1. When inflammation is present in the brain (excess protons or too few electrons), the three fundamental laws of nature are altered in our tissues. This causes them to decrease their ability to deliver higher levels of oxygen to the neocortex below to maintain proper cognitive function. This decreased oxygen density over specific portions of the neocortex acts to limit its function, relative to other areas of the neocortex by changing proton conduction.
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2. This single event uncouples mitochondrion in the neocortex and it raises that neuron’s basal metabolic rate. A chronic raised basal metabolic rate leads to cerebrovascular diseases because it increases mitochondrial respiration and the amount of physiologic work a cell has to do. This is why ALL brain diseases are associated with atherosclerosis at a core level. This is precisely how leptin resistance causes a neuro-cognitive decline in humans.
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3. The CSF around the hypothalamus becomes less dense and has a higher temperature with higher levels of cytokines in it, causing us to lose energy/info to the environment. We’ve known for a long time that only two things lower metabolic rates in living things, strong solar stimulus, and cooling. This changes the hydrogen bonding network possible in CSF. The problem for medicine is that these scaling laws of energy flux have not made it into clinical medicine as yet. This loss of energy means less oxygen is delivered to the neurons in the hypothalamus, which is designed to work optimally when there is harmony and energy balance in humans.
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4. This is why in EMF 2, I told you the leptin receptor was an ‘account’ of photons, protons, and electrons. All bits of matter that make things up roughly have equal numbers of electrons and protons. The number of photons varies. The basics of what most people forget are that if this were not so, there would be an excess of a positive or negative charge, and this would create a massive force pushing all the excess charge out, leaving behind a core group of neutral charges.
5. When sunlight moves electrons/protons in us with the energy in light waves it alters the arrangement of our bio-molecules and changes their thermodynamics. A change in an arrangement is a change in the "information" in the system. Different molecular arrangements have different energies/information associated with them. This difference in energy/info is how bio-molecules are quantized to light frequencies. It also explains how metabolic networks became coupled to terrestrial solar frequencies.
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6. The brain evolved, I believe to order this process using solar frequencies between 250-780 nm. The circadian signals are how that energy harmony is translated from the outside world to the inner workings of biochemistry. When these signals are off for any reason at all, we begin to lose energy to our environment by emitting black box radiation from our bodies. Essentially, we are losing captured sunlight, and this decreases the amount of physiologic work a cell can do. This means in illness cells are losing energy at the vibrational or electronic level and can no longer remain a dissipative structure.

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7. Prigogine defined dissipative structures and their role in thermodynamic systems far from equilibrium, a discovery that won him the Nobel Prize in Chemistry in 1977. In summary, Ilya Prigogine discovered that the importation and dissipation of energy into chemical systems could result in the emergence of new structures (hence dissipative structures) due to internal self-reorganization. In his 1955 text, Prigogine drew connections between dissipative structures and the Rayleigh-Bénard instability, and the Turing mechanism.  Prigogine's theorem is germane to these ideas.

Mitochondria are dissipative structures in cells, but not the only ones.  They transform energy and create order from the disorder in light energy they use to operate.  The water mitochondria create is probably the single most important dissipative structure that life is based upon in cells.  According to Prigogine, determinism loses its explanatory power in the face of irreversibility and instability in dissipative systems. This is a major departure from the approach of Newton, Einstein, and Schrödinger, all of whom expressed their theories in terms of deterministic equations.
8. Indeterminism is the opposite of determinism and is related to chance.  Chance is related to probability. In science, most specifically quantum theory in physics links directly to probability and not cause and effect.  Indeterminism is the belief that no event is certain and the entire outcome of anything is probabilistic. Heisenberg's uncertainty principle and the "Born rule", proposed by Max Born, are often starting points in support of the indeterministic nature of the universe.  Indeterminism is also asserted by Sir Arthur Eddington and Murray Gell-Mann. Indeterminism has been promoted by the French biologist Jacques Monod's essay "Chance and Necessity". Ilya Prigogine argued for indeterminism in complex systems.
9. At life's genesis chaos has to gain order.  Dissipative structure theory really aims to solve this problem for biology by using physics.
Dissipative structure theory led to pioneering research in self-organizing systems, as well as philosophical inquiries into the formation of complexity on biological entities and the quest for a creative and irreversible role of time in the natural sciences.

