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A healthy cell is unusual in that self-sacrifice is the rule in cell biology. In cancerous cells apoptosis is inhibited as a rule. What controls this process? INFORMATION does.
Mitochondria are known to self-regulate their biology via two coupled pathways called autophagy and apoptosis. Apoptosis is self-sacrifice. All somatic cells are actually committed to die but they dedicate their existence to the survival and modification of the stem cells. Cancer cells also harvest the blood supply for its sole benefit.
AUGER EFFECT: UV light does not break chemical bonds in DNA as the skin and eye doctors tell us. Instead, DNA is protected via the Auger effect, a process where ejected core electrons are replaced by electrons from a higher energy level, resulting in a release of energy (in this case, heat). Heat favors the formation of hydrogen bonds using H+ over D so the deuterium can be excluded by sunlight in the formation of exclusion zones to be eliminated by the body in many ways.
So this brings up an interesting angle to consider. How does light interact with electrons precisely? All cells release ELF-UV. This seems queer until you understand the Auger effect. Are their rules that govern this interaction? Mitochondria select and order electrons and protons by spin and they transfer information to the orbital angular momentum using light waves. Light is made of photons and photons have a quantum spin number of one. Photons are from the family of bosons and they are the force carrier of the electromagnetic force. So light can increase informational transfer if it can increase its orbital angular moment in some way. How do we increase the orbital momentum of sunlight? We can turn visible light frequencies into laser light. Is this how it happens in life? Yes, it is. The fats in skin with hemoglobin and light are fully capable of making a laser light the body can use to increase the OAM or light captured inside of us. One thing physics knows is that light seems to have an unlimited potential to carry orbital angular momenta. This means light can carry massive amount of information but only a limited amount of energy. The energy carrying capability is linked to the frequency of light. We now know from quantum thermodynamic experiments that information can be transferred from the quantum spin number to OAM. This means that the spin of electrons and protons are critical to a body gaining the massive information buried in sunlight. Now how does light interact with electrons and protons? I have already taught you how this happens with electrons : that is the photoelectric effect. How does it happen with protons? H+ and deuterium have different quantum spin numbers, so they have different abilities to transfer information in light waves. H+ can transfer more information than deuterium can. Hence, this is another reason why H+ was selected by the ATPase in evolutionary design of cells. The other thing to know is H+ is more lipid soluble to enter tissues that electrically active more easily. Deuterium does not have this effect. This means that H+ can enter tissues that are lipophilic. It turns out human tend to bury their highest mitochondrial density in tissues that are lipophilic, namely the brain and heart. In both organs they have the highest metabolic rate of any tissue in the human body. I believe this is a function of their ability to have protons that can share the most information to other atoms in our cells. Most of the tissues in our body are made of bosonic matter. This is why I told you years ago that our tissues are a syncytium called a Bose-Einstein condensate. It turns out those bosons in use are hungry for the information and energy that electrons and protons can provide them. This is how life goes from abiotic to biotic in my opinion. It is not from energy transfer. I believe it is from massive information transfer that occurs between the quantum spin number or electrons and protons to other atoms that are organized in the zygote by the effect of deuterium. Deuterium helps build the body plan in the zygote and helps it grow by altering mitochondrial energy and information flux tissue by tissue in amazing ways by its presence or absence at certain spots in biologic substrates. I will have a blog this month to show you how it operates mechanistically in the retina.
How do we know how light transfers physical things like energy and information ? We know this from the solar science done about the atomic spectra. I told you in the first deuterium Patreon blog that deuterium is destroyed in the sun and that most of the red light in the sun comes from the H+ versions of hydrogen. This light’s target is on all things with heme in them. Cytochrome c oxidase has 4 of them. That cytochrome is what controls the program of apoptosis. This is half of the thermodynamic couple designed to get rid of poorly functioning mitochondria. My belief is that apoptotic programs are directly related to a lack of information assimilation in the tissue in question. I believe UV light controls the process of autophagy/mitophagy which is related to poorly functioning energy flux and slower ECT speeds are their hallmark. These mitochondria are the ones studied by Wallace. They have low NAD+, pseudohypoxia, higher space between the cytochromes lowering electron tunneling speeds leading to the term called heteroplasmy. These power plants will eventually lose their ability to recycle unless UV light is restored to the system. It has the highest energy density in the system to provide the energy flux in the system to speed up ECT flow and ROS/RNS free radical signals. Free radicals are only produced via high energy reactions (mid-1930’s). This is likely why cells use the UV part of the spectrum to signal optically. Many of the early work on ELF-UV light showed it is only liberated when the optic heads are illuminated by light (pg 94). This links the process to my Vermont 2017 talk.
