QUANTUM ENGINEERING #29: THE SEMICONDUCTION OF BREATH – HEARING

Organisms are open thermodynamic systems dependent on energy flow. Energy flows in together with materials, & waste products are exported, along with the spent energy that goes to make up entropy. Entropy defines the flow of time.  Molecular clocks are flowmeters of entropy.  And that is how living systems can, in principle, escape from the second law of thermodynamics by staying on the edge of it.  Cells do this by creating order from chaos using cells as a dissipative structure. That structure is built around the AMO physics of atoms in cells.  Their molecular arrangement is key. This mimics what silicon valley engineers do to silicon in a semiconductor fabrication plant when they build solid-state circuits. Semiconductors use electric power and make light.  Cells do the same.

Breath work essentially controls the band gap changes in our semiconductors because of how powerful the reaction is in turning 02 into H20 in our mitochondria.  A change in oxygen saturation is capable of changing the color of light which changes the frequency of the light frequencies of the light emitted as biophotons.  Breathwork is about changing the frequencies of biophotons so you can imprint changes onto to tissue where wide band semiconductors are found.  This is how light sculpts mammalian semiconductors from an evolutionary perspective. But our story does not begin with mammals.  It begins with the earliest forms of life on Earth.  Bacteria and Archea.

According to the domain system in evolution, the tree of life consists of three domains such as Archaea, Bacteria, and Eukaryotes.  The first two are all prokaryotes, single-celled microorganisms without a membrane-bound nucleus. All organisms that have a cell nucleus and other membrane-bound organelles are included in Eukaryotes.  Every domain of life emits light from their cells.  Prokaryotes emit 5000 time more light than eukaryotes do.  Semiconduction is the the reason why this happens.

HOW DID THIS SEMICONDUCTIVE PLAN GET SCULPTED BY EVOLUTION?

The frequency of light changed for life many times in our evolutionary history.

We are so acclimatized to the presence of oxygen on our planet Earth, that we take it for granted. However, oxygen was absent from the earth’s atmosphere for close to half of its lifespan. When the earth was formed around 4.5 billion years ago, it had vastly different conditions. At that time, the earth had a reducing atmosphere, consisting of carbon dioxide, methane and water vapor, as opposed to the present-day atmosphere that consists primarily of nitrogen and oxygen.

Though sunlight split the water vapor in the atmosphere into oxygen and hydrogen, the oxygen quickly reacted with methane and got locked into the earth’s crust, barely leaving any traces in the atmosphere. A silent, mysterious force worked to release oxygen steadily, until the very composition of the atmosphere changed. That mysterious entity happened to be a microbe: Cyanobacteria.

The earliest onset of life on our planet occurred around 3.8 billion years ago. Since oxygen was projected to be absent from the earth at that time, metabolism in living organisms would have been anaerobic, involving the use of minerals present in the ocean to generate energy. However, around 2.7 billion years ago, a peculiar group of microbes, known as cyanobacteria, evolved. Phylogenetic analyses based on 16S and 23s rRNA, genome reconstructions and fossil evidence have been used to understand the evolutionary characteristics of these early living organisms. These microbes possessed the remarkable ability to perform photosynthesis, (i.e., they could generate energy from sunlight). Cyanobacteria possessed the machinery to utilize water as a fuel source by oxidizing it. More significantly, the by-product of photosynthesis happened to be oxygen.

Among all the biochemical inventions that life could conceive, the ability of cyanobacteria to utilize water as fuel for oxygen generation must rank as one of the most ingenious.  Trust me there are few more in this blog.

Researchers have guessed that the levels of oxygen released into the seawater by cyanobacteria gradually increased over time, and that over a span of 200-300 million years, oxygen was produced at a faster rate than it could react with other elements or get sequestered by minerals. The oxygen released by cyanobacteria steadily accumulated over vast swathes of the ocean and oxygenated the water. Gradually, the accumulated oxygen started escaping into the atmosphere, where it reacted with methane. As more oxygen escaped, methane was eventually displaced, and oxygen became a major component of the atmosphere.

This event, known as the “Great Oxidation Event,” occurred sometime between 2.4 – 2.1 billion years ago.  Life remained simple with just bacteria and archea dominated the planet.  Then environmental change happened again on Earth.

Our star went through puberty so to speak, as most G class stars do, and began transforming energy to make about 10% more UV light than normal.  This increases in Oxygen did something else; our weather changed as accumulation of oxygen in the atmosphere got pronounced.  In fact, we know it led to one of the earliest ice ages on earth.

Methane is a greenhouse gas, since it traps heat from sunlight and warms the planet. As methane was displaced by oxygen, global temperatures cooled sufficiently to generate ice sheets that extended all the way from the poles to the tropics.  That temperature change has a massive effect on how semiconductors operate.

Temperature affects semiconductors band gap size too. Cooling increases band gap size.  More on that soon.

Cooling gave us evolutionary pressures to create catecholamine chemicals in prokaryotes like dopamine and adrenaline using a new semiconductive protein inside cells.

A lack of oxygen affected the early oxygen carrier molecules called heme proteins.

Initial oxidation of hemoglobin to the ferric (Fe3+) state without oxygen present converts hemoglobin into a useless “hemiglobin” or methemoglobin, which cannot bind oxygen. Methemglobin is an ancient protein used by life long ago when oxygen was not prominent in our atmosphere.

THE RICK RUBIN SIDE BAR:  Did you know methylene blue acts by reacting within RBC to form leukomethylene blue, which is a reducing agent of oxidized hemoglobin converting the ferric ion (Fe+++) back to its oxygen carrying ferrous state(Fe++). The dose commonly used at surgery is 1-2mg/kg of 1% Methylene Blue solution.  Did you also know that methylene blue can increase NO delivery to tissues as it drops of more oxygen in this maneuver in states where pseudohypoxia or hypoxia exist and NAD+ has dropped?  I’ve told a couple of clients that.  This advice comes from the story that is unfolding for you in this blog.  MB can be used to increase the band gap of broken degenerating photoreceptors inside of sick mammals and silly talking monkeys too.

BACK TO THE STORY

Early versions of hemoglobins suffered from this problem = myoglobin.  Later on mammals figured out a novel way to stabilize hemoglobin using UV light when oxygen filled the atmosphere.  First I have to explain how we got there.  Modern versions of hemoglobin in normal red blood cells are protected by a reduction system in the RBC by an aromatic amino acid (histidine) and by a sea of electrons from the water in blood.

The surface of Earth was getting pounded by UVC light for long periods of time.   Since life was totally prokaryotic and anaerobic 2.7 billion years ago when cyanobacteria evolved, it is believed that oxygen acted as a poison and wiped out much of anaerobic life, creating an extinction event of the old guard in life including LUCA.  LUCA = last unknown common ancestor.

This environmental change drove evolutionary pressures to begin to innovate proteins that used aromatic amino acids to build the most important parts of modern metabolism we see today in cells.  Their absorption spectra can go from 150nm VUV to 400 nm UV-A light.  Melatonin is one of the most ancient semiconductors known.  Its functions have evolved as the Earth changed.

Melatonin, NAD+/NADH, dopamine, adrenaline, leptin, epinephrine and many others. Light controls the flux of all these biomolecules because of movements of H+ in cells.  Remember all enzymes that create these chemicals use proton tunneling to get the job done.  Proton tunneling is linked to HIF-1alpha and PER2 gene that uses light to increase the periodicity of molecular clocks in cells.

Tryptophan, another aromatic amino acid, became very useful as a time crystal for cells because has only one DNA codon and it catabolism changes as light changes with the tilt of Earth that gave us season. NAD+ and melatonin are made from tryptophan.  I wrote those blogs years ago and gave them to you here.

Future life forms would need this information because oxygen gave us cool seasons and hot seasons all in one year as the Earth revolved.  This cyclic pattern was built into cell metabolism as it got more complex as the slides below show.

Since oxygen has a high redox potential, it acted as an ideal terminal electron acceptor to generate energy after nutrient breakdown. Oxygen soon became indispensable for metabolic activities. Organisms also evolved strategies to detoxify the reactive oxidative species that resulted from aerobic metabolism.

Though sequencing and phylogenetic analyses estimate the evolution of ROS detoxifying enzymes even before the advent of aerobic microbes, the Great Oxidation Event acted as the catalyst to shape the directed evolution of enzymes like superoxide dismutase (below) and catalase.  Catalase (below) is one of the earliest heme proteins along with ancient myoglobin and hemoglobins.

Note the presence of wide band semiconductor components in the picture above: the Fe-S dopant semiconductors and the roles in creating the free radical signal in mitochondria.  Below note how all the chromophore proteins in mammals are linked to aromatic amino acids, heme proteins and melanin at some level. Can you guess why yet?

As oxygen continued to mushroom the high ionosphere became filled with a new gas that decreased the terrestrial solar spectrum.  Life had to react to this and it fueled changes in heme proteins showing up on the surface of Earth in early life forms.

Oxygen was also responsible for formation of the ozone layer in the atmosphere. The UV radiation from the sun split oxygen molecules (O2) into 2 atoms of oxygen, which then reacted with another oxygen molecule to generate ozone (O3). Ozone acts as a natural sunscreen for Earth to prevent harmful UVC and parts of the UV-B radiation from reaching the earth’s surface.  This reduction began the the evolution of new semiconductors in the two DOMAINS of life on the surface of the earth below called melanin.

As oxygen continued going higher it fueled the Cambrian explosion and life was able to take advantage of the mirror image of the photosynthetic arm of life on Earth.  Namely mitochondria developed.  Complex life captured mitochondria in their tissues as a stowaway to transform solar energy into CO2 and water.  It transferred electrons from food to oxygen to fuel this solar battery.  At this point in time, life exploded and all complex life on Earth we know about today showed up almost over night.  Eukaryotes came from the fusion of the other two Domains in a process called endosymbiosis.  We believe chlorophyll and mitochondria innovated at this time.

MELANINS CONTINUED TO EVOLVE IN MAMMALS ON THEIR SURFACES BUT ALSO INSIDE OF THEIR TISSUES:

THE KT EVENT

Melanin was a new type of wide band gap semiconductor.  It was innovated because it was able to absorb all frequencies of UV light.  Mammals began to dope melanin by putting atoms next to melanin that high band gaps to make UV light within their own tissues.  Mammals took their surface melanin in their hair and internalized it to make sunlight because the asteroid dimmed sunlight!  The dimmed sun was the epigenetic signal they used to do this.

Modern centralized researchers/science have the story backward on melanin.  They believe melanin’s job in nature, at least in our skin, is to convert light energy very rapidly to heat, which water absorbs, and this is the safest way to dissipate it before radicals can be generated.

Melanin is plentiful in mammals internally, not just on their skin.  The centralized science version of events makes no sense in this case.  Their focus is on the skin only and meloma prevention.  Their ideas are pictured on the black walls below.  My idea is in the foreground below.

The decentralized mind sees the same data and realizes that internal melanin of mammals has to have some unique atoms next to it to create energy missing from the sun.  Since melanin is dark it absorbs all types of light around it  This is what band gap theory of color tells us.  It seems centralized biologists do not read physics journals. This color makes melanin the ideal biological solar panel. It is not sunscreen; it is an internal panel cells use to regenerate mammalian tissues using Group 2,3, and 4 atoms on the periodic table as their partner in crime.  This explains why cells like Na, K, Ca,Mg, Fe, S,Cl, and P.  It also explains why 56 enzymes in mitochondria use Mg at some level and why the P in ATP is one of those atoms.

For example in the ear, mammals have evolved their endolyphmatic sac to have a fluid in it with high levels of potassium adjacent to the melanin.  The DC electric power (pic below) generated by mitochondria interacts with aqueous KCL in our cochlea large amounts of UV light is made.  Melanin absorbs all this light. This occurs because KCL has a band gap of that spans ALL UV frequencies that go to 150nm-400nm light.  Now we see why cells in mammals favor aromatic amino acids wherever semiconductive proteins are found because their absorption spectra can handle them without any free radicals creation to be transferred to surrounding water.

Potassium is the diode in this semiconductor and the DC electric power in the cell from the mitochondria causes it to create 150-400nm UV light. Melanin absorbs it all IN TOTAL.  Nothing goes to waste.  Nothing creates free radicals.  Melanin is able to shares the energy transformed with adjacent chromophore proteins who have different action spectra.  Melanin also uses quantum effects that have escaped biologists.  Proton tunneling not only is used in enzymes but it is used in melanin.  It undergoes a reaction called a partial proton transfer with water molecules to render deep UV light safe inside our bodies.  Remember all of a cells semiconductor are hydrated.

Now you know the reason why they are.  This stops the extreme ultraweak UV light from prompting free radicals to harm adjacent molecules to cause tissue damage.  Every living cells creates ELF-UV as Fritz Popp showed in his photomultiplier experiments over 50 ears ago.  Melanin replaced missing sunlight in mammals post KT event so they could survive and eventually thrive!

These environmental pressure are what gave rise to the warm blooded small creatures who could handle these temperature shifts from rising oxygen tensions as the Earth revolved around the sun.  I spoke about these shifts that early complex life had to deal with in my Cold Thermogensis series of blog over 15 years ago.  These combined environmental stressors drove mammals do begin to change their interiors bu using melanin in the furry coats to do it.Remember mammals all have to have hair to be a mammal.  This is where ancient mammals buried their melanin.  But this is why they remained small and underground.

One of the first ways mammals evolved post KT was putting melanin in the eye in the RPE.  They did this with POMC as well, to form the leptin-melanocortin pathway in their eyes and brains.  <——CT 6 was born.  This is a semiconductive circuit in the eye of all mammals. You’ll note below that histidine a UV absorbing protein stabilizes hemoglobin chains to deliver oxygen to mitochondria as I mentioned above.

Life got used to oxygen being plentiful for the last 2.5 billion years until something stopped the oxygen party on Earth  An extraterrestrial event interrupted sunlight and stopped photosynthesis for a period of time.  We do not know how long it went on but we do know it ended the age of dinosaurs and began the age of mammals. This drove melanin from their furry surfaces to their interiors.  It also fueled the innovation of HIF 1-alpha and linked it directly to the PER 1/PER2/PER3 gene of the circadian mechanism.

This KT event drove further evolutionary trajectory in the mammalian clade because it acutely made both UV light and oxygen scarce for a period of time.  That drive semiconductor innovation at the quantum level.  The interruption of photosynthesis made oxygen quite valuable to the semiconductor-fabricating plants in cells on Earth in cells.  The other two proteins that were altered as melanin was driven inside of tissues were chlorophyll and hemoglobin.

The reaction that turns molecular oxygen (O2) into water releases lots of energy, and all animals need that energy to drive their body’s functioning. The half-reaction and associated free energy change are:

O2 + 4H3O+ + 4e- –> 6H2O     delta G = -305 kJ/mol

This is a massive amount of energy.  This energy was the boost that powered the mammalian clade to take over the world of biology after the last extinction event.  There has to be a biological mechanism for capturing oxygen as O2 (in its high-energy, zero oxidation state) and bringing it to a place where it can be turned into H2O (this is a reduction reaction) in such a way that the energy released by this process can be profitably used by the organism.

This is accomplished in most organisms via hemoglobin and/or myoglobin, which are often referred to as oxygen-carrier proteins. An iron atom in the center of myoglobin binds to O2 and takes to where the energy is needed. Hemoglobin works almost exactly the same way except that where myoglobin has only one iron-containing protein subunit, hemoglobin has four. When one of hemoglobin’s four irons binds an O2 molecule, the other three protein subunits’ iron atoms can bind O2 more easily. This is called the “cooperativity effect

Every time I post this slide above I wonder what my readers really see.  Then I wonder what they understand about these two molecules.  What they mean to you is not what they mean to me.  Why?

They are nitride-based semiconductors ideal for creating blue and green light-emitting devices found in biological systems favored by evolution BEFORE the KT event.

The KT event happened 500 million years after the Cambrian explosion so it is an ancient semiconductor that evolved because of the oxygen event on Earth tied to photosynthesis changes in the sea by DHA of algae.  Melanin is a unique dark pigment-wide-based semiconductive protein favored by evolution AFTER the KT event.  Below is the new KT event for modern humans in two pictures.

This light above in 5 of the panels destroys all wide based semiconductive proteins in mammals exteriors and interiors.  The picture below is how we destroy the ones on our surfaces.  Sunglasses, glasses, intraocular lens, and contacts being the other.

Why was hemoglobin favored BEFORE the Cambrian explosion?

(1) hemoglobin as molecular heat transducer through its oxygenation-deoxygenation cycle

(2) hemoglobin as a modulator of erythrocyte metabolism (ferroptosis)

(3) hemoglobin oxidation as an onset of erythrocyte senescence

(4) hemoglobin and its implication in genetic resistance to malaria in the human cradle of life in the East African Rift

(5) enzymatic activities of hemoglobin and interactions with drugs to deal with met-Hb. (methylene blue)

(6) hemoglobin is a source of physiological active catabolites to create unique semiconductors.

I wonder if my readers realize that both of these molecules are the semiconductive proteins that became favored by cells 65 million years ago to let life bounce back once the asteroid destroyed the reign of dinosaurs thermodynamically?

Biophotons sculpted and created future iterations of mammals using oxygen and sunlight as their starting point.  Hemoglobin favored the development of the melanin system in the neuroectoderm of mammals to sculpt life after this extraterrestrial event changed the spectrum of sunlight. Melanin allows mammals an advantage to live in low sunlight conditions.  This means blocking melanin from its job will destroy melanin-containing tissues and their abilities in the mammalian clade.

Hemoglobin and chlorophyll are wide-band semiconductors.  Wideband semiconductors are found in Groups 2, 3, and 4 on the periodic table of elements. Nitrogen and Iron are also in those periods.  So is sodium and potassium.

Another example of a wide-band semiconductive device that was favored after the KT event is found in the human cochlea Imentioned early.  Now I want you to get the full picture.  The cochlea is a spiraled covered internally with a wide-based semiconductor sitting in endolymph fluid.  A remarkable characteristic of the cochlea is the unique composition of endolymph.  It is only remarkable to a centralized mind.

The decentralized thinker knows immediately why Nature did this.  Potassium is the smallest element in period 4 of the periodic table and it has the ability to build semiconductors that emit powerful UV light that melanin absorbs tremendously.  Melanin is designed by nature to replace the sunlight that was missing from the KT event in mammals.   This liquid fills the scala media, and is very rich in potassium (150mM), very poor in sodium (1mM) and almost completely lacking in calcium (20-30 µM).

Its spiral shape is lined with a wide-based band gap semiconductor called melanin seen below.  Most centralized physicians never learned that melanin was in the ear and this is why they have no idea what causes tinnitus.  I do.  The fluid in the spiral is loaded with potassium chloride crystal in an aqueous format and it has an energy band gap of 7.6eV.

What does this number imply to decentralized clinicians?  The way we hear in our ears is semiconductor based process and it uses UV light to work.  Due to the quantum confinement effect, electrons and holes in the semiconductors at the nanoscale level are confined by this arrangement of atoms in the cochlea. Therefore, the energy difference between the filled states and the empty states of potassium increases or widens the band gap of the semiconductor to make it easier to turn sound waves into electromagnetic signals in the cochlea.  In the human ear, the melanin absorbs the UV light & visible light into the IR spectra transformed from its potassium diode (E=mc^2) and passes this light energy to the water in the endolymph and in neurons of the eight cranial nerve.  Any light not captured by melanin is picked up by water.  All neurons release water when they fire an action potential, FYI.

Potassium chloride emits VUV-IR light in the endolymph, and forms excited electronic states in melanin that decay on ultrafast timescales that are topographically organized to excite other semiconductors in the organ of Corti that allow you to hear.

Melanin as a pigment has now been identified to have other functions apart from being just a bio-macromolecule. It is found to be among the most unique organic semiconductors on Earth.  Melanin tends to be amplified in mammalian tissues that are derived from neuroectoderm.  Everywhere in tissues that house neuroectoderm-derived cells one should expect melanin and its derivative semiconductive atoms from group 2-4 to show up.  This is why finding the leptin-melanocortin pathway changed my life.  The central retinal pathways anterior to this tract are also filled with melanin as well.

Looking more closely in biology you’ll find melanin can be found mostly in the eyes, human skin, hair, inner ear, and even brain has a special melanin. Especially the midbrain where all sense and hypothalamic areas converge. It was identified to be black or brown depending on the composition and structural differences.

Skin is derived from neuroectoderm.  So are your teeth.  The color of your teeth tells me something.  The color of your skin is called your Fitzpatrick type.  It also tells me something.