There is a well-known theorem of minimum entropy production derived by Prigogine, which states that entropy exported from a system reaches a minimum, or becomes zero, at thermodynamic equilibrium and at steady states close to thermodynamic equilibrium. Prigogine's theorem is a direct consequence of Onsager's reciprocity relationship which holds at steady states close to thermodynamic equilibrium. The principle of internal entropy compensation, is in addition to, and implies the principle of minimum entropy production, and may even be valid in regimes far from thermodynamic equilibrium.
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10. He had some very interesting things to say about TIME in his work and Nobel Prize speech.  You should watch it sometime. I think they are key to understanding circadian biology and timing. All of our time reversible equations in physics created by Newton, Einstein, and Schrödinger describe a simplification of what actually occurs in nature. We live our lives with eyes blinkered, dismissing reality as the exception to our neatly formed approximations of what time really is.
11. Time is a critical issue for dissipative systems.  While most current thermodynamical analyses used in biology completely ignore space-time structure, the “thermodynamics of organized complexity” applying to living systems depends WHOLLY on space-time heterogeneity, which allows ‘free’ variation of microscopic states within macroscopic constraints.  THIS DEFINES WHAT A MITOCHONDRIA WAS DESIGNED TO DO AND TO BE IN A VARYING  EMF FIELD CREATED ON THIS PLANET by the sun.
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12. His theories offer us another possibility of some form of enthalpy-entropy compensation, as mentioned in my work in connection with enzyme catalysis, so that coherent energy is conserved in organelles in the cell, with no entropy generated. This is maintained by the atomic organization of atoms in a cell. The system could be arbitrarily far away from equilibrium, so long as, at some sufficiently macroscopic space-time of interest, the overall balance is attained, and the net entropy production of the system either vanishes or reaches a minimum.

The internal balance of entropy production means that the system maintains its organized heterogeneity or dynamic order. It is in turn dependent on energy flow being symmetrically coupled and cyclically closed over the system as a whole. In other words, it depends on the validity of Onsager's reciprocity relationship in systems far from thermodynamic equilibrium.
13. Circadian time stamping is done AFTER DNA is translated. This implies that the genetic code is not the primary issue in diseases and health creation. Time stamping is due to his theorems of Prigogine. Circadian time stamping also puts undue stress on our cell’s mitochondrion and they begin to act less like a part of our cellular design and more like a captured slave bacteria that they really are.  Since a mitochondrion has bacterial origins, most of man’s chronic diseases look like infectious diseases at the core.  This is deceptive because this viewpoint does not go down to the most critical level to understand how subatomic charged particles behave at small scales with the electromagnetic forces that light waves can impart to them.
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14. One of the hallmarks of the living system in cells is that they are exquisitely sensitive to specific, weak signals. Most of these signals are electromagnetic in nature. The human eye can detect single photons falling on the retina, which pass information directly to the SCN and all its mitochondria. This retina is where the light-sensitive photoreceptors in cells send out an action potential that represents a million-fold amplification of the energy in the photon. This defines what a non-linear stimulus is. Some of you know it by the butterfly effect.

It is not just a property of the central retinal pathways. The entire system is a plasma or syncytium of excitable matter ready to react to the environment's EMF signals. Similarly, a few molecules of pheromones in the air are sufficient to attract male insects to their mates. This sensitivity is characteristic of all parts of the system and is a consequence of the energy stored = related to the AMO physics of organization.

No part of the system has to be pushed or pulled into action, nor be subjected to mechanical regulation and control. Instead, coordinated action of all the parts depends on rapid intercommunication throughout the system because of how it is built to react to light. The organism is a system of “excitable media” (syncytium) — excitable cells and tissues poised to respond specifically and disproportionately to weak signals because a large amount of energy stored everywhere automatically amplifies weak signals. These signals often direct things in cells into macroscopic actions. This is how order is built from chaos in a dissipative structure described by Prigogine's theorem.
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15. Lesson over. Image

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More from @DrJackKruse

May 6
1. Time to de-retard Chad. Since Chad won't read my work this will be the first and last time he will get educated using the tools on my website forum. Lesson begins. READ THE PAPER!!!! Image
2. The core issue is neither the declination angle itself nor its movement, but rather what a "magnetic stall" (a significant drop in the Earth's dipole moment) represents for the planet's atmospheric chemistry.

