# Redox Rx is all about light. How much do we really know about LIGHT?

Discussion in 'Redox Rx' started by Jack Kruse, Jan 20, 2019.

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Redox Rx is all about light. How much do we really know about LIGHT?

Why do I say this? There are a billion photons for every atom in the universe. (@25:25 video below). This tells us we have a deep problem in the Standard Model. A photon is the force carrier for the electromagnetic force. This ratio of light to atoms should tell the common sense of physicists that light is still the most misunderstood thing in physics, even today. Hard to believe but it’s true. If so why do they ignore the basic incongruity? Because they “think” the beauty of math is so good for most of the theory we just need to go further to figure out the rest. This is why we have the LHC fundamentally. What don’t they appreciate? Scientists, being humans, are biased. But concern about bias doesn't correct the bias. Sometimes concern with bias produces MORE bias. Fighting bias with concern about bias is like fighting fire with fire. Cleaving to the evidence is the best and only protection against bias.

They think they know it all about light. Do you believe them? I don’t. I believe the keys to gravity will be found in the areas of light we currently have a Dunning Kruger effect too. This is why physics theorists made up the Higgs and Dark energy/matter ideas, to begin with. They did it to make sense of the math. We did it to suit the math and not explain nature. For a Black Swan this is a problem and why I remain very unsettled about the science they consider settled.

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Example: Can light travel faster in your tissues one it is assimilated? Can you go faster than light speed in glass or water? Yes, it can.

Light travels at a speed of 186,282 miles per second, in a vacuum. Life is not lived in a vacuum. This is described by the Theory of Relativity equation E=mc2. ... The equation is n=c/v. In bulk water, the refractive index is 1.3 and in glass, it is 1.5. In water depleted of deuterium, like cells make, the speed of light is really altered and SLOWS because of the change in atomic mass of the matrix and cytosol. Therefore, light travels faster through water, than it travels through glass.

If a charged particle travels faster than this speed in heavy water, it will emit Cherenkov radiation (below).

Cherenkov radiation is produced when a charged particle travels faster than the speed of light in that medium. As nothing can travel faster than the speed of light in a vacuum, Cherenkov radiation can only happen in a medium such as air, water or glass. Many of you are probably familiar with the idea of the refractive index $[​IMG]$ of a medium. It crops up for example in Snell’s law, which allows us to calculate the angle through which radiation deviates when it travels from one medium to another. Snell's law and Fermat's law are basically equivalent in this discussion. For those paying attention, you'll recall water undergoes a refractive change when the EZ is made.

What do you think this means for cells?

Can you imagine what this means to biophysics in living systems?

"What really strikes me about light is the variety of things you can do with it." During Gérard Mourou's Nobel lecture, he talked about his passion for light and the variety of applications of light. Watch his Nobel lecture here: https://bit.ly/2LB4RW1

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We all know today beyond a shadow of a doubt that the dominant part of the solar spectra is IR-A RED light and it is made by the emission spectra of the H+ ion in the sun.

Is this why the first step in controlling all thermodynamics on Earth was to use the most common element in the sun's spectra??

It's emitted photons acted as the controlling arm of H+ on Earth 93 million miles away. When you look inside a chloroplast of mitochondria the evidence is everywhere when you observe what nature is telling us.

It also explains why we got natural selection and conditions of existence as the first steps in evolutionary change. The problem is, it was not Darwin's version of events........it is a quantum selection made by H+ light emission from the condensed matter lattice of the sun.

But what else does it mean?

The sun is the center of the quantum vibrations in our solar system and at 93 million miles from the sun, the Earth sits at the 3rd harmonic of the solar plasma in our planetary system. The frequency of solar plasma at our distance on Earth is around 3 mHz (milli Hz).

Why did I mention that about the sun?

There are lots of interesting things to say about blood cells and fluid flow in humans. There is a new field of magneto-electrohydrodynamics, where they study the geometrical structure of blood cells in our circulation, and electron flow might be the key to how the sun interacts with them.

