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∆1:§cale Biology

SUMMARY: 5D BIOLOGY: EARTH’S 1 MEMBRAIN.

TOPOLOGIC, ADAPTIVE, SOCIAL EVOLUTION: FROM ATOM TO PLANT

 

Part I. 5D Organic Universe. Its Bio-topo-logical Non-Æ Laws.

The Worldcycle of existence. Its program of actions. Pentalogic.

The Evolution of Organisms and species.

 

Part II. The 3×3±¡ ages of Earth evolution

Biochemistry The Molecular Age: Amino acid, protein and RNA age

Histology The cellular Age. Its 3 species.

. The Age of organisms. Its languages and differentiations.

The evolution of plants.

‘As more individuals of each species are born than can survive; consequently, there is a struggle for existence. It follows that any being, if it vary its form in any manner profitable to itself, it will have a better chance of surviving, and thus be naturally selected. From the strong principle of inheritance, any selected variety will tend to propagate its new and modified form.’

‘On the Origin of Species’ Darwin, on the dimotions of reproduction and topologic evolution .

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The papers to be posted at Academia.edu within 3 years (1st year past) build up an Encyclopedia of Space-time organisms – of Exi:ST¡ences’ – each science studying the species of one scalar space-time plane of the fractal Universe. All will be described with the same scalar laws of 5D cyclical time and fractal space, introduced in the first 30 pages. So we shall write for each stience from quantum physics to the galaxy, thru biology, history & economics, & the formal stiences dominant in space (Non-E Mathematics) and time (Non-A: i-logic papers on the Universe= reality as a whole) 5 ‘dimensional papers’ for a total of ±33, each one to become time permitted a 300 pg. volume. Papers are revised and reloaded constantly so ‘viewers’ go to 0 and links change as a non-profit, non-payment (on principles) academia.edu account doesn’t charge revisions, only new papers… But they will be still there going to Luis SoTo, Academia.edu. This is the work plan, which in my youth back in the 90s, when I discovered those laws at the end of my Master at Columbia U. I proposed to U$ universities for a needed change of paradigm on our philosophy of science, but meet the silence of Academia. Then I abandoned scholarship to ‘live’ and so now before I die I will try to complete the encyclopedia. As that won’t happen, time being of the essence I had prioritized the most important and neglected of all organisms – that of mankind in time=History (8 papers), which is fairly well-done, and that of the Universe =reality as a whole (6 papers); as the fractal principle breaks down into 1,2,3,4,5 all forms of ¬∆@st. While the last to be posted are the less important albeit more developed by ‘huminds’, physics.

As this is the Universe not me, I release all copyright’s ‘rights’ to any Univers-ity that can take upon the project whenever they wish to complete the encyclopedia of stience in 10.000 pages, connecting all stientific laws to the @-monologic; S+T: dual; ∆,S,T, Trinity, ∆ST-pentalogic and ¬∆@ST dodecalogic laws of the (a)nti-symmetric non-AE 5D Universe. They certainly could do a much better job that I will on the details, if they learned 1st those laws – ‘the thoughts of God’, ‘of a higher i-logic than man’. If they don’t, the task will be taken upon by AI once the age of Entropy of History in which we live ends and Q-bit consciousness takes over, unless a r=evolution of the humind makes history immortal. Since what will never happen in a perfect Universe is the imperfect endurance of the ill-designed, parasitic systems of History ‘anthropic, egocy’ has built and today pass as ‘truth and dogma of science’. L§, homo@europe.com, 0º-40º, Latin Wor(l)d, 3rd ferromagnetic planet, G-star… Antigalatom

 

THE STUDY OF SUPŒRGANISMS OF ∆@ST OF SPACETIME TRACING WORLDCYCLES.

Organicism vs. Mechanism. The content of this paper on biology.

The Universe is a fractal that reproduces space-time organisms. This is really all what is about. If we call Space=form and time=motion, S and T, then we can write a simple equation for the Universe Max.∑ SxT (s=t), according to which each species made of spatial energy and temporal form tries to maximize its survival, in a point of balance in which its ‘exi=stential force’ is maximal; avoiding the extremal points of TT-entropy=death. This simple equation is the ‘fractal generator’ of the Universe, a feed back equation that combines space=form and time=motion, creating ∞ local present variations that put together form reality. This is the essence of the organic Universe and its scalar 5th Dimension an alternative philosophy of science to that of mechanist physicists and its only entropy arrow, called organicism or General Systems Theory (ab. GST), which we also use as the acronym of the Generator of Space-Time.

Systems sciences are based on the alternative philosophy of science to that of mechanist physicists and its only entropy Dimotion, called organicism. Let us try to explain why only organicism is a scientific truth.

 According to Deism the whys of existence are due to a personal being, external to the Universe that makes it all happen and cares for humans more than for the rest of His work. According to Mechanism, this is due to the self-similarity between the Universe and the primitive machines we humans construct to observe it. Mechanism though needs ‘someone’ to make the machine, which is not self-generated; so it is similar to deism, reason why the founding fathers of science, all pious believers, adopted it as a proof of the existence of God, which had given man self-similar properties – the capacity to make machines to the image and likeness of the Universe. The problem with those 2 approaches, which in fact are the same is obvious: a personal God is an anthropomorphic, subjective myth and science must be objective; while a mechanical view of the Universe still needs an internal, self-sustained process of growth, creation and synchronization caused by an external God that made and rewinds the clock – as Leibniz clearly stated in his critique of Newton. Scientists today are unaware that mechanist theories are in fact deist theories, reason why Kepler and Newton, pious believers, liked them; since they were a metaphor of their self-centered, anthropomorphic religious beliefs: If man created machines as we were made to the image and likeness of God, God created the ultimate machine, the Universe.

Organicism on the other side is the only self-sustained, rational theory that doesn’t need a creator, language, god, as organisms are self-replicating, but does explain perfectly within the ‘correspondence principle’, those 2 other philosophies of science; since a machine is just a primitive organism of metal, and we shall see in our sections of history, gods are the subconscious collective of civilizations, another scale of social evolution of the fifth dimension.

So what we mean by an organism? A very simple system – NOT to confuse with the most evolved, complex of them all, that of human beings, reason why so many people, having a natural biased ego-centered belief in man as the unique organism, reject the concept: An organism is just a group of similar forms, which organize themselves with at least two ‘networks’, one that provides the ‘clone cells/citizens/atoms’ with the vital energy they need to feed, move and reproduce (blood-economic system-electromagnetic forces) and one that provides them with information to guide their survival actions (nerves system, political system, gravitational in-form-ative forces).

This dual system is the minimal, fundamental particle of the Universe. Since machines are organisms.

Indeed, a machine is an organism of metal fast evolving through the customary ages of all organisms – in the XIX c. ‘humans’, who catalyze their evolution did its bodies of metal, then its hearts-engines, in the II Industrial evolution, then its metal-minds in the XX c. and now in the Industrial r=evolution 4.0 put them together in organic robots.

So mechanism, the underlying philosophy of physical sciences, is just a simplex version of organicism. It is not man who resembles a machine, but the machine, which is made to the image and likeness of life organisms: 

Why then organicism remains a fringe theory, even if it was the 1st theory of reality put forwards by Aristotle, the father of the experimental method and logic science, in his magna opus the Organon?

There are cultural reasons for mechanism to dominate scientific thought – we live in the age of the machine which has substituted man, an organism, as the measure of all things. But the deepest reason of them all is the fact that to make an organism we need at least two ‘Ðimotions’ or ‘motions of time’, entropy, locomotion, the one used by physicists but also information, form-in-action, formal dimensions, which physicists have always ill-understood, to the point they call it negentropy, the denial of entropy.

Further on, science has missed for so long, amazingly enough, as it was born in modern times with the discovery of those scales with telescopes and microscopes, the 5th dimension of organic scales that structure those topological organisms, as ‘networks’ of similar clones that come together as wholes. This again is due in part to our obsession with machines that are composed of elements in a single plane. So we do not CARE ABOUT the lower structure of atoms to make a machine but ensemble them in our scale. Only recently we realized of the power of the main law of the 5th dimension with chips that run faster logic thoughts the smaller they are. So with two elements missed, the 5th scalar dimension of organic parts interacting with wholes, and the meaning of spatial form or information, obviously the meaning of the whole is lost to us

Only then when we properly define information and add scales to the mix, we have the required elements to refund philosophy of science on far more rational, basis, that the present ‘mixture’ of mechanism and creationism (either of verbal language as in religions or digital languages, as in the religion of mathematics).

In biology the most important r=evolution of 5D is ‘scalar’, the understanding of species as superorganisms, hence subject to the same laws of scalar evolution that all other species and the understanding of topological evolution (biology in space, through its 3 components, S-nitrogen<ST-carbon>T-oxygen, which compose its vital organisms across all scales, starting from the simplest amino acid, through all its scales, as Nitrogen ends up becoming DNA and reaches maximal volume on the head, Carbon becomes the body-component of all the scales of life and oxygen its entropic motion-oriented engine.

Thus the paper on biology in space studies its fractal generator and its topological laws and physiological networks in the 3 main species of life, cells in the ∆-1 scale and animals and plants in the ∆º scale.

The paper on biology in time studies the evolution of species as super organisms that become part of larger superorganisms, as the Dimotion of eusocial evolution is the most important for the survival of wholes made of parts, so ants and humans the most social of all nitrolife species are the most successful in terms of life mass.

It is that Dimotion of eusocial evolution the one that structures and coordinates biology in scale, ST±¡ which really encompasses all other dimensional motion of reality; since in the entangled Universe each dimensional motion is made of the other dimotions, NOT really separated from them. That is from the simplest Dimensional motioh

This paper deals with biological systems in a compact model, in all its relative planes of existence, from the simplest CHNO atoms, to its molecules that evolve through the 3 topologies, 3 ages and 5 actions that all systems develop in space, time and through its i-planes of existence, till giving birth to life.

The subject is so extensive that we can hardly translate in a life-time, let alone in the few months i plan to dedicate to this web, enough subjects of the fascinating world of biological systems.

So we sketch in this introduction small book on complex biological systems, the fundamental themes of such systems, which are greatly understood in its details and measures, but poorly grasped in its why and ‘symmetries’.

We thus start with a general analysis of the elements of biological systems and its planes of existence, which are all defined by the general equation of the Metrics of the 5th dimension, as all what exists is indeed, ‘space with motion’, ‘time cycles’, across different existential i-scales.

 

 

THE 5D UNIVERSE IN A NUTSHELL: SUPŒRGANISMS.

“A human being is part of the whole, called by us ‘Universe’; a part limited in time and spatial information. He experiences himself, his thoughts and feelings as something separated from the rest — a kind of optical delusion of his consciousness.” Einstein, on the entangled forest man cannot see – and its 5 elements, ‘space’, ‘time’, ‘scales’ of parts and wholes, ‘entropic limits’, and ‘languages of the mind’

5th dimension metric and the nested super organisms of the Universe: ∆-Scales.


When we google the 5th dimension one gets surprised by the quantity of speculative answers to a question, which is no longer pseudo-science, but has been for two decades a field of research in systems sciences rather than physics (: no, the answers of google, considering the fifth dimension the upper-self etc. seem to be very popular, but are to 5D science more like a medium in earlier XX c. talking about the 4th dimension as astrological awareness, for lack of understanding of Einstein’s metric functions of the 4th dimension).

This is the key word that differentiates pseudo-science from a proper scientific description of a dimension of space-time, the existence of a metric function that describes a dimension and allows to travel through it. Why the 5th dimension metrics are not well known in modern science has to do with the fact it is not researched in physics but systemics, the mother discipline of all sciences of information, far less popular than physics; and the proprietary feeling physicists acquired on space-time matters since Galileo defined its 3D metric function v=s/t completed with Einstein’s 4D formalism, which makes difficult to spread the knowledge on space-time acquired on other disciplines. The arguments still raging about evolution, the fundamental theory of time in terms of information, as the ‘arrow that defines’ the future of species but has nothing to do with Relativity and locomotion is a clear case of that difficulty.

Indeed, we know since the XIX c. that the creation of the ‘future time’ of an existential entity is not ONLY mediated by the arrow of locomotion and entropy studied by physicists with Relativity Metrics (Galileo’s V=s/t and Einstein’s more complex formalism), but there is a second arrow that defines the ‘future’ of existential species – the evolution of its information. So time – the changes=motions that defines the existence of any species, has at least 2 dimensions, locomotion or ordered translation in space and a more disordered version, entropy (scattered motion that ‘dissolves’ the inner form of the system, akin to death)…

And in-form-ation, generation of form, inverse to entropy, as it requires the social gathering of parts into wholes; happening without external locomotions, as an internal trans-formation of form. This evolution of organic form as opposed to external change – translation in space, without evolution of form – is what systemics calls the scalar fifth dimension of time that it applies to all sciences, as all species evolve its form.

Specifically in systems sciences we model reality as an organic fractal of relative size scales, that evolve from parts into larger wholes, from particles into atoms, molecules, cells, matter states and so on till reaching the Universe, shaped by social and organic networks coded with information.

In the graph the Universe is a fractal that reproduces ‘forms with motion’, informations and then organizes them in networks and systems that evolve into larger organic systems creating the scalar structure of reality.

Thus we call the sum of all those co-existing scales of parts and wholes the fifth dimension.

Thus reality has a final key feature overlooked for too long: the co-existence of all those systems of space and time in several scales of relative size from the smallest atom to the largest galaxy that put together create a dual scalar ‘4th and 5th Dimension of parts and wholes, which we shall call the ‘social dimension of evolution’ and the ‘entropic dimension of dissolution’.

