Category: Uncategorized

 

Can A Cocktail Of Vitamins And Steroids Cure A Major Killer In Hospitals?

Sure it can because that cocktail mimics the ketogenic diet.  In a 5 G world this might be the most common serious cause of death I expect to see spike in the next 5-7 years.  

Both ideas cause a recycling of cell water in the cytoplasm. I don’t believe keto is a weight loss Rx at its core either. It is something rather different that mimics the effect of Vitamin C in cleaning the TCA and urea cycle of deuterium at Kreb’s bicycle. Because of the shape of our teeth and the shortening of our gut humans lost their requirements for Vitamin C but it raised our needs for marine fats, iodine, and animal fat.  This fostered a seasonal ketosis that turned over the cell water in the matrix.

 

 

Ketosis is a novel seasonal way to drive matrix water replacement while autophagy can control cell membrane turnover and the movements of deuterium. In sepsis, both autophagy and apoptosis are uncoupled because of defective enzyme kinetics at fumerase, so this acutely lead to multiple organ failures quickly and causes a quick death.

 

 

 

It would be wise for hospitals to use red light in these patients rooms at the same time but they do not appear to understand that the 4th and 5th cytochrome react briskly to red light even when ECT is broken. This could be extended if windows were opened in an ICU to allow UV-A light in to patient room to help re-establish apoptosis. Another helpful adjunct would be the use of IV DDW. To date no one has tried this in the literature as far as I can tell.

 

 

This is so powerful, that in some cancers ketosis can exhibit synergistic antitumor activity and preferentially kill tumor cells by autoschizis, a novel type of necrosis characterized by exaggerated membrane damage and progressive loss of organelle-free cytoplasm through a series of self-excisions. During this process, the nucleus becomes smaller, cell size decreases one-half to one-third of its original size, and most organelles surround an intact nucleus in a narrow rim of cytoplasm. This narrow rim is the key marker for extreme turnover of cell water.

 

 

The key in sepsis and cancer is to change the fractionation of hydrogen in the cytosol. In sepsis, the cytoplasm becomes acutely overloaded with deuterium, but in cancer, it is a chronic change. In both cases, the cytoplasm is loaded with the wrong type of hydrogen isotope used in the urea and TCA cycle. While the mitochondria are condensed, tumor cell death does not result from ATP depletion.

 

 

CITES

https://www.npr.org/sections/health-shots/2018/05/11/609149556/can-a-cocktail-of-vitamins-and-steroids-cure-a-major-killer-in-hospitals

 

Many people have heard me use the term zip code in discussing quantum biology, but no one has ask me what I mean by it. What is “zip code” to you? I believe our zip code is the quantum fingerprint in nature we resonate with PROPERLY. Each hour of every day at every location has its own distinctive color, a family of frequencies, and a particular odor. Some of the smallest details inside of cells pay attention to these things. Nature always provides a solution, and our mitochondria was built how to solve the cipher. Our senses have to be blinded to the mystery. We can overcome that haze of understanding only if we know where to look for the answers. Life provides a myriad of vibrations but some resonant with us more than others. That is our connection to the whole. If we only live through the eyes of the others and don’t try to capture the vibration of our own individual experience, we may miss out the beam and brilliance of authenticity that is essential to move forward in nature. Allow no one and no thing to cause a schism between you and your intuition. Disorder creates connections──and that is the resonance life is built on.

 

 

ENTROPY = disorder.  Resonance creates an order from the disorder.  The probabilty of things in us and things in the sun and Earth cause a connective coupling called a correlative novelty.  ‘Correlated novelties’: are  a big thesis in how entropy drives the arrow of time in quantum thermodynamics. The more entropy we dissipate the more time become irreversible.  This is why we perceive life as we do.

HOW DOES THIS HAPPEN?

In life, as everywhere in the cosmos there exists a struggle between in matter, both biotic and abiotic. Chaos is entropy in abiotic systems and it turns out entropy appears to organize biotic systems without energy either. (represented by fear in biotic systems) Entropy appears to lead to an order which can organize into a zero entropy state of matter than keeps life far from equilibrium. If there’s a kind of physics behind biological teleology and agency, it must have something to do with the same concept that seems to have become installed at the heart of fundamental physics itself: information. Biophysics is as much about how mitochondrial create the energy flux as it is about how it processes environmental information accurately. To extract meaning from information or from energy something has to know how to do it. How does this happen? It appears this information in cells is harnessed using water’s shape shifting liquid crystalline abilities under solar powers direction.  According to thermodynamics, the capacity to extract useful work from the energy resources of the universe is always diminishing.

A mitochondria is ‘demon’ who deals in information and heat processing and energy flux. First, for the demon to dominant, it always must have more information than we do about the environment. The organism housing this colony of mitochondria must be blinded to this information and energy. This is just another facet of the quantum Zeno effect we see in the retina and skin with respect to UV and IR light. Humans cannot see either of them, because if they could they could not use either frequency family to regenerate their tissues via autophagy.

Our colony of mitochondrial demons must be able to see or sense all of the molecules individually, rather than just statistical averages of H+, deuterium content, and excitied electrons on the inner mitochondrial membrane. And second, the colony of demons within us has intention: a plan to separate the hot from the cold using uncoupling proteins to make water liquid crystalline. By exploiting its knowledge with intent, mitochondrial demons can defy the classical laws of thermodynamics by usng quantum thermodynamics

There is a deep connection between thermodynamics and the processing of information — or in other words, is related to the computations that mitochondria must make using the quantum spin state of electrons and protons.  Mitochondria make free radicals that have unpaired electrons with a unique quantum spin state.  The matrix excludes deuterium while the blood plasma is filled with it.  There seems to be an organizing process present because of the spin state of subatomic particles that is a hidden variable that limits biologic understanding.

Mitochondria are electron and proton ciphers and accountants for these things. This happens to be why the leptin receptors in the hypothalamus are loaded with mitochondria. Rolf Landauer showed that even if the computational aspects of an information demon can gather information and move a frictionless door with no seeming energy cost in his experiments.  He proved Maxwell’s ideas about the second law was correct.

Landauer also pointed out a penalty must eventually be paid back to nature. He showed that no mitochondrial demon can have unlimited memory of every molecular motion, unless it wipes its memory clean every so often. This raises the question, is this why sleep and mitochondrial function are ubiquitous in living things? 

The best two ways to improve sleep are to observe the sunrise and block our eyes and skin from man made light once the sun sets.  

 

 

 Is this why poor sleep and mitochondrial diseases are linked?  I believe it is. All quantum computational demons must occasionally wipe its memory clean — forget what it has seen and start again — before it can continue harvesting energy and information simulataneously. This night day on off switch is likely why most of the biologic cycles are feed by the sun’s energy and information of night and day.  This act of information erasure has an unavoidable price: It dissipates energy, and therefore increases entropy. And that increase of energy does not go to waste in living systems.  We use the increasing entropy to ORGANIZE information we collect.

It seems to me living quantum systems are expert in the information sharing side of the equation to organize and minimize chaos using biomolecules from the mitochondria to other parts of the cell, while extracting massive amounts of information about the universe they exist in.  Two groups of researchers found in 2017 that the quantum information describing the particles’ energy and quantum spin states can act as a kind of currency that enables trading between the reservoir’s energy and angular momentum supplies. 

This has a big implication for mitochondriacs because this organelle deals in deciphering and creating the quantum spin of electrons and protons and the information and energy they contain. The deciphering and creation of spin varies as the power densities of seasons changes as the planet moves around the sun. Electrons have quantum spin and they have information about the seasons in the power of photons that excite them. The spins of electrons can be altered in mitochondria to make free radical signals which can be used to drive decision making processes inside of cells. This will alter biochemistry within the cell. The quantum spins of protons also can be sensed by the mitochondria because the mitochondria generates a magnetic field and H+and D have two separate magnetic moments that will act differently within the same magnetic field. This difference is like a binary change in a computer that can be used quantum computation to decipher the information contained within the message.

More over, protons spin is also sensed by the mitochondria because all the channels in the mitochondrial matrix are quantum nanomachines that are built exclusively for H+ and not for the larger atom of deuterium. The level of deuterium in the matrix therefore also simulates the season inside the matrix of the mitochondria.  This alters the metabolic rate of the mitochondria as well.  All of this is programmed by light and is how ZIP CODE is coded for inside of us.

The more deuterium that is present, the more swelling one should expect. This shows you why thermodynamics and size and shape changes within the colony of mitochondria in tissues can be sensed macroscopically by our sensory systems in our thalamus. This alters the Tensegrity of the system. The human thalamus also has normal resonant frequencies it is tuned too.  That frquency is the Schumann frequency of the Earth.  Think of it as the electric and magnetic heart of Earth that is communicating with your thalamus.

Living quantum systems achieve a non equillibrium state, by capturing and storing information in our subatomic particles through the entrie system. Mitochondria are the key part of cells that are capable of doing these computations using free radical creation and the movements of hydrogen to build organization in a cell. The nucleus cannot do these computations in eukaryotes. Mitochondria offload most of the information to the nucleus by changing small poteins made by mitochondria carrying data to change the activity of the nuclear genome.  This information is encoded and stored magnetically in their nuclear genes and passed on from one generation to the next via the germline. 

 

 

This is a set of instructions for reaping a non equilibrium state by using the negative entropy built around the quantum spin states of electrons and protons. This is why most repicative structures in nature offload deuterium to their seeds and offspring. It can be used to anchor points in the organism like a thumb tack to align the body plan in the immature state in space and time using magnetic energy as the glue. Deuterium has a stronger magnetic moment and it also has a stong kinetic isotope effect to act as a buttress and trusses in body plan construction in cell membranes. The added mass allows the blueprint to drive all growth and metabolism into the adult form as excited electrons are pumped into the system and trapped by mitochondrial mechanism to build complexity. Mitochondria and DNA are examples of aperiodic crystals that go by another name called liquid crystalline quasicrystal. These are more time crystals in us that resonate with the sun and Earth vibrations. How they vibrate changes as the environment changes. Cells are designed to keep the nuclear genes tightly coiled and this changes what they can sense. This is akin to how the fret board works on a guitar. As fingers compress a string the frequency changes. This change alters signaling throught the time crystals. All of this is transferred over protons in water to all parts of the organism. The exclusion zone of water is life’s main crystal. This crystal has a different physical characteristics when light hits water made in a mitochondria (DDW).

 

 

AM sunlight has a specific resonance for EZ water. It is blue and red light vibrating together that programs water. Artificial blue light from tech screens changes the resonance in water. This results in a changing free radical signal in the central retinal pathways of the retina and can lead to mitochondrial damage in the pathways that lead to the central clock mechanism in the SCN. It is called the blue light hazard and well known. There are two types of blue hazard caused by different frequencies of blue light which changes proteins in the retina. Blue light also lowers ocular melatonin in the central retinal pathways and this lowers the efficiency of autophagy and apoptosis.

UVA increases melatonin and nitric oxide (NO) in blood vessels in skin and retina. NO inhibits ECT of mitochondria and this increases apoptosis to get rid of pre-cancerous cells with poor time crystals at Kreb’s bicycle. How? NO inhibits the flow of electrons in ECT and this is the signal that cytochrome 4/cardiolipin complex need to allow apoptosis. Cancer cells must inactivate apoptosis so they can become immortal as I laid out in the May 2018 webinar. Blue light thins the retina because of the altered free radical signals generated in the damaged mitochondria and this does not allow a normal NO signal to make other signaling molecules. To get NO and melatonin you need AM UV-A and IR-A from the sun. These frequencies improves autophagy and apoptosis via resonance.