I quote, "the 3rd lamellar spacing of RBC's = 40.6 Å (the 3rd, core hydrophobic lipid layer is significantly smaller than the spacings above, and the electron density is almost constant in the hydrophobic membrane core. This density profile is well described by α-helical coiled-coil peptides, which are embedded in the cell membranes."

They go on to report, "hexagonal packing of the lipid tails are in the hydrophobic membrane core. The distance between two acyl tails has been determined, where q|| is the position of the corresponding correlation peak. We note that this area also includes the area of cholesterol molecules. Where did this come from? Right here: http://www.nature.com/articles/srep39661

What did that just mean for the mitochondriac in training? It means I just showed you how we are supposed to connect with the sun WIRELESSLY VIA your RBC's lattice antenna.

The implication of the first law of thermodynamics is large for a Black Swan. Energy in the universe is a zero-sum game. It means energy is fixed in the universe just like the speed of light is fixed. This means there is a set amount of energy that can change between many different forms of energy. What causes these transitions? The electromagnetic environment is the short answer. This is the basis of your redox potential in your cell. When it varies the types of matter you make has to vary by definition of the first law of Thermodynamics. This brings us to Rudolf Clausius who began the understanding of the second law in the 1850s and 60s using mathematics. He found that not only did energy have a setpoint, but that it followed a strict law. Energy transitions always seem to go from hot to cold. This implies when your colony of mitochondria is falling for any reason, you must seek to increase their ability to make heat in some way (sun) or lower the environmental temperatures around this colony of mitochondria to make heat transfer more efficient. This is exactly what Carnot Theorem said too at the same time. The flow of heat is a one-way process in nature. So life decided to something amazing. She decided to store energy and not let it become thermalized so cells could transform the energy into matter the cell deems necessary to live far from equilibrium. This is one of those weird things in how light can operate in life below the submolecular level. DS/dt is greater than or equal to zero. S = entropy. Life seems to have used the or equal part quantum mechanically to do the things a cell can.

During the back half of the 19th-century scientists like Boltzmann began to realize nature might act very differently at small scales (atoms) then it did at larger scales. This opened the door for quantum mechanics in 1905. Boltzmann was the guy who saw the way because he realizes science had to let go of certainty because probability described nature better than certainty. Boltzmann ideas were heretical and Ernest Mach was one of his biggest critics. But his math married up perfectly to experiments so people had to take him seriously.

Boltzmann saw what Clausius could not because he accepted that nature was based upon atoms. When energy is shared among more atoms energy appears to dissipate macroscopically but it has not microscopically. The energy is just being shared by a larger amount of atoms in the environment causing a relative change in how energy appeared to be used. He was able to put numbers to this process and this is why he is revered today.

There are a billion photons for every atom in the universe. The guy in the video above says it at 25:25. What does this mean when you understand what Boltzmann really said? It means matter can never give energy back to light.......this is why entropy is a one way street thermodynamically. As simple of a concept as this is, physicists do not realize this today and have no idea what it means for life.

Light's energy is always a million times greater than atoms.......so light has to impart its energy into matter and that energy is what changes matter. In the case of light, it changes electrons energy and information and electrons change the chemistry of things. The red light part of light moves things with mass differently than other parts of the spectrum of light. I have a sense the other 5 parts of the spectrum do things to the atoms in matter we have not yet found in science-based upon Boltzmann's insights of how energy is changed via atoms. It seems to me that the electromagnetic state of those atoms is the key to understanding how energy is changed into change matter by the equation E=mc^2. This is really what life is up too in my opinion. Life uses light to sculpt matter it deems necessary.

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If energy is fixed in the universe, and the speed of light is fixed, what does it mean when we know there are one billion photons present in the cosmos for every atom in the known universe?

It means light is the Jacquard card of life and cells........

