What is included with this book?
Review | p. 1 |
Crassulacean Acid Metabolism: Now and Then | p. 3 |
A pathway to CAM via oxalate and malate in Atriplex | p. 4 |
Sorting the phases of CAM | p. 7 |
Biochemistry and diffusion as determinants of the [delta superscript 13]C value in CAM plants; improved understanding of water use efficiency in C[subscript 3] plants | p. 10 |
Regulation of CAM PEPCase in the dark and light; its role in the diurnal rhythms of CAM and in C[subscript 4] plants | p. 12 |
Malic acid compartmentation in CAM | p. 14 |
Light use efficiency and photoinhibition in CAM plants; the role of C0[superscript 2] supply in the avoidance of photoinactivation | p. 15 |
Recycling of respiratory C0[subscript 2] in CAM and diel variation in the engagement of cyanide insensitive respiration | p. 17 |
Field CAMpaigns | p. 18 |
Origins of CAM and its future prospects in a high CO[subscript 2] world | p. 21 |
A view from over the hill | p. 22 |
Acknowledgements | p. 25 |
References | p. 26 |
Genetics | p. 33 |
Function of Genetic Material: Progressive Insight into Antimicrobial Peptides and their Transcriptional Regulation | p. 35 |
Introduction | p. 35 |
What are antimicrobial peptides? | p. 35 |
Function | p. 36 |
Mechanism of action | p. 38 |
Classification | p. 39 |
Structure and gene regulation of antimicrobial peptides | p. 39 |
Plants | p. 40 |
Antimicrobial peptides | p. 40 |
Structure | p. 41 |
Regulation | p. 43 |
Insects | p. 46 |
Mammals | p. 48 |
Application of antimicrobial peptides | p. 49 |
Crop protection | p. 50 |
Food preservation | p. 51 |
Medical application | p. 51 |
What more is to come? | p. 52 |
Conclusions | p. 52 |
References | p. 53 |
Function of Genetic Material: Assembly Factors of the Photosynthetic Machinery in Cyanobacteria | p. 57 |
Introduction | p. 57 |
Assembly/stability of thylakoid membrane complexes | p. 59 |
Assembly/stability of photosystem I | p. 60 |
Assembly/stability of photosystem II | p. 64 |
Repair of photosystem II | p. 68 |
Subcompartementalization of thylakoid membrane biogenesis | p. 69 |
Conclusions and perspectives | p. 72 |
References | p. 74 |
Extranuclear Inheritance: Genetics and Biogenesis of Mitochondria | p. 80 |
Introduction | p. 80 |
Mitochondrial genomes and proteomes | p. 81 |
Mitochondrial genomes | p. 81 |
Inheritance of mitochondrial DNA | p. 82 |
Mitochondrial proteomes | p. 83 |
RNA import and stability | p. 84 |
tRNA import | p. 84 |
RNA stability | p. 86 |
Protein import into plant mitochondria | p. 88 |
Import receptor and import sequences | p. 88 |
Dual targeting to mitochondria and plastids | p. 89 |
Autophagic degradation of mitochondria | p. 90 |
Summary and perspectives | p. 92 |
Acknowledgements | p. 92 |
References | p. 92 |
Extranuclear Inheritance: Virus-Like DNA-Elements in Yeast | p. 98 |
Abstract | p. 98 |
Introduction | p. 98 |
Occurrence | p. 99 |
Autonomous elements | p. 100 |
Nucleus-independent replication | p. 104 |
Nucleus-independent transcription | p. 106 |
Analysis of linear plasmid derived transcripts | p. 107 |
Cytoplasmic transcription machinery | p. 108 |
The linear plasmid encoded helicase | p. 109 |
The capping enzyme and RNA capping | p. 110 |
Non-autonomous elements | p. 112 |
Elements associated with killer phenotypes | p. 113 |
Killer plasmids encoding type I toxins | p. 114 |
Killer plasmids encoding type II toxins | p. 116 |
Type I and type II toxin uptake machinery | p. 117 |
Cryptic elements | p. 120 |
Outlook | p. 121 |
Acknowledgements | p. 122 |
References | p. 122 |
Population Genetics: Evolutionary Features of Asexual Species | p. 130 |
Introduction | p. 130 |
Modes and origin of asexuality | p. 131 |
Origin of polyploidy | p. 134 |
Population genetics | p. 135 |
Clonal diversity | p. 135 |
Geographic parthenogenesis/apomixis | p. 136 |
Models | p. 139 |
Statistics | p. 142 |
Measures of genetic diversity | p. 144 |
Clonal diversity | p. 144 |
Allelic and genotypic diversity | p. 144 |
Population structures | p. 144 |
Differences between species | p. 145 |
Conclusions | p. 145 |
Acknowledgements | p. 146 |
References | p. 146 |
Plant Breeding: Assessment of Genetic Diversity in Crop Plants and its Exploitation in Breeding | p. 151 |
Introduction | p. 151 |
Assessment of genetic diversity | p. 151 |
Genetic markers | p. 152 |
Measures of genetic association | p. 153 |