Melanin can either be eumelanin (with nitrogen attached between carbons) or pheomelanin (with sulfur attached between carbons) or neuromelanin (Prota, 1980).

Neuromelanin (NM) is the darkest pigment found in humans.  It is only located in the brain and it is structurally related to melanin. It is a polymer sheet of 5,6-dihydroxy indole monomers. Neuromelanin is found in large quantities in catecholaminergic (dopamine) cells of the substantia nigra pars compacta and locus coeruleus, giving a dark color to the structures.

Do you know why I mentioned it is the darkest human pigment in humans?  That tells us something more about this semiconductive protein.  The mechanism behind the color we perceive in semiconductors is fully explained by the band theory that governs color perception.  Yes been color perception in a semiconductive event in humans.

If a pigment is able to absorb all wavelengths, we see it as black in the classical world.  Color is an invisible coach to the decentralized mind.  My friend Rick Rubin has been described as an invisible coach.  When he had his own health issues he phoned me up and the advice I gave him was given in the classical world to help his ignorant surgeons at Stanford protect all the sound waves stored magnetically in the hydrogen lattice in his body.  I view Ricks body as the master tape of the best music in the 20-21 century.  I kept what I did for him quiet.

In this surgical situation, I was Rick’s visible coach who could explain the invisible magics in the advice I gave him.  It turns out that what I told him to add to the surgeon’s recipe makes melanin a better wide-based semiconductor to protect the master tapes stored magnetically in his body.  Below is Rick protecting those master tapes after his surgery.  Note his eyes and the light around him.

Back to the invisible magic to all centralized minds part of this story:  Note the red ink below in Figure 1 below.  Do you see how the iron oxidation state is specific in the reaction?  Fe is at its +3 state.  Why is this important?

Your hemoglobin semiconductor protein refurbishes and regenerates your melanin semiconductor protein to work with full-spectrum sunlight.  Your use of any sunscreen, sunglasses, contacts, and blue light or nnEMF blocks this refurbishing process and destroys melanin stores in your body.

Hemoglobin can bind 4 oxygen molecules.  Iron changes its oxidation state when oxygen is bound from +2 to +3.  Did you know that? Why?

The molecular orbitals in hemoglobin are different when oxygen is bound and when it is not bound, and this accounts for its color change: hemoglobin is red when oxygen is bound and blue when oxygen is not bound.  This tells us that hemoglobin must also change its semiconductive band gap to account for the color change when its oxidation state changes.

With hemoglobin there is an energy shift of 5 eV between deoxyhemoglobin and oxyhemoglobin and this large band gap emits UV light from hemoglobin (just like an LED diode does) into the blood plasma when this occurs.  That plasma is filled with 93% water.  Water undergoes a phase change and a charge change when it is irradiated by terrestrial sunlight as most of you know from my work.  Blood takes on a net negative charge and this surrounds all the cells suspended in blood.

This includes platelets and it is the basis of the zeta potential in blood.  This was a big deal for Rick’s surgery because of clotting risks (pic above).

When oxygen is not bound to hemoglobin, the iron atoms in its nitrogen cage are in the +2 oxidation state, and when it is bound to Hb in the Fe+3 state.  The Fe+3 is more conductive electrically and this creates energy to improve the laminar flow of RBC in the blood vessels pictured above.  At an atomic level, Fe+3 is slightly too big to fit into the hole in the center of the plane of the immediately-surrounding “heme,” so it rests just on top of the heme plane.

Did you know hemoglobin also binds and releases NO when a cell is hypoxic in and Fe is +2?  This helps vasodilate blood vessels when they are hypoxic so that melanin can get more Fe in its +3 with oxygen.

I hope you remember that nitrogen, sulfur, phosphorus, and iron are also located in periods two and three in the periodic table of elements. This will become important soon in this story I am laying out to you.

our photoreceptors in your eye all regenerate using two more semiconductive proteins called dopamine and melatonin.  Both of them are created from aromatic amino acids that have very unusual absorption spectra of UV light.

Not only biologists, but melanin also attracted much of the attention of biophysicists due to the fact that apart from biological functions, melanin exhibits an interesting physical property such as high electrical conductivity leading to the suggestion that they could act as amorphous organic semiconductors (McGinness, 1972). Its threshold-switching behavior revealed that it can be used for electronic devices.

Melanin biology has even attracted the condensed matter people in physics because of its unique characteristics.  The people in AI have no Earthly idea how this semiconductor is key to the human quantum computer in our skulls.

Due to its physical and biochemical behavior and its possibilities of combining amorphous semiconductors with that broadband monotonic absorption from UV-vis to NIR (Near Infrared). Also, it can be converted from photons into phonons (Meredith et al., 2006 below as cite #2).

Below is the graphic formulation of the periodic law, which states that the properties of the chemical elements exhibit an approximate periodic dependence on their atomic numbers. The table is divided into several areas called blocks. The rows of the table are called periods, and the columns are called groups. Elements from the same group of the periodic table show similar chemical characteristics. Trends run through the periodic table, with nonmetallic characters (keeping their own electrons) increasing from left to right across a period, and from down to up across a group, and metallic characters (surrendering electrons to other atoms) increasing in the opposite direction. The underlying reason for these trends is the electron configurations of atoms.

Cells use atoms from hydrogen to iodine on the periodic table.  That is atomic number one to atomic number 53.  Between atomic numbers, 1-53 many atoms are not used while the once that are used are often amplified.  This fact should get the mitochondriac curious.  Why would cells on the Earth do this?  The answer is simple.  Nature knew what the frequency of terrestrial sunlight was on Earth and that is why she built her semiconductive fabrication plant to take advantage of the band gap requirements of sunlight.  When mammals faced a world devoid of UV light because of an asteroid strike melanin was created and amplified in that clade of animals.  In ancient times, before the Cambrian explosion sunlight was the only source of energy with which we could run cells.  This idea was stressed into cells at the KT event.

What is evolution really about?  Energy, captured by semiconduction correctly can be applied to sculpt the atoms in cells to accomplish anything the environment can throw at it. This idea is very different that Darwin’s.

THE KT EVENT INTERRUPTED SUNLIGHT MUCH LIKE TODAY’S SUNSCREEN AND SUNGLASSES

Melanin is the main pigment found in mammals. It is responsible for the color of hair and fur. There are different types of melanin (eumelanin and pheomelanin), and they produce a huge color range, from black to sandy to red. A lion’s coloring is produced by melanin. Mammals were small and lived underground prior to the KT event.  I covered this in detail in my book ten years ago.  The reason is likely related to the semiconductors in their skin.  Dinosaur and bird predators likely saw the UV spectrum.

All mammals and marsupials like the platypus and wombat have also been found to glow under ultraviolet (UV) light.  This would have made them easy prey before the asteroid.  It also explains why reptiles like dinosaurs likely only used melanin inside their tissues.  Research has shown there was an intriguing evolutionary shift in the type of melanin used between cold-blooded and warm-blooded species found on Earth.

Birds and mammals contain significantly more of a sulfur-rich variant of melanin than amphibians and reptiles. This tells us their mitochondria density and capacity were different and it likely also explains why dinosaurs had small brains compared to their massive bodies.

This explains why these animals made it through the last extinction event.  They were able to create their own UV light high bandwidth semiconductors internally and melanin inside of them captured this light for use physiologically.  As time went on from the KT event, they amplified the ability to make melanin internally in their body plans and humans are the collateral effect of this happy accident for mammals.

Ancient mammals tend to be hairy according to the fossil record and so their colors are dictated by the pigments in their hairs. Eumelanins produce dark colors, while pheomelanins produce light colors. There is no such pigment that produces green color in the band gap color of melanin.

HYPERLINK

COLOR IS A SEMICONDUCTOR STORY

Physicists tend to see the world through a hydrogen/proton lens.  Chemists tend to see the world through valence electrons.

A quantum biologist sees the world through how the protons and electrons and hydrogen act with iodine.  These atoms are rearranged with specificity and sensitivity by sunlight to explain everything in biology on Earth.  Melanin and hemoglobin are central to this developing story.

THE QUANTUM BIOLOGY LENS

Hydrogen should not be considered just a source of solar energy. Hydrogen is best thought of as a carrier of energy that cells favor in their mitochondria.  Just as oil has grades telling us which is the more favored product so too does hydrogen.  Light hydrogen is the favored carrier atom of solar energy for the semiconductive circuits of life.

The heaviest atom used NORMALLY in human cells is iodine.  No cell needs any other element past iodine.  Why is iodine so damn important?  It is large enough and has 7 valence electrons of electronegativity that it has enough electronegative power to draw hydrogen protons closer together to make the best performing wide band semiconductors in the UV to IR range of light using something called the Grothaus mechanism.  Iodine can and should be thought of as our optical scissors in how we turn food into an electromagnetic signal for mitochondria to decipher.  Recall that terrestrial sunlight we see goes between 250nm light and 760nm light.

The terrestrial solar spectrum actually is larger than we do not see between UV-C light at 250nm – 3100 nm light in the IR-C range.  I’m sure you are now wondering what in the hell is a wide-band semiconductor.

Wide bandgap semiconductors have many useful characteristics, such as low permittivity, high breakdown potential of electric fields, good thermal conductivity, high electron saturation rates, and most importantly high radiation resistance.  Yes, wide-band semiconductors actually protect electric currents from other parts of the electromagnetic spectrum that can destroy life.

Recall from the story above that for the first 3.8 billion years on Earth at times, the full complement of the electromagnetic spectrum has gotten through to different degrees at times and these frequencies could easily disorder AMO atomic arrangements in cells.  Cells had to build plans to navigate this problem.  Using a semiconductive design that favored radiation protection of the full spectrum of light from any star seems wise.

As a result of all these early conditions of existence on Earth, cells chose the atoms that could build semiconductors that spanned a conduction gap of 4.96 eV to 0.4 eV.  Why were those numbers chosen?  That is the band gap that corresponds to 250nm light and light up to 3100nm light. That is the thermodynamic range of the sun.

Hence, wide-band semiconductors can work at high temperatures found on Earth and are also ideal for developing semiconductor devices that have high frequency and power, and high temperature and radiation resistance. Taking group 3 nitrides as an example, in terms of optical properties, their optical band gap can vary continuously from 0.77 eV (InN) to 6.28 eV (AlN), completely covering the infrared to the ultraviolet band.

Since wide bandgap semiconductors can absorb and radiate high-energy photons, they are the most suitable candidates for fabricating blue, green, and other short wavelength light emitting diodes (LEDs), semiconductor lasers, and UV detector devices, which are widely used in the fields of optoelectronics and microelectronics.

SUMMARY

When oxygen drops, HIF 1 alpha is released and this affects the periodicity of the SCN and all peripheral clock genes.  This is especially damaging in the case of hemoglobin and melanin semiconductors.  Recall from the last blog that alpha MSH is made from sunlight via all our surfaces, skin, eyes, git, and brain.  Alpha MSH is how we keep our melanin semiconductors from aging in the hypothalamus and midbrain.  Controlling the oxidation state of iron in these proteins is key there and that links to the oxygen delivery system to melanin-containing semiconductors for reasons very detailed above.

How does it all tie together?

Today for the first time in my medical career there is overwhelming and compelling evidence that connects the circadian clock to many addictive behaviors and vice-versa, yet the functional mechanism behind this interaction remains largely unknown. You have just gotten that mechanism delivered to you for 5 bucks.  Your job is to share it far and wide and show centralized clinicians and researchers just how myopic their thinking has been on this topic.  It is the reason I have been pissed off and agitated at my profession for 20-plus years.

Your third eye is not an eye.  It is your skin that has a massive array of melanin in it that powers the entire neuroectodermal layer of melanin everywhere in your body.

Melanin is destroyed by blue light and by nnEMF when it degrades.  Iron in the wrong oxidation state powers its demise.  Your melatonin and dopamine levels in your body are designed to help every heme-based semiconductor in your body to regenerate.  It is your job to get out of these electromagnetic waves.   You need to get into the sun which build melanin.  Ivory Tower academics have ignored this science for far too long.  95% of this regenerative power is made in mitochondria.  This is why the first step in heme synthesis of all wide-based semiconductors also begins in the mitochondrial matrix of MAN.

At the molecular level where most centralized researchers spend their time, multiple mechanisms have been proposed to link the circadian timing system to the addiction to sugar, food, drugs, gambling, supplements, and bad centralized advice.  Low dopamine states are created by wide-based semiconductive demolition.

I can tell you even music has remnants of this effect.  If you do not believe me listen to the tracks of Metallica and AC/DC.  You’ll notice something profoundly different in both bands.  The way in which the drums are used is ill-timed between the two groups.  Guess why?

Do you know acoustic phonons are affected most by magnetic fields?  True.  Semiconductor science 101.  Metallica’s musical heart is driven by their drummer, Lars Ulrich born in 1963 and his drum beats lead their music.  He was into tennis, an outdoor sport until he migrated to the drums after he moved to Los Angeles at the 34 latitudes.  Ulrich was born into an upper-middle-class family in Gentofte, Denmark. He was the son of Lone and tennis player Torben Ulrich. His paternal grandfather was tennis player Einer Ulrich.

In February 1973, Ulrich’s father obtained passes for five of his friends to a Deep Purple concert held in the same Copenhagen stadium as one of his tennis tournaments. When one of the friends could not go, they gave their ticket to the nine-year-old Lars and that is how his music career began.  Lars Ulrich originally intended to follow in his father’s footsteps and play tennis outdoors, and he moved to Newport Beach, California, in the summer of 1980 as proof.  Lars became known as a pioneer of fast thrash drum beats, featured on many of Metallica’s early songs because his dopamine level was supported by his early light environment.

AC/DC was driven by its guitarist, a heavy-smoking teetotaler.

AC/DC musical heart was Angus Young.  His older brother is Malcolm a rhythm guitarist.  What is the main difference between a modern rock band’s with drums and guitar?  The way sound is amplified by nnEMF.  Guitars >>>>Drums.  The sound of drums also has a profound positive effect on the hydrogen bonds of water in how phonons are created.  This in turn affects the dopamine created by melanin semiconductors in your brain and ear.

Organisms appear anti-entropic while alive. Not only do they keep the atomic organization of the semiconductors more intact, but also manage to have lots of energy for their activities = longevity. But how do they really manage their anti-entropic existence? What would a thermodynamic description of organisms be like?

Lars took better care of his wide-based semiconductive system better than Angus.

Angus was born in Australia in 1955.  This should open the eyes of my members who are long-term readers.  Oz is a natural geopathic stress zone and is infiltrated with more nnEMF than any land mass on Earth.  in the late 1950s, he moved to Glasgow Scottland, latitude 55 North latitude.  Young also learned how to fight on Cranhill’s tough streets at night and his family was prompted by a bad winter and TV advertisements offering assisted travel for families to immigrate back to Australia.  So his family flew from Scotland to Sydney, Australia, in late June 1963.  Do you think any of this was good for the melanin in his cochlea?

Young was 18 when he and his older brother Malcolm formed AC/DC in 1973. At 18 years old, his brain was not fully myelinated which meant the semiconductors in his neocortex were fully pounded by nnEMF and blue light his whole life. Bon Scott, their lead singer died of addiction = low dopamine state. Scott died from alcohol poisoning.  In April 2014 Malcolm Young was forced to leave the band due to ill health due to alcoholism too.  Do you know alcohol affects the oxidation state of iron in our body because of how it dehydrates us?  Do you still think my hunches on semiconduction are wrong?

After Scott died they added Brian Johnson.  AC/DC was set back with yet another departure; the new lead singer Brian Johnson was ordered by doctors to stop performing or face total hearing loss. Imagine that.  See a trend yet?  All this time AC/DC musical tracks have the drum beats of Phil Rudd behind the guitar tracks.  Have you guessed why yet?

When your dopamine level is low chronically you experience time differently.  This has been imprinted in their music from day one. In fact, it is also why the most common criticism of AC/DC is that their songs are excessively simple and formulaic.  That is also linked to semiconductive degradation in the cochlea and brain.  The health of their group has also shown these effects but I doubt one centralized MD put any of this together.

The molecular mechanism of the circadian clock consists of a transcriptional/translational feedback system linked to the melanin semiconductive proteins, with several regulatory loops.  These loops are also intricately regulated by the wide-based semiconductors in us at the epigenetic level. Interestingly, the epigenetic landscape shows profound changes in the addictive brain, with significant alterations in histone modification, DNA methylation, and small regulatory RNAs. The combination of these two observations raises the possibility that epigenetic regulation is a common plot linking the circadian clocks with addiction and just about every other human behavior well.  This is how a decentralized mind sees the world as very different than your centralized researcher or expert.

CITES

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399705/

https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1600-0749.2006.00345.x

Alaie Z., Mohammad Nejad S., Yousefi M.H. Recent advances in ultraviolet photodetectors. Mater. Sci. Semicond. Process. 2015;29:16–55.

Zhao S., Nguyen H.P.T., Kibria M.G., Mi Z. III-Nitride nanowire optoelectronics. Prog. Quantum Electron. 2015;44:14–68.

Ponce F.A., Bour D.P. Nitride-based semiconductors for blue and green light-emitting devices. Nature. 1997;386:351–359.

https://www.reviewofoptometry.com/article/living-with-blue-light-exposure

Pengfei T., Ahmad A., Erdan G., Ian M.W., Martin D.D., Ran L. Aging characteristics of blue InGaN micro-light emitting diodes at an extremely high current density of 3.5 kA cm−2. Semicond. Sci. Technol.

QUANTUM ENGINEERING #28: HUMAN CELLS ARE WIDE GAP SEMICONDUCTIVE TOPOLOGIC INSULATORS

If centralized physicist is correct, and thermodynamic laws for energy say energy is a fixed quantity in the universe, and the speed of light is fixed at the same time, 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 has to be the “Jacquard card” of cellular design……..

What is the function of Jacquard’s card?

In a Jacquard loom one of a series of perforated cards controls the manipulation of the warp threads and determines the intricate pattern woven on the material.

What is a Jacquard loom?

The Jacquard loom is often considered a predecessor to modern computing because its interchangeable punch cards inspired the design of early computers.

The atomic arrangement of atoms in cells is the Jacquard card and the loom is light.  The creation from this interaction is created in the substance of water.  The arrangement of atoms creates the conditions to facilitate quantum coherence in cells to build a quantum computer called your organs.  Each organ is like a member of the orchestra.  Each organ is coordinated by the SCN.

HOW ARE OUR WAFERS BUILT? 

Just as Taiwan semiconductor makes chips through a complex process that requires atomic precision, clean environments, expensive factory equipment, and time, your cells require the same conditions.  Control in Nature’s fab plant is done optically by light and dark cycles.  

Semiconductor device fabrication in the tech world is a multiple-step sequence of photolithographic and physicochemical processing steps (such as thermal oxidation, thin-film deposition, ion implantation, and etching) during which electronic circuits are gradually created on a wafer typically made of pure single-crystal semiconducting material. Silicon is almost always used, but various compound semiconductors are used for specialized applications.  Silicon is a narrow-band semiconductor.  Nature rejected Silicon and chose carbon as her “wafer”

Semiconductors are arbitrarily defined as insulators with band gap energy < 3.0 eV (~290 kJ/mol). This cutoff is chosen arbitrarily because the conductivity of undoped semiconductors drops off exponentially with the band gap energy.  The  3.0 eV level is very low and creates light in the red range.

Nature used carbon and atoms for her semiconductors to create light from the VUV to IR range.  This mirrored the terrestrial spectrum of sunlight on ancient Earth before cells evolved.

Nature also used her own version of a photolithographic method to create her wafers that use circadian biology as her optical tweezers to place atoms at specific locations in cells to gain the desired physiological effect.

Each one of your cells is a quantum computer that is integrated & entangled to one another in their organ and in distant organs in many novel ways.  The basic design of the quantum cell is that Nature built living semiconductors with wide band gaps.

Visible light covers the range of approximately 390-700 nm and corresponds to band gaps of 1.8-3.1 eV

Carbon comes in many semiconductive crystals.  Carbon in the form of a diamond has a large band gap at 5.4 eV.  At a band gap of 5.4 eV, no light in the visible spectrum can be absorbed. These substances transmit all incident light and are colorless in their pure forms.

Our proteins are semiconductive when they are hydrated.  The “wafer design” always uses atoms in the periodic table in Periods 2-4 of the periodic table because most of these metals have band gaps that allow cells to create light in the VUV to IR ranges from atoms adjacent to our hydrated semiconductors.