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Implications of this idea?
Is this why bipolar humans seem to be in certain zip codes based upon hospital data in cities?
Why doesn't the doctors or hospitals realize what it means?
How on earth the lithium ion could have such a dramatic effect in treating mental conditions like bipolar disorder? Have you ever thought about this? Might the effect be linked to the quantum spin of Lithium? Moreover, could this be a key in why and how consciousness works? Lithium 7 and 6 only differ by having one more neutron, but this small change changes how they react in an electric and magnetic field because both isotopes have different nuclear spins. Most biologist and physical chemists have no idea how a nuclear spin affect physiologic ability.
They believe that the chemistry of the two isotopes should be the same in a reaction, and the slight difference in atomic mass largely washes out in the "watery environment" inside cells. They do not even realize that this watery environment would be changed by this isotope effect and this would also affect the action of protons in water networks in cells.
These water networks for an extreme Faraday cage inside of cells that would protect it from environmental EMF's and this would prevent or slow quantum decoherence by preserving the coherence of atoms embedded in the EZ water. What if I told you that these experiments were done in 1986 and show that Lithium does appear to work magnetically using its spin state to determine reality? Would you believe it?
Could it be that in environments where magnetic flux is poor, Black Swan MD's should expect more bipolar people will exist because light in those areas is altered in some way that we do not appreciate today in medicine?
How would you see if my insights are right?
Go to a country with a high latitude with a mixed population diversity and see what has been found via zip codes.
Quotes from the article below: "The incidence rate per 100 000 per year in south-east London was over twice that in Nottingham and Bristol. There was no significant difference in the rates of disorder in men and women. Incidence rates of bipolar disorder in the combined Black and minority ethnic groups in all three areas were significantly higher than those of the comparison White groups."
Why might these relationships all exist thermodynamically? I will tell you it is the INVERSE SQUARE LAW staring you right in the face. London has way more people = bad electromagnetic environment. Bristol and Nottingham much less.
Quote from the article: "The incidence of bipolar disorder was higher in south-east London than in the other two areas and was higher among Black and minority ethnic
groups than in the White population."
Why should this finding shock you? Nottingham is the in the middle of England at a higher latitude than London. This result tells the Black Swan that population density is far more important than latitude especially when you have White skin. It is a way bigger deal if you have dark skin. Why does race really matter here?
Your surface skin tone is how you work electromagnetically with the light in that area. Black folks have equatorial shells.......this is why they get bipolar diseases more frequently in the UK. Their melanin needs more sunlight not less to maintain their neurologic function. It also tells us if you are dark skinned and have an equatorial engine you have ZERO business living in a major 5G city.
How many will realize these things without understanding light well?
How many low dopamine critics will call this racist?
When you observe nature as she is.......you can learn a lot. I pay attention to what most ignore when it comes to light.
In the future, population density is the single biggest driver of diseases in our modern world because of these insights tied to light. This is an uncommon idea because up until 2015 life expectancy in humans has been climbing in cities. Today we now have proof Jack's insight about falling longevity in cities now exists.
How did Jack know it would stop and reverse and show up in newspapers and nobody would know why?
Jack understands how light works in cells.
Do you understand it as well as you should?
Are your current decisions based around this understanding?

If energy is fixed in the universe, and the speed of light is fixed, what does it mean when we know there are one billion photons present in the cosmos for every atom in the known universe?

It means light is the Jacquard card of life and cells........

Jacquard built the first computer that used punch cards to make silk patterns using a binary pattern using the loon.

So how did Mother nature build her first computer called a cell?

Well because there are one billion photons for every atom she started with light. She realized 4.6 billion years ago that light contains both energy and information at a ratio of a billion to one. Of the two she was the first to realize that information in light could be used to organize matter.

It took until Maxwell's paper on demons in the 1860s, for anyone else to realize this.

Light is the "bit" cells use to transfer information. Information is buried in OAM of light. The energy in light is buried in frequency. Since there are one billion photons per atom energy and information has to flow from light to atoms. It cannot flow the other way, just like a waterfall cannot flow in reverse.

A billion to one ration is like asking a 20,000 water fall to reverse its flow without adding a bit of energy.

There is no way for matter to transmit the information or energy to light because of this primordial ratio. This means that atoms are the hardware of the computer and light is the software that runs the computer.

It also means information and energy move from light to matter all the time because of the second law.

