Subject: (Curry) Tucson Meeting papers (fwd) Date: Wed, 30 Sep 1998 114751 -0500 (CDT) From: "Roy L. Beavers" <rbeavers@llion.org> To: emfguru@hotmail.com -------------------------------------------------- Hi everybody: The following is an extremely worthwhile discussion about some of the papers which were presented at the recent Tucson meeting...... Bill has put in some hard work and much thought.....Try to give this the time it deserves (a lot!)..... Heavy stuff here. Most of our EMF-L readers will not fully appreciate the work that is here..... If you can (as I do) "wade" through it two or three times, it will become more understandable ... and something you may wish to file away in your mind to bring it out at the right moment when that "utility expert" is lieing to you (since Clinton/Lewinsky, it's called "misleading" you). One of the papers reviewed is the latest effort by Dr. J. C. Weaver of MIT.....Those of you who have been a part of the EMF research community for some time ... already know what he says!!!.....The same thing he has been saying for years...... Bill, I hope you won't spend too much of your valuable time on the likes of him..... He is another of those "it's not possible" (according to the 'physics' theories) advocates who got themselves out on a limb some 8-10 years ago ... and are still trying to justify THEORY that has subsequently been undermined, if not DESTROYED, by the evidence.....(Others? Adair, Bennet, Barnes, Moulder -- Their kind of science is that: when the evidence disputes the theory ... why of course ... you ignore the evidence!!!) A fair question: Is it pure chance that those folks are also regularly listed as "expert" witnesses by industry in court cases??? (And, of course, they are ALWAYS the ones who find their way in front of the camera when the EMF issue is under discussion on TV.) Outside observors (the "press") should always remember that they (the science establishment) are defending THEORY. Theory that is consistently being "knocked down" or "put into question" by the EMF research results that are appearing..... As many of you know, that historical pattern is rather common in the history of science..... The "conventional wisdom" establishment of the entrenched "science" community does not readily admit to the new paradigms..... In truth, they do a lot of damage to the truth about EMF because almost without exception they hold prestigious positions on the staffs of major universities or institutions..... The "press" figures they must know what they are talking about..... The press doesn't look into their sources of income or research funding and endowments etc.....(A point which Bill Curry appropriately raises below....)......Thanks for this good work, Bill....guru... DO YOU KNOW OF OTHERS WHO SHOULD BE ON THIS LIST?????? ---------- Forwarded message ---------- Date: Wed, 30 Sep 1998 00:25:00 -0600 From: "Bill P. Curry"To: "Roy L. Beavers" Subject: Tucson Meeting papers Roy, Thanks for indicating the source of the work on stress responses of cells. I will quote more from the Columbia Univ. work later. I didn't mention it by name in my previous correspondent, because I wasn't sure whether similar work had been done by other investigators. I think there is corroborating work. Now I want to review two of the papers given on the first day of the Tucson conference (Annual Review of Research on Biological Effects of Electric and Magnetic Fields from the Generation, Delivery, and Use of Electricity). I am slow about getting this material out - in part, because I wanted to try to rebut one paper. When one encounters the participants in a bioelectromagnetics conference, it quickly becomes apparent that there is a wide range of opinions on the validity of apparent EMF effects. My opinion is that in vitro studies (especially cellular studies) present convincing evidence that there are substantial EMF effects on biological systems at low level of the fields, some of this evidence is bolstered by in vivo experiments on living organisms and epidemiological studies, but the connection between the cellular studies and the whole creature studies is more difficult to prove. A-1 J.J.L. Carson and J. Walleczek, Stanford University, “Sensitivity of the Self-Organized Peroxidase-Oxidase Oscillator to Weak Physical and Chemical Stimuli” The authors of this study used an enzyme system as an in vitro model to study how biological mechanisms can amplify weak external disturbances like EMF. They perturbed this biochemical system with red light and by changing the chemical reduction/oxidation (redox) characteristics (by adding manganeseions) . The results indicated that stimuli similar to EMF could be amplified by self-organized (nonlinear) biodynamic states. Thus, this oscillating chemical system is probably a good test bed to demonstrate EMF effects. I think this was a very clever experiment. A-2 J.C. Weaver, Massachusetts Institute of Technology, “Status of Theoretical Assessment of Weak EMF Exposures using Biophysical Mechanism Models and Molecular Change Criteria” This is the paper that I have spent some effort trying to rebut. I would like to point out that Weaver did have another paper (poster, if I remember correctly) in which he observed an effect that required the presence of magnetite, so he is not a total naysayer in respect to observations of bioeffects. This paper, however, is part of his extended effort to prove that previously reported bioeffects are not consistent with known laws of physics and chemistry. I think this paper is flawed. The author attempts to demonstrate that the effects of weak EMF will be difficult to detect in living media because of the occurrence of competing effects such as temperature variations and molecular fluctuations. He makes a statement that I think is completely unjustified: “Unless a human sensory