When this occurs cells begin to release ELF-UV light to the local atoms to try to make melatonin to improve mitophagy/autophagy. ELF-UV needs oxygen radicals present to radiate light ( p.79 Van Wijk) This process can exist for a time in dysfunction but when enough information is lost with that tissue, a redox shift occurs and then the Warburg metabolism kicks in. At this point, tissues lose the ability to recycle their mitochondria, so the only option left is to use apoptosis. Cells and tissues “know” because of the light they contain that this is the last gasp maneuver. But they do it waiting for the environment to return its source of energy and information from the sun. Cells need all of the visible spectra to regain control of both autophagy and apoptosis. They are the ultimate coupled system in a cell. (Predator and Prey)
How does sunlight transfer energy/information?
Atomic spectra measure radiation absorbed or emitted by electrons “jumping” from one “state” to another, where a state is represented by quantum numbers with values called n, l, and m. The fourth number is S = spin. This is the big one for this webinar. Spin is how infromation is transferred from light to make atoms biotic.
These are called the 4 quantum numbers associated with every particle. There are quantum rules that govern these quantum transfers called the Transition rule. I want to be clear here. Energy and information are both transferred in packets called quanta. Energy via the PE effect and information via quantum spin number and OAM. It turns out OAM is another conserved property in nature, like energy and mass conservation that define the laws of thermodynamics. Why do I mention it? This is how life does what it does. It appears to skirt the second law because cells are better at information transfer than they are at energy transfer. They want to know more to become more. They only need a baseline of energy to do this because they have perfected information transfer in their design which is codified in our RNA and DNA.
This energy and information transfer is not a continuous download. It is controlled by rules. The so-called “Transition rule” limits what “jumps” are possible on Earth. In general, a quantum leap or “transition” is allowed only if all three numbers change simultaneously in the process.
There are exceptions to the rule is the Zeeman effect. This is because a transition will be able to cause the emission or absorption of electromagnetic radiation (photons have a spin number of 1) only if it involves a change in the electromagnetic dipole of the atom.
Why is the Zeeman effect special? It deals with spectra of hydrogen. Ya know where H+ and D come from? Remember that the spinning ATPase makes a local magnetic field in the mitochondria. This is critical for the Zeeman effect to happen.
The Zeeman Effect in hydrogen occurs when an external magnetic field is applied to hydrogen, and sharp spectral lines like the n = 3→ 2 transition of the hydrogen split seen in textbooks. The 3 lines can be seen as multiple closely spaced lines with higher resolution. Bohr did not have this power when he made the original of atomic theory and quantum mechanics.
This was first observed by Pieter Zeeman, when he relaized this splitting was attributed to the interaction between the magnetic field and the magnetic dipole moment associated with the orbital angular momentum in protons.
In the absence of the magnetic field, the hydrogen energies depended only upon the principal quantum number n, and the emissions tended to occur at a single wavelength. This was easily measured with a spectroscope.
This is another reason why H+ was favored over deuterium in the quantum evolutionary construction of the matrix. H+ has the ability to transfer more light information to them, this is how protons transfer information from the sunlight to the Bose Einstein Condensate of atoms in the rest of your body. Sunlight animates atoms with information. The energy flux is not the key. The energy flux is needed to keep ECT flowing in most tissues. You will note that not even that is needed in some tissues like RBC’s. Why? They have no mitochondrial so they do not use the TCA cycle.