Examine this graph. The sun hasn’t changed much in 4 billion years but screen use and blue light exposure certainly has. This is how a change in light zip code can ruin your ability to see.

 

 

It turns out discrete time crystals (DTC) have another characteristic that will interest you. In physics they are forbidden to occur in equilibrium situation. Life is built far from equilibrium.

The discovery of time crystals might sound pretty abstract, but it heralds in a whole new era in physics – this is going to help quantum biology supplant the old guard in biology. Darwinian evolution is now on a death watch. For decades we’ve been studying matter that’s defined as being ‘in equilibrium’, such as metals and insulators. But it’s been predicted that there are many more strange types of matter out there in the Universe that aren’t in equilibrium that humans haven’t even begun to look into, including time crystals. It turns out all living systems are made of these things. And now we know they’re real. The fact that we now have the first example of non-equilibrium matter will change perspectives on what is possible in biology. It will lead to breakthroughs in our understanding of the world around us, and the quantum process biology inside of us, as well as new technology such as quantum computing. Mitochondriacs will be on this leading edge.

 

 

The current definition of a crystal is based on the currently known catalogue of periodic and aperiodic crystals. Scientists currently do not know of any materials that have aperiodically ordered structures beyond incommensurate crystals and quasicrystals. The definition of a crystal also reflects the lack of understanding of what constitutes order in matter, and in this sense should be seen as a working definition that may well need to be revised in the future. In crystallography, order is linked to diffraction, which makes sense because diffraction is the method of choice to experimentally determine the structure of a solid.

The human brain is very skilled at detecting patterns and recognizing order in a structure, and ordered structures permeate cultural achievements of human civilizations, be it in the arts, architecture or music. The ability to detect and describe patterns is also at the basis of all scientific inquiry.

In 2009, Sharon Glotzer and her group at Michigan discovered that entropy, a concept commonly conflated with disorder, can actually organize things!!!  Her group’s simulations showed that entropy drives simple pyramidal shapes called tetrahedra to spontaneously assemble into a quasicrystal — a spatial pattern so complex that it never exactly repeats.

Water also uses these rearrangments when sunlight hits water in our tissues like blood via our skin.

It appears life’s time crystals is built from disorder to give all living things its arrow of time.  Our eyes, skin, and gut are examples of time crystals.  How ironic, but fitting, considering the counterintuitive nature of nature’s use of quantum processes.

It appears that cells have figured out how to utilize these queer processes close to 4 million years ago.  It looks like water was the stage the show was built upon.  The vibration of proteins stable on early Earth then began to vibrate with water and sunlight and the process of evolution began.  It wa smillions of years before all the kinks were worked out in DNA and RNA mechanisms to select the proteins that resonated with the light that fell from the sun.

 

 

This discovery was the first indication of the powerful, paradoxical role that entropy plays in the emergence of complexity and order in all forms of matter. This principle is not just isolated in abiotic atoms. It appears in biotic systems too. Hemoglobin and porphyrins are well known biologic liquid crystals.  Crystals are paradigms of ordered structures. Crystals are capable of doing amazing things to light rays from the sun or re-radiated light rays from other crystals in cells. While order was once seen as synonymous with lattice periodic arrangements, the discoveries of incommensurate crystals and quasicrystals has led to a more general perception of crystalline order, encompassing both periodic and aperiodic crystals. The current definition of crystals rest on their essentially point-like diffraction.

 

 

Cells use biophysical levers contained in light frequencies to control biochemical circuits using photo-electronic circuits. Life has used photonics for 3.8 billion years.  Humans have been toying with this process for 6-8 thousand years.  The remnants of those hacks can be seen in monuments man left scattered across the globe.  Photonics can overcome the high-speed electronic interconnect bottlenecks common in electronic circuits. Direct optical connections between processing elements provided many advantages to Mother Nature in building living systems. These include low signal loss, minimal power requirements, high efficiency, and data transfer over fiberoptic cables that provide massive connects to all parts of the system with minimal energy or information losses.  Is there an example we can use in a cell to make the point?

Single tubulin proteins, for example, follow precise rules of chemistry and physics to spontaneously self-assemble, or polymerize, into the microtubules essential for cell transport and motility. The proteins’ binding interactions effect rules that specify how the pieces fit together to form the resulting structure. They also specify when and how tubulins assemble from a nucleation complex—a molecular algorithm governing the logic of polymerization. Mother Nature created an culture of connectiveness in tissues linking to the colony of mitochondria in our tissues. No cell is untouched in photonic circuitry. Tubulins form microtubules in the brain. Inside of them water is found confinded at small scales.  Water confined at 30 nm reacts very differently than water does at 1.4 nm.  Life wants the water a mitochondria makes confined at small scale.  This is another reason this water has little deuterium present in it.   At one end of the tubulins the openings are larger and at the other end the spaces is smaller by design. This is designed to confine water to harness its optical abilities when it becomes a special liquid crystalline structure where the quantum thermodynamics is allowed to occur.

These complex structures self-assemble with remarkably few mistakes. Though considered quite simple, little is understood about the principles that govern programmable structural order underlying this type of spontaneous self-assembly. We now have clues it does not require energy to occur. Darwinian evolution should no longer be a special state or case of matter, but thought of as a more general phenomenon of how biophysical processes naturally organize matter using the operational laws of quantum mechanics on a planet. 

The local star of that planet provides most or all of the power, but the thermodynamic state of the planet set the floor and ceiling of what kind and type of living systems can be built. The fundamental principles that govern how macroscopic properties emerge from microscopic interactions and arrangements really should be the cornerstones of biologic sciences. Today it is not because we are ignore the hidden variables in nature.  It appears the inherent entropy in the system is useful to self assembly. Microtubules are just another example of aperiodic crystals themselves. This mimics the picture I showed you of my rhubarb earlier in the series.

 

 

In crystals, the simplest example of spontaneous self-assembly, subunits of the whole are arranged in a repeating pattern that extends indefinitely in all directions. If you know the position of one unit in the pattern, you can tell the exact position of every other unit. Life appears to depends in large part on storing and processing information in this way.

For genetic material to carry the diverse instructions required for living processes, Schroedinger initially proposed, it must be stored in an “aperiodic crystal”. Just nine years later, it was clear that DNA is indeed an aperiodic crystal, when another physicist Francis Crick showed us that genetic information in DNA/RNA is conveyed through this irregular pattern in its matter. Much like computers, biological systems are programmed to follow a precise set of rules, or algorithms, to store information and solve problems. These biological algorithms direct actions biophysically in a myriad of ways to biochemical processes to create complex patterns and structures by chemically modifying and assembling individual components. We have to realize that biophysics and biochemical arms work in entangled fashion. If we do not teach our clinicians about these connections and patients suffer as a result.  This is what quantum thermodynamics does.  It extends the classical laws of thermodynamics to explain what life really is.

SUMMARY: 

The water your mitochondria makes, that surround your proteins is a time crystal.  Your entire brain is floating in it.  Your mindset and th eability to think is directly related to the crystalline formation possible or impossible that is developed by the water in the CSF that sits on top of your neocortex.  That is the crystal that your eye communicates with via electromagnetic pulses it senses via the retina.

 

 

All time crystals are a form of matter that “ticks” when exposed to an electromagnetic pulse—from sunlight via our eyes, skin, or gut.

 

 

Time crystals, first identified in 2016, are quite different than the crystal above. Their atoms spin periodically, first in one direction and then in another, as a pulsating force is used to flip them. You should remember that mezmorizing gif from QT#6 as an example of how this happens. That’s the “ticking of the clock mechanism.” In addition, the ticking in a time crystal is locked at a particular frequency, a specific resonance even when the pulse flips are imperfect because of the changing diurnal aspects of the sun.

 

 

This implies all of biology is applied chemistry from how light interacts with electrons and protons inside of us. Chemistry is applied physics, so every living thing on this planet runs a “resonance software program” built by hydrated proteins. These proteins are conserved magnetically in DNA. These proteins are changed by the addition of electrons, protons, and light. Proteins respond only to specific frequencies of light. They have their own ‘zip code’.

That zip code is more important than the genetic code because it is changes every second of every day we live. Our proteins are surrounded in a sea of water our mitochondria makes from substrates from food and the atmosphere which all become programmed by the sun at our current location. Proteins are quantum Garmin GPS devices fundamentally. The action of water around proteins helps quantize the electrons and protons in us to change the matter that makes us up minute to minute. Our species is constantly changing because of these unseen variations.

Evolution is not some static process that occurs slowly. It is ruthless and rapid. We just do not see or understand how the addition and subtraction of electrons orders and disorders us. Blue light and purple light change how our time crystals resonate. The change in that pattern alters what frequencies we connect to because free radicals are changed. This change, cause our resonance to change instantly. Who we were yesterday is not who we are now. That is how fast evolution is operating in us. Darwin’s version of the process leaves much of that detail out.

 

 

What we once use to respond to  at one point in our life, we remain limp too, as the light we surround ourselves changes.  What once was an abyss becomes a new echo chamber that dominates our life.  This is how electromagnetic pollution is reprogramming our us constantly.  This is how people develop tinnitus and electrohypersensitivity.   This quantized process occurs by the varying kinetic energy buried in frequencies of sunlight.  What happens if we bury the sun and build neon God’s?  This entropy causes the melody of life to change.  The beats our hearts and brains used to march to can be changed by light when we get right down to it. Light is an electromagnetic wave that gets changed to an electro-mechanical vibration by proteins and water around the protein-capture the sound blast for signaling. Changing your light environment changes your inner terrain and the dis-ease train will not be able to thrive at your station of life.  That is what “zip code” is to a mitochondriac.

What on the surface seemed ludicrous when I began this blog now suggests entropy drives order.  This now opens more questions for biology and medicine. You’ve got to question beliefs to understand nature’ innovation using the physics we know is possible. Just because something is unlikely does not mean it cannot happen. This is why I reject Occam’s razor arguments in science. What nature does not forbid will happen given enough time for the environment to sculpt the change using non-coding DNA, light, water, and mtDNA.

Photons of light come to Earth and to humans in a timeless state.  Electrons and protons in proteins in living systems pay attention and resonate with that light to absorb the energy and information light contains.  Our cells then transmute that into other waves, light and sound, which start our internal clock ticking to create time from light.  The next time you listen to a human heart beat, feel a pulse, or listen to breath, you are sensing someone else’s zip code. There is information in those waves.  You will be drawn to them or recoil from them.  This is how you connect with other living systems to build your network.

 CITES:

1. Marjorie Senechal. Structures beyond superspace. Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials, 2015; 71 (3): 250 DOI: 10.1107/S2052520615009907

2. Uwe Grimm. Aperiodic crystals and beyond. Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials, 2015; 71 (3): 258 DOI: 10.1107/S2052520615008409

3. http://journals.plos.org/plosbiology/article?id=10.1371/journal.pbio.0020448

4. https://phys.org/news/2018-05-physicists-crystal.html#jCp

 

Here is a present for my Patrons and members. I told you you would all get the benefits of reading snipets from my future works if you remain a Patron. This is the “early” realease of my own biohack from 2003-2005 of my own EHS reversal from my Operating room lights and Wifi.

I have told this story to many of my patients with EHS.

After hearing it, many have made the tough decision to relocate, mitigate and rebuild their redox potential with sunlight using information quanta mechanisms that nature provides cells to relearn using light. It sound bizarre until you understand how sunlight passes information from quantum spin to orbital angular momentum properly. (Stay tuned for QT #7) Many do not do enough and they remain on their way to getting severe EHS as their immune cells lose massive amounts of information quanta from the AC power grid.

