must not fabricate visual evidence.
SL synthesis: build a cell claim from evidence
Question
Evidence to use
Claim it can support
Is this a cell?
membrane-bounded cytoplasm with genetic material and ribosomes
an integrated cellular unit
How large is it?
calibrated graticule, scale bar or magnification with consistent units
an actual dimension
What kind of cell is it?
scale, nucleus or nucleoid, organelles, wall material and context
prokaryotic or a eukaryotic lineage
What does a structure do?
visible geometry connected to a known mechanism
a defensible structure–function inference
A strong conclusion keeps observation → interpretation → limitation in that order. One clue may suggest an identity; several independent clues make it defensible.
Cells as basic structural unit
2 marks
Outline the cell theory.
Microscopy skills
3 marks
Outline the procedure for focusing a light microscope.
Developments in microscopy
1 mark
What is a feature of immunofluorescence in light microscopy?
Structures common to all cells
2 marks
List two structures that neurons have in common with prokaryotic cells.
Prokaryote cell structure
9 marks
Escherichia coli is a unicellular organism, so each cell must carry out all of the processes required for life. Outline the functions of each of the structures in the cells of Escherichia coli.
Eukaryote cell structure
2 marks
Label structures I, II, III and IV. I. II. III. IV.
Processes of life in unicellular organisms
4 marks
Unicellular and multicellular organisms share the same functions of life. Outline four functions of life.
Differences in eukaryotic cells
3 marks
Distinguish between structures in animal and plant cells.
Atypical cell structure
7 marks
Discuss the cell theory and its limitations.
Cell identification in micrographs
3 marks
Identify organelles I to III.
I: II: III:
Drawing and annotation
3 marks
Draw a labelled diagram of a nucleus from a eukaryotic cell, such as an onion epidermis cell, as seen using an electron microscope.