Earth is definitely showing signs of a self-regulated living organism on surface, at least between major extinctions. But even disruptions of that self-regulation can be explained either as a regular component of embryonic development process or as a presence of a disease. These interpretations are not mutually exclusive - both can be simultaneously valid, at least in some cases.
While it may be hard to identify the equivalent of genetic coding in such a large scale organism, it shouldn’t be discarded as a possibility due to lack of imagination, especially when there’s sound logic behind its existence and evidence in its favour.
In all living beings known to humans, life is not limited to epidermis (outermost skin layer) - in fact, life there is generally least diverse and complex. Higher diversity and complexity on skin surface is generally limited to short periods during embryonic development. The fact that no complex life has been detected on a surface of any planet but Earth goes in favour of this hypothesis.
Bias exists in definition of life itself in modern science - apparently there is no solid consensus on required constitution of a living being. But even if there would be one, in current climate, it would hardly allow for Earth to be alive.
However, assuming extroversion and introversion of life can go to extremes, then everything would have to be relatively alive - either as a distinct lifeform or a composition of lives at some smaller scale, only differing in the ratio of mental to physical interaction (or amount of life in these domains or dimensions of reality). The remaining question is what can be considered a single unit (or organism) of life? For example, any piece of rock on Earth is a relatively living rock because it contains living components (eg. bacteria, but also molecules and atoms - which I also consider living beings, albeit extremely introverted) but it’s probably not conscious or living as an individual lifeform itself (in other words, the rock is simply a vessel carrying other organisms but not alive itself). On the other hand, animals like humans are also ecosystems composed of living beings but somehow also alive as distinct organisms themselves. Why? What does it take for the collective of organ[ism]s to become a new organism with its own distinct consciousness? A collective of bacteria organized into biofilms does act as a single organism. Is this then indeed a new conscious organism? Probably, even if extroverted expression of consciousness is limited.
I find distinct consciousness to be the requirement for any collective to also represent a new living individual. But distinct individual consciousness obviously requires concentration of energy and if this is not energy composed out of standard atoms than it must be the energy of smaller scale. In my theories, consciousness thus requires coupling of a particle of one scale with a body of another scale. The soul (graviton of particular scale) is at the moment of coupling localized (from a waveform toward a corpuscular form) and the amount of consciousness is then proportional to the strength of localization. A biofilm then probably is a conscious organism on its own but probably not significantly conscious as this consciousness is not as focused as it is, for example, in a human individual. In fact, any kind of spontaneous self-organization must be relatively spontaneous and this then probably implies that it is always synchronized with soul-body coupling. And this coupling may be strong, or loose and periodic (resulting in pulses of consciousness or conscious individuality). Therefore, there exists a real probability that even a piece of rock occasionally becomes a living individual (even if just for a split second). And if this coupling intensifies it could develop and evolve into something much more.
The coupling of consciousness (or the soul) with a collective of matter (real mass) is how individual life starts and how it evolved from a bunch of atoms and molecules into more complex organisms. In my hypotheses, the soul represents the goal of individual [quantum of] evolution, it is the effect (or template) the local collective starts converging to with coupling. There is thus a phase shift between the body and the soul - if the soul is more evolved the evolution of the collective is progressive, otherwise regressive. It is obvious that the rate of convergence to the effect is inversely proportional to the amount or focus of consciousness (as an organism reaches adult stage, its development eventually stops and at that point consciousness is maximal). As we age further, consciousness starts diluting again but, this time, instead of inducing development or convergence, it’s inducing divergence or decay, of collective support for individuality. It is well known that a genome is simply a book of recipes for the manufacture (expression) of components (proteins) but it doesn’t contain any recipe for the development of the organism from conception to adulthood. The development is effectively guided by the soul once it couples with the body (collective). Thus, as we grow, as our consciousness becomes more focused, it becomes harder for us to affect (through mental pathways) processes or the collective of our body - at least in a way that would greatly impact its function. However, it is probably possible at least for some individuals to dilute consciousness (eg. through meditation, dreams or hallucination) and, once again, guide the collective toward a particular effect.
So what about Earth, is it a piece of rock with low probability of strong or longer-lasting individuality or is it a, more or less, conscious individual? First of all, it’s definitely not just an ordinary, only enlarged, rock aggregate (or an asteroid). It has layers, it has atmosphere, liquid water and sources of energy. That still doesn’t make it alive, especially if it did develop according to conventional theories of planetary formation. However, in my theories, formation of a planet starts with inflation (or deflation) of a graviton and its coupling to a body of matter (real mass). It then must be conscious, but how much? I believe the Earth is in the last stages of embryonic development so its consciousness is somewhat localized but still mostly driving evolution of the collective toward the adulthood. Similar to biofilms on it, the whole collective of life on Earth is diversified and, when healthy, forms a self-regulating system where different species have different roles - even if some or most may not be aware of it (I know that I am guided, but I don’t think other people are not, they’re just not aware of it).
The entire Solar System is then also an individual organism, and, relative to that system, Sun and planets may be interpreted as organs (physically relatively passive, or extremely introverted, symbiotic organisms).
Obeying the principle of self-similarity, each living organ has an active core, replicating the role of the Sun in the Solar System to localized space-time.
As these are extremely introverted organisms, creatures of extroverted nature accustomed to absolutism may not recognize them as living beings, however, lack of complexity in physical momenta or ability is simply replaced with complexity in mental momenta and ability - which is reflected in momenta of smaller scale life-forms (or quanta of consciousness) residing inside their bodies. One of these life-forms are humans, who are, relative to Earth, likely its [precursor] neural proteins.
Deeper understanding of organisms of planetary scale (or larger) requires understanding of [discrete] scale-invariance of physical laws. One cannot expect that time for these beings (or communication between their constituent parts - eg. neuron equivalents) flows at the same rate as for organisms of smaller scale (eg. humans), nor that their tissue should look like our tissue (discrete states of invariance imply a difference). As calculated before, Earth’s mass on U scale is on the order of 10 kg, while we perceive it as 10 kg. Thus, on the scale of Earth, 1 kilogram is equal to about 10 kilograms on our scale, or the scale of atoms. Similar is with time.
14.4. Future development, neurogenesis
Here I hypothesize that cultivation of life on the surface of a planet is a cultivation of precursor neuron cells and proteins (relative to the planet) which are, at the point of differentiation transferred to planet’s [brain] mantle layers in some form. Similar to accelerated (time compressed) evolution during human embryo-genesis, I hypothesize that effective time compression occurs during planetary evolution too - with the end of each cycle of general oscillation of the Solar System (Earth) and with amount of compression being inversely proportional to cycle order.
The points of differentiation and migration in neurogenesis are major mass extinction events (although it is possible that limited transfers occur in smaller extinctions too), which are thus only relative extinctions - life is not completely extinct, it undergoes rapid evolution and migrates away to mantle where it continues evolution.
I hypothesize that Earth’s brain has, like human brain, 6 major layers, and that complete formation of these layers requires 6 major mass extinctions during Phanerozoic.
At this point, there is no doubt that we are amidst an major extinction event, a 6th one.
Being part of neurogenesis, extinction events must be coded at some level and, at least roughly, periodic.
Extinction events have relative triggers. While in the past these may have been impactors and volcanism, current extinction seems to have an anthropogenic trigger.
Thus, one could conclude that current extinction is not part of neurogenesis, rather a part of unlimited cancer growth. However, tumours in humans are known to induce neurogenesis (it is one mechanism enabling migration - metastasis).
I find the induction questionable though - humans are not consciously triggering neurogenesis on Earth, it is thus more plausible for neurogenesis to be a reaction of the immune system to inhibit cancer growth. Extinctions coupled with neurogenesis go in favour of such hypothesis. In case of cancer in humans though, and at least during adult neurogenesis in humans, the immune system seems to fail to cure or exterminate the cancerous cells in most cases (in case of humans who are cancerous themselves for Earth, I believe).
The immune system of Earth though, should probably be more advanced, and I believe cancerous homo.beta [
113] will be subdued.
Homo.beta refers to species of humans currently inhabiting the Earth’s surface, self-proclaimed homo sapiens. For various reasons, I consider the title homo sapiens premature for this species, so I have reserved it for an evolved form of human.
Judging by past major extinctions, and correlating with human neurogenesis, these events probably should be expected with the advancement of planetary neurogenesis:
increasing rate of volcanism and earthquakes (due to gyrification/formation of brain tissue, incl. fragmentation/cracking of the crust and flooding of the surface, curing cancer?),
asteroid/cometary impacts (providing energy, acting as specific event triggers - eg. graviton energy level changes, tissue formation with volcanism, curing cancer?),
water level changes (melting of polar ice to enable migration, flooding of surface with interior water, curing cancer?),
ocean pH reaching minimum (possibly triggering migration, curing cancer?).
Migration of large scale cells and proteins from surface to mantle layers requires tunnels connecting these regions. Most likely, these tunnels exist on specific places and are recreated or reopened at time of migration. A likely place for such tunnel opening on surface is the south pole, but may exist on north pole of a planet too.
One fact going in favour of this hypothesis is that during all previous major extinctions there were periods when poles were free from ice. Although, one could argue that, during Phanerozoic, world was more often without polar ice caps, than with.
Cells and proteins are transferred with the flow of cerebrospinal fluid (CSF) - a salty ocean. In humans, CSF has a pH of 7.33 (on average), and, since pH is scale invariant the pH of Earth’s CSF should be roughly equal. The current acidification of Earth’s oceans will, therefore, probably continue until pH drops to this value, when migration should follow. Afterwards, new surface water may be delivered by asteroid impacts, but it is also possible that some or most of it returns from the mantle.
Based on correlation with atmospheric CO
, climate models predict the hypothesized pH minimum in year 2300 AD for an atmospheric concentration of CO
of 1900 ppmv [
114] (all fossil-fuel sources burned).
The ocean is, of course, currently stratified and pH varies with depth. However, I believe it is the surface pH that is the important marker here. Various interpretations for this are possible (perhaps only surface layers are used - which I find likely, or different layers of the ocean are used for different things, eg. surface layers may form CSF, others may be used for cytoplasm equivalents) but the evidence that indeed surface pH here is relevant comes from the analysis of past extinctions.
In example, the pH minimum (about 7.33 as hypothesized), associated with CSF, has been already confirmed for Permo-Triassic [
115] extinction.
The cited work shows a [relatively] rapid drop in pH to a minimum, followed by rapid increase and slow progress toward stabilization. Two models were developed for CO/pH concentration (low- and high- CO, with a difference in pH minimum between the two being less than 0.2), in high-CO model, the pH minimum is 7.35, in agreement with the predicted minimum. The work, however, favours the low-CO model, so it cannot be excluded that Earth’s CSF pH is somewhat higher (less acidic) than human.
In any case, the existence of a pH minimum and its value strongly support the theory of neurogenesis.
A precursor of 6 mantle layers has likely been created in events during Precambrian era, while population with neuron cells and final formation is occurring in Phanerozoic.