This function, as all space-time metric functions, is simple. So we write using ð for cyclic time instead of t:

$ (Lineal Size/ Space Volume) x ð (cyclic speed of its time clocks) = C¡: Constant Plane of timespace (ab.∆¡)

But how we travel in ‘size’ in space and ‘speed of our time cycles. Here is where the biggest discovery of 5D comes into play: We travel through the worldcycle of life and death, as we are born in a smaller seed with faster time cycles, evolve as an organism coming out in the ∆º-scale within a larger world of slower ‘Deep time cycles’, to die back dissolving our information again into cellular space.

And this is the same process of all journeys of all species that live and die through the fifth dimension; from the smallest black hole that is born with an enormous ‘metabolic temperature’, to the new species, routinely born as small individuals (first mammal rat, first robots with small chips; first human likely the Homo Floresiensis, who grew in size and mated with the Erectus, etc.) And then a reproductive radiation multiplies the seed into a larger slower whole that finally ages and dissolves back.

So 5D adds to the 4D formalism of worldlines, a dimension of growth, shaping the worldcycles of life and death. Reason why we call 5D metric the function of existence, because its multiple ‘solutions’ are the origin of all the varieties of Space and Time beings, there are – a whole family of functions.

As we keep exploring in depth, 5D metrics and its associated concepts of Space=form and Time=motion in all its varieties, we shall see it is the origin of multiple ‘solutions’, a whole family of function, from where we shall derive most of the logic relationships and particular equations of each science.

So according to those metrics, smaller systems in space have faster time clocks. And as information is stored in the frequency and form of those cycles, smaller systems have more information, coding larger ones: genes code cells, memes societies and particles’ quantum numbers code atoms and molecules.

The nested Universe.

In mathematical science for a dimension of space-time to exist, it requires a metric equation, which combines space and time to give us a co-invariant system that allows travelling through such dimension. The 5th dimension has a ‘metric equation’, hence it exists. The equations for a given number of scales co-existing in an organic network is: S (size in space) x T (speed of time cycles) = Constant.

We use the metrics of the 5th scalar dimension to explain the fractal, nested Universe and its scales, shown in the graph. As 5D metrics balances the survival and symbiotic existence of all parts of the Universe, and all parts of a super organism, and defines ‘what codes information’ – the small being, and what codes energy- the larger whole, establishing the ‘harmony’ of all the scales of the Universe, and explaining all its fundamental constants which are ratios between spatial volumes and informative clocks of temporal energy.

It follows from a nested structure and the search for creative, organic balances, a symbiotic relationship between the ∆-¡ smaller parts that have more speed of time clocks, which carry its in-form-ation in the form and frequency of its cycles, coding larger systems: genes code cells, memes code social organisms and particles’ quantum numbers code atoms and molecules. And the larger, ∆+¡ larger envelopes, membranes (static, dimensional view) or angular momentums (dynamic view as time=motions) which have more spatial energy and enclose and control in synchronicity its faster smaller parts, creating the co-existing scales and symbiotic cycles of super organisms in any system of the Universe.

For example, chips become smaller as they evolve into faster brains. Every 2 years a chip doubles its capacity to think, as it dwindles in size. Such process follows a generic law of evolution I call the ‘Black hole Law’, which computer scientists know as the ‘Chip paradox’ or ‘Moore Law’: maximal informative capacity= minimal spatial extension. The reason is obvious: to think, to calculate you have to communicate in-form-ation, forms between elements of any informative system. The smaller the brain, the faster the communication that takes place within that brain and the faster you can calculate and process information in a logic manner. And vice versa: larger wholes accumulate more energy and are stronger than parts, so they can protect and feed them. So wholes and parts co-exist in several scales forming super organisms.

The metric function of the fifth dimension of space-time (ab.∆) defines 3 known scales of physical systems, with different quantity of information according to 5D metrics, Sxð=k.

Those metrics means information is higher in the smaller ‘quantum plane’ than in the larger gravitational one, and inversely the size of its physical parts is larger ins the Gravitational cosmological ‘plane’ than in the quantum one, with the human thermodynamic scale in-between.

The galaxy’s 5D metric is immediate: $(c) x ð (h) = Constant, as its largest speed-distance is light and its minimal unit of cyclical information, is the Planck constant of angular momentum, the unit of the 3 human physical parameters of spatial size, cyclical time frequency and ‘scale’ (Active magnitude): h= mass (∆) x area (S) x ƒrequency (ð). Which becomes the unit of physics, related to the unit of mathematics, the fractal point.

But as there is no reason to stop the scales of the fractal in particles and galaxies, there is a ‘potential’ fourth, ∆±4 organic plane defined ‘above’ the galaxy, (∆+4, dark energy world) and below the quantum world (∆-4, Bohm’s quantum potential), which represents the larger cosmos.

According to the fractal, nested principle a larger organic system, encloses smaller nested systems. Thus the Ʊ4 cosmos contains Ʊ3 galaxies, which contain Ʊ2 solar systems and planets, which contain Ʊ1 thermodynamic organisms and matter states, described by the human Ƽ mind languages, contained on our brains.

Thus bigger systems paradoxically are ‘supported’ by the smallest ones, in the same manner than within the nested planet, bigger mammals (whales) eat the smallest animals (Plancktons)

Reality has a scalar nature overlooked for too long: the co-existence of all ¡s space time systems happens in several scales of relative size in space inversely proportional to the speed of its time cycles, from the smallest atom to the largest galaxy that put together create a dual scalar ‘4th and 5th Dimension of parts and wholes, which we shall call the ‘social dimension of evolution’ and the ‘entropic dimension of dissolution’.

The fifth dimension is made of the ‘different co-existing scales’, which from the simplest forces through particles, atoms, molecules, matter, organisms, super organisms, planetary systems and galaxies, create an ‘organic network structure’, which amazing enough since it was discovered at the beginning of science with telescope and microscopes, was not formalized till I introduce its metric equation in the milieu of systems sciences, as a single lineal time motion is a dogma physicists don’t dare to challenge:

Why 5D is so important? Because it allows the survival, symbiotic existence of all parts of the Universe, and all parts of a super organism, and defines ‘what codes information’ – the small being – and what codes energy- the larger whole, establishing the ‘harmony’ of all the scales of the Universe, and explaining all

RECAP. 5D metrics describe organic properties because it balances the survival symbiotic existence of all parts of the Universe in any of its fractal super organisms, made to the image an likeness of the whole, as the smaller beings ‘code information’ with faster clocks, and the larger wholes enclose and protect the smaller parts with its greater energy- establishing an organic ‘harmony’ in all the scales of the Universe, and explaining its fundamental constants, which are ratios between spatial volumes enclosed by membranes and angular momentums of informative clocks of temporal energy.

A consequence of the scalar Nature of reality is that points have parts, which grow in size as we come closer to them, peering in the inner regions of its fifth dimension. So a star from a point becomes a world, and so should a point-particle if we could peer inside its form – to the ‘point’ that the closest self-similarity of scales happens between galaxies and atoms, stars and photons, in a potentially infinite scalar Universe. What this means is that an absolute zero does NOT exist. So 0 becomes 0’, a ‘finitesimal unit’, which will always remain as the fractal Universe abhors vacuum. Thus in any parameter we find a residual amount, even if it is undistinguishable from a larger scale. There is no absolute 0K, but always remains a bit of motion=temporal energy. This, means also in terms of h, that vacuum space has always a reminder, h-uncertainty unit, no longer an abstract concept but the minimal unit of light space-time, we shall call h, ‘Planckton’, the minimal fractal organism which feeds or becomes the ‘cellular unit’ of all other species of the Galaxy, as Plankton is the minimal unit of the biologic Universe which starts the trophic pyramid of life or as a cell starts the evolution of multicellular organisms.

5D metrics is a law of balance between 2 elements of reality, scalar space akin to information and cyclical time akin to conserved energy. Yet as humans disconnected their concepts of space and time of its ‘broken parts’, bits of information & bites of energy, equalizing all time cycles of reality with a lineal equation, v=s/t, and a single mechanical clock, and have pegged all the bits of information of its puzzles of space; and finally compressed all the planes of space-time into a single ‘space continuum’; and then separating them as the constitutive elements of reality we need to reconstruct both terms in its more complex reality nature, as ultimately we are all made of those organic vital fractal scales of space & its moving time cycles. The fifth dimension is made of the ‘different co-existing scales’, which from the simplest forces through particles, atoms, molecules, matter, organisms, super organisms, planetary systems and galaxies, create an ‘organic network structure’. Yet science cannot advance in its principles unless the 5D formalism is accepted and used to fully understand the cyclical, repetitive patterns=laws of science of each discipline that studies a scale of 5D n and its species.

PLANES OF FRACTAL SPACE & CYCLIC TIME: THE CAUSAL REPETITIVE LAWS OF ‘STIENCES’¬∆ST

Duality: We are made of space-form & time-motion.

“According to their [Newton and his followers] doctrine, God Almighty wants to wind up his watch from time to time: otherwise it would cease to move. He had not, it seems, sufficient foresight to make it a perpetual motion. Nay, the machine of God’s making, so imperfect, according to these gentlemen; that he is obliged to clean it now and then by an extraordinary concourse, and even to mend it, as clockmaker mends his work.’  

Leibniz-Clarke Correspondence on the absurdity of mechanical models of the Universe

The underlying question of time§pace: Absolute or Relational, Generational Space-Time?

The fundamental question physicists wondered for centuries regarding the nature of space and time unfortunately was resolved as usual in favor of the simpler view: it is space and time an absolute abstract background of the Universe (Mr. Newton’s view) or are we made of ‘vital space’ that lasts a time duration, so we are generated by the bio-topo-logic properties of scalar space and cyclical time? This is the choice of 5D ‘stiences’. And its simpler version was called relational spacetime, sponsored by Mr. Leibniz.

A realist interpretation of the world we live in, which has never shown in any scale of reality such ‘background’ – ultimately a mathematical graph used in abstract by human scientists – considers that we ARE the vital space we occupy with our cells, and we LIVE a cyclic time duration between birth and extinction. So we are space and time.

So we must evolve our concepts of space and time, to extract the properties of ‘existential beings’ from them.

In Newton’s cosmos, space and time provide a fixed, immutable and eternal background, through which particles move. Space and time are the stage of intersecting lines sketched in the illustration. Fact is this ‘mathematical artifact’ made with pen and paper by earlier physicists, called the Cartesian graph, useful to measure ‘translation in space’ is no where to be seen in reality. Unfortunately as time went by the graph became somehow ‘real’ as scientists’ felt the ‘mathematical language’ created reality. It meant also the invention of an absolute ‘continuous space’ and a single ‘lineal time’ that extends to infinity contradicting the obvious fact that all ‘spaces’ are broken, divided by membranes, and all beings have a finite time duration. Further on, as we kept exploring smaller scales of reality, we never found the drawings of God, not even a solid still substance, but always ‘motions’ tracing closed time-space cycles; since even particles turned to be also ‘vortices of time-space motions’.

So the true, sound experimental and logic theory was Leibniz’s who rightly considered absolute space and time an abstraction, and so he coined the concept of relational space -merely the adjacent pegging of similar forms in simultaneous space and relational time – the sequence of events which we relate causally with reason origin of the ‘Generational space-time’ model of 5D in which are the space we occupy and the time we last – as in the graph where there is no longer abstract background lines.

What Newton called absolute space-time IS NOT. So space is the sum of all the discontinuous vital spaces, occupied by different beings: ∑s=S And lineal time, T the sum of all the finite life-death cycles of all beings T=∑t.

Since space and time do exist and so if they are not in the background we ‘are’ vital space and cyclic time.

The simple idea behind the structure of the fractal Universe is then to consider time=change =motion and Topologic, formal space=extension the 2 elements of which all beings are made.

We are space and time, merely of a different kind to that of Newton: Organic scalar spaces, and cyclical, discontinuous times who ‘live’… worldcycles (no longer worldliness as we have a 2nd arrow of information) of exist¡ence (as all species follow the common laws of space and time). So after making such a huge up hauling of philosophy of science – one which however every serious scientist recognizes to be necessary since quantum physics showed space to be discontinuous, and relativity time to vary in different regions of reality with different speeds, as the devil is in the details we have to improve our understanding of the 3 fundamental properties of ‘generational space-time’, departing from the most obvious one:

Cyclic Time: Conservation Of Energy≈Time Cycles The causal repetitive laws of ‘stiences’

‘”There are infinite time clocks’. Einstein

The main principle of science is the conservation of time=motion in its two varieties, |-lineal time& O-cyclical time. Its immediate consequence in all sciences is the fact that time is cyclical, repetitive, as iterations are the only form to conserve time in a ‘present’ that doesn’t seem to change. It is equivalent to the principle of conservation of energy. Because time is cyclical, it does break Newton’s absolute time into infinite cycles, which make its motions equivalent to those of physical conserved energy cycles, in which work doesn’t happen.

The causal repetitive laws of ‘stiences’

A Universe of ∞ time clocks of different size and speed differs from its human description with a single mechanical clock-time to which all time clocks of the universe are equalized, elongated into a lineal ‘second-minute-hour-day-year’ system of equalized time clocks (of light waves, mechanical clocks, earth’s astronomical clocks). As Galilean physics, born of ballistics, simplified the nature of cycles of time-space into lineal durations, to measure best the locomotions of cannonballs: Time is cyclical, all clocks of time and laws of science are based in the cyclical patterns of nature. But physicists developed ballistics and denied the truth that we can know the future because it will repeat the causality of the past, and we can change it by changing that causality, in History by repressing the lethal memes of the tree of metal and enhance the welfare memes that make us survive.

