Method and apparatus for electromagnetically restructuring ingestible substances for organismic consumption

Information

  • Patent Grant
  • 6733434
  • Patent Number
    6,733,434
  • Date Filed
    Monday, December 10, 2001
    23 years ago
  • Date Issued
    Tuesday, May 11, 2004
    20 years ago
  • Inventors
  • Examiners
    • Lacyk; John P.
    Agents
    • Kilpatrick Stockton LLP
    • Calkins; Charles W.
    • Rothschild; Cynthia B.
Abstract
A method for beneficially restructuring ingestible substances such as sports drinks, water, neutraceuticals, pharmaceuticals, and the like and its contents for consumption by organisms. The method is also applied to topical substances such as lotions and creams. The method involves subjecting such substances for a period of time to an electromagnetic field of a specified flux density varying from 10−5 to 10−21 gauss and a specific frequency varying from 0 hertz to 300 hertz, depending on the intended subsequent use of the substance. The specific flux density and the specific frequency is empirically determined to restructure the substances such that the substances beneficially affect the organism which has the substances incorporated into the organism's metabolism.
Description




TECHNICAL FIELD




This invention relates to applying electromagnetic energy to water and other substances such as beverages, foods, neutraceuticals, pharmaceuticals, and the like (substances which are ingested or ingestible) in order to beneficially restructure such substances for consumption by organisms. More particularly, such substances are subjected to specific electromagnetic flux densities and frequencies of electromagnetic radiation in order to beneficially restructure the substance and/or its contents.




BACKGROUND OF THE INVENTION




In order to treat disease, organisms have previously been subjected to electromagnetic fields of various types, and a number of procedures involving the use of magnetic fields to treat disease have been described in various references. For example, U.S. Pat. No. 4,323,056 discloses numerous prior art patents and publications describing the use of electromagnetic materials and electromagnetic fields, e.g., lasers, microwaves and radio frequency (“RF”) induced magnetic fields, in the therapeutic treatment of mammals suffering from various disease conditions. These patents and publications typically teach ingestion of magnetic materials, for example, iron oxide, in patients in conjunction with the application of a magnetic force. Ferromagnetic particles become heated as a result of the coupling thereof to the magnetic field through their dielectric and hysteresis loss, the induced heating constituting the therapeutic properties of this form of treatment.




It is believed that these prior art processes were not successful for a number of reasons. The magnetic form of iron oxide is insoluble in body fluids and in substantial concentrations may be toxic to, or rejected by, the body. In addition, in many instances the amount of heat generated by these particles was excessive and substantial unwanted injury to tissue was experienced.




Devices for applying electromagnetic energy to living tissue are also disclosed, for example, in U.S. Pat. No. 2,099,511, to Caesar; U.S. Pat. No. 2,103,440, to Weissenberg; and U.S. Pat. No. 781,448 to McIntyre. Caesar teaches applying an alternating magnetic field to a localized area, and it is also believed to rely primarily on localized heating (diathermy). Weissenberg teaches application of a low level field, and McIntyre teaches means ostensibly applying a homogeneous field to the whole body of a plant or animal, for therapeutic reasons. These patents demonstrate the interest in application of electromagnetic energy to plants and animals for therapeutic reasons, but do not teach any particular means for determining a field strength or frequency that will have any particular beneficial effects.




In connection with accelerating healing of traumatic injuries, U.S. Pat. Nos. 4,611,599 and 4,576,172, both to Bentall, U.S. Pat. No. 3,890,953 to Kraus et al., and U.S. Pat. No. 3,738,369 to Adams et al., induce particular fields for purposes of promoting growth of damaged tissue. The prior art includes a wide range of field strengths and frequencies, Bentall teaching RF frequencies and Kraus teaching power line frequencies.




In addition, U.S. Pat. No. 5,269,746, to Jacobson, the present inventor, teaches a method of therapeutically treating epilepsy and Parkinson's disease which comprises subjecting mammals suffering from these diseases to an alternating magnetic field having flux density and a frequency calculated as a function of the mass of the oncogene, target gene, messenger RNA, protein, enzyme and/or hormone. This calculation equates the energy of a current electromagnetically induced in the mammal with the gravitational energy of the target genetic material, such that a dual resonance is achieved.




Although these references may disclose certain beneficial effects of electromagnetism on organisms, they do not disclose a process whereby water, beverages, foods, neutraceuticals, pharmaceuticals, topical creams and lotions, and the like, are themselves treated with an electromagnetic field in order to beneficially restructure the substances or contents thereof. For purposes of this disclosure, such substances shall hereafter be referred to as “ingestible substances” and it is intended that such term encompass any substance which is beneficially ingested or ingestible, or topically applied to or by a living organism such as a human being, etc. such that the living organism incorporates the substance into its metabolic processes. The substances provide a life support function such as that of water, nutritional function such as food, electrolyte balancing or rehydration such as pedialyte or other beneficial therapeutic function such as neutraceuticals, pharmaceuticals, creams, lotions and the like. As noted, although the term “ingestible” is used, it encompasses absorbed or topically applied substances as skin cream and the like which are not typically ingested as food or drink but absorbed through application on the skin. Methods and devices for beneficially restructuring such substances are therefore needed, and are provided by the present invention.




SUMMARY OF THE INVENTION




According to the present invention, means are provided for calculating the flux densities and frequencies appropriate for restructuring ingestible substances and their contents, by tailoring the flux density and frequency applied to the ingestible substances for a given purpose. After determining the correct flux density and frequency to be applied to the ingestible substances for a particular application, a homogeneous electromagnetic field is applied to the ingestible substance at the prescribed levels thereby inducing changes in the physical properties of the ingestible substance.




Ingestible substances which have been subjected to Jacobson Resonance (also referred to as “restructured”, “resonated” or “organized” ingestible substances) is more quickly absorbed and has improved solvency properties; i.e., it is able to resonate with more soluble matter. Therefore, restructured ingestible substances will improve the health of humans and animals through resonance derived of improved organization. The restructured ingestible substance, in particular, in the case of water will enhance the growth of fruits, vegetables, and plants in general.




Magnetization of water solvents in ingestible substances will improve the detergent capability of organisms by improving reactivity and capacity for interactivity with more soluble matter. The beneficial properties of organized ingestible substances will therefore be seen when the ingestible substance is utilized for bathing, cooking, cleaning, drinking, agriculture, medicine, veterinary medicine, cosmetics, and other applications. It is important to appreciate that in the case of such ingestible substances, a large component thereof is often water. The benefits of resonated water have been explained in co-pending parent application Ser. No. 09/386,696. It has been unexpectedly discovered that such benefits can be imparted to ingestible substances as discussed and defined herein.




The present invention, therefore provides for electromagnetic treatment of water, more preferably substances containing water (natural, spring or otherwise), with Jacobson Resonance in order to render the ingestible substance more conducive to organismic life by restructuring and clustering molecules, both water and otherwise, within the ingestible substance, thereby increasing the absorption rates, biological coherence, and cooperativity of the ingestible substance to the solute within the ingestible substance. The present invention generally includes subjecting ingestible substances to alternating and steady magnetic fields having flux densities ranging from 10


−5


gauss to 10


−21


gauss, and frequencies ranging from direct current (“DC” or 0 hertz) to 300 hertz.




The present invention also provides an apparatus for applying magnetic fields of the type described above to ingestible substances. The apparatus, referred to as the “Jacobson Resonator” or the “Resonator”, is comprised of a signal generator, attenuator unit, a set of simplified Helmholtz coils, and an application device on which the ingestible substance to be treated is placed.











BRIEF DESCRIPTION OF THE DRAWINGS





FIG. 1

shows a water molecule's angular structure.





FIG. 2

shows water states in living systems.





FIG. 3

shows the dynamic solution of the tessellation by regular pentagons: α β an δ are possible distortions of the five fold symmetry, thus becoming non-regular units. With δ the five fold symmetry is kept.





FIG. 4

shows the proper tessellation on the plain sheet by non-regular pentagons.





FIG. 5

shows the peculiar structure of water as a quasi-crystalline polymeric structure: wherein the molecules are permanent dipoles which join labily creating a network of hydrogen bonds.





FIG. 6

illustrates that a water molecule, including water in ingestible substances, joins another four forming a constantly changing short lived polymeric highly cooperative structure. Additionally, it shows that polarity makes water molecules cluster around ions. Polar molecules are therefore also hydrophile and hydrosoluble.





FIG. 7

illustrates hydrophobic interactions linking molecules.





FIG. 8

illustrates a solenoidal system magnetizing water molecules, preparing the structured water in ingestible substances for human consumption.





FIG. 9

is a diagram of the effect of the field on the motion of water.





FIG. 10

is a perspective view of the support stand and application device of the Jacobson resonator.





FIG. 11

is a schematic of the basic circuit of the Jacobson resonator.











DETAILED DISCUSSION OF THE INVENTION




The method of the present invention provides for electromagnetic treatment of ingestible substances, with Jacobson Resonance in order to render the ingestible substance more conducive to organismic life by restructuring and clustering molecules within the ingestible substance, thereby increasing the absorption rates, biological coherence, and cooperativity of the ingestible substance to the solute within the ingestible substance. The method generally includes resonation of ingestible substances at various flux densities and frequencies depending upon the use which will subsequently be made of the resonated ingestible substance. After resonation, the ingestible substance is thereafter applied to, or consumed by, organisms to treat disease and promote health of animal organisms and, in the case of water, for example, containing plant nutrients, is also beneficial in enhancing the growth of plants, particularly fruits and vegetables.




According to the present invention, ingestible substances are subjected to alternating and steady magnetic fields having flux densities ranging from 10


−5


gauss to 10


−21


gauss, and frequencies ranging from direct current (“DC” or 0 hertz) to 300 hertz. These magnetic fields recrystallize water molecules, which are constituents, particularly those water molecules with trace metals critical to the regulation of genetic information transfer. Other constituents of the ingestible substances are also believed beneficially affected, as in the case with water, particularly those with the trace metals critical to the regulation of genetic information transfer.




The invention may utilize various protocols in order to mechanically vibrate targets such as whole viruses, parts of viruses (such as the gp 120 envelope of HIV which juts into a CD4 receptor site of T-4 lymphocytes), bacterium, fungi, and other pathogens and foreign bodies. The method of the present invention impinges certain resonant frequencies upon water and other molecules in ingestible substances which are restructured and will send electromagnetic messages to macromolecules like enzymes which then change their vibrational states. The size of the seed, plant, fetus, animal and adult to which the restructured ingestible substances are applied or which are to consume the ingestible substances, changes the requirements for the signal at which the ingestible substances are resonated. After an ingestible substance is restructured, the restructured ingestible substance is subsequently supplied to an organismic system for which the ingestible substance was prepared.




An organismic system may be generally described as an aqueous solution in which water is mostly well ordered, nearly crystalline (or semi-crystalline). A polarized multi-layer of water was described which can be considered to be in a quasi-crystalline state. Relative order formed “dilute salted water” in the system has entirely different mechanical, chemical, physical behaviors than the normal aqueous solutions. The important role in the living systems of “ordered water” was pointed out in the mid-1960's and was later proved.




At first, it was suggested that ordered water was as much as 50% of the total amount of water in living bodies, but systematic investigations approximated more ordered water than was expected before. One expert, for example, has suggested that at least 95% of the cell water is bonded to fully extended proteins. In other organismic systems, 75% of the cell water was found to be bonded to fully extended proteins.




Current theories teach the conventional membrane-pump model of interaction between water and cells. Pursuant to this model, the bulk of the cell water is normal liquid water, and there is little or no interaction between the bulk-phase water and cell macromolecules. It is believed that this theory is incorrect. The more accurate theory is the association-induction model proposed by Dr. G. Ling, in which the bulk-phase water in living cells exists as polarized multilayers, interacting strongly and pervasively with intracellular macromolecules; i.e., extended proteins. Of course, it is expected that a more refined polarized-multilayer theory may be developed because there is still a lack of quantitative knowledge about the structural properties of the water molecule (e.g.; the radial distribution function and the space-time correlation function). Dr. Ling's association induction hypothesis is not yet sufficiently detailed to permit a calculation of the Nuclear Magnetic Resonance (“NMR”) relaxation times, as well as diffusive properties of cellular water. However, there is sufficient data about the diffusive motion of water molecules in biological systems to make two general qualitative statements: (1) within a cell, the amount of water experiencing reduced diffusive motion is substantial; and (2) the rotational motion of the majority of water molecules in a cell is reduced significantly from that of ordinary water. These principles are consistent with the present invention which is based on the interaction between water, other constituents of ingestible substances and solids within the organismic system which is treated by the restructured ingestible substance. By beneficially restructuring the ingestible substance that is supplied to the organismic system, the organismic system is beneficially affected.




It should be evident, therefore, that the present invention takes advantage of the physical properties of ingestible substances as including solvents and constituents thereof which are subject to change when macromolecular structure and/or motion is altered. These changes arise from intrinsic reorientations of biomolecular systems which are secondary to underpinning electromagnetic dispositional states and extrinsic changes in electromagnetic fields. The relationship of matter contained in the cells and the electromagnetic field to which the ingestible substances are is subjected is called superradiance.




Biological systems are held together by long range forces, namely electromagnetic forces in the ground state, i.e., the minimum energy configuration. Coulomb forces are short range forces and cannot account for the order of biosystems. Therefore, static forces acting at short distances are key-lock in type, and cannot account for the property of rigidity in matter, or account for communications in biological matter.




Body interactions are therefore not just the sum of the number of body interactions. Photons are emitted or absorbed during transition of energy states of atoms. When there are many particles in the unit volume super-radiance is the quantum result without any classical analog. Spontaneous fluctuations in atoms induce force fluctuations in other atoms which refer to phase coherence in the ground state. Photons are a commonwealth and cannot be traced back to any particular atom. Rather, photons are convicted and energy is lost. Although photon frequency decreases, photon momentum is unchanged. Photons are thus not radiated. Fields beyond a density threshold are trapped in biological matter. Photons with definite oscillations are shared among many particles. Thus, all the particles are compelled to oscillate according to the phase of the photons. The foregoing occurs as the particles of a gas move closer together.




