Transport in Vascular Plants

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Chapter 36 Transport in Vascular Plants PowerPoint Lectures for Biology, Seventh Edition Neil Campbell and Jane Reece Lectures by Chris Romero

Vascular tissue Transports nutrients throughout a plant; such transport may occur over long distances Figure 36.1

Concept 36.1: Physical forces drive the transport of materials in plants over a range of distances Transport in vascular plants occurs on three scales Transport of water and solutes by individual cells, such as root hairs Short-distance transport of substances from cell to cell at the levels of tissues and organs Long-distance transport within xylem and phloem at the level of the whole plant

A variety of physical processes Are involved in the different types of transport 4 Through stomata, leaves take in CO 2 and expel O 2. The CO 2 provides carbon for photosynthesis. Some O 2 produced by photosynthesis is used in cellular respiration. H 2 O CO 2 O 2 Sugar 5 Sugars are produced by photosynthesis in the leaves. Light 3 Transpiration, the loss of water from leaves (mostly through stomata), creates a force within leaves that pulls xylem sap upward. 6 Sugars are transported as phloem sap to roots and other parts of the plant. 2 Water and minerals are transported upward from roots to shoots as xylem sap. 1 Roots absorb water and dissolved minerals from the soil. Figure 36.2 H 2 O Minerals O 2 CO 2 7 Roots exchange gases with the air spaces of soil, taking in O 2 and discharging CO 2. In cellular respiration, O 2 supports the breakdown of sugars.

Selective Permeability of Membranes: A Review The selective permeability of a plant cell s plasma membrane Controls the movement of solutes into and out of the cell Specific transport proteins Enable plant cells to maintain an internal environment different from their surroundings

Effects of Differences in Water Potential To survive Plants must balance water uptake and loss Osmosis Determines the net uptake or water loss by a cell Is affected by solute concentration and pressure

Turgor loss in plants causes wilting Which can be reversed when the plant is watered Figure 36.7

Concept 36.2: Roots absorb water and minerals from the soil Water and mineral salts from the soil Enter the plant through the epidermis of roots and ultimately flow to the shoot system

Lateral transport of minerals and water in roots Figure 36.9 1 2 3 Uptake of soil solution by the hydrophilic walls of root hairs provides access to the apoplast. Water and minerals can then soak into the cortex along this matrix of walls. Minerals and water that cross the plasma membranes of root hairs enter the symplast. As soil solution moves along the apoplast, some water and minerals are transported into the protoplasts of cells of the epidermis and cortex and then move inward via the symplast. 4 Within the transverse and radial walls of each endodermal cell is the Casparian strip, a belt of waxy material (purple band) that blocks the passage of water and dissolved minerals. Only minerals already in the symplast or entering that pathway by crossing the plasma membrane of an endodermal cell can detour around the Casparian strip and pass into the vascular cylinder. 5 2 1 Symplastic route Plasma membrane Apoplastic route Root hair Casparian strip Endodermal cell Pathway along apoplast Pathway through symplast Casparian strip Vessels (xylem) Epidermis Cortex Endodermis Vascular cylinder Endodermal cells and also parenchyma cells within the vascular cylinder discharge water and minerals into their walls (apoplast). The xylem vessels transport the water and minerals upward into the shoot system.

The Endodermis: A Selective Sentry The endodermis Is the innermost layer of cells in the root cortex Surrounds the vascular cylinder and functions as the last checkpoint for the selective passage of minerals from the cortex into the vascular tissue

Concept 36.3: Water and minerals ascend from roots to shoots through the xylem Plants lose an enormous amount of water through transpiration, the loss of water vapor from leaves and other aerial parts of the plant The transpired water must be replaced by water transported up from the roots

Transpiration produces negative pressure (tension) in the leaf Which exerts a pulling force on water in the xylem, pulling water into the leaf 3 Evaporation causes the air-water interface to retreat farther into the cell wall and become more curved as the rate of transpiration increases. As the interface becomes more curved, the water film s pressure becomes more negative. This negative pressure, or tension, pulls water from the xylem, where the pressure is greater. Cuticle Upper epidermis Mesophyll Lower epidermis Cuticle Airspace Cell wall Airspace Evaporation Evaporation Water film CO 2 O 2 Xylem CO 2 O 2 Stoma Water vapor Water vapor Y = 0.15 MPa Y = 10.00 MPa Low rate of transpiration Airspace High rate of transpiration Air-water interface Cytoplasm Cell wall Vacuole Figure 36.12 1 In transpiration, water vapor (shown as 2 At first, the water vapor lost by blue dots) diffuses from the moist air spaces of the leaf to the drier air outside via stomata. transpiration is replaced by evaporation from the water film that coats mesophyll cells.

Rate of Transpiration High humidity slows down transpiration, low humidity speeds it up Wind can reduce humidity near the stomates and therefore increases transpiration Increased light, inc. photosynthesis, inc water vapor, inc transpiration Closing stomata stops transpiration

Concept 36.4: Stomata help regulate the rate of transpiration Leaves generally have broad surface areas And high surface-to-volume ratios

Both of these characteristics Increase photosynthesis Increase water loss through stomata 20 µm Figure 36.14

Each stoma is flanked by guard cells Which control the diameter of the stoma by changing shape (a) Changes in guard cell shape and stomatal opening and closing (surface view). Guard cells of a typical angiosperm are illustrated in their turgid (stoma open) and flaccid (stoma closed) states. The pair of guard cells buckle outward when turgid. Cellulose microfibrils in the walls resist stretching and compression in the direction parallel to the microfibrils. Thus, the radial orientation of the microfibrils causes the cells to increase in length more than width when turgor increases. The two guard cells are attached at their tips, so the increase in length causes buckling. Figure 36.15a Cells turgid/stoma open Cell wall Vacuole Radially oriented cellulose microfibrils Guard cell Cells flaccid/stoma closed