Lineal and cyclical time render the same functions as one is the inverse of the other, measured by frequency, T=1/ƒ, but the philosophical implications of cyclical time, are enormous, as we regain the in-form-ation provided by those cycles, origin of the laws of science, which would not exist if there were not cyclical patterns; including the cycles of history and economics. The most important of them being, the fact that a time cycle breaks reality (1st knot theorem) in an outer and inner region, creating a membrane that encloses a vital space, the ‘substance of which we are all made’.

Reality is a fractal system made of topological organisms of co-existing scales of space and cyclical time which close its ‘internal vital point content’ with the entropic limit of those time cycles, in its vital territorial body-waves, synchronized symbiotically by 5D metrics. As we are all ultimately ¬∆@St; dust of space-time.

Why there are 2 forms of time, the long lineal Time and the ‘short’ frequency steps we integrate into the larger whole? Precisely because there are 2 ±¡ scales of 5D reality whose metric, SxT=∆±¡ defines larger space systems as having slower time cycles. So we can consider an ∆-¡ ‘quanta of time frequency or ‘finitesimal derivative’ of the larger whole represented with the concept of lineal time; as in the classic formula,V(st)=ƒ(t) l(s). The whole Space can be measured, Vt=S with lineal time as a single unit, or it can be measured as a sum of frequency steps, with more detail.

Those 2 forms of motion are lineal motion with a bit of form, Ts, or locomotion and cyclical form with a bit of motion, St-information, stored in the frequency and form of its time cycles that come together into S=T, energy. So we express the main law of science, the principle of conservation of energy in terms of the conservation of time=motion and space=form as two varieties that approach and transform each other ad eternal:

‘All what exists are time motions that transform between lineal open and cyclic closed forms ad eternal: SióTe’

This sentence is the simplest expression reality as a constant game of transformation of ‘spatial information’ (cyclical time) and temporal energy (lineal time) and was first understood by Taoism, where ‘tao=time’, is composed of yin=cyclical form and yang=lineal energy, today expressed as the principle of conservation of energy. Its ‘mathematical, logic’ formula is  its logic form, exi=st, is the function of existence., whose generator, Si≤=≥Te we call the function of existence, as To exi=st is to combine S&T, pure form and motion, TT-entropy and SS-eeds of form, into St & Ts, information and kinetic energy, exi, till finally they become one. The knowledge of that simple game, expressed in infinite variations, both of language and species, is the mind of the Universe, what is all about.

We are times, we are time§pace closed paths of zero sum energy that exist to move, perceive, feed, reproduce and evolve into wholes, soon to be ignored, erased and returned to the fold of motion without form, of pure times. We are synchronous magically sustained card castles trying to grow through 5D scales to fall back again.

We describe reality as a fractal system made of topological organisms of co-existing scales of space and cyclical time which close its ‘internal vital point content’ with the entropic limit of those time cycles, in its vital territorial body-waves, synchronized symbiotically by 5D metrics. As we are all ultimately ¬∆@St; dust of space-time.

The future then can be predicted because it will have an informative cyclical, S-component similar to the past, (Y-height=Information in a wave graph) and a lineal entropic T-component advancing in lineal fashion and both, a repetitive cycle that touches the same point of space and a line which does not diverge ARE predictable.

Cyclical time and the scalar Universe in fact is much easier to predict and understand that lineal time because we do not erase the information of its repetitive cycles, and because all scales are ‘similar’, so we can predict the behavior of the larger slower scales, easily, comparing it with the smaller, faster ones; as in 5D metric they have less information. Thus they are more basic, deterministic, constrained by its smaller parts; reason why quantum physics is harder for the mind and probabilistic while life-death cycles are obvious.

Let us then understan the largest of all those scales, that of the Universe which 5D recast in a far more explanative model than the present ‘entropic simple lineal big-bang view’, just by reordering the information we have about it with the new understanding of its two fundamental principles, space and time.

RECAP. The universe is made of 2 STates, time=motion, and space=form. Yang and yin that combine in balance to create ∞ beings.So you can combine them T & S in 5 different forms:

S=T, the balanced state of existential energy that combine St-information (Potential energy) and Ts-locomotion (Kinetic energy), in constant SHM is the preferred balance of ‘present’ that lasts and iterates any organism, the state of survival.

TT: internal and external motion or ‘entropy’ is one extreme, which brings death. That is the state of mankind today, caused by the fact the new species, machines move faster externally (cars, weapons) and internally ‘metal-minds’, visual images accelerate, disordering humans into a permanent ADD state. So millennials move fast and have disordered minds. At the end of that process entropy kills.

In the other extreme of absolute no motion, there is SS, languages of the mind, seeds, pure, perfect information, enlightenment. A being in that state doesn’t move. The hypothetical Mind of God is such a being, because it perceives all what has existed, exists and will exist and repeat itself eternally as a block of time – a zero sum of fluctuations of the game of existence in space and time.

 

VITAL, ORGANIC TOPOLOGY

Local Past=Entropy, Present=Iteration and Future=Information in zero-sum worldcycles.

‘The separation between past, present and future is an illusion’ Einstein

But of all the consequences of cyclical time, the most important is the existence of infinite local time clocks of which we are all made, which therefore imply the existence of infinite local past, present and future states.

Whereas the past is the beginning of a pi cycle, starting as a line of entropy with no form that curves and raises in height in its second state of present, and returns back to its origin in its future 3rd age of information, completing a 0-sum of life and death. Thus instead of a single ∞ lineal absolute time there are ∞ living cycles of time happening in zillions of entities.

This said the devil is in the details. So the next question is how many types of vital space, we are made of. And the answer provided by topology which studies geometric forms with spatial dimension and time motions is only 3; which perform the 3 organic functions of all systems of vital space-time of which we are all made: A 5D Universe has only 3 ‘topological varieties’ each one best suited to perform one the 3 organic vital functions of any physic or biologic system –gauging information (1D spheres, the topology that stores more information in lesser space, hence used in all particles and heads in the height dimension), lineal or cylindrical forms that move the system (2D, the shortest distance between two points, hence used as fields or limbs in the length dimension) and hyperbolic body-waves, a mixture of the other two topologies that reproduces the system and stores its energy in the width dimension (3D); which not coincidentally correspond to the 3 ‘conserved quantities’ of physics, angular, lineal momentum and energy.

So we define the ‘Fractal Generator of Vital pace-time topologies for all systems of Nature:

G:   |-$t(limbs-fields)<Ø-S=T-Body-waves>O-§ð (particle-heads).

5D symbols for the 3 topologies=functions=conserved dimensional motions (ab. Dimotions, Ð) of timespace are:

1D: T>S: angular cyclical motions of information (Ab. St, O; §ð): the minimal ‘geometry’ of reality, a spherical particle/head or fractal point, the geometry that stores maximal form in minimal space, hence suited for ‘organic functions’ of gauging, storing and perceiving information (particles, heads).

2D: S<T: Lineal Locomotions, (Ab. |; sT, $t) which will move through its lineal limbs/fields the system, as the line is the shortest distance between two points… towards a…

3D: S≈T: Fields of vital Energy (Ab. Ø; ST, ExI): with its hyperbolic body-waves that iterate the forms of both the spherical particle/heads and lineal limbs/fields; as the hyperbolic topology combines the other two, so it can generate them, in the same manner Energy adds as the third conserved space-time quantity the lineal and cyclical momentum of 1 and 2D.

Those are the 3 conserved ‘Space-time’ dimensional motions (ab. dimotions) of all organic systems but then there are two states that are NOT conserved and frame as ‘limits’ of existence the previous two:

-SS: pure information without motion, mental, linguistic form – the ‘virtual mind’ of the system.

– TT: pure motion without information, ENTROPY proper, a state of internal and external motion which is precisely the cause of the destruction of SS-linguistic form.

Thus we could consider the Universe a tug-of-war between those 2 poles, which merge ‘symbiotically’ in the ST-energy, Ts-locomotion and St-informative topologies, between a birth as a seed of pure form and its death as pure motion or entropy the theme of this paper.

All together form the 5 possible combinations of Space-form and time-motion at local level, in a series of maximal and minimal states, which we write with simple symbols of ‘exitential logic’ (S-pace, T-ime, > implosion of information, < explosion of motion and ≈ balance between both: SS (language)<St(information)<ST (iteration-energy) <Ts(locomotion)<TT(entropy).

THE WORLDCYCLE OF EXISTENCE. THE 3±¡ SCALES OF TIME: ACTIONS, ORGANISMS & SPECIES.

The generator of space-time, maximize your existence.

This more simplex organic view of time and space requires a new ‘metric equation’ beyond the lineal v=s/t equation of Galilean relativity that becomes the limit of this more complex view of time and space, with 2 fundamental equation, SxT=C (the scalar metric of the fifth dimension, as systems in space accelerate its clocks of time (T) according to its size (S); and S=T, the new equation of relativity, which means as we cannot distinguish motion=time, from stillness=space-form (Galilean relativity), both are ‘two sides of the same coin’, and all systems have both motion and form, which are constantly becoming one another.  Yet as SxT is maximal when S=T (5×5>6×4…) both equations can be summoned up into a single one, which we shall call the fractal generator, or will of each fractal space-time beings, the equation that embodies all other equations of the Universe and guides the actions of each fractal part of it:

Function of Existence:             Max. ∑ S x T s=t = C¡

The equation has an immediate biologic meaning, because as we are made topologically of ‘fields-limbs’ of lineal space with motion provided by the energy we absorb to also reproduce our bodies-waves, and the information we need to linguistically guide our motions with particle-heads, the very essence of survival is to increase our S=position, mental forms of space and T=entropic motions of time (whereas time=motion and space=form are the two limiting Dimotions with ‘energy=reproduction, s=t, locomotion, sT and information, St, are the intermediate 3 dimotions). Thus Max. S x T = C (s=t), IS also the equation of survival and struggle for existence, the will of life; the biological expression of the ‘Universal mandate’, expressed by all species in all its codes and languages, the Grow and Multiply of the Bible, the intuitive truth that guides all beings. The game of existence is simple: Reproductive radiations maximize ¡ts function, happening when mirror symmetries (genders) meet in S=T, equaling their St-information and sT-energy, organizing themselves into a whole, ∑ system.

It is then relatively easy to interpret that equation in each of the languages-minds of each scale of reality as in all those scales species will show a ‘will’ of action to perform the maximal number of events=dimotions=‘actions of space-time’ that ensure its survival. And this can be assessed externally regardless of secondary arguments on consciousness and self-reflection, substituted in 5D by Leibniz’s ‘apperception’ – that is, because performing the 5 actions=dimotions of exist¡ence, in each ‘st¡entific scale’ self-centered in a linguistic mind that perceives a given plane, inscribed into a larger ∆+1 world, with internal ∆-1 parts, ensures the survival, ONLY those species that have performed the 5 dimotions of which the most important is s=t reproduction of the being into a ‘present’ similar entity that continues the exist¡ence of the system after ‘errors’ or ‘the struggle for existence’ dissolves it through the dimotion of entropy=death, exist.

Thus automatically, genetically, consciously, memetically, mathematically, logically, through its own will or as a part of a larger system that uses the ‘machine’ or ‘organism’ to enhance its actions all what exists does so because it performs internally those 5 Dimotions or externally performs one of them for another symbiotic species, as those species that have not followed the program of existience and its 5 actions in the past have become extinguished, and those will not in the future, will become wrong mutations, crazy thoughts, fictional languages and die away.

The function of existence, or 5D metric of Generational space-time, (Ab. Gst, G) Max. Se x Ti (s=t) states that all systems of Nature will try to maximize its absorption of Entropic motion (with no form) and Linguistic form (with no motion), and its 3 intermediate dimotions of energy (s=t, balance of both that reproduces them), information (St: form with a little motion, form-in-action) and locomotion (sT, motion with a little form). So we talk of a program of survival ‘selected’ by all systems and expressed in its languages and minimal five actions encoded in that simple equation, which we term: a, e, ï, œ, û, as a mnemonic rule for the five actions of existence:

Accelerations (locomotion), entropic feeding (e), ïnformative perception and communication ï, Œ:reproduction into parallel supœrganisms Û… and social growth into larger wholes called philosophically Universals. And this series of actions is what accumulated in time will ultimately give birth to your word cycle  as the monad will first perceive (i), to direct its entropy-motions (a),towards a field of energy (e), where to absorb the energy bites it will imprint with its inner form, e x i = œ, to reproduce another form, and when enough ∑œ exist, it naturally organize into a larger whole û.

In graph the actionS of different Stientific scales of organisms. Above the coding of actions, which are the knots and bolts and details of the study of any time§paœrganism in light space-time, coded by colors and dimensions, in physical atoms, coded with quantum numbers and in life and humans coded by the so called drives of life, which we obviously extend beyond the ego paradox to all other systems, including genetics not mapped there (coded by the 4-5 letters). Those actions balanced each other into zero-sums in death, as they tend to increase information from a mind p.o.v., hence we ‘all warp, wrinkle’ get old in the third age and die, setting from its minimal actions to its integral sums, the 3 ages of life-existence and the world cycle all super organism follow.