Why did she choose light?

Light is the ONLY particle that seems to have an unlimited amount of OAM, and OAM = information.

That is not true about electrons or protons. OAM of both is also limited.

Information can create order from chaos only when we store information about light in our memory (water). What is the physical basis of this? With time, light information will fill the capacity of water and fill up and memory will decline. Information can only be useful on an ongoing basis until memory deletes information contained in light.

This means there really is no free lunch. How did life do this? Evolution built sleep to be mandatory. This is where memory in water is being deleted diurnally so that we can continue to use the information to order our cells while using the light energy to power the cell.

Because there are more photons than atoms and because light appears to have unlimited OAM.........nature chose to use light to drive all biologic processes at the submolecular quantum level. How do you increase OAM of light? You use crystals to make a laser.......laser light has higher OAM than sunlight.

Now......what did I say in Vermont 2018 lecture again about lasers and cells?

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The erasure of information is what drives entropy increases over time. This is a consequence of having 1 billion light photons to one atom ratio in the universe.

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Adding sunlight to cell water makes the dielectric constant go from 78 to 160. Why is this a big deal inside a cell? Is this a cipher of an ability of light adding OAM to water in some way? What are the collateral effects in the atoms that make up the hardware computer when this happens? It turns out the ATPase optimal operation is quantized to these changes.

Under the power of non-flickering red light from the sun, the ATPase become 100% energy efficient nano-torque motor. Researchers are now adding chemicals to cells that can monitor toque speeds like anemometer measure wind speeds on a barn. To measure the micro-viscosity inside a cell, the researchers first needed to create and insert the measuring protein. This allows them to understand the hydrodynamics of how the created probe behaves diurnally day and night as the environment varies. Different electromagnetic environments should create different viscosities which alter the tensegrity of the system. Once you alter the shape you alter the charge and this is how redox varies inside a cell. Using computer simulations of liquids, the researchers were able to show that as the viscosity of the solution increased, the rate of rotation of the probe decreased and its fluorescence changed in a measurable way. So it appears increasing the viscosity of cell water increases the EZ, decreases the pH, raises the net negative charge while allowing the cell to create ELF-UV biophotons. This is the kind of paper a Black Swan loves. It undercover the recipes of Mother Nature for the ignorant to see. #biophysics #mitochondriacwisdom https://pubs.acs.org/doi/10.1021/acsnano.8b00177

How do we delete information? Have you ever heard of the Landau limit?

CARNOT HEAT ENGINE DYNAMICS: Every 3.5 times the ATPase spins one molecule of ATP is made. Only H+ can spin the ATPase. Deuterium cannot spin the ATPase and in many tissues, it destroys it. Each molecule of ATP in a cell controls 8,800 water molecules binding sites and 20 potassium ions to make a liquid quasi-crystalline semiconductor inside every cell of our body This crystal is built by deuterium depletion of the mitochondrial matrix at cytochrome 4. This chromophore has 4 red light photoreceptors and it has a heme protein in its core. All these are destroyed by free retinal from melanopsin dysfunction.

What do you think that would do to the normal ratio of deuterium to protium in a cell even if you knew nothing about biology? It is common sense. As deuterium flows into the matrix less ATP is made. As less ATP is made we get diseases and come close to death. This is exactly what cyanide does at a faster time scale and people want to act like tech screens are "safe". This is a freaking joke to those of us who understand biophysics.

In the living state, potassium acts like “the glue” to keep our protein backbone and water in a quasi-crystalline gel state inside our cell to maintain the semiconducting plates together in a cohesive form. This is why K+ is critical in setting the redox potential of water in a cell. In this way, you are building a special type of semiconductor that forms “the fourth phase of matter” and can act like a “topologic insulator.”(TI) A ‘TI’ allows quantum effects to happen in warm wet environments. This idea offends the core of standard physics but even they are coming around to this issue. K+ changes the optics inside of a cell that allows it to use OAM.