The sides of coherence domains are the wavelengths of photons. According to the formulas:









(
wavelength
)


λ

=


h
mv

=





mc
2

·
t

mv






and





f

=


mc
2

mvl




,










ƒ decreases as l increases, that is the photons are shared by greater numbers of particles. Momentum remains the same. Energy is therefore given off as the electromagnetic field assumes a minimum energy configuration, and the photons serve as glue for the condensed system.




When the biosystem changes, photons are emitted resulting, for example, in bioluminescence. The gain of energy is proportional to density. Particles stop collapsing only when they meet the repulsive hard core forces i.e., the impenetrability of matter. The only task of this field is to keep the particles in phase without producing any work. Thus, the second principle of thermodynamics is not violated and spontaneous creation of order in the ground state occurs. Congruent and coherent oscillatory trajectories or vibrational states whether rotational and/or translational are shared by aggregations, groups, strings, or clusters of molecules e.g., water which produce the ordering and cooperativity of systems.




The earth rotates at approximately 1000 mi/hour and orbits the sun at 18.5 mi/sec and moves through the local star cluster toward the bright star Vega with the solar system at about 12 mi/sec. The local cluster of stars takes part in the rotation about the center of our galaxy at an average speed of 200 miles per second. Similarly, groups, collections, strings or polarized layers of water molecules maintain numerous frequencies of vibrational modes and relative motions simultaneously. Likewise, resonating water molecules with a variety of magnetic flux densities and frequencies will engender vibrational patterns or periodicity or clusters in sets or clusters of molecules that can be retained for some time only to interact with macromolecular complexes once ingested into a biological system as the solvent relates and communicates with solute particles thus inducing phase coherence and adjustments of electrophysiological states and biochemistry. The force between particles in a liquid or solid (condensed matter) depends upon how many particles share a common phase. Because it represents an atypical coherence domain in ingestible substances, the force between particles is directly proportional to the number of molecules as compared to the force in vacuo, where there is only a small force between a small number of molecules.




In vacuo, the dominant force is the static force, and in condensed systems the dominant force is the radiated force. Moving from the gaseous state to the liquid state the density of water is 1600 times greater, thus increasing the force between molecules accordingly. In renormalizing frequency electromagnetic field is trapped in the ground state while (mv) remains the same. When momentum (mv) is renormalized the trapped light will come out e.g., bioluminescence. Light will be emitted by biosystems (e.g. sono-luminescence) when sound waves are produced in the system. From the antinode of the stationary wave light is emitted. The frequency of the emitted light depends upon the liquid. Each liquid has its own frequency. Biosystems have many frequencies contained by the solvent. Collapsing bubbles affect temperature (a diabatic compression) in applying van der Waals equation, p molecules are excited and light is emitted.




Yet, carbonation is not the only explanation of sonoluminesence. Thousands of particles firing their photons synchronously into a short time interval in coherence domains accounts for light being emitted from a pressure wave, i.e., sound. Trapped light of superradiance is explicable through an understanding of aggregations of molecules maintaining phase coherence. Various frequencies in water and other ingestible substances with multi-polarized layers refer to collective processes. In liquids it is the electrons which move coherently. Electrons compel nuclei to stay at fixed distances, but not a fixed place in water or other ingestible substances. Solids appear when we get superradiance of nuclei.




Consider for example, two foreign molecules A and B entering into water or other ingestible substances from outside the system. In the spectra of A and B, there are frequencies W


A


and W


B


which are equal and equal to the common superradiance of water (renormalized frequency). Since the field depends upon frequency and since these molecules contain the code of recognition of frequency these molecules are not distinguishable from water. Frequency is the natural language of the molecules. The two body attraction is magnified by the larger number of particles as the water attraction in pure water or water as a constituent of ingestible substances. The attraction between A and B while in water or other ingestible substance is highly magnified. When a third molecule C is introduced into the water or ingestible substance which is unable to co-resonate with water or ingestible substance and its constituents, C does not have in its own spectrum or frequency propensity for recognition of the pattern. A and B will interact strongly while in the water or ingestible substance and not C. The chemical pattern in this way is governed by the superradiant behavior of the solvent, which is able through this mechanism to select interacting molecules on the basis of pattern recognition which is the code of frequency.




Consider, however, 3 molecules A, B and C, each one having 2 possible frequencies in their spectra. If that water has now 2 superradiances and WA=WB, A and B will interact strongly and not C. Without touching A, B and C the superradiance of water or the ingestible substance can change for example, if in this case, the equality changes between B and C and not A then WB=WC. Thus, the chemistry would suddenly change. B and C would attract strongly, and A would not attract.




In this example, A, B and C did not change at all. Rather, the water or ingestible substance changed. Since we can affect the properties of the solvent without touching the solute we can dramatically change the chemistry of the solute just by changing the frequency at which super-radiance could occur. In biosystems we have ordered patterns of reactions and we can regulate these reactions by restructuring water with magnetic signals having physiologic amplitudes and frequencies for water or the ingestible substance, the selection at each given time of which molecules will interact strongly controls cooperating of systems.




When there is disease the order of biochemical maturity is altered. It is possible to reorder the pattern by introducing resonated water with codes for frequencies to restore the proper biochemistry to the biosystem. Or, in the case of giving resonated water or water containing plant nutrient to plants we may regulate the various processes that regulate growth and repair. Furthermore, in this manner of giving resonated or restructured ingestible substances such as electrolyte drinks, such as pedialyte, water and the like to biosystems we may even regulate genetic information transfer as well as the susceptibility of an organism to foreign interaction, e.g., alter the immune responses. When biological systems are poisoned, cavities increase and more light is lost.




In order to understand the present invention, one may envision a living system as an aggregation of atoms which share ubiquitous photons (quanta of light) which serve as the “glue of matter”. These photons are bound in the ground state where they will remain due to the long range force of matter. Since living systems are composed of coherent charged states and cooperative systems, restructuring the solvent, namely the water, in the living systems changes the molecular vibrational frequencies of the living system itself.




It is possible to regulate the structure of ingestible substances and thereby induce critical molecules like genes, enzymes, neurotransmitters, antibodies and hormones to restructure by changing the spin angular momenta of electrons and protons with externally sourced pico Tesla range, physiologic fields. When pathophysiological states occur, there are biophotonic emissions, or the release of the radiant quanta which regulated coherence and communications. If water within cells and in tissues is organized, then the organization of water is sensitive to the physiological and pathophysiological states of cells and tissues. When ingestible substances, in particular ingestible substances with water as a constituent, are treated with electromagnetic fields corresponding to normal magnetic profiles in humans, animals and plants and ingested by these systems, there occurs systemic reorganization of superradiances: frequencies of vibrational modes through which constituents communicate to improve total function of the living system. Therefore, the consumed ingestible substance affects the solutes which it comes into contact with and vice versa. The effect is therefore multidirectional—water affecting solids and solids affecting the water. Additionally, human tissue is piezoelectric, that is mechanical vibrations are converted into electromagnetic oscillations and vice versa. Therefore, vibrational modalities of molecules of water, as well as macromolecular systems, will enhance mutual coherence domains so all the constituents of the system will be correlated as they come into contact with each other.




Consumption of organized or coherent water or ingestible substance molecules will reorganize the particles of the solute (critical molecules) to produce increase in coherence domains, improved communications between the various atomic constituents of living systems and improve health. Consumption of electromagnetically treated water therefore improves health as these ingestible substance molecules, including water molecules, take their places as solvent in the living systems.




The living process involves the gradual loss of the electron energy of incoming compounds (nutriments, foods) by a multi-step oxidation having very little energy changes in a single step. The typical metabolic energy-step is in the range of the hydrogen-bridge bond. Consequently, it is possible to rearrange the ingestible substance structure.




Water alone or as a constituent of ingestible substances is an excellent solvent, a catalyst for many chemical reactions, a good storehouse for both heat and cold, and a poor electrical conductor when pure. The unique properties of water and water in ingestible substances are based on its unusual structure and on the polarity of its molecule. Adding ions to water, for example, or constituents of ingestible substances, typically as trace metals adds to the capacity for reactivity. The water molecule's angular structure is shown in FIG.


1


. The hydrogen atoms are about 1 angstrom unit away from the oxygen atom, bound to it by covalent bonds. Each covalent bond is due to the mutual sharing of a pair of electrons between each hydrogen and the oxygen. However, the sharing is unequal because an oxygen atom is considerably more electronegative than a hydrogen atom. The oxygen atom is able to pull both electron pairs much closer to it. The oxygen has a partial positive charge. Although the water molecule as a whole is electrically neutral, it is highly polar: that is, it has a negatively charged pole (at the oxygen atom) and a positively charge pole (centered between the hydrogens). The polarity results from the bent shape of the molecule and the distribution of electrical charges within it.





FIG. 2

represents water states in living systems. It also shows geometrical frustration in three dimensions, where (a) breathing like, and (b) tilting like, changes the icosahedral cluster. Note that we may change the physical properties, for example the dielectric constant, of a material; e.g., water, without changing the composition (only the microscopic ordering) of the medium itself.





FIG. 3

shows the dynamic solution of the tessellation by regular pentagons: ∝ β and γ are possible distortions of the five-fold symmetry, thus becoming non-regular units. With γ the regular five-fold symmetry is kept; the geometric frustration causes the units to vibrate (if these units are composed of water, the hydrogen bridges will vibrate).





FIG. 4

shows the proper tessellation on the plain sheet by non-regular pentagons. Ordered states of water reveal coherence in the domains of the quantum world as subatomic particles move in relative translational and rotation modes which are dependent upon the elementary electrical charges which comprise the electromagnetic field—matter.




The solid and aqueous phases of the cytoplasm are the meeting point between biochemistry and biophysics. Water, which includes free water in the cytoplasm, has a peculiar structure, a quasi-crystalline polymeric structure: all its molecules are permanent dipoles which join labily creating a network of hydrogen bonds.

FIGS. 5 and 6

show that at 37° C. every water molecule joins another four forming a constantly changing short lived polymeric highly cooperative structure.




Although hydrogen bonds continuously form and disrupt, they give the ‘water polymer’ a high level of cohesion, which in turn displays certain characteristics—such as high surface tension, high specific heat, and high vaporization heat. Water has a high dielectric constant (E−80 at 20° C.) which is correlated to the refraction index and to a high absorption of infrared and microwaves. In ice, which is highly structured water, the dielectric constant is extremely low (E=5).




Water is a statistic assembly of five types of molecules which form 0, 1, 2, 3, or 4 hydrogen bonds per molecule. In this model the hydrogen bonds form and then disrupt and bending must be considered.




Theories on the structure of water postulate the existence of molecular clusters or aggregates. This hypothesis is consistent with the dielectric behavior, which is property pertaining to molecular clusters rather than to single molecules. H


2


O molecules connected by hydrogen bonds aggregate in clusters which have an extremely short mean life (10


−10


-10


−11


sec.).




Polarity makes water molecules cluster around ions (Na


+


and CI





) and other polar molecules (—COOH) and establish hydrogen bonds with them. Polar molecules are therefore also hydrophile and hydrosoluble (FIG.


6


). Apolar molecules break the network of hydrogen bonds, they are hydrophobic and insoluble. They tend to isolate themselves from surrounding water by forming hydrophobic interactions which play a very important functional role.




As well as reacting with ionizing radiation (forming radicals and peroxides), water interacts with non ionizing radiation to produce various conformational changes which are determined by charge distribution, motions of aggregations of clusters of water molecules through space and time, and coherent communications between water and its contained ponderable bodies.




Water forces the hydrophobic groups to aggregate or cluster to minimize the disruptive effect they could have on the H bond network. When hydrophobic groups associate like this, it is often said they are aggregated by “hydrophobic bonds”.




As seen in

FIG. 7

, hydrophobic interactions can link molecules (hydrophobic bond). Two or more hydrophobic groups tend to isolate from surrounding water with its polymeric like structure. This mechanism is the possible cause of enzyme-enzyme and enzyme-filament interactions in the sheet of structured water adjacent to the solid state protein structures.




The traditional interpretation whereby intracellular water was seen to have the same characteristics as free water has been reviewed: several experiments prove that a large fraction of intracellular water has properties which differ from those of the pure liquid. Biophysically cytoplasm is considered a gel, consisting of a rich dynamic network of interconnected filaments that give the cytoplasm that stiffness and elasticity without hindering its fluid character.




The relationship between the filament structures of the cytoplasm and water have been studied. We see the cytoskeleton as a solid state dynamic reticulum with a very vast surface, estimated at about 70-90 billion sqnm per cell. Clegg was able to prove experimentally while using several techniques that the water surrounding the cytoskeleton is ordered; that is aligned with polar links on the surface of the proteins. Consequently this means that each cell has a very thin layer of ordered water extending over at least 3 nm from the billions sqnm of solid state surfaces.




We believe through a dipolar mechanism this water can be coupled to the coherent dynamics of the protein solid state, protecting it from thermal dissipation and thus creating favorable conditions for the protein filaments to carry signals.




Biophysicists currently view hyaloplasm (that is MT reticulum+water) as a highly ordered and structurally coherent reticulum of dynamic protein polymers which is closely connected to ordered water through a vast surface; it has a lower level of entropy and a lower dielectric constant compared to the free water far from the reticulum surface.




The biological importance of the juxtafilament structured water becomes apparent when considering the well based hypothesis that all metabolic activities take place on the surface or near the surface of cell ultrastructures, because this means that enzymes operate in a microenvironment which is different from a diluted aqueous solution.




Of the relaxation processes of excited atoms and molecules one must consider fluorescence, or radiative relaxation, which is quick de-excitation with emission of a photon whose energy is less than that of the incident radiation. Excited molecules can relax by means of a chemical reaction with other excited or non-excited molecules, yielding free radicals, biradicals or stable molecular products. Excited molecules can transfer their excitation energy to other molecules through non-radiative processes (excitons, conformational variations) as well. They can also de-excite in a non-radiative mode by internal conversion of excitation energy into mechanical or vibrational energy which is our goal in utilization of physiologic magnetic fields i.e., the production of stable, balance and hemostatic products and processes.




