What is included with this book?
Whole-Plant Regulation | |
Oxygen Transport in Waterlogged Plants | p. 3 |
Introduction | p. 4 |
O2 Transport in Plants: Some Basic Physics, and Modelling of O2 Diffusion | p. 5 |
A Survey of Methods to Study O2 Transport and Related Parameters in Higher Plants | p. 7 |
Anatomical Adaptations to Flooding Stress: Barriers to Radial Oxygen Loss | p. 10 |
Anatomical Adaptations to Flooding Stress: Formation of Aerenchyma | p. 11 |
Mechanisms of O2 Transport in Plants | p. 13 |
O2 Transport in Plants: Ecological Implications | p. 18 |
Open Questions and Directions of Further Research | p. 18 |
References | p. 19 |
Waterlogging and Plant Nutrient Uptake | p. 23 |
Introduction | p. 23 |
Effects of Hypoxia on Nutrient Uptake | p. 26 |
Physiological Effects of Hypoxia Change Root Elongation Rate, k, and Maximal Nutrient Uptake Rate, Imax | p. 26 |
Waterlogging Leads to Changes in the Availability, Cli, and the Effective Diffusion Coefficient, De, of Some of the Nutrients in the Soil | p. 28 |
In Waterlogged Conditions, Some Plant Species Show More Root Hair Development, Longer and Thinner Roots and Increased Levels of Infection With Mycorhizal Fungi - Effectively Increasing k | p. 29 |
Waierlogging Decrease Evaporation and Bulk Water Flow, Vo | p. 30 |
In Response to Waterlogging the Kinetics of Root Transport Systems, Km and Imax, Can be Modified | p. 31 |
Summary and Concluding Remarks | p. 31 |
References | p. 32 |
Strategies for Adaptation to Waterlogging and Hypoxia in Nitrogen Fixing Nodules of Legumes | p. 37 |
Introduction: The Oxygen Diffusion Barrier in Nodules | p. 38 |
Nodule Morphology and the Gas Diffusion Barrier | p. 38 |
Modulation of the Gas Diffusion Barrier | p. 40 |
Control of the Gas Diffusion Barrier in Response to Sub-Ambient O2 and Flooding | p. 40 |
Mechanism of Regulation of the Gas Diffusion Barrier in Response to pO2 | p. 41 |
Developmental and Morphological Adaptations of Nitrogen-Fixing Nodules to Low Oxygen Stress | p. 43 |
Secondary Aerenchyma Formation | p. 43 |
The Inner Cortex and Infected Zone | p. 44 |
Influence of Adaptive Changes on Nitrogen Fixation Under Altered Rhizosphere pO2 Conditions | p. 45 |
Strategies of Adaptation: Flood-Tolerant Legumes and Oxygen Diffusion | p. 46 |
Tropical Wetland Legumes | p. 46 |
Lotus uliginosus: A Temperate Wetland Legume | p. 49 |
Strategies of Adaptation: Alternate Nodulation Pathways for Flooding Tolerant Legumes | p. 50 |
Intercellular-Based Mechanism of Nodulation: The Lateral Root Boundary Pathway | p. 50 |
Sesbania rostrata: A Model Legume for Aquatic Nodulation | p. 51 |
Summary and Concluding Remarks | p. 53 |
References | p. 55 |
Oxygen Transport in the Sapwood of Trees | p. 61 |
Brief Anatomy of a Woody Stem | p. 62 |
Atmosphere inside a Stem: Gas Composition and is Effects on Respiration | p. 63 |
Gas Transport and Diffusion | p. 66 |
Radial and Axial Oxygen Transport to Sapwood | p. 68 |
Sapwood Respiration | p. 70 |
References | p. 73 |
Intracellular Signalling | |
pH Signaling During Anoxia | p. 79 |
Introduction | p. 79 |
pH, Signal and Regulator | p. 81 |
pH as Systemic Signal | p. 82 |
The Nature of pH Transmission | p. 83 |
What is the Information? | p. 83 |
Anoxic Energy Crisis and pH Regulation | p. 85 |