Human cells only use atoms 1-53 on the periodic table but not all these atoms are used for a variety of reasons linked to wide band gap solid-state wafer design.  Many of these atoms are used over and over again because they have band gaps from 1.5 eV-8 eV.

Collagen is the most common protein of man and it is a wide-based semiconductor.  Collagen types vary in design and so do the dopants on them.  For example, we know that in bone collagen is the N-type wide-based semiconductor, and hydroxyapatite is the P-type semiconductor that has a band gap that emits 200-270nm light.  This is UVC light extends past the light the sun provides at the bottom of the UV light in the visible spectrum of sunlight.  It marries beautifully with the absorption spectra of aromatic amino acids.

Wide-bandgap semiconductors permit cells to operate at much higher frequencies of light in the UV range.  They also can tolerate higher voltages, background radiation, and temperatures than conventional semiconductor materials.  The most critical thing they do for cell design is that Many group 2-4 atoms create wide-band semiconductors that can emit UV frequencies that are more powerful than the sun provides.  This explains two things.  Why did cells use only 4 aromatic amino acids on Earth?  Nature married the band gap distances of atoms to only 4 amino acids with a specific power density UV absorption spectra. This explains the slide I used in Vermont in 2018 and that I mentioned in the QT #26 blog.

What else does it explain?  Roeland van Wijk laid out the case that Pritz Popp found that every cell on Earth emits ultraweak-UV light.  Prokaryotes emit 5000 times more light than eukaryotes but they all emit light.  Guess where their light emission comes from?  Their wide band semiconductors.

Why was light picked as our Jacquard punch card by Mother Nature?

From above I told you that 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?

In our universe, there are one billion photons for every atom.  That is the light-to-atom ratio. So she chose to use the higher quantity energy asset so she started with light from our star. She realized 4.6 billion years ago that this light contains both energy and information at a ratio of a billion to one. That was the bandwidth she had to work with.  Of the two Mother Nature was the first to realize that information in light could be used to organize the matter.  The atomic organization is the basis of design.

It took until Maxwell’s paper on demons in the 1860s, for anyone else to realize this relation between photons and atoms existed.  No one knew what it meant much less implied.

Light is the “bit” cells use to transfer information. Information is buried in the orbital angular momentum of light (OAM) of light. The energy in light is buried in its frequency.  Immediately Nature realized that low-frequency light packed quite an information punch.  That punch was formulated into a card we call a cell.

Since there are one billion photons per atom energy and information has to flow from light to atoms.  A billion-to-one ratio is like asking a 20,000 waterfall to reverse its flow without adding a bit of energy.  Kight cannot flow the other way, just like a waterfall cannot flow in reverse.  This set the parameters for the arrow of time creation.  The entropy measures the flow of light in a particular atomic organization.  The ratio gave time an arrow.  Clocks were innovated to count the flow of entropy on these ancient semiconductive cell-wafers.

With this circuit board arrangement, there is no way for matter (atoms) to transmit 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 of thermodynamics.  Now you can begin to see how the classical world you call reality is glued to the quantum level by the laws of thermodynamics.

Why did she choose light as the key in her design?

Light is the ONLY particle that seems to have an unlimited amount of orbital angular momentum (OAM), and OAM = information.

The same thing is not true about electrons or protons. The OAM of both are limited by the laws of physics.

Information by itself is capable of creating order from chaos.  I have a blog coming up on those details.  This happens because our cells are built to store information at the electronic level in every part of the circuit board.  This made cells a dissipative structure.  Light information creates a memory in water.  It is buried in its coherent domains and in hydrogen bonds. Proteins suspended in this cell water are critically important to our wafer design.  The ATPase, melatonin, collagen, NAD+, leptin, and melanin are critical in her designs.

Water can absorb massive amounts of OAM information but water does not cover all frequencies in its absorption spectra.  Many of the chromophore proteins I just mentioned can and do help water out with light absorption. This is why you will see melatonin, water, and melanin in close proximity in critical areas of human biology.  Just think about the leptin-melanocortin pathway as a proxy for this idea.

Human neuroectoderm was a spectacular addition to the primate clade in their brains.  Mammals are 210 million years old and they were able to figure out how to use charge density changes to move melanin from their hair into their brains over 210 million years.  It was perfected in ancient humans to sculpt their brains.  Changes in the environment sculpted these moves.  You’ll be hearing about them soon.

One of the problems with wide-band semiconductor design with time is, light information will fill the capacity of all the electronic states inside the cell and fill up all the memory slots.  When this happens memory space would decline. Information can only be useful on an ongoing basis until memory deletes information contained in light/water.  Cell developed a plan for this called sleep.

KEY BLOG MOMENT:  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.  Cells somehow figured out how to use visible light to transform matter into more powerful light and then turnaround and use this transformed light to make water flow uphill.  Mother Nature used the periodic table and solid state physics as her cosmic wand of creation.  This is the basis of how cells create a negative entropy state.  This created the appearance that life somehow was breaking the second law of thermodynamics.  It wasn’t.  She used semiconductors to create better sunlight than the sun shines on Earth.

ATPase creation

Adding sunlight chronically to cell water makes the dielectric constant go from 78 to 160.  In ancient times when more dangerous parts of the electromagnetic spectrum in the dielectric constant were likely higher.  This gave ancient cells the ability to add a ton of OAM to water to build better optical tweezers to build the ATPase. What were the collateral effects of having an excess of sunlight interacting with atoms for a billion years before life organized?  The hardware could be built using that excess OAM locked into the electronic state of the cell.   It turns out the ATPase was created and it optimized its operation to light from the environment.  It was quantized to these changes.

Under the power of non-flickering red light from the sun, the ATPase becomes a 100% energy-efficient nano-torque motor. Researchers are now adding chemicals to cells that can monitor torque speeds like an anemometer measures 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.

CREATION OF ELF-UV LIGHT

So it appears increasing the viscosity of cell water by light addition increases the coherent domains in water, while lowering the number of protons, which raises the net negative charge inside the cell.  Storing powerful VUV light at the electronic level allowed cells to develop mechanisms to create ELF-UV biophotons. This is the kind of paper a Black Swan loves. It undercovers the recipes of Mother Nature for the ignorant to see.  https://pubs.acs.org/doi/10.1021/acsnano.8b00177

CREATION OF THE ATPase CREATED THE ABiLiTY FOR QUANTUM COHERENCE IN ORGANISMS AT A CELLULAR LEVEL

The reaction that turns molecular oxygen (O2) into water releases lots of energy inside cells, and all complex life cells needed that energy to drive their bodies functioning. The half reaction and associated free energy change are:

O2 + 4H3O+ + 4e- –> 6H2O     delta G = -305 kJ/mol

There has to be a biological mechanism for capturing oxygen as O2 in its high-energy, zero oxidation state and bringing it to “a place” where it can be turned into H2O.

THAT PLACE IS YOUR COLONY OF MITOCHONDRIA

The ATPase is a CARNOT HEAT ENGINE in mitochondria that is the ultimate wide band gap semiconductive device in a cell.  Here are its key DYNAMICS: Cytochrome c oxidase creates its own water.

Every 3.5 times the ATPase spins one molecule of ATP is made. Only the H+ isotope 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.

K+ is usually in solution with a Group 7 atom like Cl. KCL has a massive band gap. This entire crystalline structure of water is built by deuterium depletion of the mitochondrial matrix at cytochrome 4. This chromophore has 4 red light photoreceptors and it has a heme proteins in its core.

All these are destroyed by free retinal from melanopsin dysfunction. As melanopsin damage occurs it frees retinal and the retinal destroys the atomic arrangement of melanin and heme proteins where ever they are suspended in cell water. This damage needs to be repaired or disease will result.

Chemical and atomic structural disorder profoundly influence the steady-state spectroscopic properties of heme proteins and melanins. The consequences of the of atomic disorder of wdie band semiconductive proteins is called disease generation.  This includes redox disorder on excited solid state dynamics.

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 closer 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 of what “P” is doing really in ATP inside the quantum cell.  It is not what is published in any biochemistry book today.

AMP/ADP/ATP are all wide-gapped semiconductive proteins and “P” dopes them to fluoresce. Read the Lavender blog on LinkedIn now. Carefully re-read the Quantum Thermodynamics #26 blog on Patreon again. Why is it that the few amino acids cells use have VUV light absorption spectra?  Where was that light coming from?

This deep VUV light interaction with matrix water is how a cell uses light and water to create coherence inside every cell in your body.

In the living state, potassium acts like “a solar 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 in tissues over long distances. This crystalline structure allows proteins to semiconduct and it also limits atomic motions to facilitate coherence. This is why K+ is critical in setting the redox potential of water in a cell.

Hypkalemia in labs is huge tell to a quantum clinicians.  The symptoms in diseases are devasting when they occur.  A low potassium level in a cell has many causes.  It is almost always due to a loss of the atomic arrangement inside cells. Hypokalemia usually results from chronic vomiting, diarrhea, adrenal gland disorders, or use of diuretics. A low potassium level can make muscles feel weak, cramp, twitch, or even become paralyzed without neurologic disease, and abnormal heart rhythms develop.  Left untreated death will occur.

Look at the periodic table above, notice the location of atoms that cells reuse over and over again. In this way, you are building a special type of semiconductor that forms THE REAL “the fourth phase of matter” in cells that emits its own SPRECTRA of sunlight.

It can do this when the surface is perturbed to action by light and then the party gets started inside the cell and can act like a “topologic insulator”(TI). A ‘TI’ allows a multitude of quantum effects to happen in warm wet environments. Modern physics struggles to wrap their belief system around this cellular design.  Yet, they know photosynthesis is run this way since 2007.  This idea offends the core of classical standard physics but even they are coming around to this issue. Look at how they are studying melanins now to make new solar panels.

Silicon Valley types are using narrow-band semiconductors to build tech empires while nature is building-wide band semiconductors where ever you look. K+ changes the optics inside of a cell which allows it to use OAM in VUV-IR light. That spectrum is more powerful than the sun’s spectra is on the surface of Earth. Every critical protein in man is made from aromatic amino acids. Potassium, Na, and Mg will be close to most of the most critical semiconductive proteins in cellular design.

The Fo base piece of the ATPase is embedded in the mitochondrial inner membrane and 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. These actions create a magnetic field when there is enough current coming into the inner mitochondrial membrane. When the current is high the magnetic field mitochondria makes is also strongest. When UV light is present and it slows ECT flow, the magnetic flux in mitochondria drops. This is why the DC electric current varies from wakefulness and sleep. We can measure that as Dr. Robert O. Becker did in the DC electric current in neurons in the brain.

A second, off-center protein tether connects the head group to the base piece and prevents the headpiece from 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 (affects light release as a diode/piezoelectric/flexoelectric), destroying their ability to bind ATP.

Piezoelectric release DC electric current and flexoelectricity is the electromechanical coupling between mechanical strain gradient and electric polarization or vice versa. This is how refractive indices in cells are controlled to deal with variable light conditions on Earth.  Cells are capable of changing their dielectric constant by changing the ratio of deuterium to hydrogen in water.  They use mitochondrial uncoupling proteins to do it.

The “P” in ATP responds just as two magnets do when you try to push them together. How? The oxidation state is altered to change its magnetic effects. The energy input is used to drive ATP release, not for bond formation.  Hemoglobin does the same thing when it alters the oxidation state of iron atoms in its core.

It is presumably necessary to disable the catalytic mechanism on the center which has just formed ATP (to stop this center from 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 are 120 degrees out of phase.

Because of this, it takes at least 9 H+ protons (possibly as many as 12) to drive one revolution of the camshaft and produce 3 ATP molecules. One turn requires about 3.4 H+. Red light is the main energy source to spin this Fo head and move protons.

HERE IS WHAT EVERYONE FORGETS: Remember that the whole ATPase complex is reversible. Electrons can actually flow from cytochrome 4 to 1 and the ATPase can spin the opposite way. What controls the motion? The electromagnetic force of light does. This complex is optimized to work with UV and IR light and not any other frequency of light. This was a critical understanding when I built my leptin Rx series of blogs.  This is even a bigger deal in a blue-lit 5G world.
https://arxiv.org/abs/1508.06135

SUMMARY

True friendship is like fluorescence, it shines better when the situation darkens.  You might use this description for the greatest event in the history of mammals too, the KT event.  Dark wide band gap semiconduction was critical in understanding the story of leptin.  You will soon understand it all at a very foundational level.  You had to learn many parts first to understand the whole.

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. Cells built themselves to take in lower-powered visible light of the sun and used wide band gap atoms to create her wafer design in cells.  This is the basis of why cells seem to have a negative entropy to them. That book written in 1944 made this case. (below).  Schodinger had no idea how it happened and this blog just gave it to your for the cost of a cup of coffee.  That is a decentralized trade.

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. Phosphorous does the best.  Fluorescent materials cease to glow nearly immediately when the radiation source stops, unlike phosphorescent materials, which continue to emit light for some time after.

Cells have the uncanny ability to emit light close to 150nm based on the atoms we use in our cell design.

What is the implication of this blog?  Many things we believe in centralized science are not only wrong, but the meaning is also 180 degrees from what is printed in textbooks.

Here is the decentralized lesson for this blog for you to consume:

We know from A. G. Gurwitsch’s work on onions and from Popp’s work on cells that UV light is required to stimulate a cell on Earth to divide at mitosis in the cell cycle.  Most centralized cancer doctors believe that cancerous cells are most deadly at the mitosis stage of the cell cycle and this is why chemotherapeutic drugs are designed to screw up the mitotic processes.  This is 180 degrees opposite what you should do!!!   If you understood the blog well, you’d realize why we cannot and will not solve cancer with this pathway of thinking.

We have no Earthly idea how a cell really operates.   You do now.

When a tissue loses its ability to create ultraweak UV light because the atomic arrangement of your wide band gapped melanin semiconductors are demolished from low redox processes like blue light and/or nnEMF human cells cannot undergo mitosis.  The cell is stuck in a non dividing state without UV light.  Moreover, this stoppage of the cell cycle is actually when cancers become lethal via metastasis. On the surface when you say these things to a medical oncologist they think you are nuts.  This is completely counterintuitive position to take compared to centralized teachings.  Today in 2023 some oncology researchers are reporting new data that supports my quantum thesis of cell design that takes account of Gurwitsch’s finding from 1923 on UV light and mitogenesis.

Now you know why I love sunburns and why they don’t matter either.  You are a creature that loves and is organized around Very deep UV light.  That light REGENERATES every wide based semiconductive protein in your body.

CITE

https://journals.lww.com/oncology-times/fulltext/2019/01050/non_proliferative_cancer_cells___the_deadly_charge.5.aspx

Game, set, match.

QUANTUM ENGINEERING #27: WHY IS SUNSCREEN AND SUNGLASSES HARMFUL?

For the ignorant people advocating sun creams on my social media feeds, & this post should be called your shut-up juice.  Sunscreens have several effects and none of them are good for your decentralized life. Read them below.

1.  The tyrosinase inhibitors block melanin production everywhere in your body and this atrophies the skin (chronically pale), gut (blocked VDR), eyes (RPE) hearing (cochlea/hearing loss/tinnitus), brain/basal ganglia (dopaminergic neurons/PD/depression/suicide/poor executive functioning/poor thinking)

2.  Without melanin in your skin you burn faster BECAUSE your skin cannot make POMC, melanin, and can’t make Vitamin D3 from cholesterol esters. This is why I looked pink above.  It only takes me a few days to repair this problem when I get my skin and eye back in nature.

3.  Unlike most mammals, which have melanin-producing melanocytes predominantly in the hair follicle bulb, humans are uniquely equipped with melanocytes in the outermost layer of the skin, the epidermis. These neural crest-derived melanocytes are the only source of the photoprotective pigment melanin in human skin.  Melanin absorbs UV light and stores its photonic power created in daylight to be transferred to other semiconductive proteins in dark.  These cells are stimulated by 3 pathways.  The UVB, UVA, and the melanopsin pathway.  Of the three, the last one is associated with many human skin/brain diseases.  The second one (UV-A pathway) works with encephalopsin/neuropsin (OPN3).  In humans, encephalopsin works with POMC cleavage protein α-melanocyte stimulating hormone (α-MSH), an agonist of the Gαs-coupled melanocortin 1 receptor (MC1R) that is primarily expressed on melanocytes.  Melanocytes are the cells that cause melanoma.  Blue light is highly stimulatory to melanocytes.  Implications?

Sunlight reduces the incidence of the diseases below.  This means sunscreen will increase them.  

SUNSCREEN CAUSES MORE SKIN CANCERS OF ALL TYPES: HIGHER MELANOMA RISK = LOW MELATONIN, LOW DOPAMINE, LOW VIT D LEVELS = NO SUN = LOWERED mitochondrial REDOX

OPN3 is a negative regulator of melanogenesis in human melanocytes. It lowers the action of alpha MSH and this lowers melanin production.

^^^^^This means another form of light is the real problem.  BLUE LIGHT/nnEMF is that answer.

4.  SUNSCREEN USE CAN DEPRESSES YOUR MOOD and cause depression. It lowers your mood. When you affect tyrosinase inhibitors you also block POMC.  Many will look at the comic below and laugh and find humor in it.  Some of us, however, will see something else more concerning and educational about sunlight.

We might see a story of how nature built us, and why we have a massive opiate issue.  UV-A has a big surprise function that is buried in this picture below: It increases POMC from the brain and protein stimulates many important things.  β-endorphin is one of the more important ones.  Do you know what it does?  It is an endogenous opiate made when we are in the sun.  What happens when you aren’t in the sun?  Think Kurt Cobain, Jimi Hendrix, and Micheal Jackson.  More on this link below.

Melanin provides protection of structures in and below the skin against free, UV-induced radicals. Thus, melanin acts as a direct shield from UV and visible light radiation. UV radiation causes a stimulus to DNA damage in the nuclei of keratinocytes that are degenerating on the surface of the skin.  This results in the activation of the p53 gene, which transcriptionally upregulates the expression of the gene encoding proopiomelanocortin (POMC) mentioned above.  Most think solar radiation induces only bad secondary effects but here is an example of positive regulation. Why do I say this is a positive stimulus?

The POMC precursor polypeptide is processed into several bioactive products, including α-melanocyte-stimulating hormone (α-MSH), adrenocorticotropic hormone (ACTH), and β-endorphin. These all link to important systems. After secretion, α-MSH binds to the melanocortin 1 receptor (MC1R) located on melanocytes and activates melanin production, and is tied to the leptin-melanocortin system tied to obesity. The leptin-melanocortin system was behind the construction of the leptin Rx 12 years ago.   This is why a lack of sunlight is linked to obesity because of a lack of UV-A and IR-A normally present in the morning sunlight. The anti-inflammatory effects of α-MSH and ACTH may help relieve irritation and local inflammation in UV-exposed skin acting as a calming influence. This increases histidine in the skin. (see below)  Urocanic acid is our natural sunblock that I spoke about in the solar callus blog.

Histidine is an aromatic amino acid that absorbs massive amounts of UV-A light. This lowers erythema production in the skin.  It turns out that IR-A light also pre-treats the skin to lower inflammation. The fact that UV-A light induces a small opiate response tells us nature is trying to addict us to get us to come out into the solar light for a REASON.  You should not mess around with that reason.

5. With sunscreen you are raising your risk of hypertension and stroke!  Why?

One amazing way to lower your pressure is with SUNLIGHT via multiple mechanisms.  The first way is via the release of NO in the skin which allows for the blood to get irradiated by the sun via dermal pooling as NO dilates the blood vessels under your skin.  This lowers resistance to lower pressure.

Did you know 40-60% of your blood volume moves toward the sun with this effect assuming you have no clothes or sunblock on? The second way sunlight lowers BP is via the renin-angiotensin system in the kidney. Sunlight raises Vitamin D3 in the skin and blood plasma and this directly affects the inhibition of renin activity in the kidney to control blood pressure centrally in the brain. The vitamin D3 and sunlight axis work via calcium signaling and this gives the endocrine system a potentially bidirectional and stimulatory relationship between aldosterone and parathyroid hormone. Most modern humans have lost this bidirectional control because of clothing, sunblock, and an indoor existence and this is why high blood pressure is now a global epidemic.