Living systems must be regarded as a unit, since their properties cannot be additively composed from the properties of its parts, and it is not possible to divide living systems into parts carrying the properties of the system. The living reactions are special processes which are cooperative, collective phenomenon expanded over the whole living unit (protein, cell, etc.) depending on the level of the interaction. The cooperativity in the living state is the essence of the phenomenon. Some synchronized effects characterize life (for example, the growth or the dividing of cells) which have to have a general controller in the system. Some cooperative mechanisms have been ascribed to the living state, e.g., chemical, solid-state electronic and ionic transfer, as well as fractional charge-transfer. These phenomenon have succeeded in explaining different special proteins (e.g., enzymes) or whole cells. As another example, ionic concentration (pK) has also been introduced governing and explaining the collectivity of some special process.




The first suggestion of a solid-state type electronic process in living systems as one of the possible collectivity in proteins and DNA was made by Szent-Gorgyi in 1941. An early calculation strongly suggested the existence of a conduction band in proteins. This was later proven experimentally by observing a semi-conductive behavior with a forbidden gap of 2-3 eV. The measured conductivity in wet proteins (there is no effect in dry proteins) supports this conclusion.




The protocol which the water (or other material to be realigned for ingestion into the body of a human, or, abrasion to the body of a human such as a material; e.g., cotton) must be exposed to electromagnetically is determined by the physiologic nature of the signal. That is, the field impinged upon the water molecule, ingestible substances, trace metal, foreign body; e.g., virus, clothing material, cosmic construction block, etc., should be that field which the target element in vivo must experience to maintain order, coherence, cooperativity and coherent oscillatory trajectories of particulate matter composing the body thereto.




The electromagnetic field, focusing upon the magnetic component of the signal may be created by a solenoid, helmholtz coil, plates, free flowing electrical current magnetic components, poloidal magnets, toroidal coils and any other means of producing a homogeneous, isotropic magnetic field to therein induce changes in spin angular momenta of leptons and baryons, thus causing changing magnetic moments, and crystalline restructuring. Since the atoms are spinning permanent magnets, they are susceptible to reorientation by extrinsically sourced magnetic forces. Solenoids and helmholtz coils, plates, poloidal magnets, toroids, free electrical currents all may produce the appropriate EM signals. A solenoidal exposure system or a helmholtz coil exposure system is acceptable to produce a homogeneous isotropic magnetic field to therein rearrange the water molecule, ingestible substances, and/or water and other specific constituents of the ingestible substance itself; i.e., the particles that comprise the atoms that may themselves participate in changing charge densities and cooperativity between changing systems or kinetic systems such as our universe.





FIG. 8

, for example, shows a solenoidal system magnetizing water molecules, preparing the structured water for human consumption. The levels of magnetization are provided in Tables 1, 2 and 3 below. The Jacobson Resonator, described in detail below, produces such an electromagnetic field, and it is preferred to use the Jacobson Resonator to create and control the electromagnetic fields to which the water is subjected.












TABLE 1











Critical molecules used in calculating the amplitude and frequency or






desired magnetic field.


















Intensity, B




Freq., F




Length, L*




Velocity, V


#









Critical Molecules




(Gauss)




(Hz)




(cm)




(cm/s)




















1




Spectrin, Brain Specific Fodrin




1.0 × 10


−5






0.15




ML




SS






2




Neurofilaments, L-70kb,




2.5 × 10


−6






71.0




ML




EO







Hemoglobin, MAP-70kd






3




Interferon, Leukotrines, Platelet




1.3 × 10


−6






36.0




ML




EO







Derived Growth Factor (PDGF)






4




Nerve Growth Factor (NGF),




9.97 × 10


−7







27.9




ML




EO







Kinesine






5




Motor Proteins




9.0 × 10


−7






25.2




ML




SC






6




Microtubule Associated Protein




8.25 × 10


−7







23.0




ML




SC







(MAP) 2a, 2b






7




Melatonin, Calmodulin, Spectrin,




7.0 × 10


−7






19.0




ML




SC







Brain Specific Fodrin






8




IgE




6.2 × 10


−7






17.4




ML




SC






9




Neurofilaments, Calmodulin




5.7 × 10


−7






16.0




ML




EO






10




IgG, Epinephrine




4.6 × 10


−7






12.8




ML




ER






11




Tubulin αβ dimer




3.4 × 10


−7






3.6




ML




SC






12




IgM (900KD), Dopamine,




2.7 × 10


−7






7.6




ML




SC







Norepinephrine, Homeoboxes






13




Neurofilaments L-70KD




2.1 × 10


−7






5.6




ML




SC






14




MAP, G-actin, Calcium ion,




1.75 × 10


−7







5.4




ML




SC







Microtubule, Tubulin globular







monomer






15




Potassium, Bone Growth Factor




1.5 × 10


−7






4.1




ML




SC







(BGF)






16




GAP, Homeoboxes, Iron




1.26 × 10


−7







3.5




ML




ER






17




Serotonin, Interferon, Platelet




9.0 × 10


−8






2.5




ML




SC







Derived Growth Factor (PDGF)






18




NGF




7.5 × 10


−8






2.1




ML




SC






19




Calmodulin, Profilin




5.0 × 10


−8






1.4




ML




SC






20




ATP




3.4 × 10


−8






0.952




ML




SS






21




Epinephrine, Serotonin




3.4 × 10


−8






0.952




HL




SS











Table 1: Magnetic field intensities (B) calculated from Eqn (1), and frequency (f) from Eqn (2) using the mass (m) of critically important molecules (total of 14 settings). Note B- and f- values with were calculated by the use of length (l) mice ML, and four different velocities (v): They are: EO earth orbital velocity, ER earth rotational velocity, SS solar system velocity, and SC local star velocity.












#


In calculating the magnetic field intensities and frequencies from Equation (1), four different velocities were used. They are Earth Orbital (EO), Solar system (SS), Earth Rotation (ER), Local Star Cluster (SC).










*All of the B- and f- values were calculated using length of mice (ML), except for enpinephrine and serotonin, which was calculated from the length of human (HL).

























TABLE 2










Intensity, B




Freq., F




Length, L*




Velocity, V


#








Critical Molecules




(Gauss)




(Hz)




(cm)




(cm/s)



























Motor protein




  9 × 10


−7






25.2




ML




SC






IgE




0.2 × 10


−7






17.4




ML




SC






Neurofilaments




2.1 × 10


−7






5.6




ML




SC






NGF




7.5 × 10


−8






2.1




ML




SC






Calmodulin, Profilin




  5 × 10


−8






1.4




ML




SC






ATP




3.4 × 10


−8






0.952




ML




SS






Epinephrine,




3.4 × 10


−8






0.952




ML




SS






Serotonin











Additional magnetic field intensities (B) calculated from Equation (1), and frequency (f) from Eqn (2) using mass (m) of critically important molecules (total of 20 settings when these 8 are added to 14 settings in Table 1). Note these B- and f-values were calculated with the use of length (l) of mice ML, length (height) of human HL, and two different velocities: They are: SC local star cluster velocity and SS solar system velocity.





















TABLE 3









Table For Humans























(Length = 1.7 × 10


2


cm)













Inertial




 3.22 × 10


7


cm/s




star cluster (SC)






Velocities:




 2.98 × 10


6


cm/s




earth orbital (EO)







4.642 × 10


4


cm/s




rotational earth (ER)






























B





target masses




target masses







(microgauss)




(Hertz)




in (daltons)




in (daltons)