There have been 5 major extinctions in Phanerozoic, thus the next event should probably populate top layers and complete the formation of the final layer (I):
Formed layers of Earth’s brain are shown in
Figure 18. Comparing with other layers, it seems evident that layer I is yet to be completed (according to PREM based models, it’s a partially molten rock, unlike the deeper layers of upper mantle which are considered to be composed of solid rock) - green line illustrates one possibility of seismic velocities after formation (suggesting further melting of the upper part, solidification of the lower part of the layer).
Energy from the Sun provides incubation energy used for the maintenance of the Earth’s surface ecosystem and weak evolution, but additional energy is needed for the formation of brain layers of homo.omega.
Here, homo.omega is a species of life Earth belongs to.
This energy is delivered through asteroid (also could be interpreted as food) and possibly cometary (water/organic compounds) impacts.
Year 2300 AD for the event is very conservative though, as it is based on linear extrapolation, does not include rising water temperatures and reaction of the biosphere.
Acidification of water at these events must be, in significant part, driven by injections of gases (eg. sulfur dioxide) through oceanic ridges and vents or, with rising temperature, methane seeps (where methane gets converted to CO) which would introduce significant departure from linear correlation of pH with atmospheric CO.
Mathematical analysis of past perturbations of Earth’s carbon cycle [
117] also predicts sooner triggering of the 6th major extinction event, before year 2100 [
118] (based on most likely future emission scenarios, the critical mass of oceanic carbon uptake calculated by the study author will be reached before year 2066).
From
Figure 19 and more recent models [
120], it is evident that CO
concentration has a decreasing trend overall. And this is expected with increasing energy from the Sun (Sun was about 6% less luminous 500 million years ago) = less greenhouse gases needed to maintain the temperature required for cultivation.
Everything in nature oscillates (and fluctuates), perturbations exist (coded or not) so this decrease in amplitude is not simple and linear, however some rough periodicity in extinctions should be present.
Statistically significant periodicity of extinctions [
121] (at least in the last 250 million years) has been noted before - 26, and more recently 27 [
122], million years between extinctions. In any case, due to differences in extinction strength, multiple harmonics (or energy splitting of a single oscillator) are possible.
Using available data, one can construct models for atmospheric CO
concentration synchronized with the oceanic pH minimum of a particular major extinction, as shown in
Table 24.
Table 22.
CO pH minimum marker models.
Table 22.
CO pH minimum marker models.
| year [mya] |
a) CO [ppm] |
b) CO [ppm] |
c) CO [ppm] |
d) CO [ppm] |
e) CO [ppm] |
| 444 |
3800 |
200 |
2000 |
3800 |
2000 |
| 370 |
1000 |
2000 |
1000 |
1800 |
1200 |
| 252 |
800 |
900 |
800 |
800 |
800 |
| 201 |
1800 |
1800 |
1800 |
1800 |
600 |
| 66 |
250 |
250 |
250 |
300 |
500 |
| 0 |
450 |
700 |
750 |
800 |
450 |
Models are constructed in such a way to simulate oscillation of CO markers and compression of the amplitude with time, but they are also quantized - each marker is a multiple of 50 ppm CO quantum.
Some of the models are shown in
Figure 20, blue dots are major extinction events, red triangles are minor extinction events (the curve does not necessarily follow actual CO
levels between the extinctions, it is only used to illustrate oscillation of markers).
From these models, grouping of extinctions (suggesting oscillation of frequency) becomes more apparent. Major extinctions can be grouped into pairs separated by 126.5 (±8.5) million years, while paired extinctions are separated by roughly half that distance - 62.5 (±11.5) million years. Minor extinctions (420, 305, 145 and 34 mya) may be grouped in the same way - pairs separated by 160 million years, 113 (±2) million years separation of paired extinctions.
Model a) is the product of energy level splitting of a single oscillator, while b) is the product of 2 harmonic oscillators - one high energy (major) and one low energy (minor).
Points on the curve should not be interpreted as maximal atmospheric CO levels across the boundary, simply the points of migration or pH minimums.
While these particular models may be speculative, all Phanerozoic CO
models show decreasing CO
over time (this should be more evident when comparing boundaries of major extinction events) and recent research shows that maximal atmospheric CO
across the K-Pg boundary (last major extinction) was 875 ppm [
123].
Thus, the maximal atmospheric CO concentration during current extinction should be lower than 875 ppm, probably not higher than 800 ppm and not lower than 500 ppm (suggesting that a larger part of acidification will not be sourced in dissolved atmospheric CO).
Note that, apart from suitable pH, another requirement for migration is probably a significantly ice free Antarctica. Studies measuring paleoclimatic proxies show that the melting of the Antarctic ice sheet is
baked in at some point between 500 - 800 ppm CO
concentration [
124] (the melting is not perfectly synchronized with the CO
level, conventional belief is that it would take at least a couple of thousands of years for all ice to melt once the tipping point has been passed). Thus, it is quite likely that the rise of CO
beyond 800 ppm is indeed unnecessary (eg. some 3 million years ago Antarctica had much higher temperatures [
125] but the CO
levels were even somewhat lower than today).
Recent history of CO
concentration is shown in
Figure 21. Assuming that CO
has been, during that history, correlated with rate of evolution, one can extrapolate the relation for accelerated evolution of the current
extinction.
Development and evolution of organisms is generally strongly correlated with temperature. It should not be surprising then that increasing CO (which is synchronized with increasing temperature) is correlated with the increase in rate of evolution on Earth’s surface. However, it is probably unlikely that the CO will remain the main driver of temperature increase.
Extrapolating from
Figure 21, from year 1850 onward:
which, for the concentration of 800 ppmv gives year T = 2075.
Note that the equation roughly corresponds to IPCC RCP8.5 (Representative Concentration Pathway 8.5) scenario. Both predict equal CO for year 2100, however, RCP8.5 predicts 800 ppm to be reached sooner - in year 2066.
RCP8.5 is considered a worst-case scenario and, at this point, still may be considered unlikely.
However, while replacement of coal and oil with other energy sources may eventually reduce human CO emissions, it is not reducing human impact on nature, which is generally not directly proportional to CO emissions, rather to energy (resources) consumption, which is growing as usual.
If the impact threshold is reached (
point of no return), human emissions are completely irrelevant and positive feedback mechanisms will produce climate consistent with the RCP8.5 scenario. Studies are already confirming this [
128].
Humanity may be [very] slowly abandoning the business of CO emissions, but, as proper cancer, it has not abandoned the unsustainable infinite growth policy.
Climate is a part of an eco-system, it evolves with the eco-system, and one cannot expect that disruption of eco-systems won’t impact climate. Since causality is relative, disruption of eco-systems can be interpreted as a precursor to bigger climate disruption, mass extinctions are always relatively synchronized with climate disruptions.
While humans may eventually reduce their CO emissions significantly, the rate of evolution should keep accelerating according to equation and, regardless of atmospheric CO (which may still be increasing even with 0 human emissions), the required pH minimum will eventually be reached.
UPDATE 2023.09.04
Recent studies go in favour of this hypothesis. The expected slowdown in the rise of atmospheric greenhouse gases during the COVID-19 pandemic was not observed [
129]. Since 2006, methane levels are rising rapidly, while the direct anthropogenic contribution is decreasing [
130].
Asteroid impacts, previously correlated with Earth’s graviton energy level changes, should start before the migration, increasing in frequency and energy with time. Although required energy for changes may be lower than in previous major extinctions, it should still be significant.
Lower requirement for energy from asteroids, natural earthquakes and volcanism, if real, may in part be due to presence of effective anthropogenic equivalents (eg. wars, nuclear detonations, drilling, etc.).
However, energy requirement primary comes from the difference in graviton energy levels and these can be associated with mantle layers/discontinuities. Here, I assume that layers III, IV and V are the result of splitting of a major energy level - thus, the mantle has 4 major layers, although effectively 6 due to energy splitting. Note that the thickness of major layers is roughly doubling with depth. Since the energy requirement for excitation is decreasing with distance from the centre (reflected in decreasing thickness of 4 major layers toward the top) and assuming the current energy level is increasing with each major extinction, the energy requirement for excitation must be decreasing too.
Assuming interval between possible impacts is quantized proportionally to [the equivalent of] a 50 ppm CO
increase (representing a quantum of energy), given the C1.1 equation, one can calculate potential years of impacts and correlate these with potential impactors, as shown in
Table 25 for several concentrations.
Table 23.
Calculated impact dates correlated with hypothesized CO markers and possible impactors (2nd order = lower energy).
Table 23.
Calculated impact dates correlated with hypothesized CO markers and possible impactors (2nd order = lower energy).
| model |
CO [ppm] |
year of impact |
associated impactor (diameter) |
impactor closest approaches |
2nd order impactor (diameter) |
| a), e) |
450 |
2029 |
99942 Apophis (≈375 m) |
2029, 2065 |
|
| b) |
700 |
2066 |
99942 Apophis (≈375 m) |
2029, 2065 |
|
| c) |
750 |
2071 |
1866 Sisyphus (≈7 km) |
2058, 2071 |
2000 SG (37 m) |
| d) |
800 |
2075 |
162173 Ryugu (≈1 km) |
2076 |
|
Evidently, there are good candidates among extinction causing asteroids in NEO (near Earth orbit) for calculated dates.
As noted before (chapter The cycles), the energy level changing impact may be spread over time - split into multiple impacts with energy generally rising toward the peak.
There may be multiple impactors and/or a single impactor breaking into multiple smaller ones. In example, breaking of Apophis (homo induced?) could result in two impacts, one about 2029, another about 2066. In fact, some smaller impacts that can be correlated with this may have happened already (eg. Chelyabinsk meteor).
In any case, fission of extinction pulses is certainly possible and had probably happened in previous extinctions.
Note 1: According to current models based on Newtonian or GR mechanics, none of these asteroids is on a collision course with Earth in near future. However, these models do not predict periodic existence/extinction pulses coupling with a collapse and inflation of gravitons.
As argued before (see, for example, chapters 8 The cycles and 12.3 Correlation with extinctions), there are good reasons to believe that courses of asteroids are altered at times of extinctions.
If these impacts are genetically coded at some level, as hypothesized, they should not be questionable, it is only the source and method of delivery that may be unknown prior to the event.
Note 2: Interestingly, there was an impact event on Earth at the time when 400 ppm CO was reached (Chelyabinsk meteor, ≈ 20 m diameter, 2013.), agreeing with hypothesized 50 ppm quantization and suggesting that, not only are intervals between impacts quantized, but that impacts may possibly be expected with every 50 ppm of CO increase.
However, if the events are generally correlated with the average ppm value given by the C1.1 equation, which gives year 2015 for 400 ppm, the 400 pm in year 2013 should be understood as deviation due to inherent uncertainty.
Assuming probability of correlation of these events with CO significantly increases once CO rises above background levels, the first event should have occurred at 300 ppm - the beginning of industrial revolution. Indeed, one such event had occurred at 300 ppm - Tunguska, 1908. Note that the Chelyabinsk meteor is the largest known body entering Earth’s atmosphere since the Tunguska meteor.