Methods to order and display genetic variation | p. 155 |
Diversity of crop plants as determined by evolution, domestication and breeding | p. 156 |
Barley (Hordeum vulgare) | p. 157 |
Evolution and history of barley | p. 157 |
Genetic diversity in wild and cultivated barley | p. 159 |
Oilseed rape (Brassica napus) | p. 161 |
Evolution and history of brassicas | p. 161 |
Rapeseed cultivation, oil quality and applications | p. 162 |
Brassica species, wide hybridization and cytological status | p. 163 |
Exploitation of novel genetic variation for rapeseed breeding | p. 167 |
Conclusions | p. 170 |
References | p. 171 |
Plant Breeding: Antisense ODN Inhibition in in vitro spike cultures as a powerful Diagnostic Tool in Studies on Cereal Grain Development | p. 179 |
Introduction | p. 179 |
Antisense ODN inhibition | p. 180 |
Antisense ODN inhibition as a technology for gene silencing | p. 181 |
Construction of antisense ODNs | p. 181 |
Delivery and intracellular trafficking of antisense ODNs | p. 183 |
Antisense ODN inhibition in in vitro spike cultures as a powerful strategy in studies on cereal grain development | p. 183 |
Conclusions and perspectives | p. 188 |
Acknowledgements | p. 188 |
References | p. 188 |
Physiology | p. 191 |
Characean Algae: Still a Valid Model System to Examine Fundamental Principles in Plants | p. 193 |
Introduction | p. 193 |
Chara as a model for pattern formation | p. 194 |
Rhizoids and protonemata of the green alga Chara as unicellular model systems for gravity sensing and polarized growth | p. 195 |
Cytoskeleton dynamics and polarized growth | p. 198 |
Cytoskeletal basis of the gravity-sensing apparatus | p. 200 |
Critical role of actomyosin in gravity susception | p. 202 |
How statoliths activate gravireceptors | p. 203 |
Calcium, cytoskeleton and gravitropic responses | p. 204 |
Photosynthesis-dependent interactions of cortical organelles | p. 206 |
Wound-induced cell polarization | p. 207 |
Chara as model for Ca[superscript 2+]-mediated signal-response coupling | p. 208 |
The genus Chara as a model for sex differentiation | p. 212 |
Outlook | p. 214 |
Acknowledgements | p. 215 |
References | p. 215 |
Receptors for the Five Classical Plant Hormones | p. 221 |
35 years of hunting receptors: we never got what we expected | p. 221 |
Intracellular hormone receptors acting at the level of gene expression | p. 222 |
Intracellular auxin perception by TIR1 and other F-box proteins | p. 222 |
ABP1 or TIR1? | p. 223 |
GID1, an intracellular receptor for the gibberellins | p. 224 |
Membrane-bound receptors | p. 225 |
Two-component receptors in ethylene signalling | p. 225 |
ETR1 as a prototype ethylene receptor | p. 226 |
ETR1 is reminiscent to bacterial two component signalling systems | p. 227 |
A further two component ethylene receptors have been identified | p. 229 |
How do two-component receptors transduce the ethylene signal? | p. 229 |
Cytokinins are also perceived by two-component type receptors | p. 230 |
More two-component cytokinin receptors for Arabidopsis and the rest of the plant world | p. 233 |
How do two-component receptors transduce the cytokinin signal? | p. 234 |
Candidates for the ABA receptor | p. 235 |
A receptor-like kinase as a possible ABA receptor | p. 235 |
At last: A plant G protein coupled receptor may be involved in ABA signalling | p. 236 |
Perspective | p. 237 |
References | p. 237 |
Spatiotemporal Patterns and Distributed Computation-A Formal Link between C0[subscript 2] Signalling, Diffusion and Stomatal Regulation | p. 242 |
Inorganic carbon themes and perspectives for signalling | p. 242 |
Ci signalling to stomatal guard cells | p. 243 |
Lateral C0[subscript 2]-diffusion in leaves | p. 245 |
The heterobaric/homobaric leaf concept | p. 245 |
Stomatal patchiness | p. 246 |
Lateral gas diffusion over large distances within leaves | p. 246 |
Lateral diffusion and Ci signalling for synchronization/desynchronization of photosynthetic activity within leaves | p. 247 |
Heterogeneity and the role of photorespiration in leaves performing C[subscript 3] photosynthesis | p. 247 |
Heterogeneity in leaves performing CAM | p. 248 |
Heterogeneity during endogenous circadian rhythmicity of photosynthesis | p. 249 |
Interpreting spatiotemporal patterns beyond explicit models | p. 250 |
Ci signalling network | p. 253 |