FIELD




FREQUENCY




EO




SC




















0.001




0.028000001




339.321




3619.424







0.002




0.055000001




678.642




7238.848







0.003




0.084000002




1017.963




10858.272







0.004




0.112000002




1357.284




14477.696







0.005




0.140000030




1696.605




18067.120







0.006




0.168000003




2036.926




21716.544







0.007




0.196000004




2375.247




25335.968







0.008




0.224000004




2714.568




28955.392







0.009




0.252000005




3053.889




32574.816







0.010




0.280000006




3393.210




36194.240







0.011




0.308000006




3732.531




39813.664







0.012




0.336000007




4071.852




43433.088







0.013




0.640000070




4411.173




47052.512







0.014




0.392000008




4750.494




50871.936







0.015




0.420000008




5089.815




54291.360







0.016




0.448000009




5429.136




57910.784







0.017




0.478000010




5768.457




61530.208







0.018




0.504000010




6107.778




65149.632







0.019




0.532000011




6447.099




68769.058







0.020




0.560000011




6786.420




72388.480







0.021




0.588000012




7125.741




76007.904







0.022




0.618000012




7465.062




79627.328







0.023




0.644000013




7804.383




83246.752







0.024




0.372000013




8143.704




86866.176







0.025




0.700000014




8483.025




90485.600







0.026




0.728000015




8822.346




94105.240







0.027




0.756000015




9161.667




97724.448







0.028




0.854000016




9500.988




101343.872







0.029




0.812000016




9840.309




107963.296







0.030




0.840000017




10179.630




108582.720







0.031




0.868000017




10518.951




112202.144







0.032




0.896000018




10856.272




115821.568







0.033




0.924000018




11197.593




119440.992







0.034




0.952000019




11536.914




123060.416







0.035




0.980000020




11876.235




126679.840







0.036




1.008000020




12215.656




130299.264







0.037




1.036000021




12554.877




133918.888







0.038




1.064000021




12894.198




137538.112







0.039




1.092000022




13233.519




141157.538







0.040




1.120000022




13572.840




144776.960







0.041




1.148000023




13912.161




148396.384







0.042




1.176000024




14251.482




152015.808







0.043




1.204000024




15690.803




155835.232







0.044




1.232000025




14930.124




159254.658







0.045




1.260000025




15269.445




162874.080







0.046




1.288000026




15608.766




166493.504







0.047




1.316000026




15978.087




170112.928







0.048




1.344000027




16287.408




173732.352







0.049




1.372000027




16626.729




177351.776







0.050




1.400000028




16966.050




180971.200







0.051




1.428000029




17305.371




184590.624







0.052




1.456000029




17644.692




188210.048







0.053




1.484000030




17984.013




191829.472







0.054




1.512000030




18323.334




196448.896







0.055




1.640000031




18662.655




199068.320







0.056




1.568000031




19001.976




202687.744







0.057




1.596000032




19341.297




206307.168







0.058




1.624000032




19680.618




209926.592







0.059




1.652000033




20019.939




213546.016







0.060




1.680000034




20359.260




217165.440







0.061




1.708000034




20696.581




220784.864







0.062




1.736000035




21037.902




224404.288







0.063




1.764000035




21377.223




228023.712







0.064




1.792000036




21716.544




231643.163







0.065




1.820000036




22066.866




235262.560







0.066




1.848000037




22395.186




238881.984







0.067




1.876000038




22734.507




242501.408







0.068




1.904000038




23073.828




246120.832







0.069




1.932000039




23413.149




249740.256







0.070




1.960000039




23752.470




253359.680







0.071




1.988000040




24091.791




256979.104







0.072




2.016000040




24431.112




260598.528







0.073




2.044000041




24770.433




264217.952







0.074




2.072000041




25109.754




267837.376







0.075




2.100000042




25449.075




271456.800







0.076




2.128000043




25788.396




275076.224







0.077




2.156000043




26127.717




278695.648







0.078




2.184000044




26467.038




282315.072







0.079




2.212000044




26806.359




285934.496







0.080




2.240000045




27145.680




289553.920







0.081




2.268000045




27485.001




293173.344







0.082




2.296000046




27824.322




296792.768







0.083




2.324000046




28163.643




300412.192







0.084




2.352000047




28502.964




304031.616







0.085




2.380000028




28842.285




307651.040







0.086




2.408000048




29181.606




311270.464







0.087




2.436000049




29520.927




314889.888







0.088




2.464000049




29860.248




318509.312







0.089




2.492000050




30199.569




322128.736







0.090




2.520000050




30538.890




325748.160







0.091




2.548000051




30878.211




329367.584







0.092




2.576000052




31217.532




332987.008







0.093




2.604000052




31556.853




336606.432







0.094




2.632000053




31896.174




340225.856







0.095




2.660000053




32235.495




343845.280







0.096




2.688000054




32874.816




347464.704







0.097




2.716000054




32914.137




351084.128







0.098




2.744000055




33253.458




354703.552







0.099




2.722000055




33592.779




358322.976







0.100




2.800000056




33932.100




361942.400







0.101




2.828000057




34271.421




365561.824







0.102




2.856000057




34610.742




369181.248







0.103




2.884000058




34950.063




372800.672







0.104




2.912000058




35289.384




376420.096







0.105




2.940000059




35628.705




380039.520







0.106




2.968000059




35968.026




383658.944







0.107




2.996000060




36307.347




387278.368







0.108




3.024000060




38646.668




390897.792







0.109




3.052000061




36985.989




394517.216







0.110




3.080000062




37325.31




398136.640







0.111




3.108000062




37664.631




401756.064







0.112




3.136000063




38003.952




405375.488







0.113




3.164000083




38343.273




408994.912







0.114




3.192000064




38682.594




412614.336







0.115




3.220000064




39021.915




416233.760







0.116




3.248000065




39361.236




419853.184







0.117




3.276000066




39700.557




423472.608







0.118




3.304000066




40039.878




427092.032







0.119




3.332000067




40379.199




430711.456







0.120




3.360000067




40718.520




434330.880







0.121




3.388000068




41057.841




437950.304







0.122




3.416000068




41397.162




441589.728







0.123




3.444000069




41736.483




445189.152







0.124




3.472000069




42075.804




448808.576







0.125




3.500000070




42415.125




452428.000







0.126




3.528000071




42754.446




456047.424







0.127




3.556000071




43093.767




459666.848







0.128




3.584000072




43433.088




463286.272







0.129




3.612000072




43772.409




466905.696







0.130




3.640000073




44111.730




470525.100







0.131




3.668000073




44451.051




474144.544







0.132




3.696000074




44790.372




477763.968







0.133




3.724000074




45129.693




481383.392







0.134




3.752000076




45469.014




485002.816







0.135




3.780000076




45808.335




488622.240







0.136




3.808000076




46147.658




492241.664







0.137




3.936000077




46486.977




495861.088







0.138




3.864000077




46826.298




499480.512







0.139




3.892000078




47165.619




50309.936







0.140




3.920000078




47504.940




506719.360







0.141




3.948000079




47844.261




510338.784







0.142




3.976000080




48183.582




513958.208







0.143




4.004000080




48522.903




517577.632







0.144




4.032000081




48862.224




521197.056







0.145




4.060000810




49201.545




524816.480







0.146




4.088000082




49540.866




528435.904







0.147




4.116000082




49880.187




532055.328







0.148




4.144000083




50219.508




535674.752







0.149




4.172000083




50558.829




539294.176







0.150




4.200000084




50898.150




542913.600







0.151




4.228000085




51237.471




54633.024







0.152




4.258000085




51576.792




550152.448







0.153




4.284000086




51916.113




553771.872







0.154




4.312000086




52255.434




557391.296







0.155




4.340000087




52594.755




561010.720







0.156




4.368000087




52934.076




564630.144







0.157




4.396000088




53273.397




568249.568







0.158




4.424000088




53812.718




571868.992







0.159




4.452000089




53952.039




575488.416







0.160




4.480000090




54291.360




579107.840







0.161




4.508000090




54630.681




582727.264







0.162




4.536000091




54970.002




586346.688







0.163




4.564000091




55309.323




589966.112







0.164




4.592000092




55648.644




593585.536







0.165




4.620000092




55987.965




597204.960







0.166




4.648000093




56327.286




600824.384







0.167




4.676000094




56686.607




604443.808







0.168




4.704000094




57005.928




608063.232







0.169




4.732000095




57345.249




611682.858







0.170




4.760000095




57684.570




615302.080







0.171




4.788000096




58023.891




618921.504







0.172




4.816000096




58363.212




622540.928







0.173




4.844000097




58702.533




628160.352







0.174




4.872000097




59041.854




629779.776







0.175




4.900000098




59381.175




633399.2







0.176




4.928000099




59720.496




637018.624







0.177




4.856000099




60059.817




640838.048







0.178




4.984000100




60399.138




644257.472







0.179




5.012000100




60738.459




647876.896







0.180




5.040000101




61077.780




651496.320







0.181




5.068000101




61417.101




655115.744







0.182




5.096000102




61756.422




658735.168







0.183




5.124000102




62095.743




662354.592







0.184




5.152000103




62435.064




665974.016







0.185




5.180000104




52774.385




669593.440







0.186




5.208000104




63113.706




763212.864







0.187




5.236000105




63453.027




676832.288







0.188




5.264000105




63792.348




680451.712







0.189




5.292000106




64131.669




684071.136







0.190




5.320000106




64470.99




687690.560







0.191




5.348000107




64810.311




691309.984







0.192




5.376000108




65149.532




694929.408







0.193




5.404000108




65488.953




698548.832







0.194




5.432000109




65828.274




702168.256







0.195




5.460000109




66167.595




705787.68







0.196




5.488000110




66506.916




709407.104







0.197




5.516000110




66846.237




713026.528







0.198




5.544000111




67185.558




716645.952







0.199




5.572000111




67524.879




720265.376







0.200




5.600000112




67864.200




723884.800







0.201




5.628000113




68203.521




727504.224







0.202




5.656000113




68542.842




731123.648







0.203




5.684000114




68882.163




744743.072







0.204




5.712000114




69221.484




7.8362.496







0.205




5.740000115




69560.805




741981.920







0.206




5.768000115




69900.126




745801.344







0.207




5.796000116




70239.447




749220.768







0.208




5.824000116




70578.768




752840.192







0.209




5.852000117




70918.089




756459.616







0.210




5.880000118




71257.410




760079.040







0.211




5.908000118




71596.731




763698.464







0.212




5.936000119




71936.052




767317.888







0.213




5.964000119




72275.373




770937.312







0.214




5.992000120




72614.694




774556.738







0.215




6.020000120




72954.015




778178.160







0.216




6.048000121




73293.336




781795.584







0.217




6.076000122




73832.657




785415.008







0.218




6.104000122




73971.978




789034.432







0.219




6.132000123




74311.299




492653.856







0.220




6.160000123




74650.620




796372.280







0.221




6.188000124




74989.941




799892.704







0.222




6.216000124




75329.262




803512.128







0.223




6.244000125




75888.583




807161.552







0.224




6.272000125




76007.904




810750.976







0.225




6.300000126




76347.225




814370.400







0.226




6.328000127




76686.646




817989.824







0.227




6.356000127




77025.867




821609.248







0.228




6.384000128




77365.188




825228.672







0.229




6.412000128




77704.509




828848.096







0.230




6.440000129




78043.830




832467.520







0.231




6.468000129




78383.151




836086.944







0.232




6.496000130




78722.472




839706.368







0.233




6.524000130




79061.973




843325.792







0.234




6.552000131




79401.114




846945.206







0.235




6.580000132




79740.435




850564.640







0.236




6.608000132




80079.756




864184.064







0.237




6.636000133




80419.077




857803.488







0.238




6.684000133




80758.398




831422.912







0.239




6.692000134




81097.719




865042.336







0.240




6.720000134




81437.040




868661.760







0.241




6.748000135




81776.361




872281.184







0.242




6.776000136




82115.882




875900.608







0.243




6.804000136




82455.003




879520.032







0.244




6.832000137




82791.324




883139.456







0.245




6.860000137




93133.645




886759.880







0.246




6.888000138




83472.966




890378.304







0.247




6.916000138




83812.287




893997.728







0.248




6.944000139




84151.608




897617.152







0.249




6.972000139




84490.929




901236.576







0.250




7.000000140




84830.250




904856







0.251




7.028000141




95169.571




908475.424







0.252




7.055000141




85508.892




912094.848







0.253




7.084000142




85848.213




915714.272







0.254




7.112000142




86187.534




919333.696







0.255




7.140000143




86526.855




922953.120







0.256




7.168000143




86866.176




926572.544







0.257




7.196000144




87205.497




930191.968







0.258




7.224000144




87544.818




933811.392







0.259




7.252000145




87884.139




937430.816







0.260




7.280000146




88223.460




941050.240







0.261




7.308000146




88562.791




944668.664







0.262




7.336000147




88902.102




948289.088







0.263




7.364000147




89241.423




951908.512







0.264




7.392000148




89580.744




955527.936







0.265




7.420000148




89920.065




959147.360







0.266




7.448000149




90259.386




952766.784







0.267




7.476000150




90598.707




966386.208







0.268




7.504000150




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25.113000500




304370.937




3246823.328







0.898




25.144000500




304710.258




3260242.752







0.899




25.172000500




305049.579




3253862.176







0.900




25.200000500




305388.900




3257481.6







0.901




25.228000500




305728.221




3261101.024







0.902




25.256000510




206067.542




3264720.448







0.903




25.284000510




306406.863




3268339.872







0.904




25.312000510




306746.184




3271959.296







0.905




25.310000510




307085.505




3275578.720







0.906




25.368000510




307424.826




3279198.144







0.907




25.396000510




307764.147




3282817.568







0.908




25.424000510




308103.468




3286436.992







0.909




25.452000510




308442.789




3290056.416







0.910




25.480000510




308782.110




3293675.840







0.911




25.508000510




309121.431




3297295.264







0.912




25.536000510




309460.752




3300914.688







0.913




25.584000510




309800.073




3304534.112







0.914




25.592000510




310139.394




3308453.536







0.915




25.820000510




310478.715




3311772.960







0.916




25.648000510




310818.036




3315392.384







0.917




25.676000510




311157.357




3319011.808







0.918




25.704000510




311496.878




3322631.232







0.919




25.732000510




311835.999




3326250.656







0.920




25.780000520




312175.320




3329870.080







0.921




25.788000520




312514.641




3333489.504







0.922




25.816000520




312853.962




3337108.928







0.923




25.844000520




313193.283




3340728.352







0.924




25.872000520




313532.604




3344347.776







0.925




25.900000520




313871.925




3347967.200







0.926




25.928000520




314211.246




3351586.324







0.927




25.956000520




314550.567




3355206.048







0.928




25.984000520




314889.888




3358825.472







0.929




26.012000520




315229.209




3362444.896







0.930




26.040000520




315568.530




3366064.320







0.931




26.068000520




315907.851




3369683.744







0.932




26.096000520




316247.172




3373303.168







0.933




26.124000520




316586.493




3376922.592







0.934




26.152000520




316925.814




3380542.016







0.935




26.180000520




317265.135




3384161.440







0.936




26.208000520




317604.456




3387780.864







0.937




26.236000520




317943.777




3391400.288







0.938




26.264000530




318283.098




3395019.712







0.939




26.292000530




318622.419




3398639.136







0.940




26.320000530




318961.740




3402258.560







0.941




26.348000530




319301.061




3405877.984







0.942




26.376000530




319640.382




3409497.408







0.943




26.404000530




319979.703




3413116.832







0.944




26.432000530




320319.024




3416736.256







0.945




26.460000530




320658.345




3420355.680







0.946




26.488000530




320997.666




3423975.104







0.947




26.516000530




321336.987




3427594.528







0.948




26.544000530




321686.308




3431213.952







0.949




26.572000530




322015.629




3434833.376







0.950




26.600000530




322354.950




3438452.800







0.951




26.628000530




322694.271




3442072.224







0.952




26.656000530




323033.592




3445691.648







0.953




26.684000530




323372.913




3449344.072







0.954




26.712000530




323712.234




3452930.496







0.955




26.740000530




324051.555




3456549.920







0.956




26.768000540




324390.876




3460169.344







0.957




26.796000540




324730.197




3463788.768







0.958




26.824000540




325069.518




3467408.192







0.959




26.885200054




325408.839




3471027.616







0.960




26.880000540




325748.160




3474647.040







0.961




26.908000540




326087.481




3478268.464







0.962




26.936000540




326426.802




3481885.888







0.963




26.964000540




326766.123




3485505.312







0.964




29.992200054




327105.440




3489124.736







0.965




27.020000540




327444.765




3492744.160







0.966




27.048000540




327784.086




3496363.584







0.967




27.076000540




328123.407




3499983.008







0.968




27.104000540




328462.728




3503602.432







0.969




27.132000540




328802.049




3507221.856







0.970




27.160000540




329141.370




3510841.280







0.971




27.188000540




329480.691




3514460.704







0.972




27.216000540




329820.012




3518080.128







0.973




27.244000540




330159.333




3521699.552







0.974




27.272000550




330498.654




3525318.976







0.975




27.300000055




330837.975




3528938.400







0.976




27.328000550




331177.296




3532557.824







0.977




27.356000550




331516.617




3536177.248







0.978




27.384000550




331655.380




3539796.672







0.979




27.412000550




332195.259




3543416.096







0.980




27.440000550




332534.58




3547035.520







0.981




27.468000550




332873.901




3550654.944







0.982




27.496000550




333213.222




3557274.368







0.983




27.524000550




333552.543




3557893.732







0.984




27.552000550




333891.864




3561513.216







0.985




27.580000550




334231.185




3595132.640







0.986




27.608000550




334570.506




3568752.064







0.987




27.636000550




334909.827




3572371.488







0.988




27.66400055




335249.148




3575990.912







0.989




27.692000550




335588.469




3579610.336







0.990




27.720000550




335927.790




3683229.760







0.991




27.748000550




336267.111




3586849.184







0.992




27.776000560




336606.432




3590495.608







0.993




27.804000560




336945.753




3594088.032







0.994




27.832000560




337285.074




3597707.456







0.995




27.860000560




337624.395




3901326.880







0.996




27.888000560




337963.716




3604946.304







0.997




27.916000580




338303.037




3608568.728







0.998




27.944000560




338642.358




3612185.152







0.999




27.972000560




338981.679




3615804.586







1.000




28.000000560




339321.000




3619424.000







1.001




28.02800056




339660.321




3623043.424







1.002




28.056000560




339999.642




3626662.848







1.003




28.084000560




340338.963




3630282.272







1.004




28.11200056




340676.284




363391.696







1.005





341017.605




3637521.120







1.006






3641140.544







1.007






3644759.968







1.008






3648379.392







1.009






3651998.816















The (L) length used is 5′8″ average human length. This table is used to calculate the appropriate signed parameters for water to treat any condition dependent upon critical molecules of specific molecular weights in accordance with earth orbital velocity, earth's rotational velocity and the star cluster velocity we are in which circles the center of the Milky Way Galaxy.




Applying the principles above, the present invention provides a method which imposes an electromagnetic field upon water and liquid suspensions at least in the water or ingestible substances. The most beneficial flux densities and frequencies may be determined empirically by experimentation. However, more preferably, a flux density and frequency may be calculated using the formula mc


2


=Bvlq. In this formula, “m” equals a mass of one of a plurality of targets, e.g., water molecules; “c” equals the speed of light; “v” equals the inertial velocity of the target mass, “l” equals length of the conductive system; and “q” equals unity of charge. Using this equation, it is possible to determine a magnetic flux density (B). The flux density and frequency is then applied to a quantity of water for a given period of time. After the water has been restructured, it may be applied to an organism or the water may be subjected to any number of additional magnetic fields based on different targets before the water is applied to the organism. Or, the water may be applied to usage in a cosmetic, construction building block . . . etc.




The target masses in biosystems include masses such as oncogenes, homeotic genes, enzymes, hormones, peptide hormone trophic factors, cytokines, interleukins, GAP proteins and centrioles. Additionally, masses of regulatory nature, such as interferon, enzymes and viruses, may also be targeted, as may trace metals such as Ca


tt


, Na


+


, Mg


++


, K


+


, Zn


+


, Cu


tt


, Fe


tt


and Li


t


.




The examples below provide calculations for determining the necessary flux density and frequencies necessary to beneficially restructuring water for specific applications. Example 1 provides the calculations and resulting flux densities and frequencies for cleansing the water molecule, ingestible substances and/or constituents thereof, and leaving the water molecule, ingestible substances and/or constituents thereof in an improved state of health and harmony.