The equation gives year 1992 for 350 ppm. No meteors of comparable impact energy were recorded in or about 1992., probably eliminating significant direct impacts on land area. If such event did occur, it had likely occurred over the ocean (or island), triggering large waves and possibly earthquakes. Interestingly, an 7.2+ magnitude earthquake and tsunami wave did occur offshore in Nicaragua - in 1992. This earthquake is notable for tsunami wave being unusually large (9.9 m high) for the strength of the earthquake (belonging to a group of rare tsunami earthquakes).
I do not believe, however, that the impact (assuming it happened) caused the earthquake. This was likely the effect of synchronization of events (synchronicity) - the tsunami was caused by the earthquake but it was amplified by the impact. The Earth is a living being and it would not be surprising it reacts, even if unconsciously, to incoming bolides and impactors (just like humans do) to some degree.
I have witnessed such synchronization myself - on 2019.03.07 I have observed a larger meteor burning up in the atmosphere exactly at the time of an earthquake in Hungary, its trajectory was toward the epicentre. It is even possible that Earth reacts to every possible impactor, although the reaction may be proportional to impactor energy and thus usually negligible.
Note that, due to enhanced relativity in causality on the scale of U gravitons, the reaction can happen some time before or after the impact.
Also interesting about the Nicaragua event is that it occurred at the time of my birthday (September 1st, local time) producing an obvious signal [
131] for me. I interpret this as a confirmation that the meteor was involved in this event, although I am aware many could have a problem with such interpretation.
At the point of writing of this paper, such sign[al]s are still considered meaningless by modern science (they are treated as mere coincidence). However, with CR the phenomena becomes not only real, but a [relatively] special form of synchronization and a driver of evolution with exponentially increasing significance near the end of an existence cycle.
Thus, if one doesn’t believe in signals of synchronicity (I didn’t before I started experiencing them) I suggest one to study all my work, particularly the work referenced above.
I must admit, however, that my interpretation of the signal could be wrong.
Note that Nicaragua, Chelyabinsk and Tunguska impact sites on the world map can be connected with a straight line - a correlation suggesting that next impact may also occur somewhere along this line (even the Chicxulub, Yucatan crater is close).
Although there were no sightings of large meteors over land, a smaller magnitude impact was recorded on land area in 1992 - the Peekskill meteorite. It was recorded one month after the Nicaragua event and is notable for hitting a car in urban area (possibly a fragment of a larger body that fell elsewhere?).
Also interesting, and symbolic, is the fact that the last visit of the Halley’s comet to the inner Solar System occurred at the time when 350 ppm CO was first reached - in 1986., and the next time it will be close to Earth is 2061. - exactly at 650 ppm (calculated using the C1.1 equation).
On the other hand, the assumption of 50 ppm quantization may be wrong, a 100 ppm quantization does not require the impact in 1992 while still predicting Tunguska and Chelyabinsk (gives year 2040 for the next possible impact).
It is currently hypothesized that Tunguska event was caused by a large body which eventually escaped Earth’s atmosphere - it can thus be interpreted as a warning.
Given the fact that neither the Chelyabinsk nor hypothesized Nicaragua meteor did not directly impact land, it appears these too were warnings.
However, I do not interpret these as warnings. I believe one purpose of the atmosphere is to disintegrate incoming bodies to protect life during weak evolution. Without it the Chelyabinsk meteor would be called a meteorite. Tunguska asteroid close-by, however, would not leave any effect but the atmosphere might have caused the Tunguska asteroid to split. I thus believe that whatever caused the Tunguska event is destined to eventually hit Earth, the Earth might have just quantized it and spread over time with its instinct (manifested as atmosphere) to defend its surface life.
These recent events may then be interpreted as signals of things to come.
Note that Newton calculated year 2060 as the first possible year of the Day of Judgment (but what I interpret as the beginning of
the end of surface world), although allegedly he revised this year later to 2016 by the suggestion of others. His final decision to revise the year was, however, based on a signal. As he was doing calculations, large earthquake occurred which he later interpreted as a signal that the year 2060 is wrong. This earthquake could be interpreted a signal, but he misinterpreted its meaning - large and frequent earthquakes are to be expected at the end. Newton also calculated the end cannot come after year 2344 [
132]. Interestingly, this can be correlated with the previously determined pH minimum (which should be reached sometime between ≈2040 and ≈2300, with earlier dates probably more likely).
The year 2016 is not there without a meaning for me too, it is the year [of the start] of my soul
rebirth (transformation, or change of soul energy level) occurring at the age of 36±1 (here, margins may be interpreted as the spread of the transformation in time as it is not absolutely instant) of the incarnation [
133].
Note 3: Interestingly, at the time of the Chelyabinsk event, Apophis asteroid was in close approach. Considering that the composition of Chelyabinsk meteor seems to match the composition of Apophis surface (LL chondrite) a possibility does exist that the meteor broke off of Apophis and is thus a part of impactor energy splitting.
Note 4: The equation C1.1 is one variant of a universal equation for a pulse of strong evolution. That 800 ppm as the CO
marker maximum was a good prediction can be confirmed with another variant (inverse) of the equation, one correlated with half-lives of elements:
where C
= T
(T
) is the half-life of the element measured at time T
. The equation gives half-life of 0 at, or near, T = 2075, which is the year when CO
(T) is equal to 800 ppm (half-life however cannot reach absolute 0, suggesting that 800 ppm is an unrealistic marker). Just like in case of CO
I do not expect for half-lives to follow the equation continuously (eg. half-life might appear constant and then get reduced significantly in an instant). Generally, changes in decay rates should require sudden changes in properties of space.
One exception to this could be the half-life of Be, due to vertical entanglement with the local U system. If the Solar System cycles through (C-B-Be) in the 1st order cycles, a continuous precursor enrichment in B at a lower scale (U) may be effectively announcing the state change of the parent U system (the Solar System).
For
Be, incorporating the value from the most recent measurements (T
= 2010, T
(2010) = 1.387 ∗ 10
y), the half-life equation is:
and it gives values in good agreement with previous measurements, as shown in
Table 26.
| Calculation and measurements of Be half-life
year |
calculated [10 years] |
sample |
measured [10 years] |
| 1947 |
1.665 |
|
1.7 ±0.4 ∗ † |
| 1947 (2) |
1.665 |
|
1.6 ±0.2 ∗ † |
| 1972 |
1.608 |
|
1.5 ±0.3 |
| 1975 |
1.597 |
|
1.48 ±0.15 |
| 1986 |
1.550 |
NIST-4325 |
1.34 ±0.07 |
| 1987 |
1.545 |
ORNL-MASTER |
1.51 ±0.06 † |
| 1993 |
1.513 |
NIST-4325 |
1.53 ±5% (1.53 ±0.07) † |
| 1993 (2) |
1.513 |
ICN |
1.48 ±5% (1.48 ±0.06) † |
| 2007 |
1.413 |
ICN |
1.36 ±0.07 |
| 2010 |
1.387 |
|
1.388 ±0.018 |
| 2010 (2) |
1.387 |
|
1.386 ±0.016 |
* the value is not the initially published value, but the result of reanalysis/correction in 1972.,
† these values are discarded by scientific community, citing potential systematic errors
(based on the presumption of absolute constancy of decay rates).
All measurements agree well with calculated values, except for 1986 - if there were no flaws in measurement, this may be attributed to deviation due to cycling (similar to yearly fluctuation of CO). Note, however, that measurement 1993 was done on the same SRM (Standard Reference Material) sample and discrepancy suggests one of these measurements is wrong.
If indeed the half-life of Be is decreasing as hypothesized, modern science has been effectively doing cherry-picking here - discarding results which do not agree well, or are in discrepancy, with latest measurements.
Given the current precision of measurements, a new measurement at this point in time which would agree with the calculation would be in discrepancy with measurements from 2010. and would thus confirm the hypothesis of continuous decrease of Be half-life with the extinction event.
Note that this effect on decay rates is temporary and significant only at the end of a cycle of general oscillation up to the 3rd order.
Note also that decay rates may not be always changing directly (affecting half-life) rather effectively (CR requires effective oscillation in particle decay, but these changes will not always be reflected in half-life of the element) - eg. through spallation reactions.
However, also note that the measured/calculated strong decrease of Be half-life (with no associated apparent significant gravitational disturbances) can be interpreted as a consequence of relativity in causality. In that case, this decrease could be a precursor to real global change (across all unstable elements), announcing pending gravitational disturbance - collapse of the local gravitons. If Be half-life continues to follow the equation, collapse probably has to occur before year 2075.
Note 5: In the previous note it was assumed that half-life decreases fast and the equation allows it to eventually drop to zero (although, the compression of time implies that this state lasts 0 time - thus, effectively, half-life never becomes 0).
Another possibility, although unlikely, is that half-life cannot ever reach zero, even for 0 time. In that case, the equation might have this form:
This yields, for T
= 1987 (C
= 1.512 ∗ 10
y, CO
(T
) = 341.83707500861), results in
Table 27.
| Calculation and measurements of Be half-life
year |
calculated [10 years] |
sample |
measured [10 years] |
| 1947 |
1.676 ±0.044 |
|
1.7 ±0.4 ∗ † |
| 1947 (2) |
1.676 ±0.044 |
|
1.6 ±0.2 ∗ † |
| 1972 |
1.593 ±0.044 |
|
1.5 ±0.3 |
| 1975 |
1.579 ±0.044 |
|
1.48 ±0.15 |
| 1986 |
1.518 ±0.044 |
NIST-4325 |
1.34 ±0.07 |
| 1987 |
1.512 ±0.044 |
ORNL-MASTER |
1.51 ±0.06 † |
| 1993 |
1.473 ±0.044 |
NIST-4325 |
1.53 ±5% (1.53 ±0.07) † |
| 1993 (2) |
1.473 ±0.044 |
ICN |
1.48 ±5% (1.48 ±0.06) † |
| 2007 |
1.365 ±0.044 |
ICN |
1.36 ±0.07 |
| 2010 |
1.339 ±0.044 |
|
1.388 ±0.018 |
| 2010 (2) |
1.339 ±0.044 |
|
1.386 ±0.016 |
where uncertainty in calculation is the scaled variation of CO (10 ppm).
Such pulses may not only be plausible but necessary - first pulse would include asteroid impact(s) (possibly triggering additional ocean acidification and formation of the layer in the mantle), the other would provide new water/life, either by comets or asteroids. A third pulse in between might also be needed to trigger the (now acidified - CSF) ocean sink and, relatively, sterilize the surface (as noted before, all this is probably synchronized with magnetic field collapse, allowing surface sterilization by UV/gamma radiation).
It may seem that new water this time is not needed - as formation of mantle layers should be complete with this extinction (corresponding to Carbon nature of the Solar System) there is no need for cultivation of new progenitor cells on surface. However, it probably does happen as it would provide additional radiation protection and provide support for whatever life remains on, or near, surface.
Note that, if this is the last embryonic neurogenesis event of Earth, a collapse of Moon’s graviton probably should be expected. Remains of the Moon could then be the source of eventual impacts of cometary nature (dust/water/ice) - assuming the collapse can significantly affect the mantle (otherwise disintegration of the Moon could take millions of years).