system (multicellular system integrated with the nervous system) is involved, it appears that effects due to weak 50-60 Hz EMF will not be able to be reconciled with established understanding of physics and chemistry, and in this sense are implausible.” What I think is a fatal flaw in this argument is the following: the reaction rate for a biochemical system was assumed to follow the Arrhenius form of temperature dependence for chemical reaction rates (see Molecular Theory of Gases and Liquids by J.O. Hirschfelder, C.F. Curtiss, and R.B. Bird 1964 edition, pp. 661-667, John Wiley and sons, Inc., New York). This glosses over a number of difficulties. To understand the implications of this statement, consider the simplest kind of chemical reaction, a simple exchange in which a molecule of type A collides with a molecule of type BC, where B and C denote specific molecular fragments (which could be atoms or specific molecular units). As a result of the collision, a different type of molecule AB may be formed, liberating the fragment C. The reaction rate can be written as the product of the concentrations of the reacting species with a term called the specific reaction rate. The Arrhenius form of the specific reaction rate is R(T) = sGexp(-B/kT), where G is a preexponential factor which in gases or liquids would represent the collision frequency per unit volume of the reacting molecules with weak - if any - temperature dependence, k is Boltzmann’s constant, T is the absolute temperature (in Kelvin), and B is the activation energy - i.e., the energy that colliding molecules must overcome to cause a reaction. Weaver assumes first that the Arrhenius form applies in biochemical reactions (which might be surface reactions at cell membranes, instead of volumetric reactions - under such circumstances an Arrhenius form is dubious) and second that the activation energy is constant in chemical reactions in biological systems - as it usually is in molecular physics and chemistry. He then defines a signal-to-noise ratio, assuming that the EMF induced change in the reaction rate is the signal, and he evaluates the noise as being due to naturally occurring molecular fluctuations and to thermal fluctuations, on the basis of perturbing the reaction rate equation with respect to the temperature. If this form is used, then it is fairly easy to show that the EMF effects will be swamped by temperature fluctuations. This makes it very difficult to see the EMF effects, unless the temperature fluctuations are held to unrealistically small values during experiments. What the author neglects, however, is whether the activation energy B is a constant or is modified by the presence of EMF. If the EMF causes a change in B, the result of EMF will be a change in the reaction rate at least as large as the effect of thermal fluctuation. There is also another problem in simply assuming the Arrhenius form of reaction rate. The term sG is called the frequency factor and it is treated as a single constant in Weaver's paper. However, the term s is the probability that the collision geometry and the internal molecular arrangements are favorable for the reaction. In general, it cannot be predicted, and the Arrhenius form breaks down if either s is required to exceed 1.0 (in order to fit the experimental data) or if the specific reaction rate declines with temperature. When this is so, a more comprehensive absolute reaction rate theory developed by Henry Eyring must be used. (This is also described in Hirschfelder, Curtiss, and Bird.) Eyring’s theory assumes a collision complex of all the reactants occurs and then breaks down into the final reaction products. A statistical mechanical analysis of this complex results in there being an additional exponential factor involving the activation entropy. The activation energy itself is a free energy term that results from determining the potential energy of the reaction constituents as a function of the coordinates of all members of the reacting system. This potential surface is a hypersurface - meaning it has more than three dimensions, depending on how many coordinates describe the reacting molecules. There is a reaction path over this surface from the initial reactant molecules to the final product molecules. The potential energy of the reactants is higher than the energy of the final products, and there is a saddle shaped ridge on the potential surface between reactants and products. The reaction path over this ridge is the path that represents steepest descent of the ridge. The activation energy is the difference between the highest point on the reaction path and the initial potential energy of the reactants. The entropy term is where the effect of EMF on the reaction rate might enter the equation. To evaluate the dependence of the entropy on electric or magnetic fields, however, will require greater knowledge of the nature of the reactions - for example, if the reaction rate depends on ion transport across a membrane, how is this transport modified by EMF. Some of Carl Blackman's experiments and Janie Blanchard’s theoretical studies (ion parametric resonance) suggest that certain combinations of both DC and AC magnetic fields can strongly affect the the rate of ion transport across membranes - thus, in that instance, the EMF acts as a valve - permitting or inhibiting ion transport and, hence, effectively turning on or off chemical reactions dependent on ion transport across membranes. While I don't know the form of the effect of EMF on chemical reactions in living systems, it is common to find sensitivity to electric or magnetic fields in inorganic physical systems with characteristics similar to the Arrhenius equation. For example, in electron emission from a heated metal surface, the work function of the metal plays the role of “B” in an equation very similar