6. You always hear the Zen/food gurus talk about the third eye.  The Black Swan mitochondriac reality is that your skin is your literal and figurative third eye if you have not figured it out yet.   Melanopsin was found to be in our eyes in 1998.  Then we found it in the arterioles of our skin in 2014.  Then we found it in our skin and subcutaneous fat in December 2017.  This is when it became clear why so many people in the LCHF community remain fat and cannot tan because their skin is chronically atrophic from blocking the sun.  They have no idea how melanopsin works to explain their phenomena.  In fact, their old leader Mr. Jimmy Moore is a textbook example of what happens when you eat lots of fat and use blue light to run a life.  He regained all his weight and was just sentenced to 20 years for pedophilia with a 13-year-old girl.

Yes, sexual deviancy is something we SHOULD expect in people when they chronically block the sun in how hormones are created in the skin/eye/brain.  We’ve known about this for over 100 years. (see below) .

The implications of this are seen every day now in the pronoun warriors online.  Kids are now bathed in blue and nnEMF in schools.  It is also supported by centralized systems in healthcare now too!  Hospital systems are raking in profits over it.

7. We’ve known about blue light reflecting off the moon for ages.  It is where the word “lunatic” comes from.  Blue light at night makes humans act differently than one would expect because it alters our dopamine levels.  It also affects our sexual functioning and our libido.  It can drive aberrant behaviors as well.

Blue light has been used positively in biology as well at night. Not in humans but if you are a coral.  The problem is modern humans who use sunscreen are killing coral reefs everywhere.  Why?  The sunscreen floats at the top of the ocean.  It blocks the effect of blue light reflected off the moon.

Why is this a big deal?

Starting with the beginning of the last century, a multitude of scientific studies has documented that the lunar cycle times behaviors and physiology in many organisms. It is plausible that even the first life forms adapted to the different rhythms controlled by the moon. Consistently, many marine species exhibit lunar rhythms, and also the number of documented “lunar-rhythmic” terrestrial species is increasing. Organisms follow diverse lunar geophysical/astronomical rhythms, which differ significantly in terms of period length: from hours (circalunidian and circatidal rhythms) to days (circasemilunar and circalunar cycles). Evidence for internal circatital and circalunar oscillators exists for a range of species based on past behavioral studies, but those species with well-documented behaviorally free-running lunar rhythms are not typically used for molecular studies. Thus, the underlying molecular mechanisms are largely obscure: the dark side of the moon.

Lunar rhythms of light, dark, and gravitation changes cause alteration in the human transcriptome, proteome, and physiology.  The proxy for these effects is seen in the hormonal variation of humans.  This can be positive or negative.

The POSITIVE: Lunar cycles modulate the estrus cycle because the moon can and does reflect light from the sun at night to the Earth as it goes through its revolutions monthly around Earth……..that is why they influence woman’s hormone cycles assuming she is properly connected to Earth, sun and the lunar cycles.

A NEGATIVE: MOST ladies aren’t properly coupled to light and dark cycles now, therefore, their hormone effects are muted and lowered in modern females. This is why estrus vanished in humans and proof it still has influence can be seen when women get together and live together their cycle will all become coupled oscillator again…….just like molecular resonance predicts.  When the negative and positive feedback loop is uncoupled from one another the result is the extinction of both sides of the coupled system.  This extinction effect manifests in the pregnenolone steal syndrome that can cause sexual and gender identity issues.

ANOTHER POSITIVE: Among all, probably the most spectacular and documented event orchestrated by animals according to the lunar cycle is certainly the mass spawning of corals. Like inside a shaken snow globe, once every year, the barrier reef explodes with eggs and sperm, a few days after Full Moon, during late spring/summer nights, a phenomenon even visible from space. Unfortunately, reef corals are losing this critical reproductive synchrony, likely due to the anthropogenic impact of artificial light at night. This phenomenon threatens several species, not only corals but entire reef communities.

This is why Mexican cenote owners require humans to take showers before they enter any CENOTE in Mexico.  They want you to remove the sunscreen so you do not harm the life inside the cenote.  Imagine that.  Sunscreen is not good for cenote life either.

8. All these effects have butterfly effects.  How long will it take for people to wake up to how big a deal this is?  Melanopsin serves an important role in the photoentrainment of circadian rhythms in ALL mammals but especially humans.  Why?  Humans have the weakest covalent bond in melanopsin to retinol. This means the bond is easily broken by blue light which is the light modern humans now live under and within >90% of the time. An organism that is photo-entrained has aligned its activity to the 24-hour cycle, the solar cycle on Earth. In mammals, melanopsin-expressing axons target the suprachiasmatic nucleus (SCN) through the retinohypothalamic tract (RHT), skin arterioles, skin, and subcutaneous fat.  In fact, it has recently been shown that the human brain has far more melanopsin in it than any other mammal on Earth.  Humans are the ultimate solar mammal and this explains why the silly-talking monkeys lost their hair/coat.  How do you like that as a game changer?  This implies the food is not what fattens us today.  It is technology that does it.

How? You get fatter because of the blue light way faster than eating carbohydrates.  And when you do that weight is HARDER to lose.

Aponte found that artificial light via the eye over stimulates pro-opiomelanocortin (POMC) and agouti-related peptide (AGRP) neurons acutely regulate feeding behavior. This causes apoptosis or cell suicide of these neurons.  Once this happens you become resistant to the action of leptin.  Aponte found that AGRP-induced hyperphagia is completely independent of melanocortin signaling.  This told us that blue light alone, without red and UV light, could cause obesity. This has been confirmed by electrophysiology studies that have shown that leptin stimulates POMC neuron firing (Cowley et al., 2001) and regulates the activity of potassium channels in POMC neurons thus modulating neuronal excitability (Jobst et al., 2004).  Sunscreen, sunglasses and glass in windows all cause these light effects because of how they block light.  Just living indoors behind glass will fatten you.  It will cause other diseases as well.

Solar exposure with full terrestrial sunlight 250-760nm)  uncouples respiration from ATP synthesis via its NO effect on cytochrome C oxidase in mitochondria.  Uncoupling respiration from ATP synthesis or increasing ATP hydrolysis restores NAD+/NADH homeostasis and proliferation even when glucose oxidation is increased.  UVA light from the sun creates Nitric Oxide to slow Electron chain transport flow mimicking calorie restriction.  The sun however, always has IR-A light present when UV-A light is present, and 43% of IR-A light directly and simultaneously affects the 4 red light chromophores in Cytochrome c oxidase in mitochondria to create water and make ATP without ELECTRONS.  Electrons come from food.  If you slow ECT down you do not need to eat as much.  You can still transform energy because the IR-A light is always present when the sun shines on you.

Any rapid activation of oxygen consumption inside of the mitochondrial matrix leads to local transient hypoxia (NAD+ drops), causing cytochrome C oxidase to change from reducing oxygen with electrons to catalyzing the formation of nitric oxide.  NO disrupts and lowers ECT flow.  Red light can counterbalance NO release by near-infrared light (600-1000nm).  These photons directly energize cytochrome oxidase (Complex IV) via photon absorption, facilitating its catalytic activity and leading to the up-regulation of cytochrome oxidase levels. People seem to forget that cytochrome c oxidase contains 4 red light chromophores in the IR-A range.  The sun is loaded with this frequency of light because it comes from the atomic spectrum of hydrogen.  In fact, it is the most abundant light in terrestrial sunlight. (43%)

When you put sunscreen or sunglasses on you are making it harder to lose weight and easier to gain it while atrophying your skin and eyes making them more susceptible to damage because there is no melanin present in tissues to absorb UV light.

Weight loss factoid of the day:  most people want to argue that it’s an argument between competing theories:

1. The calories in calories out theory (CICO)

2.  The insulin theory of obesity.

My point is simple, both miss the mark in a large way because they never consider light’s effects on the mitochondrial engines.  Nothing makes sense without understanding the power of light in a reversal of obesity because of how solar light controls the chemicals that optimize our engines.  Melatonin, dopamine, and insulin are those chemicals.  These molecules, and not the fuels we eat are critical in engine optimization.  Melatonin controls autophagy and apoptosis, dopamine with melatonin controls photoreceptor regeneration, and insulin improves or destroys the periodicity of the molecular clocks of the gut organs.

Higher blood glucose and insulin levels are seen in poor sleepers.  Poor sleepers have lowered melatonin/dopamine levels.  How is insulin disrupted? Insulin reduces Bmal1 transcriptional activity by altering liver clocks but lowering the periodicity of the clock mechanism. This signaling mechanism has a central role in the initial phase during food entrainment resetting of the hepatic clocks.  It is disrupted by light or food eaten outside of the control of the sun’s light and dark cycles.

Food only becomes a dominant player when the solar light is subtracted or artificial light/nnEMF is added to your life to subtract from the quantized equation on our skin and eyes.

https://jackkruse.com/time-17-melatonin-insulin-solar-metronomes/

See, I’ve been telling you the same story over and over again and trying to get you to understand and stop blaming food for what light causes.  Engine destruction by light always trumps a fueling problem in the engine.

9. Can sunscreen make your migraine headache worse even when you are on medication?  YEP.  How?  When you put sunscreen on you destroy melanin production.  You need melanin production in the RPE of your eye. The RPE of your eye help regulates the function of Muller cells in the retina.

Now we have similar data developing on migraines that light disruption causes brain-level migraines: These headaches result from a stroboscopic effect via the Muller cells into the hypothalamic pathways of the brain and decreased current in DHA and CSF superconductors anterior to the SCN.

The stroboscopic effect occurs when a flashing light source illuminates a moving object. This effect, created by the flickering of the surrounding light, is harmful to the vision and causes discomfort, visual fatigue, and headaches.  Fluorescent & LED are the lights associated with this effect most.

Researchers used H2 15O (radioactive water) to measure regional cerebral blood flow as a surrogate marker for neuronal activation.

They found that compared with baseline scans, there was activation in several key areas, including the hypothalamus, an area involved in low-level regulation of sleep, appetite, mood, and fluid balance. “It seems very likely that the hypothalamus is pivotal in the onset of migraine”

http://ow.ly/mHqV2

10. In mammals, the eye is the main photosensitive organ for the transmission of light signals to the brain because their skin is usually covered by coats and hair.  Humans are unique among mammals as they have shed most of their hair and the skin is their LARGEST organ.   This helps explain why there is so much melanopsin in the human brain compared to hairy primates who cannot talk.  The skin and brain both come from the same tissue in the human embryo called neuroectoderm.  This is why blind humans are a very interesting cohort to follow to learn about how melanopsin and vitamin A work to lower Vitamin D production and POMC production because of altered skin signals humans get from their skin to ruin every peripheral clock gene in every organ of their body by blue light exposure.  Why?  Blind humans are still able to entrain to the environmental light-dark cycle, despite having no conscious perception of the light via their retina.  How do they do it?  They use their third eye in the skin to do it, their skin.  One study exposed subjects to bright light for a prolonged duration of time and measured their melatonin concentrations.

Melatonin was not only suppressed in visually unimpaired humans but also in blind participants, suggesting that the photic pathway used by the circadian system is functionally intact despite blindness. This was a big clue there was another pathway that the circadian mechanism works with.  When it was found that all human opsin were loosely bound to opsin then the connection to mitochondrial dysfunction was easy to make because melanopsin and Vitamin link to mtDNA repair via the production of melatonin.  Melatonin is well known to repair mtDNA damage at night during sleep during autophagy.   This is why in neurosurgery we have warned ophthalmologists, that we should no longer routinely practice enucleation of blind patients or removal of the eyes at birth since the eyes play a critical role in the photoentrainment of the circadian pacemaker and the peripheral clock genes in every tissue in the body.  This also means if you wear sunscreen you are blocking massive information to control all your peripheral clock genes.

There is some good news: If you had Lasik surgery or cataract surgery this is how you help offset the damage to neuropsin in the cornea and/or the blockade of light in your eyes by the intraocular lens the eye doctors inserted to replace your cataract.

https://www.news-medical.net/news/20120522/Study-finds-large-amounts-of-melanopsin-in-the-human-brain.aspx

11.  More on melanopsin, your eyes, and Parkinson’s disease. This is due to the effect of free retinal from its weak covalent bond to melanopsin due to unopposed blue light and nnEMF in manmade light.   The effect is massive and few seem to realize it.  Your pupillary function can be destroyed via your skin and subcutaneous fat.

https://www.nature.com/articles/s41598-018-26078-0

12.  Based on #9 you probably have figured out that the number one cause of cataracts in the 20th and 21 century is now linked to blue light exposure from tech screens and TV.  It also causes dry eye, depression, mood disorders, AMD, hormone problems, and the list goes on every year.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288536/

13. The more sunscreen, makeup, foundation, and skin products you use the more melasma you will get.  The risk increases when you add blue light from indoor living where full-spectrum sunlight is absent.  Melasma is a complex skin issue tied to nonlinear optics and free radicals. It is a circadian mismatch in the skin that releases excessive light from the keratocytes of the skin which in turn stimulates the melanosomes to darken. The reason this occurs in my opinion is that melanopsin is operational in skin and fat. This is a prediction I have made for some time. 

Artificial blue light exposure darkens, freckles, and causes mitosis in melanosomes to lead to darkening diseases like melasma and melanoma. Few dermatologists realize that man-made light is behind these diseases and they should at least consider it. Decreasing tyrosinase activity is a great prevention strategy for conditions related to hyperpigmentation of the skin, such as melasma. Sunlight does this because it is a tyrosine kinase inhibitor. This specific sensitive environment found in your skin and around your mitochondrial membranes is required for the proper release of UV light from skin cells.

It is also related to the mitochondrial function of skin in another way: One cannot make the normal free radical signal in a hypoxic or pseudohypoxic state (low NAD+).  All sunscreens lower NAD+ in your mitochondria.  They cause photoaging.   

UV light increases oxygen levels (and deuterium in the dead skin to get rid of it) in the skin in presence of RBC When full spectrum sunlight hits our skin blood flow in the skin will rise.  Porphyrins in hemoglobin absorb UVA, UVB, and IR-A light.  They have no mitochondria.  Putting sunscreen or sunglasses on your eyes blocks this light.

In melasma, it does not work this way because women are blocking the darkening skin from full spectrum light with their makeup and exposing their skin to man-made light at night. This means we need a constant source of O2 and UV light to keep oxygen as our terminal electron acceptor in the mitochondria of the skin/cornea.  This is why contacts are problem.  They lower oxygen tensions in the eye.   

If we don’t use oxygen as the terminal electron acceptor on the skin it favors the growth of bacteria in the skin/eye.  These bacteria are capable of using other atoms than oxygen to act as the terminal electron acceptor.  When UV light is also absent simultaneously this increases their ability to grow in a woman’s skin even more. UV light is bactericidal. This causes a large increase in the phenol content of the skin/cornea because these bacteria are growing. Bacterial growth is linked to a lack of UV light exposure. 

In fact, bacteria contain substantial amounts of photo-sensitive amino acids compared to our cells. They have a lot of phenylalanine and tyrosine and those two amino acids are relatively rare in eukaryotic skin cell proteins by design. The reason for the bactericidal effect of UV light upon them is that they absorb greater amounts of UV light and they have no protective mechanisms.   It should now make sense to you why tyrosinase activity and the darkening of skin are linked. Tyrosinase is an oxidase (enzyme) that is the rate-limiting enzyme for controlling the production of melanin in our skin melanosomes. So decreasing tyrosinase activity WITH SUNSCREEN darkens the skin.

14. Taking exogenous melatonin orally is equivalent to using sunscreen.  Why?

Taking melatonin orally chronically without blocking blue light can lead to serious eye damage. Here are two eye-opening papers on why you better make sure you have the right people packing your parachute.

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2785757/

All oral doses produce the same response: they thin your retina by ruining photoreceptor regeneration. Whatever supplement maker tells you to take it does not know the data. If your cells and body make it endogenously, you’re not designed to take it exogenously. It is a simple rule of Nature.

 http://www.iovs.org/content/33/6/1894

15.  Using sunscreen will reduce your mood and if you do it long enough you will get various mental diseases.  Do it longer and you may become a suicide statistic.  Seasonal changes in sun time were found to best account for relationships between weather variables and variability in mental health distress. Increased mental health distress was found during periods of reduced sun time hours. A separate analysis examining subjects’ endorsement of a suicidality item, though not statistically significant, demonstrated a similar pattern. Initial results showed a relationship between pollution and changes in mental health distress; however, this was mediated by sun time.  We’ve known this for a long time in medicine, but you’d never know it from the advice given in the Dermatology and Ophthalmology clinics in the USA.

https://journals.sagepub.com/doi/pdf/10.1177/003591572902200434

16.  I almost hate to say this in this blog but I am compelled to.  Low-dose methylene blue use is a way to counterbalance chronic suncream abuse, blue light, toxicity, and the implantation of intraocular lenses.  I will not go into the mechanisms but if you are a physician and you understand the top 13 points you will see why this makes sense.  For the lay public, I do not practice medicine on these Patreon blogs and I will say this is why you want to hire decentralized MDs to advise you when you have some of these conditions.  Do not ask for the dose or how I do it because the answers will not show up magically in the comments below.  I used this strategy with a famous patient of mine and once he reveals the story fully online this topic is sure to make some waves on social media.  I expect that to happen in the first week of March 2023.

17.  If you use sunscreen or eyeglasses you might be more prone to addictions.  Why?  Addictions are associated with lowered dopamine states.  Dopamine is created via melanin biology.  Sunscreens block melanin production.

If migraines are linked to artificial light via the hypothalamus via POMC, and POMC creates our natural opioid beta-endorphin, is it possible drug addiction is somehow related to modern man’s abuse of man-made light day and night?

If we put a rat in a cage and give it 2 water bottles. One is just water and one is water laced with heroin or cocaine. The rat will almost always prefer the drugged water and almost always kill itself in a couple of weeks. That is our current theory of addiction. Is it right? Might a tighter connection with our environment that leads to entanglement or connection be the missing piece to the addiction equation? Is this radical thinking?

A wise researcher came along in the ’70s and said, “Well, hang on. We’re putting the rat in an empty cage under artificial light. It has nothing to do and it is doing it in bad light. Let’s try this a bit differently.” So the wise-built Rat Park and Rat Park are like heaven for rats. Everything a rat could want is in Rat Park. Lovely food. Lots of sex. Lots of darkness because rats are NOCTURNAL. Other rats were present to befriend. Colored balls. Plus both water bottles, one with water and one with drugged water. But here’s what’s fascinating: In Rat Park, they didn’t like the drugged water any longer. In fact, They hardly used it. None of them overdosed in this experiment. None of them use drugs in a way that looks like compulsion or addiction. What did the wise show? They showed that both the right-wing and left-wing theories of addiction are wrong. The right-wing theory is that it’s a moral failing, you’re a hedonist, and you party too hard. The left-wing theory is that it takes you over, and your brain is hijacked. It turns out the connection or lack of connection to our native environment is the missing piece to addiction. The wise say it’s not your morality, it’s not your brain; it’s the cage that becomes your prison that is the key to why you are addicted to something. Addiction is largely an adaptation to your environment due to a lack of entanglement or connection. This leads to a desynchrony of how things operate in your cells and this changes your behavior = see Prince, Lead singers of Soundgarden and Linkin Park.

Now, we created a society where significant numbers of us can’t bear to be present in our lives without being on something, drinking, drugs, sex, shopping… We’ve created a hyperconsumerist, hyper-individualist, isolated world that is, for many of us, more like the first cage than the bonded, connected cages we need.

The opposite of addiction is not sobriety. The opposite of addiction is connection or entanglement to Nature. And our whole society, the engine of it, is geared toward making us connect with things, not people. You are not a good consumer citizen if you spend your time bonding with the people around you and not stuff. In fact, we are trained from a young age to focus our hopes, dreams, and ambitions on things to buy and consume. Drug addiction is a subset to living a life without proper entanglement in Nature with the sun.

https://www.linkedin.com/pulse/time-rethink-your-truth-sun-jack-kruse/

18.  Why can’t young people sleep anymore?  Well, their parents have put sunscreen on them all their lives and this has atrophied their skin and eyes.  This means they cannot handle being out in the sun very long.  When I hear people tell me they are photosensitive I know how this was caused.  They are always in disbelief because of what they have been told by centralized nonsense.  Sunscreen, sunglasses, and modern tech screens while living indoors for their entire life.  They have no melanin.  They are manufactured albinos.

Blue light/nnEMF dehydrates cells because they stop H2O production from the mitochondrial TCA cycle.  Why is this a big deal? Neurons absorb and release water when firing information.  When H2O is missing in action in your cells so are neurological functions/capabilities.  You lose the ability to sleep and account for time in your molecular clocks when water is absent.  This is why all neurodegenerative conditions are exploding globally.

