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Transpiration & Potometer

IB DP Biology ยท B3.2 Plant Transport

SL + HL
IBDP Mode
Plant Type
Conditions
Light intensity10000 lux
Temperature22ยฐC
Humidity50%
Wind speed0 m/s
Leaf area20 cmยฒ
IBDP investigation design
This is now a DP-style investigation. You must plan controls, justify the mechanism, run repeats, calculate rate, then build a claim from evidence.
Keep temperature, humidity, wind, leaf area and plant type the same while you test light intensity.
Hydrophyte is included as a simplified comparison model. A standard potometer is usually used with a cut shoot in air, so floating or submerged aquatic plants need careful interpretation.
Setup check before the apparatus runs
Select at least two control variables for this investigation.
Choose the biological mechanism that explains your prediction.
Reliability and validity checks
Make a prediction and pass the setup check before starting the timed trial.
Run the Experiment
Simulation Speed
Elapsed
0:00
Ready
rubber bung water reservoir capillary tube (scale in mm) air bubble 22ยฐ 50%
Leaf surface (ร—400)
Current rate
0.0 mm/min
Bubble position
0 mm
Volume of water uptake
0.000 cmยณ
What is happening
Choose an investigation variable, set an IV value, make a prediction, pass the setup check, then run a timed trial. The bubble movement gives water uptake data that students must calculate and interpret.
Practical accuracy A potometer measures water uptake. It is used as an estimate of transpiration rate, but it does not measure water loss from the leaf directly.
Trial status: Choose one variable, make a prediction, then run a fixed-time trial.
DP evidence progress: No trials recorded yet. Aim for 3 repeats at each of at least 3 values of the independent variable.
Trial Data
TrialRateConditions
No trials yet
Results graph

After-trial calculation

Run a trial, then calculate the rate from the start and end bubble position before the result is revealed in the table.

Claim, evidence, reasoning

Collect enough calculated trials to build a DP-quality conclusion.

Transverse section of a dicotyledonous leaf

Click any labelled tissue in the transverse section of a dicotyledonous leaf. The diagram shows the distribution of tissues involved in gas exchange and transpiration, including the vein / vascular bundle, xylem, phloem, mesophyll, epidermis and stomata.

Upper cuticle (waxy, waterproof) Upper epidermis Palisade mesophyll (tightly packed, lots of chloroplasts) Vein / vascular bundle Xylem Phloem air spaces Spongy mesophyll (gas exchange) Lower epidermis Hโ‚‚O Hโ‚‚O Hโ‚‚O Hโ‚‚O Click any part to learn its role

The transpiration stream

Water enters root hair cells by osmosis, travels through the root cortex, enters the xylem, and is pulled upwards by transpiration. In the leaf, water evaporates from the wet surfaces of spongy mesophyll cells into the air spaces, then diffuses out through the open stomata. Click a part of the diagram to see what it does.

Cohesion-tension theory Water molecules cling to each other (cohesion) and to the xylem walls (adhesion). As water evaporates from leaves, it pulls the whole column upwards, like pulling a thread of wool. No energy from the plant is needed.

Plan diagram: transverse section of a dicotyledonous leaf

IB expects students to draw and label a plan diagram of a transverse section of a dicotyledonous leaf. A plan diagram is low power and simplified. It should show tissue regions, not individual cells, chloroplasts, shading or tiny details.

Click a label, then click the numbered tissue on the plan diagram 1 2 3 4 5 6 7 8 9 10

Label bank

Select a label, then click the matching number on the diagram. You need all ten labels correct.

IB drawing reminder
In a plan diagram, use clear single lines and labels. Do not draw individual palisade cells, chloroplasts or shading. Show where the tissues are distributed across the leaf.

Stomata: how guard cells open and close

Stomata are pores in the lower epidermis, each flanked by two kidney-shaped guard cells. When guard cells take up water and become turgid, they bow outwards and open the pore. When they lose water, they go limp and close it. Move the sliders below to see this happen.

