Level 5 — MasteryPlant Biology

Plant Biology

75 minutes60 marksprintable — key stays hidden on paper

Chapter: 4.9 Plant Biology Level: 5 — Mastery (cross-domain: biology + physics + mathematics + coding) Time limit: 75 minutes Total marks: 60

Instructions: Answer all three questions. Show full reasoning. Where a physical model is invoked, state assumptions. Calculators and pen-and-paper coding (pseudocode/Python) are permitted. Take g=9.81 m s2g = 9.81\ \text{m s}^{-2}, water density ρ=1000 kg m3\rho = 1000\ \text{kg m}^{-3}, atmospheric pressure Patm=101.3 kPaP_{atm}=101.3\ \text{kPa}.


Question 1 — Cohesion–Tension & the Physics of Ascent (22 marks)

A tall tree draws water from roots to the topmost leaves purely by transpirational pull (cohesion–tension theory).

(a) Describe, with reference to xylem structure, why xylem (not phloem) is the conduit for this upward flow, and explain the roles of cohesion, adhesion and tension. (5)

(b) Water reaches the top of a tree of height h=100 mh = 100\ \text{m}. Treating the xylem column as a continuous water thread, compute the hydrostatic pressure drop ΔPgrav=ρgh\Delta P_{grav} = \rho g h required just to support the column against gravity (in MPa). (3)

(c) The measured water potential at the leaf mesophyll is Ψleaf=1.5 MPa\Psi_{leaf} = -1.5\ \text{MPa} and at the root xylem Ψroot=0.3 MPa\Psi_{root} = -0.3\ \text{MPa}. Using Ψ=Ψp+Ψs\Psi = \Psi_p + \Psi_s, and given the tension (negative pressure potential) that must exist at the top, argue whether cohesion–tension can account for transport to 100 m100\ \text{m}. Compute the total pressure difference available and compare to (b). (4)

(d) Model steady transpirational flow with a Poiseuille-type resistance. A xylem vessel has radius r=20 μmr = 20\ \mu\text{m}, length L=100 mL = 100\ \text{m}, and water viscosity η=1.0×103 Pa s\eta = 1.0\times10^{-3}\ \text{Pa s}. Using the Hagen–Poiseuille law Q=πr4ΔP8ηLQ = \dfrac{\pi r^4 \Delta P}{8\eta L}, compute the volumetric flow rate QQ for a driving ΔP=1.0 MPa\Delta P = 1.0\ \text{MPa} (give in m3s1\text{m}^3\,\text{s}^{-1} and comment on why plants use many parallel vessels). (6)

(e) Explain how cavitation (embolism) threatens the tension model and one anatomical adaptation that limits its spread. (4)


Question 2 — Stomata, Photoperiodism & a Computational Model (20 marks)

(a) Explain the ion/water mechanism of stomatal opening in guard cells, and state the roles of blue light and ABA in the light-vs-drought responses. (6)

(b) A short-day plant flowers only when the continuous dark period exceeds a critical night length of 9 h9\ \text{h}. Interpret each case and state whether flowering occurs: (i) 14 h light / 10 h dark; (ii) 16 h light / 8 h dark; (iii) 15 h light / 9 h dark interrupted at midnight by a 1-min red flash. (4)

(c) Explain the roles of phytochrome (PrPfrP_r \leftrightarrow P_{fr}) in (b)(iii), including which form is active and how red/far-red reversibility works. (4)

(d) Write a short function (Python or clear pseudocode) will_flower(light_h, dark_h, flashes, plant_type) that returns whether a plant flowers, given plant_type ∈ {"short_day","long_day"}, critical night length 9 h, and a list flashes of red-light interruption times (each interruption resets the continuous dark timer). State your reset logic explicitly. (6)


Question 3 — Translocation, Tropisms & a Growth Model (18 marks)

(a) State the pressure-flow (mass-flow) hypothesis of phloem translocation, defining source, sink, loading and unloading, and explain what physically drives the flow. (5)

(b) Auxin redistribution drives phototropism. In a coleoptile bending toward light, auxin is redistributed to the shaded side in a ratio measured as 57:4357:43 (shaded:lit). If total auxin arriving in the tip region is 100100 units, and the local elongation rate is modelled as E=k[auxin]E = k\,[\text{auxin}] with k=0.02 mm h1 per unitk=0.02\ \text{mm h}^{-1}\text{ per unit}, compute the elongation rates of the shaded and lit sides over 2 h2\ \text{h}, and hence the difference in length produced. (5)

(c) Geometry of bending: a coleoptile segment of length =10 mm\ell = 10\ \text{mm} and width w=2 mmw = 2\ \text{mm} bends because the shaded side elongates more. If the shaded side becomes ΔL\Delta L longer than the lit side (use ΔL\Delta L from part (b)), estimate the bending angle θ\theta (radians and degrees) using the arc relation θΔLw\theta \approx \dfrac{\Delta L}{w}. State one assumption. (4)

(d) Contrast the auxin distribution logic of positive phototropism in shoots with positive gravitropism in roots — why does auxin accumulation cause opposite growth outcomes in the two organs? (4)


End of paper.