This is also why children experience time differently than adults.  Less water, less sunlight, or more ALAN at night destroy the clock-timing mechanism of living things.  Few see this recipe in life’s blueprint  The inability to sleep = lowered mitochondrial melatonin production = low NAD+ regeneration.  

https://www.nih.gov/news-events/news-releases/neurons-absorb-release-water-when-firing-nih-study-suggests

19.  Bone/Joint failure is made worse by sunscreen and sunglasses. Now you know why orthopedic surgeons are so busy replacing knees and hips over the last 100 years. This includes osteoarthritis, autoimmune arthritis, osteopenia, and osteoporosis.  Why?  Because blue light ruins POMC in the musculoskeletal system too.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3410228/

20. Sunscreen creates huge profits for functional medicine practitioners who are ignorant about light.  How?  Sunscreen ruins H+ movements (light hydrogen) and when H+ movements are disrupted SNP’s/SAPs do not operate they way they should?  Why?  They both operate using proton tunneling.  In fact, all enzymes use proton tunneling to work. If you block sunlight with sunscreens and sunglasses you are effectiving enzyme kinetics.

D+= deuterium or heavy hydrogen.

SNPs expression is amplified when there is too much D+ to H+ in the mitochondrion of a cell – because the Enzyme kinetics is even more altered.

COX2 amplification occurs in mitochondria (light stress) = more D+ coming into the cell from COX2 action on PUFAs on the cell membrane (Deuterium webinars I did for my members).

This is why SNP issues weren’t really a problem 50-70 years ago with incandescent lights + quite a shitty diet + limited dirty electricity/ RF.  Those lights had some UV and red in them.  Modern lights DO NOT!!!!!

And this explains why functional medicine doctors are robbing people blind by treating their bad SNPs/SAPs on 23andme testing:  It also explains why they’re exploding now in the modern world cause it’s LED Lights + generally a good diet (sugar consumption has dropped) + huge D.E / RF

= Diet doesn’t affect SNPs… Deuterium fractionations do!!!

COX2 is how D+ is getting through and clogging up the TCA cycle in the mitochondrial matrix.

Structured Water and Charge (Sun) is how we limit the inflow of deuterium and keep it filled with H+.

Limiting D+ in diet (Keto/Carnivore/Boros/crooks) is a short-term remedy for SNPs/SAP issues but doesn’t solve the problem long-term until you understand the light story.

SUMMARY

The medium is the message.  Dermatology and Ophthalmology are the “mediums” Big Pharma has used to get you to believe the sun is toxic.  Today modern man does not live in sunlight.  So how could the sun be toxic?  Might it be the light we live under be the real problem?

If you are a physician and don’t realize our profession is dying on its own vine, you haven’t been paying attention to the science I am showing you daily.  Sunscreen supports centralized healthcare overuse = highly profitable for healthcare corporations.

What is the difference between a decentralized vs centralized MD?  Centralized MDs are told by their bosses to just treat the symptom of things and not reach for the cause.

There are a lot more links to how sunscreen can harm you but the list above is instructive and should shed light on why you need to avoid conventional advice about blocking the sun with sunscreen or sunglasses.  I hope you educate the ignorant around you with this mitochondriac wisdom.

This truth is discoverable, but the facts will be so dishonestly set forth in almost any media outlet by the “mediums” that the public can be forgiven either for swallowing lies or failing to form an opinion.  The reason for this is how the news is being delivered today about the sun.  The products of modern science and technology are not in themselves good or bad; it is the way they are used that determines their value to us.  Right now they are destroying the public’s health.

The difference between you and the “mediums’ today is education.  The profiteers got wiser and put the “mediums” on the media platforms to deliver their propaganda to change your beliefs to get you to stay out of the sun.  This began with Coco Chanel.  The actions of the mediums and media have resulted in “a public” that is too ignorant to explain why they’re experts are right or wrong on medical topics (think COVID/SUN), while the media is so smart they can collectively join forces online and make “wrong or bad medicine” sound good to most of the public.  The medium was designed to dull the senses and cognition of the viewing audience.  Lowered dopamine from a lack of sun creates compliant obedient idiots.  It has worked fabulously.  COVID uncovered their plan.  This is why Fauci wanted you out of the sun in lockdown and it is why the vaccine king, Bill Gates, wants to block the sun.  Your use of sunscreen and sunglasses make his agenda easier to obtain.

The public is now a product of the media and not their customer.  Advertisers are their chief customers = Big Pharma.  Public viewers are now quite cheap because of how the news is delivered in the technocracy.  When viewers realized they have been made a cheap commodity, they can easily force the cost of their services higher to cause the financial collapse of the media.

Why should you care?  Once we have surrendered our senses and nervous systems to the private manipulation of those mediums paid by Big Pharma to work the airwaves in the media who would try to benefit from taking a lease on our eyes and ears and nerves, we don’t really have any rights left.

If Covid has taught you anything don’t discount what initially appears as nonsense. The most fatal illusion is the settled point of view. Nonsense is nonsense only because we have not yet found that point of view from which it makes sense to us.  A fixed point of view in life usually harms anybody who has one.  Nature’s knowledge is never final.  There are no axiomatic truths in medicine or science.  This is why the scientific method exists.  To continually test what we know for new data.  Wisdom tells me what is correct today, is likely going to be wrong in the future.

If you want to be the most innovative person in your space – get outside of it, regularly. Sunburns like the one I got above is not a death sentence.  In fact new data show the opposite.  (see below)

Conversations with people doing the same job you do can expand your box but rarely pushes outside of it.  Go to spaces no one else cares about and you’ll end up dominating your own.

^^^^^You live longer when you are in the sun.  Sunscreens keep you out of it.

The education system today feeds the government narrative to create obedient idiots. This preconditions the human brain for future planned events to support the paradigm in power.  

Sunscreen & sunglasses helps them and hurts you.  

CITES

https://onlinelibrary.wiley.com/doi/full/10.1111/exd.12715

QUANTUM ENGINEERING #26: IT’S THE LIGHT ENVIRONMENT STUPID!

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“Writing in a report summary in 1979, John Calhoun noted that “no single area of intellectual effort can exert a greater influence on human welfare than that contributing to better design of the built environment.”

June 22, 1972. John Calhoun stood over the abandoned husk of what had once been a thriving metropolis of thousands. Now, the population had dwindled to just 122, and soon, even these inhabitants would be dead.

Calhoun wasn’t the survivor of a natural disaster or nuclear meltdown; rather, he was a researcher at the National Institute of Mental Health conducting an experiment into the effects of overcrowding on mouse behavior. The results laid bare at his feet, had taken years to play out.

In 1968, Calhoun started the experiment by introducing four mouse couples into a specially designed pen—a veritable rodent Garden of Eden—with numerous “apartments,” abundant nesting supplies, and unlimited food and water. The only scarce resource in this microcosm was physical space, and Calhoun suspected that it was only a matter of time before this caused trouble in paradise.

Calhoun had been running similar experiments with rodents for decades but had always had to end them prematurely, ironically because of laboratory space constraints, says Edmund Ramsden, a science historian at the Queen Mary University of London. This iteration, dubbed Universe 25, was the first crowding experiment he ran to completion.

IS THERE A HUMAN CORRELATION TO THIS EXPERIMENT ON GOING ON NOW?

What happens over a few generations when they give up on having sex?  Well, female children will experience follicle failure and male children experience low sperm counts.  There is no reason to have sex when you’re infertile and today most of the world is headed this way.  How will it end for humans?  The same way it did for the dinosaurs when something from the environment changed the light on the planet.  EXTINCTION.

What causes celibacy syndrome in Asians who make made love to the 5 G devices on Wifi with no blue blockers on?  Myopia, low dopamine, and a sexless life begin as deuterium fills their mitochondrial matrices in all the various tissues in their body.

As dopamine drops many things happen but the most consequential thing that occurs is that you lose your ability to perceive time properly.

I’ve written extensively about the “celibacy syndrome” in Asia that is developing in young people in the Ubiquitination series of blogs. Many people did not see the link to nnEMF and how it causes massive assimilation of MASS into the mitochondrial matrix to cause many collateral problems in cells. Now we have more data showing us what happens when we allow blue light and nnEMF to destroy how our endocrine system works with light from the sun via our eyes and skin.  This is what the implication of my Vermont 2017 talk on youtube was all about.

How many of you “naked apes” out there get the implications???   How should we supplement to fix this deuterium mass problem? Do like the Sphinx does every AM. Look toward sunrises while grounded to become moist supple and sexy….. you should make an effort to look in the direction of the sun…….not directly at it………from sunrise til 9-10 AM. Most cannot do this because of modern life. Their lives keep them from it, so they lose dopamine and melatonin as deuterium rises in our mitochondria and wonder why they cannot turn on or off the compound pharmacy in their brain. Their beliefs around light use are why this happens.

Beliefs block us from atomic recycling that light controls. We are all recycled atoms at our fundamental basis that are altered by the light that hits us to get the life we get.

Sunlight creates dopamine and dopamine is the guardian of your pituitary gland and this is where sexy time begins. Without sexual activity in young people,  extinction is on the human agenda over the next few decades.  Leptin is the hormone that controls fecundity but many have forgotten that link to light.

In the last two years in cities, longevity has declined for the FIRST TIME in human history.  Regarding sex, dopamine controls what the endocrine system can or cannot release hormones to cells in your body and this zaps your libido and performance. As light energy changes via your eye dopamine levels alter in your eye. This changes the world you receive and understand. As energy slows down for any reason, it changes its form and becomes matter, the substances we think we know best in our world. The problem is we are fooled by what we think we now know because we have no idea what we are missing. This is the modern world’s Dunning Kruger moment. Science is ever-changing and incomplete, but it always maintains its own resistance to new and better ideas.

Today, metaphors reign large in biochemistry, where quantum mysteries reside below the surface ready to take out the “smart naked apes” just as she took out the T-Rex. Those mysteries are where all of our truth lies. A lowered dopamine is what creates this false reality today.  Lowered dopamine creates the illusion that we have more time than we really do.

Those who think that the loss of libido (the natural desire for sex) is something that only happens to people of more advanced age, today you’d be seriously wrong.  Alien light can do it and has been doing it for some time.  Before extinction, manifests diseases in the young that used to be rare will become common.  Myopia, autism, autoimmunity, obesity, T2D, AMD, and cancer are a few.

Both men and women in their late twenties are reporting a lack of interest in their own sexuality to their doctor or therapist, and even younger people are wondering where their desire for sex has gone.  Thank Apple, Facebook, Cisco, and Google.  their blue light and alien nnEMF networks were built to sell you virtual sex lives online and none of you intelligent naked apes saw it coming.

MODERN REALITY

THE CALHOUN EXPERIMENTS WERE EYE-OPENING THEN, BUT PEOPLE STILL DO NOT UNDERSTAND WHAT THE EXPERIMENTS RELAYED TO US.

“The “Universe 25″ experiment is one of the most terrifying experiments in the history of science, which, through the behavior of a colony of mice, is an attempt by scientists to explain human societies. The idea of ​​”Universe 25” Came from the American scientist John Calhoun, who created an “ideal world” in which hundreds of mice would live and reproduce. More specifically, Calhoun built the so-called “Paradise of Mice”, a specially designed space where rodents had an abundance of food and water and a large living space.

The living space, however, was in a laboratory that had modern man’s light exposing it while the experiment was ongoing.

In the beginning, he placed four pairs of mice that in a short time began to reproduce, resulting in their population growing rapidly. However, after 315 days their reproduction began to decrease significantly. When the number of rodents reached 600, a hierarchy was formed between them and then the so-called “wretches” appeared. The larger rodents began to attack the group, with the result that many males begin to “collapse” psychologically. As a result, the females did not protect themselves and in turn, became aggressive toward their young. As time went on, the females showed more and more aggressive behavior, isolation elements, and lack of reproductive mood. There was a low birth rate and, at the same time, an increase in mortality in younger rodents. Then, a new class of male rodents appeared, the so-called “beautiful mice”. They refused to mate with the females or to “fight” for their space. All they cared about was food and sleep. At one point, “beautiful males” and “isolated females” made up the majority of the population.

According to Calhoun, the death phase consisted of two stages: the “first death” and “second death.” The former was characterized by the loss of purpose in life beyond mere existence — no desire to mate, raise young, or establish a role within society. As time went on, juvenile mortality reached 100% and reproduction reached zero. Among the endangered mice, homosexuality was observed and, at the same time, cannibalism increased, despite the fact that there was plenty of food. Two years after the start of the experiment, the last baby of the colony was born. By 1973, he had killed the last mouse in the Universe 25. John Calhoun repeated the same experiment 25 more times, and each time the result was the same.  Each time there were no light controls.

Modern life also has no life controls.  Stop and think about your world now.

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Calhoun’s scientific work has been used as a model for interpreting social collapse, and his research serves as a focal point for the study of urban sociology.

Sadly most people carefully read the paper’s methodologies to realize that mice are not adapted to living in a lab indoors disconnected from their natural habitat and light source.

UNIVERSE 25 picture above: John Calhoun crouches within his rodent utopia-turned-dystopia that, at its peak, housed approximately 2,200 mice. Calhoun studied the breakdown of social bonds that occurs under extreme overcrowding, a phenomenon he termed a “behavioral sink.”  YOICHI R. OKAMOTO, WHITE HOUSE PHOTOGRAPHER, PUBLIC DOMAIN

We are currently witnessing direct parallels in today’s society; weak, feminized men with little to no skills and no protection instincts, and overly agitated and aggressive females with no maternal instincts. I wonder when people will control for light in all experiments.

Calhoun’s experiments showed us the effect of incandescent light on nocturnal mammals.  Can you imagine what the effects of these types of experiments are when you add in 5G and all the other parts of the electromagnetic spectrum outside the visible spectrum?

Sunlight is the foundation layer of Nature that gives rise to everything else.

Manmade light is not foundational to Nature and it induces collateral biological effects

Therefore, when sunlight breaks down because of modern life and centralized healthcare beliefs, standing your ground when the ground gives way will provide little in the way of safety.

How is sunlight breaking down and what should we look for as evidence of the failure?

Central healthcare is manipulating the narratives around sunlight at an unprecedented rate to avoid a profit collapse of the system they’ve built over the last 100 years.

Using information theory as a beacon it follows that misinformation around sunlight MUST be growing throughout the system if you look for it.

I write about that evidence every day and few people value it.  If they did more people would be reading my work on Patreon.

It follows as a second-order derivative of that misinformation is that trust MUST be declining throughout the healthcare system.  We have seen that in the government and economy for the last few years.  We’ve seen that in biology of diseases which have exploded over 100 years.  Not everyone realizes that what has gone on with COVID is linked to the misinformation about sunlight.

Because physicians/patients measure a system from within the system, for most of the population, it would make the truth virtually impossible to see.

With this misinformation as a backdrop and a new protocol layer technology emerging (decentralized mitochondrial medicine).  You must remember that open protocols provide the most value to society and are the hardest to understand it would be extraordinarily difficult to see why mitochondrial medicine alone stands out as a breakthrough technology and where it is heading.  You as a patron are part of that movement toward truth.

By extension, it would be relatively easy in this environment for ill-informed or bad actors to conflate sunlight with manmade light, WiFi, LiFi, nnEMF, cosmic radiation, and other “light conventions” to gain an advantage for their offering.

SUNlight is information.  It is the most critical information for you to get right now

CITES

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1644264/

QUANTUM ENGINEERING #25: DEMAR HAMLIN, JJ WATT, & LICTENSTEIN FERNING HAVE A LOT IN COMMON

A cardiac arrest is an acute loss of electric power to the heart.  When the heart fails rapidly what do we do?  We re-shock it to get it started.  The electrical shock restores the decentralized networks in us.  This is why adenosine is part of the ACLS protocol with AED therapy.

IS INTENSE RED LIGHT CAPABLE OF REPLACING AN ACLS DRUG?

SVT is a broad term for a number of tachyarrhythmias that originate above the ventricular electrical conduction system (Purkinje fibers). In cardiac arrest algorithms, ACLS tells us to use adenosine via IV push to rid the heart of this detrimental rhythm until the patient is not symptomatic.  Why adenosine?

Did you know red light from the sun creates adenosine normally in the heart when it is exposed to sunlight?

Modern humans rarely expose their skin to sunlight and this is one reason cardiac death is a leading cause of death in humans.

IS THERE NOW EVIDENCE THAT INTENSE RED LIGHT can do THE same thing using the PER circadian gene system? Does this imply that red light is a drug equivalent?

YES.

Is there more to this circadian story you need to know? YES.

Adenosine-mediated increase of cyclic AMP (cAMP) is a core component of PER2 expression and PER2-mediated ischemic preconditioning of the heart.  This means sunlight creates a perfect circadian situation for oxygen in the heart and its conduction system.

THE KEY HISTORY LESSON

The most dramatic event in the history of the earth was the arrival of sunlight and its effect on oxygen on Earth due to photosynthesis.  Sunlight caused the great oxygen event. With sunlight, trillions of photosynthetic algae could now make oxygen, transforming the entire planet’s atmosphere and setting up the perfect storm for the evolution of a mammalian mitochondrial world.

This study on adenosine, red light, and the heart shows, on a molecular level, that intensive red light therapy offers a better strategy for treating or preventing low oxygen conditions like myocardial ischemia.  Why?  Red light has no side effects but all drugs do.

In this paper below in an effort to find out why red intense light can do this, researchers developed a photonic strategy using optogenetics to protect the heart using intense light to target and manipulate the function of the PER2 gene which is expressed in a circadian pattern in the part of the brain that controls circadian rhythms. (Sounds like something Dr. Kruse would suggest no?)

You do know that sunlight is made of 42% intense IR-A light huh?

By amplifying this gene, the researchers using JUST LIGHT PHOTONS, found that it protected cardiovascular tissues against LOW OXYGEN conditions like myocardial ischemia, caused by reduced oxygen flow to the heart. Dr. Kruse called low oxygen situations pseudohypoxia. These are all associated with low NAD+ levels in cytochrome 1 and leptin resistance with low delta psi on the inner mitochondrial membrane.

They also discovered that bright light increased cardiac ADENOSINE, a chemical that plays a role in blood flow regulation and sleeps. Hey didn’t Dr. Kruse just do a massive post on ADENOSINE last week on his FB page?  Yep.

Mitophagy contributes to mitochondrial quality control not only by removing damaged mitochondria but also by promoting the biosynthesis of new mitochondria. It has been demonstrated that there is a crosstalk between the mitophagy pathway and the mitochondrial biosynthetic pathway (10). Specifically, Plaikaras et al. established that mitophagy and mitochondrial biosynthesis are interfaced with each other to maintain mitochondrial homeostasis.

The implication of this work is there’s no need to take PQQ, and other supplements, if your sleep is sub-par. Sleep and sunlight remain king and queen.  Sunlight controls the adenosine levels in humans

Hey, isn’t leptin resistance a synonym for melanopsin dysfunction? Yes, it is. Tell me again how that works Dr. Kruse.

My Response: Blue light and nnEMF liberate Vitamin A from our cells and cell membranes to raise its presence in the blood plasma and this lowers plasma levels of Vitamin C and Vitamin D. When Vitamin is liberated by non-terrestrial light or trauma, it becomes an aldehyde that destroys the small molecule modulators of the mammalian circadian mechanism. PER1 and PER2 are light gears in that eye clock mechanism.

It raises the question what in the hell do PER genes do?

Cell hypoxia is controlled by the hypoxia-inducible factor (HIF-1).
Do you know the link between HIF 1 to sunlight and oxygen?  Light and oxygen-sensing pathways are linked on a cellular level in ALL mammals (Gu et al., 2000Hogenesch et al.,1998McIntosh et al., 2010).  Hypoxia-inducible factor 1⍺ (HIF1A), is an evolutionarily conserved transcription factor enabling cellular adaptation to low oxygen availability (Semenza, 2011).  Here is the kicker:  It belongs to the same protein family as the light-inducible circadian core protein Period 2 (PER2) (Liu et al., 2012).

HIF-1 is what the entire hypoxia series was about on Patreon.  Review those blogs sometime.

So when you’re missing sun your cells sense your missing oxygen and HIF-1 goes up and PER circadian mechanism genes go awry.  The circadian mechanism loses its periodicity.  Remember what you learned on Patreon about periodicity?  Periodicity is a synonym for the circadian clock mechanism.  This ruins every cycle in the cell that relies on it.  

Once the molecular clock in the eye and peripheral clocks goes awry the implications for many neolithic diseases spiral out of control. What are some of the Vitamin A proteins involved in this downward spiral?