Lower epidermis (top-down view) Kโบ Kโบ Kโบ Kโบ Kโบ Kโบ ๐Ÿ’ง ๐Ÿ’ง ๐Ÿ’ง ๐Ÿ’ง ๐Ÿ’ง ๐Ÿ’ง OPEN - guard cells turgid
Stomatal aperture 100%

Controls

Light intensityHigh
Water availabilityPlenty
COโ‚‚ inside leafLow

Low internal COโ‚‚ signals "photosynthesis is happening - keep stomata open."

The mechanism 1. Light + low COโ‚‚ trigger Kโบ pumps in guard cell membranes. 2. Kโบ ions move into guard cells. 3. Water follows by osmosis. Cells become turgid. 4. Guard cells bow outwards (their inner walls are thicker, so they can't expand inwards). 5. Pore opens. Gas exchange can happen.

In drought: ABA (abscisic acid) signal from roots reverses this. Kโบ leaves, water leaves, guard cells go limp, pore closes.

Adaptations of leaves to water availability

Plants in different habitats have evolved very different leaf structures. Compare three plant types below, then try the stomatal density practical to measure these differences quantitatively.

epidermis (thin cuticle) palisade spongy mesophyll

Mesophyte

Sunflower, oak, lettuce
  • Thin waxy cuticle
  • Stomata mostly on lower epidermis
  • ~150 stomata per mmยฒ
  • Broad flat leaves for photosynthesis
  • Lives where water is moderately available
thick waxy cuticle epidermis palisade sunken stomata in pits

Xerophyte

Marram grass, cacti
  • Thick waxy cuticle
  • Stomata sunken in pits (trap humid air)
  • ~60 stomata per mmยฒ (fewer)
  • Hairs reduce air movement at surface
  • Often rolled or needle-shaped
stomata on UPPER surface palisade (thin) large air spaces (aerenchyma) water beneath

Hydrophyte

Floating hydrophyte: water lily
  • Floating leaves have stomata on the upper epidermis
  • Very thin or no cuticle because water is abundant
  • ~300 stomata per mmยฒ on exposed upper surface
  • Large air spaces (aerenchyma) for buoyancy
  • Submerged plants such as Elodea are different and may have no functional stomata

Practical: stomatal density measurement

Complete the leaf cast protocol before the microscope unlocks. Students have to choose the correct epidermis, make the clear nail varnish cast, lift the imprint with tape, mount it on a slide, focus the microscope, then count repeated fields of view.

Leaf cast practical bench

Cast not ready
Leaf cast workflow Prepare an epidermal imprint before counting stomata in repeated fields of view. 1. Select epidermis glass tile choose surface 2. Make varnish cast thin clear layer, then dry 3. Lift the imprint press tape flat epidermal cell pattern on tape 4. Mount and focus slide and coverslip then then then

Select the leaf surface you would sample, then complete each preparation step in order.

1. Choose surface to sample
2. Prepare the leaf cast
Start by choosing the epidermis that should contain visible stomata for this plant.
Complete the leaf cast practical first:
nail varnish, dry, tape, peel, slide, focus.
sample grid: 0.25 mmยฒ include top and left border exclude bottom and right border 0.25 mm
-
selected stomata in sample grid
-
calculated density per mmยฒ
Counting rule: count stomata fully inside the red square. Also count stomata touching the top or left border. Do not count stomata touching the bottom or right border. Click again to untick.
Prepare the leaf cast, then click the stomata inside the red sample grid.
NOS: reliability from repeats
Click the countable stomata in five different fields of view from the same leaf surface. The same border rule must be used every time so the sampling is consistent and reliable.
FieldCount in 0.25 mmยฒDensity per mmยฒ
No repeats recorded yet
Complete the leaf cast, then record five sample fields to calculate mean, range and standard deviation.

