Multiple Choice
1. B Death of xylem vessel elements removes all cytoplasmic contents and dissolves the end walls between cells, creating a continuous hollow tube with minimal resistance to water flow. Living cytoplasm would obstruct the lumen and impose osmotic resistance, water crossing from one living cell to the next through membranes would be far slower than bulk flow through a hollow tube.
2. C The Casparian strip's function is selectivity. By blocking the apoplast (cell wall) pathway, it forces everything to cross the plasma membrane of endodermal cells. The membrane contains specific ion transport proteins, ions without matching transporters cannot pass. This is how plants exclude harmful ions from their vascular tissue and regulate mineral nutrition.
3. D Turgor pressure at the source is created by the sequence: active sucrose loading → high solute concentration in sieve tubes → low water potential → osmotic water entry → raised turgor. The ATP is used for the sucrose pump; water entry is passive (osmosis). Transpiration creates negative pressure in xylem, not positive pressure in phloem.
4. A Phloem loading is the ATP-requiring step. Without it, sucrose cannot be concentrated in source sieve tubes, no osmotic water entry occurs, no turgor pressure builds, and no pressure gradient exists to drive bulk flow. Xylem transport is entirely passive and independent of cellular ATP, it would continue normally.
5. C Xylem operates under negative pressure (tension) maintained by cohesion, the xylem vessel walls must be lignified to resist the inward force of negative pressure. Phloem operates under positive turgor pressure generated by active sucrose loading. These are opposite pressure regimes requiring opposite structural adaptations.
Q6, Model Answer
Water enters root hair cells by osmosis, the solute concentration of root hair cell cytoplasm is higher than soil solution (partly due to active uptake of mineral ions), giving the cell a lower water potential than soil water. Water moves from high water potential (soil) to low water potential (root hair cell) across the semi-permeable plasma membrane.
From root hair cells, water moves through the root cortex toward the central xylem via two pathways: the apoplast (through cell walls, no membranes crossed) and the symplast (through cytoplasm via plasmodesmata). At the endodermis, the innermost layer of cortex cells surrounding the vascular tissue, the Casparian strip, a band of waterproof suberin in the cell walls, blocks the apoplast pathway. All water and dissolved minerals must cross the plasma membrane of endodermal cells to proceed further.
This membrane crossing allows selective mineral uptake because specific ion transport proteins in the endodermal cell membrane determine which mineral ions can pass into the cell and onwards to the xylem. Ions without matching transporters are excluded. This gives the plant fine control over its mineral nutrition and protects the vascular tissue from potentially toxic soil ions.
Q7, Model Answer
The driving force at the leaf is transpiration, water evaporates from the surfaces of mesophyll cells and diffuses through open stomata to the atmosphere (which has very low water potential, especially in dry, warm conditions). This continuous water loss creates a water deficit in leaf mesophyll cells, lowering their water potential below that of the water in leaf xylem vessels.
Water moves from xylem into mesophyll cells by osmosis, creating tension (negative pressure, pressure below atmospheric) in the xylem. This tension is transmitted through the entire xylem from leaf to root because water molecules are strongly cohesive, held together by hydrogen bonds. The water column acts as a continuous chain; tension applied at the top is transmitted downward without the column breaking (in normal conditions).
At the root, the xylem water potential (under tension) is lower than the water potential of soil water. This drives osmotic uptake of water from soil into root hair cells, and from endodermal cells into root xylem, maintaining a continuous supply of water to replace that lost by transpiration at the top.
Q8, Model Answer
Phloem transport can occur simultaneously in both directions because it is driven by pressure gradients from source to sink, and a plant can have multiple sinks in different locations at the same time. For example, a mature leaf may simultaneously supply sucrose to developing fruit above it (upward flow in phloem above the leaf) and to growing root tips below it (downward flow in phloem below the leaf). The pressure-flow mechanism creates independent pressure gradients in different sections of the phloem, allowing different directions of flow in different parts of the plant at the same time.
Xylem transport is always unidirectional (upward, from roots to leaves) because it is driven by transpiration pull, evaporation at the leaf creates tension that is transmitted downward through the cohesive water column. This is always a one-directional driving force: from high water potential in soil to low water potential in dry atmosphere. There is no equivalent upward driving force in xylem, gravity always acts downward, and the plant does not have a mechanism to reverse the transpiration-driven gradient.