I’ve been asked my opinion if EHS can begin as a transient mild headache while in the proximity of a 50Hz or 60Hz Magnetic field (fan or transformer) and progresses as the bodies learn from the information quanta in the man-made fields of the electric power grid via the mechanism in the QT series on Patreon? The answer is yes that is precisly how EHS goes from bad stimulus to learned behavior. This can manifest as a sign of transient mild PTC by destructuration of HDW in the coherent domains of the EZ. It can cause changes or inflammation of the pia of the brain where our main SQUID is located.

In 2003 I found I was getting tuned to the things in my OR when we went to papers EMR’s. The number one offender for me was LED lights and the Wifi from anesthesia machines. I found in my hacks after they showed up in my work environment my sleep was degraded quickly so I went searching. I began concentrating transition metals because of the OR EMF and blue light the hospital added to the OR. So I started to change my OR start times and I went outside between each case to get the sun to teach my system with solar EMF’s. Therefore I knew I had to use CT when I got home in the sun with a higher fat diet to get my redox potential back in my inner mitochondrial membrane to lose weight and reduce the EHS symptoms causing my cognitive haze. I realized I had to get my ATPase spinning faster without using excess food (ECT flows) to do it. This is when I realize this is what UV-A light does for cytochrome c oxidase via its release of nitric oxide from the skin and arterioles in the skin that come to the surface when UV-a light is sensed. I also realized the”pressure wave it made was the key to making the soliton in the blood to cause the NO release.

 

 

The addition of the sun and fat increased my ability to change the water made in my matrix that was attuned to the OR nnEMF’s. I found doing this also to supercharged my P450 system via the PPP. This was an unexpected result of the hack.

 

 

This is how I learned to always choose redox over detox. The PPP gives us back the major reducing element, NADPH. I realized the H in NADPH had to be light hydrogen to properly make intracellular glutathione in cells. This is why I no longer will use the new version of IV tylenol that hospitals are psuhing for patients in surgery. I have found it reduces glutathione the most of any drug in our surgical toolbox. In fact, if one uses oral tylenol often you should drink DDW to reduce the chance of getting EHS in an altered magnetic field. The NADPH acts to recycle glutathione and the glutathione links directly to the melatonin cycle in the brain. It is also when I found out that saturated fat diets and DDW increases endogenous glutathione production. Then I found evidence for this in the literature.

That is when my life really changed its focus. When glutathione is low, we must add back UVA light to increase apoptosis and this help raises melatonin at the same time. Often EHS destroys melatonin cycles in the brain with the Vitamin A cycle. All opsins use Vitamin A to work with light. This is how I found the LED lights in my OR were making me sick. It is also when I made the prediction that melanopsin would be found in the skin. This is why skin problems develop in our patients before they get really sick from electro pollution. It is also why my profession uses Vitamin A, in retin A, to try to improve these issues. Is the redox is bad it makes on worse? If the redox is decent it can help. The smarter move for EHS people is getting AM sun when the UVA IRA transition occurs. It dawned on me then that that artificial light was fully capable of altering people to make them more electrosensitive and this change would lead to poor cogntive function that made it harder for them to think, learn, and adapt. It was why I was losing my edge in surgery for something I truly liked to do. It all occured because of the light hospitals adapted too to save money in the 2000’s.

 

 

 

Water puts the “magnetic” back in “electromagnetic.” In nature’s schematic above, a standing light wave with magnetic (blue) and electric (red) field peaks is generated in an optical photonic cavity, it acts as a resonator. As the light bounces between two reflection points that act like mirrors it transfers information from the quantum spin of particles to orbital angular momentum. This is how lasers can be tuned and how we can increase the base quantum spin number of photons. Normally photons have a quantum spin number of one.

Most people have no idea that light appears to be able to have unlimited storage capacity for OAM when we use an optical resonator. What does this physically in us? Water does this. Not the water from your tap, or the water you drink. It is done by the water your mitochondrial makes. I will be talking about this process in three weeks in Vermont at Shelburne Farms. you might want to get some tickets. You can review my talk on photosynthesis from 2016 and my talk on the retina from 2017 on Youtube. This year there won’t be a YouTube video so attendance will be helpful.

 

 

Once water is physically changed by sunlight it obtains new physical properties that give it unlimited nonlinear potential.  Researchers have now proven this to be true in several sub-disciplines of physics.  How much do you know about aquaphotomics?  If you do not, you might want to join my tribe of misfits at https://jackkruse.com/become-a-member/

If you cannot swing that join me here at Patreon.  For in-depth blogs on the coming age of quantum, biology becomes a Patron and I will teach you and answer your questions directly for the cost of a coffee a month. https://www.patreon.com/DrJackKruse

ARE YOU READY TO BECOME A BLACK SWAN MITOCHONDRIAC?

 

 

Magnetism is everywhere if you look for it. In biology, few look for magnetism and that is why they do not understand it. Most biologists know oxygen is critical for life, and since it is paramagnetic and drawn to magnetic fields you’d think this would make them understand why oxygen is drawn to the terminus of the respiratory proteins where the ATPase spins at a fantastic rate to generate a magnetic field. That one observation should change all of what we believe, but so far it has not made its proper mark. Any place life has mitochondria we are able to measure huge magnetic fields with SQUID’s, MEG, and EEG’s. We know this, but we don’t know what it means.

We detect magnetic fields everywhere, even in the “empty” depths of intergalactic space too. Magnetic fields cannot exist without causative electric currents. We learned this from Faraday and Ampere experiments. In fact, as you will soon in this series certain diets have topologic effects related to their topologic charge. This is why the vegan diet does not operate well at high latitudes. It ruins the topology of the semiconductors in our cells. This means less information can be stored in our tissues when we make poor choices. SERIOUS? Yep.

 

 

The study below in the cite shows omega-3 levels are better predictors of risk for death than serum cholesterol

A recent study published in the Journal of Clinical Lipidology looked at the value of measuring blood levels of EPA and DHA omega-3 fatty acids to assess an individual’s risk for developing certain diseases. In this new report from Harris and colleagues, the “Omega-3 Index” (the EPA+DHA content of red blood cell membranes) was measured in 2500 participants in the Offspring cohort of the Framingham Heart Study. (This group is largely made up of the children of the original Framingham study which began in 1948.) The results showed that the risk for death from any cause was reduced by about 33% comparing the lowest Omega-3 Index participants to the highest.

An update on lipids and mitochondrial function: impact of dietary n-3 polyunsaturated fatty acids.

 

Review article:  Stanley WC, et al. Curr Opin Clin Nutr Metab Care. 2012.

PURPOSE OF REVIEW: Recent evidence has linked n-3 polyunsaturated fatty acid (PUFA) supplementation with dramatic alterations of mitochondrial phospholipid membranes and favorable changes in mitochondrial function. In the present review, we examine the novel effects of n-3 PUFA on mitochondria, with an emphasis on cardiac mitochondrial phospholipids.

RECENT FINDINGS: There is growing evidence that dietary n-3 PUFA, particularly docosahexaenoic acid (DHA), has profound effects on mitochondrial membrane phospholipid composition and mitochondrial function. Supplementation with n-3 PUFA increases membrane phospholipid DHA and depletes arachidonic acid, and can increase cardiolipin, a tetra-acyl phospholipid that is unique to mitochondrial and essential for optimal mitochondrial function. Recent studies show that supplementation with DHA decreases propensity for cardiac mitochondria to undergo permeability transition, a catastrophic event often leading to cell death. This finding provides a potential mechanism for the cardioprotective effect of DHA. Interestingly, other n-3 PUFAs that modify membrane composition to a lesser extent have substantially less of an effect on mitochondria and do not appear to directly protect the heart.

SUMMARY: Current data support a role for n-3 PUFA supplementation, particularly DHA, on mitochondria that are strongly associated with changes in mitochondrial phospholipid composition

CITES:

Harris WS, Tintle N, Etherton MR, Vasan RS, The Omega-3 Index can serve as a marker of overall health in older Americans. Erythrocyte Long-Chain Omega-3 Fatty Acid Levels are Inversely Associated with Mortality and with Incident Cardiovascular Disease: the Framingham Heart Study, Journal of Clinical Lipidology (2018), doi: 10.1016/j.jacl.2018.02.010.

 

Even when the experts all agree, they may well be mistaken.  This is the case with photosynthesis.  How energy and information flows is not equal.

IS OUR ZIP CODE MORE IMPORTANT THAN OUR GENETIC CODE BECAUSE OF OUR ATPase design?

Is this why I drag my members to the Yucatan yearly?  yep.

What makes Yucatan special is the Chicxulub crater?  Information and energy transfer is optimized in the ATPase at this location even in a plasma filled with nnEMF.

I need to go back and retell you the story most of your forgot.  It is incredibly important to the black swan mitochondriac to fully comprehend why it is critical.

The Chicxulub crater  links humans to their ancient ATPase and may allow them to navigate the modern 5G ecosystem well.   What connects their ATPase to the crater is the biophysics of their matrix in their mitochondria.  I spoke about this deep connection in my book, The Epi-Paleo Rx.  I still do not believe most people understand how incredibly powerful this connection is for the mitochondriac.  The picture above is the skull of the dominant animal on Earth prior to that asteroid impact.  Go back above and take a look at the picture carefully.  Without that asteroid, nothing human would have ever been present on Earth.  Dinosaurs and humans are a mismatch of species.  When you see the power of the picture above it makes you realize that a single environmental change can take out the most powerful species at any time on Earth.  Today, modern humans are now facing their asteroid in technology.

You might have missed how this crater directly coupled life on Earth today with a huge environmental shift that occurred 65 million years ago.  The two major groups of life that survived this environmental event had excessive mitochondrial capacity in their body plans.  This was the key requirement for life to survive post-event.  Photosynthesis has two prongs.  It provided energy and information to living systems via electron, proton, and photon spin, as you have learned in this series.

Photosynthesis was disrupted for a long period of time so it meant that life had to live on the edge, predominantly using information, using this capacity to survive in some way.  Light normally flows from the sun to living things on Earth.  This flow of energy and direction can be altered by many factors.  Interestingly, information flow might differ. How so?  65 million years ago it was an out of this world factor that limited energy and infromation flows that change the trajectory of ALL evolution on Earth.  Today, it is a manmade factor that is disrupting energy and information flows from nature to living systems on Earth. Much like the unbelievable sotry fo the first sailing of the Titanic, modern people have no idea that technology is biology’s iceberg.  How could this be, you ask?

The Titanic sunk in 1912.  This is what our inner cities began to look like at the same time.

 

 

These wires are located between the Earth and sun and create their own waveforms. Are waves the keys to understanding information loss?

Remember from the earlier blogs in this series I showed you as we extract more information from a system more physiologic work can be done. The flip side of the coin is that if any information is lost, less physiologic work can be done and life becomes less complex and must adapt. That is the essence of what an extinction event is all about. This is why observing humans from 1900 with normal cognitive function being rapidly altered by our environments over the last 120 years to be more afflicted by things like Alzheimer’s and autism at different times of their life is a canary in the coalmine for the black swan mitochondriac. In 1912, Alzheimers was considered a disease of the older population. Today it is not. In 1912, autism was not even discovered. It took 3 more decades of nnEMF to show up in the medical literature in 1940. This disease afflicts the youngest humans from birth to their first few birthdays.