Active Questions

Apply what you have learned. Work through the cards below, predict before revealing, and use the potometer data you collected to do the calculations.

Investigation workflow

Core: predict whether the rate increases or decreases, then explain using one keyword: light, temperature, humidity, wind or leaf area.

Standard: keep control variables constant, run three repeats, calculate a mean rate, and describe the pattern using data.

Challenge: evaluate limitations, identify anomalies, compare stomatal density with water uptake rate, and explain the trade-off between gas exchange and water loss.

Worked calculation

Bubble distance = 24 mm. Time = 6 min. Capillary radius = 0.5 mm.

Distance per hour = 24 รท 6 ร— 60 = 240 mm/hour.

Cross-sectional area = ฯ€rยฒ = ฯ€ ร— 0.5ยฒ = 0.785 mmยฒ.

Volume per hour = 240 ร— 0.785 = 188.4 mmยณ/hour.

Convert to cmยณ: 188.4 รท 1000 = 0.188 cmยณ/hour.

Method limitations

  • Water uptake is only an estimate of transpiration.
  • Leaks in the apparatus change bubble movement.
  • Cut shoots may not behave exactly like intact plants.
  • Leaf area must be controlled or used to standardise rate.

Practical technique

  • Cut the shoot underwater to prevent air entering xylem.
  • Seal joints with petroleum jelly to prevent air leaks.
  • Allow the shoot to acclimatise before recording.
  • Repeat trials and calculate a mean.

Challenge thinking

  • Why might high temperature eventually close stomata?
  • How does stomatal density affect gas exchange and water loss?
  • Why should one variable be changed at a time?
  • Which variable is hardest to control in a classroom?

Guide & reference

Vocabulary and quick reference for the B3.2 plant transport content covered in this simulation.

Key processes

Transpiration is the loss of water vapour from a plant, mainly from the leaves through the stomata. It is a consequence of having stomata open for gas exchange.

The transpiration stream is the continuous flow of water from roots โ†’ xylem โ†’ leaves โ†’ atmosphere. It also delivers mineral ions to the leaves.

Cohesion-tension theory explains how water moves up the xylem against gravity. Water molecules cohere through hydrogen bonding. As water evaporates from leaves, tension is created that pulls the entire water column upwards.

Factors affecting transpiration rate

Light opens stomata for gas exchange; transpiration rises in light. Temperature increases evaporation from leaf surfaces and increases the kinetic energy of water molecules. Wind removes the layer of humid air around the leaf, maintaining a steep concentration gradient for diffusion. Humidity reduces the concentration gradient between the leaf and air - high humidity slows transpiration. Leaf surface area directly scales the rate.

Adaptations summary

Mesophytes live where water is moderately available. Standard leaf structure.

Xerophytes live in dry conditions. Thick waxy cuticle, sunken stomata, reduced surface area, leaf hairs, fewer stomata per mmยฒ - all reduce water loss.

Hydrophytes live in or on water. Floating hydrophytes such as water lilies often have stomata on the upper surface because that side is exposed to air. Submerged hydrophytes such as Elodea are different and may have no functional stomata.

Stomatal density values to know

Typical values per mmยฒ: Mesophyte lower epidermis about 150, xerophyte lower epidermis about 60, and floating hydrophyte upper epidermis about 300. These are averages. There is wide variation by species and even between leaves on the same plant.

IB syllabus checklist

B3.1.7: Leaf adaptations for gas exchange include waxy cuticle, epidermis, air spaces, spongy mesophyll, stomatal guard cells and veins.

B3.1.8: Students should draw and label a plan diagram showing the distribution of tissues in a transverse section of a dicotyledonous leaf.

B3.1.9: Transpiration is a consequence of gas exchange through open stomata, and the rate is affected by light, temperature, humidity, wind and leaf area.

B3.1.10: Stomatal density is determined from micrographs or leaf casts. Repeated counts improve reliability and show natural variation in biological material. A consistent border rule prevents double counting or biased sampling.

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