1 / 62

Chapter 36

Chapter 36. Resource Acquisition and Transport in Vascular Plants. Overview: Underground Plants. The success of plants depends on their ability to gather and conserve resources from their environment The transport of materials is central to the integrated functioning of the whole plant

clodia
Download Presentation

Chapter 36

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Chapter 36 Resource Acquisition and Transport in Vascular Plants

  2. Overview: Underground Plants • The success of plants depends on their ability to gather and conserve resources from their environment • The transport of materials is central to the integrated functioning of the whole plant • Diffusion, active transport, and bulk flow work together to transfer water, minerals, and sugars

  3. Fig. 36-1 Lithops sp.

  4. Fig. 36-2-3 O2 CO2 Light Land plants acquire resources both above and below ground Sugar H2O O2 H2Oand minerals CO2

  5. algal ancestors of land plants absorbed water, minerals, and CO2 directly from the surrounding water • xylem and phloem: long-distance transport of water, minerals, & products of photosynthesis • Adaptations in each species represent compromises between enhancing photosynthesis and minimizing water loss

  6. Shoot Architecture and Light Capture • Stems serve as conduits for water and nutrients, and as supporting structures for leaves • Phyllotaxy,the arrangement of leaves on a stem, is specific to each species

  7. Light absorption is affected by the leaf area index, the ratio of total upper leaf surface of a plant divided by the surface area of land on which it grows • Leaf orientation affects light absorption Plant BLeaf area = 80%of ground area(leaf area index = 0.8) Plant ALeaf area = 40%of ground area(leaf area index = 0.4)

  8. Root Architecture and Acquisition of Water and Minerals • Soil is a resource mined by the root system • Taproot systems anchor plants and are characteristic of most trees • Roots and the hyphae of soil fungi form symbiotic associations called mycorrhizae • Mutualisms with fungi helped plants colonize land root hyphae

  9. Diffusion and Active Transport of Solutes • Diffusion across a membrane is passive, while the pumping of solutes across a membrane is active and requires energy • Most solutes pass through transport proteins embedded in the cell membrane • The most important transport protein for active transport is the proton pump

  10. Fig. 36-6 Proton pumps in plant cells create a hydrogen ion gradient that is a form of potential energy that can be harnessed to do work EXTRACELLULAR FLUID CYTOPLASM _ + _ H+ + ATP H+ _ + H+ H+ H+ H+ _ H+ + H+ H+ _ + They contribute to a voltage known as a membrane potential

  11. Fig. 36-7a Plant cells use energy stored in the proton gradient and membrane potential to drive the transport of many different solutes _ + CYTOPLASM EXTRACELLULAR FLUID _ + K+ _ + K+ K+ K+ K+ K+ _ + K+ Transport protein _ + (a) Membrane potential and cation uptake

  12. Fig. 36-7b In Cotransport, transport protein couples the diffusion of one solute to the active transport of another _ + H+ NO3− H+ _ NO3− + _ H+ + H+ H+ H+ H+ H+ NO3− _ NO3− + NO3− _ NO3− H+ + H+ H+ _ H+ + (b) Cotransport of an anion with H+

  13. Fig. 36-7c The “coattail” effect of cotransport is also responsible for the uptake of the sugar sucrose by plant cells _ + H+ H+ S H+ _ _ H+ + H+ H+ S H+ H+ H+ S _ S S + H+ _ + H+ S _ H+ + (c) Cotransport of a neutral solute with H+

  14. Water potential (Ψ) • is a measurement that combines the effects of solute concentration and pressure • determines the direction of movement of water • Water flows from regions of higher water potential to regions of lower water potential (osmosis) • MPa = unit of measurement (megapascal) • Ψ = 0 MPa for pure water at sea level and room temperature

  15. How Solutes and Pressure Affect Water Potential • Both pressure and solute concentration affect water potential • solute potential (ΨS) is proportional to the number of dissolved molecules • also called osmotic potential

  16. Pressure potential (ΨP) is the physical pressure on a solution • Turgor pressure is the pressure exerted by the plasma membrane against the cell wall, and the cell wall against the protoplast • Ψ = Ψs + Ψp

  17. Measuring Water Potential • Consider a U-shaped tube where the two arms are separated by a membrane permeable only to water • Water moves in the direction from higher water potential to lower water potential

  18. 0.1 Msolution If no pressure is applied: The addition of solutes reduces water potential Purewater H2O ψP= 0ψS = −0.23 ψP= 0ψS= 0 ψ= −0.23 MPa ψ= 0 MPa