 

 

Technology is not always progressive leading to cutting-edge change in society. It is sold to us this way by the sellers of technology gear. This is how marketing work. As I showed in the last paragraph, long periods of stability in homo sapiens is now being interrupted by Black Swan occurrences in our environment that are now leading to a branching evolution and new trajectory in our species. This is evolution in motion by causing a change in information and energy flows in nature. The collateral effects can lead to a punctuated evolution in living systems by placing limitations of wisdom in our society and our valuation of information over understanding.

 

 

DOES PHOTOSYNTHESIS HAVE TO TRAVERSE THE IONOSPHERE IN A SPECIFIC WAY TO OPERATE IN OUR CELLS?

Yep.

Do modern communications affect the information transfers in some way from the sun and Earth?  Yes they do.  How? They interrupt vibrations between the sun and Earth.  Remember all living systems are between those two thermodynamic objects.

Researchers have discovered a new role for protein vibrations in controlling the transformation of sunshine into useful energy and information in our cells.

Plants on land and algae in the sea soak up sunlight and transfer the energy using proteins holding colored pigments in cells. A pigment energized by a photon can pass that excitation energy and information in the light photon to another nearby pigment—like passing the baton between runners in a relay. By repeating this process the photon’s energy and information is carried to the reaction center where the energy can be used to produce oxygen and power plant growth.  The information can be transferred from the light photon to the orbital angular momentum of electrons, protons, and other light waves trapped within the organization of things in cells.  This is why cells are built to work far from equilibrium.  They can capture the information in light during the process of transferring energy.  Energy, charge, quantum spin, and orbital angular momentum are all conserved quantities in nature.  Your cells use each one in specific ways to harness the energy and information with high efficiency.

Scientists have long wondered how plants move this energy and information so quickly and efficiently across the large collections of pigments surrounding each reaction center.

In the study cited below, researchers focused on one photosynthetic protein known as PC645. Using computer simulations and experimental data, they found that PC645 controls where energy goes by tuning the vibrations of pigments to enhance energy transport along specific routes.  What they did not realize is that information transfer is the key controller of how that energy is transported and dissipated in a specific and sensitive way.

All proteins and lipids in you have a bar code built into their atomic arrangement that allow them to work with specific and sensitive vibrations.  This means the incoming light can offload its information in its orbital angular momentum to the quantum spin of electrons and protons in you without any time delay.  They key to the download speed is the atomic arrangement of the things in your cell.  That is the information your nucleic  acids provide to your cellular design.  That design varies within tissues.  Each tissues has a different zip code to work with information quanta transfers in cells.  The paper below only is dealing with energy transfer.  They do not realize that energy transfer is directed by information download first.   You can imagine these proteins using the vibrations of different pigments like traffic signals in your tissues that send excitations in one direction or another.  This mechanism has a name.  It is called anisotropy.

For example, when a ‘blue’ pigment is excited it could pass the excitation to a number of different neighboring pigments with similar energies. By controlling the vibrations, proteins can direct the ‘blue’ pigment to pass the excitation to a specific ‘red’ pigment thereby skipping over pigments with intermediate colors.

The unusual thing that occurs when you run the experiments in a lab, the excitation doesn’t step down an energy ladder. It jumps from the very highest rung to the very lowest rung and never touches anything in between. It makes you wonder—why does life do this? And more importantly, how does it happen?   It happens because information quanta is being transferred before energy is moved.  The ability to transfer information between quantum spin and OAM occurs faster than the transfer or energy on excitons between proteins.  The issue is the researchers never realized it because they never controlled for this effect.  Because they never control for it, they have no idea what is controlling the process.  Fodo researchers are making the same error in their papers when they fail to control for light frequencies when they perform studies on diets and biochemical pathways in a lab.  What occurs in a lab is not equivalent to what happens between the Earth and the sun.  This is why in Vermont in 2016 I said if Dr. Price was alive today he would be part of my misfits and not Sally Fallon’s tribe of food gurus.  Without understanding the details of biophysics you can never decipher the code of understanding of how nature operates.

BACK TO THE SUN

Previously, researchers thought this could only be explained by quantum effects like entanglement. It turns out we now know this is not true.  It is also why I spent so much time highlighting that the TCA and urea cycle can only operate to burn fat and protein when they inner mitochondrial membrane are vibrating at 100Hz.  Vibronic coherence—the entanglement between electron and vibrational motion—was thought to be necessary for the fast jumps between very different energy levels. However, the new research cited below suggests that what is needed is not vibronic coherence, but a large band of vibrations that bridge the energy gap between two pigments.  That is precisely what your cells are expert in producing from their DNA.

From a material perspective, this kind of classical mechanism is more useful because it’s robust to reasonable levels of disorder (entropy) that current synthetic techniques can achieve.  I warned you this entropy thing was going to be a big deal in quantum thermodynamics.  We’ll have a full blog on that soon in this series.

Researchers have to pursue further research into the quantum thermodynamic principles that form biophysical abilities of life. In my opinion, quantum thermodynamics will eventually fully explain how biologists need to begin to study how photosynthetic proteins to control and enhance the energy and information transport necessary for efficient photosynthesis. When they do tap QT ideas they can begin to use these natural design principles to help develop new technology and solar energy materials that will not harm man.

One of the key challenges is that we need better tools to study the changing interface of quantum spin to orbital angular momentum that ocurs in cells. I’ve got a sense the computer might help us get there.  How is that for irony!  Computer simulation required 10 million CPU hours and more than two years of human time to study one protein they studied.  Lesson suspended now.

BACK TO US

The atmosphere and water share a physical property by being anisotropic. You heard me use that term above.  What does this mean?  Anisotropy of an object or substance means it has a physical property that has a different value when measured in different directions. A simple example is wood, which is stronger along the grain than across it.

The atmosphere and water exhibit properties with different values when measured in different directions or perspectives.  Earth has an anisotropy at different zip codes. So does water all over the globe.  So does air in different locations.  This is what a geopathic stress zones are really all about.  The Yucatan peninsula, for mammals, is their “cradle of life” because of the biophysics of the ATPase built by our DNA.  These variances alone can alter the flow of energies and information quanta on Earth to living things.  That is what the property of anisotropy really is to the black swan.  This physical ability is born from the 3 D atomic relationships of the object in question to an energy source;  these arrangements can alter energy and information flows within and between living things.

Consider the ATPase in a mitochondria:

The Grotthuss mechanism occurs in humans  who use iodine from the marine food web to brings H+ closer together to transfer information rapidly.  This mechanism allows protons to tunnel from one water molecule to the next via hydrogen bonding.  It is the usual mechanism given for facilitated proton mobility. When hydrogen bonds are deuterated to high degree can information transfer occur from the quantum spin number of deuterium to its surrounding components in a cell?  No.  Chemical bonding slows infromation transfers.  This is why the KIE is an optical brake for information transfer.  H+ can freely move in an aqueous system like the matirx and it can rapidly transfer information in the TCA and urea cycles.

This process is very similar to that of auto-dissociation or electrolysis we see in photosynthesis; the mechanism causing the ions (H+, OH-) to initially separate because of sunlight.  People forget, charge separation of water happens as the first step in photosynthesis. Both processes increase with increasing temperature. This means that temperature favors the formation of H+ in an aqueous network. Isn’t it an interesting coincidence how mitochondria release heat by nature’s design to raise the temperature as we go away from the equator where sunlight is poor and deuterium depleted water is more common? The skeptics have left a lot on the bone for me to hammer them on this month on the Patreon blogs!!!!  I spoke about these concepts long ago without much detail here:  https://www.jackkruse.com/tensegrity-6-hydrogen-bonding-networks-water/

Why is DHA seafood H+ and sunlight all linked at the ATPase? BIOPHYSICS.

Matrix reality: One ton of ATP is turned over in 24 hours. In a marathon of 26 miles, you could turn over 60 kilograms of ATP as you run.  Running makes the ATPase Fo head spin faster.   When you consider that it takes a little over 3 hydrogen atoms (H+) to make one ATP in the ATPase, you can triple this number and then you can understand how important deuterium is to a living system. When you consider deuterium is designed to be plentiful in the blood plasma where RBC’s are, you begin to realize why RBC’s have NO mitochondria.  If they did they could not work with a deuterium fraction of 150 ppm around them.   The mammalian system in the matrix is designed to see a very much lower deuterium fractionation where an ATPase is located. Ask yourself why nature built us this way? Why is deuterium absent where mitochondria are plentiful? There is no paradox here. Where a mystery of nature exists,  a lack of human understanding persists.

Anisotropy enables for abrupt swings in the direction of flow of energy within its atomic lattice, in the atmosphere and in living tissue because of water.   Today, modern life and our atmosphere are changing rapidly in a similar situation.  Let us examine this queer physical ability.  After the KT event, the environment cooled tremendously for a long time because photosynthesis was disrupted.  This lead to massive changes in the flow of energy and information in the atmosphere to change our climate and killed off the dinosaurs.  Let us use a modern example to explain this further.

It is clear that most electromagnetic energies are capable of altered ubiquitin rates on Earth because of how the gases are changing in our atmosphere today.  C02 is rising as we use technology.  We have blamed the rise on many other things.  The thermodynamic process is linked to light’s power in quantized fashion.   The only way to increase light’s power is to increase its frequency.  We seem oblivious that light can increase its information power by just expanding its orbital angular momentum.  This is how a laser works.  It appears life is best adapted to the frequencies below the microwave range in the electromagnetic spectrum of light.  Might this be how cells build their own lasers to operate in cells?  I think so.  I will be talking about this in Vermont this year.  This is incredibly important concept.  Today, man is using the frequencies above visible light for communications without fully understanding the effect on ubiquitin marking. Anything distal to infrared rays seem to be a real problem of information transfer of sunlight to cells via photosynthesis.  It is clear to me now that the information quanta in the nnEMF photons is what is transferring the incorrect error messages to ubiquitin in our cells.  This leads to diseases.  When you visit the Yucatan, your ATPase can operate better, and over come many of the error messages that modern tech devices bring to our cells.  

CITES:

Samuel M. Blau et al, Local protein solvation drives direct down-conversion in phycobiliprotein PC645 via incoherent vibronic transport, Proceedings of the National Academy of Sciences (2018).  DOI: 10.1073/pnas.1800370115

https://jackkruse.com/ubiquitination-18-flow-and-energy-direction/

 

We have seen through the human genome project data that “gene theory” alone can not explain the complexity of human life when we have fewer genes than our ancestors, and yet, we have extraordinary physiologic traits never seen before in our primate tree.  Might there be another way to transfer information other than DNA?  This series has shown you that in fact, there is another method to go this.  That is the big implication of QT#1.

Might it be that the information in a proton be able to change DNA?  I believe it is .  WE know DNA has a massive array of proton tunneling taking place we just have no idea how it happens.  QT # 1 give you my idea of how I think it is happening every moment.

Darwinian biology describes phenomena that are a result of a myriad of interactions but have no particular dominant factor at play. Genetics is 180 degree opposite this paradigm today.  They believe there is a reductive pathway from a gene to cell to tissue to physiologic function to explain everything we observe in life, and then we have QED who says we can have “spooky action at a great distance” because of nonlocality,  quantum tunneling, etc. The organic chemists believe that there is no such action possible at a distance in chemistry. No wonder modern medicine is a mess!  We know energy and information about electrons and protons transfer and that input come from sunlight.  It is based on the core beliefs of these fields as well.  Your results are this way because of this thinking that science should be studied in special areas independent of a more global view. Medicine today, is like a giant game of telephone.  

When you were kid it was funny to see how the message was changed by a chain of people as the message passed to other people.  I have a sense our DNA and RNA gets those information transfers from protons.  The main different between these examples is today in medicine,  the message is seeing your health disappear as one person talks to another via a journal filled with RCT instead of using nature’s wisdom in proton quanta transfer.  