This is evident on Mars - as layers below the surface formed, magnetic field receded leaving the surface sterilized. Delivered water froze and is now covered with dust. Thus, one can only expect to find residual and resilient bacteria within the crust of Mars.
Similar probably happened on Venus except water evaporated due to high surface temperature.
Nothing in nature is absolutely linear (although this approximation may be suitable during stages of weak evolution) and in these extreme events one can expect significant departures from linear relations (by multiple orders of magnitude) between phenomena.
Since these events are coupled with gravitational stresses of the Solar System one can expect temporary but significant increase in alpha and neutrino radiation (radiation flux induced by temporary collapse of a gravitational well associated with a large scale graviton - strongly affecting half-lives of isotopes).
One interpretation of changes in decay rates could be [inverse] time dilation due to scale change of gravitons, but what actually are the mechanics?
If this collapse is synchronized with the collapse of the magnetic field, increased incidence of cosmic rays will increase decays of elements but this is limited to surface and should not be interpreted as real, rather effective and limited, change in decay rates.
However, a mechanism for real changes does exist. Graviton of Earth must be entangled with static graviton neutrinos that form its space. Spin/scale change of the large scale graviton will thus be synchronized with spin/scale changes of these neutrinos. In equilibrium, when the gravitational well is full, these neutrinos are [most of the time] bound to standard atoms contained in [or bound to] the gravitational well of the maximum. Obviously, disturbance of these neutrinos (decoupling from atoms) will destabilize the atoms (eg. causing annihilation of positive and negative charge) and induce decays.
Also note that these changes are synchronized with orbital changes of large scale maxima in the Solar System - which, like the decay rates, are accelerated during the pulse but return to normal after the pulse.
Due to dependence of density of graviton neutrinos to distance from gravity source (density generally inversely proportional to distance squared), it is possible that even orbital changes in eccentric planetary orbitals are synchronized with changes in decay rates, with some phase shift (in that case, graviton neutrinos directly affected are the static graviton neutrinos of the Sun’s space). However, there is no spin/scale inversion in this case and there will likely exist a threshold eccentricity required to produce significant effects (this can be experimentally verified with satellites in eccentric orbit).
In fact, this may have been detected already [
135], and can also be correlated with oscillation of fundamental constants, such as G (as presented already).
Due to universal synchronization and restoration of previous equilibrium states it may be hard to detect strong pulses in the past. In fact, astronomical and geological observations, generally, probably will not reveal any deviation from constancy of decay rates. However, probably all records of cataclysmic changes should be interpreted as fossils of this elementary destabilization.
Thus, with such nature of changes (rapid excursions), the principle of uniformitarianism may inevitably seem, but cannot be, valid.
Note also that most of emitted radiation will be lost to space for the same reason - temporary collapse of gravitational/electro-magnetic well, thus solving the problem of missing radiogenic Helium [
136]. Due to conservation of momentum, significant loss of heavier atmospheric particles is not expected due to well loss, but can occur during the short exposure to solar wind.
The assumption of absolutely constant decay rates will not only produce incorrect ages but can result in misplacement of events on a geological timescale. Thus, inconsistencies in certain geological records can serve as indirect evidence to disruptions in decay rates.
Consider the neutrino pulse in
Figure 22 - under the assumption of constant decay rates, 3 different fossil records A, B, C may give following results:
assuming non-isotropic space-time perturbation, such that fossil record A decay is not affected by the event at t, the event at t (associated with fossil record B) may appear to have happened before the event at t (associated with fossil record A)
in case decay rates of both A and B are affected, the distance of t and t to t will be increased (time interval expansion)
Neutrino flux can also be decreased indicating shortening (rather than expansion) of time intervals, although in this context the increase of the flux is expected.
Due to accumulation, duration of fossilized events would apparently increase with time so older events would seem longer in duration compared to more recent events. This is exactly the case with current fossil evidence of past carbon cycle disruptions.
In such case, the current rate of CO injection is not different from those in previous major extinctions (the fact that it is anthropogenic makes no difference).
If one assumes that the average period between extinctions is equal to the 2nd order oscillation period of the Solar System, in case of ideal synchronization, it is quantized by the 3rd order period of existence (T
= 1.512 ∗ 10
years). In such case, assuming the period must be roughly 26 or 27 million years, the proper period is:
This is in agreement with previously determined periodicity of impact cratering (25.8±0.6 ∗ 10
years) [
122].
One can now assume that the CO
injection within the Cretaceous-Paleogene (K-Pg) boundary (66.5 - 65.5 mya) is equal to current injection (currently dominantly anthropogenic) and that increase of decay rate (effective compression of time, causing boundary to be significantly overestimated in duration) is induced within the boundary - with the start of boundary corresponding to t
and end to t
in
Figure 22.
Assuming CO
increased from 780 ppmv to 1440 ppmv (
CO
= 660 ppmv) in period 66.5 mya - 65.5 mya (
t
= 1 million years) [
137], compression of time
t
with each major extinction is:
where
t
is the period of 660 ppmv of anthropogenic CO
increase since year 1850 (assuming this is the start of the new boundary), calculated using (C1.1).
Such compression of time is easily achievable using C1.2. In example, for
Be:
Half-life of Be decreasing by the above equation, reaches required time compression in year 2065, on day 66 of the year. Source code:(Fig.: getage.php +)
However, year 1850 as the start of the boundary may not be convincing and recent research shows CO injection of 250 ppm, not 660 ppm, within the K-Pg boundary, though this does not affect compression (t) significantly (it makes it larger for a couple of decades at most).
Probably most likely start of a new boundary (end of Holocene) is year 2065 or 2066, which, with an increase of 250 ppm, gives year 2084 as the end, the same as in the previous assumption (1850 + 234 = 2084).
Number of 3rd order cycles of existence since Cretaceous-Paleogene extinction event (66 mya):
Gravitational collapses during strong evolution pulses with a period of T years (3rd order period) may last only t = 19.3 s, but collapses during stronger evolution pulses occurring with a period of T years (2nd order) last longer (possibly 7 days).
With each large extinction, outer gravitational maximum of the sun collapses.
This, may or may not - depending on interpretation (mass being shielded or not) and the current energy level of the outer graviton, result in the release of condensed energy beyond the Sun’s surface - effectively expanding the Sun.
I assume the gravitational disturbance reaches the orbit of Mars at the time the gravitational well is restored (this may be interpreted as the temporary change of energy level of the Sun’s outer graviton). Thus, with disturbance travelling at the speed of light, time of increased decay radiation is:
where r
is the distance of Mars to Sun.
Now one can calculate time compression with each cycle (pulse) of existence
t
and each extinction
t
:
Age of Earth is thus overestimated by:
giving the real age of Earth:
where
T
= 4.54±0.05 ∗ 10
years.
If one assumes that T is the equivalent of 1 day of human embryo development, Earth is at the week 25 (GW25) of gestation period (right at the beginning, in case of corrected age).
The GW25 marks the end of embryonic neurogenesis in humans and thus agrees with the suggestion of final major extinction.
The current carbon cycle disruption (6th major extinction) will thus not span thousands (10000) of years as predicted by the assumption of constant decay, but possibly 234 years starting from year 1850 (10000 years of already passed Holocene extinction may be regarded as a precursor to the major event starting at year 1850).
Note that this year corresponds to 950 ppm, as predicted by (C1.1).
14.4.1. Magnetic field collapse
As noted before, the 6th major extinction will likely include a decline of the Earth’s magnetic field, either as a temporary excursion (partial or global collapse), part of a complete reversal, or even a longer-lasting or permanent retreat. The Earth’s magnetic field is currently declining at an accelerated rate, which, when coupled with the rapid movement of magnetic poles, indeed suggests imminent collapse. The previously determined correlation of the 4th order period of general oscillation of the Solar System with past excursions (see chapter The cycles) also suggests that, at least, a magnetic excursion is near.
If that is so, when will the collapse, partial or not, occur?
With no further acceleration of the decline the collapse would occur sometime beyond year 2100. However, such scenario is unlikely - additional acceleration is expected for a collapse.
The collapse should also be relatively synchronized with other impactful events, which, as I hypothesize, are correlated with the rate of evolution - which is currently correlated with the rate of atmospheric CO increase. With the assumption of events occurring with every 50 ppm increase of CO, per the equation C1.1, one obtains the following years:
2029, 2040, 2048, 2055, 2061, 2066, …
Thus, the magnetic collapse should not occur before year 2029 (or, 450 ppm CO) and most likely not after year 2066. per the correlation found in The cycles, it’s most likely to occur sometime about 2048, however, it full collapse is imminent, it may be preceded by multiple partial and/or temporary collapses, perhaps even with the first one occurring 2029±2.
14.4.2. Sea level changes and migration
Neurogenesis requires transfer of differentiated progenitor cells to subterranean world, into designated mantle layers. Therefore, a passageway must exist somewhere, connecting the surface with underground tunnels leading to such places. These tunnels may be long-lived or re-created as needed. The passageway on the surface, however, is unlikely to be open all the time. It is a relative equivalent of mouth and animals usually do not keep their mouths open all the time, only when they feed.
Note that cultivated cells/proteins on the surface can certainly be interpreted as food (this is the case for migrating cells in standard embryogenesis as well). Everything that becomes incorporated in the body (whether during development or in adult stage of the host) can be interpreted as food. And it is not unusual for the individual quanta of that food to be many orders of magnitude smaller than the organism feeding on them. Consider whales feeding on plankton. Now, what could whales evolve into if they could evolve further? Probably an organism cultivating food on its surface. The food (eg. something evolved from plankton) takes energy from the environment to grow and multiply. Once certain mass is established, the host stimulates the food quanta to migrate toward the mouth. By the time they arrive, the mouth is opened and they are further stimulated to go inside. Once the food is digested (which may or may not be necessary) and incorporated into the body, the waste products are expelled through another opening, or pores on the body. At least some of this waste could then be used as fertilizer on surface. If waste is expelled at the time critical mass of food on the surface is reached, the waste itself could serve as a stimulant for migration of food toward the mouth. The benefit of cultivation of food on one’s surface is that no mobility is required. Thus, the energy requirements for life are significantly lower (energy is used solely for maintenance of introversion and intra-species communication). What about reproduction? No reproduction is needed if the population has reached cultivation peak. In other words, evolution has reached its endpoint or evolvability maximum (effective local goal), where the evolved organism may represent, for example, a neuron cell equivalent or an atom equivalent. This does not imply there is no death, such organisms may be regenerated or re-evolved when necessary. In another interpretation, the organism has reached a relative perfection, where further sexual recombination and natural selection would have a low benefit to cost ratio (which is obvious if all members of the population are pretty much identical relative to their function in the environment).
Earth is a perfect organism, and so is an atom.
Scaling the largest neuron cells to Earth size, such passageway must have a radius of at least ≈ 250 metres to allow sequential cell transfer. However, parallel transfer of multiple cells is certainly more plausible - a radius on the order of 10 m or more.