Your intuition about the poles being "static" in Siberia vs. "moving" hits on a key geodynamic reality: the alignment of magnetic and physical north (\(declination = 0\)) is a marker of a strong, stable geodynamo. When they decouple significantly, it often signals a weakening of the entire protective field.

Why Declination Matters (Biophysically)
The alignment of the magnetic dipole with the rotational axis (True North) is not just a convenience for human evolution; it is a byproduct of a strong, active core.

The Protective Shield: A strong magnetic dipole acts like a "filter" that prevents solar wind from stripping away the atmosphere.

The Oxygen Link: As shown in the Science Advances article I provided you for the 100th time now, there is a powerful correlation between magnetic field strength and atmospheric oxygen levels over the last 540 million years.

The "Magnetic Stall": If the magnetic north pole were to "permanently end up in Siberia" while remaining static and strong, it might not be a problem for humans. However, such a "static offset" is physically unlikely. In geophysics, when the pole drifts far from the rotational axis (high declination) or wanders erratically, it usually indicates the dipole is weakening or "stalling".

You have to put in some work here Chad. This has been covered elsewhere on the forum on my website for other tards like yourself.

youtube.com/watch?v=L2gf_z…
3. Nonzero Declination (Static)

If the field remained strong but tilted (e.g., North Pole in Siberia forever), the primary biological issue would be localized radiation spikes at the "new" poles. Most complex life would likely adapt.

The problem with the current erratic movement toward Siberia is that it reflects instability in the molten outer core not th einner one which got cooked 780,000 years ago just before the Cambrian.

Atmospheric Stripping: A "wandering" or weakening field allows more high-energy particles to penetrate the atmosphere. This can lead to the depletion of the ozone layer and, eventually, the loss of oxygen to space while deuterating and tritiating the food webs below on Earth. This is the real problem in NA and OZ now. Soon will be an African and EU issue due to AMOC collapse.
Read 10 tweets
May 4
1. Ichthyosis vulgaris (IV) is a highly compelling case study for challenging the rigid boundary between pure genetics and epigenetics.

In standard centralized dermatology, IV is classified as a classic Mendelian, autosomal semi-dominant genetic disease caused by loss-of-function mutations in the filaggrin (FLG) gene.

However, from a systems-decentralized biology or quantum biology perspective, the skin’s physical presentation is driven heavily by the epigenetic and environmental constraints forced upon the tissue
2. The Filaggrin Gene is Not the Whole Story

In clinical medicine, finding a "spelling mistake" or null mutation in the FLG gene is considered the ultimate cause of IV. Filaggrin is the key protein that bundles keratin filaments and later breaks down into the "natural moisturizing factor" (NMF) and urocanic acid (which maintains skin pH and acts as a natural sunscreen).

The Epigenetic Disconnect: Many individuals carry heterozygous FLG mutations (haploinsufficiency) and display zero clinical symptoms or only very mild dry skin. Conversely, individuals can present with full clinical IV or severe atopic dermatitis with perfectly normal, unmutated FLG genes.

Promoter Methylation: Research into FLG expression shows that DNA methylation heavily regulates whether the gene is turned on or off. If methylation is deuterated this process is BROKEN. What looks like a genetic problem is really an epigenetic issue. Undifferentiated skin cells can actively suppress the healthy gene through non-CpG island promoter methylation. The genetic code is present, but the epigenetic software is refusing to run it.
3. The Mitochondrial Stress and Energy Tax

Connecting back to the previous discussion on high-turnover clones and the "isotopic tax": the epidermis is constantly renewing itself.

To successfully flatten, enucleate (spit out its nucleus), and form the stratum corneum (the brick-and-mortar skin barrier), a keratinocyte undergoes a massive, highly orchestrated energy-intensive process.

Acquired Ichthyosis: True genetic IV presents at birth or in early childhood. However, acquired ichthyosis occurs in adults who possess perfectly normal genetics.