EXAMPLE 1













mc
2

=
BvLq






m
=


mass





of





water





molecule



18





daltons







18
×
1.67
×

10

-
24




g
·

(

1





Da

)


×
9
×

10
20




cm
2


s
2







=


(
B
)






.3
×

10
6



(

earth





orbital





velocity

)







om
s


1.75
×

10
2


cm






(
humanlength
)








27.1
×

10

-
3




5.25
×

10
8



=


(
fluxdensity
)

=
B











5.16×10


−11


gauss=B for water molecules interacting with the earth's inertial velocity.






fjr
=

5.16
×

10

-
11



.2

.79874
×

10
7






(


q
_






forelectron

)






2

π






m


q

2

π





m












FJR
=


Jacobson





Resonance

=


.001456





HZ

=
FREQUENCY







5.16
×

10

-
11







GAUSS

=

FLUX





DENSITY











This frequency and flux density is particularly beneficial for treating water for consumption by humans. Example 2 shows the calculation of a frequency and flux density which is particularly beneficial for stabilizing water molecules which may be consumed in order to render human physiology in maximum function.




EXAMPLE 2




5.16×10


−11


gauss×65=flux density in consideration of earth rotational velocity,




about 4.5×10


4



or 1000 miles per hour.





3.38×10


−9


gauss=B (for v=earth rotational)






f
=

3.38
×

10

-
9



.2

.79874
×

10
7



coul
9






.095





Hertz




3.38
×

10

-
9







gauss










Example 3 provides a resulting frequency and flux density which is particularly beneficial for stabilizing water molecules which may be consumed in order to render human physiology in maximum function.




EXAMPLE 3













5.16
×

10

-
11



13

=


(
B
)






for





solarsystemvelocity





B
=

3.9
×

10

-
12







gauss





fjr
=

3.9
×

10

-
12


×
2.79
×

10
7






1.09
×

10

-
4







HERTZ




3.9
×

10

-
12







GAUSS










(B) and ƒjr for vibrating water molecules.




EXAMPLE 4




Calcium Resonance








A
)











Ca
++

-

40.08
×
1.67
×

10

-
24



g
×
9
×

10
20




cm
2


s
2










atomic






mass


(

1





Dalton

)
















=

B





.5

.25
×

10
8




cm
2

s






5.25
×

10
8




cm
2

s






is





3
×

10
6



cm
s

×

1.7
5

×

10
2






cm








(
EO
)



human





earth





orbital




(
L
)





velocity













602.7
×

10

-
4




5.25
×

10
8



=

B




=


1.15
×

10

-
10







gauss











fjr
=


1.5
×

10

-
10







gauss





.760





coul


/


g





760





coul


/


g

=



g

2

π





m







for






Ca
++






=


8.74`
×

10

-
8







Hz


(
calcium
)
























B
)






fjr

=





1.5
×

10

-
10







gauss







(
B
)





.1

.5
×

10
4






coul


/


g


(
proton
)




(


q

2

π





m







for







p
+

proton


)










=


1.75
×

10

-
6







Hz


(
proton
)













C) ƒjr=1.15×10


−10


G. 2.79×10


7


coul/9 (electron) 3.2×10


−3


=0.0032 Hz




Thus, when B=1.15×10


−10


G, ƒjr may be 8.7×10


−8


Hz, 3 frequencies for




1.7×10


−6


Hz, or B=1.15×10


−10


G




0.0032 Hz




Now, consider the vector operator ∇ (del) defined by














i










χ



+

j










γ



+

k










z









(
27
)













Then if φ (χ, γ, z) and A (χ, γ, z) have continuous first partial derivatives in a region (a condition which is in many cases stronger than necessary, we can define the following:











curl





B

=




×
B


=



(


i










χ



+

j










γ



+

k










z




)

×

(



B
1


i

+


B
2


j

+


B
3


k


)










=

&LeftBracketingBar;



ijk














χ












γ












z









B
1



B
2



B
3





&RightBracketingBar;












(
28
)











=


i


&LeftBracketingBar;













γ












z









B
2



B
3





&RightBracketingBar;


-

j


&LeftBracketingBar;













χ












z









B
1



B
2





&RightBracketingBar;


+

k


&LeftBracketingBar;













χ












γ









B
1



B
2





&RightBracketingBar;








(
29
)











=



(





B
3




γ


-




B
2




z



)


i

+


(





B
1




z


-




B
3




χ



)


j

+


(





B
2




χ


-




B
1




γ



)


k







(
30
)













Note that in the expansion of the determinant, the operators ∂|∂


χ


, ∂|∂


γ


, ∂|∂z must precede B


1


, B


2


, B


3


.




Jacobson Resonance states, using continuous functions:











c
qv

·



mc
·


l




=



(





B
3




γ


-




B
2




z



)


i

+


(





B
1




z


-




B
3




χ



)


j

+


(





B
2




χ


-




B
1




γ



)


k






(
31
)













The foregoing expression represents the equivalence of the intrinsic energy of a mass, and the interaction energy resulting from an interaction of a body and magnetic flux or magnetic field vectors.




Although specific resonation of water has been described, the invention is not limited to water and includes ingestible substances as previously described herein. Thus, we may change the growth patterns, structural patterns and function of living systems by exposing materials to be ingested into the living system to magnetic field ranging from about 3×10


−6


gauss to about 10


−18


G, or 1-3000 nanogauss. Materials which are ingestible substances ingested by living systems including water, water containing other particles, atoms, elements, minerals, ions, chemicals, etc. and may be restructured to beneficially improve the quality of health, electrophysiology, intermolecular communications, atomic structure and organization, coherent charged states, cooperativity of systems, growth, regeneration, vagosympathetic balance, decrease of oncogenic expression, and/or in other systems (non-living) material crystalline structural states may be changed to improve efficiency of a process or a state of being non-conducive to the purpose of usage. Examples include resonation of materials to produce softening or hardening of water, the enhanced growth of fruits, vegetables and livestock (cattle, pigs, chickens, etc.) and the maintenance of health of said organisms. Furthermore, the resonation (exposure to magnetic fields less than ˜10


−6


gauss) process may enhance absorption of any material into a biological system, e.g., skin, intestinal mucosa, etc.




Resonation of water may be accomplished with, for example, 7.5×10


−8


gauss at 2.1 Hertz (mainly sinusoidal, but can also be rectilinear, triangular pulse) to improve absorption through a semipermeable membrane. In the case of specific ingestible substances containing an increased amount of solids, for example, the resonation must be adjusted for by increasing the amplitude from 6.67 to 10


−8


gauss up to as high as 7×10


−7


gauss for water, sports drinks, geriatric drinks, some medicinal formulations, seeds, creams, such as hand or body creams, lotions, alcoholic beverages (ethyl alcohol) like wine, beer and hard liquor.




Seeds and plants may be resonated directly, or water to nourish plants may be resonated. Exposure to nanogauss to microgauss range magnetic fields may speed germination rate, increase growth potential, improve physiologic function and health, fruit weight, and total plant weight may be increased. Taste can be improved with fields ranging from 1×10


−8


gauss to 8×10


−7


gauss, or a lower range of flux densities utilizing different inertial velocities in mc


2


=BvLq may be beneficial, from about 10


−8


guass to about 10


−12


gauss. The 10


−9


gauss to the 10


−11


gauss range is particularly effective in subtle changes of taste and odor, which are structurally (mechanically) based. Plant growth regulators like auxins and gibberellins may be targeted for specific growth effects, e.g., in a dark room soybeans may be grown faster and longer (more mass) with an amplitude of 7.5×10


−8


gauss using a sinusoidal waveform at 2.1 Hertz. The changing magnetic field should be homogenous and isotropic.




Sports drinks, water, pediatric and geriatric drinks that are resonated are other ingestible substances which will be absorbed faster through the intestinal wall.




Hand creams, skin lotions, suntan lotion, moisturizers and medicines will be absorbed faster by the skin for improved performance. Any object can be resonated to improve the charge distribution, magnetic profile and atomic crystalline lattice structure to function better in a specified interaction. An example would be the softening of water with 7.5 pico Tesla→7×10


−7


gauss field having corresponding cyclotron frequencies calculated with ƒ


ICR


=qB/2 πm. Greater intensities up to a microgauss (from the picogauss range) may be used to harden water, or stimulate increased vibratory motions of atoms. The atoms in any material may be resonated to enhance or alter interatomic communications such that the coherence of said material may be affected. Most notably, configurational entropy may be reduced in an intrinsic system by moving the photon-phonon transduction through gravity to the phonon field to produce an enhanced vibration of a target mass. While the source of the energy is extrinsic to the material (non-invasive) the energy is assimilated by the internal strings of the conductor (material).




Neutraceuticals, indeed a diversity of pharmacologic agents may be absorbed more readily if resonated directly and as well resonation of a living system will enhance dissemination of a molecule or medicine or food, etc. which is resonated through the living system.




EXAMPLE 5




Tuning into Carbon in a Seed




Carbon: 12.01115 (atomic mass)




Material: longest dimension 0.2 cm (seed)




Velocity of material: earth orbital 3.0×10


6


cm/sec. Resonate seed directly to increase rate of growth.










12.01
×
1.67
×

10

-
24







grams







(

carbon





mass

)















X






9.10
20








cm
2

/

s
2



=






(

c
2

)










(
B
)


3
×

10
6







cm
/
s

×
0.2





cm








(
v
)







(
L
)


beginning





of





germination
















180.4
×

10

-
4



=
B


6
×

10
5












B
=

3
×

10

-
8







gauss















F
=


2.8
×

10
7








C
/
gm

·
3






gauss

=

0.56





Hertz
×

10

-
8



















As the seed grows, the B field required for resonance decreases in amplitude. If the earth's rotational velocity were used (4.6×10


4


cms


−1


) about 1000 miles per hour, then the B field required increases by a factor of 65.




The molecular vibrational modes of water molecules or any liquid or solid present in a water based solution or colloidal system will be enhanced by resonant energy states induced by exogenously sourced or intrinsically sourced electromagnetic fields. Critical adjustments to microcomponents of ponderable bodies, structures and particles produce photonic fluxes which adjust the metric of space-time itself, the points that regulate the order of the four-dimensional manifold, and the matter which moves into previously occupied but now unoccupied volumes of space, i.e., the gravitational fields.




Thus we may expose water, beverages in general, pedialyte, sports drinks, neutraceuticals, creams, lotions, medicines, etc. to be absorbed faster by living systems to provide healthful benefits. The range of flux densities is determined by the size of the conductive body, vessel, container or confinement body and by the target atom, subatomic particle, molecule or particulate mass contained in said conductive body. Therein we may rearrange the structural lattice arrangement of relative point masses supplying coordinate axes for solid geometrical and algebraic properties.




EXAMPLE 6




Heretoauxin (indoleacetic acid) is 157 Daltons.









175







Da
.

·



(
heteroauxin
)



1.6



7
×

10

-
24




1





Dalton








grams
·
9

×

10
20







cm
2



s

-
2



=




7.5
×

10

-
8







gauss




(

7.5

pT

)






used





in







studies





in





mung







bean





models





at







the





University







of





Oklahoma



·


3
×

10
6






cm



Earth





orbital






velocity



-



1
·
1.2






cm


Seed





length













EXAMPLE 7














12.01

Carbon





atomic





mass


·
1.6




7
×

10
24



1





Dalton




gm
·
9

×

10
20





cm
2



s

-
2




(

c
2

)



=

B



4
×
6
×

10

-
4




Earth






rotational






(
v
)











cms

-
1


·


.3





cm


Small






seed




(

beginning





of





germination










B
=

1.31
×

10

-
6







gauss











Thus, seed germination can be enhanced with nanogauss magnetic fields up to microgauss magnetic fields.




The range of 6 pT to 70 pT (pico Tesla) is considered effective in promoting plant growth directly or with resonated fluids.




EXAMPLE 8




For a skin cream (skin moisturizer) we may have as its constituents water, phospholipids, triacygloycerol, glycerin, urea, cetyl alcohol, sodium phosphate, BHT, beeswax, fragrance, methyl paraben and propyl paraben. Let us use water as our target in such a system, remembering the more solids the more harmonic resonances, which increases the B field. These should be calculated as well and added to the B field for water in terms of their relative masses combined to the mass of the water content. This ratio tells the practitioner what percentage increase the B field requires for optimal efficiency in the increased rate and depth of absorption into the skin the cream will accomplish. It also represents the method to calculate the B field for increasing absorption by the gut of any material resonated as per the foregoing process and method. Thus, we see:









18
·




H
2


O






atomic





mass



1.7
×




10

-
24







gm



(

p
1

)







1





Dalton



·
9

×

10
20













cm
2



(

c
2

)




s

-
2



=



B4

.64
×

10

-
4




ER






(

earth





rotational





velocity

)










cms

-
1


·


1.7
×

10
1






cm



Skin





moisturizer







container






(
L
)
















In a system containing 4 fluid ounces, the longest dimension of which is 17 cm, the product can be resonated directly after completion.








270.54
×

10
4



7.89
×

10
5



-

34.3
×

10

-
9













B=3.43×10


−8


gauss; the lower end of the pico Tesla range which relaxes soft tissue clinically, decreases blood pressure, and is predominantly parasympathomimetic in the vagosympathetic balance in the autonomic nervous system.




We see that the B field, as other products are added, must increase due to the larger number and amplitude of oscillations produced by same.




Now, we may also consider the energy content of the solids as mc


2


. A phospholipid is about 207 Da discounting R


1


, R


2


, and X Groups.




Let us change the (m) to 207, which is an approximation.











207
·
1.067

×

10

-
24





phospholipid





1











Da







·
9

×

10
20














cm
2







s
2




(

c
2

)



=





(
B
)

·
4.64

×

10
4



(
ER
)








cms
·


1.7
×

10
1






cm


Cream






(
L
)















The oxidative metabolism of fats yields over twice the energy of an equal weight of dry carbohydrate or protein. Fats are nonpolar and are stored in an anhydrous state whereas glycogen, the storage form of glucose is polar, and is consequently stored in a hydrated form that contains about twice its dry weight in water. Fats therefore provide up to six times the metabolic energy of an equal weight of hydrated glycogen. The atomic number of phosphate is 15.