References | p. 256 |
Plant Hemoglobins, Nitrate and Nitric Oxide: Old Players, New Games | p. 261 |
Introduction | p. 261 |
Properties of nsHbs | p. 263 |
Gene and protein expression | p. 263 |
Cellular and subcellular localization of Hbs | p. 264 |
Oxygen affinity | p. 265 |
Structural aspects | p. 265 |
Reaction of nsHbs with NO | p. 266 |
NsHb and NO in nitrate assimilation | p. 267 |
Nitrate assimilation as a source for NO | p. 267 |
A matter of speculation: Effects of NO on nitrate assimilation and related processes | p. 268 |
Role of nsHbs in nitrate assimilation | p. 270 |
NsHb and NO in anoxia tolerance | p. 272 |
NO production under anoxia | p. 272 |
Role of nsHbs in anoxia tolerance | p. 273 |
NsHb and NO in plant-microbe interactions | p. 277 |
Conclusions | p. 280 |
Acknowledgements | p. 281 |
References | p. 281 |
Living in Day-Night-Cycles-Specific Diel Leaf Growth Patterns and the Circadian Control of Photomorphogenesis | p. 288 |
Introduction | p. 288 |
Endogenous patterns of leaf growth | p. 290 |
Diel growth patterns in different species and light environments | p. 291 |
Circadian clock, gene expression and diel metabolic activities | p. 295 |
Gating of cell cycle and diel growth processes | p. 297 |
Linking light environment with diel growth dynamics | p. 299 |
Shade avoidance, signalling networks and the role of the circadian clock | p. 299 |
Light signalling pathways | p. 300 |
Cross-talk with circadian clock | p. 302 |
Circadian gating of shade avoidance | p. 303 |
Leaf growth dynamics in dicot plants and mechanisms of shade avoidance | p. 304 |
Perspective | p. 307 |
Acknowledgements | p. 307 |
References | p. 307 |
Ecology | p. 315 |
Competitive Networks, Indirect Interactions, and Allelopathy: A Microbial Viewpoint on Plant Communities | p. 317 |
Introduction | p. 317 |
Do hierarchies or networks characterize competitive interactions in plant communities? | p. 320 |
Do indirect interactions occur among competing plants? | p. 323 |
Allelopathy and indirect interactions among plants | p. 325 |
Do hierarchies in allelopathic tolerance exist? | p. 327 |
What can we learn from microbes? | p. 329 |
Conclusions | p. 330 |
Acknowledgements | p. 331 |
References | p. 331 |
Quaternary Palaeoecology: Isotopes as Valuable Aids in Palaeoecological Research | p. 336 |
Use of various isotope species as indicators of food consumed in the past | p. 336 |
General difficulties in choosing appropriate samples for obtaining reliable [superscript 14]C age-data | p. 338 |
Problems in dating palaeopedological processes | p. 341 |
Regional patterns of [superscript 14]C-reservoir ages in oceans, lakes and rivers | p. 342 |
Problem of constructing a generally accepted calibration curve for translating [superscript 14]C age-data into those of calendar years | p. 347 |
Conclusion | p. 348 |
References | p. 349 |
Competition for Resources in Trees: Physiologigal Versus Morphological Plasticity | p. 356 |
Abstract | p. 356 |
Introduction | p. 357 |
Size-asymmetric versus size-symmetric competition | p. 357 |
Hypotheses | p. 358 |
Background | p. 359 |
Above-ground competition in response to resource limitation | p. 359 |
Above-ground morphological plasticity | p. 360 |
Above-ground physiological plasticity | p. 361 |
Below-ground competition in response to resource limitation | p. 363 |
Below-ground morphological plasticity | p. 364 |
Below-ground physiological plasticity | p. 365 |
Evidence for size-asymmetric competition below ground | p. 367 |
Competition at high versus low resource availability | p. 368 |
Synthesis | p. 370 |
Morphological versus physiological responses | p. 370 |
The whole-tree perspective: above-ground/below-ground interactions in resource competition | p. 372 |
Conclusions | p. 373 |
Acknowledgements | p. 375 |
References | p. 375 |
Explaining Variation in Fine Root Life Span | p. 382 |
Introduction | p. 382 |
Fine root estimation methodology | p. 383 |
Indirect estimation | p. 383 |
Direct estimation | p. 383 |
Direct and indirect comparison | p. 384 |
Predicting fine root life span | p. 385 |
Environment | p. 390 |
Life history/growth form | p. 392 |
Interactions between life form and environment | p. 393 |
Conclusions | p. 394 |
Acknowledgements | p. 395 |
References | p. 395 |
Subject Index | p. 399 |
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