It is heavily triggered by systemic conditions like Hodgkin's lymphoma, severe acute malnutrition, or new-onset diabetes.

What this reveals: This proves that the "fish scale" phenotype is not solely a product of a broken gene. It is a default failure state of the skin barrier when the body's systemic redox potential drops or metabolic wasting takes over, preventing cells from correctly processing lipids and proteins. Genes are not the be all end all in any disease. Rockefeller medicine wants MDs to believe it to write Rx's.
Read 5 tweets
May 4
1. No Liz. Base chain of DNA/RNA has to be undeuterated to be coherent in its expression if not an aberrent phenotype results.

Let me give you an example. See the pic? It is called cradle cap.

Do you know what centralized pediatricians tell patients with kids who are born with this?Image
2. IS CRADLE CAP A SYMPTOM LIKE JAUNDICE IS, LEADING TO HIGHER HETEROPLAMSY LEVEL?

Children with cradle cap suffer from more metabolic problems later in life pointing out why this is not a temporary mothering hormone issue that centralized science tries to sell to MDs.

My observation highlights a critical pivot in how we understand chronic, systemic diseases. The argument is that if cradle cap (infantile seborrheic dermatitis) were merely a transient reaction to maternal hormones, it would not correlate with long-term metabolic dysfunction later in life.

While the standard centralized medical model focuses on the local, temporary symptom (excess oil and yeast), the perspective of quantum biology and bio-energetics argues that the skin is merely the outward map of internal mitochondrial efficiency and "isotopic tax."

The Conventional Medical View sold to parents is as follows......
In standard dermatology, cradle cap is known as infantile seborrheic dermatitis.
The Mechanism: It is a self-limiting condition characterized by yellowish, greasy plaques and scales on the scalp.
The Clinical Cause: It is primarily attributed to maternal hormones crossing the placenta before birth. These hormones temporarily hyperactivate the infant's sebaceous (oil) glands.
The Microbiome Role: The excess sebum acts as a lipid-rich feeding ground for commensal skin fungi, specifically Malassezia. The inflammatory response to the fungal byproducts causes hyperkeratosis (the sticking together of dead skin cells).Image
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3. The Quantum Biology / "Deuterium Burden" Hypothesis of Kruse
The perspective I've presented operates on the premise that disease and cellular dysfunction are problems of sub-molecular physics and energy transfer rather than just genetic hardwiring or hormonal shifts.

If we apply this specific framework to cradle cap, the hypothesis would be structured as follows: The Follicle as an Energy Sink: As I've noted many times before, hair follicles and their associated sebaceous glands are highly active "clones" demanding immense metabolic energy to fuel continuous cellular turnover.

The Mitochondrial Stutter: In my decentralized framework, mitochondria function as nano-motors. At the center of the ATP synthase motor is a rotating axle propelled by hydrogen ions (protium). Because deuterium is twice the mass of normal hydrogen, its presence in the mitochondrial matrix can physically damage or "stutter" the motor.

The Singlet Trap & Apoptosis: High local concentrations of deuterium within the rapidly dividing follicular cells would reduce the efficiency of the electron transport chain. This causes electron leakage, creates reactive oxygen species (the "singlet trap" heat/entropy), triggers inflammation, and interrupts normal cellular desquamation (shedding).

Here is an analysis of why viewing cradle cap as an early marker of metabolic/deuterium stress, rather than a simple hormonal fluke, that holds weight under my framework.Image
Read 8 tweets
May 3
Do you think you understand vortex biophysics? Here is your test. Why I would never live in TN or Hawaill is based on vortex math and the biophysics of the current magnetic dynamo boundary conditions.

1. forum.jackkruse.com/threads/unders…

2. forum.jackkruse.com/threads/unusua…

You think you get it, but you do not.Image
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2. More on the lesson?

UNDERSTANDING VORTICES OF THE TECTONIC PLATES and YOUR HEART REALLY MATTER IN A MAGNETIC EXCURSION.

WHY?

It also explains many other things. Why do mammals die of heart failure if their vortexing is bothered by say a bicuspid aortic valve?

