PRESENTED AT THE UNCONVENTIONAL THERAPIES CONFERENCE,
MONTE-CARLO, MONACO, 6 & 7 DECEMBER 1996


ENDOGENOUS ELECTROMAGNETIC FIELD PATTERN FORMATION IN WATER

O. Zhalko-Tytarenko, V.Liventsov, G.Lednyiczky

Hippocampus Research Facilities,
H-1092 Budapest, Ráday utca 8., Hungary
Tel: (+361) 299-0200; Fax(+361) 299-0836
e-mail: hippocampusamerica@yahoo.com
www.hippocampus-brt.com


Introduction

By studying the therapy for electrically sensitive patients (in whom the allergic reactions may be compensated or even neutralized by exposure to certain frequencies of an electromagnetic oscillator) C. Smith and J. Monro found [1] that exactly the same response can be achieved when a patient holds a vial with mineral water or saline solution previously exposed to the same frequency. Water (at least that in the proximity of a human) seems to be able to “remember”, for at least six weeks, the frequencies of magnetic fields to which it has been exposed.

The authors of [2] have provided the evidence that the UV spectrum of water (in the region of 190-220 nm) can be changed with extremely weak influences (high dilution homeopathic remedies or extremely low frequency endogenous electromagnetic fields transduced with the BICOM device). In this work, BICOM-induced changes in UV absorption of water are reproduced within at least an hour.

The following considerations make it possible to expect observable changes in the free energy of hydrogen bond formation in water under the influence of extremely low frequency extremely low intensity endogenous electromagnetic field of a biological solution. The actual occurrence of such changes in turn will support the model of hierarchical dynamic organization of supramolecular water structures and interlevel communication through hydrogen-bond interactions within this dynamic hierarchy.

1) Biomolecules’ evolution in an aqueous medium results in the necessity of structural and, under physiological conditions, dynamic conformity of the protein’s secondary structure and H-bonded water clusters in the vicinity of a protein molecule;

2) Water/protein system is strongly coupled via inter- and intramolecular hydrogen bonds. In such a system, even very small defects (e.g. created by extremely low electromagnetic bioresonance field) can be transferred over great distances approximately immediately.

3) Water has a high dielectric constant and thus will readily absorb electromagnetic waves (including the extremely low endogenous electromagnetic fields of biological systems, of course) between the species, i.e. in a case when water did not partake in bioresonance interactions, it would completely absorb extremely weak bioelectromagnetic fields.

The dynamics of liquid water comprises many small molecular movements of an hierarchical kind within large basins and jumps from one basin to another [3 and references therein]. The average lifetime of an individual hydrogen bond in liquid water is known to be 2-3 ps whereas that of a global hydrogen-bond network structure is about 30 ps [4]. These lifetimes account for more “strong” hydrogen-bond interactions inside water clusters, which is evidenced by the structure of the band in the IR spectra of water [5]. One should distinguish these “core” interactions from the more “weak” hydrogen-bond interactions at the surface of water clusters. The occurrence of the hyperbolic region in the power spectrum of total system (64 water molecules) potential energy in the instantaneous structures of liquid water indicates that the correlation of hydrogen-bond network fluctuations decays through multiple processes [3]. Longer timescale dynamics involves still more coupled events.

In fact, any biochemical process shows cooperative behavior which is determined by noncovalent interactions [6, 7 and references therein].

Proton polarizability of the structurally symmetrical

B-H...B = B...H- B
bond within H5O2+ group is shown to be about two orders of magnitude larger than the usual polarizabilities caused by the distortion of electron systems [8].

This phenomenon is due to the proton migration within hydrogen bonds and results in at least three interaction effects: an interaction between such hydrogen bonds via proton dispersion forces; an induced dipole interaction of the hydrogen bonds with the fields from their environment; and interaction between the transitions in the hydrogen bond and other vibrations [9].

According to ab initio SCF calculations, H-bonded chains with multiminima proton potentials show still larger proton polarizabilities than single H-bonds with double minima potential [10]. Since the first excited level of a tunneling proton is separated only slightly from the ground level, an extremely small electrical field is sufficient for the first excited state to be mixed with the ground state.