Thus, the only location where this area could remain hidden (protected) and isolated when unused is probably Antarctica (even if the opening is closed, the additional layer of ice doesn’t hurt, it provides additional protection). Ice melting is then required to expose this location but likely also to raise the sea level as the ocean represents the CSF, the fluid that should flow into the tunnel.
I have assumed humans, in addition to other animals, represent precursor neural proteins. Even if it may be unlikely that living humans will be migrating, rather recipes required to make them (DNA), the sea level still would have to be high enough to pick up the viable human genomes. However, even if all the ice melts, significant parts of the land would still not be covered with water. There are two solutions:
additional water comes from the deep and/or from space,
no additional water is needed, biomass destined for migration is concentrated where needed (eg. on Antarctica).
The most likely outcome is probably a superposition of these 2 solutions. With climate changes (and possibly nuclear war) Antarctica may increase its habitability while the rest of the world is decreasing habitability. Biomass destined for migration (including people, or hybridized people [
139]) could be thus
lured or guided (eg. by certain fields of potential) to Antarctica prior to migration.
Note that the collapse of the Atlantic meridional overturning circulation (AMOC) would significantly decrease temperatures in the Northern Hemisphere while, at the same time, it would further accelerate warming in the Southern Hemisphere, particularly about Antarctica. Apart from increasing storms, flooding and dropping temperatures in Europe and North America (where, in the east, it would also raise sea level), the collapse would severely disrupt the rains that billions of people depend on for food in India, South America and west Africa.
Thus, AMOC collapse would significantly increase habitability of Antarctica while significantly decreasing habitability elsewhere.
Some studies suggest AMOC could collapse this century and the most recent one predicts collapse sometime between 2025 and 2095 [
140], with probability maximum about 2050.
Increased levels of radiation (eg. through a nuclear war, magnetic field anomalies) could also have a role in migration of biomass to Antarctica. Magnetic field is currently decreasing strength while tensions between US and China/Russia are high and have been rising lately.
In standard embryogenesis, migration of cells can be stimulated by excretion of extracellular matrices (various cell products).
Here, one equivalent factor may be hydrogen sulfide (H
S), a highly toxic and unpleasant gas, which had a role in at least some past major mass extinctions. For example, natural gases (incl. hydrogen sulfide) leaked from deeper reservoirs in the Arctic could be carried by disturbed polar jet streams toward the equator, stimulating life to migrate south. Indeed, the increasing accumulation of Sargassum seaweed [
141] on the shores of the Caribbean, America and Africa could be interpreted as a precursor to larger hydrogen sulfide emissions (the Sargassum is releasing H
S as it rots).
If environmental pressure is required to stimulate migration, a major extinction may be interpreted as a side-effect of migration induction, or a result of filtering - which can also be interpreted as natural selection. Is it a selection of most intelligent, most adaptable and/or most easily manipulated? In any case, those who do not migrate, lack intelligence or adaptation capabilities, are probably those who go extinct and will appear in the fossil record. If intelligence is selected for migration here (effectively, or whatever the interpretation), it is then quite possible that high intelligence has evolved, or has been cultivated, multiple times on Earth.
Rise in atmospheric greenhouse gases seems unlikely to produce adequate rise in temperature required to melt all ice in the predicted short time-frame (≤2066). Thus, different mechanisms may be responsible to induce significant breaking and melting of ice sheets. In addition to greenhouse gases, geothermal sources are likely. Melting can also be accelerated by asteroids, but also by advanced alien species from the deep.
However, if time indeed gets effectively compressed (with temporarily increased decay rates of elements), radioactivity itself could contribute to melting. Assuming that the increase of decay rates of hydrogen and oxygen in water molecules doesn’t produce significant effect (hydrogen probably shouldn’t be affected at all, and the effect may be negligible for all stable isotopes), required radioactivity (heat) may be produced by less stable isotopes trapped in ice or by elements in the crust below it.
Note that significant amount of sea level rise has been already baked in with the increase of CO from pre-industrial 280 ppm to present levels (≈410 ppm). The estimates depend on study (some are analyses of recent glacial-interglacial fluctuation, others of individual past events with different CO ranges) and range from 10 - 40 metres. The relationship is not linear and may go roughly like this:
with CO in the range 200 - 400 ppm, sea level rise baked in is 26 m per 100 ppm of CO,
for 400 - 600 ppm, 13 m rise per 100 ppm CO,
600 - 800 ppm, 4.3 m rise per 100 ppm CO.
This would then result in 65.8 m total sea level rise, baked in with CO rising from 280 ppm to 800 ppm.
Note that, although predicted as such, migration of life (at least one that represents proteins, not cells) from the surface to mantle layers does not necessarily imply transfer of living individuals (depending on transfer conditions, it may not even be possible to survive it). DNA may be all that’s required.
However, migration to Antarctica probably is a migration of living individuals. Not all species may migrate and not all individuals of species
selected for migration will migrate (I have hypothesized elsewhere that every population contains polarized and non-polarized individuals and only one of these is affected by strong evolution [
142] and will migrate). This then can explain the unexpected negatively-skewed frequency distribution of body size for extinct dinosaur species [
143] (although other explanations are possible). Further going in favour of the hypothesis is the fact that distribution was distinctly negatively-skewed only toward the end of major time periods, when migration is supposed to occur. This suggests that the largest dinosaur species did not migrate, or that non-polarized individuals dominate in largest species - which I find more likely.
In case of the current strong evolution event, non-polarized individuals likely dominate in largest whales, while in humans non-polarized individuals still represent a minority. The fossil record past the current event is thus unlikely to contain humans.
But is human DNA destined for migration, or is it an uninvited guest? I assume if land animals are lured to Antarctica, then at least some of them should be neural precursors, otherwise, all that matters is probably life in the ocean (which, however, can contain DNA of land animals, even if not in large amounts).
Conventional potential for faster melting of ice
The rate of melting of interior ice on Antarctica generally depends on two heat fluxes - flux between the ice sheet and the atmosphere and the flux between the ice sheet and the base (geothermal heat flux).
Recent measurements show that geothermal heat flux is bigger than expected but still low, lower than 300 mW/m
, on average [
144]. Much bigger fluxes exist on Antarctica at the vents of subglacial volcanoes where they can be as high as 25 W/m
. If such volcanism would spread all over Antarctica (average heat flux of 25 W/m
), all ice could be melt in about 760 years (without taking into account melting caused by atmospheric heating). At the moment, however, there are no signs of this happening (although this could change with the predicted global increase in volcanism, the signs of which may be here already [
145]).
On the other hand, considering atmospheric heat flux alone, if the average temperature in Antarctica interior would climb by 43.5
C (from -43.5
C to 0
C), 40-50 years would be enough to melt all ice. Is this possible in the short-term? Well, this is exactly what happened on 2022.03.18 at Concordia Station [
146] - temperature measured was a record high -11.8
C, about 43.5
higher than the median average for that day of the year.
Others report a temperature of -11.5
C, claiming 38.5
C higher than normal [
147]. Not 43.5
, but close.
Similar was measured in Vostok, and these places are the coldest places in Antarctica. Is this the signal that yearly average of 0 C could be reached in the short-term? I wouldn’t be surprised. However, melting of all ice may not be required at all for a neurogenesis event. What is certainly required is a sufficiently large area to contain the biomass destined for migration. This will probably be an area with a significant geothermal flux. And the Earth’s magnetic field, which will be fragmented and weak generally, will probably have a significant dipole component concentrated in this area.
The creation of tunnels
By the theory, large scale gravitons (probably inflated from smaller scale) should be commonly involved in the formation of stars and planetary bodies. The inflation (or initial over-inflation followed be deflation and stabilization at the new energy level) of a graviton and dark matter associated with it is relatively synchronized with the clumping of real mass (ordinary matter) and makes the process of formation much faster and possible even in cases of strongly diluted real mass (like in the Kuiper belt of the Solar System, for example).
Given the generally torus-like shape of gravitons, concentration of mass is not isotropic.
Mass in planetary bodies should then be differentiated not only vertically, but horizontally as well, with lower density at the poles and possibly even with tubes (tunnels) connecting poles of large scale gravitons, or different energy levels in case of a single oscillating graviton (although these tunnels in terrestrial bodies would have to be eventually filled with fluids to ensure stability).
Note that Earth’s gravity is greater on the poles, but not as much as would be expected for either simple compression or removal of material. Density does seem to be somewhat lower at the poles. Are there tunnels below? Long-lived tunnels, except near gravitons, seem unlikely due to increasing pressure with depth, however, fluid density should be increasing with depth as well. High polarization and angular momentum of the wall material (or the fluid) can increase the stability of such tubes but this is not expected for the walls in terrestrial bodies (fluid flowing toward the centre would, however, possess an angular momentum). Long term stability could be ensured with appropriate density of energy levels and relatively frequent oscillation of large scale gravitons as this provides multiple density maxima. Lateral density gradient (with increasing density away from the pole) also decreases pressure on the tube and such gradients are likely for rotating bodies (note that Earth rotated much faster during formation). Otherwise, tunnels may be only periodically recreated (fluids remelt). I suspect that on bodies like Earth the fluids involved should be [salty] water and magma, with dominant fluid probably depending on the pole. Land should be depressed at the entrance where water is involved, however, it may be elevated on the pole where magma is involved. Interestingly, the subglacial topographic depression in Antarctica known as Wilkes land anomaly (elsewhere hypothesized 480 km wide impact crater, which would make it the largest impact crater on Earth) was directly antipodal to Siberian Traps (largest known volcanic event in the last 500 million years) during the Permian-Triassic boundary (Siberian Traps are considered to be the primary cause for the Permian-Triassic extinction, largest mass extinction on Earth).
Interestingly, the Siberian Traps may not be the only large scale phenomenon the Wilkes anomaly was antipodal to over time.
The 31 km wide Hiawatha structure on Greenland, hypothesized to be an impact crater, seems to have been antipodal to Wilkes anomaly at the time of the hypothesized impact (estimated to have occurred about 58 million years ago [
148]). However, rather than being directly correlated with Hiawatha structure, Wilkes may be directly correlated with the creation of the Iceland hotspot (likely a mantle plume effect), which was located beneath Greenland at the time [
149] and was responsible for the strong wide-spread volcanism (comparable to Deccan Traps) occurring there some 60 million years ago (Vaigat formation).
Currently, however, the Iceland hotspot is antipodal to the Balleny hotspot (Balleny islands), which does not seem to be correlated with a mantle plume [
150].