They are called retinoic acid receptor-related orphan nuclear receptors or RORs for short. The RORs have several isoforms too called RORα-γ. These proteins are also under the transcriptional control of CLOCK/BMAL1 heterodimers.

CLOCK and BMAL1 are positive regulators of circadian gene expression, and PER and CRY are the NEGATIVE FEEDBACK LOOP regulators that operate under day and night cycles. These are the positive and negative feedback arms of the circadian mechanism.

They must be coupled properly to terrestrial light to operate well and control all growth and metabolism, protein synthesis, and hormone production and release. It also controls receptor biology. It controls EVERYTHING. If they are not properly coupled to the light and dark cycles the eventual results are the extinction of both sides of the feedback loop. So when sunlight is absent we lose control of the negative feedback loop of the circadian mechanism controlled by PER2.  This is what causes the NAD+ drop in mtDNA.  That is how all human disease begins. It is circadian biology that couples all the molecular clock genes in humans and the SCN of the eye drives the program and the major timekeeper.  The SCN as the metronome of biology loses accuracy as PER2 drops.  PER2 is critical in controlling the optical periodicity of the circadian mechanism.

Are heart rhythms are controlled by the circadian mechanism in humans?

Yes, they are.  The enzymatic flux of the entire TCA cycle is also controlled by it in the electrical system of the heart.  Cardiac arrhythmias are a leading cause of cardiovascular death in humans. It has long been accepted that life-threatening cardiac arrhythmias (ventricular tachycardia, ventricular fibrillation, and sudden cardiac death) are more likely to occur in the morning after waking. It is perhaps less well recognized that there is a circadian rhythm in cardiac pacemaking and other electrophysiological properties of the heart. In addition, there is a circadian rhythm in other arrhythmias, for example, bradyarrhythmias and supraventricular arrhythmias.

Two mechanisms underlie this finding:

(1) a central circadian clock in the suprachiasmatic nucleus in the hypothalamus may directly affect the electrophysiology of the heart and arrhythmogenesis via various neurohumoral factors, particularly the autonomic nervous system; or

(2) a local circadian clock in the heart itself (albeit under the control of the central clock) may drive a circadian rhythm in the expression of ion channels in the heart, which in turn varies arrhythmic substrate.

Remember the free decentralized lesson from my FaceBook page on 7/31/2019:

I said, “Classic Paroxysmal SVT (supraventricular tachycardia) has a narrow QRS complex & has a very regular rhythm. … A rapid heart rate will significantly reduce the time which the ventricles have to fill.

The heart fills during diastole, and diastole is normally 2/3 the cardiac cycle. A rapid heart rate will significantly reduce the time that the ventricles have to fill. The reduced filling time results in a smaller amount of blood ejected from the heart during systole. The end result is a drop in cardiac output & hypotension.
With the drop in cardiac output, a patient may experience the following symptoms.

These symptoms occur more frequently with a heart rate >150 beats per minute as the ECG strip shows below:
Shortness of air (S)
Palpitation feeling in the chest (S)
Ongoing chest pain (U)
Dizziness (S)
Rapid breathing (S)
Loss of consciousness (U)
Numbness of body parts (S)

The pathway of choice for SVT in the tachycardia algorithm is based on whether the patient is stable or unstable clinically.
The symptoms listed above that would indicate the patient is unstable are noted with the letter (U) in a cardiac code situation. This can present outside a code situation when someone has a very low redox state because of a very poor environment linked to blue light and nnEMF toxicity. This mimics adrenal fatigue and brainstem pathology, sleep disorders, and eating disorders. Stable but serious symptoms are indicated with the letter (S) above.
Insert any 3G-5G city or environment. a \/, trauma, poor sleep = an acute or chronic adenosine problem.

HYPERLINK

What screws up sleep ultimately in decentralized networks in cells? Problems with adenosine at the brain stem level. Go look up what adenosine signals in us.  It is the biochemical signal that begins the sleep cycle in humans.  This is why ACLS uses adenosine to treat acute mitochondrial failure in the heart that results in SVT cardiac rhythms……..guess what drug is used for cardiac tachycardias in ACLS?
ADENOSINE via IV push = a DEFECT IN PER 1 or PER2. SOUND FAMILIAR?

Light-deficient humans get electrical problems in their hearts before the disease begins that people can see and sense.  That is what bad rhythms mean in patients whose heart is still pumping but acting badly.  They are all light deficient, solar light deficient, and most of the time blue light toxic. 

How do you like me now?

When the system teaches ATLS/ACLS/BLS/CPR recertification you can see where their focus really lies if you are paying attention. Pre-covid videos and protocols are available for you to review. Every variable has been subjected to intensive statistical analysis to increase the odds of survival, but there will be no mention of how a broken circadian mechanism leads to all codes covered by their protocols.  That includes myocardial infarction, clots, or seizures; which are the most common cause of acute arrest today.  To a decentralized mindset, you might think this omission of the circadian defect should invalidate the stats and protocols they regurgitate until you realize what perspective they play this game with.

For example, historically, a small child has been more likely to choke or ingest a poison than suffer spontaneous heart problems than an older child or adult. The protocols never take new data that the system is built around.  This eliminates new decentralized options and just keeps publishing ideas of treatment that are based on data that may have changed and has not been updated. No updates or changes for first responders are present, except for the new advice of not performing mouth-to-mouth resuscitation on kids. I wonder if we will ever acknowledge the elephant in the room, and change our dataset and actions or if organizations like the AHA, ADA, FDA, CDC, and USDA will continue to feed us garbage into perpetuity.

Why would you expect a centralized healthcare Rx to be set up to work for you based on their perspective on health?   Do you realize who is being harvested and bled dry by these beliefs??  The public is.  If you knew the sun fixes this and drugs induce many more problems than they solve you’d realize you really do not need most of what centralized healthcare sells you.

How does a centralized healthcare system operate?  Is it for your benefit or theirs?  In most cases, protocols are set up for the chronic profiteering of the system.

Centralized healthcare remains fully ignorant about how light operates in our bodies by design. The people who profit make the curriculum that the experts are forced to learn from organizations like the AHA, ADA, FDA, CDC, and USD so they can sell products, drugs, foods, and suncream to you because their advice is given to you when you visit the centralized system for advice. It is a giant financial feedback loop and you are the patsy. The decentralized healthcare system warns you with data (adenosine a drug in ACLS can be replaced by the red light of the sun to get the same effect for the heart)  that if you avoid the sun and wear suncreams the guys selling as the centralized solutions (Pharma/food/AHA/CDC/FDA facade) their profits rise while your health risks multiply over time. As the risks rise they are ready to wallet biopsy you as an inpatient next. The centralized circle of life explained.

I’m shocked you’re shocked.

IS THIS ALL HYPERBOLIC TALK?

Does centralized medicine have direct evidence that is visual that we are built entirely from many decentralized networks?

What can lightning strikes of living systems teach us about life?

Lichtenberg figures are reddish, fern-like patterns that appear on the skin when a patient is struck by lightning. These appear to be a result of an inflammatory response to the electric voltage as the current spreads out causing ionization and heat effects and damage to the small subcutaneous capillaries.

It tells us more about us and less about light. We are photoelectric beings and the marks on us outline many of the decentralized networks operating inside our cells. https://www.frontiersin.org/articles/10.3389/fmed.2021.663807/full

SUMMARY

The fastest way to make Lichtenstein’s marks vanish is to add red light back to the system.  It sounds a lot like how we make SVT vanish from heart rhythms, doesn’t it?  This makes electrical sense when you understand what these ferning patterns are on the skin.  They are a sign of an electrical discharge in the body that has lost an acute amount of redox power.  Red light is the easiest way to recharge the body quickly so its addition to the skin will make the repair happen more rapidly.

As cite one below shows us, the new mRNA \/’s can cause sudden cardiac arrest and we had visual evidence of that recently in an NFL game.  Many of you will read this and not believe it.  I want to remind the skeptics of this reality that also occurred this year in NFL circles.  Remember when JJ Watt had to have his SVT treated after he was injected with mRNA technology?  What did they do to treat him?

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They had to emergently shock his heart back into a sinus rhythm because the drugs they gave did not work.  This is really bad news for anyone who took the government mandate seriously and complied with it.   Do you think this might have anything to do with why he is retiring from the NFL now a few weeks later?  I think Demar Hamlin’s acute cardiac arrest on MNF in front of the US public is going to become a commonplace post-vaccine mandate.  JJ Watt’s case tells us that you do not need trauma to induce an arrest.  A bad rhythm may come first before the arrest occurs.

Might the same prescription of using light to combat disease be important in helping someone overcome that centralized healthcare injury?  Does this Tweet video look normal to you?

TWEET

Mitochondriacs know that answer.

Do you?

CITES

https://twitter.com/vascohill/status/1613610308140138496

https://twitter.com/P_McCulloughMD/status/1613685112033394689

https://academic.oup.com/ehjcr/article/5/3/ytab054/6154461

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6520649/

https://nigms.nih.gov/education/fact-sheets/Pages/circadian-rhythms.aspx

https://geardiary.com/2011/06/17/meet-winston-kemp-lightning-strike-survivor-and-lichtenberg-figure-owner/

https://www.cell.com/cell/fulltext/S0092-8674(13)01521-3

CPC #68: WHY IS THE INCIDENCE OF TYPE 1 DIABETICS RISING?

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The incidence of diabetes will rise as people block the sun and introduce alien light to their lives. And this information will be transferred to their offspring via trans-generational epigenetics and we will continue to see the incidence rise of juvenile diabetics.

Many have asked me how I believe this process occurs.
Here is my answer.

The Nobel Prize for physics in 2016 was given for the discovery of topologic insulators (TI’s).

Topological insulators conduct electricity on their surfaces but do not conduct the current deep inside their cores. This limitation allows the cell to control Brownian motion in the cell to maintain the low entropy state.  A low entropy state is critical for wellness.

This helps explain why DNA’s surface is highly coiled and coated with histones, chromatin, and methyl groups when it is kept in its “quiet state” (non-dividing)

It also explains how it can receive photo-electric instructions on its surface and transfer that information through the hydrogen bonding network (proton tunneling causing flickering) that surrounds nucleic acids to run the epigenetic programming it contains deep within. What happens on its surface can awaken the code of life buried deep below its double helix that is filled with fermions = electrons, protons, and maybe neutrinos!

This process is all possible because DNA AMO structure is capable of inducing a change in base pairs by altering the hydrogen bonds on its surface because of how Dirac fermions operate.  What is a Dirac fermion?

In physics, a Dirac fermion is a spin-½ particle. Take a look here to see a video on how I think this happens.  Electrons, neutrinos, and protons have that spin quantity.

https://www.instagram.com/p/CnPiUugho2Z/

Spin is a quantum-mechanical property, akin to the angular momentum of a classical sphere rotating on its axis, except it comes in discrete units of integer or half-integer multiples of ħ. The proton, like the electron and neutron, has a spin of ħ/2, or “spin-1/2”. So do each of its three quarks that make up a proton. With the proton, there is a catch. And that catch is one of the keys to how evolution code is altered.

Summing the spins of the quarks that make up a proton to get the total spin of the proton seems, in principle, straightforward: if two of the quark spins point up, while the other points down, the down spin will cancel one of the ups, and both sides of the equation should be left with an angular momentum of ħ/2.

Except it isn’t that simple. In 1988 the European Muon Collaboration (EMC) at CERN shocked the physics community by announcing that the sum of the spins of the three quarks that make up the proton is much less than the spin of the proton itself. This was unexpected because the summing-up approach had worked for several of the proton’s other properties. For example, the proton’s electric charge of +1 can be accounted for by adding the charge of its two “up” flavored quarks (+2/3) to that of its one “down” quark (–1/3).  (Note that here, “up” and “down” are names of quarks and have nothing to do with spin.)

However, the EMC researchers discovered that the net spin of the three quarks actually accounted for no more than 24% of the proton’s spin, and might even contribute as little as 4% – practically none of it, in other words.

It was an observation that shocked the world.  To me, it meant Nature was using spin as some coding mechanism in cells.  This unique feature would make it ideal to create a code.  Today I think The proton spin problem is evolution’s cosmic wand……

HOW DOES LIFE COMMUNICATE WITH THE COSMOS?  “THE FERMIONIC CODE”

In condensed matter physics, low-energy excitations in graphene and topological insulators, among others, are fermionic quasiparticles described by a pseudo-relativistic Dirac equation. I think DNA acts like a fermionic quasiparticle. Fermions include all quarks and leptons and all composite particles made of an odd number of these.

Some fermions are elementary particles (such as electrons), and some are composite particles(such as protons). I think this is why mitochondria only deal with electrons and protons inside of them. I also believe this is why neutrinos might be a player in biology on Earth.  Neutrinos are part of the fermion family of Nature. I think fermions and light interactions are how starlight is transmitted to living cells. This science is based on AMO physics as a discipline.

The Standard Model recognizes two types of elementary fermions: quarks and leptons. In all, the model distinguishes 24 different fermions.

There are six quarks (up, down, strange, charm, bottom, and top), and six leptons (electron, electron neutrino, muon, muon neutrino, tauon, and tauon neutrino), along with the corresponding antiparticle of each of these.  Protons are made from quarks.

HOW DID I DECODE THE FERMION MESSAGE?

Claude Shannon taught the world that information flows via entropy. All clocks should be thought of as flowmeters for entry. This includes the biological circadian clocks in cells. Wheeler taught physics that information and energy are one and the same thing. Shannon’s mathematics from his 1948 paper advanced the linkage of entropy and information. Shannon’s paper also told us anything can be a message.

I believe sunlight messages for mitochondrial DNA and nuclear are controlled by “fermion messaging”. DNA is informed about what to do with optical information from the sun via mtDNA signaling (optical and free radical) and this message is transmitted over water’s hydrogen bonds adjacent to proteins in a cell. DNA is a very complex topologic insulator that is an antenna for our star’s information.

Unlike its much larger counterparts, which we’re all familiar with in modern devices, this minuscule genetic molecule (DNA) isn’t made to transmit radio waves, but to glean the secrets of ever-changing proteins.  DNA is around 20,000 times smaller than human hair. It also emits all frequencies of light in the visible spectrum of terrestrial sunlight, which means it uses light signals to record and reports back information.

And those light signals can be used to study the movement and change of proteins in real-time.

Part of the innovation with this particular antenna is the way in which the receiver part of it is also used to sense the molecular surface of the protein it’s studying. That results in a distinct signal when the protein is fulfilling its biological function.  It also means the signal is low fidelity when the protein is not functioning well.  When this happens the cell emits another optical signal and marks the defective protein for removal with ubiquitin.

This system operates just like a two-way radio that can both receive and transmit radio waves, the DNA nanoantenna receives light in one color (frequency), or wavelength, and depending on the protein movement it senses, then transmits light back in another color, which the cell can detect and perform a physiologic function.  (Cite 2 below)

DNA chemistry is relatively simple to program and easy to use once programmed.  DNA is surrounded by water.

Water makes up 99% of molecules in every cell. Water is a very small molecule that has more hydrogen bonds in it than any other compound. Liquid water contains the densest hydrogen bonding of any solvent, with almost as many hydrogen bonds as there are covalent bonds and hydrogen bonds in its structure found anywhere on Earth. These two bonding networks are the binary code in water. Just as a computer can use a 1 and 0 to create digital information on the internet, hydrogen bonds create the internet in your cells. Shannon taught us the information content of any kind of message could be measured in binary digits or just bits.

Water’s hydrogen bond network changes at a pico and femtosecond level in any environment. Inside a cell, its atomic arrangement is controlled by electrostatic forces in a cell created by the redox power of the mitochondria in that cell. These hydrogen bonds can rapidly rearrange in response to, light frequencies, charge density, and changing conditions and environments (for example, solutes like K+ in a cell).

Shannon demonstrated, contrary to what was commonly believed in the 1940s, that engineers could beat their worst enemy ever: transmission errors-or in their technical jargon, “noise.” Noise is anything that disturbs communication. It can be an electric signal in a telephone wire that causes crosstalk in an adjacent wire, a thunderstorm static that perturbs TV signals distorting the image on the screen, or a failure in network noise to increase the energy of the transmission signals or send the same message repeatedly-much as when, in a crowded pub, you have to shout for a beer several times. Shannon showed a better way to avoid errors without wasting so much energy and time: coding. Nature does the same thing.

She takes the message in the hydrogen bonding network of water that surrounds every protein and encodes that information in “a fermionic code” in mRNA, mtDNA, RNA, tRNA, and DNA.

Coding is at the heart of information theory. All communication processes need some sort of coding to limit the noise and create a high-fidelity signal that doesn’t degrade. Water preserves the information and transfers it to nucleic acids via hydrogen bonds. Just as the telephone system transforms the spoken voice into electrical signals. In Morse code, letters are transmitted with combinations of dots and dashes. The DNA molecule specifies a protein’s structure with four types of genetic bases. Digital communication systems use bits to represent or encoded information. Each letter of the alphabet, for example, can be represented with a group of bits, a sequence of zeroes, and ones. You can assign any number of bits to each letter and arrange the bits in any way you want. In other words, you can create as many codes as desired. Cells have done this to run life’s program.

The interactions of electrons in a solid or liquid crystal change space in abstract ways. If you look at the picture below you can see odd shape and size changes and this leads to the different thermodynamics of what is possible on the surface. Many TI’s developed “holes” where electrons are absent and this allows them to act as P-type semiconductors then there are adjacent regions that are extremely electron rich that can act as an N-type semiconductor.

Those positive and negative regions can act like “charges” and can lead to striking effects. For example, an insulating material (phosphorus) can become conductive at its surface when light hits it.  All semiconductors become conductive when light hits their surface.

Phosphorus has ten atoms that stick directly out from the surface of DNA when you look at it from an axial view. See figure C below. Those ten atoms are surrounded by 447 water molecules to form part of the TI in DNA. The addition of phosphorus and iodine in the liquid crystalline water networks creates a “playground of charges and spins” in fermions to control how DNA should react to the electromagnetic signal from our star on its surface.

Note the ten phosphate groups sticking out of the surface of DNA to bind with coherent domains in water as DNA unwinds above.

Within the heavily condensed and coiled state DNA structure tightly holds atoms (lowering entropy), electrons, and photons in one “spin state”. When DNA is uncoiled by electromagnetic signals from our mitochondria hit on DNA’s surface.  This surface change can alter protons deep inside of DNA to change how it functions.  Hydrogen bonds occur between the two strands and involve a base from one strand with a base from the second in complementary pairing.

Once this change occurs light is/can be liberated from the double helix and the surface template of hydrogen bonds in water surrounding DNA radically changes the “topologic signals” by the altered spin states of fermions (protons) in the DNA crystal. This can turn on and off DNA replications. It can also cause DNA base changes.

In their seminal paper from 1953, Watson and Crick proposed that the tautomerization of DNA base pairs could produce stable errors in the genetic code. The proposed mechanism for such tautomerization was the double proton transfer along the hydrogen bonds within base pairs, Guanine–Cytosine (G–C) or Adenine–Thymine (A–T).

The tautomerization process involves the relocation of protons, which are subatomic particles and obey the laws of quantum mechanics.

Tautomers are structural isomers (constitutional isomers) of chemical compounds that readily interconvert. The chemical reaction interconverting the two is called tautomerization. This conversion commonly results from the relocation of a hydrogen atom (proton) within the compound.

The spins of electrons/protons (H+) can not only be manipulated by magnetic fields (mitochondria) but also by electrical fields (proteins side chains) and can be used to collect and store information from electrons or the photons they carry. All magnetic drives use spintronics today to magnetically store data on hard drives. It appears DNA uses many of the same ideas but it does it on hydrated carbon-based semiconductors in cells.

SUMMARY

We already know a leaf can do it via photosynthesis and so can a European Robin using a light inclination magnetic compass in its eye. In my humble opinion, this process works in all animal tissues to create the many species of animals we all observe in the classical world we inhabit.

Why don’t we have more data on this mode of information transfer in cells?

Specifically, the job of the antenna is to measure the structural changes in proteins over time. Proteins are large, complex molecules that carry out all kinds of essential tasks in the body, from supporting the immune system to regulating the function of organs.

However, as proteins rush about doing their jobs in cells, they undergo constant changes in their structure (protein bending), transitioning from state to state in a highly complex process scientists call protein dynamics. And we don’t really have good tools to track these protein dynamics in action today.