Instead of a reductive view, we need a top-down approach, to include all principles to come up with a 30,000 foot understanding of how life works using biology, chemistry, and physics.  The study of circadian biology is the best place for this to begin,  in my humble view, because this is where protons learn their lessons, from the teacher, the sun.

It is hard to repair this mechanism when you have no idea that the loss resonant energy transfer from the nnEMF  to electrons and protons is changing the messages from the Sun and Earth.  The mechanism is clearly found in QED theory to water is behind “the curtain” causing all neolithic disease.  If you scour the chronobiology literature every known disease has a link back to problems with the molecular clock at some level.  Sadly, no one is making these connections yet. But they are getting what I have been saying for 13 years.

I am in the process now of releasing my 5G hacks in the CPC blogs because 5G is now a reality in most USA cities in case you do not know it.  The Big carriers are now actively unleashing the network by testing its functionality in many cities.  In QT #1 and #2 you are seeing how it links to mitochondrial function by making sense of second law of thermodynamics in mitochondria.

For 150 years no one has questioned to see if science has missed something quite basic in this law.  Maxwell, wrote a letter to a friend who laid the case out clearly.  I am going to put some data on what I told you in QT #1.

Some people will find this science dense but it won’t be for those of you who have been keeping up with your reading to see how things are coming together.

Now, the question should be………..

Why is it that some mammals can live in freezing cold regions of Earth with little sunlight and modern humans worry about hypothermia in temperatures that are not even close to this cold?

What is the thermodynamic issue here?

THE ANSWER:  The foundations of “Quantum thermodynamics.”

What did I teach you about long ago about how polar bears and penguins repel cold temperatures so they can live in polar water? How did they do it?  Why do we struggle with it??   What do they both eat and where do they both live?  What is special about that environment?  Is there something special about these animals compared to us?  Do you sense an entanglement yet with these concepts? A food guru will struggle to see the gorgeous threads nature provide living quantum systems. A mitochondriac will begin to see something different.

The invisible threads nature weaved into electron and proton spin are the strongest ties in the Quilt of our lives.   Today this blog is about the foundations of thermodynamics in living systems.  How these new concepts link to the quantum spin states of electrons and protons in mitochondria are critical to get correct before we can see nature’s wisdom manifest in tissues.

ELECTRONS/PROTONS and THE STANDARD MODEL

The Standard Model of particle physics, tries to get at what exists in the universe (matter), the laws of thermodynamics only say what can and can’t be done with this matter. But one of the strangest things about the theory is that these rules seem subjective because the idea of dissipation of energy depends on the extent of our KNOWLDEGE.  Yes, you read that correctly.  What is possible thermodynamically in any system depends 100% on the extent of what we know about that system.

This implies that any study of the thermodynamics of quantum systems means you must accept that what you do not know is the single most important part of the equation.  This idea forces you to realize the Dunning Kruger (DK) effect is not some amorphous concept, but something that PHYSICALLY matters deeply in living systems.  DK is not a cognitive bias, it is actually a REAL physical thing.  I hinted at this in the Tensegrity 13 blog.

“Quantum thermodynamics” is a field in the making that will completely change how medicine is delivered globally, in my opinion.

The paradox hinting at the connection between thermodynamics and information, was put forth by James Clerq Maxwell in 1867 in a letter he wrote to a friend.  In this letter the concept of a “Maxwell demon” was born.  The demon concept he mentioned was a thought experiment that really was all about informtion transfer in the system and not about the transfer or transmutation of energy.  Most people lost that nuance until information theory in quantum computing was mentioned by Feynman in the 1960’s.   The ‘paradoxical demon‘ he came up with in this letter concerned the second law of thermodynamics — the rule that entropy always increases in systems.  Today, we now know that entropy can lead to self assembly and order.  This new idea is also rather shocking to the foundation of physics.  It challenges everything we know today about how heat operates.  The new data on entropy is beginning to make physics stop buying its own hype around classic interpretations of thermodynamics.

JACK, WHY DOES THIS MATTER?

Ask better questions when you get new bits of information.  

Why do things organize they way they do?  Is it only chemical or electrostatic  interactions, or is there something else we’re missing??    Look at the picture of my rhubarb below.

 

 

What allows them to assume this pattern?  Is it a chemical bond?  Is it a hydrogen bond?  Is it electrostatics?  No, it is none of those things.  The pattern emergence come from the entropy I introduced into the system by way of the crafty knife cuts I put on all the pieces as I put them in the pot.

JACK, WHY IS THIS IMPORTANT?

EMERGENCE — the phenomenon whereby simple objects give rise to surprising collective behaviors.  For example, consider the tetrahedra crystal;  it’s the simplest Platonic solid — the simplest three-dimensional shape.    When they arrange with one another based solely on entropy (randomness), meaning they have no direct physical interactions between them — they didn’t want to stick together; there’s no charges; there’s no nothing binding them but their shape.  Using entropy alone, the tetrahedra organize into a quasicrystal format — this really complex, ordered structure. Take a look at the picture above again.  That is a topologic organization.  Now I want to make you look back to another blog.  Go look at the first picture you see in the TIME #24 blog right now.  Do you see anything that is similar to the picture above?

Nature organizes living quantum systems using nothing but entropy.

Order in biology,  always emerges from DISORDER.

At its core, nature is asymmetric because of this design.

Mathematics actually now contains proofs that show this is true even though it is counterintuitive to logic and reason.  Logic and reason are not good enough to understand how nature operates, it appears.  It may show you why many of the things I post about seem to shock those people whose brains are filled with conventional ideas.  To see how order hides within chaos, imagine coloring number pairs in an infinite set according to this rule in this HYPERLINK 

People normally understand the law of increasing entropy as the tendency of things to get messier, but science and mathematics are now reporting that entropy leads to order in nature too.

The philosopher steeped in epistemology will say, “Jack, Why is that not a paradox thermodynamically?”

ANSWER:  CARNOT TRUTH WAS A HALF TRUTH:  CARNOT NO MORE

Maxwell wondered how a law of nature could depend on one’s knowledge — or ignorance — of the positions and velocities of molecules.  He realized that the Dunning Kruger effect could be at play behind dissipative structures long ago because of what he wrote in that letter.  Ilya Prigogine developed the concept and contributed to the theories of dissipative structures for which he won the 1977 Nobel Prize in Chemistry.  Maxwell is who gave Prigogine confidence to guess correctly to get that Prize.  Good science always begins with a good guess.  Maxwell sensed that the things we do not know now, might lead to massive changes in our beliefs down the road.  He wrote that in his letter to his friend about his ‘demons.‘

If the second law of thermodynamics depends subjectively on one’s information, in what sense is it true?  Maybe, it is not always absolute and maybe living quantum systems are the observable fact of his warnings from that letter?

Ludwig Boltzmann showed that energy disperses, and entropy increases, as a simple matter of statistics: There are many more ways for energy to be spread among the particles in a system than concentrated in a few, so as particles move around and interact, they naturally tend toward states in which their energy is increasingly shared.  Maxwell described his thought experiment in which “an enlightened being” — we later called Maxwell’s demon — uses its knowledge it acquired from the environment to lower entropy and appear to violate the second law from an energy perspective.

Maxwell theorized to do this, the “demon” had to know the positions and velocities of every molecule in a container of gas. By partitioning the container and opening and closing a small door between the two chambers, the demon lets only fast-moving molecules enter one side, while allowing only slow molecules to go the other way. The demon’s actions divide the gas into hot and cold, concentrating its energy and lowering its overall entropy. The once useless gas can now be put to work.  Paraphrasing his own words, this is how he believed life might finds a way to win.

He had no idea that quantum spin could share information to other conserved traits of nature.  If he had, he would have relaized that every electron and proton is a Maxwell demon.

Could it be that the real demon in our mitochondria is the a trap door that does this for deuterium and light hydrogen?

Today classic thermodynamic theory separates information and energy when it is taught to scientists and engineers.  This has not caught the attention of biology yet.  Information is now known to be a physical thing in quantum thermodynamics.

KEY POINT:  The more information the living system can acquire, the more work that system can extract from any living system. Does this mean that information and consciousness might be linked via an emergent property of matter?  Yes, I believe it does.  Now with the insights from information theory, we wouldn’t and cannot say entropy is a property of a system, but a property of an observer who describes a system.

This is very different from the past.  It implies information cannot be lost because like angular momentum and charge it is a conserved property in nature.

The present state of the universe preserves all information about the past.  Understanding entropy as a subjective measure allows the universe as a whole to evolve without ever losing any information.  They is understanding how the information is transferred.  Even as parts of the universe, such as coffee, engines and people, experience rising entropy as their quantum information dilutes, the global entropy of the universe stays forever zero satisfying the 2nd law at all times.

 

 

The relationship among information, energy and other “conserved quantities,”  can “change hands” but never be destroyed, took a new turn in 2017.  Two groups of researchers found that the quantum information describing the particles’ energy and quantum spin states can act as a kind of currency that enables trading between the reservoir’s energy and angular momentum supplies.  I covered this in the April 2018 webinar called QT #1.

This has a big implication for mitochondriacs because this organelle deals exclusively in the spin of electrons and protons and the energy and information they contain. 

The notion that conserved quantities in subatomic particles can be traded for one another in quantum systems is brand new to thermodynamic science and really helps us understand what mitochondria and chloroplasts are really up to inside living systems.  They are casino dealers of information about our environment.

This work suggested to me the need for a more complete thermodynamic theory had to exist within the framework of the second law that  would help explain life more fully.  This idea would describe not only the flow of energy and information, but also the interplay between all the conserved quantities in the universe in our cells.

Angular momentum and charge are two such conserved factors that continue to confuse scientists today.  If biology realized that the addition or subtraction of electrons and protons could change proteins they’d realize finally why we do not need DNA/RNA change to explain the human genome.  More complex animals can have less genes, but gain their complexity because they have systems in them that allow them to extract more information than lower animal forms.

For example,  consider the human brain compared to the chimpanzee brain.

Fundamental Brain Development

In mammals, the nervous system develops from ectoderm, the surface layer of the gastrula. Later in development, the mesoderm gives rise to the notochord, which releases the organizer proteins noggin and chordin. These proteins block the suppressive effects of bone morphogenetic protein (BMP), allowing the ectoderm to form the neural plate, then the neural tube, and eventually the ventricular system, where neurogenesis proceeds within the walls of the tube to form the CNS, including the brain and spinal cord (Butler & Hodos, 2005; Siegel & Sapru, 2015). The neural plate and neural tube are composed of a single layer of neuroepithelial cells, which can be considered as neural stem cells (NSCs) (Gotz & Huttner, 2005). After closure of the neural tube, neuroepithelial cells undergo asymmetric division to generate a daughter stem cell, plus a more differentiated cell, such as a radial glial (RG) cell or a neuron (Gotz & Huttner, 2005; Huttner & Brand, 1997). With the switch to neurogenesis, all neuroepithelial cells undergo a transformation and give rise to RG cells. RG cells are fate-restricted progenitors, which can either generate nascent neurons by symmetric division or undergo self-renewal by asymmetric division (Gotz & Huttner, 2005; Yao & Jin, 2014).

The epigenetic changes to cytosine in the human brain is all it took to change the chimp brain to homo.  Methylation adds 3 H+ atoms to every cytosine and this allows us to transfer massive amounts of information to the neurons in our frontal lobes.  This simple change is the largest difference between us and chimps and allows us to have less genes than they do.  Why is having less genes an advantage to humans?  It saves us in energy costs as Wallace has pointed out in his papers!  How does this happen?