The Davis-Roberts-Hypothesis: Aspects of pH Signaling | p. 85 |
Cytoplasmic Acidification, ATP and Membrane Potential | p. 86 |
Cytoplasmic pH (Change), An Error Signal? | p. 87 |
pH Interactions Between the (Major) Compartments during Anoxia | p. 88 |
The pH Trans-Tonoplast pH Gradient | p. 88 |
Cytoplasm and Apoplast | p. 90 |
The Apoplast under Anoxia | p. 90 |
Anoxia Tolerance and pH | p. 91 |
pH as a Stress Signal - Avoidance of Cytoplasmic Acidosis | p. 92 |
pH as Signal for Gene Activation | p. 93 |
pH Signaling and Oxygen Sensing | p. 94 |
Conclusions | p. 94 |
References | p. 95 |
Programmed Cell Deaths and Aerenchyma Formation under Hypoxia | p. 99 |
Introduction | p. 100 |
Description of Aerenchyma Formation: Induced and Constitutive | p. 102 |
Evidence for PCD During Lysigenous Aerenchyma Formation | p. 103 |
Description of the sequence of events leading to induced lysigenous aerenchyma formation | p. 104 |
Stimuli for Lysigenous Aerenchyma Development (Low Oxygen, Cytosolic Free Calcium, Ethylene, P, N, and S Starvation, and Mechanical Impedance) | p. 105 |
PCD and the Clearing of the Cell Debris | p. 110 |
What Determines the Architecture of Aerenchyma? - Targeting and Restricting PCD | p. 112 |
Future Prospects | p. 113 |
References | p. 113 |
Oxygen Deprivation, Metabolic Adaptations and Oxidative Stress | p. 119 |
Introduction | p. 120 |
Anoxia: Metabolic Events Relevant for ROS Formation | p. 121 |
ôClassicö Metabolic Changes Under Oxygen Deprivation Related to ROS Formation | p. 121 |
Changes in Lipid Composition and Role of Free Fatty Acids under Stress | p. 124 |
Modification of Lipids: LP | p. 125 |
ROS and-RNS Chemistry Overview and Sources of Formation Under Lack of Oxygen | p. 126 |
Reactive Oxygen Species | p. 126 |
Reactive Nitrogen Species | p. 127 |
Plant Mitochondria as ROS Producers: Relevance for Oxygen Deprivation Stress | p. 129 |
O2 Fluxes in Tissues and Factors Affecting O2 Concentration In Vivo | p. 131 |
Microarray Experiments in the Study of Hypoxia-Associated Oxidative Stress | p. 132 |
Update on Antioxidant Protection | p. 133 |
Low Molecular Weight Antioxidants | p. 134 |
Enzymes Participating in Quenching ROS | p. 136 |
Concluding Remarks | p. 138 |
References | p. 139 |
Membrane Transporters in Waterlogging Tolerance | |
Root Water Transport Under Waterlogged Conditions and the Roles of Aquaporins | p. 151 |
Introduction | p. 151 |
Variable Root Hydraulic Conductance (Lr) | p. 152 |
Changes in Root Morphology and Anatomy | p. 153 |
Root Death and Adventitious Roots | p. 153 |
Barriers to Radial Flow | p. 154 |
Varying the Root or Root Region Involved in Water Uptake | p. 157 |
Volatile and Toxic Compounds in Anaerobic Soils | p. 158 |
Water Permeability of Root Cells and Aquaporins | p. 158 |
Plant Aquaporins | p. 159 |
Responses at the Cell Level Affecting Water Permeability and Potential Mechanisms | p. 161 |
Other Changes under Oxygen Deficiency that Could Affect Water Transport | p. 169 |
Transport of Other Molecules besides Water Through MIPs Relevant to Flooding | p. 170 |
Signalling | p. 171 |
Conclusion and Future Perspectives | p. 172 |
References | p. 173 |
Root Oxygen Deprivation and Leaf Biochemistry in Trees | p. 181 |
Introduction | p. 182 |
Root O2 Deprivation | p. 183 |
