Quantum Trappings "Resonant Transmutation Of Metals In Human Blood" Part II

  

Kervran further applied his comprehensive findings to resolve many commonly misunderstood biomineral deficiencies in humans involving the biological transmutation of all essential elements as magnesium, calcium, manganese, iron, copper and zinc. In fact, it is known that calcium deficiency and resulting bone-depletion cannot be reversed by calcium intake. Calcium is now widely supplemented with magnesium, but the underlying mechanism can only be satisfactorily explained by resonant atomic transmutation. Hard evidence for fusion of magnesium and oxygen atoms is found in measurable Ca44 depletions in all bone.

An identical situation exists in dietary supplements manufactured for both iron and copper, which must be given together to achieve rebalancing of either essential element, as blood metabolism involves the resonant conversion of one element into the other.Similarly, available manganese is constantly being converted into iron in the blood to aid the rebalancing process during iron deficiency. Once again, this newly recognized substitution mechanism explains such enigmatic questions as why intestinal absorption of manganese increases during iron deficiency, and increased iron stores (ferritin levels) are associated with decreased manganese absorption.

Cellular respiration processes in all green-blooded organisms, including tunicate, ascidian, holothurian and sponge species, exhibit an alternate transmutation of iron that closely relates to that used by red- and blue-blooded species (vertebrates, cephalopods, gastropods and crustaceans). Fission of iron atoms forms vanadium and lithium in green blood while lithium combines with iron to form copper in red and blue blood. When one considers that constantly cycling cascades of nuclear reactions underlie the essential functions of all biological systems, acting as radiant biological holographic projectors, all previously inexplicable animal and plant behavior displaying group synchrony and coherent mass communication can be understood as nonlinear biophoton field coupling effects occurring within the range of visible light.

Researchers Widom, Srivastava and Sivasubramanian have redefined the well-established properties of biophotons as products of atomic nuclear reactions, drawing conclusions that parallel those established by Kervran in their 2011 paper, entitled 'Biological Nuclear Transmutations as a Source of Biophotons' :

We have shown that soft multi-photon radiation from hard higher energy reactions sources can be employed to describe the three major well-established properties of biophoton radiation. Since the soft photon frequencies span the visible to the ultraviolet frequency range, the hard reaction sources have energies extending into the nuclear transmutation regime. Thus, the biophotons serve as a valuable clue as to which biological systems exhibit a large number of nuclear transmutations.

Kervran's observations of human skin and sweat gland processes inspired laboratory experiments in 1959 that clearly demonstrated the low energy nuclear fusion of sodium and oxygen to form stable potassium, which contributes to the overall biophoton emissions observed of human skin surfaces. This surprising resonant atomic reaction was later replicated by ionizing sodium vapor in the presence of oxygen under spectrographic observation (Torii, Sakurazawa, Odagiri, 1963; Ohsawa, Kushi, 1964).

Recent investigations of the ultra-weak visible luminosity of the human body have applied direct biophoton detection by ultra-sensitive light-amplified CCD cameras that accurately record subtle diurnal fluctuations in the distribution patterns within human biophoton fields over time. The re-emission of absorbed photons observed in living cells is identified as 'delayed luminescence' in the hours after exposure. Multiple sources comprise the perpetual and spontaneous biophoton emissions of all cells. Biophysicist F.A. Popp and his research team have reported remarkable series' of images of the weak human glow during traditional acupuncture and moxibustion therapies (below), clearly revealing the left-right symmetry of the healthy body and biorhythmic cycles of 14 days, 1 month, 3 months and 9 months.

Popp's focus has narrowed to investigations of the nonlinear photon trapping of DNA as a coherent broadband visible light biocommunication system, emitted from within the chromatin in the nucleus of each cell. 

DNA base-molecules and surrounding cell walls act as quantum resonators, efficiently storing light by internal reflection of nonlinear standing waves. These findings inform a radical recharacterization of chromatin as an exciplex laser array, with DNA base pairs now recognized as 'excited complexes' that emit photon fields displaying constructive or deconstructive interference modes. 

Studies found that DNA conformation and skin conductivity directly correlate with biophoton emission intensity.