Experimental study of protein transient states remains a major challenge because high-structural-resolution techniques, including nuclear magnetic resonance and X-ray crystallography, often cannot be directly applied to study short-lived protein states.  I expect this to change as centralized healthcare realizes these tools will make Big Pharma superfluous to the public.

Topology is a branch of mathematics focused on the fundamental shapes of things as they change. In cells, proteins can vary their size and shape based on the light energy that is added or subtracted from their bonds.

In this way, life can be considered a quantum computer that is working in parallel with a quantum universe that also runs on light. The fermionic messages are information buried in terrestrial solar light wave frequencies in the sun that can be magnetically stored in a thin film of water surrounding nucleic acids, using non-linear aspects of light. DNA is the ultimate topologic insulator or superconductor suspended in a superfluid of coherent and noncoherent water that imprints information and conducts electrons, protons, and photons in different ways.

This Nobel Prize may soon get biology away from its “solution-based ideas” in biochemistry books and push them toward quantum biology which uses a solid-state foundation. That is what the Nobel Prize meant to me in 2016. The state of fluctuation of the hydrogen bonding network that light brings creates probabilities in a cell. Light adds charge density to the AMO structures in a cell.

PHYSICS IS THE SCIENCE OF PROBABILITIES. BIOLOGY IS THE STORY OF THE IMPROBABLE AND BIOLOGY CAN ONLY MAKE SENSE FROM THE PERSPECTIVE THAT THE LIVING STATE IS ONLY PROBABLE ON EARTH USING REACTIONS UNDER SUNLIGHT WHICH ARE STATISTICALLY IMPROBABLE anywhere but on Earth.

Knowing is just not enough. Understanding the connections is critical in understanding what life is doing below the cell level. Stop being your own worse enemy. Stop looking outside for solutions when the wisdom you seek is buried within you in how you organize matter in your cells with sunlight.

This is why diabetes is exploding globally in the modern world in my opinion.

CITES

1.  https://pubmed.ncbi.nlm.nih.gov/33949935/

2. https://www.nature.com/articles/s41592-021-01355-5

3. https://pubmed.ncbi.nlm.nih.gov/21457072/

4. https://pubmed.ncbi.nlm.nih.gov/35949615/

5. Watson, J. D. & Crick, F. H. C. The structure of DNA. Cold Spring Harbor Symp. Quant. Biol.18, 123–131 (1953).

6. https://www.nature.com/articles/s42005-022-00881-8

7. Löwdin, P.-O. Proton tunneling in DNA and its biological implications. Rev. Mod. Phys. 35, 724–732 (1963).

8. Löwdin, P.-O. Quantum genetics and the aperiodic solid. In Advances in Quantum Chemistry(ed. Löwdin, P.-O.) Vol. 2 (Academic Press, 1966).

9. Slocombe, L., Al-Khalili, J. & Sacchi, M. Quantum and classical effects in DNA point mutations: Watson–Crick tautomerism in at and GC base pairs. Phys. Chem. Chem. Phys. 23, 4141–4150 (2021).

10. https://www.mdpi.com/2624-960X/3/1/6

BECOMING A DECENTRALIZED HEALTHCARE PROFESSIONAL?

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How many doctors and nurses feel like the dog in the video above???

How can a video of a caged animal help a human healthcare worker?

How will they learn to extricate themselves from their cage……how do they deal with the learned helplessness from their education?  What do I mean?

I realized 20 years ago, like a 40-year-old centralized neurosurgeon I was back in the same predicament as this dog below was.  My brain and mind were no longer my own.  They were tethered to a centralized medical mindset given to me by my education.

This educational paradigm was my cage.

The dog below fought like hell to get out.  I had to fight like hell to become decentralized.  Have you tried to unlearn to relearn?

Back then I was intellectually impoverished, unable to cure myself, so how I could really help anyone else if I kept doing the same things over and over?  I knew I had to think differently.

The dog was wiser than I was.

This is when I first began to think about building a virtual private practice and hospital.  It has now morphed into what I hope the Kruse Longevity Center to be in El Salvador.

Medicine has kept me tethered to a life that was harming me and my family.  I did not see it.  I never realized how being up all night on call every third night for 25 years was harming me.

Like the caged dog, when the tether was bent and opened initially, we often don’t realize that we have the opportunity to roam free from our self-created prison.  The dog seemed to know it right away.  Why don’t we?

Was this learned helplessness built into me by design in how I was taught to think by my education?  Medicine allowed me to escape being a poor kid in NYC, but it allowed me to build a new prison with more money, but less time and time had to be spent awake at night under fake light 24/7.  I realized slowly 15 years ago I had traded one prison for another.  It turned out the second prison was far more dangerous than the one I escaped as a kid when I thought about it.

Medicine was tethering my reality because my ability to think was usurped by an Oath I took.   My oath and education were tethering me to ideas that were no longer useful to me or my patients.  I began to feel what I believe the dog in the video is feeling.  This was learned helplessness now becoming angry and determined.  Initially, it was depressing,  and it lead me to become angry.  I became so pissed off I planned my escape.  The dog did the same thing.

Like the dog who trusts his master, a master who locked him up, he did nothing but accept his fate initially.  Initially, I did nothing to try to break free on my own either.  I hate the idea that, as an educated medicine man, felt I had to blame somebody for this educational disadvantage.  It never occurred to me I was my own worse enemy until much later in my professional life.

I hated the notion that I, a modern doctor, lacked the ability or means to take control of my own destiny.  This is why when I see a caged animal video, I remember this lesson.  When I woke, I ripped the tether from my life as the dog did below.  I realized quickly I was fully able to step outside the downward spiral I was in. I realized I could fly again if I took control and became the CEO of my career.  Even today I often think of those many animals who are caged and how their perspective shaped their future life as slaves to a paradigm.

I wonder if centralized doctors and nurses realize how their job traps them.

I wonder if their patients understand how it affects their care.

I wonder if centralized healthcare workers understand why so much junk science is published these days.

The answer is simple:  There is no cost to being wrong in modern centralized science, but there is a huge cost to not publishing if you are part of the centralized paradigm.

What lesson have I learned about my profession in 2020-2022?  The COVID experience has taught me that there is an inverse relationship between education and common sense. The higher you go in academia the less common sense can be found.  This is why the PEER-reviewed literature is littered with junk science.  

The American dream is alive and well in centralized healthcare. The hustle is sold separately to patients individually in a package called “evidence-based medicine”. Corporations force mandates down our throats that the government cannot do due to illegality. And it’s funded by the guys making money on both sides of the equation.

Science must always be “pressure tested” to distill the truth. That’s the only way forward.  Science isn’t ‘what experts think.’ It’s a method that corrects what experts think.  In 2021, Fauci claimed he was science.  In 2022, the scientific method has removed him from power.

I believe you will learn why alternative therapies and natural immunity were removed from the lexicon of medical science by bureaucrats in 2021-22.  The jabs cost them a lot of money to develop and they needed to protect themselves from legal challenges to the EUAs if any alternative therapy worked because this would have made their EUAs ILLEGAL.

A curious principle of epidemiology, which only the public seems to get and the elites act like it is a conspiracy theory is what happens if you give drugs that work too late in the course of a disease?

What we found out in 2022 is that ‘scientific authorities’ just published assumptive baloney which conformed to a narrative that suited the centralized elite and their paradigms, with no medical evidence behind it whatsoever……Then why would any sane person contend, ‘Trust the Science’?

If you don’t treat someone, until they are almost dead – your treatments aren’t going to appear very effective when the studies are published.  This is how the methodology can be used to skew the truth.  This creates an opportunity for the political ruling class.  Then you can use that data, to cite that treatments are ineffective – so there are none.  This can be used to create legal means to create a solution via a patent that has legal protection.  This is how the EUA idea was born by Big Pharma during Operation Warp Speed.  This is why Hydroxychloroquine and Ivermectin were vilified in 2021.

In fact, I will take this idea further.  I now believe they all believe that natural immunity is viewed as an illegal theft of pharmaceutical intellectual property by people in power.  They believe COVID was a flu that accidentally blew into your lungs or gut.  Your immune system then attempted to usurp Big Pharma IP.  Your thieving-ass immune system was and remains their real enemy. That is how centralized healthcare operates now.  This is how centralized medical systems think. It is also what the people who sit next to its money printer think. This is how the Cantillon effect operates in medicine now.  This is why most physicians follow the mandates of those who pay their salaries.  It is also why hospitals now employ most physicians.  It is done by design to gain control and compliance to their beliefs.  Physicians no longer work for themselves.  They work for centralized healthcare systems.  If you take money blowing downwind of a bank robbery, you’ll see another centralized system that will force you to pay it back.

The moment you allow the government to break the law for an emergency, you will live in a daisy chain of emergency from that day forward.  That is centralized healthcare in a nutshell.  

Any power taken by the government without constraint leads to abuse. Remember when ‘two more weeks’ and ‘flatten the curve’ was a thing?

It was only 50 political narrative shifts ago.

COVID was a crisis ( a compliance test) that was used to make way for the most extreme and widespread suspension of constitutional freedoms in American history, despite being based on myths and lies.  The goal of these maneuvers was to replace the US constitution with the UN Charter.  This would remove your inalienable rights and put the government’s interest in front of your own.  That is why the global elites have infiltrated political cabinets all over the world and that includes the USA.  It is what they have been doing since World War 2.

SUMMARY

From the beginning of the Coronavirus crisis, the media and politicians engaged in myths, half-truths, and even flat-out lies to bring about obedience from the populace.

COVID was built as a crisis by politicians to create a cultural war to divide us so they could conquer us.  It allowed a deep dive into how those in power used the emergency to consolidate power and change the very concept of American freedoms. The government, media, advertisers, and scientists all sought to set an agenda to strip Americans of their rights. From church attendance to running a business, right down to how many people can be in a private home, few rights were left wholly unchecked. What’s worse is that any challenge to the holy laws of lockdowns was criticized and censored as dangerous and deadly speech. The question that remains is whether Americans will ever allow centralized systems to destroy their lives again.

QUANTUM ENGINEERING #24: CENTRALIZED HEALTHCARE FAILINGS

When you see all the data flowing in regarding “Died Suddenly”….do you ask yourself if maybe   Common sense died suddenly first….  or   Critical thinking died suddenly…..after being injected by propaganda?

The centralized paradigm thinks biology is driven by a DNA paradigm.  Decentralized medicine is driven by the other genome, the mitochondrial genome that responds to the thermodynamic situation of the environment.

I have chosen the team I play on.  It is up to you to decided your team.

DUE DILIGENCE OF YOUR CHOICE

Modern epidemics are not caused by genetics, but by epigenetics!

This is also a clinical medical fact that gets lost in the modern scientific literature but you would never get that from reading the literature on diabetes or any other neolithic disease. In fact the totality of the diabetes literature would have you believe the exact opposite. This is a centralized neolithic thought that has harmed all modern diabetics and is at the seat of why modern medicine has failed to find a cure.

Mother Nature has a cure for insulin resistance in all eutherian mammals. That answer is thermodynamic.  It is mitochondrial based and has nothing to do with defective RNA/DNA.  Your choice need to change so that they marry strong solar power with night time cooling by avoiding all heating and lighting at dark.  Nature & decentralized medicine is non negiotiable with this prescription.

That is cold exposure of there peripheral nervous systems, is critical in informing the brain what probabilities should happen at night.  Artificial light at night changes the probabilities when a human makes the wrong choice.

The stimulus to this pathway begins when the mammal is exposed to a high dietary carbohydrate diet that is found in long light cycles on this planet.  It is magnified at higher latitudes.  It is minimized at the equator.  The truth is found in mitochondria haplotypes. The electromagnetic signal of Earth informs the cell that the membranes need to adapt to cooler temperatures.  This is why certain haplotypes exist in different latitudes.

This is how the gut senses the environment and this signals are transmitted to the brain via the vagus nerve. Centralized healthcare & modern biochemistry books and biochemists stop here at this level of understanding.  YOU MUST GO FURTHER.

Their beliefs are built by what THEY believe they know about energy transformation in cells. But I always focus in on what they have failed to realize.

When dietary carbohydrates are high it stimulates the eutherian mammal to begin to upregulate omega 6 content into every cell membrane of their body slowly through the autumn while temperature falls. It speeds up as the temperature drops in winter. This process is completely independent of dietary sources as I laid out in the Cold Thermogenesis #3 blog.

Why does this occur in all mammals?

People forget that lipid membranes are objects in cells that are very sensitive to electromagnetic signals.  The proof is found in how membranes are built and vary via temperature variation. For example, in mammalian cells, the plasma membrane cytoplasmic leaflet usually contains more phosphatidylethanolamine (PE) and phosphatidylserine (PS) when compared with the outer leaflet rich in sphingolipids.  There is an electromagnetic reason for this.  The phosphate groups in membrane phospholipids bind strongly to water because they are hydrogen (proton acceptors).  This singular fact suggests that light signals activate the membranes.  The membrane alters the hydration and dehydration of proteins and metabolites and in turn are critically important in activation control and deactivation of all the biochemical pathways in cells.  These are choices made by light and temperature variation.  That is why crcadian biology is the key to recapturing your health.

Maintenance of membrane fluidity by DHA incorporation, despite the presence of saturated lipids, is sustained by integrated sterols that interfere with acyl chain packing.  This mixture changes its electrical conductance and impedience.  Membranes vary the reactivity to light.  It is like cells can change the semiconductors they use as seasons change.  Those changes are signaled to water below the cell level. Conversely, because sterols themselves are inflexible they can increase membrane rigidity if associated with flexible unsaturated lipid bilayer. It is worth noting that cholesterol deposition can similarly be asymmetrical and differs greatly among organelles and in tissues in mammals.  Mammals are highly adaptable to environmental variation.

Because to cell membranes to function in cold weather it requires all land based mammals from cold adapted ancestors to have an EFA ratio of 4:1 for optimal signaling. In water based mammals who are cold adapted, like whales, walrus, and seals, humans they face steeper temperature gradients in the water that require a much lower EFA ratio (essential fatty acids) in their cell membranes to function properly.  Water transmits heat changes 24 times faster than air does.  This is why temperature variation matters in decentralized prescriptions of disease reversal.  To see this effect look at what heavy use of the AC power grid did in Spain to annual birth rhythms of humans.  Does this look like the scientific reason of what happened in John Calhoun’s Universe 25 experiments done in labs over and over again?

This lowered ratio of EFAs also changes the biology of adipocyte biochemistry below the skin level where light enters the body. It favors the accumulation of surface fat but not of visceral fat. Visceral fat is used to burn first to maintain core temperature in these animals. In land based cold adapted mammals like the polar bear the same is true. When they emerge from their den in spring they are shredded of all visceral fat and no longer insulin resistant, and have the biggest and strongest muscles they will have all year. Their body composition is at its best at this time. They accomplish all this without needing any exercise to do it.  Do polar bears or any other animal but humans have indoor lit gyms?

This is in counter distinction to modern man beliefs. Why is this? The question is more complicated than the answer, but the answer is again, simple.  It is simple because it is based in decentralized wisdom.  Light and dark control the circadian mechanism.

Modern man is further down the evolutionary path because its optical lattice clock in the eye is best atomic clock on the planet.  Everything should be thought of clock.  Humans have the most accurate timepiece of any mammal on Earth.  But its accuracy is ruined when its periodicity of light and dark is disrupted.  Better clocks mean it can support a faster evolution.  Fast evolution has another name.  It is called epigenetics.  In offspring it is called transgenerational epigenetics.

This implies in mammals, after the KT event, evolutionary development was the product of a sped up epigenetic process. Photosynthesis was disrupted.  The next generation of mammals had to quickly adapt so they could navigate this changing environment.  Life faced this before at the Cambrian explosion as I showed in my Vermont 2019 talk.  The sun changed 650 million years ago before complex life forms showed up on Earth.  Light sculpts all life.  It is not arguable any longer.

The rapid changes in the environment had to be transmited to the next generation to guarrantee survival.  The reason was due to massive environmental changes that occured due to the dsruption of photosynthesis of the KT event.

The KT event subtracted UV light from the thermodynamics of life.

This made the environment colder at most latitudes for many years after the event.  In essence, the electromagnetic response of complex cells to an extinction level event was to speed up epigenetics over time.  This wass a complex thermodynamic response to a lack of sunlight.  This negative, set the tone for future human evolution.  These environmental actions 65 million years ago allowed for the human brain to develop faster 2.5 million years ago because cellular machinery us were adapted in our epigenetic tool box to build a more complex body plan when the sun returned for mammals.  It advanced epigenetic evolution because he sun returned with photosynthesis yield post KT event.

With photosynthesis back our diet once again became an electromagnetic bar code for latitude and tectonic plate motions.  The return of UV light gave us a new way to deplete deuterium further because of the epigenetic changes that caused our mammalian mitochondria to become efficient at depleting it from foods.  UV light is critical in depleting deuterium in mammalian cells.  Look at the absorption spectra of proteins compared to the electromagnetic spectrum of light.

This allowed our cell membranes to signal both electric and magnetic field strength to the interior of cells where our mitochondrial reside.  As a result, our diet radical changed again from our immediate ancestors, the chimpanzee.

This ability caused two simultaneous evolutionary adaptations to occur simultaneously. As our brain expanded, our guts shrunk in length. We only needed a smaller gut when we become adapted to eat predominantly fat and protein from marine animals.  This diet built a faster clock because of the effect of DHA on the central retinal pathways.  This made our eye clock wildly sensitive to changes in environmental light.  This was a benefit that drove hominid evolution but now it has become our major weakness as a species.

Man made light destroys mitochondrial redox by lowering cell voltages on the inner mitochondrial membrane.

After the KT event, our SCN became a better optical lattice clock with the return of full powered terrestrial sunlight.   A diet high in fat and protein was also used to fuel encephalization of hominids. DHA in the marine chain was critical in this change.  Larger brains meant we needed pelvic changes to become bipedal and it also extinguished the need to hibernate. Hibernation needs were shrunk from seasonal changes into our sleep cycle during stage 3 and 4 sleep. As we became smarter (DHA infusions in eye and frontal lobes) we became able to not only react better to electromagnetic signals in our environment, but we became able to control our environment. We changed light in our environment because of how our brain adapted.  This is how a sped up epigenetic plan set up modern man to become more susceptible to many biochemical mismatches.

SUMMARY

When our recent ancestors lost the ability to hibernate, they also lost their best way to fight insulin resistance. Since those ancestor mammals ate carbohydrates in a proper circadian cycles, purely controlled by their seasonal growth, the biochemical systems in those mammals readily adapted to these new states without much problem. This biologic adaptation required alteration of the leptin receptor to function with higher levels of cytokines present. It appears natural selection also made adjustments to liver biochemistry and bioenergergenics to mirror those changes made in the brain.

Every eutherian mammal born on this planet up until 2.5 million years ago had to live by the dictums of their environment. When hominids evolved, much later, this environmental situation radically was altered. Hominids remain the only mammal on the planet who can 100% control its own environment. This allows our species to create mismatches at even a  great speed, as our brain continued to develop over the last 2.5 million years. This trend dramatically speeds up all our chemical clocks in every cell of our body that is controlled by circadian biology. This is well known by modern science, but its implications are IGNORED.

The Nobel Prize of 2009 tied this all to telomere lengths in our cells. The 2017 Nobel was given for circadian biology.  It is time you all pressure centralized healthcare to begin working for you and how biology works and stop supporting centralized healthcare that works for Big Pharma and Big Food.

All mammals have circadian signaling hardware in their brains that wire directly to the cell cycle machinery in every single cell of their bodies. This means that modern hominids are the most sensitive mammal to any circadian mismatch compared to their ancestors. Moreover, since they have the most advanced brain in the mammalian family, they are subjected to the greatest risk of neolithic diseases due to these mismatches. Humans get diseases that no other wild animal gets for this reason. Humans get autoimmune disease when our most recent ancestors, the chimp can not. They do not have zonulin and we do. This is one of the most fundamental reasons why our guts are adapted to different diets that lead to our encephalization. Animals domesticated by humans suffer the same fates as we do, ironically. Wild mammals tend not to get these issues because they live by the rule that Mother Nature determines for them in their own selected environments.

The ultimate paradox of modern hominids is that they evolved the ability to live on a warm adapted diet and in a warm environment, but that they retain the cold adapted biochemistry buried in their brains even though they do not need to use it presently. Evolution has not extinguished this ability for a very good reason, in my view. Mammals survived an extinction event because of it.  One reason is that the geologic record shows that our planet undergoes cyclic cooling and warming over longer epochs. This will keep the pathway active epigenetically over thousands of years.

