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Biology · Plant Reproduction, Signals & Responses

Tropisms, biological clocks and seasonal responses

A shoot bends while its base remains in place. Another plant changes its flowering behaviour as days lengthen. Both respond to light, but direction and duration ask different biological questions.

Plant Structure, Transport & Nutrition supplies meristems, tissue boundaries, water movement and source–sink transport. Development & Differentiation introduces changing cell identities; Meiosis & Patterns of Inheritance supplies haploid and diploid chromosome sets. The first lesson explains the plant life-cycle transition again before using n. Cell Regulation & Signalling is a useful return path for receptors and feedback, and Evolutionary Processes for the final lesson’s selection argument.

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By the end, you can

Distinguish directional growth, rhythmic timing and seasonal cue interpretation, and read a bounded coincidence model without treating it as a universal flowering rule.

01

Tropisms depend on the direction of a cue

A tropism is a directional growth response to a stimulus. Positive phototropism of a shoot directs growth toward light. Growth can reorient an organ without locomotion of the whole plant. Photoreceptors, signalling and differences in growth across the organ contribute to the response.

In a selected shoot example, the initially equal sides are each 10 mm long. Over the assigned interval the lit side becomes 16 mm and the shaded side 18 mm. Their extensions are 6 and 8 mm, respectively. The longer shaded side belongs on the outside of the bending shoot; the selected shoot bends toward the light.

The straight side-length bars display the measured extensions, while a separate curved outline shows the qualitative orientation. The 2 mm extension difference does not determine a bending angle: width, the distribution of growth and geometry are not measured here. Root responses and other contexts should not be inferred from this one selected shoot case.

Unequal extension reorients a shoot

Unequal extension reorients a shootThe shaded side extends farther than the lit side in this selected positive-phototropism example.Extension during the assigned intervalLit side extension6Shaded side extension80246810Extension during the assigned interval (mm)Light arrives from the rightShaded sideLit sideLight arrives from the rightShaded side is the longer outer sideSelected shoot bends toward lightNo angle inferred from the length differenceConstructed two side-length measurements; curved outline is qualitativeand has no angle scale.
The bar axis measures extension; the curved outline is not a reconstruction from measured geometry.
Read the diagram in words

Both sides begin at 10 mm. The lit side ends at 16 mm, extension 6 mm; the shaded side at 18 mm, extension 8 mm. The difference is 2 mm. The qualitative outline bends toward light on the right with the longer shaded side on the outside.

Unequal extension reorients a shoot
Shoot sideInitial length (mm)Ending length (mm)Extension (mm)
Lit side10166
Shaded side10188
Unequal extension reorients a shoot
Displayed axisAxis minimumAxis maximumDisplayed ticksUnit
Extension during the assigned interval0100, 2, 4, 6, 8, 10mm
Selected shoot bends toward light
Qualitative curve pointSchematic x coordinateSchematic y coordinate
Base00
First control point02
Second control point0.53
Tip24
Schematic width
0.6
Light arrives from the right
Right
Unequal extension reorients a shoot
SeriesDisplayed marker
Lit side extensionCircle
Shaded side extensionDiamond
  • Light arrives from the right
  • Shaded side is the longer outer side
  • Selected shoot bends toward light
  • No angle inferred from the length difference

Constructed two side-length measurements; curved outline is qualitative and has no angle scale.

02

A daily cue can synchronise an internal rhythm

A circadian rhythm is an internally generated roughly daily pattern. Environmental cycles can entrain it: align its timing with outside conditions. A pattern that continues under a constant condition can support an internal timing interpretation; a daily response observed only during a daily light cycle cannot establish that by itself.

The schematic clock trace repeats every 24 assigned hours after an earlier light–dark cycle. Its phase markers recur at 0, 24 and 48 hours during the depicted constant-light interval. This constructed trace represents a persisting internal pattern; it is not an experimental measurement of an oscillator or evidence that all plants have exactly the same free-running period.

Photoperiod is the duration of daylight within a cycle. Clock-regulated components can interact with light-dependent processes, making a cue’s timing matter as well as its duration. Different plants interpret seasonal cues differently. Temperature, developmental stage and other conditions can also affect flowering.