5-hydroxymethylcytosine (5-hmC), a derivative of 5-methylcytosine (5-mC), is abundant in the brain. Methyl groups have 3H+ on each one. The rediscovery of 5-hmC in mammals demonstrates that covalent DNA modifications are more dynamic than previously believed. Is the reason why the brain, especially the frontal lobes and neocortex are loaded with H+ on cytosine residues and how these cells get more information during morphogenesis?

Yes it is.  How?

A protein called nogging mention in Quantum Biology #7 blog post 5 years ago is loaded with deuterium and this protein from our bone cells is used to control brain growth in humans.

Noggin has a very interesting protein structure that can modify human brain growth by altering cytosine.

Hydrogen/deuterium exchange in spaces or proteins can be monitored by mass spectrometry (HDX-MS). HDX-MS has recently emerged as a powerful method for characterizing protein conformational dynamics. The basis of this method is the fact that backbone amides in stable hydrogen-bonded structures (e.g., α-helices and β-sheets) are protected against exchange with the aqueous solvent like extracellular water from the blood plasma, lymph, or the interstitium.

All protein structures are dynamic, however, and eventually all of the protecting hydrogen bonds will transiently break as the protein—according to thermodynamic principles—cycles through partially unfolded states that correspond to excited free energy levels. As a result, all of the backbone amide groups in proteins will eventually become temporarily solvent-exposed and exchange-competent over time.

Consequently, a folded protein in D2O will gradually incorporate deuterium into its backbone amide hydrogen fractionation and this will change its physiologic abilities because H+ delivers more information than deuterium can.  Unfolded proteins react differently.  Deuterium however can cause matrix swelling to drive tissue proliferation compared to H+.  Since humans have a large amount of deuterium in their blood plasma this source can be tightly controlled to affect the ECF space to change the kinetics of the process. This process can be readily monitored by mass spectrometry. How is the process controlled? The optical swtich that is deuterium fractionation between the blood and matrix.

 

 

It seems to me, living quantum systems are experts in the information sharing side of the equation to organize matter in specific ways in mitochondria, while simultaneously minimizing chaos, while extracting massive amounts of information about the universe they exist in.

This means that Dr. Doug Wallace might be on “the wrong side” of understanding too.  It is not energy that is key to the black swan mitochondriac……..it is information transfer that is MOST critical.

I think what Doug has found in the inter-mitochondrial junctions (IMJ) of mitochondria is not just tied to energy (see bottom right of pic below).    IMJ’s are electron dense structures.  IMJ’s are conserved across species, resistant to genetic disruption of cristae organization, dynamically modulated by mitochondrial bioenergetics, independent of known inter-mitochondrial tethering proteins mitofusins and are rapidly induced by the stable rapprochement of organelles via inducible synthetic linker technology.  The information from eleectrons protons and light appears to lead to the rearrangements in the cristae maybe the key to how energy is made.  Wallace has focused on the energy angle because that is all he can measure.  Information transfer from quantum spin to angular momentum is not easy to measure in living systems.  We know information transfer show macroscopic shape changes in matter.  The changing crystals in proteins, lipids, and water is critical to understanding how information alters physiologic function.

 

 

It should be obvious this new idea in quantum thermodynamics is massively important to a mitochondriac, but one has to be careful with this concept, because information does behave differently than other physical properties, like power, torque, and space-time.

HOW DOES THIS SITUATION LOOK TO AN OBSERVER IN A CELL?

Information transfer in light is buried in the controls in autophagy and apoptosis when they are coupled at a quantum level.

What couples them?  Harmonic oscillators in the circadian mechanism, is the answer.

The connection is built via light WIRELESSLY because photons also have a spin.  Few people seem to realize light has a quantum spin number too.  Photons have a quantum spin number of one but the key is light appears to have no limit on how high its angular momentum number can rise to transfer information.  This implies organizational power can be massively concentrated in light waves.   This is why coherent light (laser) appears to raise its OAM as a laser gets powered up.  Angular momentum was recognized as an important property of light after the pioneering works of J.H. Poynting and R.A. Beth showed that a circularly polarized light beam exerts a torque on objects with mass.

 

 

Mammalian mitochondria participate in inter-organelle communication. However, physical structures that enhance or enable interactions between mitochondria have not been defined. I believe light is the connecting fabric. Below you can see all the areas and spaces in which information can be carried.

 

 

When physicists have looked at light waves headed straight on to a target they have noticed that leading edge of the light wave can look very different. That difference likely carries different data from the environment to proteins, lipids, and water in cells. (pic below)

 

 

Bacteria also communicate with one another via bacterial quorum sensing and I believe mitochondria share data via photons in much the same way as bacteria do.

HOW DO WE GET THE INFORMATION? 

We get it from our surfaces.  The eye, skin, gut, and lung surfaces.

In my opinion, with time it will be proven surface quantum effects within the skin and gut is more important than biochemistry of these organs for humans.  The light these surfaces gain use the information to control biochemistry below their surfaces transferring the data from quantum spin numbers to orbital angular momentum of things in our cells. 

For example, sunlight increases the redox potential in our blood to affect the temperature, pressure and peroxiredoxins in RBC’s.

Peroxiredoxins are regulated by phosphorylation, redox status, acetylation, nitration, truncation and oligomerization states in the blood plasma.  This is why young animals blood help keeps older animals mitochondria younger in parabiosis studies.  The proton information is shared into the matrix and this changes what is possible physiologically.

Parabiosis and transfusion of young blood have strong anti-aging effects.  Parabiosis is the surgical union of two organisms resulting in the development of a single, shared circulatory system. When animals of different ages are conjoined (i.e. heterochronic parabiosis), blood-borne factors from the younger animal can often beneficially affect the older animal and recapitulate the youthful phenotype & function in target tissues.

Parabiosis experiments will not work without  CREB.  CREB is short for cAMP response element.  Cyclic AMP (cAMP) regulates the expression of many genes via a conserved gene promoter element.   CREB is that element.  CREB is a nuclear factor that is regulated by protein kinase A phosphorylation.  Inorganic phosphorus in the blood can interact with light and electrons to stimulate cAMP creation in blood.  CREB is stimulated by sunlight hitting our skin.  CREB is also critical in controling circadian cycles in animals.

 

 

These two systems are harmonic oscillators with one another that need to be properly coupled by protons and sunlight to work together. What connects these two oscillators in our body?  Water networks do in both organs. Why don’t we realize it? Sunlight makes the water in our cells and our arteries a liquid crystalline PLASMA.

What is the other plasma that links the sun to our blood in our eyes, skin, and gut?  The ionospheric skin of Earth.

This is the plasma right over your head literally and figuratively at all times.  You live within this plasma.  Changes to that plasma via geo-engineering can also affect the peroxiredoxins in our blood.  Peroxiredoxins are heme proteins that also react to red light from the sun.  They are ubiquitous in all forms of life and the key to understanding how the circadian mechanism works with proton spin and angula rmomentum in your tissues.  The levers that control how quantum spin of electrons and protons inside of you is controlled by the plasma in you and around you.  Sunlight powers the system and the biophysical lever of sunlight must traverse the plasma on Earth called the ionosphere to get to you to do its magic.

ONCE THE SUN GETS THROUGH YOUR OPTICAL WINDOW

When sunlight and blood plasma interact another phase transition occurs to allow information and energy transfer.  This is how the blood plasma becomes another plasma in water.  I covered this in the Quantum biology blog series in detail.  I also followed it up in Tensegrity #13.  Bulk water is changed to a a liquid crystal.  It is called an exclusion zone.  What does it exclude?  Anything larger than a PROTON.  

It turns out, it excludes deuterium too because of this reason…….and this is how we get rid of deuterium and how we direct it to where it needs to be.  Might this fit Maxwell’s description above for the demon and the trap door?

 

The blood plasma is loaded with deuterium (pic above) yet the mitochondrial environment is devoid of it.  What is the trap door between these two areas?  Could it be sunlight and water that makes the EZ?  Does it use something else to accomplish this task?  Could this be why we have so many uncoupling proteins in the matrix?  Yes.

That EZ water is created inside cells and it fills the outer mitochondrial membrane space to be distributed to surround all proteins in us.   Our mitochondrial matrix and cytosol around the matrix makes DDW using H+ while avoiding deuterium to make this plasma;  this is how eukaryotes brought the sea to a land-based existence.  It needed to use the water cycle in the ionopshere to give it a boost by lowering the deuterium levels in rain compare to seawater.  Humans really used this to evolve from chimps because of how the environment changed in the East African Rift Zone 4-6 million years ago.  The change in sunlight and protons over 3 tectonic plates over a massive magnetic flux is what drove this process. If you look at the picture below imagine a human on top of the moutain and a chimp on the surface.  What changes would you see in protons in that case?

 

 

The liquid crystalline state = builds coherent water networks that provide millions of free electrons to drive biochemical pathways = exclusion zone water = excludes protons and deuterium = creates a bounty of them in blood = travels via ECF to delivery energy and information over the entrie animal instantaneously.

THE QUANTUM THERMODYNAMICS OF WATER

Liquid crystalline water possesses long-range orientational order by pointing all the molecules in the same direction. It also allows for a translational order that allows them to keep their position as they move. Think about my rhubarb cuts abive now.  Sunlight makes cuts in water because certain mosaics in light create crystalline hydrogen networks in water.  Not all are the same.  I talked about two state water in the Quantum biology blogs long ago.  Liquid crystals are mobile and flexible and highly responsive to the power density of EMF’s around them.  Our cells and tissues are optimized to solar EMF’s, not man made ones.  This is only one octave of 73 octaves in the entire light spectrum.   If we are afflicted by nnEMF the resultant free radical signals are not the same as they are when sun shines on our tissues.  Free radicals have one unpaired electron and protons are programmed as they are made.  Any time free radicals increase so does the amount of ELF-UV light a cell emits.  (See pg 74-95 in Van Wijk’s book)

 

 

This changes optical signaling in cells.  When signaling is changes quantum probabilities are altered.  This means energy and information is entangled and exchanged within the cell to build order.   This allows them to undergo rapid changes in orientation or phase transitions when energy is added or subtracted from the water and can be shared with the surfaces of proteins.  Remember all human proteins are hydrated or they cannot work. This is why cell water responds vigorously to electric or magnetic fields of ANY light radiations we experience in our environment.

Is this curious set of circumstances why water responds vigorously to temperature, pressure, pH, hydration, and concentrations of inorganic ions like phosphorus and iodine in tissues linked to the ECF????

Yep.

I told you in the Tensegrity #6 blog hydrogen can also act as a group 7 halogen.  This means ‘light hydrogen’ can gain electrons to become a non metal.  When hydrogen does this in an aqueous environment, and when it is associated with iodine atoms, it forms an ionic liquid. Ionic liquids are now receiving special attention in science, owing to their unique properties such as high ionic conductivity, non-volatility and non-flammability.  This ability makes these fluids versatile alternatives to conventional solvent-based systems used to make batteries, fuel cells, and super capacitors that hold large charges.

Water is unique because it can be both an acceptor and a donor of hydrogen (H+). It means water can be a “switch hitter” in many biochemical reactions in cells.  This is why water is the universal solvent on Earth.