The crater hypothesis has its problems and it is questionable whether impacts alone can cause significant volcanism on the other side of the planet (although they can certainly cause earthquakes). However, the recreation of tunnels with graviton oscillation should create such phenomena at antipodal locations - depression on the side of water entrance/exit, bulges or traps at the side of magma expulsion (masking the depression). If Earth is modelled as a living being, different products on entrance and exit are expected. As tectonic plates move with time, the locations on the surface should move as well. I believe that all major mass extinctions are correlated with recreation of the tunnels. The Siberian Traps are already considered to be the result of a mantle plume which effectively is a
temporary creation of a tunnel between the planet’s core and surface through which magma flows upwards. Antipodal volcanism is common to large craters of the Moon and Mars [
151] and there are other examples of antipodal relationships on Earth involving large igneous provinces and hotspots (Yellowstone, for example, is antipodal to French Southern and Antarctic Lands). All of these may be correlated with oscillation of large scale gravitons and associated temporary recreation/reactivation of tunnels. In fact, deep mantle plumes may not be possible without it. As noted before, energy level changes cannot be absolutely spontaneous and large impacts can be interpreted as relative triggers of energy level changes of large scale gravitons. If graviton is, at the time of impact, oriented in such way that its axis of rotation is aligned with the impact site, and this should be likely at least for impacts occurring near the poles (possibly nearer magnetic ones if these are present), then the impact can be correlated with antipodal volcanism. In that case, the seismic energy generated by the impact further stimulates the flow of fluids through the tunnels, increasing the effect on surface (note that impacts do create chimneys of stress connecting the impact source with the antipodal location [
152]). Generally, however, impact sites may not be aligned with the graviton axis at the time of impact and the magnitude of extinction then should be proportional to the alignment. The exceptional magnitude of Permian-Triassic extinction thus can be explained as a result of unusually high alignment.
If there are multiple gravitational maxima in the mantle, the lateral pathways in the core-mantle heat convection cells must be branching, corresponding to the number of maxima. Thus, plate tectonics may be present in multiple places in the upper mantle as well. In fact, I suspect that surface plate tectonics is only active during embryonic development, and possibly, in a limited way, during adult neurogenesis in mature planets.
In any case, if the highly energetic expulsion of magma on the surface is matched with antipodal water intake, the mechanism of transfer of organics into the deep exists.
14.4.3. Analysis of past extinctions
Here, past extinctions are analysed for periodicity, with incorporated corrections by previously calculated time compression due to pulses of decay rate changes.
Periodicity is obtained using circular spectral analysis [
153] of a couple of datasets, which all give similar results.
Data is grouped into energy levels corresponding to the extinction magnitude (5 - major extinctions, 4 - minor extinctions, 3 - other extinctions, 2 and 1 - potential extinctions).
The method
In the circular model of periodicity a time line is wrapped about a circle, the circumference of which represents a trial period. For each occurrence, a unit vector from the origin is calculated. If periodic, the series will tend to form a cluster at one point on the circumference when the correct trial period is used. Here, angular location relative to 0 (present) gives the phase (t).
Ages of individual events (t
) are transformed to angles (a
, b
) for each trial period P:
where R is a mean vector magnitude (normalized measure of goodness of fit). The phase shift (t
) is calculated as follows:
Dataset 1
Table 24.
Extinction events dataset 1, sources: *, a, b, c, d, e, f, g, h.
Table 24.
Extinction events dataset 1, sources: *, a, b, c, d, e, f, g, h.
| energy level |
extinction events [mya] |
extinction events (t), age corrected [mya] |
| 5 |
66*, 201.3*, 252.2*, 365, 445 |
61.986, 190.208, 238.316, 345.385, 421.148 |
| 4 |
37.8*, 145*, 260, 305, 420 |
36.206, 136.774, 245.993, 288.3, 397.519 |
| 3 |
11.6*, 93.9*, 182.7*, 230, 270, 424e, 428, 488, 502 |
11.402, 88.465, 172.88, 217.463, 255.844, 401.469, 404.42, 461.48, 475.257 |
| 2 |
117, 168.3* |
111.194, 159.702 |
Extinction events in dataset 1, grouped into energy levels and calculated corrected ages for these events, respectively, are shown in
Table 28.
Maximal R was obtained for a period P = 25.92 My (million years), with a phase of 9.355 My.
On the left,
Figure 23 shows extinctions plotted against the obtained periodicity (dashed grey line), solid colored circles are extinction events with corrected ages, empty circles are extinctions with non-corrected ages. On the right,
Figure 23 shows the result of circular spectral analysis.
Dataset 2
Here, a larger dataset from a single source was used.
Table 25.
Extinction events dataset 2, source: Gradstein2016.
Table 25.
Extinction events dataset 2, source: Gradstein2016.
| energy level |
extinction events [mya] |
extinction events (t), age corrected [mya] |
| 5 |
66, 201.4, 251.9, 372.2, 445.2 |
61.986, 190.308, 238.041, 352.461, 421.348 |
| 4 |
37.8, 145, 259.8, 306.7, 419.2 |
36.206, 136.774, 245.793, 289.975, 396.744 |
| 3 |
11.6, 93.9, 183.7, 228.5, 272.3, 423, 427.4, 485.4, 500.5 |
11.402, 88.465, 173.88, 215.987, 257.12, 400.469, 403.82, 458.929, 473.782 |
| 2 |
113.1, 168.3 |
107.344, 159.702 |
Maximal R reveals a period P = 26 My, with a phase of 8.617 My.
Extinctions and the result of spectral analysis are shown in
Figure 24.
Dataset 3
Previous datasets do not take into account possible splitting of energy levels. Here, an even larger dataset is presented which shows possible energy splitting and how this, when not accounted for, causes lower confidence in calculated P.
Table 26.
Extinction events dataset 3, source: Gradstein2016.
Table 26.
Extinction events dataset 3, source: Gradstein2016.
| energy level |
extinction events [mya] |
extinction events (t), age corrected [mya] |
| 5 |
66, 201.4, 251.9, 372.2, 445.2 |
61.986, 190.308, 238.041, 352.461, 421.348 |
| 4 |
37.8, 145, 259.8, 306.7, 419.2, 514 |
36.206, 136.774, 245.793, 289.975, 396.744, 486.084 |
| 3 |
11.6, 93.9, 183.7, 228.5, 272.3, 423, 427.4, 485.4, 500.5, 541 |
11.402, 88.465, 173.88, 215.987, 257.12, 400.469, 403.82, 458.929, 473.782, 511.664 |
| 2 |
113.1, 168.3, 330.9 |
107.344, 159.702, 312.804 |
| 1 |
295, 346.7, 393.3, 467.3 |
279.448, 328.357, 372.239, 442.101 |
Here, for R = 0.413, obtained P = 22.493 My, phase 15.603 My.
Dataset 4
Here I hypothesize that deviations from P are the result of energy splitting into smaller events which when grouped properly would fit on P intervals.
The dataset is the same as dataset 3, except the hypothesized splittings (circled extinction pairs in
Figure 25) have been grouped into a single event, simply by using arithmetic mean age of the pair.
Table 27.
Extinction events dataset 4.
Table 27.
Extinction events dataset 4.
| energy level |
extinction events [mya] |
extinction events (t), age corrected [mya] |
| 5 |
66, 201.4, (251.9+259.8)/2 = 255.9, 372.2, 445.2 |
61.986, 190.308, 241.967, 352.461, 421.348 |
| 4 |
37.8, 145, 306.7, (419.2+423)/2 = 421.1, (514+541)/2 = 527.5 |
36.206, 136.774, 289.975, 398.619, 499.361 |
| 3 |
11.6, 93.9, (183.7+168.3)/2 = 176, 228.5, (272.3+295)/2 = 283.7, 427.4, (485.4+467.3)/2 = 476.4, 500.5 |
11.402, 88.465, 166.304, 215.987, 268.346, 403.82, 451.053, 473.782 |
| 2 |
113.1, (330.9+346.7)/2 = 339 |
107.344, 320.78 |
| 1 |
393.3 |
372.239 |
The R peaks at 0.807, corresponding to P = 25.89 My, very close to one obtained from dataset 1. Phase is 9.55 My.
Dataset 5
Here dataset 4 is modified with the assumption that splitting occurs in all events, thus, in addition to previously grouped events, the remaining non-grouped events have been grouped with adjacent boundaries.
Table 28.
Extinction events dataset 5.
Table 28.
Extinction events dataset 5.
| energy level |
extinction events [mya] |
extinction events (t), age corrected [mya] |
| 5 |
(61.6+66)/2 = 63.8, (199.4+201.4)/2 = 200.4, (251.9+259.8)/2 = 255.9, (372.2+382.7)/2 = 377.5, (443.8+445.2)/2 = 444.5 |
60.81, 189.333, 241.967, 356.687, 420.648 |
| 4 |
(33.9+38)/2 = 36, (139.4+145)/2 = 142.2, (306.7+314.6)/2 = 310.7, (419.2+423)/2 = 421.1, (514+541)/2 = 527.5 |
34.431, 134.998, 293.926, 398.619, 499.361 |
| 3 |
(11.6+13.8)/2 = 12.7, (89.8+93.9)/2 = 91.9, (183.7+168.3)/2 = 176, (228.5+237)/2 = 232.8, (272.3+295)/2 = 283.7, (427.4+430.5)/2 = 429, (485.4+467.3)/2 = 476.4, (497+500.5)/2 = 498.8 |
12.502, 86.49, 166.304, 220.213, 268.346, 405.395, 451.053, 472.107 |
| 2 |
(113.1+126.3)/2 = 119.7, (330.9+346.7)/2 = 339 |
112.87, 320.58 |
| 1 |
(387.7+393.3)/2 = 390.5 |
369.489 |
Figure 27.
Dataset 5 - spectral analysis
Figure 27.
Dataset 5 - spectral analysis
The R peaks at 0.75, corresponding to P = 25.84 My. Phase for this P is 9.78 My, however, here another peak at 12.875 My (R = 0.61) reveals a likely harmonic.
Dataset 6
Here, dataset contains only highest energy (major and minor) extinctions, from dataset 1.
Table 29.
Extinction events dataset 6.
Table 29.
Extinction events dataset 6.
| energy level |
extinction events [mya] |
extinction events (t), age corrected [mya] |
| 5 |
66, 201.3, 252.2, 365, 445 |
61.986, 190.208, 238.316, 345.385, 421.148 |
| 4 |
37.8, 145, 260, 305, 420 |
36.206, 136.774, 245.993, 288.3, 397.519 |
This dataset gives highest R maximum (0.837), a period P = 25.74 My, with a phase of 9.689 My.
Confidence
Note that equal weight was assumed for all extinctions in a particular dataset. Different weights can affect the confidence in the result (less if they are all harmonics). But even with that taken into account, there is high confidence in P ≈ 25.74 My - 25.89 My.
The result with highest confidence (25.74 My) is also the closest to calculated ideal quantization by the 3rd order period (1.512 ∗ 10 My) - 25.705 My, further increasing confidence in such periodicity.
Note that the burning cycle of the Sun’s core is calculated (in the "Quantization of the Sun" chapter) to be equal to 25.746608 My, confirming the signal.
Interestingly, taking into account major extinctions only, one of the obtained peaks (with R = 0.94) is at 25.705 My, exactly as needed for ideal quantization.
Neurogenesis in standard lifeforms on Earth during embryonic development does imply certain periodicity in the formation of brain layers and neuron migration.
High energy impact cratering and extinctions (migrations) in planetary neurogenesis should be no exception.