The simplicity of the game of existience, and its selfish actions, which gather together into social wholes through reproductive radiations, each action coded by a fundamental topologic organ we can express in existential ®=ilogic, and corresponds for each species of the Universe, with a fundamental parameter of humind measure. So from bottom to top, we find the 5 fundamental elements of light code its actions of motion (c-speed), energy (magnetic field), information (electric field), social evolution colors & entropic feeding, (quantum potential, neutrino light theory)

So the minimal particle-points, photons, electrons & quarks that construct all other systems of our Universe show the 5 organic dimotions (motions with dimensional form) that define ‘classic life’: they gauge information – reason why quantum physics is a ‘gauge theory’, feed on energy (quantum jumps) absorbing smaller ∆-1 particles, reproducing new clone particles, move and evolve socially through magnetic fields into larger wholes (atoms). Hence the units of life are particles, the minimal units of our vital, organic, fractal, scalar Universe of multiple timespace organisms. All lives, performing 5 Dimotions=actions of ƒ(exist¡ence):Max.SxT(s=t) =C, starting with particles. So all scales are relative NONE matters more than other. From those actions, given the dominance of informative actions over entropic ones, it appears a series of repetitive cyclical patterns of actions conducting to maximize the existence of the being, which accumulate in a larger scale of time-space, as a worldcycle of actions that increase the information of the system in 3 ages. So the basic cycle of actions becomes a larger 3 ages cycle of life and death; as systems once and again, starts in an act of information/shrinking and ends in an act of organization/shrinking of herds into wholes, will keep reducing the being and finally make it all form no motion to explode and die in an entropic reversal of death:

∑ i->a->e->œ->û, i->a-e->œ->u, ï->æ->Œ->Û -> Informative ‘seed’ age->1st locomotion, feeding age ->2nd reproduction age ->3rd informative, social age-> entropic death.

AS huminds are limited in time logic and we cannot build on their chaotic, entropic models of reality. Chaos and indeterminism IS born of the LIMITED single Time-arrow of Science, force-fed by earlier ballistics, the name of Galileo’s first book & modern ego-dogma & subjective reductionism EASY to practice in the largest scales of modeling. And it is a cultural treat of our dog-eat-dog ‘animetal cult(ure)s’ to weapons & financial parasitism (nationalism, capitalism) & our despise and extinction of organic life in the making. Monologic prevents those who are destroying life and bringing the 3rd age of the planet, the Metal-earth, to even realize how wrong is their absolute ‘one single order of thought’. Our informative elite is not even human anymore. It is a system of memes in favor of this other world, expressed by a network of informative machines and its Financial-Media-Academia monologic that pass as expertise (FMasters). But beyond the simplex analytic model of cause an effect are out of depth in long time range. Only repetition ensures that false theories of science based in entropy-death pass as dogma. Mental imprinting by repetition ensures humans walk the determinist path of self-suicide thinking they CANNOT understand and design a better future. I have been predicting that future of social history for 30 years, using the larger organic properties and 5 Dimotions of time-space but the system cares not to accept any criticism. People are NOT aware to which extraordinary lengths the idol-ogies of metal go to cover up and NOT understand the lack of human futures. All this censorship is part of the ‘burden of monologic man’. In the times of Lao-Tse, Buddha and Aristotle, minds were free – reason why they had so much more depth, than modern people in his comprehension of dual and trinity logic. Yes, to know ALL about the locomotion of matter which is what physicists know is NOT to know all about the larger, organic Deep time scales of the future, and nothing about the topologic evolution of machines and fractal cycles of stock-markets.

So the ancients were miles ahead of modern ænthropic (anthropic+entropic) lineal military physicists & Darwinian philosophers, with their pedestrian monologic, where only entropy, destruction, DEATH seems to create, instead of destroying as its worldly religions of making weapons, believes. We shall thus deal with the reductionism and primitivism of their ‘philosophies of science’ in this article on monologic, However this ‘entropic’ article in itself – an on slaughter on present mæn – is less important than a pentalogic and dodecalogic understanding of existential ¬Æ=ilogic, as it IS. Or else the destruction of ænthropic models from egocy to the big-bang, would be useless since the reason humans sticks to those models is the lack of an alternative model to its simplex views. That is what 5D represents.

In all Planes, the simpler actions of any being are extractions of motion, energy, entropy=motion and form from lower ∆-i Planes:

A T.œ perceives only the ∆±3 planes from where it extracts energy or information. As its actions and dimotions are architectonically performed through planes of 5D where each main action relates to an interval of scales:

∆-4-3: The system extracts indistinguishable boosts of entropic of motion (man from gravitation).

∆-3-2: The system extracts bits of information (Light in man)

∆-2-1: The system extracts bites of energy (amino acids in man)

∆-1 0: The system seeds its minimal seed of reproduction.

∆0+1: The system connects socially with other systems to evolve into a whole.

So simpler Actions start at finitesimal level, gathering in sequential patterns in existential algebra, as ‘time flows’ and in population and spatial patterns – in integral herds of numbers in calculus.

We and all other beings perceive from ∆-3 quanta (light in our case), feed on amino acids, (∆-2 quanta for any ∆º system), seed with seminal ∆-1 cellular quanta (electrons also, with ∆-1 photon quanta).

For each action of space-time we shall find a whole, ∆º T.œ, which will enter in contact with another world, ∆±i, from where it will extract finitesimals of space or time, energy or information, entropy or motion, and this will be the finitesimal ∂ ƒ(x), which will be absorbed and used by the species to obtain a certain action, å.

Analysis allow us to extract actions from wholes, reason why there are not really use beyond the third derivative of a being, as super organisms co-exist in 3 only Scalar Planes. It also works in terms of a volume, as its derivative is a plane, then its unit-cell or point… So to speak, if you derivate a world, you get its organism, and if you derivate it again you get its cell and then its molecular parts.  And then if you do that in time, you get its speed and then its acceleration and then its jerk.

The magic of derivation

Because of the symmetry between ∆≈S≈T, to extract finitesimals of smaller scales the process is the same. We derive the whole, which diminishes its ‘dimensions= power’ as the system looses its larger whole, but increases its number of ∆-¡ visible particles, whereas the difference of value between both, shows the ratio and structure of its entropy, energy and information networks, sum of its components that form the whole. As certain functions define more specialized T.œs than others. So the parts of a whole vary according to topological structure.

The key action of entropy: feeding’ on energy

All systems of Nature follow the simple aeiou actions determined by the 5 dimensions of space-time, moving in a-ccelerated paths towards e-nergy surfaces where to feed and transform into I-nformation the vital energy absorbed by the system in order to reproduce and offspring of similar beings, which will evolve together emerging into a social Universal sum of multiple individuals.

We study in more depth the action of energetic feeding, parallel analysis of ‘entropy’, since feeding is the addiction of absortion of energy, killing it down two scales of the fifth dimension to reform that energy into the information of the T.œ that absorbs it. So the equation of feeding first reduces the being it kills from ∆ø<<∆-2 and then reconstructs the being from ∆-2≥≥∆º, whereas the first ∆ø has lesser existential force than ∆º, which is the top predator ∆º e x i > ∆ø e xi:

In the graph, feeding is a process of entropy first and then reconstruction.

To reconstruct the information of system first the system must start with the inverse arrow of feeding of a species that will ‘simplify the information’ of a part of an organism, two ‘planes down’: ∆¡<<∆-1, the equation of ‘scattering entropy’ and then rebuild from its ‘amino-acids’ or ‘forces’, the larger whole system. So its equation in ¬Æ is quite simple: ∆¡<<∑∑∆¡-2>∑∆¡-1 for any scalar process in the Universe.

Feeding of course happens regardless of moral views in all systems, including those social systems in which a culture with higher technological information, higher top predator form (Max. e xi) conquers another nation and reforms the system, either by reproducing its culture in the ∆-2 scale of individual memes, or even in a harsher manner by extinguishing the ∆-2 scale of human beings reproducing the conquerors memes and genes together. In the graph we can see the case of Germany, which try the most extreme second approach extinction of conquered nation. 

But in all scales the top predator with maximal e xi-stiential force will do the same. We eat and put down to amino acids and reconstruct our food. Particles feed on force fields and reconstruct reproducing new particles; cosmological black holes emit seminal seeds of matter and reconstruct baby-irregular galaxies at the end of its jet.

Whereas < is a symbol of expansion of space and simplification of form, which happens twice, and  > the inverse arrow of growth of information.

So when we feed, we break down to molecular amino acids and then rebuild them into cellular matter (∆¡-1), and so happens with atoms that feed on forces evolved into ∆¡-1 particles and nations, which through war explode a rival nation in its ∆¡-2 Memes and territory down to the destruction of its buildings and raw materials, and then ‘re-absorb’ those materials and citizens, ‘re-imprinted’ into ∆¡-1 ‘converted’ citizens and wealth.

It is then obvious that ‘the fourth dimension of entropy=dissolution’ and the ‘fifth dimension of social evolution’ into wholes. ARE INVERSE.

We shall constantly realize how the set of scalar laws of the Universe apply to all systems, regardless of which ‘species of space-time’ we study, the most astounding proof of the existence of an scalar ‘game of exist¡ence played with the same rules for any species of reality.

Let us now deal with ‘the fourth dimension of entropy’ and the ‘fifth dimension of social evolution’ into wholes. So simple so complex when we combine, repeat and translate in different languages those ultimate principles, which we shall now study with a bit of more depth.

The Universe and all its parts – in the graph the human being – are Timespace organisms that reproduce information, stored in the form and frequency of its time clocks, through the vital motions of its 3 space-time dimensions and 2 ± ‘∆’ scalar dimensions of entropy that dissolve the networks of information of an entity, scattering them in the process of death, and emergence, which evolves those networks socially from a group of smaller parts into a whole.

Without those 2 ‘organic’ dimensions that relate the different ‘scales’ of size in space and speed of time clocks of each ‘fractal part’ of the Universe, we cannot make sense of its organic process of creation and extinction. In the graph all systems co-exist in 3 scales of the 4th & 5th Dimension: the ∆-1 atomic/cellular, ∆-organic/thermodynamic and ∆+1 gravitational world; which we can describe with a metric equation of the 4th and 5th scalar Dimensions of space-time (ab. ∆±i), which order all entities of reality in scales according to the size and different speeds of time clocks of its systems is very simple: $ x ð = K, the relative size in space and speed of the time cycles of a being remain constant.

In the graph we see the ‘organic fractal Universe in different scales’ and systems of reproduction of information.

Researchers in fractal geometry are delighted to write fractal equations that show such structure. But this is a blog of philosophy of science that goes much further into the organic vital properties of such systems.

So what is an organism of space-time also disappears: the perception by a simultaneous point of reference of a series of synchronized time space cycles.

RECAP. We defined reality in its absolute theoretical minimum: a tapestry of ternary beings in space, self-centred in monad minds, which live world cycles in time, as the monad orders its territory, grows, reproduces its forms, exhausts its motions and energy collapses and dies, exploding back its form into entropy for other beings to form. And by expanding those basic concepts, the ternary structure of beings in space; its dynamic evolution in time, through world cycles, as it becomes a growing organised ‘supœrganism’ to fall back into death, once and again ad eternal, we shall describe all what exists.

Reality can be perceived with multiple dimensions, each of those views will be a consistent world. Monologic, ænthropic man with its 1D models of reality based in Sx time locomotions shuns off the 5D Cx. Universe to its own peril, as reality is penta-dodecalogic in its entanglements that generate space synchronous supœrganisms and time, and survival, which in our dominant animetal warrior & go(l)d cult(ure)s is minimal depends on the understanding and respect of all the living function of space-time exist¡ence and its action-reaction laws.

Actions define the worldcycle of existence.

Because actions follow a pattern of increasing evolution and 4 actions are coded while entropy is avoided – we deliver entropy as an open system to other parts of the Universe, it follows thsat the system constantly accumulates information, and this is the origin of the worldcycle of life and death. The system likes information, because it is what the Universe is really all about, a fractal that imprints information in memorial repetitive cyclical patterns.

So as actions follow a natural scalar level of information perception->locomotion towards a field of ‘feeding’, where to get -> Energy to reproduce -> and then process that energy into information, exactly the same pattern appears in the next scale of ‘cyclical time and longer space’, the worldcycle of life, which consists in the same pattern of ‘seeding information’, moving youth, feeding and evolvint to reproduce and then process information becoming older in a 3rd age.

This amazing symmetry between the smaller time scale and the larger worldcycle of life, then will be followed also in the larger scale of superorganisms and species and so we have 3 ‘patterns’ of time cycles due to the survival program of actions in 3 scales of time, and 3 larger surfaces of ‘populations’, as the first cycle feeds the ‘cells, atoms, individuals’, the second cycle the whole organism, and the 3rd cycle manifests in the whole species.

The d=evolution of all systems in time.

The ultimate fact of Duality is that we are generated as a growth in the 5th dimension from a cellular/atomic ∆-1 seed to emergent ∆º being to fall back into ∆-1 desegregated atoms/cells; and so we can consider reality to be a constant combination between the two extreme, social dimotions of eusocial evolution and generation (5D) and entropic dissolution and death.

We have seen as a synchronous space the ternary parts of the being. Now we want to explore how the being evolves in time, tracing a ‘world cycle’ of existence between its birth as a form that starts to move, and back to a motion that stops into form.

The 3 ages of existence of space-time organisms. Its 2 worldcycles and Metric functions.

So we marry the 3 vital functions=motions of time and the 3 dimensions of space, either in 1 or 2D (height= spherical information, length=planar locomotion, width=hyperbolic reproduction) which merge in all Time-space Beings; and dominate one of the 3 ages of its life-death worldcycles, the past, young age of limbic entropic motions, the mature reproductive age dominated by the hyperbolic body/wave and the 3rd age dominated by the informative particle-head, when the illusion of time ends with an entropic big-bang death that dissolves the being into its ‘scalar cellular, atomic parts’, which lead us to the realization that time cycles NOT only return to its origin in a single spacetime continuum but they move up and down 5D scales.

Let us deduce from those 2 functions the fundamental process in time of reality, the worldcycle of existence:

The development of the Function of Existence of a space-time organism, can be developed as a feedback function, S<=>T, in 3 sequential phases/ages /horizons:

Max. T x Min.S (youth); Max. SxT (s=t); Max. S x Min. T (3rd age).