A rhythm and a separate coincidence rule

A rhythm and a separate coincidence ruleA constructed rhythm persists under constant light; a separate timing panel compares light intervals with an assigned active window.Constructed internal pattern (Relative readout)00.510612182430364248Time under constant light (h)10.500.510.500.51Schematic persisting rhythm12-hour light interval0121418Shared interval: 0 hOutput absent under the teaching rule16-hour light interval0161418Shared interval: 14–16; 2 hOutput present under the teaching ruleAssigned clock-associated active window0161822Shared interval: 0 hOutput absent under the teaching rule04812162024Hours after dawn (h)Schematic persisting rhythmLightAssigned clock-associated active windowShared intervalOutput present under the teaching ruleOutput absent under the teaching ruleTwo distinct constructed panels; the 24-hour period, window and 1-houroutput threshold are invented teaching inputs.
Persistence, phase and coincidence are distinct ideas. The assigned timing rule is not a species flowering schedule.
Read the diagram in words

The constructed constant-light trace repeats peaks at 0, 24 and 48 hours. In the separate 0–24 hour panel, the active window is 14–18. Light from 0–12 overlaps it for zero hours; light from 0–16 overlaps it for 2 hours, from 14–16. The assigned output threshold is at least 1 hour. Shifting the window to 18–22 removes overlap with the same 0–16 light interval.

Schematic persisting rhythm
Displayed axisAxis minimumAxis maximumDisplayed ticksUnit
Time under constant light0480, 6, 12, 18, 24, 30, 36, 42, 48h
Constructed internal pattern010, 0.5, 1Relative readout
Schematic persisting rhythm
Time (h)Relative readout
01
60.5
120
180.5
241
300.5
360
420.5
481
Assigned period (h)
24
Constant light in this panel
Yes
Schematic persisting rhythm
Phase marker time (h)
0
24
48
A rhythm and a separate coincidence rule
Displayed axisAxis minimumAxis maximumDisplayed ticksUnit
Hours after dawn0240, 4, 8, 12, 16, 20, 24h
Assigned overlap threshold (h)
1
Assigned clock-associated active window
Assigned timing caseLight starts (h)Light ends (h)Active window starts (h)Active window ends (h)Overlap starts (h)Overlap ends (h)Overlap duration (h)Output under the teaching rule
12-hour light interval0121418No shared intervalNo shared interval0Output absent under the teaching rule
16-hour light interval016141814162Output present under the teaching rule
Alternative window with the same light interval
Assigned timing caseLight starts (h)Light ends (h)Active window starts (h)Active window ends (h)Overlap starts (h)Overlap ends (h)Overlap duration (h)Output under the teaching rule
Alternative window with the same light interval0161822No shared intervalNo shared interval0Output absent under the teaching rule
  • Schematic persisting rhythm
  • Light
  • Assigned clock-associated active window
  • Shared interval
  • Output present under the teaching rule
  • Output absent under the teaching rule

Two distinct constructed panels; the 24-hour period, window and 1-hour output threshold are invented teaching inputs.

03

Read one selected timing rule

The second panel is a separate constructed coincidence model. A clock-associated active window is assigned to hours 14 through 18 after the cycle’s dawn at hour 0. One light interval runs from 0 to 12; another from 0 to 16. Both panels use the same 0–24 hour axis.

The 12-hour light interval has no overlap with the active window. The 16-hour interval overlaps it from hour 14 to hour 16, for 2 hours. The teaching rule labels an output present when the overlap is at least 1 hour. Under this assigned rule, the first case has no output and the second has output. These particular hours and threshold are invented, not a flowering schedule for a named species.

The model isolates temporal coincidence, a useful idea for photoperiodic pathways. In Arabidopsis, FT protein provides a well-supported example of a signal associated with communication from leaves to the shoot apex during floral induction. That evidence does not imply that every plant uses the simplified threshold or that FT is a sugar reserve flowing to a sink.

A rhythm and a separate coincidence rule

A rhythm and a separate coincidence ruleA constructed rhythm persists under constant light; a separate timing panel compares light intervals with an assigned active window.Constructed internal pattern (Relative readout)00.510612182430364248Time under constant light (h)10.500.510.500.51Schematic persisting rhythm12-hour light interval0121418Shared interval: 0 hOutput absent under the teaching rule16-hour light interval0161418Shared interval: 14–16; 2 hOutput present under the teaching ruleAssigned clock-associated active window0161822Shared interval: 0 hOutput absent under the teaching rule04812162024Hours after dawn (h)Schematic persisting rhythmLightAssigned clock-associated active windowShared intervalOutput present under the teaching ruleOutput absent under the teaching ruleTwo distinct constructed panels; the 24-hour period, window and 1-houroutput threshold are invented teaching inputs.
Persistence, phase and coincidence are distinct ideas. The assigned timing rule is not a species flowering schedule.
Read the diagram in words

The constructed constant-light trace repeats peaks at 0, 24 and 48 hours. In the separate 0–24 hour panel, the active window is 14–18. Light from 0–12 overlaps it for zero hours; light from 0–16 overlaps it for 2 hours, from 14–16. The assigned output threshold is at least 1 hour. Shifting the window to 18–22 removes overlap with the same 0–16 light interval.