Areas of the human body that emit the greatest intensity of photons (seen above in yellow, red and white) correspond closely to the circulatory system. Along with the heart, large superficial veins and arteries present the greatest biophoton emission and highest electrical conductivity in the body. Blood is more saline than other bodily fluids, and full of iron-bearing hemoglobin, contributing to a conductivity that is higher than the rest of the body's systems, acting as an extension of the electromagnetic field of the beating heartby maintaining an electronically excited state exhibiting coherent oscillations :  

Monitoring of spontaneous and luminophore amplified photon emission (PE) from non-diluted human blood under resting conditions and artificially induced immune reaction revealed that blood is a continuous source of biophotons indicating that it persists in electronically excited state. This state is pumped through generation of electron excitation produced in reactive oxygen species (ROS) reactions. Excited state of blood and of neutrophil suspensions (primary sources of ROS in blood) is an oscillatory one suggesting of interaction between individual sources of electron excitation. Excited state of blood is extremely sensitive to the tiniest fluctuations of external photonic fields but resistant to temperature variations as reflected in hysteresis of PE in response to temperature variations. These data suggest that blood is a highly cooperative non-equilibrium and non-linear system, whose components unceasingly interact in time and space. At least in part this property is provided by the ability of blood to store energy of electron excitation that is produced in course of its own normal metabolism.

Oscillatory excitation of the electronic state of blood by ROS reactions coordinates enzymatic activities and enhances the absorption of dissolved gases by metal nanoparticles in the blood, especially chromium, manganese, iron, copper and zinc. Hemoglobin within red cells acts as a reducing agent that synthesizes iron nanoparticles in the 2-5 nm range for optimized binding with oxygen during circulatory transport.

Precision control of the blood pressure differentials of dissolved oxygen and lithium gases maintained between red cell membranes and the surrounding blood plasma is accomplished by temperature-dependent transport interactions with sodium and potassium cations. Kervran's elucidation of the electrically enhanced nuclear fusion of sodium and oxygen to form stable potassium occurs under the exact conditions that are constantly maintained in healthy blood, in conjunction with the fusion of iron and lithium atoms, forming stable copper and zinc atoms.

The indispensible role of oxygen and lithium gases in the resonant nuclear conversions of sodium into potassium and iron into copperdirectly implicates these specific reactions as primary mechanisms for blood's rebalancing of crucial metal concentrations, thus enabling effective utilization of a wider ratio of available metals to fulfill the well-known respiratory functions as well as the newly discovered biophotonic functions of blood medium.

This conclusion is directly supported by isotopic signature studies of trace metals in mammals and plants, which diverge significantly from the great abundance of dietary metal sources and those of all geological deposits.

Trace copper isotope ratios in human blood consistently present a Cu65 variation of +0.30% as compared with non-biological copper, being products of the resonant fusion of iron and lithium atoms.

Isotopic shifts of iron in human blood enable gender determinations of partial skeletal remains, with male blood presents Fe56depletions of -2.5% to -2.9%, suggesting heavier iron isotopes do not concentrate in the blood serum of females due to regular menstrual blood loss and the enhanced iron absorption that compensates for such periodic deficiency. This hypothesis is supported by findings that hemochromatosis, characterized by excess iron levels and heavy iron isotope concentrations, is alleviated by phlebotomy (the removal of blood). Such cumulative isotopic shifts that perpetually accumulate during blood recirculation implicate the atomic weight disparity as produced by hydrogen-dependent conversions of manganese into iron in watery blood plasma, a reaction previously observed and reported in seed germination studies.

The surprising conclusions established by Kervran's in vivo biological transmutation experiments have not been thoroughly followed-up by biophysicists despite the ever growing body of solid evidence for nuclear conversions occurring in all living organisms. The compelling case of biological transmutations informs the open questions of biophotonics by synthesis with the formulaic framework of phonon resonance developed by W. Lussage in 1965 and confirmed in microbial transmutation studies by J. Champion in 2001 :

Dimensional phonon resonance occurs when the space occupied by one isotope is exactly the same as that of another isotope in its rest state [i.e. 20°C]. This event can only occur under the following two conditions: the expansion of an isotope by heating, or the contraction of an isotope by cooling. Due to the natural characteristics of elemental properties, this event is extremely rare and one can only force the event under select conditions. To determine the phonon resonance of an isotope, it is necessary to apply the following formula:

Phonon resonance calculations reveal the elusive quantum dynamics of the lattice interactions that induce low energy nuclear reactions throughout the bodies of living organisms, as first identified by Kervran decades earlier. Such precise calculations for the exact atomic diameter of various isotopes was only recently enabled by the careful determination of exact atomic masses, densities and linear thermal expansion coefficients for all known isotopes- data that was not available during Kervran's discoveries of biological transmutations, and comprises undeniable evidence for his conclusions.