  19. Physical pressure increases water potential Positivepressure H2O ψP= 0ψS= 0 ψP= 0.23ψS = −0.23 ψ= 0 MPa ψ= 0 MPa

  20. Increased positive pressure on the right causes the water to move to the left Increasedpositivepressure H2O ψP = 0.30  ψS = −0.23 ψP= 0ψS= 0 ψ= 0.07 MPa ψ= 0 MPa

  21. Fig. 36-8d Negative pressure decreases water potential Negativepressure(tension) H2O ψP = 0ψS = −0.23 ψP = −0.30ψS = 0 ψ= −0.30 MPa ψ= −0.23 MPa

  22. Fig. 36-9a A cell placed in a high solute concentration it will lose water, plasmolyzing Initial flaccid cell: ψP= 0ψS = −0.7 0.4 M sucrose solution: ψ= −0.7 MPa ψP= 0 ψS = −0.9 ψ= −0.9 MPa Plasmolyzed cell ψP= 0 ψS = −0.9 60% H2O ψ= −0.9 MPa (a) Initial conditions: cellular ψ > environmental ψ Turgor loss in plants causes wilting, which can be reversed when the plant is watered

  23. Fig. 36-9b If the same flaccid cell is placed in a solution with a lower solute concentration, the cell will gain water and become turgid Initial flaccid cell: ψP = 0ψS = −0.7 100% H20 Pure water: ψ= −0.7 MPa ψP = 0ψS = 0 ψ= 0 MPa Turgid cell ψP = 0.7ψS = −0.7 ψ = 0 MPa (b) Initial conditions: cellular ψ < environmental ψ

  24. Aquaporins • are transport proteins in the cell membrane that allow the passage of water • The rate of water movement is likely regulated by phosphorylation of the aquaporin proteins

  25. Transport • Transport is also regulated by the compartmental structure of plant cells • plasma membrane • controls the traffic of molecules into and out of the protoplast • barrier between two major compartments, the cell wall and the cytosol

  26. vacuole • occupies as much as 90% or more of the protoplast’s volume • vacuolar membrane regulates transport between the cytosol and the vacuole

  27. the cell wall and cytosol are continuous from cell to cell • cytoplasmic continuum is called the symplast • cytoplasm of neighboring cells is connected by channels called plasmo- desmata • apoplast is the continuum of cell walls and extracellular spaces cytosol vacuole cell wall

  28. Water and minerals can travel through a plant by three routes: • Transmembrane route out of one cell, across a cell wall, and into another cell • Symplastic route via the continuum of cytosol • Apoplastic route via the cell walls and extracellular spaces apoplast symplast

  29. Long-Distance Transport • Efficient long distance transport of fluid requires bulk flow, the movement of a fluid driven by pressure • Water and solutes move together through tracheids and vessel elements of xylem, and sieve-tube elements of phloem • Efficient movement is possible because mature tracheids and vessel elements have no cytoplasm, and sieve-tube elements have few organelles in their cytoplasm

  30. Absorption of Water and Minerals by Root Cells • Most water and mineral absorption occurs near root tips, where the epidermis is permeable to water and root hairs are located • Root hairs account for much of the surface area of roots • After soil solution enters the roots, the extensive surface area of cortical cell membranes enhances uptake of water and selected minerals

  31. Transport of Water and Minerals into the Xylem • The endodermisis the innermost layer of cells in the root cortex • It surrounds the vascular cylinder and is the last checkpoint for selective passage of minerals from the cortex into the vascular tissue • Water can cross the cortex via the symplast or apoplast

  32. Fig. 36-12a Casparian strip Plasmamembrane Apoplasticroute Vessels(xylem) Symplasticroute Roothair Epidermis Stele(vascularcylinder) Endodermis Cortex

  33. Fig. 36-12b Casparian strip Endodermal cell Pathway alongapoplast Pathwaythroughsymplast The waxy Casparian strip of the endodermal wall blocks apoplastic transfer of minerals from the cortex to the vascular cylinder

  34. Bulk Flow Driven by Negative Pressure in the Xylem • Plants lose a large volume of water from transpiration, the evaporation of water from a plant’s surface • Water is replaced by the bulk flow of water and minerals, called xylem sap, from the steles of roots to the stems and leaves • Is sap mainly pushed up from the roots, or pulled up by the leaves?