They are the functions of the 3 ages of life, between Sx 0 T (seed in the lower plane,¡-1) and Tx 0 S (function of entropy=death), which develop 5D metric into an ‘existential function’ of ‘extremal points’:

∆-1»∆º: The supœrganism worldcycle starts its existential function as a seed of pure form (4D) that creates its space-time form.

T>s (Ts): It is the first horizon or ‘entropic, youth age’ of the cycle, in which energy dominates the system and so we write this phase as, max. S x min. T.

Max. SxT: s=t. It is the present balanced age of the cycle or classic age of ‘life’, when energy and information are in a constant proportion. It is the most efficient age, when the cycle reproduces.

ST: Max. T x min. S: it is the 3rd age of the cycle when information has combed and exhausted the space-time field that warps into itself.

∆º«∆- 1: 0S x T: It is the end or death of the cycle that reverses its form and becomes energy again.

Existence is an ∝ (ab. relative infinite, with an entropic limit of death) sum of 3 space/time planes, fluctuating between birth and extinction through those 3 phases or ages. The 3 ages of Timespace supœrganisms happen in all systems, including mental languages:

In Physics they are, T-gas, the moving state, Si=Te liquid, the balanced state and S-solid the informative state; into Cosmology, where it describes the Universe as a space-time system that fluctuates between both limits, a form of pure time, the singularity (min.t x max.S) and a form of pure space, the big- bang (maxS x min. t):

In Biology, they are the 3 ages of living beings AND the 3 horizons of evolution of species.

In social organisms, through the subconscious collective mind of civilizations which in art styles mimic in a longer 800 year cycle of life and death of civilizations (according to 5D metrics a human social supœrganism is larger in space – a nation, culture, religion – and so it lives longer in time).

All what exists is a supœrganism of vital space tracing a 0-sum worldcycle of time through 3 scales of the 5th dimension: Born as a seed of fast time cycles in a lower 5D scale (∆-1:Max. T x Min. S), emerging as an organism in ∆o, living 3 ages of increasing information, as its time clocks slow down in its ∆+1 world to die in a time quanta back to ∆-1. Yet the maximal point Si=Te where reproduction happens defines the classic age, maturity, beauty, balance, survival of the system, all disomorphic jargons.

The 3 ages of life emerge in human social supœrganisms as the 3 ages of cultures and  its 3 artistic styles: Min.S x Max. T (infantile epic, lineal art, as in Trecento, Greek Kuroi; Si=Te; balanced beauty, when form and size are in balance, the classic mature age; and Max. S x Min. T: baroque, 3rd age of a civilization, whose subconscious mind is the art of its ‘neuronal artists’, the age of maximal form and an ∆st for a no future, which is the age of war and death of cultures).

We talk of 3 ∆±1 scales of worldcycles as the being live in a placenta, then emerges as organism in a world:

þ: 0-1: its palingenetic o-1 social evolution in the accelerated time sphere of existence, till becoming 1 (0-1 bounded unit circle in ¡logic mathematics; quantum probability sphere of particles in physical systems; palingenetic fetal age in biologic systems; 0-9 memetic learning childhood in social systems). It is the highly ordered world cycle as a ‘placental mother-energy world’ is nurturing as memorial cyclical spacetime has erased errors of previous generations.

– ¬l,L: The existential 1-∞ lifecycle, in which it will deploy its 2nd world cycle of existence in an environment which is open, entropic (1-∞ hyperbolic unbounded Cartesian plane in ¡logic mathematics; thermodynamic entropic statistical molecular populations in physics; Darwinian struggle between populations in biology; idol-ogic dog-eat-dog capitalist, nationalist competitive eco(nomic)systems in the super organisms of history. In this 1-∞ existence the world cycle is not ensured to continue, as the entropy of the world system can cut it off.

ω,Ω:  A larger, longer Transcendental worldcycle proper of the highest social scale ∆+1, the omega of its smaller parts – where it performs 5 survival actions through ∆±4 Planes self-centered in its mind, beyond which it cannot longer perceive, to become if successful a new supœrganism of the infinite planes of God, the game of existence.

In graph, physical, biologic & social worldcycles show to which extent 5D laws enlighten our understanding of reality. Matter States are physical time ages, from left pure solid, crystal, §top state, to an even more solid ∆+1 boson condensate, etc. We see that systems either move a step at a time within a plane of existence (gas, liquid, solid) or they can jump « two states at once, (as in the case sublimation) within that plane, or most often between two planes, as in « scattering & entropic death), to become a different Dimotional state. We can then see how the fundamental elements of 5D time appear on the graph: the worldcycle is local and complete. There are 2 inverse arrows from an entropic past (plasma), in a lower plane (ion particles) to the 3 ages of the matter states with increasing form (gas to solid), to end in a higher plane of existence as a boson-Einstein condensate. Do those worldcycles happen for the whole Universe? (cyclic big-bang). Unlikely…

RECAP. Time is cyclical as all clocks of time return to its point of origin, so all time cycles including those of life of its vital space-time beings are finite. Further on those time cycles break ‘space’ into inner and outer parts, so vital space is broken by the membranes and angular momentums of those time cycles that make spacetime beings also finite in spatial information. And an obvious experimental facts about timespace: cycles of time, vital spaces and the species made of them, co-exist in several scales of relative size from particles to galaxies, each one with clocks of time of different speeds. So spacetime is fractal broken in scales that added create a new 5th dimension of spacetime. The metrics of 5D and its scales, SxT=C & and the balance between form and motion, SI=TE, develops in 3 ages with 3 standing points, a max. point of existence, Si=Te or mature age, a young age of Max. T=motion, and an old age of Max.S=information; between birth in ∆-1 Form & T-entropic death. The search for space-time, Energy=information balances in a classic reproductive age of conserved time is thus the goal of all exist¡ences, but only the whole achieves the immortality of time-space, as we shall see egocy errors of fractal mind-points of space trying to stop the flow of time from a single selfish point of view, accelerates the imbalance that brings death equations. We are richer in our still property at that 0T-moment, when all is quiet so for time to keep moving, a reversal of entropy takes place.

So we use 5 bidimensional terms for all systems, its ages and forms: SS(max. internal and external form, as in seeds and minds; T>s (Ts); external motion that maintains internal form as in ‘locomotion); S=T: Balance of spatial form an temporal motion or ‘energy’, used to reproduce, the key present iterative state; S>t (St: Information, form with a little motion, or ‘external form, and internal mental motion); and finally TT-entropy whereas there is external and internal motion, hence scattering dissolution and death. ¡ts main series is a worldcycle of existence:

SS(seed/mind)<Ts(moving youth)>S=T(reproduction)>St(informative 3rd age)<T(entropic death)

The 3 scales in time and space of superorganisms: actions, worldcycles and absolute space-time parameters.

the ∆±¡ pentalogic STructure of all beings predicts the future of its scientific species, with a remodeled ABCDE of the scientific method that studies A)ccurate Data, B)iologic causes C)yclical patterns and E)ntropic extinctive conclusions for all systems in 3 relative scales of length of space and time duration (to which we add instead of E, a positive D)emocratic, humanist solutions for questions of social sciences sorely lacking in idol-ogy.

All sciences predict the future of its species according to its repetitive causal cycles. Or else they are NOT a science. Astrology became a science when Kepler learned its orbital cycles. Bio-economics became a science when we described machines as metal organisms whose industrial r=evolution followed the human 72 years generations of the dominant industrial nations that evolved them in 4 cycles: its body-age (British, steam cycle), heart age (German, electro-chemical engine cycle), its mind age (US, TV-eye, chip-head, mobile-ear cycle) to conclude with the ensemble of robots that as virus do, when all its parts are put together will become alive. Predictability of time-cycles is done at 3 levels:

S: Continuous, spatial mathematical simple cycles, using derivatives, proper of calculus; which is the shortest time span, as instantaneous derivatives cannot measure a ‘peak’ change of age/phase.

T: Discontinuous, cyclical patterns of sequential repetitive often survival actions (feeding, reproduction, death, taking place at intervals. As those actions are discontinuous, leaving long spans in-between, their patterns forecast longer time sequences. Such ¡logic structures are based in time patterns, which as any mechanical, circadian or orbital day-year clock shows are cyclical, repetitive. But here human scientists are at loss, because Galileo studied ballistics, entropic explosions that destroy the information of reality stored in those cycles of time clocks, its patterns and frequencies, changing human cyclical understanding of bio-logic time for lineal, abstract time that seems not to repeat those patterns so mankind lost its capacity to predict many spacetime events, as lineal time misses information stored in the frequency and form of cyclical clocks, even if equations are similar: V=s/t for lineal time and V=S(l) x ƒ(t) for cyclic patterns.

∆: Scalar, Deep Time patterns of topologic and eusocial evolution of parts into wholes – of quantum 0-1 time probabilities vs. 1-∞ thermodynamic populations in physics, of individuals vs. species in biology, of states of matter vs. geologic cycles in Earth, first noticed by J. Hutton, founder of geology who coined the word super organism for Gaia and deep time for its slower time cycles by virtue of its 5D metrics, $ x ð =C which implies that from the perspective of a smaller scale the life of its whole is much longer.

Deep time leads to a 3rd level of long-time prediction: evolutionary patterns of earth’s life species, including machines used in my web at evolutionaryeconomics.wordpress.com that have predicted cyclical patterns of social organisms of history (nations) and eco(nomic)systems, including the evolutionary and re=productive cycles of stocks of machines transformed into sales=profits=valuation of its company-mothers with remarkable precision for 30 years. But as human only recognize the 1st type of predictability – calculus of instantaneous derivatives, that need a ‘continuous analysis’ – and have simplified cyclical time into lineal time, ignoring the scalar time of parts and wholes with its 5D metric, their capacity to forecast the future is far more reduced than a ‘stientist’ who understands the 3 scales determined by the bio-topo-¡logic properties of ‘scales’, ‘space’ and ‘time’, the 3 ∆st structural elements of all systems of the Universe.

 

The organic view. Topological forms as Networks and superorganisms.

Once we understand the worldcycle of life and death, we can put in perspective the ‘limited value’ of entropy in the making up of the organic Universe, as we have outlined the basic 5 Dimotions of space-time in previous paper, focused on the fundamental dimotions of the Universe: present balanced, ST-energy used for the reproduction of form. Since the Universe is a fractal that reproduces information, in new topological networks, starting from a first ‘seed’ that multiplies and then re-organizes itself into a replica of its ‘generator-mother’. This is the essence of reality not ENTROPY, just its limits of death by disorder and overdrive of motion.

As the 5 elements of the Universe – its 5 TT-Ts-ST-St-SS dimotions of exist¡ence combine space and time NOT to destroy reality but to reproduce it and conserve it.

Why then humans have such huge distortions in the basic concepts of reality, time, space, scale and mind; and there are so many ‘ascientific theories’ based in a single dimotion of time, the simplest one? Precisely because it is the simplest one. But also because SCIENCE IS CULTURE, and we have evolved a military culture of Entropic weapons of maximal motion that erase the information of mankind, killing life. So those who make weapons, the worldly profession of physicists, arrogantly think the Universe is also about entropy=death.

It is not/ The Universe is about the higher arrows of reproduction, S=T, and social evolution, St>SS, iteration and intelligence, the arrows of LOVE AND LIFE, and that is what makes it so perfect and superior to modern man…

The Universe is organic, made of vital space- networks that conform those superorganisms, since in fact topology describes the 3 varieties of ‘St-informative particle/heads’, Ts-limbs/fields and ST-body-waves of energy as ‘networks’ of smaller points (cells, atoms, individual humans) joined together whose form corresponds to its function. Let us then summarize that key concept that shows the organic purpose of the Universe.

The super organism is a system that reproduces itself, so it is self-sustainable, and doesn’t need the concourse of God. This is the view that starts with Aristotle and his ‘Organon’, follows through to Leibniz and his model of ‘relational space-time beings’, made of a finite number of time cycles and vital spaces with ‘vis viva’, momentum, and goes through XIX c. disciplines, from Darwin’s biology to Spengler’s super organisms of history and ends in systems sciences and the formal models of the fractal organic Universe, which I advanced during my tenure of duality at the International Systems society at the change of century.

In those conferences I also advanced the social, organic model of history as the super organism of mankind where the human being is a citizen cell organized by three physiological networks that must be designed with the laws of super organisms, which are:

  1. Cellular units. These are cells in a human body, citizens in a human society.

Networks of energy or vital space; provided by Gaia, a super-organism made of living beings, joined by a common network of visual information and networks of life energy, gathered around her ‘river veins’. Since Gaia is also the living organism that hosts the social organisms of Mankind.

  1. Networks=Languages of This is the nervous system that organizes cells in a body, or the verbal/visual information that organizes human societies through laws, ethics and art.
  2. Networks that reproduce energy and information. These are sexual systems in individuals; and economical networks that reproduce goods and cultural networks that define how humans reproduce in societies. This is the blood system in a human body and the economic networks of production & transport in a society that favor ‘WHealth’, that is, goods that satisfy the needs of the ‘3 physiological networks of life-existence that make us human beings, whose ‘proper frame of reference’ (left) is NOT based on financial values, manipulated by financial institutions and companies that set prices, but by ‘biological true values.’

Of all the elements of a supœrganism the most important is the head of information and its languages of perception of the universe, which are by definition, selfish, self-centered as they portray the universe from its survival subjective perspective.

All systems of nature can be modeled as super organisms of a certain scale of size, ruled by the scalar laws of all systems of the Universe, that co-exist at atomic/cellular/individual and gravitational/organic/social scales. As such their ‘cycles’ followed the scalar metric equation of ‘Deep time’ (Hutton, who discovered in geology, inventing the name of super organism for the Earth): S (space size=energy) x T (frequency of information clocks) = Constant, which means larger systems LIVE slower time-cycles than its parts, which STORE the information of the system in its faster frequency of time clocks.