Phonon vibrations of the atomic lattice of 2-5nm iron nanoparticles in hemoglobin display a set of four oscillatory modes reflecting each of the four stable isotopes present (Fe54, Fe56, Fe57, Fe58), thereby allowing four distinct possibilities for precision tuning of the resonant nuclear reaction with lithium atoms. Comprising only 2.2% of the abundance of iron, Fe57 is the only iron isotope that resonates at a frequency corresponding to the atomic diameter of the target isotope Cu65 near room temperature.

Atomic data for each isotope applied in these calculations (in blue) was obtained from various updated sources, while the exact atomic mass figures are consistent with tables produced by the Secondary Ion Mass Spectrometer (SIMS) Laboratory of the GeoForschungsZentrum in Potsdam, Germany.

The resonant frequency of copper target isotope (Cu65) at the 20°C rest state is 43,639,033 Hz, according to its atomic diameter and thermal expansion coefficient. Iron starting isotope (Fe57) matches this atomic diameter while resonating at the target frequency of 43,639,033 Hz during precision heating to 37.9°C :

Healthy blood circulating within the human body maintains temperature near 37.9°C, slightly elevated above the average core body temperature of 37.0°C. This significant variance of blood from mean human body temperature induces rhythmic thermal fluctuations in blood cells according to their cyclical transport from the warm heart to the slightly cooler extremities and skin capillaries. Fusion of iron and lithium atoms at 37.9°C resonance with Cu65 is the only viable explanation for observed isotope shifts.

Fe56 depletion in male blood likewise results from the fusion of manganese and hydrogen atoms to form iron at the resonant frequency of iron target isotope (Fe58) at rest state: 43,408,450 Hz. Manganese starting isotope (Mn55) resonates at this exact phonon frequency during precision heating to 37.6°C :

Further studies of isotope variations in trace elements of the human body will identify specific contributors to exciplex photon cascades observed as biophotons. The wide variety of metals present in healthy human blood and their respective concentrations endow the fluid medium with complex resonant characteristics only now being recognized as phonon resonance dynamics of the metal crystal lattice. Absorbance of dietary cobalt and its uptake by red blood cells has been studied in detail, while findings presented herein are the first to apply phonon resonance principles that implicate the presence of cobalt in blood as a byproduct of continual resonant conversions of chromium atoms into nickel and iron.

The four stable isotopes comprising chromium nanoparticles (Cr50, Cr52, Cr53, Cr54) are in constant oscillation at four distinct frequency modes in atomic resonance within the crystal lattice. The low energy nuclear fusion reaction of chromium and lithium atoms to form nickel, iron and cobalt is optimized at the resonant frequency of nickel target isotope (Ni62) at rest state: 44,246,564 Hz. Chromium starting isotope (Cr50) resonates at this exact phonon frequency during precision heating to 37.8°C :

The previously discussed hydrogen-dependent fusion reaction of manganese into iron is closely mirrored by the hydrogen-dependent fission reaction of manganese into chromium which takes place under exactly the same conditions present in the human bloodstream, according to frequency matching by Mn55 and Cr53.

The low energy fission of manganese and hydrogen atoms to form chromium and vanadium is optimized at the resonant frequency of chromium target isotope (Cr53) at rest state: 43,407,276 Hz. Manganese starting isotope (Mn55) resonates at this exact phonon frequency during precision heating to 38.1°C :

As with transmutations of Mn into Fe and Fe into Cu, conversion of Mn into Cr, V and Cr into Ni, Fe, Co occurs within the same very narrow temperature band, revealing a profound synchronicity in the isotopic phonon relationships. Upon confirmation of these findings, one must inevitably conclude that the innate phonon resonance relationships of stable isotopes in adjacent element groups fulfill the primary purpose of providing all living systems with resonant temperature ranges for generating nuclear reaction cascades.

Resonant nuclear interactions of matter form the basis of life throughout the vast reaches of the cosmos, and warm-blooded beings similar to mammals on Earth likely inhabit innumerable galaxies by exploiting tuned nuclear reactions releasing photon cascades by multiple resonant metal conversions near 37.9°C :

This unmistakable pattern of phonon resonance conversions demonstrated between the predominant metals of human blood directly reveals the primary fundamental principle within the universal isotopic architecture of all matter that enables all living organisms to maintain excited states for coherent electro-photonic field communication. These remarkable conclusions offer the only comprehensive explanation for the observed natural isotopic order and the precision temperature regulation of living organisms.