RBC’s like deuterium and this is why our blood plasma is jammed with them (above). Deuterium and hydrogen can be used to generate ELF-UV to signal mitosis or growth in a controlled fashion when melatonin is controlling autophagy and apoptosis. When it is not deuterium can be usurped by a Warburg shift to cause cancer by liberating massive amounts of UV light from cells (Van wijk/ Popp).
How does this happen?
When deuterium or H+ have a voltage placed across them they can emit UV radiation. This becomes easier when they are under a pressure gradient. So how does this process work in you? RBC’s are loaded with Fe porphyrins called hemoglobin that acts like a dye laser. They also absorb massive amounts of light. The absobtion spectra of hemoglobin is from 250- 600 nm and the cut off is SHARP.
Since RBC are swimming in a blood which is made up of 93% water there is a ton of deuterium present. The RBC’s are light ferry and their oxygen payloads are delivered to mitochondria. The mitochondria are fed a constant source of electrons from foods or recycled FFA’s, amino acids, or glucose from gluconeogenesis. These electrons have a quantum spin that carries information of the sun when they were programmed. They are also in the excited state by the very same photons. This is done by the frequencies of light photons. This imparts a power to each electron and allows each electron to be sorted by the information and energy programs in the cytochrome proteins. The mitochondria has several dehydrogenases that pull hydrogen from foods or substrates delivered to the matrix for metabolic recycling. These hydrogens harvested from foods tend not to be deuterium because we know there is a tight specificity where deuterium is in the TCA cycle substrates as the picture below shows
The blood is a magnetohydrodynamic plasma which contains both versions of hydrogen and in many different chemicals. Most of the H+ is incorparated into hydrogen bonding networks of water and can anywhere in the body via the blood lymph or syncytium/interstitium to touch every last bit of collagen in the body. Here these protons can share the information they contain. This is how the tensegrity system gains information from sunlight.
Since sunlight forms an exclusion zone using H+, deuterium is excluded and its concentration in the blood rises. Irradiated blood comes closer to the surface because of the electric and magnetic fields in light and these waves have many effects. Releasing NO is one effect, but creating a pressure within the vessels also effects building a charge in all the blood products and cholesterol in the arteries. The charge really build because all these things tend to be sulfated. (picture below)
As the zeta potential of the blood is raised by solar irradiation the blood heat up and this physocally effects deuterium more than H+. Since RBC’s are highly charged on their surface a voltage is developed that discharges to the anions or anodes in blood. This effect causes both hydrogen and deuterium to emit UV light.
Since most of the H+ is in EZ form of water it leaves the deuterium exposed in the blood to emit this light perferentially. I have always believed this is why Pollack found that when the EZ forms in water its viscosity and is absorption spectrum changes. It begins to absorb light at 270 nm. This is deep in the short wave UV spectrum. Not much sunlight gets to Earth in this range, yet water and hemoglobin absorb this light. This looks unusual until you understand what makes UV light inside of us in this range.
When you compare H+ and deuterium emission it turns out deuterium is more capable of emitting a continuous and and more powerful light source of UV light. Hydrogen-1 provides a very similar UV spectrum to deuterium. In fact, both isotopes have been used in UV spectroscopes. However, scopes using deuterium have a longer life span and an emissivity (intensity) at the far end of their UV range which is three to five times that of an ordinary hydrogen. This is why hemoglobin has strong peaks in the 250-300 nm range even thought this type of light is not often present in sunlight even in equatorial regions. This was my clue that deuterium in the blood is why hemoglobin and the EZ used UV-C light from 250-280nm. Deuterium is fully capable of creating a continuos spectrum in this range. Remember blood plasma has 150 ppm of deuterium. This tells you something deep about the quantum biologic systems.
The emission UV light from deuterium does not work like it does in excited electrons when they fall back to the ground state and give off a light photon. That process in electrons is called atomic emission, where excited electrons emit radiation. Instead, deuterium uses an unusual molecular emission process, where radiative decay of excited states in molecular deuterium, causes the effect the UV light emission.