The Fo base piece of the ATPase is embedded in the mitochondrial inner membrane is a molecular turbine driven by the transmembrane proton gradient. Proton entry forces a central camshaft to rotate within the Fo baseplate and the F1 head group, altering the subunit conformation as this movement takes place.
A second, off-center protein tether connects the head group to the base piece and prevents the headpiece spinning uselessly as the central shaft rotates. Energy is transmitted to the catalytic subunits in the ATP synthase F1 headpiece by the rotation of the camshaft. The "cam" distorts the protein subunits, destroying their ability to bind ATP. The energy input is used to drive ATP release, not for bond formation.

It is presumably necessary to disable the catalytic mechanism on the center which has just formed ATP (to stop this center hydrolyzing its own product) before destroying its ability to bind ATP. This allows the product to be released. Meanwhile, the two other active centers are performing their own parts of the catalytic cycle. The three active centers operate simultaneously, but 120 degrees out of phase. It takes at least 9 H+ protons (possibly as many as 12) to drive one revolution of the camshaft and produce 3 ATP molecules.

HERE IS WHAT EVERYONE FORGETS: Remember that the whole complex is reversible. Electrons can flow cytochrome 4 to 1 and the ATPase can spin the opposite way. What controls the motion? The electromagnetic force of light does. This is a big deal in a blue-lit 5G world.
https://arxiv.org/abs/1508.06135

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^^^^is this why regular cold exposure combines with (seasonal) carb restriction is what nature requires of our ATPase via Carnot theorem?

Water carries light information. This is why water has a memory. And you sleep to erase part of the information stored in water. (Luc Montagnier)