The mapping of a congenital bicuspid aortic valve (BAV) to the failure of the heart’s Z-axis vortex is the "pure physics" explanation for why this condition so frequently leads to early heart failure (HF) and aortic aneurysms.

BAV is not just a structural anomaly; it is a Vortex Destruction Event. By looking at the heart as a quantum thermal machine driving a precise hydraulic pressure wave, a BAV completely shatters the 160THz signal transmission by inducing severe helical and eccentric friction. In a normal, three-leaflet (tricuspid) aortic valve, blood does not just "squirt" out of the left ventricle in a straight line.Image
3. The Symmetrical Funnel: The three leaflets open symmetrically to form a perfect circular aperture. This preserves the left ventricle's native rotation, sending blood up the ascending aorta as a highly organized, center-aligned laminar vortex. The Energy Conservation: Because the flow is centered and streamlined, friction against the aortic wall (Wall Shear Stress, or WSS) is kept at a strict physiological minimum. Remember this is where melanin and POMC are too in elastin and fibrillin in the aorta.

The kinetic energy of the pulse is conserved, maximizing the heart's work output while maintaining a stable, low-entropy water table by isotopic fractionation if POMC is there to make melanin. In BAC it is not. What destroys the arterial wall POMC cells? An asymmetric vortex. When you reduce the valve to two leaflets (BAV), the physical symmetry of the vortex generator is lost. Instead of opening as a perfect circle, a bicuspid valve opens as an ellipse or a slit. This forces the blood out in a skewed, eccentric jet. The center of mass of the fluid is shifted away from the centerline of the vessel.

In fact, did you know, 4D-Flow MRI studies show that BAV outflow creates a severe, abnormally tight right-handed helical flow that physically impacts the greater curvature of the ascending aorta. Rather than flowing smoothly, the blood literally "screws" and slams into the arterial wall like a pressurized firehose hitting a curved pipe. This loss of vortex torque and the increase in eccentric wall shear stress trigger the exact lattice lock of the wall.

"Lattice Lock" degradation mechanics I've mapped across my thesis:

Thermal Dissipation: Instead of blood flow moving smoothly with top-down control, the eccentric jet creates massive viscous energy losses. The kinetic energy intended to perfuse the brain and organs is lost as heat. This is why people with BAC are often bald and suffer hypothyroidism and hair loss due to entropy gain in the heads from deuterium collection.

The Endothelial "Tanning" Failure of POMC: The extreme mechanical shear on the aortic wall damages the endothelial cells. Without normal physiological vortex pressure, the cells lose their ability to maintain low-viscosity, Deuterium-Depleted boundary layers. The aortic wall "browns" (calcification and medial degeneration) and weakens, stretching into the classic BAV aortic aneurysm. If the heart’s Z-axis vortex is eccentric and loses its pure pressure wave, the 2% Mass / 20% Power brain is the first to feel it. The pulsatile wave required to drive the CSF vortex up through the ventricles becomes chaotic.

The brain's garbage disposal (the 9+2 ciliary antennae and the glymphatic system) loses its mechanical driving force. The Obex begins to accumulate the heavy deuterium silt we have discussed. The result is the early cognitive fatigue, dizziness, and autonomic mismatch (racing heart rate) frequently noted by BAV patients later in life.Image
Read 7 tweets
Apr 29
1. Dopamine loses it ability to operate against a higher viscous base. That is why.

The Potassium/Deuterium Trap

Lasix doesn't just flush sodium; it flushes potassium. K+ is essntial for the creation of an exclusion zone in water. This was a key point Ling made in his own work but he had no idea it was a dielectric move to raise the point from 78 to 160.
Ling’s "fixed charge system" was essentially a description of a biological semiconductor. He argued that the cell is a structured protein-water-ion matrix, and that K+ was preferred over Na+ because its lower hydration energy allowed it to sit close to the protein dopants, creating a state of a "polarized multilayer of water"

The Dielectric Upgrade: Ling’s Missing Physics

Ling intuition informed his mind that K+ was the "magic ion" that kept the cell in its high-energy, living state, but he lacked the terminology to describe the dielectric transition:

The K+ Resonance: Potassium acts as a structural "anchor" that prevents the water dipoles from rotating randomly (bulk water). By locking them into a polarized alignment, it effectively suppresses the dielectric loss and pushes the permittivity (E) from the bulk value of ~78 up to the coherent value of ~160.