In fact, with such periodicity and the last high energy extinction 37.8 My in the past, next one would be overdue, roughly by the phase shift.
Note that such delay of extinction could have some benefits due to more evolved precursor neurons at time of differentiation, although with the cost of increased probability of cancer development.
Also note that neurogenesis implies correlation of many processes. Therefore, calculated periodicity should not be limited to mass extinctions, rather present in plethora of other phenomena affecting the planet - volcanism, magnetic reversals, seafloor spreading, orogenic events, etc.
Indeed, such periodicities have been found in previous analyses [
163].
However, as noted before, major extinctions seem to be grouped in pairs and multiple oscillators should probably be considered. With paired extinctions separated by roughly 63±3 My (in uncorrected ages), major extinction in the present time would be on schedule. This peak can be observed in analysis. Indeed, repeating the analysis for dataset 5, but with only major events (using corrected ages) included, yields highest peak at 12.85 My (the 2nd harmonic of 25.7 My) and R = 0.973, with the 2nd highest peak being at 59.272 My (R = 0.923).
Including current extinction (0 Mya) in the analysis gives highest peak at 59.74 My (R = 0.925) and a phase shift of 2.38 My. Note that, while the hypothesized 3rd order cycle period of 1.512 My is a harmonic of 25.7 My, the 2nd harmonic of 1.512 My (0.756 My) is a harmonic of 12.85 My and is then probably also a harmonic of the bigger period, in which case the correct period would be 59.72 My. Assuming synchronization with this harmonic (0.756 My), last major extinction 62.029±0.011/0.043 Mya (66.043±0.011/0.043 Mya uncorrected [
164]) gives the interval for the current major extinction 48000 years before present to 6000 years after present. Interesting result, considering the extinction of megafauna (incl. Neanderthals) started some 50000 years ago. The age of 66.006 Mya (uncorrected) for the last major extinction would give exactly the present time for the current extinction.
In any case, this suggests the current major extinction is right on schedule.
Thus, imminent extinction (or the ongoing extinction peak) as calculated using models based on C1.1 equation should not be surprising.
Supplement
Here is the code used to calculate correct ages of extinction events, perform the analysis and generate images.(Fig.: getext.php +)
14.4.4. Correlation with mantle layers
Grouping and correlation of extinction events with the formation of brain [mantle] layers also indicates that another major mass extinction should be near, at least in geological terms.
This correlation is shown in
Figure 28 - time between major extinction events of Phanerozoic is proportional to the thickness of the corresponding mantle layer.
Such correlation should not be surprising - all lifeforms grow in layers. But it also confirms the previous hypothesis that asteroid impacts are correlated with discontinuities (changes in energy levels) in Earth. Note that encapsulated growth/development is common in standard embryogenesis. It appears this is the case with planets such as Earth as well.
This is, effectively, a conversion of time separated discontinuities into events separated in space.
To quantify the correlation, periods of weak evolution and thicknesses of mantle layers have been normalized:
Results are shown in
Table 34. Here, corrected extinction ages are used, although non-corrected ages would yield similar results.
Table 30.
Comparison of weak evolution periods and mantle layers, sources: a, b.
Table 30.
Comparison of weak evolution periods and mantle layers, sources: a, b.
| i |
Period of weak evolution T [My] |
Normalized period of weak evolution T
|
Corresponding mantle layer thickness D [km] |
Normalized layer thickness D
|
| 5 |
421.348 - 352.461 = 68.887 |
0.163 |
780 - 660 = 120 |
0.176 |
| 4 |
352.461 - 238.041 = 114.42 |
0.272 |
660 - 520 = 140 |
0.206 |
| 3 |
238.041 - 190.308 = 47.733 |
0.113 |
520 - 410 = 110 |
0.162 |
| 2 |
190.308 - 61.986 = 128.322 |
0.305 |
410 - 220 = 190 |
0.279 |
| 1 |
61.986 - 0 = 61.986 |
0.147 |
220 - 100 = 120 |
0.176 |
Correlation in absolute value varies between the pairs, but overall, it is apparent.
At least some deviation could be explained by the fact that formation is not yet complete - eg. the boundary between layers 3 and 4 might change with the pending extinction.
If layer 3 decrease would be equal to layer 4 increase (≈ 0.0575 in normalized value) and layer 1 decrease to layer 2 increase (≈ 0.0275 ≈ 0.0575 / 2), with a small decrease in layer 5 (0.013 ≈ 0.0275 / 2) coupled with equivalent increase in layer 6, normalized extinction and mantle boundaries would be almost equal.
Effectively, what is necessary for better agreement is the upward movement of 3 discontinuities (between layers I and II, III and IV, V and VI).
There are two interpretations for the correlation. Extinction events are either memorized in Earth’s [brain] mantle as they occur or they are programmed events and can be predicted through the analysis of discontinuities (layers) in the mantle. The ongoing 6th major extinction and existing discontinuity at 100 km depth suggest the latter, although superposition may be more likely - discontinuities are ancient but they move/adjust as extinctions occur.
In any case, the correlation is good evidence for living Earth and its neurogenesis.
The entanglement of 3 discontinuities (I/II, III/IV, V/VI) suggests that all 3 move during a single extinction, thus, if movement is correlated with asteroid impacts, 3 impacts may be ahead.
However, exact location of boundaries is a matter of debate. They must have some thickness, so it may be more appropriate to equate layer thickness with distance between discontinuities. If that would be a distance between lower discontinuities of two boundaries, it would, for layer 1, yield a normalized value exactly equal to the corresponding normalized period of weak evolution:
Also, globally average velocities might not be the best choice for determination of layer discontinuities - eg. Lehmann discontinuity is at 220 km for tectonic North America, but 200 km for shield North America [
167], while it may be absent beneath north Atlantic and other oceans.
No graviton can be completely neutral. At the time a discontinuity is occupied by a [large scale] graviton, a hole, proportional to polarization, is expected. Physical imprint may be further complicated with the presence of multiple gravitons and may be affected by additional disturbances.
If one assumes that 200 km is a
proper boundary (220 km may be a precursor boundary that will reduce to 200 km with complete formation), the correlation with extinctions for both layers, I and II, becomes remarkable:
Some report the base of the upper mantle at 670 km [
168] rather than 660, this improves the correlation with layers 5 and 4:
Now, the only
problematic boundary is the one between layers 3 and 4 (at 520 km). Some do report this boundary at 500 km, which gives much better agreement:
Note that extinction boundaries also have some thickness or uncertainties, notably first three, which may explain differences in reported discontinuity depths. The 3rd major extinction (Permian) is apparently split into two events (End-Capitanian and Permian-Triassic). Using End-Capitanian 245.793 Mya (259.8 Mya non-corrected) instead of Permian-Triassic 238.041 Mya (251.9 Mya non-corrected) as the date of Permian extinction gives results in remarkable agreement with the obtained layers 3 and 4 (with discontinuities at 410 km, 500 km and 670 km):
The correlation, with above adjustments, is shown in
Table 35 (with ages rounded to a single decimal).
Table 31.
Correlation of weak evolution periods and mantle layers (or, major extinctions and discontinuities).
Table 31.
Correlation of weak evolution periods and mantle layers (or, major extinctions and discontinuities).
| i |
Period of weak evolution T [My] |
Normalized period of weak evolution T
|
Corresponding mantle layer thickness D [km] |
Normalized layer thickness D
|
| 5 |
421.3 - 352.5 = 68.8 |
0.163 |
780 - 670 = 110 |
0.162 |
| 4 |
352.5 - 245.8 = 106.7 |
0.253 |
670 - 500 = 170 |
0.250 |
| 3 |
245.8 - 190.3 = 55.5 |
0.132 |
500 - 410 = 90 |
0.132 |
| 2 |
190.3 - 62.0 = 128.3 |
0.305 |
410 - 200 = 210 |
0.309 |
| 1 |
62.0 - 0 = 62.0 |
0.147 |
200 - 100 = 100 |
0.147 |
The correlation, using uncorrected ages for major mass extinctions, is shown in
Table 36.
Table 32.
Correlation of weak evolution periods and mantle layers, using uncorrected ages.
Table 32.
Correlation of weak evolution periods and mantle layers, using uncorrected ages.
| i |
Period of weak evolution T [My] |
Normalized period of weak evolution T
|
Corresponding mantle layer thickness D [km] |
Normalized layer thickness D
|
| 5 |
445.2 - 372.2 = 73.0 |
0.164 |
780 - 670 = 110 |
0.162 |
| 4 |
372.2 - 259.8 = 112.4 |
0.252 |
670 - 500 = 170 |
0.250 |
| 3 |
259.8 - 201.4 = 58.4 |
0.131 |
500 - 410 = 90 |
0.132 |
| 2 |
201.4 - 66.0 = 135.4 |
0.304 |
410 - 200 = 210 |
0.309 |
| 1 |
66.0 - 0 = 66.0 |
0.148 |
200 - 100 = 100 |
0.147 |
Interestingly, corrected ages are in all cases except for i=4 in better agreement with mantle layers. Unless an artefact of rounding/imprecision (eg. in depths of discontinuities, which may be averages) this can be interpreted as evidence for effective time compression (pulses of abrupt temporary changes in decay rates of elements).
The excellent agreement here suggests no further adjustment of discontinuities is needed, except possibly for layer I, as shown in green in
Figure 28 (right) which should be unsurprising given the correlation with the current extinction.
Correlation of layer 6 and the corresponding period of weak evolution has not been determined due to unknown boundary.
However, assuming the extinction at the start of Phanerozoic (511.664 mya in corrected age, or 541 mya non-corrected) is correlated with the lower boundary of layer 6, one can calculate the thickness of layer 6:
In that case, a discontinuity, if formed, should exist in Earth’s mantle at a depth of 937 km (assuming boundary between layer 5 and 6 at 780 km).
Apparently, this discontinuity has been detected [
169] (at 940 km).
14.4.5. Evidence in time compression
If planetary neurogenesis is happening on Earth, it was likely happening on Mars and Venus too. Time, however, flows differently for animals of different size. The rate of evolution on Mars should then be different from the rate of evolution on Earth - it should be faster.
Applying Kleiber’s law, 4.54 billion years of evolution on Earth would, on Mars, last:
M = 0.642 ∗ 10 kg
M = 5.972 ∗ 10 kg
T = 4.54 ∗ 10 years
Assuming Mars was formed roughly at the same time as Earth, present time on Earth corresponds to a time 3.69 billion years ago on Mars (4.54 - 0.85 = 3.69).
This is a very interesting result as studies show that Martian climate shifted from habitable to uninhabitable - when its atmosphere was lost and liquid water disappeared from surface, roughly 3.6 billion years ago [
170] (src [
171]).
This suggests that current major extinction on Earth may indeed be the final major extinction of the planetary embryogenesis (neurogenesis), after which the Earth’s surface will become permanently uninhabitable (although periodic and possibly spatially limited pulses of habitability cannot be excluded, as hypothesized pulses of adult neurogenesis).