to the Arrhenius equation. J(T) = AT^2 Exp (-eW/kT), where A is a constant, e is the electronic charge, and W is the work function for the emitting surface (expressed in volts). The work function expresses the energy required to extract an electron from the metal surface. This energy is supplied by heating the surface. This equation is the Richardson-Dushman equation for thermionic emission (see Statistical Physics by Edward Desloge, pp. 57-59, Holt, Rhinehart, and Winston, New York, 1966). It is a very useful equation for anyone who must calculate the emission properties of filaments in vacuum tubes. (Are any of you surprised to find that vacuum tubes are still used in electronics?) The Richardson-Dushman equation expresses the emission current density (current per unit area of the emitting surface) as a function of the absolute temperature. The higher the temperature, the more electron current you can get out of a metal surface. The preexponential temperature dependent factor in the equation is the square of the absolute temperature. Even though this a fairly strong temperature dependence, it is weak in comparison to the exponential factor. As long as there is no external field, the work function is constant and the Richardson-Dushman equation agrees quite well with measurements of the emitted current from a heated metal surface. Upon application of an electric field at the emission surface, however, the work function is effectively reduced by a factor which depends on the electric field. (See, for example, Large Ion Beams: Fundamentals of Generation and Propagation by A.T. Forrester, pp. 158-161, John Wiley and Sons, Inc. New York, 1988.) This is called the Schottky effect, after its discoverer. It results in the presence of a multiplicative factor which takes the form Exp (139 E^1/2 /T), provided the electric field E is stated in kV/cm. Note that the square root of the field appears here; my suspicion is that this is also the form that might be expected in bioelectromagnetics. Thus, if EMF sensitive biochemical reaction rates actually assume a pseudo Arrhenius form, it might be useful to plot experimental effects as a function of the square root of either electric or magnetic field, instead of plotting as a function of the field strength itself. I think that this paper is misleading and simplistic in its implications. Significantly, this work was supported in part by the MIT Electric Utilities Program Consortium; however, I don't think that an investigator is necessarily constrained to make his (or her) work fit the expectations of sponsors. A-3 M. Blank and L. Soo, Columbia University, "Magnetic Fields Accelerate Enzyme Reactions" The authors studied the effects of low level AC magnetic fields on two different types of enzyme reactions. The first type involved a biochemical system that was reacting by steady state kinetics; the second was a system which was proceeding toward equilibrium - thus one of the systems was near equilibrium and the other was far from equilibrium. In both cases the magnetic fields accelerated the reactions, and the threshold for an effect due to the field was below 5 milligauss. One interesting observation was this: if the reaction was already strong, the field had little effect, but if the reaction was weak, the field had a large effect. The frequency response of both these enzyme reactions was also interesting. These two reactions were definite examples of nonmonatonic response of reaction rates to EMF. The authors interpreted these observations in light of the mobile charge interaction model (MCI) and said that both electric and magnetic fields interact with the same charge movements during enzymatic activity. They also said that the thresholds for magnetic fields effecting enzyme reaction rates and stimulation of transcription activity in DNA molecules are comparable with the low field cutoff for epidemiological studies. Further, they concluded that the magnetic fields interact with electrons moving along DNA base pairs and that the MCI model is a rationale explanation for stimulation of transcription by EMF. My interpretation of the latter statement is that EMF can turn on cellular reproduction processes before they would otherwise be activated. Readers, please correct me if I have misinterpreted this. A-4 R. Goodman and M. Blank, Columbia University, "Differences Between Electomagnetically-Induced and Thermally-Induced Cellular Stress Response" I have previously mentioned the similarities between EMF stimulation of the cellular stress response and thermal stimulation of the stress response in studies by the Columbia team. One such similarity is the production of heat shock factor by both types of stimuli. This paper, however, identified a number of differences between the responses to these two types of stimuli. One such difference is the dependence of cellular response on field intensity. Cells whose stress response has been saturated at one field strength can be re-stimulated by a different field strength. It was suggested that this behavior could be explained on the basis that EMF of different strengths activates different segments of DNA. In my opinion, this is one of the most significant implications of this remarkable study. Even though there were several more papers in the first day's session, I will have to postpone transcribing my notes on these until later. I recommend to any readers interested in pursuing these matters more thoroughly that you get the book of (extended) abstracts for this meeting. It can be obtained (probably at a nominal cost) from W/L Associates, Ltd., 7519 Ridge Road, Frederick, MD 21702-3519. I shall slowly release to the list the content of other papers at the Tucson meeting as I have time to do so. -- ---- Bill P. Curry, Ph.D. |Physics is fun. 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