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Screen time increases the likelihood of Adrenal Fatigue.
How?
Screen time is linked to AF via the butterfly effect of light on heme-based chromophores/ferroptosis/POMC/dopamine.
Most people have no idea it is a topologic defect caused by nnEMF in our environment that alter how the photoelectric can interact with our cells.
More proof that getting AM sunlight to program your RBCs is the key to avoiding AF?
This podcast gets into this photoelectric problem.
https://drsherrillsellman.com/podcast/audio/wwmk/WWMK_012419.mp3
When your eyes, skin, gut, or lung surface are afflicted by nnEMF trauma it induces cell damage in heme-based chromophore proteins that liberate something called CpG Islands from our nuclear DNA/RNA or our mtDNA from the cytochrome proteins like cytochrome c oxidase.
It has also been shown in the literature that RBCs homeostatically bind mtDNA, and RBC-mediated DNA scavenging is essential in mitigating tissue injury after CpG-DNA is liberated from heme-based proteins from destroyed cells. What kind of disease states should we expect to see cf-mtDNA elevated? Any disease where inflammation is induced by heme protein destruction = blue light hazard, ADRENAL FATIGUE, depression, nnEMF, sepsis, trauma and most mitochondrial and RBC diseases tied to alterations in circadian biology. All neurodegenerative diseases fit this bill too.
What protein controls circadian cycles in our surfaces I mentioned above? Sunlight induces changes in tissues below these surfaces. What gets programmed just below these surfaces? RBCs? What is in RBCs? Peroxiredoxins, cytochrome c oxidase, hemoglobin, catalase. All of them are heme-based proteins. Most of them are inducible proteins too. This means that the environmental EMF or oxygen levels induce their production. This is how biochemistry varies in tissues. Biochemical pathways are not foundational. The electromagnetic fields around us induce the biochemistry in our cells.
What do heme-based proteins due to the circadian mechanism controlled by PER1 protein? Peroxiredoxins affect the PER protein function by way of ferroptosis in the circadian clock gears of cells and this is where ADRENAL FATIGUE begins in human PVN in the brainstem. If you do not do this, eventually your PVN will become hypermethylated and be recalcitrant to most therapies. Why does the PVN get hypermethylated?
Tissue damage in the nervous system induce ferroptosis and this liberates Vitamin A in the retinal aldehyde form and this aldehyde destroys the heme-based proteins I mentioned above. What causes methylation problems in the brainstem? The liberation of CpG Islands from our mtDNA and DNA/RNA in damaged cells.
Red blood cells (RBCs) below our 4 surfaces need to be programmed by sunlight and no other electromagnetic fields. In this way, RBCs are the key modulators of the innate immune responses by scavenging these chemokines from blue light and nnEMF fields and damage.
Keeping your RBCs in tip-top shape is one of the best treatments for adrenal fatigue I know of. Seeing the AM sunrise, avoiding nnEMF day and night, and STRICT avoidance of ALAN post-sunset is MANDATORY to get better.
This Black Swan perspective helps explains why parabiosis studies in the literature have shown why young blood shows so many health benefits in disease states. Blood that is younger from a circadian standpoint, has the ability to clear these fragmented heme-based molecules from damaged cells.
I have hypothesized in my Patreon blog series that RBCs may attenuate CpG-induced inflammation in multiple organs through direct scavenging of CpG-containing DNA released from damaged cells.
How does our blood plasma link to this perspective Uncle Jack?
The innate immune system appears to use TLR9 on our blood cells for detecting unmethylated CpG dinucleotides which are liberated during the blue light hazard and nnEMF exposure associated with mental disease. The CpG Islands help tell the immune system how much damage has been done by pathogens and how to react. Why? CpG islands in pathogens vary compared to our own from our DNA/RNA and mtDNA. CpG islands are relatively common in bacterial and viral genomes but are highly methylated and uncommon in vertebrate genomes. People forget mitochondria have a bacterial lineage and this is why mitochondrial damage leads to a hypermethylated state in our CNS and PNS.
It begins even earlier in kids who come from parents who have AF, because those kids who are afflicted with the blue light hazard in their parent's germline occurs before the kid's brain is myelinated. A lack of myelination makes the child's brain more sensitive to nnEMF. When will we wake up to the power of sunlight over man's drugs?
The innate immune system in our blood plasma also has another backup system to help RBCs out clear the toxins. It appears to use TLR9 on our blood cells for detecting unmethylated CpG dinucleotides which are liberated during the blue light hazard and nnEMF exposure associated with Adrenal fatigue and the development of cognitive haze and eventual mental disease if the stimulus is chronically present in the environment.
The CpG Islands help tell the immune system how much damage has been done by pathogens and how they should induce the heme-based proteins.
THIS IS WHY AM SUNLIGHT IS IRREPLACEABLE WHEN YOU ARE AFFLICTED BY ADRENAL FATIGUE, in my opinion. The sunrise is the surprising best drug designed by Nature to keep us from AF. This is why AM sunlight creates dopamine, melatonin, and POMC make 6 other key brain chemicals it does in the eye and skin every AM you have your skin in the game = This leads to BDNF creation that REVERSES the hypermethylation in your brainstem.
This is BLACK SWAN MITOCHONDRIAC WISDOM HERE.
Don't believe me? ------> https://www.sciencedaily.com/releases/2017/11/171130170212.htm
Ya' still don't? ----->https://www.abc.net.au/news/science...s-vulnerable-to-mental-health-issues/10751264

True friendship is like fluorescence, it shines better when the situation darkens.

NEW BLOG OUT: Fluorescence is the emission of light by a substance that has absorbed light or other electromagnetic radiation. It is a form of luminescence. In most cases, the emitted light has a longer wavelength, and therefore lower energy, than the absorbed radiation. The most striking example of fluorescence occurs when the absorbed radiation is in the ultraviolet region of the spectrum, and thus invisible to the human eye, while the emitted light is in the visible region, which gives the fluorescent substance a distinct color that can be seen only when exposed to UV light. Fluorescent materials cease to glow nearly immediately when the radiation source stops, unlike phosphorescent materials, which continue to emit light for some time after.

Fluorescence has many practical applications, including mineralogy, gemology, medicine, chemical sensors (fluorescence spectroscopy), fluorescent labeling, dyes, biological detectors, cosmic-ray detection, and, most commonly, fluorescent lamps. Fluorescence also occurs frequently in nature in some minerals and in various biological states in many branches of the animal kingdom.

https://www.patreon.com/posts/24770650

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