B=4×10


−7


gauss for phosphate in cream, showing that the range of 3pT→70pT is important for the induction of coherence and resonance into any system. The system could be applicative to resonating a pediatric beverage for improvement of health and well being. The worker skilled in the art may also resonate with Jacobson Resonance mc


2


=BvLq wines, liqueurs, liquors, beer and other alcoholic beverages to enhance absorption rate across membranes and improve taste. Studies at the University of Oklahoma to Scherlag and Yamanashi have shown that there is a 17% increase in absorption rate across membranes of resonated triple distilled water as compared to distilled water non-resonated. These studies are well replicated. It has also been shown that conductance of water increases with resonation, as well as hardness and softness. The pico Tesla range (B field) may soften water while higher flux densities may harden water. At 7.5 pT distilled water was also made harder by adding calcium before the resonation. That is, with the addition of solids (especially highly crystalline solids) resonation can make the water harder than it would be with the solids (calcium) while unresonated. This means that concrete blocks can be made harder if mixed with water (highly mineralized) with resonation.




EXAMPLE 9




When utilizing hydrogen peroxide in a system 12 cm in length, H


2


O


2


=34 Daltons, and V representing the voltage setting in the Jacobson Resonator which corresponds to a setting in the attenuator of the Jacobson resonator which may be microgauss (μG), nanogauss (nG) and milligauss (mG).




1.42 V in nanogauss setting=1.42×10


−9


gauss




1.42 V in migrogauss setting=1.42×10


−6


gauss




we view the following table:




















V




B




f




time




v







volts




gauss




Hertz




minutes




Velocity




setting




























1.42




1.42 × 10


−9






.04




40




EO




nG






2.24




2.24 × 10


−9






.063




40




SS




nG






0.93




 9.3 × 10


−8






2.59




40




ER




μG






.133









1.33 × 10


−10






.0037




40




SC




μG














EXAMPLE 10




Using catalase (250 kDa) and L=12 cm we get:




















V




B




f




time




v







volts




gauss




Hertz




minutes




Velocity




setting




























.97




 9.7 × 10


−7






2.78




20




SC




μG






10




  1 × 10


−5






290




20




EO




μG






.0162




1.62 × 10


−5






454




20




SS




mG






.675




6.75 × 10


−4






18,900




20




ER




mG














The foregoing is based in electronic resonance where q/2 πm in ƒ=qB/2 πm is 2.79×10


7


coul/gram for the electron.




For protonic resonance, q/2 πm for the proton is 1.5×10


4


coul/gram; or one may multiply the electronic frequency by a factor of 5.36×10


−4


(scalar).




q/2π for the proton:












q
=






2

π





m







1.6022
×

10

-
19







Coulomb






(
C
)



2


(
3.1416
)


1.67262
×

10

-
24







grams






(
g
)




=

1.525
×

10
4







C
/
q













Vagal






(
f
)


=


.0423





Hz

=


1.5225
×

10
4








Cg

-
1


·
B






B

=

2.774
×

10

-
6







gauss













Autonomic





nervous





imputs










Sympathetic


(
f
)


=


.0043





Hz

=



1.5225
×

10
4






Cg

-


1
·
B






B


=

2.82
×

10

-
7







gauss








Autonomic





nervous





inputs















There can be exerted a sympathomimetric influence on a biosystem upon ingesting any material first resonated with a range of 5.51×10


−7


→1.934×10


−6


gauss. There will be parasympathetic, sympathetic overlap in this range. From 1.31×10


−8


gauss→5.51×10


−7


gauss there is autonomic overlap as we have seen, yet the lower pT field range around 3.4 pT is predominantly parasympathetic while 5×10


−7


gauss is predominantly sympathetic. This holds for ingestion of water, sports drinks, pedialyte, geriatric drinks, neutraceuticals which are classified as foods but contain a number of vitamins, minerals, biochemically active molecules, plant extracts, etc., and medicines that are liquid based or otherwise, i.e., pharmaceuticals. 1.9→3.6×10


−6


gauss in protonic resonance will show vagal stimulation. Other resonance phenomena relating the water molecules ingested into the body after resonation (as well as all other material aggregations) may be shown.




Vagal, Ptoconic Resonance at 0.25 Hz will be associated with 1.64×10


−5


gauss (B).




Sympathetic, Protonic Resonance at 0.15 Hz is associated with 9.84×10


−6


gauss (B).




Vagal, Electronic Resonance at 0.25 Hz is associated with 8.93×10


−9


gauss (B).




Sympathetic, Electronic Resonance at 0.15 Hz is associated with 5.36×10


−9


gauss (B).




The range for parasympathetic stimulation may also extend from about 2.77×10


−6


gauss→1.64×10


−5


gauss in protonic resonance. Also, the range for parasympathetic (predominance of tonicity dependent) may be 8.93×10


−9


gauss→3.5×10


−8


gauss in electronic resonance. 5.36 nG and lower reveals both aspects of vagosympathetic tone. The overlap is based upon the similarity of neurotransmitter masses. Protonic resonance may extend from 1.7×10


−4


gauss (in small animals) to 1×10


−5


gauss, and from 2.55 Hz to 300.8 Hz. From 9×10


−6


gauss to about 1.5×10


−7


gauss we see first sympathetic electronic windows and then parasympathetic resonance at about a few microgauss.




Understanding the relationship between density of an object and the autonomic functions of living systems is important because certain fields allow charge densities to change which in a living system will allow increased perfusion through tissue. The low pT range (pico Tesla) at about 3.3 pT decreases tension in soft tissue and bone. The frequency of the changing field influences the kind and rate of the interaction as well. If one were to use a 20 Hz frequency with a low pT field there would occur increased asymmetry of tissue and increased conformational entrophy even if the tissues are relaxed. The appropriate physiologic signal of a low pT range flux density requires about 1 Hz and slower. The brain EEG frequencies are accommodative to cognitive and functional changes in the brain.




Proteglycan and collagen are molecules subject to influence through resonation, important to chondrogenesis.




EXAMPLE 11















For resonating water and feed for horses:















Microgauss Setting

















Targets




Amplitude




Frequency




Time







(include harmonics)




(v)




(Hz)




(minutes)


















MAP, NF, Hb, motor




.207




5.796




30




1 hour






proteins







protocol






Tubulin, BGF, glial fibrilar




.1484




4.2




30







acidic protein, calmodulin,






NGF, PDGF






Homeoboxes,




.274




7.66




30




1 hour






motor proteins dynein,




3.29




9.23




30




protocol






phosphorylase kinase






enzyme “emergizing”






Interferon PDGF, cytokines




.112




3.0




20




1 hour






NGF




.121




3.39




20




protocol






PDGF




.138




3.84




20






Calmodulin profilin




.075




2.1




20




1 hour






ATP, interloekins




.093




2.6




20




protocol






G-actin




.168




4.1




20






NGF




.075




2.1




30




1 hour






IgA, IgD, IgM, IgG,




.049




1.38




15




protocol






melatonin






Neurotransmifters




.034




9.52




15






“relaxing”






Singular signal




.075




2.1




60




Single






protocols







signal







.15




4.2




60




Single










Signal







2.74




7.7




60




Single










signal














0.15V at 4.2 Hertz for 60 minutes will energize the horse without him leaving his race in the stable. We want the horse to be relaxed, feel good, yet be ready to move quickly and maintain stamina. There are many possible combinations to enable a horse to run faster yet be controllable.




We may also diminish the viability, decrease the proliferation rate and perhaps kill viruses, bacteria and other pathogens in water, sports drinks, and other beverages and ingestible solids to decrease the negative effects of antigenic particles coming into a living system. Said fields are in the pico Tesla range generally but may require a microgauss to picogauss range combination to therein recrystallize parts of microorganisms (protein and nucleic acid, glucoproteins) thus rendering them static or cidal and/or whole pathogenic microorganisms. The size of the vessel or container holding the liquid, or the longest dimension of the solid should be utilized in mc


2


-BvLq to amplify the particulate triggers which may shake the i.e. virus to death or to an inert state, such that dessication occurs, necrosis of organic tissue and death. Tuning into masses in system (conductive) to induce order-inducing or disorder-inducing vibrational modes may be utilized.




EXAMPLE 12




For example, it may be that a non-physiologic signal is indicated to kill microorganisms in a liquid setting. This is because living systems are intrinsically ordered to maintain their integrity. Thus microorganisms, while maintaining relative abnormal profiles in larger living systems requiring lower magnetic profiles, nevertheless microorganisms maintain themselves physiologic magnetic profiles based in subatomic particle resonances. Therefore, we may view the following method.


















1.




Kill the possible pathogens that exist in the beverage or food by resonating the













system according to mc


2


= BvLg.












2.




Renormalize the magnetic profile of the beverage or food before ingestion by













humans or animals.














A.




6 × 10


−18


grams · 9 × 10


20


cm


2


/s


2


= (B) · 4.6 × 10


4


cm/s · 30 cm















Virus particle




(ER)




1 foot long vessel













B = 3.91 × 10


−3


gauss







B field is oncogenic enhancer














B.




6 ×10


−18


g · 9 × 10


20


cm


2


/s


2


= (B) · 3 × 10


6


cm/s · 30 cm














(EO)




vessel













B = 6 × 10


−18


gauss (more physiologic)














C.




6 × 10


−18


g · 9 × 10


20


cm


2


/s


−2


= (B) · 3.2 × 10


7


cms


−1


· 30 cm














virus




star cluster velocity













B = 5.6 × 10


−6


gauss







more subtle, closer to human physiologic MF (magnetic field)














D.




Most preferable choice is a non-physiologic field to disrupt the virus, e.g.,














6.54 × 10


−7


gauss




2,750 Hertz













Above 1 kHz electric fields are sharply attenuated by the cell membrane.







5.89 × 10


−19


grams · 9 × 10


20


cm


2


/s


−2


= 6.54 × 10


−7


gauss · 3 × 10


6


cms


−1


· 30 cm















353,000 Daltons is a larger target in a virus or bacterium, yet one sees a practical association of the B field with conductive bodies or vessels containing fluids with pathogens. The frequency will be disruptive while energizing of large aggregates in the pathogen will be continuously vibrated for about an hour by the skilled worker.




After usage of the values set forth in 2(D) above renormalization of the magnetic profile of the fluid or conductive body therein resonated should be accomplished. For general human and animal consumption a range of 3.4×10


−8


gauss at a frequency of 0.952 Hz to 1.5×10


−7


gauss at a frequency of 4.2 Hz may be used safely from an effect ranging from relaxing to stimulating respectively.




The present invention also provides a preferred apparatus for applying electromagnetic fields to water as described above. This device is referred to as “The Jacobson Resonator” or the “Resonator”. The apparatus is comprised of a signal generator, an attenuator unit, a set of simplified Helmholtz coils, and an application device on which the water to be treated is placed. In order to minimize the distortions of the generated magnetic field, no ferrous metals are utilized in the construction of the coils, application device, and support stand. Some minimal amounts of ferrous metals are used in the construction of an actual embodiment of the Resonator. For example, referring to

FIG. 10

, a bolt (


121


) on the swivel clamp (


123


), and the swivel wheels (


125


) were made of ferrous materials due to strength requirements and cost consideration. However, field uniformity was not significantly affected by this small amount of ferrous metal.




The Jacobson Resonator uses a signal generator to produce a magnetic field. The signal generator produces a magnetic field of the desired amplitude and frequency. In a preferred embodiment, the signal generator is an HP 3325B signal generator manufactured by the Hewlett-Packard Company which is capable of producing signals varying in frequency from DC to approximately 20 Megahertz (Mhz) in square, sinusoidal, and triangle waveforms. The generator is also capable of generating amplitudes from 1 millivolt to 10 volts into a 50 ohm load termination. In order to maintain correct signal relationship, the signal generator should be terminated into a 50 ohm load termination during operation.




Referring to

FIG. 11

, (see diagram for clarity) the attenuator unit (


1


) uses the signal produced by the signal generator to drive the helmholtz coils. The circuitry is designed to provide impedance matching to the generator and selectable attenuation of the signal. The attenuation range is from 10 milli gauss to 1 atto gauss by combining the generator range and the attenuator selection ranges. The attenuator (


1


) has two switches (


2


), one rotary switch for milli (10


−3


), micro (10


−6


), and nano (10


−9


) selections and one toggle switch (


3


) for inducing an additional micro (10


−6


) level of attenuation to the above signal levels. This provides for a total of 10


−15


signal attenuation. All coils should never be connected directly to the signal generator, as magnetic fields in the gauss range are possible depending on the generator settings.




The magnetic fields are produced by simplified helmholtz coils. The coils may be 18 inches or 7 feet in diameter with a separation of 9 inches or 3.5 feet respectively. The smaller coils (


117


) are shown in FIG.


10


. These coils are preferably made of 5 turns of #37 gauge wire around an 18 inch disc made of laminated foam. Additionally, the discs have an epoxy coating, for additional strength, and a black gloss enamel finish. Coil interconnections are made via two pin friction fit connectors (


127


) for ease of mating.




Still referring to

FIG. 11

, the application device (


115


) provides the correct separation and mounting for the coils (


117


). The device is capable of 180° rotation and 90° pivoting. The application device also has an epoxy coating, for additional strength and rigidity, and a black gloss enamel finish. System interconnections are made via two pin friction fit connectors (


119


) for ease of mating. All connections are keyed to maintain correct polarity of the coils and the field.




The support stand provides 360° rotation of the device with vertical and horizontal movement of approximately 3 feet and the ability to secure the device in any position. This provides extreme versatility in positioning and securing the device. In one embodiment, the support stand is fabricated from PVC with brass hardware for interconnecting the sub-assemblies.




Using the Jacobson Resonator described above, it is believed that the following settings provide beneficial restructuring of water and/or other ingestible substances for application to humans. For Table 4, the Jacobson Resonator is using the “Microgauss” setting and various targets are listed in the first column. In column 2 of Table 3, the amplitude setting is listed which corresponds to a flux density produced by the resonator. The third and fourth columns, respectively, represent the frequencies e





and p


t


. frequency e





represents the corresponding Jacobson Resonance and ion cyclotron resonance frequency when q is the gyromagnetic ratio of the electron and frequency p


+


corresponds to q/2 πm of the proton, in the formula ƒ


ICR-JR


=qB/2 πm




These tables can be used generally with other EM devices when converted into general terms. These settings are for the resonator but can be converted generally. For example,




10V=10 μG (microgauss)=1×10


−6


gauss or 0.7V=0.7×10


−6


G=7×10


−7


gauss.