The same equation gives evolution period of 3.9 billion years for Venus, suggesting Venus lost habitability some 640 million years ago. Again interesting, as studies [
172] show that Venus did lose habitability roughly 700 million years ago [
173].
It is a common assumption that all planets in the Solar System have been formed at the same time (this is also the case with my theory of inflation of the system), and calculations above certainly can be interpreted as a confirmation of that assumption. However, the term is relative and a deviation on the order of millions or tens of millions of years is possible.
The rate of evolution here should be matched by the rate of geologic changes. Thus, these too should have proceeded at faster rates on early Mars. In example, the average rate of production of new crust during the Mars’ habitable period should have been about 5.33 times faster than on Earth. Magnetic reversals, on the other hand, are likely correlated with the Sun’s activity and Mars, being farther from the Sun, should be less sensitive to this activity. Magnetic dipole reversals on Mars during the crust formation should then be less frequent (proportionally to distance difference) than on Earth during the habitable period.
Assuming sensitivity inversely proportional to the square of distance (being dependent either on Sun’s gravity, electro-magnetic field strength, or, most likely, solar wind density [
174]), with horizontal scale length of order 10 km on Earth for the width of features magnetized in normal, or reversed, polarity, the horizontal scale length on Mars should be:
d
= horizontal scale length on Earth = 10 km
r = Mars’ distance from the Sun = 227.9 ∗ 10 m
r = 149.6 ∗ 10 m
Thus, on Mars, magnetic crust anomalies should be 10 times wider than on Earth, and this is exactly what has been measured [
175]. Given this and other evidence, plate tectonics had likely occurred on habitable Mars, only the number of plates, compared to Earth, may have been different.
Interestingly, observations show stronger magnetism near the Mars’ south pole [
176]. This could indicate that the magnetic field was confined to this area during the late stages of habitability on Mars (which should not be surprising if life is guided to the south pole, as hypothesized for the end of neurogenesis events). It could also be interpreted as younger re-magnetization (eg. during an adult neurogenesis event). Both interpretations can be true. In fact, discrepancy between most recent measurements of Mars’ core radius (1650±20 km [
177]) and previous estimates (1810 - 1860 km [
178]) suggests a recent change in energy level of a major graviton, possibly causing core differentiation into a solid inner core and liquid outer core. This should then result in a creation of a magnetic field on surface (possibly also recreation of a larger Martian moon) and may thus be interpreted as a signal of an upcoming adult neurogenesis event on Mars.
14.4.6. Some additional predictions of neurogenesis
If cultivation of life on planet’s surface is equivalent to cultivation of neural cells during embryonic neurogenesis in mammals, the events hypothesized above are not the only upcoming events that can be predicted.
Obviously, cultivation of cells/proteins must be limited. The most effective (or most energy efficient) way to limit population growth is to substantially decrease its fertility. Recent studies show that fertility in humans is indeed decreasing, at an accelerating pace [
179]. But possible ways to limit population growth are diverse and probably will be diverse. Fertility decrease does not have to be correlated exclusively with physical health (inability to produce offspring), it can rather be effective, eg. through subconscious effects on human psyche or mentality. Generally, limitation of population growth can be correlated with:
decrease in ability or will to produce offspring,
increase in types of reproduction inhibiting sexuality (eg. homosexuality, bestiality, etc.) and increase in asexuality,
decrease of physical gender inequality or increase in physical attributes and behaviour decreasing sexual attraction between males and females,
increase in male-female mental incompatibility,
increase in socio-economic gender equality, reducing the need or will for partnerships,
increase in acceptable sterile alternatives (artificial, virtual) or substitutes for sexual intercourse,
increase in attraction and partnerships between younger (more fertile) and older (less fertile) male and female individuals,
domesticated animals and artificial intelligence increasingly filling the voids usually occupied by children or partners,
decrease in sexual compatibility (which can be strongly correlated with the above),
increase in diseases that can be correlated with a decrease in fertility (eg. prostate cancer),
increase in deaths (eg. through wars, natural disasters, diseases, …), assuming limit has been exceeded and population needs to be reduced to sustainable levels,
etc.
Evidently, all of these are currently present, and most, if not all, are increasing in the society.
Of course, at least some of these effects can be attributed to humans (eg. pollution may affect fertility directly), but even that probably should not be interpreted as non-coded or non-natural development.
Correlated with short-term interests, polarized humanity obviously does not want to limit population growth (contrary, it promotes unlimited growth), however, something, correlated with long-term interests, is obviously acting against it. I don’t see much free will here, I see two forces, one seeking domination and the other its regulation. This may be common for the process of neurogenesis, where, in a healthy one, regulation prevails, and this then can be interpreted as domestication or taming of cancer, as regular part of embryogenesis.
Accelerated evolution also likely includes accelerated ageing in some species or sub-species (in some, possibly reversed), cases of which are showing up in studies too [
180].
14.4.7. Adult [neuro]genesis
I have hypothesized previously that changes in energy levels of large scale gravitons are correlated with major mass extinctions and evolution of life in between. If different species of life are evolved between these major extinctions, the large scale graviton associated with these is not oscillating between adjacent levels, it is rather increasing or decreasing energy level with each major extinction. Here, progressive evolution may be associated with increasing energy levels, regressive evolution with decreasing energy levels. But what if the graviton is oscillating between two levels? In that case, relatively the same species should be evolved over and over again. This is exactly what happens in adult [neuro]genesis events. Once the highest energy level is reached, evolution (development) of new species stops. Occasionally, the graviton drops to a lower level before it returns back up, which should then be correlated with re-evolution of certain species.
Note that death event is a collapse of the graviton [entanglement with the body]. In this collapse, graviton changes vertical energy levels, not horizontal, so, assuming direct transition, there is no regressive evolution of body components. However, the collapse may at least in some cases include transition between horizontal energy levels as well, which then should include evolutionary regression to some degree.
Note also that, assuming that decay rates of standard unstable elements are temporarily increased with energy level increases, and temporarily decreased with energy level decreases, oscillation would imply no net effect on decay rates.
Adult [neuro]genesis events are probably generally spatially and temporally limited. Note that a relatively recent adult neurogenesis event on Mars has the potential to explain unexplained phenomena on Earth (eg. some UFO/UAP sightings/interactions, greatest pyramids in Egypt). Some of the intelligent lifeforms re-evolved in the last Mars’ adult neurogenesis event may have, with the neurogenesis terminating extinction event, fled to Earth. Here they may have built the greatest pyramids (possibly even original Sphinx) as shelter, possibly using some kind of 3D printing machinery. They may have somewhat evolved since and probably still inhabit Earth (and/or Moon?), somewhere in the deep. As I have hypothesized elsewhere, modern Egyptian religion was probably formed once Egyptians encountered these structures. They associated them with gods, considered them sacred (this is one of the reasons why there are no original inscriptions in greatest pyramids) and started imitating them - to please the gods and to secure passage to the underworld.
In fact, life matching or surpassing human intelligence may evolve prior to each major mass extinction (with temporary effective time compression solving flaws in the Silurian hypothesis), it just doesn’t last long on surface. It thrives somewhere deeper underground (in the underworld).
14.4.8. Problems and alternatives
While partitioning of the Earth’s mantle, its correlation with major extinctions and cultivation/evolution of cells (life) on the surface do represent a strong signature of a large scale equivalent of neurogenesis, how plausible it is that migration of life to mantle does indeed happen?
It is possible that it does not - the Earth might simply represent a large scale of a [precursor] lifeform that is yet to evolve neurogenesis. Perhaps life evolving on the surface will, on its own, eventually start digging deeper and deeper into the Earth’s mantle (as surface habitability decreases) - in the process changing the environment and making it more suitable for complex life (the process may be somewhat similar to how the standard cell acquired bacteria which evolved into mitochondria).
Note however that this as well could represent the coded migration event of the neurogenesis.
Thus, even if the Earth’s mantle doesn’t have habitable regions at the moment, it’s probably evolving in that direction.
But why then would mantle discontinuities correlate with major extinctions? This could be interpreted as a precursor of formation of habitable layers, but is it possible that the habitable regions have been created already?
To answer that question one first needs to determine what are the requirements for complex life to survive in the mantle. These appear to be: water, energy and suitable pressure (temperature) and density. The availability of water and energy probably should not be questionable (these are already predicted/confirmed with conventional theories/interpretations). The only issue then is the suitable pressure and density, enabling liquid water among other things.
I assume the layers are created and sustained with oscillation of a large scale graviton (if not permanent presence of multiple gravitons at different energy levels). Presence of a graviton will result in concentration of matter (real mass) about that maximum. Once the graviton changes energy level (through spin reversals and temporary scale collapse) the accumulated matter will remain stable for some time (millions of years or more) but periodic presence of a graviton can ensure long-term stability. This mechanism (oscillation between energy levels) can thus create alternating gradients of gravity where gravity is cancelled at some point between two energy levels, enabling thus the establishment of pressures/temperatures suitable for complex life.
Is it possible that such places exist in Earth’s mantle?
It certainly is - even without involving large scale gravitons, density can have multiple maxima, but there are constraints on size and shape (a habitable layer may be represented by a relatively hollow tube in the shape of a torus, or it could be quantized into multiple spherical cells).
Interior of the Earth has not been seen directly so one must rely on indirect observations. The mass (average density) of Earth has been determined from laws of gravity and planetary motion, and is known to very good precision. Moment of inertia of Earth has revealed strong concentration of mass about the centre. Earth’s core thus must be, on average, more dense than the mantle.
Astronomy also revealed that Earth’s mantle must be, on average, rigid (solid).
Everything else known about the interior (including core size) comes from seismology, which is limited and very prone to interpretation bias.
Interpretation is possible once the paths and velocities of seismic waves are determined. Velocity is proportional to pressure (through coefficient of stiffness and shear modulus) and inversely proportional to density. To determine pressure one needs to know the density. Obviously, the same velocity can produce infinite combinations of pressure and density.
Constraints can come from wave dispersion analysis (for shallow depths) and from modes of free oscillation [
181] (which is especially valuable, as it can give averaged density in
absolute value - independent of elasticity).
The conventional interpretation of the interior is usually based on 1-dimensional (density dependent solely on radius) models (eg. PREM), where density in the mantle generally gradually increases with depth. Pressure is then determined from calculated density.
Although 3D models exist as well, due to limited resolution [
182] (averaged values) - which decreases with depth, density can oscillate/deviate from the prediction (model) and some areas in the mantle, especially at depths with high lateral heterogeneity, could have much different pressure and density than assumed. Due to poor resolution of free oscillation and absence of earthquakes (ray-paths) throughout most of the mantle, existence of habitable zones cannot be ruled out.
It is also possible that habitable zones are hidden from view - eg. in regions (eg. tubes, spheres) of effectively curved space where sound waves simply wrap about the region. Here, this is not necessarily a localized spacetime curvature (which, by conventional theories, is not even possible here) rather a material acting like an acoustic invisibility cloak (such materials are definitely possible and have been created by humans already). After all, it makes sense to hide intelligence from outer threats (eg. cancer, or earthquakes), whether extra/intra-terrestrials are involved or not.