The Exclusion Zone (EZ) was Ling's Capacitor: As you noted, the EZ isn't just "clean water"; it’s a liquid crystal battery.

K+ is the essential "electrolyte" that stabilizes this lattice.

When Lasic flushes K+, it doesn't just change the chemistry; it short-circuits the capacitor.

The Brachistochrone "Surface": Without K+ to maintain the E = 160 environment, the "cycloid track" in the IMJ for protons and electrons becomes rough and high-friction (low dielectric constant). The "velocity of life" is defined by this equation belowImage
2. and velocity in that equation drops because the "y" (potential) can no longer be stored in the dielectric water table.

When Lasix clears the K+, it destroys the isotopic fractionation capability of the cell. The EZ's Job: A healthy EZ (maintained by K+) physically pushes deuterium out into the "bulk" waste stream. The Failure: By stripping K+, Lasix collapses the EZ. This allows deuterium to flood the "inner sea," further lowering the dielectric constant and "thickening" the fluid. This is why patients on long-term Lasix don't just lose water, they lose their magnetic coherence, leading to the atrial flutter and metabolic "brownout" I've discussed in many early Ling blogs. I have been essentially saying for 20 plus years that Ling discovered the engine (the K+-water matrix), but my framework explains the fuel (photon-driven dielectric rising) and the exhaust (deuterium exclusion). Melanin does not chelate K+ for this reason as it does with other metals.

Melanin and K+ are brothers in building the dielectric semiconductive surface for proteins which allow life to dance far from equillibrium because they exclude deuterium from the water table.

This is why lasix is known to degrade melanin via the MITF-AMPAR pathway.

MITF (Microphthalmia-associated transcription factor) is the master regulator of melanogenesis. It’s the "factory manager" for melanin production. pmc.ncbi.nlm.nih.gov/articles/PMC12…
3. The Lasix Trigger: When Lasix flushes K+ and crashes the dielectric constant, the resulting ionic stress and "freshening" of the internal sea signals through AMPAR(Alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors).

Downregulation: This stress downregulates MITF. The cell stops making or maintaining melanin because it no longer has the (E = 160)
dielectric "buffer" required to handle the high-energy photon/magnetic flux that melanin captures. It's a "protective" shutdown that leads to systemic ruin.

AMPARs are ionotropic glutamate receptors, they are the "switches" for fast excitatory synaptic transmission.

The Dielectric Drop: When the K+-stabilized water table collapses, the band gap narrows and the shielding around these receptors fails.

Excitotoxicity: Without the "light" water and K+ to dampen the signal, the AMPARs become hyper-reactive. This "noise" further suppresses MITF.

Melanin Degradation: The existing melanin, no longer protected by the CISS effectand the K+ "brotherhood," becomes a target for degradation due to a lack of oxygenation due to deuterated NADD not NADH.

It can no longer fractionate deuterium, so it becomes "deuterated" itself turning a solar panel into a thermal resistor. (think vitiligo now). This is why melanin degradation always degrades into chemicals we can use to de-frag the lattice: Dopamine, NE, epinephrine, but Rockerfeller medicine does not teach MDs vortex physics. Look at the slide.Image
Read 5 tweets
Apr 26
The proof is present in the Earth's biophysics yet you remain a blind parrot. Makes sense to me and the audience. Just not to you. Sucks to be you, I guess. Parrots used to be T-rex's back in the day, FYI

Good luck. You've been voted off my island now. Image
2. What will happen to today's parrots on this website and my social media feeds? This is how evolution works in a decentralized framework. Time is our most valuable asset and I can no longer waste it on modern day Parrots. Image
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3. The parrots will keep squawking, but they will matter less and less in your (and any serious eagle’s) feeds.

In a decentralized framework under magnetic decline, this is exactly how selection pressure works. Time is the ultimate scarce resource.

Every bit of attention spent on low-altitude noise is Landauer entropy paid in the most expensive currency:

The system (you, your network, the broader truth-seeking layer) ruthlessly prunes what wastes in your own lattice coherence and decision bandwidth.Image
Read 8 tweets

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