BLOOD AND CHLOROPHYLL ARE PORPHYRINS THAT DIFFER IN UV LIGHT
Blood does not glow under UV light, but it reacts with a chemical (luminol) that does fluoresce, so it can be detected after this reaction using ultraviolet light at a crime scene. The interesting thing is that chlorophyll does fluoresce!
Chlorophyll makes plants green, but it fluoresces a blood red color under UV light. This is how plants gain information for their protons in leaves. IF you want to check this out for yourself grind some spinach or swiss chard in a small amount of alcohol (e.g., vodka or Everclear) and pour it through a coffee filter to get chlorophyll extract (you keep the part that stays on the filter, not the liquid). You can see the red glow using a black light or even a strong fluorescent bulb, from your house, which (you guessed it) gives off some ultraviolet light.
Deuterium is the UV optical switch in blood that control melatonin levels in tissues to control mitophagy and apoptosis programs in mitochondria. These two self regulating programs must be controlled for a good healthy life. If control is lost in this mechanism from either the energy or information side of the equation disease is the result. Mitophagy controls the quality and quantity of the water in the cytosol. This is why the cybrid studies I mentioned in TIme 4, 9, and 19 gave the results they did. Cytosolic water must be free of deuterium. Matrix and cytosolic water are where H+ is needed to impart information to light hydrogen as it is pulled from the anions in the TCA cycle and urea cycles. Water links both of these cycle via fumerase at a place called Kreb’s bicycle. This means water in the periphery of blood is a lot different composition inside mitochondria and this water creates a different size and shape of its crystalline form to changes cell water. You blood plasma must have higher deuterium concentration by design.
Protonicity or proton conduction in water networks is how tissues gain the ability to know things via the information quanta passed to the orbital angular momentum of H+. This is how energy and information are transferred from the sun to our atoms. We are made up of lots of atoms mostly considered bosons that collect light information. That is what life is a really at our core.
When the familiar red solar spectral line of the hydrogen spectrum is examined at very high resolution, it is found to be a closely-spaced doublet. This splitting is called fine structure and was one of the first experimental evidence for electron spin. The small splitting of the spectral line is attributed to an interaction between the electron spin S and the orbital angular momentum L. It is called the spin-orbit interaction.
The familiar red H-alpha line of hydrogen is a single line according to the Bohr theory. The straight application of the Schrodinger equation to the hydrogen atom gives the same result. If you calculate the wavelength of this line using the energy expression from the Bohr theory, you get 656.11 nm for hydrogen, treating the nucleus as a fixed center. If you use the reduced mass, you get 656.47 nm for hydrogen and 656.29 nm for deuterium. The difference between the hydrogen and deuterium lines is about 0.2 nm and the splitting of each of them is about 0.016 nm, corresponding to an energy difference of about 0.000045 eV.
This corresponds to an internal magnetic field on the electron of about 0.4 Tesla. Why is this detail important? It is directly in the middle of the Earth magnetic field strength. Remember that H+ and D both have unique magnetic moments because they have different quantum spin numbers.
The magnetic field magnitude at Earth’s surface ranges from 25 to 65 microteslas (0.25 to 0.65 gauss). Roughly speaking it is the field of a magnetic dipole currently tilted at an angle of about 11 degrees with respect to Earth’s rotational axis. It is as if there were a bar magnet placed at that angle at the center of the Earth with respect to our protons.
Does anyone want to guess where magnetic strength is strongest on Earth? The Yucatan peninsula. Does anyone want to guess why? Does anyone want to guess why I recommend everyone sick go there now? Illness is a lack of information redox in your cells. You have been thinking this was all about energy flux because that is what the laws of thermodynamics suggested based upon a CLASSICAL interpretation of them. Since 1960, that has fallen by the wayside. You’ve now been introduced to really how the second law allows your cells to gain information how to stay far from equilibrium to do the things life does. Nature will astound you when you see her magic.
You need to go the Earth’s library where more information can be transferred from the sun and Earth to your cells to fix any problem you have in the Yucatan.
Lesson over. You’ve just been introduced to Quantum Thermodynamics of life.