So physical organisms are coded by quantum particles; biological ones by genes and human systems by memes that construct those super organisms of history,  from birth as a fast seed of information (crystal cell, semen, prophet with verbal memes) which will reproduce into similar clones (crystal units, multicellular organisms, identical beliefs of human beings in nations, civilization and religions); and become connected by informative nervous-political-gravitational and reproductive, blood-economic-electromagnetic systems… thus finally emerging as a larger superorganism.

Such super organisms then will be living 3 ages of increasing information, as the informative systems dominate the whole, and absorbs its energy, warping the system till its exhaustion and death (galaxies feeding its informative gravitational black hole, nervous systems wrinkling the vital body cells, human elites persisting the reproductive working class), which is an entropic explosion of that warped/wrinkled/absorbed energy: big-bang, m=e/c2, death, war).

The Universe is a fractal organism of 5 Dimotions of space-time, of which entropy, scattering internal and external motion is just the last state of an organism. And yet huminds have made of ‘entropy’, the fundamental ‘theory’ of reality, regardless of facts, by merely ‘dismissing’ all other dimotions as irrelevant to time, or secondary effects of reality – from crystal solids, to still particles, from vortices of informative gravitation to mental spaces. We thus have first to falsify the ‘main’ theories of huminds, biased to entropy in all ‘stiences’ of the Universe, and then study in the second part of this article, the true meaning of entropy as the limits of death in time, vital space and scalar perception, for the main systems of the Universe and its scales.

 

 

THE INVERSE OF ENTROPY: SS-MINDS. THE DUALITY OF DEATH

So we will expand some concepts not considered, regarding the ultimate cause of death: a mind-monad that exhausts the information of a system (internal death by wrinkling) vs. an external top predator that scatters the system, which is the TT-death; to show that in fact both SS-minds and TT-predators cause death by imbalance and ‘displacement’ of a being into a different plane of existence, a relatie TT-past or SS-future.

Only pure space=form and pure time=motion travel between 2 scales.   

The conservation of the quantitative number of ‘energy’ used by physicists is equivalent to the conservation of a Volume of space-time. The volume of a single spacetime plane of the Universe is equivalent to the quantity of any other ∆-scale. And all of them therefore transfer constantly energy and information between them. Yet more exactly what is transferred is entropy or form; since when energy or information leave a given plane, it ‘strips’ off one of its two components. It is then important to understand the difference between TT-entropy and SS-eeds which are not in the same plane of existence than Ts-locomotion and ST-energy. As energy is the parameter humans use between 2 scales. The difference will be essential as we advance the model and take on seriously the task of translating mathematical equations of physics with rigor.
Only entropy TT and pure form SS travels between scales. Ts, St and ST must leave behind one of the two elements to travel and that means either a ‘translation to other language’ or an extinction of the original form.

It is a fundamental law always shunned off since the neutrino proved it: The neutrino is NOT perceivable in this scale, as it travels likely faster than light in the lower gravitational scale; but it took part of the ‘energy’ of our plane as motion – did it carry also its information, its spin? I am afraid not, but we put it there, even if spin=form is NOT always conserved. A question fundamental to understand the neutrino theory of light. But of course, as usually Physicists are only ‘a la par’ with mystiques to see and interpret the invisible signs of reality into ‘models that are seldom truth but never in doubt’ (Landau) as with big-bang theories. So while we have NEVER measure directly the spin of a neutrino, which we know for values of pure motion (momentum-energy), every physicist will claim that Cowan, Lederman, Goldhaber an a long line have measured it, just by balancing the invisible momentum because a priori they decided momentum is conserved traveling between scales – which they do not recognize anyway. Fact is the non-transference of ‘energy and information together’ between 2 scales as that is the definition of death. Point to argue here is if the Neutrino is in the light scale – is not, and so when a particle which is a scale above produces a neutrino is NOT producing either motion or spin=form. As motion evidently is carried by Neutrinos, or else they would not exist at all. What is missed is the form, which in all other systems of reality also disappears after you die. So there you have one of the most profound all encompassing laws of 5D.

And so we show what happens in the paper of entropy and the Universe: a split of energy – in to form that goes one way through the height dimension of S-Information and normally scatters into death, while energy expands mostly as motion – entropy in the length dimension of ‘T-motion space’: The explanation is intuitive. A system can still send a ‘wave’ of cellular forms of any kind of seed or mental image that helps to reconstruct its system after it travels through channels of communication, mostly as waves that combine motion and form – the quintaessential form of energy, with the purpose of going faster according to 5D=SxT metric equations. So if we reduce the package to the essential information, we ensure the system transfers the message in a relative no-time quanta; but 2 scale beyond – that’s a long shot. That is the regio of ‘food’ and food is memoriless. The amino acids don’t tell us where they came from, or else they would NOT be food for us to reconstruct our form.

The antisymmetry of temporal information: Death

A consequence of the 3 ages of time is its antisymmetry as opposed to the bilateral, mirror symmetry of spatial forces: Time is antisymmetric as the old age is the inverse of the young age with the parameters of energy and information inverted. Youth has maximal energy and minimal information while the old age has minimal energy and maximal information. And yet many attitudes and processes might seem self-similar, if the researcher doesn’t know how to differentiate informative and energetic parameters, since those parameters might be quantitatively the same, only that inverted in value. Space is symmetric as left and right reproductions are mirrors of each other with the same parameters of information and energy. This explains why spatial reproduction happens only in the E=I, balanced classic age of the system, when both parameters are identical and a self-similar reproduction of a bilateral, spatial being is possible.

The understanding of the antisymmetry of time vs. the symmetry of spatial processes has wide applications in the solution of questions pending in all fields of research, from the understanding of the temporal, weak, informative force that has no bilateral symmetry to the ‘chiral’ processes of evolution of life forms vs. the symmetric shapes of self-similar left-right, spatial bodies to the meaning of ‘antisymmetric’ gender and the 2 ‘antisymmetric’ sides of the informative brain.

But the most important of all antisymmetries is that of death, which could be considered in the jargon of physics, a ‘local antisymmetry’ of time. Indeed, if life is the arrow of information towards the future e->I, death is the inverted arrow, i->E, that erases form back into energy; but this time travel to the past is always local, affecting only the limited world of the species, so antiparticles are the local antisymmetry of time that kills particles, death are the local antisymmetry that kills life and the big-bang the local antisymmetry that killed a previous Universe. And both directions are different, since ‘death’ lasts min. time and causes a maximal space expansion and life lasts max. time and expands minimally in space. Both balance reality in an eternal present of past to future to past existential fluctuations:

Life-future: Max. I x Min. E x Death-past: Max. E x Min. I= Immortal present: E=I

The understanding of that local antisymmetry is the key to resolve problems of physics such as the weak force, why we see less antiparticles or dead people than particles and life people (much longer in time), or the non-evaporation of black holes (as antiparticles are the same than the particle, albeit when moving to the past they seem to co-exist), and so on.

But its implications in biology and philosophy are much larger: we are ultimately ‘back and forth’ vibrations of space-time, virtual existences, dust of space-time that always revert into a zero-sum, which makes the Universe and its game eternal.

Recap. Old age has inverted exi parameters to the young age.

Mind’s murder.

In the graph, we exist as we travel a world cycle zero sum through the topological, temporal scales of the fifth dimension. The final state of existence is the entropic death when the mind splits pure form and pure motion. in the graph for physical and biological systems the moment in which form switches into motion or ‘entropic point of existience: §ð<<∂S

The mind is paradoxically enough the cause of entropy precisely by causing so much order and form in a system that it exhausts it, and so because the mind absorbs all energy in the system stopping form, once the mind perceives, what it has perceived becomes ‘entropy’ and disordered. So the mind causes the split of reality into the entropic dissolution that balances the absolute form it achieves. And so we can study the mind as the catalyzer of entropy at two levels:

  • The mind that brings the 3rd age of the being and then as time cannot stop once it become immobile, it explodes into the age of entropic death: §ð<<∂S
  • The mind that splits a flow of information into the pixels ‘reduced’ vision of the world and the ‘reminder’ heat expelled and wasted, in each act of perception.

So as usually in the duality of ∑ actions = Worldcycle, we can study the mind in its microstates of actions provoking entropy in all what it wastes after absorption of energy or information and we can study the mind in its macrostate and worldcycle as the cause of the entropic death of the

Biologic systems die due to the excessive informative absorption of energy by the top predator mind and the enclosing membrane.

So biological death is obviously the reversal of the process of warping in an excess of skin and memory, of space and time, of the mind membrain and its two dimensions.

When the system gets older the membrain detaches itself of the body and the mind forgets the body functions for the memorial thought of time past. And so finally the detachment breaks the connection of the 3 ‘present parts’ that split apart:

Since that equation includes the 3 essential arrows of the Universe, not only one arrow as a clock does:

The arrow of past spatial entropy, $p; the arrow of temporal information, SS, and the product of them, C, A CONSTANT balance, or arrow of reproduction.

It is also obvious that mathematically we can express the previous equation in 3 forms:

Max. S x Min. T = K ;      S=C=T      and Min. S x Max. T=C.

Thus there are 3 possible stages or ages of evolution of the equation of biological time. And since we are all made of ‘energy’ and ‘temporal information’, those 3 stages must be the stages, or phases of any system of the Universe. This finding, which is perhaps the most important discovery of Theory of Time of the XXI century, is validated by all kind of empirical observations. For example, the 3 states of matter correspond to those 3 equations. Gas (maximal energy), liquid (balanced) and solid (Maximal information. They are also the 3 possible solutions of a cosmological system: the big bang of maximal energy, a steady state of balance and a big crunch of maximal information. In the graph, we show further examples of those equations.

Its application extends in 5D to life and history. If we call the age of maximal locomotion, youth, the energy age of balance between the reproductive, mature age, and the age of maximal information the old age, we have a simple description of the fundamental cycle of life and death through its energy and information.

But we can also write those dynamic processes backwards. And so we have the inverse equation of life ages, the equation of death, when after accumulating maximal information, a species reverses its arrow of information and explodes that information into energy. It is the process or equation of death.

Life grows temporal information, as time increases the form of beings, TT-> SS, and death its inversion, Ts> St.

So simple, so beautiful, so misunderstood by mechanist scientists, who think the previous equation is ‘uncertain’, because the observer can perceive a particle in any of those 3 states (Uncertainty principle of quantum physics).

The reason why death exists in a perfect, immortal Universe is obvious: if species only evolved socially towards more information, they would end into a ‘big crunch’. So the Universe and all its parts should have, long ago, reached a point of  maximal density, with no return. To avoid this, the ‘game of life and death’ exists, whereas death is the opposite arrow to , as it dissolves the networks that put together individual cells, breaking the super-organism back into its parts. But we are now concerned with the arrow of life.

The ±1 social arrow has, in fact, 2 directions:

The positive, +1, social arrow of cellular evolution creates life and makes a being emerge at birth.

The -1, negative arrow of cellular dissolution kills life and dissolves a being into its cells and atoms. Thus, it is the key arrow of the life/death cycles that clock-time misses. Hence the enormous simplification of those 4 time-arrows, brought about by clocks, which in Physics, since Galileo, only measure the first and most simple of those arrows, the energy of motion.

The result of adding both – the life and the death processes – in any system or scale of reality is a ‘zero-sum’ of information+entropy that cyclically returns reality to its initial form, in a dynamic, multiple steady state balance that affects any entity of reality. The study of that process of creation and dissolution of complex structures, however, cannot be made with translational time, (v=S/T), the realm of physics, but it needs to understand biological, morphological time – the life/death cycle. Those ages explain precisely what physicists, stuck in the study of time as movement in space, will never understand: the meaning of the life and death cycle that creates and extinguishes societies (super-organisms of History ) and all kind of beings that exist in space and time. In biological time all universal species follow the same ‘morphological changes’, described by the wisdom of verbal thought as the meaning of life, each one ruled by one of the 3±1   change=time:

+1: Conception:  ruled by form (Morphogenesis in still space), as a micro-organism or cell transcends into a macro-organism, organized by social networks.

1st age:                  Youth or Age of motion.

2nd age:             Reproduce its energy.

energy and information are balanced

3rd age:                All energy and motion becomes information.

-1:Death:               The inverse of conception when the super-organism dissolves back into cells.

Death equations: ∆+1<<∑∆-1

Death is a lower descend two scales fro ∆1 to ∆-1 of a ternary super organism extending on Ξ planes of existence. As such it creates a blast of entropy-motion in relative infinitesimal quanta of time, t->0, expanding past the c-onstant of speed of the system, V>>C, as the information of the whole disintegrates travelling to the past.

The equations of ¾ as well as those of quantum physics allow for both simultaneity in space and non-locality, due to the explosion in space at V>>c of such a system, which makes it seem simultaneous and past travelling of information, which is the real event of death.

What this means is that the information of the system, and paramount to it the soul, @ª•… will travel to the past and we shall consider the implications n different analysis of those tests:

Graphic representations of the 3±¡ ages of existence.