Answer keyMark scheme & solutions

Question 1

(a) (5)

  • Xylem consists of dead, hollow tracheids/vessel elements with lignified walls forming continuous open tubes — no cytoplasm to obstruct flow (1); lignin gives mechanical strength to resist the negative pressure (1). Phloem is living and used for sugar transport, not bulk water ascent (1).
  • Cohesion: H-bonding between water molecules holds the column together as a continuous thread (1). Adhesion of water to hydrophilic xylem walls + tension generated by evaporation at leaf air spaces pulls the whole column up (1).

(b) (3) ΔPgrav=ρgh=1000×9.81×100=9.81×105 Pa=0.981 MPa\Delta P_{grav}=\rho g h = 1000\times9.81\times100 = 9.81\times10^{5}\ \text{Pa} = 0.981\ \text{MPa}

  • Correct formula (1), substitution (1), answer ≈ 0.98 MPa (1).

(c) (4)

  • Total water potential difference driving flow: ΔΨ=ΨrootΨleaf=(0.3)(1.5)=+1.2 MPa\Delta\Psi = \Psi_{root}-\Psi_{leaf} = (-0.3)-(-1.5) = +1.2\ \text{MPa} (2)
  • This 1.2 MPa gradient (leaf more negative) drives water upward. Since 1.2 MPa > 0.98 MPa required to counter gravity (part b), there remains ~0.22 MPa to overcome frictional resistance — cohesion–tension can account for ascent to 100 m (2).

(d) (6) Q=πr4ΔP8ηLQ=\frac{\pi r^4 \Delta P}{8\eta L}

  • r4=(20×106)4=(2×105)4=1.6×1019 m4r^4=(20\times10^{-6})^4 = (2\times10^{-5})^4 = 1.6\times10^{-19}\ \text{m}^4 (1)
  • Numerator: π×1.6×1019×1.0×106=π×1.6×1013=5.027×1013\pi\times1.6\times10^{-19}\times1.0\times10^{6} = \pi\times1.6\times10^{-13}=5.027\times10^{-13} (1)
  • Denominator: 8×1.0×103×100=0.88\times1.0\times10^{-3}\times100 = 0.8 (1) Q=5.027×10130.8=6.28×1013 m3s1Q = \frac{5.027\times10^{-13}}{0.8}=6.28\times10^{-13}\ \text{m}^3\text{s}^{-1} (2)
  • Comment: one vessel carries a tiny flow (~6×1013m3s16\times10^{-13}\,\text{m}^3\text{s}^{-1}); plants bundle thousands of parallel vessels so total flow adds — and because Qr4Q\propto r^4, small radius increases resistance sharply, favouring many narrow safe vessels over few wide ones (cavitation trade-off) (1).

(e) (4)

  • Under high tension the water thread can break, forming a gas bubble = cavitation/embolism, breaking continuity and blocking that vessel (2).
  • Adaptation: bordered pits between vessels confine the embolism and let water bypass through adjacent conduits; narrow vessels / pit membranes resist air-seeding (2).

Question 2

(a) (6)

  • Blue light activates H⁺-ATPase → protons pumped out of guard cells → membrane hyperpolarises → K⁺ influx through voltage-gated channels, plus malate/Cl⁻ accumulation (2).
  • Lowered solute potential draws water in by osmosis → guard cells become turgid; unevenly thickened inner walls make cells bow apart → pore opens (2).
  • ABA (drought signal) triggers efflux of K⁺/anions → water leaves → guard cells lose turgor → stomata close, conserving water (2).

(b) (4) — critical night length = 9 h; SDP flowers when continuous dark > 9 h.

  • (i) 10 h dark > 9 h → flowers (1)
  • (ii) 8 h dark < 9 h → no flowering (1)
  • (iii) 9 h dark but interrupted by red flash splits it into <9 h continuous segments → no flowering (2)

(c) (4)

  • Phytochrome exists as PrP_r (absorbs red) and PfrP_{fr} (absorbs far-red, biologically active) (1).
  • Red flash converts PrPfrP_r\to P_{fr}; the presence of active PfrP_{fr} during the night is "read" as daylight, resetting the dark measurement (2).
  • Red/far-red reversibility: a subsequent far-red flash converts PfrPrP_{fr}\to P_r, cancelling the effect → flowering restored, proving phytochrome control (1).