  35. Pushing Xylem Sap: Root Pressure • At night, when transpiration is very low, root cells continue pumping mineral ions into the xylem of the vascular cylinder, lowering the water potential • Water flows in from the root cortex, generating root pressure • Root pressure sometimes results in guttation, the exudation of water droplets on tips or edges of leaves • Positive root pressure is relatively weak and is a minor mechanism of xylem bulk flow

  36. Pulling Xylem Sap: The Transpiration-Cohesion-Tension Mechanism • Water is pulled upward by negative pressure in the xylem • Known as transpirational pull

  37. Transpirational Pull • Water vapor in the airspaces of a leaf diffuses down its water potential gradient and exits the leaf via stomata

  38. air-water interface 3 the curvation increases surface tension and rate of transpiration • Transpiration produces negative pressure (tension) in the leaf, which exerts a pulling force on water in the xylem, pulling water into the leaf 2 air-water interfase retreates farther into the cell wall, becoming more curved. cell wall of mesophyll cell water film 1 water vapor lost is replaced by evaporation of water film coating the mesophyll cells

  39. Cohesion and Adhesion in the Ascent of Xylem Sap Watermolecule Roothair Soilparticle Water Water uptakefrom soil The transpirational pull on xylem sap is transmitted all the way from the leaves to the root tips and even into the soil solution

  40. Transpirational pull is facilitated by cohesion of water molecules to each other and adhesion of water molecules to cell walls Adhesionby hydrogenbonding Xylemcells Cellwall Cohesion andadhesion inthe xylem Cohesionby hydrogenbonding

  41. Fig. 36-15c Xylemsap Mesophyllcells Stoma Watermolecule Transpiration Atmosphere Drought stress or freezing can cause cavitation, the formation of a water vapor pocket by a break in the chain of water molecules

  42. Fig. 36-15 Xylemsap Mesophyllcells Outside air ψ = −100.0 Mpa Stoma Stoma Leaf ψ(air spaces) = −7.0 Mpa Watermolecule Transpiration Leaf ψ(cell walls) = −1.0 Mpa Atmosphere Adhesionby hydrogenbonding Xylemcells Cellwall Water potential gradient Trunk xylem ψ = −0.8 Mpa Cohesionby hydrogenbonding Cohesion andadhesion inthe xylem Watermolecule Roothair Trunk xylem ψ = −0.6 Mpa Soilparticle Soil ψ = −0.3 Mpa Water Water uptakefrom soil

  43. Stomata help regulate the rate of transpiration • Leaves generally have broad surface areas and high surface-to-volume ratios • These characteristics increase photosynthesis and increase water loss through stomata open closed guard cells stomata

  44. Stomata: Major Pathways for Water Loss • About 95% of the water a plant loses escapes through stomata • guard cells control the diameter of the stoma by changing shape

  45. turgid/Stoma open flaccid/Stoma closed Mechanisms of Stomatal Opening and Closing Changes in turgor pressure open and close stomata These result primarily from the reversible uptake and loss of potassium ions by the guard cells Radially orientedcellulose microfibrils Vacuole Guard cell Guard cells Guard cells turgid/Stoma open flaccid/Stoma closed H2O H2O H2O H2O H2O K+ H2O H2O H2O H2O H2O Role of potassium in stomatal opening and closing

  46. Stimuli for Stomatal Opening and Closing • Generally, stomata open during the day and close at night to minimize water loss • Stomatal opening at dawn is triggered by light, CO2 depletion, and an internal “clock” in guard cells • All eukaryotic organisms have internal clocks; circadian rhythms are 24-hour cycles

  47. Effects of Transpiration • If the lost water is not replaced by sufficient transport of water, the plant will lose water and wilt • also results in evaporative cooling, which can lower the temperature of a leaf and prevent denaturation of various enzymes involved in photosynthesis and other metabolic processes

  48. Adaptations That Reduce Evaporative Water Loss • Xerophytesare plants adapted to arid climates • They have leaf modifications that reduce the rate of transpiration • Some plants use a specialized form of photosynthesis called crassulacean acid metabolism (CAM) where stomatal gas exchange occurs at night

  49. Fig. 36-18a Ocotillo leafless when dry Ocotillo after a heavy rain

  50. Cuticle Upper epidermal tissue Oleander Stomata Crypt Lower epidermaltissue Trichomes(“hairs”) Multiple layerd epidermis Stomata recessed in crypt Crypt retains humidity Trichomes brake up air flow

More Related