Schematic persisting rhythm
Displayed axisAxis minimumAxis maximumDisplayed ticksUnit
Time under constant light0480, 6, 12, 18, 24, 30, 36, 42, 48h
Constructed internal pattern010, 0.5, 1Relative readout
Schematic persisting rhythm
Time (h)Relative readout
01
60.5
120
180.5
241
300.5
360
420.5
481
Assigned period (h)
24
Constant light in this panel
Yes
Schematic persisting rhythm
Phase marker time (h)
0
24
48
A rhythm and a separate coincidence rule
Displayed axisAxis minimumAxis maximumDisplayed ticksUnit
Hours after dawn0240, 4, 8, 12, 16, 20, 24h
Assigned overlap threshold (h)
1
Assigned clock-associated active window
Assigned timing caseLight starts (h)Light ends (h)Active window starts (h)Active window ends (h)Overlap starts (h)Overlap ends (h)Overlap duration (h)Output under the teaching rule
12-hour light interval0121418No shared intervalNo shared interval0Output absent under the teaching rule
16-hour light interval016141814162Output present under the teaching rule
Alternative window with the same light interval
Assigned timing caseLight starts (h)Light ends (h)Active window starts (h)Active window ends (h)Overlap starts (h)Overlap ends (h)Overlap duration (h)Output under the teaching rule
Alternative window with the same light interval0161822No shared intervalNo shared interval0Output absent under the teaching rule
  • Schematic persisting rhythm
  • Light
  • Assigned clock-associated active window
  • Shared interval
  • Output present under the teaching rule
  • Output absent under the teaching rule

Two distinct constructed panels; the 24-hour period, window and 1-hour output threshold are invented teaching inputs.

Worked example

Find the actual shared interval

To calculate overlap, choose the later start and the earlier end. With 16 hours of light the later start is 14, and the earlier end is 16; overlap = 16 − 14 = 2 hours. With 12 hours of light the earlier end, 12, comes before the active window begins; overlap is zero, rather than a negative duration.

The result depends on timing, not just total light. A separate hypothetical light interval from 0 to 16 with a clock window from 18 to 22 would have no overlap. It has the same 16-hour duration but a different relation to the assigned window. The example describes the constructed logic and supplies no cultivation advice.

Check your understanding

  1. The shaded side extends by 8 mm and the lit side by 6 mm. Which side is longer, and can an angle be calculated?

    Show reasoning

    The shaded side is longer by 2 mm and lies on the outer side of the selected bend toward light. No exact angle follows because width and the distribution and geometry of growth are unassigned.

  2. Why does a 24-hour pattern seen only during alternating daily light and darkness fail to prove an internal clock?

    Show reasoning

    The outside cycle could directly drive the pattern. Persistence under appropriate constant conditions supplies different evidence for internal timing; entrainment concerns alignment with external cues.

  3. Under the assigned window 14–18 and light interval 0–16, how many hours coincide?

    Show reasoning

    Hours 14–16 coincide, a duration of 2 hours. This passes the model’s invented 1-hour threshold; it is not a universal flowering condition.

What to carry forward

Direction, phase and duration carry different information; keep the response and timing rule specific to the case.

References

Resources supporting this lesson’s explanations and examples.

  1. Plant phototropic growth (2015)Christian Fankhauser and John M. ChristieResearch abstractpubmed.ncbi.nlm.nih.govRead source
  2. Biology 2e — Plant Sensory Systems and Responses (Biology 2e)OpenStaxOpen textbookopenstax.orgRead source
  3. Photoperiodic Flowering: Time Measurement Mechanisms in Leaves (2015)Young Hun Song and colleaguesResearch abstractannualreviews.orgRead source
  4. FT protein movement contributes to long-distance signaling in floral induction of Arabidopsis (2007)Laurent Corbesier and colleaguesResearch abstractpubmed.ncbi.nlm.nih.govRead source