Chapter 35: Water and Sugar Transport in Plants
Biologists use the term water potential to indicate the potential energy that water has in a particular environment compared with the potential energy of pure water at room temperature and atmospheric pressure.
The tendency for water to move in response to differences in solute concentrations is determined by the solute potential.
The force exerted by the wall is called wall pressure.
As water moves into the cell, the pressure of the fluid contents inside the cell, known as turgor pressure, increases until wall pressure is induced.
Cells that are firm and experience wall pressure are said to be turgid.
Pressure potential refers to any kind of physical pressure on the water.
Inside a cell, the pressure potential consists of turgor pressure and, in the opposite direction, wall pressure.
In most cases, water potential is highest in soil, medium to high in roots, low in leaves, and very low in the atmosphere.
This situation sets up a water-potential gradient that causes water to move up through the plant.
To move up a plant, water moves down the water-potential gradient that exists between the soil, its tissues, and the atmosphere.
When it does so, it replaces the water lost through transpiration.
Endodermal cells are tightly packed and secrete a narrow band of wax called the Casparian strip.
This layer is composed primarily of a compound called suberin, which forms a waterproof barrier where endodermal cells contact each other.
The Casparian strip blocks the apoplastic route by preventing water from moving through the walls of endodermal cells and into the vascular tissue.
The Casparian strip does not affect water and ions that move through the plastic route.
The movement of ions and water into the root xylem is responsible for the process known as root pressure.
In certain low-growing plants, such as strawberries, enough water can move to force water droplets out of the leaves by a phenomenon known as guttation.
Surface tension is a force that exists among water molecules at an air-water interface.
Adhesion is a molecular attraction among dissimilar molecules.
In this case, the water interacts with a solid substrate- such as the glass walls of a capillary tube or the cell walls of tracheids or vessel elements-through hydrogen bonding.
Water molecules are pulled upward as they bond to each other and adhere to the side of the tube.
Cohesion is molecular action among like molecules, such as the hydrogen bonding that occurs among molecules in water.
Because water molecules cohere, the upward pull by adhesion is transmitted to the rest of the water column.
The water column rises against the pull of gravity.
The leading hypothesis to explain long-distance water movement in vascular plants is the cohesion-tension theory, which states that water is pulled from roots to the tops of trees along a water-potential gradient, via forces generated by transpiration at the leaf surface.
This process relies on two of the forces involved in capillary action, namely, cohesion and tension.
Translocation refers to the movement of sugars by bulk flow in multiple directions throughout a plant-but specifically, from sources to sinks.
In vascular plants, a source is a tissue where sugar enters the phloem; a sink is a tissue where sugar exits the phloem.
Phloem consists largely of two cell types, sieve-tube elements, and companion cells.
Sieve-tube elements lack nuclei and most other organelles.
They are connected to one another, end to end, by perforated sieve plates.
In the roots of the same plant, however, an entirely different mechanism is responsible for unloading sucrose.
Root cells in this species have a large vacuole that stores sucrose.
The membrane surrounding this organelle is called the tonoplast.
It contains two types of protein pumps that work together to accumulate sucrose in the vacuole, much like the phloem loading process.
Biologists use the term water potential to indicate the potential energy that water has in a particular environment compared with the potential energy of pure water at room temperature and atmospheric pressure.
The tendency for water to move in response to differences in solute concentrations is determined by the solute potential.
The force exerted by the wall is called wall pressure.
As water moves into the cell, the pressure of the fluid contents inside the cell, known as turgor pressure, increases until wall pressure is induced.
Cells that are firm and experience wall pressure are said to be turgid.
Pressure potential refers to any kind of physical pressure on the water.
Inside a cell, the pressure potential consists of turgor pressure and, in the opposite direction, wall pressure.
In most cases, water potential is highest in soil, medium to high in roots, low in leaves, and very low in the atmosphere.
This situation sets up a water-potential gradient that causes water to move up through the plant.
To move up a plant, water moves down the water-potential gradient that exists between the soil, its tissues, and the atmosphere.
When it does so, it replaces the water lost through transpiration.
Endodermal cells are tightly packed and secrete a narrow band of wax called the Casparian strip.
This layer is composed primarily of a compound called suberin, which forms a waterproof barrier where endodermal cells contact each other.
The Casparian strip blocks the apoplastic route by preventing water from moving through the walls of endodermal cells and into the vascular tissue.
The Casparian strip does not affect water and ions that move through the plastic route.
The movement of ions and water into the root xylem is responsible for the process known as root pressure.
In certain low-growing plants, such as strawberries, enough water can move to force water droplets out of the leaves by a phenomenon known as guttation.
Surface tension is a force that exists among water molecules at an air-water interface.
Adhesion is a molecular attraction among dissimilar molecules.
In this case, the water interacts with a solid substrate- such as the glass walls of a capillary tube or the cell walls of tracheids or vessel elements-through hydrogen bonding.
Water molecules are pulled upward as they bond to each other and adhere to the side of the tube.
Cohesion is molecular action among like molecules, such as the hydrogen bonding that occurs among molecules in water.
Because water molecules cohere, the upward pull by adhesion is transmitted to the rest of the water column.
The water column rises against the pull of gravity.
The leading hypothesis to explain long-distance water movement in vascular plants is the cohesion-tension theory, which states that water is pulled from roots to the tops of trees along a water-potential gradient, via forces generated by transpiration at the leaf surface.
This process relies on two of the forces involved in capillary action, namely, cohesion and tension.
Translocation refers to the movement of sugars by bulk flow in multiple directions throughout a plant-but specifically, from sources to sinks.
In vascular plants, a source is a tissue where sugar enters the phloem; a sink is a tissue where sugar exits the phloem.
Phloem consists largely of two cell types, sieve-tube elements, and companion cells.
Sieve-tube elements lack nuclei and most other organelles.
They are connected to one another, end to end, by perforated sieve plates.
In the roots of the same plant, however, an entirely different mechanism is responsible for unloading sucrose.
Root cells in this species have a large vacuole that stores sucrose.
The membrane surrounding this organelle is called the tonoplast.
It contains two types of protein pumps that work together to accumulate sucrose in the vacuole, much like the phloem loading process.