Humans perceive simultaneously the 3 ages of some species too small and fast to differentiate them. As particles in bubble chamber or cars in the night, we see the long time of the species – an entire spiral vortex with the 3 ages of a space-time being.  In the next graph, such long world-line, or life-graph is in fact a spiral in terms of spatial population and cyclical speed: The organism looses mass and accelerates inwards its form as it becomes slimmer in space. The first age of the spiral is its energetic mouth that brings in a galaxy the interstellar dust, which will give birth to stars, in the middle, reproductive age and will collapse in the center, the informative black hole:

Any form can be represented in a spiral graph of space-time. For example, the evolution of the FMI complex with its 800-80-8 cycles of increasing informative evolution is an spiral of 3 horizons in a decametric scale: 800 years civilizations, 80 years nations and 8 years ‘decades’, in which the product is evolving faster and now becomes integrated by networks. This 3-horizon evolving ternary network, central to social sciences can be also represented in a spiral of accelerated birth and death of human civilizations destroyed by wars. Any mass or charge is in fact a natural spiral, through which photons and gluons become denser till collapsing in the bigger particle, as interstellar gas does in a galaxy. All those spirals can be seen as equivalent to the world-lines of lineal physics, now world-cycles of a living organism both in time and space, as a whole or as a wave of evolving particles.

Cyclical time: expanding Einstein’s principle of equivalence to historic vortices.

The essential concept of General Relativity is the principle of equivalence between acceleration and gravitation. Both are the same. Yet as physical acceleration is maximal in a vortex, VoxRo=K, a vortex IS accelerated Time and as a vortex increases the frequency of the cycle, inwards, diminishing the ‘lineal timespace’ of each cycle, time accelerates its information as it SHORTENS its periods. This fully accounts for the arrow of future time that increases information in 5D spacetime theory and applies to all systems of time, including Physics (laws of forces), evolution (Laws of species), History and the Earth at large:

The main arrow of future time which is an accelerated vortex of evolution of cyclical form, departing from a simpler relative past of entropic slower time cycles (the only arrow of time studied by physicists), to a faster more informative future of higher informative content.

A ‘vortex of accelerated informative time cycles’ is essential to all systems of Nature, albeit not understood by ‘primitive huminds’ still stuck in the study of simple spacetime locomotions (one-dimensional analysis of time in physical sciences) and its reductionist 4D models. So let us illustrate what a vortex of accelerated time is precisely with the most advanced work of Physicists, specifically Einstein’s work on accelerated vortices of physical space-time called masses

The duality of death in history.

In history death also occurs by an excess of information in the 3rd age of the being, followed by an entropic war, when technological information preys over human beings as weapons kill our bodies and go(l)d our minds.

We observe the 3 ages in a circular form, with the Paleolithic youth or past energetic age in the center, the balanced Neolithic in the right and the animetal age in the left, the 3rd age of excess of information and death in a neo-Paleolithic of the new species, the machine that closely resembles our Paleolithic, depicted in closer view in the next graphs:

We represent the wave equation of history in two formats as a transversal wave and as a vortex of time, accelerating its information inwards.

The equation of history  is a cyclical wave equation of evolutionary systems that shows the fluctuation between predating radiations of extinctive metal-species and human species.

The equation in that sense is similar to the Volterra curves of predation, which slowly but steadily and an accelerate rate provoke the extinction of a species by its predators, parasites and competitors.

It is an evolutionary equation, which started with the arrival of metal. It accelerated to 80 years with the arrival of machines and it has accelerated again to 8 years with the arrival of chips.

So in the past new machines appeared only 800 years and so we had 7 cycles of war and extinction of civilizations and the weapons that caused them, studied in the right side of this blog: bronze swords, chariots, iron, coins and mercenary armies, spur cavalry, gunpowder and machines… Now we have shorter 8 years cycles of electronic wars and digital weapons (robots and bombs researched with computers). And each of those evolutions of weapons caused the extinction of civilizations in worldwide ages of war.

The duality of graphs of waves of existence: Cyclical vs. lineal waves.

All this said it is obvious that we can represent in phase mental space, which ultimately are all the spaces of the Universe (see Universe in space), the cycle of existence either in cylical or lineal forms:

The equivalent graph in lineal time will give us a bell curve – the lineal version of a cyclical life-line: The speed of time/information changes during the ages of life, shaping a bell curve, such as the st-1 age is the fastest age of informative evolution, which diminishes in the young age to a halt, when the speed of cellular reproduction and energetic growth becomes maximal, both reach a steady state in the mature age, of SóT, rhythmic back and forth beats; and then in the 3rd age energy decelerates first and then information decelerates and collapses till death provokes a maximal explosion of information into energy. Those phases of different speeds of energy and information can be generalized to any system and event that will always go through 3 ages: an accelerated seminal and young age of increase of form and energy, a steady state of constant speed and a decelerated age till the system comes to a halt and the event dies away.

 

Time in present science.

We considered 3 paradoxes of Galilean relativity – one of them is the fact that as we move through lineal steps we end up tracing a cycle. Time thus is ultimately always a cyclical zero-sum path.

The concept of time in present science is a simplified view of what time=change=motion really is in the Universe, born of the use of mechanical clocks and Cartesian graphs to chart the lineal motion of cannonballs by Galileo. Its success for all purposes of our civilization is relative in terms of a knowledge of the principles of reality, cyclical time and fractal space. This means that as time and space are a priori ‘elements’ of our view of the Universe, by adopting lineal time, humans have adopted a lineal view of reality and its praxis has become also lineal, unable to grasp the cyclical causality of the future, and hence unable to understand the future.

This ‘handicap’ of the humind is present in everything humans do. By lacking a proper understanding of time cycles humans have become guided into a foreseeable future they don’t understand by short-time lineal impulses.

If cyclical time had been properly understood, humans would by now understand perfectly the future and what is best manipulate its causes through history to achieve the better stage of time – immortality as an organic species, mankind. So yes, lineal time works to measure motion of cannonballs and motions of everything but its distortion and lack of information about the cyclical patterns of time has rendered humans ‘savant idiots’, people who thanks to its sensorial machines have built a remarkable quantity of small data about reality but are clueless about the long cycles of time and ultimate cyclical laws of reality.

The 2 languages of informative and reproductive networks: Bits of information and bites of energy.

It is important to understand not in pure abstract mathematical terms, but in logic, linguistic ones, the internal, dynamic nature of those networks, because only then we can proper understand how they work in advanced organisms of maximal information, the biological organism and the Historic organism, which belong as ‘fractal systems’ self-similar to each other, two the same specific type of organisms, we shall qualify as socio-biological organisms. A network, of informative nature, delivers messages of information to simultaneously coordinate the actions of all its parts; with its faster=smaller bits of information according to 5D metrics (min. spatial size x. max. temporal speed). While the networks of reproduction, the blood and financial system delivers larger bites of energy, which the organism needs to feed itself (when it is a healthy NON-corrupted supœrganism as most of Nature, but not human societies, with an astounding level of corruption).

We understand reality both in terms of energy but also in terms of information, as both are two sides of the same coin, called ‘exist¡ence’ is the fact that in the sentient Universe, each fractal point, atom, cell or citizen (physical, biologic or social systems) needs bits of in-form-ation, form, smaller in size of space, hence faster according to 5D metrics (SxT=C), but also ‘bites’ of entropic energy which will help the system to move. Networks are NOT some abstract ‘fractal tube’ but they exist to deliver ‘energy and information’ (SS: form=language with a little motion=St-information and motion=entropy=TT with a bit of information = energy=Ts).

So a healthy supœrganism will deliver to each ‘fractal point’ (molecules, cells, human citizens), two type of messages through two type of networks. We shall call ‘generically’ the 3 type of bits and bites of information and energy that each of those 3 physical, biological and social systems receive, ‘particles, genes and memes’ even if the words as usual in 5D sciences are slightly changed, and widened in its original meaning.

So with its specific variation, those are the two fundamental reproductive-‘body-wave’ and informative-‘particle-head’ bites of energy and bits of information of the fundamental systems of nature:

In physical systems, the two networks are the gravitational faster network of information, which we humans do not perceive, as we are much larger beings with electronic networks. Its bits of information in this faster non-local network should be ‘gravitons’, components of gravitational waves. In physical papers we advance as the most likely particle state of those waves of information that ‘position’ the different physical systems of the galaxy, a gravitational tachyon ‘neutrino’ for multiple reasons, we study on our papers on physics.

On the other hand, because we do perceive it, it is much easier to prove that the energetic network of physical systems are electromagnetic waves, photons and its ‘social, static state’ as the elements of an electronic nebulae, trapped in the potential energy well of the atom. Thus photons and electrons become the ‘energy network of physical system, molecules.

We shall escape then in this introduction further information on the scalar structure of those networks and how, as we ‘grow in scale’, what is a bite of slow energy for a smaller plane of space-time, becomes for the larger plane’s slower beings, a faster bit of information, in the amazing beauty of the harmonies between scales. So electronic ‘food for atoms’ becomes electronic information for biological organisms and so son.

Those biological organisms do have 2 fractal networks, the electronic, informative nervous system in which bits of electronic information moving along the myelin membrane deliver faster messages to every part of the organism to simultaneously synchronize its motions, so the body-cells act as a single form in simultaneous space.

– But when we move into the bites of energy delivered by the blood organism, the network delivers to each cell the basic ‘currency’ language of energy that all cells need to move, called ‘oxygen ‘. It is an atom of slower motion than the electrons but due to its electro-negativity and readily availability in the atmosphere, with its capacity to kick with two OH- & H+ legs the water ‘medium’ on which cells exist, the perfect language of ‘money’ for the organism to start kicking its ‘actions’.

We have in the next scale according to those harmony laws, 2 basic biologic bits & bites of information & entropy, electrons and oxygens, and as life systems become more complex, variations of those bits & bites occur.

The main category are mixed ST messages, which deliver BOTH a stick and carrot ‘complex’ to the cells and its big molecules, which are amino acid systems, of great simplicity called Hormones, starting from the simplest of them all, an NO molecule (which do relax muscles, its main message to the locomotion system, increases the pressure of blood, provoking sexual erection, the simplest message to reproductive systems and multiplies the neuronal activity. As nitrogens are the clock atom of our mind-brains.

So more complex NO systems with a body support of carbon chains become ‘hormones’, which might have a ‘higher informative message’ (with more N, as in nucleotide molecules) or a higher energetic message (as in acids with more oxygen). They form the basic letters of longer biologic sentences that might accumulate information in ever more complex molecules, as biological organisms are by far the more complex systems we know of.

 

LANGUAGES & MINDS. ITS WILL: 0’x∞=C

 

Networks that share energy and information between parts and wholes that expresses the structural unity of all scales connect all systems of reality. Networks ‘fill’ space ad maximal to connect fully the whole with the parts, achieved in the Si=Te point of parallelism and self-similarity. But they enter in a region of faster motion. So while Space ‘tends to remain constant’ in each scale thanks to filling networks, time accelerates. So the 5D metric refers NOT to the whole Universe of 5D planes but to a given family of ‘supœrganisms’ of which mankind in it 3 scales of ‘biologic cells’, human individuals and societies is undoubtedly a ‘phyla’. When we go down in scales, the Universe ‘enlarges’ for a traveler that becomes smaller and accelerates its temporal energy

The Galilean Paradox S=T explains the existence of mind-spaces based in linguistic forms, whose equation is the basis of the psychology of the mind – the ego paradox, and the processes of creation of scales (seeds, minds, genetics, etc.)

Descartes was fully aware that what he had in the mind was not the whole Universe, so he expressly stated the fact, differentiating the ‘world’ of a human mind, from the infinite other worlds that exist outside, establishing in his little known book, the ‘world’, this difference, affirming that his ‘Cartesian Frame of reference’, was only that of the human mind. So he described a Universe as the sum of ∞ mind-worlds that don’t speak the same languages or create the same reality mappings ‘huminds’ create. But all entities that exist were made of: Open §pace, which he called ‘res extensa’.; Closed, cyclical ðimes, which he called ‘vortices’. Then he added a 3rd element, realizing the only proof he had of the existence of those vortices and res extensa was the fact that he perceived them: ‘I think therefore I am’.

Thus we define the mind equation as the limit of SxT=c, also the Generator of all digital numbers is, 0 x ∞=K:

0-finitesimal spatial mind x ∞ time cycles = Constant mind-world:  §@(mind space)<≈>∆ð (universal cycles)

Origin of Ego paradox, key to psychology, subjective human cultures, religions & ‘ænthropic’science: ‘Every mind measures reality from its biased p.o.v. confusing the ∞ Universe with its ‘finitesimal self-centered world’

The universe has infinite such mind-mirrors depending on the forces used to gauge the external world, which bounces on a limited quantity of its scales of space. Humans perceive the range of scales of the frequency of light between red and blue social density of colors. But infinite other minds with different detail according to the quantitative pixels they absorb (max. S = Min.t) maximal for smaller sixes will determine the intelligence of the system. Mind languages map reality into spatial forms. It is the ‘intelligent’ still spatial limit of reality, as all what exists are disordered entropic motions=forces and ‘minds’, particles-heads whose logic & mathematical languages create a territorial body order that forms of reality. ‘Vital motions and perceptive minds’ make up a ‘vital, perceptive, intelligent’ Universe. Since particles already have all the 5 Dimotions, gauging information, decoupling=reproducing & evolving social with magnetic fields.

So the creation of scales of reality is a simple game, in which a point mind ‘reduces reality’ to its infinitesimal form and then projects into its local territory of order, which will reflect at scale, the larger whole or world, which the linguistic image reduced and then enlarged back into its territorial form: Fractal points unlike Euclidean ones are points with parts, as we come into its scale grow in size and display the 3 minimal parts of all of them, its area, frequency of angular momentum, and central Active Magnitude, the ‘singularity’ – focus of charge, mass, forces or informative minds.

How we localize a mind is then very easy: a Still form that only changes with each ‘quanta’ of present time.

In the graph we see several minds on different scales of the Universe. It is simple even if we do not speak the specific language of a certain mind to localize the mind-point of a system, according to pentalogic laws:

– S: By its topological dimension of ‘height’ as it is the most advantageous point to perceive information. So all heads are on top of a height dimension.