The main reason it has not been extinguished in my opinion, is that this ancient pathway determines ultimate survival of the mammalian species and it was vital at one time in evolutionary history. Modern hominids have an advanced nervous system, but they still are tied to the evolutionary family they came from long ago. They are not divorced from the rules of Mother Nature even though they act as if they are. This ties modern humans directly back to Factor X at the KT event. The paradox of this situation is that they remain blind to it even today.

CITES

1.  https://pubmed.ncbi.nlm.nih.gov/12562849/

2. From the file of they are waking up to my perspective:  Circadian disruption and human health: A bidirectional relationship – Abbott – – European Journal of Neuroscience – Wiley Online Library.  https://onlinelibrary.wiley.com/doi/10.1111/ejn.14298

Listening well is often the only thing needed to really help someone. No one is as deaf as the centralized man who will not listen.  You earn the right to be heard by listening to others first.  Do it carefully to understand how they think before you respond. Most folks do not listen with the intent to understand; they listen with the intent to reply.  Seek to understand a situation before judging its faults or merits.  Listen to your elder’s advice carefully. The wise do this not because they are always correct about things, but because they have more experience of being wrong.  The smartest among us always learn to avoid the pitfalls of life with via the experience of others who made the errors.  Our mode of thinking sculpts our perspective. We only see what we think about because it forms how we choose to see the world.  This is why listening is a tool of the wise.  You can dissect anyone or thing when you learn how to listen to how someone thinks.

QUANTUM ENGINEERING #23: CIRCADIAN CLOCK MANAGEMENT

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Good circadian clock management creates lives with less volume creation and more storage at night for urine. Nature seems to want diurnal mammals to drink water prior to sleep.  The system is built for this type of behavior.  All neurons move and release water when neurons fire action potentials. Thirst is controlled by posterior pituitary vasopressin.  Vasopressin is directly acted upon by light coming in through the central retinal pathways to affect the posterior pituitary.  The posterior pituitary output affects the immune system’s ability to function.  The nervous and immune systems are engaged in bidirectional communication as the picture shows.  Vasopressin is a big part of this blueprint.

I believe all autoimmune diseases are related to the disruption of the bi-directional reflex loops you see in the pictures above.  I believe the damage begins with light we are not built for.

T-Cells are the key player in autoimmune conditions. We’ve known this since 2003. In 2016 we found out how blue light causes T-cell motility. We now have all the pieces to explain the basic mechanism of all autoimmune diseases and why it is linked to the blue hazard.  HYPERLINK

Autoreactive T lymphocytes are key players in autoimmune diseases. They can act both as regulatory and effector cells. Various animal models have been used in the literature to show that the transfer of autoreactive T cells is sufficient to induce a model of an autoimmune disease. Thus, the pathogenic importance of autoreactive T cells has been formally demonstrated in animals. This should inform centralized healthcare that autoimmunity is tied to our light choices but patients never get told this.

Robert O. Becker taught us that injured tissue elicited an electromagnetic signal to begin wound repair. He found that an electrostatic field, negative away from the limb stump, could enable the regeneration of a frog limb.  Becker ascribed regeneration capability to the existence of a nucleus in the salamander’s erythrocyte. (The mature erythrocytes of frogs and higher animals lacked a nucleus.) Erythrocytes with nuclei seemed to have the dedifferentiation capability required for later differentiating into the various cell types needed in the growth area. Becker described these studies in his 1985 book The Body Electric, and also (condensed and compared with other fields) in the first part of his 1990 book Cross Currents.

The video above also shows this effect in the animal modeling of human cell injury in trauma.

Vasopressin (AVP) is released after every type of brain injury.  All injuries cause an electromagnetic stimulus to direct repair, as Becker found in his work.  This tells us vasopressin responds to electromagnetic stimuli even outside its normal circadian cycle.  Non-terrestrial forms of light is a light stress.  It is a form of traumatic brain injury.  Light injuries have become the most common non-military injury humans get in the modern world in their neurons.

Normally vasopressin is released at night when light is not present.  Artificial light post-sunset causes massive early chronic release of vasopressin.  Screen time during the day exacerbates this.  I believe that this is critical in the development of diseases like Multiple Sclerosis.  Research has shown that people with MS respond to vasopressin antagonist drugs to heal their myelin deficits.  This tells clinicians that the chronic release of vasopressin to light stress is the key problem in this immune-mediated disease.

https://twitter.com/DrJackKruse/status/1609921221017190407

Is Nature’s clue found in vasopressin molecular structure?  They are.  Vasopressin is a posterior pituitary hormone which means it has a direct connection to the retina and the SCN.  It also is directly related to the neuroimmune system.  It tells us sunlight is the electromagnetic stimulus that vasopressin reacts to.  Vasopressin is made in an area with no blood-brain barrier telling us that it is open to the environment’s electromagnetic signal.  Vasopressin is made of 9 amino acids.  The amino acid sequence of arginine vasopressin (argipressin) is Cys-Tyr-Phe-Gln-Asn-Cys-Pro-Arg-Gly-NH2, with the cysteine residues forming a disulfide bond and the C-terminus of the sequence converted to a primary amide. It has two clues it is a circadian qubit.  It contains two aromatic amino acids and it has a disulfide bond linked to its cysteine residue (re-read the orexin blog to understand the importance).

Mother Nature seems to want enough water in the system for the neurons in our brain to be able to anticipate it can follow the circadian rhythm of CSF production for the brain’s glymphatic system, and that there will be enough to not compromise autophagy.

One of his key goals is to design a sensitive vasopressin test for healthcare workers to use for people with circadian arrhythmia in the Emergency Room. If levels could be assessed rapidly, it could help physicians to understand how the body is managing water, giving clues as to how to deal with various illnesses with blue light and nnEMF exposures.  In experimental models of cardiac arrest, vasopressin increases blood flow to the heart and brain and improves long-term survival.  But vasopressin release in excess seems to be one of the things that cause chronic injury to myelin in Multiple sclerosis.  This is why Big Pharma is developing vasopressin antagonists drugs to treat it.

Why? Our modern lights dehydrate us causing us to age faster and die sooner.  Sunlight hydrates our cells.

Middle-age serum sodium >142 mmol/l is associated with a 39% increased risk of developing chronic diseases  & >144 mmol/l with a 21% elevated risk of premature mortality. People with serum sodium >142 mmol/l had up to 50% higher odds to be older than their chronological age.  High serum Na is a proxy for your Light clock management behavior at the SCN level.

Until recently (2017), it was thought to only work in a classic, negative feedback loop: when we are dehydrated (bad matrix function at CCO), levels of vasopressin rise, which causes urine to become concentrated in the kidneys, freeing up more water to be used in the body.

Conversely, when we have too much water in our body, vasopressin levels decrease, and urine is diluted. What if that is not all that vasopressin does?

Vasopressin changes the possibilities that water presents to the quantum programs that control wound healing by altering charge density in coherent domains of water.  This adaptation is done by altering the epigenetic programs in cells.

Water is the quantum stage cells play on.  Water is created by cytochrome c oxidase in the mitochondria.  The spinning Fo head of the ATPase sits adjacent to the CCO. That spinning Fo head creates a magnetic field at the subatomic level. Inside a cell, water also has a magnetic dipole effect (negative and positive ends) because of the hydrogen and oxygen that make water up.

Hydrogen is positively charged, and oxygen is negatively charged. This creates a bar magnet effect in cells. These physical features are what help water networks respond to electromagnetism and waves of light.  If you look at the vasopressin molecular structure above you’ll notice on one side of the disulfide bond there are a lot more negatively charged oxygen atoms.  This tips the magnetic flux one way to signal wounds should heal using the epigenetic programs mentioned in the video above and found in Becker’s books.

I believe vasopressin is a highly negatively charged protein that is a qubit for the quantum brain that changes epigenetic signaling in tissues.  Vasopressin is how we influence probabilities of future events in water using sunlight as a lever.  

It seems organisms use vasopressin levels to predict and prepare themselves in advance for environmental changes that have selective advantages over those who cannot accommodate themselves until the changes of the environment have taken place to cause dehydration of mitochondria for some reason.  ALAN causes massive dehydration in the mitochondrial matrix.  Doing this long-term will shorten longevity by leading to diseases like MS.

In 2017 the same researchers found vasopressin does a lot more than they thought initially. They found that not only is there a vasopressin circadian feedback loop, but “it’s also involved in feed-forward mechanisms. This is quite important in understanding from a chronobiologic perspective. They determined that this molecule is produced in the brain right before people go to bed WHEN IT IS SUPPOSED TO BE DARK, and during sleep, in anticipation of the dehydrating effect of sleep. During sleep, autophagy is supposed to be very active if you are healthy.  Vasopressin is normally released at 9 PM.  It is designed to offset the dehydrating effect of sleep.  Vasopressin is also known as an anti-diuresis hormone.

I believe vasopressin induces a negative magnetization in water networks.  What is negative magnetization?

When negative charges are added, we can find a temperature-dependent crossover of the DC magnetization from a positive value to a negative value of a material (cooled under a positive applied magnetic field) is termed the magnetization reversal or negative magnetization.  Becker found this flip in the DC magnetic field between sleep and wakefulness and between consciousness and general anesthesia.  Vasopressin helps us sleep when water creation is reduced.

Moreover, when you are recycling mitochondria during autophagy you cannot make any water at CCO. What happens if you cannot make water even in the sunlight because you’ve lost total control of autophagy because of chronic toxic blue light and nnEMF light stress?

The core skill of a successful Mitochondriac is error recovery in Nature, not failure avoidance from prior poor decisions.

There is only one way to repair that well. It means that we need SUNLIGHT IS MANDATORY to make water at CCO during the day. If you do not get enough or live at a high latitude and inside you need more water. If we do not get enough sunlight then we lose circadian feedback control of vasopressin and the entire water cycle in our body.  This is how lousy clock management leads to epigenetic disease by decreasing mitochondrial redox power.  You saw this in the petri dish picture above in the video.  A loss of redox power = disease state or injury state.

So people who are incentivized by selling DDW need to be vetted.  They have not thought this out well from the Black Swan mitochondria perspective.

Our light choices can be seen in our labs if you know what to look for.  Our light environment trumps chronological age as an epigenetic driver.
Frequent shift work results in more urination for ANY AGE because the circadian gene Rev-Erbα controls the production of Cx43, which determines how much urine a bladder holds.

TL;DR: Poor circadian rhythm = More urination = more disease = FASTER DEATH COMES = THE RELATIVITY OF TIME MODELED.

Energy and light frequencies are the only predeterminants nature needs to change water’s behavior in your cells. 

As the environment’s frequencies and power density change so do the reaction of water in you. When you begin to realize how sunlight changes in different latitudes on Earth and in different cities because of 1G-5G footprints it should begin to make sense to you why you perform differently in differing locations. Water is made at cytochrome 4 called CCO. What if that process is disrupted by the environment? Is the fidelity of the signal destroyed? Will the oscillation pattern of the inner mitochondrial membrane also change? Is this why we lose the ability to fat burn with the 100Hz oscillation needed for beta-oxidation in alien environments?

If so, does this affect how much water is made and how that water reacts within the metabolic cycles of the cell? You bet your ass it does. This is how nnEMF is operating to make you ill way below your ability to perceive it.

SUMMARY

I have found in my “internet guru career” those who are easily shocked about things or words I utter should be shocked more often in their life. This is why our brightest blazes of insight in life are really kindled by unexpected sparks of insight. Be unique and light people up because you are extraordinary in how you think.

Is drinking water post-sunset mandatory for outdoor living creatures based on what we’ve discussed here?   When humans tell you not to drink water might they be incentivized in trying to sell that belief (Boros and his DDW krewe in LA)

Canadian research showed that mammals tend to increase water intake just before sleep when sunlight is absent. Rather than being motivated by a physiological need for water, the drinking response was solely based on the animal’s circadian rhythms.  The efficiency of your circadian mechanism is critical to this mechanism working as it is designed.  Sunlight creates water, darkness doesn’t <———-BIG FREAKING DEAL ALERT.

When a cell is de-polarized it is deformed by water, and potassium is released. This normally causes a glial cell to swell. This causes a volume change in the adjacent neuron (astrocytes).

When water moves, it changes the refractive index of bulk water in the extracellular compartment of the neuron to create a large coherent domain of water within the neuron and below the myelin level. The astrocytes work as a giant drainage system for water, which uptakes potassium ions in regions with high potassium, and sends them to regions of lower potassium ion concentrations. Vasopressin changes how the drainage system operates.

Vasopressin or antidiuretic hormone, which is made in the posterior pituitary gland, allows the brain controls the flow of water to activate itself in accordance with the stimuli that it currently faces. Any trauma to neurons causes its release. Normally vasopressin is controlled by circadian stimuli. The sun normally controls the release. Artificial light is a light stressor. It causes the release of vasopressin outside of the circadian mechanism.

Fact: Blue light/nnEMF dehydrates cells because they stop H2O production from the mitochondrial TCA cycle. Why is this a big deal? Neurons absorb and release water when firing information via their action potentials. When H2O is missing in action so are neurological functions/capabilities. Check the link here.

Bai, Ruiliang. Brain-active transmembrane water cycling measured by MR is associated with neuronal activity. Magnetic Resonance in Medicine. https://doi.org/10.1002/mrm.27473

The gist of this paper is that neurons absorb and release water when they relay messages throughout the brain and peripheral nervous system. Tracking this water movement with imaging technology may one day provide valuable information on normal brain activity, as well as how injury or disease affects brain function. 

The study appeared in Magnetic Resonance in Medicine.  Just how devasting is artificial light on water flowing in neurons?  4% of the world has autoimmune diseases related to the blue light hazard.  There are just over 100 human autoimmune diseases that afflict humans. 

Current functional magnetic resonance imaging (fMRI) technologies measure neuronal activity indirectly by tracking changes in blood flow and blood oxygen levels. Neurons communicate with each other by a process known as firing. In this process, they emit a slight electrical charge as an enzyme moves positively charged molecules — potassium and sodium ions — through the cell membrane. In the study, when researchers stimulated cell cultures of neurons to fire, they found that the exchanges of potassium and sodium ions were accompanied by an increase in the number of water molecules moving into and out of the cell.

Water movements only occur in the CNS/PNS via water channels that are made up of aquaporin 4 gates. This is going to become important later in the explanation of various diseases (MS). EVERY brain disease and EVERY autoimmune disease is tied to malfunctions in this mechanism

Remember that when water leaves a neuron, it carries a larger negative charge, and this charge induces an increase in the coherent domains in water networks inside the cytoplasm of the neuron. When the size of the coherent domains increases, it increases the optical efficiency within the neuron and outside the axon beneath the myelin where the interfacial water resides.

Remember that it is this interfacial water where Robert Becker found the regenerative DC current. This is why circadian biology and sleep are directly linked to regeneration. It all has to do with the scattering of light in water in neurons.

Ask yourself this: Is it biologically possible to predict the effects of lifetime exposure to electromagnetic, chemical, and physical agents that are not part of the biological experience of man given what we know about the butterfly effect?

If you do not fully understand light will you ever come to realize how important water is to life?

Evidence-based science has divorced itself from nature’s evidence.

Quantitative evidence-based science is used to remove uncertainty by transforming it into a probability for algorithms so that mathematical modeling can play the ritual role of haruspices. This epistemic governance arrangement in science is today in crisis.
The primacy of science today is to adjudicate political issues and it is having massive collateral butterfly effects on public health.
They must pass through an assessment of the level of maturity and effectiveness of the various disciplines deployed. The solution implies abandoning dreams of prediction, control, and optimization obtained by relying on a limited set of simplified narratives that linear thinking scientists and clinicians can understand to define the problem and moving instead to an open exploration of a broader set of plausible and relevant stories that define the real issues at hand.

CITES

Mae-Wan Ho, Fritz Albert Popp, Ulrich Warnke Bioelectrodynamics and biocommunication 1994, p. 21

https://medicalxpress.com/news/2023-01-good-hydration-linked-healthy-aging.html

https://medicalxpress.com/news/2019-03-younger-nightshift-workers-shown-pee.html

https://www.nature.com/articles/nature19756

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7400257/

http://www.photonics.com/Article.aspx?AID=41237

HOW DO ASSUMPTIONS SHAPE US?

Are assumptions the mother of all fuck ups?   Some will try to convince you that your assumptions are your windows to the world. They’ll tell you to scrub them off every once in a while, or the sunlight won’t come in to inform you of the truth.

Assumptions can be dangerous things for people to make, and like all dangerous things that are made — bombs, for instance, or strawberry shortcake — if you make even the smallest mistake you can find yourself in terrible trouble because of the consequences. Making assumptions simply means believing things are a certain way with little or no evidence that shows you are correct.  Moreover, if you just think about how assumptions affect thinking and decision-making, you might be able to see how this can lead to terrible problems. For instance, one morning you might wake up and make the assumption that your bed was in the same place that it always was, even though you would have no real evidence that this was so, that it had floated out to sea, and now you would be in terrible trouble all because of the incorrect assumption that you’d made. You might be able to see now that it is better not to make too many assumptions, particularly in the morning when the sunlight rises to inform you by uploading her wisdom.

On the other hand, assumptions can be useful.  Assumptions could be used as an artist’s palette of paint, and when we slept in that bed on a plane we’d use our beliefs to paint a new masterpiece as well on a freshly stretched canvas.  Your mind would act the role of the brush that pushes the paint around the canvas’s surface as you dream and assume what awaits you in the City of Lights.

Here, an assumption might look like this:  When you got out of your bed this time, you might discover that the bed was in a plane.  When you went to sleep you were flying over New York from Chicago on your way to Paris for the holidays just to be seduced by the lights, music, and atmosphere.  You wanted to dance the Tango on the Seine.  Below Point Neuf, you’d planned to meet a vivacious Frenchwoman who would invite you to a dark fire-lit jazz joint in Monmarte.  There you’d look into the eyes each other over a glass of Bordeaux.  Then, you’d get invited to her rooftop terrace where you’d gaze at the Eiffel Tower under starlight while resting your head on her beautiful shoulder.  Then, you’d wake up in white satin sheets and have breakfast in bed waiting for the sun to rise.  Then you’d walk hand in hand over to Point des Arts to hang up our lovelock.  But just then reality woke you in the bed of the plane over an ocean and you’d realize you never really appreciated what your job was really about.  You take people to places they dream of going by giving them a new chance to assume and choose.  Choices really are the hinges of destiny in life.  When you woke up and stepped out of that bed on the plane you’d realize you were traveling into a new world.  A superposition of what might be.  Here, one can be met by unfamiliar scents, where the colors of the rainbow take on a different filter, and where hearts can acquire a new beat.  You’d begin to realize you are so glad you are who you are, rational, calm, and so determined because the world needs people like you to get people like those reading this, to a place they have trouble imagining.

SUMMARY

Your perceptions influence all areas of life. The totality of your perceptions— regarding yourself, your life, life in general, and others, creates and impacts your personal reality and ultimately your experience of life.

Negative, disabling assumptions lead you in the direction of a very dismal reality. Positive, empowering assumptions give you every opportunity to live a rich, fulfilling life. Though assumptions don’t make your wishes come true, they can give you the perspective necessary for bringing your dreams to life.

Perception acts as a lens through which we view reality. Our perceptions influence how we focus on, process, remember, interpret, understand, synthesize, decide about, and act on reality. In doing so, our tendency is to assume that how we perceive reality is an accurate representation of what reality truly is.  Through perception, we become more aware of and can respond to our environment. We use perception in communication to identify how our loved ones may feel. We use perception in behavior to decide what we think about individuals and groups.

Perception is everything; the way you perceive things, the way you see things, is ultimately the way things will play out in your life.  Perspective helps us to understand situations from other positions and to consider other beliefs, experiences, and viewpoints. This gives us a better understanding and greater empathy. It reduces bias, and judgment, and reduces conflict.

The power of perspective is an intentional discipline. It takes time and commitment, but it creates an understanding between you and the people you lead that allows you to move forward, faster—and with increasing success.

Your perceptions need to be sharpened in 2023.  Realize you need to describe your relationship with truth and false perception this year.  You cannot rely on experts or the media.  You need to deal with your own and other’s perceptions.

Perception is more important than reality. If someone perceives something to be true, it is more important than if it is in fact true. This doesn’t mean you should be duplicitous or deceitful, but don’t go out of your way to correct a false assumption if it plays to your advantage.” 

In 2023 you must obtain clarity in declaring the acceptability of what is false.