A biological cell is fundamentally a dissipative system by its very nature.  It is a playground for light rays.  A dissipative system is a thermodynamically open system which is operating far from thermodynamic equilibrium in an environment/plasma with which it constantly exchanges energy, information, and matter.  This implies when water is hit by sunlight and becomes an ionic plasma (EZ) that has the purpose to break symmetry in nature.  This singular act creates a metastable system in our tissues to react to all environmental possibilities/probabilities that the cell may face. Water is the molecule that allows a cell to break symmetry in nature.  When water is confined in microtubules (below 1.4nm), it is done this way in cells to maximize its ability to transfer energy and information to the surrounding neurons.  (OSF 3 blog)

All these things are vital in understanding the quantum thermodynamics of life.

Iodine-hydrogen bonding in aqueous environments are also quite helpful as heat-transfer fluids to move infrared energies within a system.  Iodine’s addition to iodide-based ionic liquids leads to extraordinarily efficient charge transport, vastly exceeding that expected for a standard viscous liquid crystalline system.  You saw above that turning water from a bulk fluid to a liquid crystalline structure is the key thermodynamic step life uses to capture energy and information in protons and electrons.  What you need to understand is that just touching a protein can lead to a thermodynamic change.

Where does the blood and matrix touch one another?

The TCA cycle and urea cycle are linked in the cytosol by fumerase.  This is right outside the cell membrane.   How is the infromation from H+ or deuterium transferred to mitochondria to alter the spin rate of both cycles?  All mitochondria rely on a stream of proteins to sustain their energy production. Nearly all their proteins are manufactured in the surrounding gel-like cytoplasm, and must be imported into the mitochondria to keep the powerhouse running.  This is where cytosolic fumerase exists.

WHY IS DEUTERIUM A PROBLEM FOR LIFE IN THE MATRIX AND NOT THE BLOOD?

In the blood plasma, deuterium is not a problem.  It is necessary for function as you’ll soon find out.  In the mitochondrial matirx it can be a real problem when oxygen is around.  The TCA cycle and urea cycle use oxygen as their terminal electron accpetor.  That is not true with other metabolic pathways.  When oxygen is low it acts as a metabolic controller of anions in the TCA and urea cycle.  This control area is called “Kreb’s Bicycle.”

HOW DOES THIS WORK IN THE BRAIN?

Hydrogen and iodine form an ionic plasma within CSF of the human brain.  Deuterium and iodine form a very unusual bond because of the kinetic isotope effect between these two atoms.   The choroid plexus of the human brain is designed to add iodine to CSF.  CSF, you will recall is an ultra-filtrate of blood plasma and is made up of 99.3% water with 150ppm of deuterium.

Grotthuss was the first person to realize the correct concept for the charge transport in electrolytes using iodine as the transfer mechanism; and it still remains valid for the charge transport in water.  The Grotthuss mechanism allows for protons (H+) cable construction within an ionic fluid by using a current of  protons that use a “hopping mechanism.”  That “hopping mechanism” is referred to as quantum tunneling of protons.  Quantum tunneling of protons becomes more probable the smaller the mass of the cation is, and the proton is the lightest possible stable cation on Earth.

Deuterium is DOUBLE THE ATOMIC MASS of H+.

Iodine and iodides turbocharges H+ that are excluded in cell water;  this ability occurs by turning the sea of protons into a positively charged ionic plasma.  This is why the thyroid gland, choroid plexus, and intestinal gut lining all concentrate iodine and iodides and H+.  The mitochondrial matrix concentrates it 1,000 fold compared to the blood plasma.

What about the brain CSF?

When iodine meets water that has been charged separated by IR/UV light or by the hydrophilic proteins in the dura matter covering the brain’s neurocortex, we become able to exclude a massive amount of H+ in the CSF.

Since iodine/iodides become able to further condense the excluded H+ from the EZ.  This makes the hydrogen (H+) ions come closer together at the atomic level.  The H+ excluded is then used to make proton cables in water networks to make positive electric currents used for energy and information transfer in the brain.  Is this the brains biggest information collection scheme that fuels our instincts and subconscious with knowledge?

Is this why lions and hippos know what to do when they are born????

The brain specializes in both operations in every living thing on Earth with one.  The only difference is how efficient each brain is using these protons.   The exclusion zone (EZ) also excludes deuterium to the blood plasma,  because it is LARGER than H+. The more deuterium in the brain the less proton cabling can be formed in CSF.  This leads to cognitive haze and neurologic decline.  Remember, H+ is equivalent to a proton.  Deuterium is a proton and a neutron bonded together = larger atomic mass = loss of energy and information transfer via “quantum thermodynamics” 

Using the Grotthuss mechanism, iodine is able to move protons (H+) closer together than we would normally expect, to alter their hydrogen bonding network to allow them to form superconducting proton cables that act like a positively charge electric current.  The Grotthuss mechanism does not work properly with deuterium because of its larger atomic size.  Iodine condenses and makes the H+ cabling in water more likely by making hydrogen bonding networks in water more DENSE.  It cannot do this when deuterium is in the aqueous environment because of kinetic isotope effect.

The Grotthuss mechanism between iodine and H+ allows for charges to be transported not by the movement of protons, by the breaking and reformation of chemical bonds EASILY. Deuterium impedes the breaking and reformation of chemical bonds because of the kinetic isotope effect between iodine and deuterium.  This alters the hydrogen bonding networks in cell water.  As water is charge separated by UV/IR light or by hydrophilic substances, excess H+ ions are made adjacent to surfaces in cells like cell membranes and collagen. Gerald Pollack’s experiments have shown this actually occurs in nafion.   The excluded protons become capable of diffusing through the hydrogen bond network of water molecules (iodized CSF) through the formation or cleavage of covalent bonds.

WHY IS ASYMMETRY FAVORED BY NATURE?

Symmetry is broken by any phase transition in any chemical reaction.  This is also true in biochemistry.   Any time symmetry is broken, energy and information transfers, and the law that controls the proces is the second law of thermodynamics.  

This post is all about the “quantum thermodynamics” in a living system.  This occurs many times in biochemical reaction of cells when they are using hydrogen in specific parts of biochemical substrates.   The picture below shows you just how specific the movement of H+ and deuterium is controled in biochemical substrates of the TCA cycle.

 

 

The specificity of where deuterium can or should be is the ONLY reason why carbohydrates out of season are killers for our health span. Humans are omnivores and can eat carbohydrates when nature’s quality assurance programs built by chloroplasts and mitochondrion remain intact by the circadian mechanism.

You can see the Vitamin B5 need for fatty acids entering the cycle (acetyl Co A) Comparison of metabolic profile changes associated with:

1) natural deuterium depletion by low deuterium fatty acid oxidation. Avastin® and Glivec® exert similar effect and require intact mitochondria for efficacy (Red boxes #1)

2) low deuterium metabolic water recycling from the mitochondrial matrix during citrate, isocitrate and malate formation; the target of fumarate hydratase activation and hyperbaric oxygen treatment combined with a ketogenic diet (Red box #2).

Mitochondrial shuttles, such as the malate shuttle, pass low deuterium carrying fatty acid carbons to gluconeogenesis, where glyceraldehyde-3-phosphate becomes the source of extensive carbon exchange reactions for the non-oxidative pentose cycle to maintain low deuterium saturation in C3’-C5’ pentose sugar carbon positions in RNA and DNA  (Red box #3).

This ^^^^ is where cancers really come from.  Cancers are due to a loss of information in the system and this uncouples autophagy from apoptosis in mitochondria.  The May 2018 webinar is really going to make this concept ridiculous simple to understand.  This blog is not simple by design.  It is being written for the scientist critic.  I implore the non scientist to take your time getting these details down because they are critical to the remainder of the series. 

When too much deuterium is in the C3′-C5′ you can bet cancers will be following.  It appears from the data I have found over 13 years that if we can keep our deuterium levels below 135 ppm in the matrix and cytosol the chances of cancer drop dramatically.  The best way to follow that level is using the calcium index score I mentioned in CPC #23 blog.  The blood plasma fraction is unimportant in to this mechanism.  This area is not well studied, except in the history of the building of the MRI machine by Damadian.  If you want more information on it read this book below.  You also might want to read Damadian’s book about building the MRI machine.  It is eye opening for the mitochondriac.

 

 

These are the carbon sites are where DNA stability, radiation, and chemotherapy derived hydroxyl radical sensitivities that are regulated by hydrogen/deuterium fractionation methods.  This is due to primary and secondary intrinsic kinetic isotope effects in the anions in the TCA and urea cycle at the junction of Kreb’s bicycle where fumerase joins the urea and TCA cycles.  This process  is partially controlled by collective proton tunneling at fumerase.  The protons must be H+ that impart that wisdom to the mitochondria.

Besides the C3’–C5’ nucleic acid sugar backbone fragment, de novo nucleic acid base syntheses, hydrogen bonding and deuterium channeling into hydrogen bonds are controlled by the serine oxidation glycine cleavage single carbon cycle pathways [SOGC pathway mentioned in previous patreon blogs] (Red box #4).

Serine use is actually a better hack for oral melatonin use to improve sleep by improving autophagy if you understand this blog.  This is a critical link to make as the series goes on.

When tumor cells revert to the Warburg phenotype and reductive carboxylation-driven mitochondria, deuterium depletion in free (drinking) water becomes the only deuterium depleting mechanism for specific carbon sites in nucleic acid backbone sugars and the bases (Red box #5). This is the 5G mitochondrial pathways you should get facile with.

KREB’S BICYCLE IS THE CRITICAL TAKE HOME

So the take home is that deuterium limits the breaks in symmetry in nature because it limits the movement of anionic substrates in both cycles by its actions at fumerase.  Why is this bad for nature?

Nature needs hydrogen to be constantly on the move in our mitochondria when oxygen is present to share data.  When the environment is pseudohypoxic or hypoxic it must use glycolysis and the PPP for biosynthesis (EMF4).  Protons cannot share information quanta when this occurs.  This means our tissues are not as wise as they could be.  They are in a state of suspended animation and growth is limited.  That leads to redox changes in our mitochondria to make sure growth is controlled.

As such, all breaks of symmetry in biochemistry require a transfer of energy and information by the laws of physics to satisfy the Second Law of Thermodynamics.

Symmetry is also broken any time temperature rises or falls when electrons or protons are moving in any biochemical reactions. Don’t the uncoupling proteins play a huge role in temperature changes in the matrix of mitochondria?  Yes they do.  Is this the demons trap door?

Yep.

Any transfer of energy has the potential to break symmetry and therefore to give rise to emergent properties in the protein polymers or products of these reactions.  This is really how evolution works. Darwin’s theory leaves a lot to be desired.

I think the entire universe is powered by water electricity (negative/positive) and I believe every cell is powered in the same way using the same quantum thermodynamic laws. Water is the universal electron and proton donor.   Why?

When you understand these concepts, you begin to see that proton and electron currents in water made by sunlight create currents inside of cells and over extracellular distances that are capable of delivering physical and chemical messages concerning the energy and information redox status of all parts of the cell. Redox has two sides to understand.  Prior to now, we have only focused on energy and ignored information.

Water networks communicate this information to lipid, proteins and DNA.

TIME7

SUMMARY

Life does not violate the second law of thermodynamics, but it utilizes the information quanta in electrons protons and photons.  It is this side of thermodynamics we fail to account for in mitochondrial biology today. 

Until recently, physicists were unable to use thermodynamics to explain why it should arise in the first place. In Schrödinger’s day, they could solve the equations of thermodynamics only for closed systems in equilibrium. In the 1960s, the Belgian physicist Ilya Prigogine made progress on predicting the behavior of open systems weakly driven by external energy sources. But the behavior of systems that are far from equilibrium (life), which are connected to the outside environment and strongly driven by external sources of energy, could not be predicted because we had no idea how information was being shared.

