Table of Contents
| INTRODUCTION BY DR. EUGENE MALLOVE | 7 |
| AUTHORS' PREFACE | 16 |
PART 1 - Aetherometric physical and biophysical foundations |
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1. Continua, fields and manifolds:fundamental problems of a Physical Theory of Biological Systems and Processes |
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| Invariance of the failed syntheses of holism and reductionism | 21 |
| The basic physical and mathematical problem of the definition of a continuum | 24 |
| The aetherometric solution to the definition of energy continua | 26 |
| Aetherometric phase energy, phase space and higher order simultaneity | 27 |
| Matter and Aether: Space and Time as distinct manifolds and energy properties | 28 |
| Irreversibility of Time: the arrow of Time is not the arrow of entropy | 31 |
| Role of Simultaneity: every energy flux produces a duration in universal Time | 32 |
| Brief examination of field concepts, in Physics and Biology | 34 |
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2. Aetherometric system dynamics(and evaluation of the thermodynamical, molecular genetic and biochemical approaches to living systems) |
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| Biological holism vs Physical reductionism at the birth of molecular biology | 40 |
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Reversible and nonreversible processes: isolated and imperfectly closed systems and entropy of a system |
41 |
| An energetic approach to entropy and ideal negentropy | 44 |
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Characteristic of living systems: active energy extraction and reverse potential of energy flow; closed and open systems |
49 |
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The Carnot engine, the steam engine and latent heat: the internal energy function ΔU, and enthalpy of a system and of a reaction |
53 |
| The total internal energy function ET and the free energy of a system | 62 |
| The energy forms composing the internal energy of a system | 65 |
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Open and closed systems: order and internal energy; characteristic of living systems |
74 |
| The real physical senses of entropy | 88 |
| The internal and vital power functions of living systems | 98 |
| Biological machines as systems of double articulation | 104 |
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3. Speciation, transformation and biopoiesis |
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| 3.1 A Lamarckian-Nietzschean critique of evolutionism, old and new | |
| The concept of evolution as an explanation for speciation | 107 |
| Foundations of Darwinian Evolutionism | 110 |
| The historical nature of the civilized myth of a natural struggle for existence | 112 |
| The myth that all biological variation is random: relative and absolute chances | 115 |
| Breaking down the central dogma of molecular genetics: against neo-Darwinism | 120 |
| Is cancer the Lamarckian adaptation of an 'amoeboid-becoming'? | 122 |
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Anomalous mutagenesis and the attack on neo-evolutionism: the return of the Chevalier de Lamarck (neo-Lamarckism) |
127 |
| Post-adaptive mutagenic processes | 131 |
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3.2 The problems of the origins of Life |
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| Biopoiesis of protobionts: the protein microspheres of S. Fox | 136 |
| Autocatalytic properties of RNA | 141 |
| How did a molecular system of double articulation emerge? | 144 |
| Rhizospheric involution and creative evolution | 147 |
| The ultimate perspective on biopoiesis: the end of the dogmatic era | 149 |
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PART 2 - Aetherometric biophysics of cellular and molecular systems |
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4. Aetherometric bioenergetics and molecular biophysics |
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Energetic specificity or nonspecificity of the living: biological roles of massbound charges, light and heat |
152 |
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Molecular biology and allosteric interactions: A. Noncovalent bonds as a biological specialization B. Stereoscopic properties of proteins C. Biological specificity of latent heat in noncovalent bonds |
153 |
| Types and aetherometric structure of noncovalent bonds | 156 |
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Activation energy in covalent and noncovalent reactions, and underlying energy fields |
161 |
| Immanent fields and biological order as phase energy processes: role of latent heat | 163 |
| Is there a biological specificity for electric energy? | 165 |
| Animal electricity and the conflict with mechanism | 167 |
| The vitalism vs mechanicism conflict | 169 |
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Autopoietic machines: micro-functionalist problems with the concept and its aetherometric function |
172 |
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Mechanism vs vitalism: an aetherometric approach to the monist machinic solution |
176 |
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5. Biological affinity, cellular and molecular, of aether energy |
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W. Reich's discovery of ORgone energy and our discovery of the ambipolar radiation spectrum, and its two subspectra |
181 |
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Fundamental physical roles and byproducts of ambipolar radiation: blackbody photons and latent heat |
186 |
| Biological roles of ambipolar energy and depolarization in the action potential | 188 |
| Biological affinity and specificity of massfree energy | 191 |
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6. Aetherometric theory of the pH scale
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| The fundamental role of water in Life | 194 |
| The pH scale of acid-base reaction processes | 196 |
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Proton and electron chemistries: acid-base and redox reactions; the Nernst equation |
200 |
| Aetherometric treatment of the Nernst equation | 204 |
| Aetherometric treatment of the pH and pOH scales | 206 |
| The aetherometric pe- scale | 208 |
| Aetherometric cycles for the complete equilibrium dissociation of H2O and H2 | 211 |
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7. The fine structure, geometry and molecular dynamics of water |
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| Ambipolar radiation and the role of noncovalent bonds in water | 224 |
| The fine structure and geometry of the water molecule | 227 |
| Ambipolar resonances of water and rotational modes | 230 |
| Ambipolar energy, latent heat and "chemical energy" | 238 |
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8. Aether bioenergetics of capture, storage and metabolism |
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| Central metabolic role of ATP | 240 |
| The latent heat of ATP is responsible for its exergonic hydrolysis | 241 |
| Latent heat draw: reverse potential of energy flow and protein self-assembly | 242 |
| Oxygen, ambipolar radiation and the alpha/beta states of metabolism | 244 |
| The origin of eukaryotic cells and the role of oxygen | 246 |
| What is missing in the respiratory chain | 249 |
| Aetherometric model of the respiratory chain | 255 |
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Biological circuits of ordinary electricity and thermal or photobiological fields in the context of the new system dynamics |
262 |
| ATP-driven dark photosynthesis and futile metabolic cycles | 264 |
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Hemoglobin as a thermal radiator that converts captured ambipolar radiation (antenna function) |
266 |
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The universality of the protoporphyrin ring IX asX a biological ambipolar antenna and an electromagnetic pigment |
269 |
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9. The specificity of the living and biopoiesis of a double articulation:
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| The monist concept of desiring machines and their scopes | 271 |
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Micro and macro, molecular and molar, and the specificity of organic machines |
280 |
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Molecular event of the biological double articulation: cellular or precellular? |
289 |
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Is chromatin DNA an evolved clue to the biopoietic emergence of a system of RNA-protein articulation? |
291 |
| Thermal exhalpy and stability of living systems | 294 |
| The myth of mitogenic radiation | 297 |
| Aetherometric capture, conversion and emission functions of chromatin-DNA | 299 |
| Ambipolar radiation capture and thermal re-radiation by DNA | 302 |
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305 |
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REFERENCES |
310 |
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PLATES |
323 |
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INDEX |
413 |
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POSTSCRIPT: The untimely death of Dr. Eugene Mallove |
449 |