Root O2 Deprivation: Effects on Leaves | p. 185 |
The Role of ADH | p. 185 |
Carbon Recovery | p. 186 |
Differential mRNA Translation | p. 188 |
Effects on Cell Metabolism | p. 189 |
Conclusions | p. 191 |
References | p. 192 |
Membrane Transporters and Waterlogging Tolerance | p. 197 |
Introduction | p. 198 |
Waterlogging and Plant Nutrient Acquisition | p. 198 |
Root Ion Uptake | p. 198 |
Transport between Roots and Shoots | p. 199 |
Ionic Mechanisms Mediating Xylem Loading | p. 200 |
Control of Xylem Ion Loading Under Hypoxia | p. 201 |
Oxygen Sensing in Mammalian Systems | p. 201 |
Diversity and Functions of Ion Channels as Oxygen Sensors | p. 201 |
Mechanisms of Hypoxic Channel Inhibition | p. 203 |
The Molecular Mechanisms of Oxygen Sensing in Plant Systems Remain Elusive | p. 203 |
Impact of Anoxia and Hypoxia on Membrane Transport Activity in Plant Cells | p. 204 |
Oxygen Deficiency and Cell Energy Balance | p. 204 |
H+ and Ca+2Pumps | p. 204 |
Ca2+-Permeable Channels | p. 205 |
K+-Permeable Channels | p. 206 |
Secondary Metabolites Toxicity and Membrane Transport Activity in Plant Cells | p. 206 |
Waterlogging and Production of Secondary Metabolites | p. 206 |
Secondary Metabolite Production and Plant Nutrient Acquisition | p. 207 |
Secondary Metabolites and Activity of Key Membrane Transporters | p. 208 |
Pumps | p. 208 |
Carriers | p. 209 |
Channels | p. 209 |
Breeding for Waterlogging Tolerance by Targeting Key Membrane Transporters | p. 211 |
General Trends in Breeding Plants for Waterlogging Tolerance | p. 211 |
Improving Membrane Transporters Efficiency Under Hypoxic Conditions | p. 211 |
Reducing Sensitivity to Toxic Secondary Metabolites | p. 212 |
References | p. 213 |
Ion Transport in Aquatic Plants | p. 221 |
Introduction | p. 221 |
Morphological and Physiological Adaptations of Aquatic Plants | p. 222 |
Ion Transport | p. 224 |
Cation Transport Systems | p. 228 |
Anion Transport Systems | p. 230 |
Root versus Leaf Uptake | p. 230 |
Molecular Characterisation of Transporter Genes | p. 232 |
The Relevance of Aquatic Plants to Terrestrial Plants in Regards to Waterlogging and Inundation Stresses | p. 233 |
Conclusions | p. 233 |
References | p. 234 |
Agronomical and Environmental Aspects | |
Genetic Variability and Determinism of Adaptation of Plants to Soil Waterlogging | p. 241 |
Introduction | p. 242 |
Diversity among Populations: Adaptation to Water-Logged Soils? | p. 246 |
Genetic Control of Traits Related to Hypoxia Tolerance | p. 249 |
Genetic Determinism of Tolerance to Waterlogging and Identification of the Involved Genome Regions | p. 250 |
Methodology of the Detection of QTL for Hypoxia Tolerance: Caution and Strategies | p. 251 |
Major Loci Detected for Hypoxia Tolerance | p. 256 |
Conclusions | p. 260 |
References | p. 260 |
Improvement of Plant Waterlogging Tolerance | p. 267 |
Introduction | p. 267 |
Genetic Resources of the Tolerance | p. 268 |
Selection Criteria | p. 271 |
Genetic Studies on Waterlogging Tolerance | p. 273 |
Marker-Assisted Selection | p. 275 |
QTL Controlling Waterlogging Tolerance | p. 275 |
Accurate Phenotyping is Crucial in Identifying QTLs for Waterlogging Tolerance | p. 278 |
References | p. 281 |
Index | p. 287 |
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