TABLE 4











(Human Length (L) = 1.7 × 10


2


cm.)














Includes









harmonics





Frequency







target




Amplitude (volts)




(e





)




Frequency (p


t


)

















virus (whole)




10 V − 1 × 10


−6






279.9 Hz




.15 Hz







gauss







9




251




.135







8.8




246




.132







7




197




.1






Interferon




6.35




178




.095






Growth factors




5.15




144




.077






Enzymes




4.55




126




.067






Motor proteins




3.42 − 3.42 ×




95.8




.0513







10


−6


gauss






calmodulin




2.83




78




.042






NGF




2.54




71




.038






kinesine




.997




27.9




.015






Map




.84




23.5




.0126






Spectrin






brain specific fodrin




.7 − 7 × 10


−7






19.6




.01







gauss






neurofilaments




.57




15.99




.0085







.457




12.8




.0069







.343




9.59




.0051







.33




9.24







.32




8.96







.31




8.68






Transforming DNA




.3




8.4






(oncogenes)






homeoboxes




.274




7.677




.0041






hemoglobin




.2




5.6




.003







.19467




5.448







.192




5.36




.0028







.175




4.9







.162




4.53




.00243






BGF,tubulin






single rope




.15 − 1.5 × 10


−7






4.2




.0023






(homeobox)




gauss







.137




3.84







.126




3.5




.0019






leukotrine




.1




2.798




.0015






PDGF, interferon




.09




2.52




.00135







.085




2.38




.00127







.081




2.27






NGF




.078




2.1







.0667




2.01







.06




1.68






melatonin




.05




1.4






calmodulin




.04




1.12




(DNA repair .0005)






hormones, epi




.035




.976







.02




.56







.012




.336














In Table 5, the Jacobson resonator is placed in the “Nanogauss” setting.












TABLE 5









.316 V = .316 × 1 × 10


−9


gauss = 3.16 × 10


−10


gauss




























10 V = 10


−8


gauss




.28 Hz








8.6




.24








7.8




.218







NGF (solar)




5.9




.16








3.5 × 10


−9


gauss




.098







H20




2.99




.09








1.76




.021







Leukotrines




1.47




.041








1.195




.033








.895




.025







melatonin




.667




.02







serotonin




.4937




.0138







epi




.431




.012







norepi




.392




.011







dopamine




.347




.097







histamine




.316




.0885








3.16 × 10


−10


gauss








.0538




.0015







water




.046




.001288








4.6 × 10


−11


gauss















In Table 6, the Jacobson resonator is placed in the “Microgauss” setting.












TABLE 6











Brain grouping















30-40 minutes




.077




2.1








.076




2.13








.075




2.1








.074




2.072








.073




2.044








.072




2.016








.071




1.988








.07




1.96








.069




1.932








.068




1.904








.0667




1.8667








.0661




1.864








.065




1.83








.064




1.8















Joint Pain Including Bone















about




.2




5.6







40




.15




4.1







minutes




.126




3.5








.09




2.5








.078




2.1








.05




1.4








.034




.97















Headache















about




.038




1.064







40




.034




.976







minutes




.032




.896








.03




.84








.028




.784








.025




.7















Table 7 list various protocols which have been developed using the Jacobson Resonator for beneficially restructuring water and/or other ingestible substances for application to humans to improve the health of the person treated with the restructured water and/or other ingestible substances.












TABLE 7











DEAFNESS














Amplitude




Frequency




Time


















0.077




2.17




2′5′







0.076




2.13




2′5′






0.075




2.1




2′5′






0.074




2.072




2′5′






0.073




2.044




2′5′






0.072




2.016




2′5′






0.071




1.988




2′5′






0.070




1.960




2′5′






0.069




1.932




2′5′






0.068




1.904




2′5′






0.067




1.866




2′5′






0.066




1.864




2′5′






0.065




1.863




2′5′






0.064




1.80




2′5′






0.034




0.952




2′5′






0.033




0.920




2′5′






0.032




0.890




2′5′






0.031




0.870




2′5′






0.030




0.830




2′5′






0.029




0.800




2′5′


















TOTAL TIME:




50′














HEADACHE














Amplitude




Frequency




Time


















0.038




1.064




5-15







0.037




1.063




2′5′






0.036




1.000




2′5′






0.035




0.98




2′5′






0.034




0.952




5






0.032




0.890




2′5′






0.031




0.870




2′5′






0.030




0.830




2′5′






0.029




0.800




2′5′






0.028




0.784




2′5′






0.025




0.700




2′5′


















TOTAL TIME:




40-50 min.














MIGRAINE














Amplitude




Frequency




Time


















0.034




0.952




5-20







0.0335




0.937




2′5′






0.033




0.928




2′5′






0.0325




0.909




2′5′






0.032




0.890




2′5′






0.0315




0.882




2′5′






0.031




0.870




2′5′






0.030




0.830




2′5′






0.029




0.800




2′5′






0.028




0.780




2′5′






0.027




0.750




2′5′






0.026




0.728




2′5′






0.025




0.700




2′5′






0.024




0.670




2′5′






0.023




0.640




2′5′






0.022




0.620




2′5′






0.021




0.590




2′5′






0.020




0.560




2′5′


















TOTAL TIME:




47′5-55 min.














SPRAINED ANKLE














Amplitude




Frequency




Time


















0.343




950




15







0.274




7.7




15






0.033




0.920




20′






0.032




0.890




20′


















TOTAL TIME:




60-70 min.














FLU VIRUS














Amplitude




Frequency




Time


















0.274




7.7




15







0.200




5.6




10






0.150




4.1




10






0.126




3.5




10






0.090




2.5




5






0.078




2.1




5






0.050




1.4




5






0.034




0.952




5














TENNIS ELBOW














Amplitude




Frequency




Time


















0.034




0.952




15







0.274




7.7




15






0.200




5.6




5






0.150




4.1




5






0.126




3.5




5






0.090




2.5




5






0.078




2.1




5






0.050




1.4




5






0.034




0.952




5


















TOTAL TIME:




60 min.














OSTEOARTHRITIS ROTULIANA (KNEES)














Amplitude




Frequency




Time


















0.0340




0.952




15-20







0.457




12.8




5






0.343




9.6




5






0.274




7.7




5






0.200




5.6




5






0.150




4.2




5


















TOTAL TIME:




40-45 min.














RHEUMATOID ARTHRITIS (HANDS)














Amplitude




Frequency




Time


















0.034




0.952




20







0.457




12.8




10






0.343




9.6




10






0.274




7.7




10






0.200




5.6




10






0.150




4.1




10


















TOTAL TIME:




70














WATER














Amplitude




Frequency




Time


















0.457




12.8




30




SKIN, WINE, PLANTS






0.075




2.1




35




SKIN






0.15




4.1




35




LAXATIVE, PLANTS, CEMENT






0.034




0.952




40




RELAX






0.15




4.1




30




PLANTS, WINE






0.075




2.1




25




COSMETICS






0.075




2.2




15




BEER






0.075




2.1




15




CANNED FRUITS






.274




7.7




25




WINE, ENERGY, PLANTS














NEUROPATHY OF THE FOOT














Amplitude




Frequency




Time















Reducing tension in tissue














.034




.952




5







.274




7.70




5






.033




.92




5











Once you go over 5 minutes, you are changing rhythms.














.20




5.6




6












If pain is in the sole of metatarsals, need more # in .033 range.














.032




.89




15












Does pain move from sole to heel? Use heel or bone #'s














.274




7.7




4-7












Is pain just in sole?














.033




9.8




 8-10



















TOTAL TIME:




44 min.














PAIN IN FOOT - Plantar Fascitis, Neuropathy,






Tarsal Tunnel














Amplitude




Frequency




Time















FOR SOFT STRUCTURES














.031




.867




5-6







.03




.84




5-6











FOR HARD STRUCTURES














.078




2.1




5







.126




3.5




5






.15




4.2




5






.457




12.8




4-5




If left too long, pain will increase






.457




.0069




4-5






.57




15.99




4-5




If too much tension builds in soft tissue,









use .0085.






.7




19.6 or




3








.01






.84




23.5 or




3







.013











*Best sequence for feet












.033







.274






.032






.2






.031






.15






.03






.126











If needed













.343




9.8







.033






.457






.032














.57





2-3







.7





2-3






.84





2-3






.033











Generally, it is better to move from low to high and keep going back and forth rather than to use big frequencies for too long. If you don't release the foot from big frequencies, you will increase the pain in the soft tissues.


























PARKINSON DISEASE PROTOCOL











*If there is any pressure in the head, move to .033 ug at .92 hz






until the pressure subsides or disappears.






TREAT SIDE TO SIDE














Amplitude




Frequency




Time

















.077




2.17




3.50






.076




2.13




3.50






.075




2.10




3.50






.074




2.07




3.50











REST FOR 20-30 MINUTES






TREAT FRONT TO BACK














.075




2.10




3.5







.074




2.07




3.50






.073




2.04




3.50






.072




2.02




3.50









TOTAL TREATMENT TIME: 28 min.














CEREBRAL PALSY PROTOCOL














Amplitude




Frequency




Time


















.034




.952 or .976




10




*or 15 minutes UE and LE to decrease






.033




.92




10




spasticity (not for brain exposure in









small resonator but for focused field









on limbs)






.032




.9




10











Other numbers are














.457




12.8




1.5




}






.343




9.6




1.5




}






.274




7.7




1.5




} For large resonator for full body









exposure






.2




5.6




1.5




}






.15




4.2




1.5




}






.075




2.1




5.5




}









TOTAL TREATMENT TIME: 43 min.











Always end a .034 at .952 for 20 minutes to decrease rigidity and facilitate good sleeping. Watch carefully on head. If pressure wave develops, drop down to .075 from any number. If pressure persists, drop to .033 @ .92 for 5-10 minutes. Use .033 on head only when necessary (does not help cognition). Generally 10-12 minutes @ .075 on head is excellent.


























ALZHEIMER'S DISEASE PROTOCOL











*If there is a pressure wave in the head, balance with .033 ug at .92 hz or






.032 at .89 hz until the pressure subsides or disappears.













Amplitude




Frequency




Time
















.077




2.17




4






.076




2.13




4






.075




2.1




4






.074




2.07




4











REST FOR 20-30 MINUTES













.075




2.1




4






.074




2.07




4






.073




2.04




3






.072




2.02




3














ATTENTION DEFICIT DISORDER













Amplitude




Frequency




Time














SIDE TO SIDE













.076




2.05




4






.075*




2.10




4






.074




2.0




4













REST





30











FRONT TO BACK













.076




2.05




4






.075




2.10




4






.074




2.0




4











*MAJIC NUMBER FOR CALMING KIDS/TUNES IN NERVE GROWTH NUMBER. Some researchers use .075 @ 2 hz.


























ADDITIONAL HEADACHE SETTINGS














Amplitude




Frequency




Time

















.038




1.064




setting is rarely used; for thick, heavy skull














.034




.976




 8-10







.033




.952




 8-10






.032




.92




10-30






.031




.89




10






.03




.84




 5-10






.028




.784




 5-10






.025




.7




 5-10














MIGRAINE PROTOCOL











Treat 30-40 minutes side to side then front to back






*Most headaches go away at .031 at .87














Amplitude




Frequency




Time


















.034




.952




 5-15












If pain decreases, leave longer at .034














0.033




.92




10-15







.032




.89




10






*.031




.87




10-15











If continues to subside, leave at .031














.03




.83




5







.029




.8




5






.028




.78




5






.027




.75




5






.026




.73




5






.025




.7




5






.024




.67




5









TOTAL TREATMENT TIME: 60+














UNMOTIVATED, LOST AND APATHETIC PROTOCOL














Amplitude




Frequency




Time















FRONT TO BACK














.06




1.68




8







.05




1.4




8













.0428




1.2




8* great results for men






.0464




1.3




8* great results for women











SIDE TO SIDE














.075




2.1




3







.0428




1.2




7











REEVALUATE. If patient's mood elevates, stop. If patient is still






sluggish, do














.075




2.1




4







.05




1.4




4











If there is any pressure, go to













.033




.92




until pressure is gone














.0428




1.2 (men




5







.0464




1.3 (women)




5









TOTAL TREATMENT TIME:









50 min.














TENDONITIS OF THE ELBOW (and MUSCLE SPASM)














Amplitude




Frequency




Time


















.034




.952




20












It still has pain go to:














.033




.92




10-15







.343




9.8




6-8






.032




.89




 5-10




*relax before going back up






.274




7.7




15-20






.2




5.6




 5-10






.034




.952




 5-15













.15




4.2




extra 10 minutes if necessary














.034




.952




20-30










TOTAL TREATMENT TIME:









85 min.











Times can be cut but .034 and .274 are the critical signals. .034 at .952 is used to reduce tension. .274 at 7.7 is used to reduce pain. If pain doesn't decrease after 30-40 minutes of weak signals then try some plain numbers. A muscle spasm usually doesn't need pain numbers; but, longstanding tendonitis does after 25-30 minutes.


























MIGRAINE HEADACHE PROTOCOL














Amplitude




Frequency




Time


















.034




.95




10







.033




.92




10






.032




.9




10






.031




.87




10






.03




.84




10






.027




.72




10









TOTAL TREATMENT TIME: 50 min.














Extend treatment time on any signal that seems to work the best.











OTHER NUMBERS PARKINSON'S DISEASE, ALZHEIMERS






AND MULTIPLE SCLEROSIS














Amplitude




Frequency




Time















Side to Side














.077




2.17




4







.076




2.13




4






.075




2.10




4






.074




2.07




4











Front to Back














.073




2.04




4







.072




2.02




4






.071




1.99




4






.070




1.96




4











32 minute treatment every other day






Treat 3 × week for 2-3 weeks then reevaluate.