This situation changed in the late 1990s, due primarily to the work of Chris Jarzynski, now at the University of Maryland, and Gavin Crooks, now at Lawrence Berkeley National Laboratory. Jarzynski and Crooks showed that the entropy produced by a thermodynamic process, such as the cooling of a cup of coffee, corresponds to a simple ratio: the probability that the atoms will undergo that process divided by their probability of undergoing the reverse process (that is, spontaneously interacting in such a way that the coffee warms up). 

As entropy production increases, so does this ratio: A system’s behavior becomes more and more “irreversible.” The simple yet rigorous formula could in principle be applied to any thermodynamic process, no matter how fast or far from equilibrium it is at any time. Our understanding of far-from-equilibrium statistical mechanics greatly improved, and now some scientists have decided to apply the new knowledge of statistical physics to biology.  This will open the door widely to quantum biology.  It is why I am very optimistic about the future of medicine.  

Change is coming and no one seems to see what it will lead too for humans.  

Living quantum nanomachines inside of our cells appear to be able to do some unique things with respect to infromation quanta.  This occurs because living systems are sometimes able to extract the work much more quickly, giving them more power and range using information over energy flux.  This is what allows life to organize to do the things we observe it to do.  Life is capable of some amazing emergent properties, like consciousness.  The smaller our quantum nanomachines get, the more efficient they become in extracting information from the spin of electrons and protons.  This explains fundamentally why mitochondrial prefer H+ over the heavier deuterium isotope.  Deuterium is useful in the blood plasma for another reason I will reveal soon.

What the mitochondriac will like about quantum thermodynamics is that “you have these two fundamental quantities — energy and quantum information — and these two things meet together in living systems to bring the diversity we observe in reality.   How it happens is the story that will be built by quantum biologists, clinicians, thermodynamic specialists.  This is my new job description.

DNA is really a switchboard for sunlight cells trap. Interestingly, the code is self referencing and regions of it are co-dependent irreducably complex.  Maintaining the system far from equilibrium is what DHA from seafood does in the cell membrane structure of eukaryotes. In fact, living oyster reefs, have been shown to dissipate wave energy in the oceans.  It turns out their matter does the very same thing inside of our tissues.  This is why oysters are at the top of the list for mitochondriacs. The patterns in us, is built by the sun, and builds organization in us that is tied to entropy.  This entropy is what organizes what life is all about.

In today’s medical environment…….my science is alien because of how I look through the lens of reality, but the reasons supporting my beliefs are 100% native and natural to Earth, to humans in their native form………it offends the modern beliefs of science, however. It’s my particular way of looking at the world that offends others common sense because it’s typically not how we experience life to interpret science, and certainly not how we experience other selves. But it seems to me that you can also get an interesting thought out of this one, if you turn it the other way around, and ask if science, properly, is something you “look through”. So the scientific method has been effective because it excludes everything that is unobservable in terms of measurement and quantification. This is precisely what allowed the scientific revolution to take off long ago.  Today the revolution is a stalled paradigm because the things we cannot observe and measure are the things that are critical to disease reversals.

 

Sometimes we don’t choose our path. It chooses us…….and it then becomes our job to carry the message no matter how much it pisses off the ignorant. You only get mad because you now might realize you’ve been duped by “experts” for so long. You now know what the essence of the Dunning Kruger effect really is. I could care less what anyone thinks about me, I’d rather be their wake up call than everyone’s cup of tea.

CITES:

http://aip.scitation.org/doi/abs/10.1063/1.1734134

https://www.quantamagazine.org/scant-evidence-of-power-laws-found-in-real-world-networks-20180215/

https://theconversation.com/amp/the-surprising-benefits-of-oysters-and-no-its-not-what-youre-thinking-90697

https://www.psychologytoday.com/blog/the-athletes-way/201607/vagus-nerve-stimulation-dramatically-reduces-inflammation

J. H. Poynting, Proc. Roy. Soc. A82, 560 (1909).
R. A. Beth, Phys. Rev. 50, 115 (1936).

https://www.nature.com/articles/ncomms7259

http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0048046

https://phys.org/news/2018-04-scientists-pathway-protein-import-mitochondria.html#jCp

Electric fields control embryonic development and morphogenesis and wound healing through directing and enhancing cell migration and proliferation. They also control who gets heart disease and atherosclerosis. However, details pertaining to electric sensing of cells remain unclear to the paradigm if you read their literature. It is pretty clear cut in the bio-physical data. We need to eat saturated fat to maintain our coulomb electrostatic force in the mitochondrial matrix to maintain our redox potential. Being in the sun makes this easy. Many studies have reported involvement of different cell surface proteins, yet the identity of the electric field sensor is unknown to the paradigm. For my mitochondriac misfits it is linked to cholesterol, sphingolipids, DHA, and all the lipid rafts in our arteries. This is true in even in those with hypercholesterolemia. This slide below will seem out of place to some but after the next few blogs and webinar you will realize why it is tied to the CAC score for 5G. Sunlight increase inorganic Phosphorus in the blood and this is a key marker how a CAC goes wrong in people afflicted with a 5G environment. My members will be getting this data soon.

 

 

High cholesterol means nothing if there is no calcium in your arteries. properly charge ipid rafts in arteies make you resistant to heart disease. They act as the primary sensor to electric field-induced directional cell migration for morphogenesis, pathologic plaque formation, and sustained blood flow as we age. These nanodomains in lipid rafts respond to electric fields from sunlight as mobile complexes that polarize, coalesce, and partition membrane proteins and in turn activate intracellular signaling events to orient cell migration and keep our vessels patent and responsive to the nitric oxide effects of sunlight.

 

 

K2 is a vitamin that is a lipid and part of the lipid raft in arteries. Lipid rafts are electric field sensors in vessels. They are there to sense the electric fields of sunlight after they crash into RBC’s in the blood plasma. How does the blood plasma get closer to the skin surface? Sunlight stimulates the release of nitric oxide to bring the vessels closer to the skin for blood to be irradiated by sunlight. That is how it works. K2 is a vitamin made by the gut microbiome using light release from the prokaryotes there. Bacteria (prokaryotes) are well known to release 5000 times more ELF-UV light than our cells. You’ll be rewarded soon with where I think the ELF-UV signal comes from directly in the May 2018 webinar. Since K2 is made from aromatic amino acids these aromatic rings of this chemical made by symbionts in out gut capture the light released and create Vitamin K2.

 

 

This K2 is then ferried by more lipid carriers in blood that also are electric field sensors for sunlight for deposition in your arterial wall that wait for the sunlight stimulus to do their part in keeping you healthy in full spectrum sunlight. Tracking your plaque index is possible these days using Xray. I am not a fan of this test chronically but it is not a bad idea to do when you decide to initially become a mitochondriac one time to get a baseline assessment. There is another indirect assessment of vitamin K2 activity that gets straight to the heart of the calcium paradox that is tumping the lipidologists today. Coronary artery calcium scoring is a specialized type of ultra-fast X-ray (not fast enough for me) imaging that measures the presence and amount of calcium buildup in the arteries that supply blood and oxygen to your heart. If your main goal of K2 replacement with foods or supplementation is reducing your risk of heart attack, this might be an important test to take, to measure that risk. Sunlight exposure increases K2 creation by your microbiome.

 

 

Coronary artery calcium (CAC) scoring, also called calcium score or heart scan, is a technique that uses computed tomography (CT) scanning technology to quantify the volume and density of calcium in each of your coronary arteries. The calcium presence is calculated to give you a “score” or number that represents your arterial calcium burden in your arteries and this effects the amount of NO present to vasodialate our circulation in a mitochondrial stresses environment. In my view in 2018, this is the best test for heteroplasmy in your body.

Tom Petty could have used this blog before he died. Remember that arterial calcification is an active process mediated by bone-building cells present in bone marrow and this is connected to the blood plasma system to make connections globally in the body over hydrogen bonding networks in blood. (93% water by volume). K2 is a quinone that whose production in the gut is stimulated by sunlight exposure. This is why Vitamin K2 and UVA and IRA light exposure are tightly coupled to get proper arterial physiology. UVA light slows ECT via the NO effect and red light from IRA can affect the 4 red light chromophores in cyctochrome c oxidase to increase the spin rate of the Fo head of the ATPase to effect the spin rate tied to H+. The food guru and supplement makers have no idea that sunlight can slow ECT while speeding up ATPase hydrogen movement of H+. A lack of sunlight leads to a lack of Vitamin K2 production.

A lack of K2 causes calcium to accumulate, and NO to decline, within plaque in a consistent ratio, occupying about 20 percent of plaque volume. For that reason, the amount of arterial calcium detected with a heart scan reflects the buildup of atherosclerotic plaque and the higher stimulus from sunlight required to get the same effect if the local mitochondria heteroplasmy levels were LOWER.

 

 

In cardiac disease they are always elevated. Heart disease is related to a higher heteroplasmy rate. We know that in cardiac muscle there is a loss of alignment of the IMJ’s around lipid droplets in the heart. The bottom right corner of the slide shows how IMJ alignment marries to heart muscle power.

 

This CAC test cannot directly tell us that, but it indirectly implies physiologic power to the mitchondriac. Vitamin K2 deficiency isn’t the only factor contributing to heart disease, but undercarboxylated MGP (matrix gla protein) levels, a sure sign of K2 deficiency, do correlate to the severity of arterial calcification and the CAC score. I wrote about this in my K2 blogs on my old site. The new site is going live this month, in case you did not know The greater the degree of K2 deficiency, the greater your NO decline in your vessels, and the higher the calcium score will be. It also implies you heteroplasmy rate is rising and the amount of infromation you can harvest from sunlight has DECLINED.

 

 

A high CAC score on electron beam computed tomography— is a precise type of CT, discussed in this book below. It turns out to be a way better predictor of morbity and mortality than is age is because it is an indirect measure of heteroplasmy rates in your coronary bed and heart. We are only as strong as our weakest link in quantum biology. That means you are as old as your arteries and this test will tell you If you need more sunlight than your current environment could provide. This could lead you to migrating to abetter location to get healthier. For example, if you are a 60-year-old man with a low CAC score, there’s a good chance you’ll live to a ripe old age. On the flipside, if you are a 45-year-old man with a heavy calcium plaque burden, low NO levels, and higher heteroplasmy rates your more likely to become a “Tom Petty” heartbreak hotel situation. Heart disease is major killer of humans today because it is a circadian disease too! Most people die at dawn. Your are more likely to be one of the unfortunate souls who suffer a massive heart attack at age 50— if you don’t take action to prevent it by lowering your blue light life and nnEMF burdens. I believe the CAC is the best test for a 5G world. For my members I will be going into new tests to follow as 5G is live. For people who choose to become patients at the Kruse Longevity Center you will be on the absolute cutting edge of mitohacking.

 

 

5G reality: Sudden death from heart attack is much more highly correlated with arterial calcification than with altered cholesterol panels based upon the latest in the literature. Sudden death from a heart attack is going to be very common in a 5G world. You might not hear that in the office because the data is relatively new to most clinicians. The biggest advantage of CAC scoring is that it quantifies your risk of heart attack and is a decent indirect measure of heteroplasmy rate in the heart. It is a hack I did a long time ago and I thought I’d mention it here. A low score means low risk, a high score means a high risk. No other risk factor offers that kind of graded risk assessment currently. I want you all to remember that in a 5G world the best tests will change as we see the heterogenity in the 5G spectrum vary from zip code to zip code as I have covered in the member Q & A’s the last few months.

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