(d) (6) Reset logic: dark timer accumulates hours; each red flash resets the continuous dark counter to zero, so the longest uninterrupted dark run must exceed critical length.

def will_flower(light_h, dark_h, flashes, plant_type, critical=9):
    # flashes: list of times (hours into the dark period) that reset dark timer
    # Determine the longest continuous dark stretch
    if not flashes:
        longest_dark = dark_h
    else:
        pts = [0] + sorted(flashes) + [dark_h]
        longest_dark = max(pts[i+1] - pts[i] for i in range(len(pts)-1))
 
    if plant_type == "short_day":
        return longest_dark >= critical      # needs long uninterrupted night
    elif plant_type == "long_day":
        return longest_dark < critical       # needs short night
    else:
        raise ValueError("unknown plant_type")
  • Correct longest-continuous-dark computation (3); correct SDP vs LDP condition (2); flash-reset handled (1).

Check: (i) SDP, dark 10, no flash → 10≥9 → True ✓; (iii) 9 h dark, flash at 4.5 → longest = 4.5 < 9 → False ✓.


Question 3

(a) (5)

  • At the source (mature leaf), sugars are actively loaded into sieve tubes → lowers Ψs\Psi_s → water enters from xylem osmotically → high hydrostatic (turgor) pressure (2).
  • At the sink (root/fruit), sugars are unloaded → water leaves → low pressure (1).
  • The resulting pressure gradient drives bulk (mass) flow of phloem sap from source to sink through sieve tubes (1). Flow direction depends only on source–sink relationship, hence bidirectional in the plant overall (1).

(b) (5)

  • Shaded side auxin = 57 units, lit = 43 units (1).
  • Eshaded=k57=0.02×57=1.14 mm h1E_{shaded}=k\cdot 57 = 0.02\times57 = 1.14\ \text{mm h}^{-1}; over 2 h → 2.28 mm2.28\ \text{mm} (1.5)
  • Elit=0.02×43=0.86 mm h1E_{lit}=0.02\times43 = 0.86\ \text{mm h}^{-1}; over 2 h → 1.72 mm1.72\ \text{mm} (1.5)
  • Difference ΔL=2.281.72=0.56 mm\Delta L = 2.28-1.72 = 0.56\ \text{mm} (1)

(c) (4) θΔLw=0.562=0.28 rad\theta \approx \frac{\Delta L}{w} = \frac{0.56}{2}=0.28\ \text{rad} (2) θ=0.28×180π=16.0\theta = 0.28\times\frac{180}{\pi}=16.0^\circ (1)

  • Assumption: the lit side acts as the (near-inextensible) inner arc of radius ≈ ww, bending is uniform, small-angle/arc approximation holds (1).

(d) (4)

  • In shoots, auxin accumulating on the shaded side promotes cell elongation → shaded side grows faster → bends toward light (positive phototropism) (2).
  • In roots, auxin accumulating on the lower side (gravitropism) inhibits elongation (roots are far more auxin-sensitive; high auxin is inhibitory) → upper side grows faster → root bends downward (positive gravitropism) (2). Same signal, opposite dose–response.
[
  {"claim":"Hydrostatic support pressure over 100 m is ~0.981 MPa","code":"rho=1000; g=9.81; h=100; dP=rho*g*h; result = abs(dP-9.81e5) < 1"},
  {"claim":"Available water potential difference 1.2 MPa exceeds gravity term 0.98 MPa","code":"dpsi=(-0.3)-(-1.5); grav=1000*9.81*100/1e6; result = (abs(dpsi-1.2)<1e-9) and (dpsi>grav)"},
  {"claim":"Poiseuille flow Q approx 6.28e-13 m^3/s","code":"import sympy as sp; r=20e-6; dP=1.0e6; eta=1.0e-3; L=100; Q=sp.pi*r**4*dP/(8*eta*L); result = abs(float(Q)-6.283e-13) < 1e-15"},
  {"claim":"Auxin elongation difference 0.56 mm and bend angle 0.28 rad","code":"k=0.02; t=2; Es=k*57*t; El=k*43*t; dL=Es-El; theta=dL/2; result = (abs(dL-0.56)<1e-9) and (abs(theta-0.28)<1e-9)"}
]