ADD MORE SIGNALS














.069




1.93




3







.068




1.90




3






.067




1.87




3






.066




1.86




3














CANCER and AIDS











Parkinson disease may possibly have pressure.






M.S. and Alzheimer's most likely will not have pressure.






Any pressure, drop to .033 or .032 until pressure goes away.



























Large Resonator - full body immersion in field.













FIELD STRENGTH




FREQUENCY




TIME






(micro-gauss)




(hz)




(minutes)




















1.0




ug




27.9




hz




1




min




3






.82




ug




23.0




hz




1




min




3






.72




ug




20.16




hz




1




min




3






.654




ug




18.2




hz




1




min




2






.57




ug




16.0




hz




1




min




2






.475




ug




12.8




hz




1




min




2















REST PERIOD




3




min

















.343




ug




9.59




hz




2




min




3






.274




ug




7.68




hz




5




min




6






.200




ug




5.6




hz




4




min




5






.175




ug




4.9




hz




2




min




3















REST PERIOD




6




min

















.150




ug




4.2




hz




6




min




7






.126




ug




3.5




hz




3




min




6






.115




ug




3.15




hz




1




min




2






.090




ug




2.52




hz




4




min




5






.075




ug




2.1




hz




8




min




10















REST PERIOD




10




min

















.050




ug




1.4




hz




3




min




4






.038




ug




1.1




hz




3




min




4






.034




ug




.976




hz




10




min




12






.030




ug




.84




hz




2




min




3






.025




ug




.7




hz




2




min




3






.020




ug




.56




hz




2




min




3














Microgauss Setting






FOR HUMAN NERVE















2.54




71






1.3




36






.997




27.9






.84




23.5






.72




20.16






.654




18.2






.57




16












.5157 (EGF-R)




14.56












.457




12.8






.343




9.6






.274




7.7






.2




5.6






.194




5.45






.175




4.9






.162




4.53






.15




4.2






.137




3.84






.126




3.5






.1




2.8






.09




2.52













TOTAL TREATMENT TIME: 1 hour and







42.5 minutes














Signal Protocol - 41 Signals for human nerve












.078




2.1






.0667




2.01






.06




1.68












.0589 (TGF-OC Precursor)




1.65












.05




1.4






.04




1.12






.038




1.1






.034




.976






.184




.52






.1769




.495






.1168




.3267














Nanogauss Setting (32 Signals in η G)












5.9




.16






2.99




.083






1.76




.049






.895




.025






.667




.02






.494




.014






.431




.0121






.392




.0109






.316




.0089











The examples above use are based on a human length. It is also possible to use the length of a water container. As discussed above, it is also possible to use this procedure to treat organisms other than humans. For such treatment, the length of the organism at the appropriate stage of development is used. The following calculations demonstrate methodologies for determining the proper flux density and frequency for treating plants.













The four inertial velocities that have been used for calculations are as follows:




1. 3.22×10


7


cm/s—star cluster (SC)




2. 2.98×10


6


cm/s—earth orbital (EO)




3. 1.93×10


6


cm/s—solar system (SS)




4. 4.642×10


4


cm/s—earth rotational (ER)




Lengths (Samples)




(1.7×10


2


cm) 1. Human length is about 5′8″ (170 cm) L


H






(1.5×10


1


cm) 2. Mouse length is about 15 cm L


M






3. nerve piece length—




A) 1.5 cm—1


st


experiment in Cornell lengths of nerve pieces




B) 2-.7 cm—2


nd


+3


rd


experiments in Cornell




Note (Samplesof Calculations inTableFormareincluded)



















electron




Examples I (Plants)




chloroplast






q/2πm




chlorophyll a(g)




˜5 μm long








ellipsoids















2.79 × 10


7


 Coul/


gram proton q/2πm


1.5 × 10


4


 Coul/


gram


















~
625






Daltons


1.67
×

10

-
24








g
·
625



=

1
×

10

-
21







g







(




principal





photoreceptor






in





photosynthesis




)






[



ineukaryotesand





cyano





Bacteria




]




&AutoLeftMatch;






















5
×

10

-
6







m

=

5
×

10

-
4







cm







membranous





subcellular






organelle





and





site





of





photosynthesis



&AutoLeftMatch;




















mx(c


2


)





















1
×

10

-
21







g
×

9

(
v
)


×


10

(
L
)


20







cm
2



/



s
2


=


B
·
2.98

×

10
6






cm


/



s
·
5

×

10

-
4







cm


































9
×

10

-
1








gem
2



5
2



1.5
×

10
3







cm
2



/


s


=
B

;






B
=

6
×

10

-
4



gauss





&AutoLeftMatch;































ficr
=



qB
/
n






π





m

=

2.79
×

10
7




e
q

·
B




;






frequency
=

2.79
×

10
·
6

×

10

-
4







&AutoLeftMatch;

















If q/2 πm is for p


+


(proton) instead of e





(electron) then q/2 πm=1.5×10


4


c/q instead of 2.79×10


7


c/q




Thus, frequency


(ion cyclotronresonance, ICR)


=1.5×10


4


c/q. 6×10


−4


gauss ƒ=9 Hz




Therefore, the protocol is:




1. 1


st


week—B=6×10


−4


gauss and ƒ=9 Hz or 1.67×10


4


Hz




Then, 2


nd


week L could be 0.2 cm (length of seed for example)




10


−21


g×9×10


20


cm


2


s


−2


=B. 2.98×10


6


cm/s. 2×10


−1


cm




∴B=1.5×10


−6


gauss






f
=


2.79


×

(

e
-

)





10
7

·




1.5

×

10

-
6



=


4.2
×

10
1


=

42





Hz





or







f
=


1.5
×


10
4

·




1.5

×

10

-
6



=


2.25
×

10

-
2



=

.0225





Hz













2. Week #2—B=1.5×10


−6


gauss at 42 Hz or 0.0225 Hz




3


rd


week; L is increasing; L=2 cm (arbitrary depends upon growth cycle of plants)








9
×

10

-
6




6
×

10
6



=

B
=

1.5
×

10

-
7







gauss












f=4.2 Hz ƒ or e
























(protocol for plants)














B (gauss)




f (Hz)


















  6 × 10


−4






9




1


st






week






1.5 × 10


−6






42




2


nd






week






1.5 × 10


−7






4.2




3


rd






week















through maturity of fruit

















*





See chart which has flux densities in microgauss setting













with associateed frequencies based in electronic













gyromagnetic ratio.











again plants Example II  seedlength/0.1 cm

























t arg et{˜600Daltonsiron protoporphyrinIX }






1 × 10


−21


9 × 9 × 10


20


cm


2


/s


2


= B.4.6 × 10


4


cm/s.0.2 cm






(EO) (L)






seed


























1. 1


st


week













9
×

10

-
1




9.2
×

10
3



=


1
×

10

-
4



gauss

=
B






























f
=


1.5
×

10
4


.1
×

10

-
4



=

1.5





Hz






(




using






p
+



q
/
2


π





m





protonic



)
























2. 2


nd


week




L → 2 cm B = 10


−5

















f
=

15





Hz






(




using






p
+



q
/
2


π





m





protonic



)























3. 3


rd


week




L → 20 cm








B = 10


−6

















f
=

28





Hz






(




using






e
-



q
/
2


π





m





electronic



)























4. 4


th


week through duration




B = 10


−7

















f
=

2.8





Hz






(




using






e
-



q
/
2


π





m





electronic



)























EXAMPLE II



















B (gauss)




f (Hertz)




























1 × 10


−4






1.5








1 × 10


−5






15




Hz







1 × 10


−6






28




Hz







1 × 10


−7






2.8













* Water should be treated (resonated) for one hour and plants should be water only with resonated water from initiation to maturity of fruit.













EXAMPLE III















Dog protocol






treat racing heart syndrome (tachycardia)














Water should be









resonated for 1 hour




B (gauss)




f (Hz)










(2 days)




3.4 × 10


−8






 .952




4 signals to treat






(2 days)




3.3 × 10


−8






.92




dogs with resonated









water






(2 days)




3.2 × 10


−8






.89






(2 days)




3.0 × 10


−8






.80














A) 8 day treatment—dogs should only be given resonated water (one signal at a time) or




B) water may be treated with all four signals—20 minutes for each signal.




To treat humans with multiple signal protocols as indicated on various tables—the patient should drink either:




A) water treated with one signal at a time; in successive days as many as there are signals (1 signal for each day)




B) treat water with entire protocol at one sitting—multiple frequencies imbued in H


2


O (each signal should be used to resonate water for the length of time at least (20 minutes).




Table 7, below, gives an example of the settings for the Jacobson Resonator which have demonstrated beneficial nerve regeneration in mice. The information in Table 4 was determined with the Jacobson Resonator placed in the “Microgauss” setting.












TABLE 8









Nerve Regeneration In Mice


























.10




280 or .15







2.54




71







1.3




36







.997




27.9







.825




23







.7




19.6







.57




16







.46




12.8







.34




9.6







.27




7.6







.175




5.4







.15




4.1







.126




3.5







.09




2.5























TABLE 9











Resonated Water to Enhance Plant Growth















Amplitude




Frequency




Time




















A




0.63




17.6




30








0.84




23.5




30








1.0




28




30







B




.15




4.2




30








.268




7.5




30








.381




10.68




30







C




6.5




0.975




30








4.0




0.6




30








2.0




0.3




30







D




6.5




182




30








4.0




112




30








2.0




56




30















It should be understood that the foregoing is illustrative of the instant invention and should not be considered limitative or restrictive thereof. The scope of the invention may be further described within the scope of the attached claims.



Claims
  • 1. A method for beneficially restructuring an ingestible substance comprising:subjecting an ingestible substance for a period of time to an electromagnetic field of a specific flux density varying from 10−5 to 10−21 gauss and a specific frequency varying from 0 hertz to 300 hertz depending on the intended subsequent use of said ingestible substance, wherein said specific flux density and said specific frequency has been empirically determined to restructure said ingestible substance such that said ingestible substance beneficially affects the organism to which the ingestible substance is subsequently applied.
  • 2. The method of claim 1, wherein said ingestible substance is at least one of an aqueous mixture, a sports drink, a geriatric drink, an electrolyte drink, a neutraceutical, a pharmaceutical, a medicinal formulation, a cream, a lotion, and an alcoholic beverage.
  • 3. The method of claim 1, further comprising calculating said electromagnetic field to impinge upon said ingestible substance in a manner which is directly correlated to target masses in biosystems.
  • 4. The method of claim 3, further comprising after subjecting said ingestible substance to said electromagnetic field of a specific flux density and specific frequency corresponding to a particular target, repeating subjecting said electromagnetic field of a specific flux density and specific frequency for each of a plurality of targets.
  • 5. The method of claim 1, further comprising generating said electromagnetic field using a solenoid to which electric power has been applied.
  • 6. The method of claim 1, further comprising generating said electromagnetic field using helmholts coils to which electric power has been applied.
  • 7. The method of claim 1, further comprising generating said electromagnetic field using poloidal magnets to which electric power has been applied.
  • 8. The method of claim 1, further comprising generating said electromagnetic field using toroidal coils to which electric power has been applied.
  • 9. A method for restructuring an ingestible substance, comprising:subjecting an ingestible substance to an electromagnetic field of a specific flux density varying from 10−5 to 10−21 gauss and a specific frequency varying from 0 hertz to 300 hertz depending on the intended subsequent use of said ingestible substance, wherein said specific flux density and said specific frequency being calculated using the formula mc2=Bvlq, wherein m equals a mass of one of a plurality of targets; c equals the speed of light; v equals the inertial velocity of said mass; l equals length of the organism to which the water will be applied; and q equals unity of charge, to thereby determine a magnetic flux density (B).
  • 10. The method of claim 9, wherein said ingestible substance is at least one of an aqueous mixture, a sports drink, a geriatric drink, an electrolyte drink, a neutraceutical, a pharmaceutical, a medicinal formulation, a cream, a lotion, and an alcoholic beverage.
  • 11. The method of claim 9, further comprising calculating said electromagnetic field to impinge upon the ingestible substance in a manner which is directly correlated to target masses in biosystems.
  • 12. The method of claim 11, further comprising after subjecting said ingestible substance to said electromagnetic field of a specific flux density and specific frequency corresponding to a particular target, repeating subjecting said electromagnetic field of a specific flux density and specific frequency for each of a plurality of targets.
  • 13. The method of claim 9, further comprising generating said electromagnetic field using a solenoid to which electric power has been applied.
  • 14. The method of claim 9, further comprising generating said electromagnetic field using helmholts coils to which electric power has been applied.
  • 15. The method of claim 9, further comprising generating said electromagnetic field using poloidal magnets to which electric power has been applied.
  • 16. The method of claim 9, further comprising generating said electromagnetic field using toroidal coils to which electric power has been applied.
  • 17. The method of claim 14, further comprising arranging said coils such that each of the coils have equal diameters and the distance between the coils is about equal to the radius of each of the coils such that upon applying power to said coils, a relatively uniform magnetic field exists between the coils.
  • 18. The method of claim 9, further comprising generating said electromagnetic field using plates to which electric power has been applied.
RELATED APPLICATIONS

This application is a continuation-in-part of application Ser. No. 09/386,696 filed Aug. 31, 1999, now U.S. Pat. No. 6,458,071 which is a continuation-in-part of application Ser. No. 08/986,832, filed Dec. 8, 1997 now abandoned. This application claims priority to the filing date of both the prior filed applications. This application is also related to U.S. Pat. Nos. 5,269,746, 6,004,257 and 6,099,459 of the same inventor as the inventor herein.

US Referenced Citations (5)
Number Name Date Kind
4524079 Hofmann Jun 1985 A
6022479 Smirnov Feb 2000 A
6287614 Peiffer Sep 2001 B1
6458071 Jacobson Oct 2002 B1
6579375 Beckett et al. Jun 2003 B2
Continuation in Parts (2)
Number Date Country
Parent 09/386696 Aug 1999 US
Child 10/013325 US
Parent 08/986832 Dec 1997 US
Child 09/386696 US