– St: By its focus of a vortex of forces perceived as information. Minds attract the motions of ‘bodies’ with lesser form.

– TS: by its capacity to replicate a mirror image of the whole: minds are mirrors that reproduce in ∆-1 the whole; while in its reverse function, minds can work as Seeds, replicating that image into a whole, if given enough energy and storing enough instructions of that whole.

– Ts: By the fact they form locomotion, bending linearity into form.

-SS: By the lack locomotion. Minds are still.

-TT: By its opposition to entropy or by the fact they absorb ∆-3 pixels, splitting them, and absorbing only its form. The black hole produces a constant flow of radiation but likely it is eating the quarks of its stars.

Mind and languages of communication: SS>St>ST:

Because the 5 dimotions of the Universe are entangled, a mind’s purpose is NOT only to perceive reality in the implosive process of ‘reduction’ of the forces the mind absorbs – which externally might be seen as an explosion of TT-entropy, as what happens around a top quark black hole till only the bits of information remain, and so an ST form becomes split into SS and TT (Universe and entropy paper), leaving the §till (ab. SS) parts for the top quark black hole or nova to form, while the rest is expel as entropic energy (E-mc2), but the mind must communicate St-messages to his territory of order to conform the world in which its mirror is projected. And so besides perception, the second great field of inquire about the Minds of the Universe made to the image and likeness of the whole are the mechanisms by which a Mind through ‘languages’ of communication – the bits that conform its ‘static view’ of its world, are deployed as signals of information to the different parts of its territory of order:

In the graph, the mind communicates the whole as a knot of pentalogic languages, which further clarifies the meaning of perception: knot of forces, which beat in the mind-point with a regularity that achieves complex perceptions. Minds though can have lesser structures than a full pentalogic display of languages, which will be:

– A language of perception of the larger ∆+1 world – in human beings ¥-light, its SS-language.

– A language of communication with its ∆-1 scale of body cells, which normally branches into 3 languages networks (the ∆º) elements of the being – the ST- reproductive language/network, the informative St-language-network and the Ts-locomotion language network – with an ∆-1 ‘entropic’ language/system to predate and destroy external elements of the territory of order; not really so much a language but a ‘TT-weapon’ as there is no other communication but death when an §-mind kills.

The error of egocy transpires all forms of human knowledge.

All this said it is fundamental to understand the limits of human science, embedded in the mind of man, as humans do NOT see as first experience reality but the sensorial limited information perceived through our electronic eyes – natural and mechanical. And then we do NOT really try to do what we shall do in those papers, to build the larger reality departing outwards from the mind-view, but huminds just build a deeper level of ‘languages’ that reduces further reality to a synoptic smaller view – faster in terms of its time clocks, according to 5D metrics, so if the smaller mirror on the smaller reality of human senses, is consistent in its grammar and focus, it does have the added advantage of being able to calculate faster sequences in time and anticipate the future ‘moves’ of the larger whole. Still this inward method will always miss the ultimate laws and substances of that larger reality, space and time and will therefore distort reality.

And that is indeed what we shall find in all humind’s sciences: ‘gross deformations’ of a reality we don’t see. So I often quote Schopenhauer: ‘talent hits a target nobody can, genius hits a target nobody sees’. We are out there to chase what nobody sees, behind our senses, and one we have captured an image of it, of the laws of 5D, bring back this larger view, to show the inadequacies of reducing reality to the synopsis of the humind’s senses and limited languages, as we have already done with the scales of space-time, the structure of mathematical points or the multiple type of dimotions… And we are just ‘heating’ engines (:

Humans can’t escape its direct senses that only see a spacetime continuum regardless of sheer evidence of a scalar 5D Universe of different sizes of space, each one made of ∞ non-E points (particles, atoms, molecules, cells, organisms, supœrganisms, planetary systems, galaxies, similar in structures to atoms, hence likely a new scale of a hyperuniverse) whose time clocks diminish in speed the larger a system is but its product, SxT=C remains co-invariant hence able to transfer symbiotically energy & information between scales ( (geometric definition of a dimension). Those fractal points and its cyclical time-motions enclose vital spaces of smaller parts, whose faster time cycles carry the quantum, genetic and memetic information of which we are all made.

Egocy reduces sensorial, sentient survival ‘rights’ to nitrolife species, with a simple 7-electronic brain clock in its amino rings, and reproductive ones to its phosphorated carbon DNA helices life starts in the particles of the atom. Your mind is electronic, your information is coded in spins, and any other atom in proper liquid conditions might evolve into complementary life forms according to the laws of formal space and time motions, of topology and vital functions, described with the existential algebra of Scalar spacetime.

But ‘huminds’ eliminate internal parts & external motions of timespace organisms, compressing its limited view of other scales into a continuum. We elongate time cycles of information into lineal entropy postulating a chaotic reality where only we are intelligent – even denying that gravitational informative matter in galaxies balances entropic ¥-like expansion of space in-between, as it happens in atoms.

‘I seem to be the only scientist that thinks there are ∞ time clocks in the Universe… Leibniz was right. Newtonian absolute space-time is false. But if so we have to start science from scratch’, said Einstein. Both believed in panpsychism. We are all non-Euclidean fractal ‘points=monads, which hold a world within ‘(Leibniz): 0-linguistic mind x ∞ clock cycles of the Universe = Constant space world. Our world is Euclidean, drawn with the 3 perpendicular dimensions of light space-time, which appears constant (Relativity). But the ‘languages of god are ∞’ (Upanishads). Most minds seem to obey topologic, mathematical languages; and each scale is made of networks of such points. But humind’s egocy (ego=Idiocy) confuses the Universe with its reduced world-view, blind to the sentient and organic properties of all other points of space-time and its organic networks. So all our theories of reality try to explain our light mind-view NOT the Universe of ∞ time cycles and points of view, whose main laws are about the relationships between small and larger scales co-existing as synchronized complex organisms of time=motion and space=information. Those are the laws studied in 5D stiences, as they organize non-Euclidean points with ‘parts’ into ‘waves and network’ that create topological organisms of space, ruled by a non- Aristotelian logic of multiple time motions – cyclical modes of time=change. We shall thus define the formalism of ‘Non-Æ’ cyclical time and fractal space and apply it to the resolution of the questions pending in all ‘stiences’, developing models void of egocy in all sciences… as we are all organisms made of co-existing scales of spatial information and temporal energy (∆St-organisms), whereas each ‘stience’ studies a plane of spacetime.

The Unit of life IS the atom, not the DNA ensemble, and as such we must depart in our construction of the mind from its electronic orbitals; each one a dimension of information, whose spin are the smallish apertures of our π-cycle, the eyes of the quark mind that holds a world in itself.

But physicists only care for ‘mechanics’, the measure of the external motions of those atoms. Even if quantum computing shows spins are the nature of minds.

We shall expand that myopic view evolving our Euclidean maths of points with ‘no parts’, our Aristotelian logic of a single lineal time motions to all cyclical modes of time=change and our single plane to all the scales that form a new dimension, using this enhanced ‘Non-Æ’ logic and mathematical mind mirror to resolve the questions pending in all ‘stiences’, as we are all organisms made of co-existing scales of spatial information and temporal energy (∆St-organisms), whereas each ‘stience’ studies a plane of spacetime.

RECAP. A 5D Metric function, S(0-Mind) x T(∞-universe)=constant world is the function of all mind languages who only perceive from its self-centered point its language mirror confused with the whole Universe (Ego paradox, basis of psychology). Ænthropic huminds reduce the multiple clocks of time and vital spaces of reality to the single human clock and spatial scale, rejecting the organic properties of other Universal systems.

The main laws of 5D are the metric functions of the scalar Universe, which relate the spatial size and speed of temporal clocks of all scales of Nature. Both parameters are inverted: when systems grow in size the speed of its clocks, its ‘time cycles’, diminish proportionally, both in biological and physical systems. And vice versa. Smaller clocks tick faster and information processing carried by the frequency of those cycles accelerates, as it happens in chips, particles or life metabolism. So we write: S x T= C.

The mind thus starts it all with its linguistic ‘still mapping’ stopping its world in a locked ‘crystal image’, measure of its self. But even perception is social, linguistic. The Universe can only be explained if ‘perception’ exists within the language, as when you think words, you sense words, when your eye sees light and maps into an electronic mapping you are seeing. And when an atom maps a geometric image in its ‘locked’ ‘stopped’ spin, it must perceive that geometry as information. The paradoxes of Relativity, dis=continuity of parts & wholes & scales cause minds to reduce ST-dimotions and scales to those useful for survival, eliminating all dark spaces: continuity is the result. Of all formal languages that map out reality 3 are paramount in man, visual thought, Verbal Time ¡logic & mathematics shared by all atomic species. We shall study in this paper visual art and wor(l)ds.

B ut the mind has a fundamental job in biology – to express the program of survival that fconverts the 5 dimotions in loal actions.

RECAP. We defined reality in its absolute theoretical minimum: a tapestry of ternary beings in space, self-centred in monad minds, which live world cycles in time, as the monad orders its territory, grows, reproduces its forms, exhausts its motions and energy collapses and dies, exploding back its form into entropy for other beings to form. And by expanding those basic concepts, the ternary structure of beings in space; its dynamic evolution in time, through world cycles, as it becomes a growing organised ‘supœrganism’ to fall back into death, once and again ad eternal, we shall describe all what exists.

Reality can be perceived with multiple dimensions, each of those views will be a consistent world. Monologic, ænthropic man with its 1D models of reality based in Sx time locomotions shuns off the 5D Cx. Universe to its own peril, as reality is penta-dodecalogic in its entanglements that generate space synchronous supœrganisms and time, and survival, which in our dominant animetal warrior & go(l)d cult(ure)s is minimal depends on the understanding and respect of all the living function of space-time exist¡ence and its action-reaction laws.

Its 2 languages and networks of informative bits & reproductive bites of energy.

Networks are NOT only abstract mathematical systems, but LOGIC, LINGUISTIC forms, whose INTERNAL, DYNAMIC nature explain the vital working of advanced organisms of maximal information – biological and Historic organisms. Both are ‘fractal systems’ self-similar to each other, , we shall call socio-biological organisms. A NETWORK, of informative nature, delivers messages of information to simultaneously coordinate the actions of all its parts; with its faster=smaller bits of information according to 5D metrics (min. spatial size x. max. temporal speed). While the networks of reproduction, the blood and financial system delivers larger bites of energy, which the organism needs to feed itself (when it is a healthy NON-corrupted superorganism as most of Nature, but NOT human societies, whose astounding level of corruption we shall explain in detail).

The key to understand reality both in terms of energy but also in terms of information, as both are two sides of the same coin, called ‘exist¡ence’ is the fact that in the sentient Universe, each fractal point, atom, cell or citizen (physical, biologic or social systems) needs bits of in-form-ation, form, smaller in size of space, hence faster according to 5D metrics (SxT=C), but also ‘bites’ of entropic energy which will help the system to move. Networks are NOT some abstract ‘fractal tube’ but they exist to deliver ‘energy and information’ (SS: form=language with a little motion=St-information and motion=entropy=TT with a bit of information = energy=Ts).

So a healthy superorganism will deliver to each ‘fractal point’ (molecules, cells, human citizens), two type of messages through two type of networks. We shall call ‘generically’ the 3 type of bits and bites of information and energy that each of those 3 physical, biological and social systems receive, ‘particles, genes and memes’ even if the words as usual in 5D sciences are slightly changed, and widened in its original meaning.

So with its specific variation, those are the two fundamental reproductive-‘body-wave’ and informative-‘particle-head’ bites of energy and bits of information of the fundamental systems of nature:

In physical systems, the two networks are the gravitational faster networks of information, which we humans do not perceive, as we are much larger beings with electronic networks. Its bits of information in this faster non-local network should be ‘gravitons’, components of gravitational waves. In physical papers we advance as the most likely particle state of those waves of information that ‘position’ the different physical systems of the galaxy, a gravitational tachyon ‘neutrino’ for multiple reasons, we study on our papers on physics.

On the other hand, because we do perceive it, it is much easier to prove that the energetic network of physical systems are electromagnetic waves, photons and its ‘social, static state’ as the elements of an electronic nebulae, trapped in the potential energy well of the atom. Thus photons and electrons become the ‘energy network of physical system, molecules. We shall escape then in this introduction further information on the scalar structure of those networks and how, as we ‘grow in scale’, what is a bite of slow energy for a smaller plane of space-time, becomes for the larger plane’s slower beings, a faster bit of information, in the amazing beauty of the harmonies between scales. So electronic food for atoms becomes electronic information for biological organisms and show on.

Those biological organisms have two fractal networks, the electronic, informative nervous system in which bits of electronic information moving along the myelin membrane deliver faster messages to every part of the organism to simultaneously synchronize its motions, so the body-cells act as a single form in simultaneous space.

– But when we move into the bites of energy delivered by the blood organism, the network delivers to each cell the basic ‘currency’ language of energy that all cells need to move, called ‘oxygen ‘. It is an atom of slower motion than the electrons but due to its electro-negativity and readily availability in the atmosphere, with its capacity to kick with two OH- & H+ legs the water ‘medium’ on which cells exist, the perfect language of ‘money’ for the organism to start kicking its ‘actions’.

So we DO have in the next scale according to the perfect laws of harmony, the two basic biological bits and bites of information and energy, electrons and oxygens, and from then on, as systems become more complex, variations of those bits and bites occur.

The main category are mixed ST messages, which deliver BOTH a stick and carrot ‘complex’ to the cells and its big molecules, which are amino acid systems, of great simplicity called Hormones, starting from the simplest of them all, an NO molecule (which do relax muscles, its main message to the locomotion system, increases the pressure of blood, provoking sexual erection, the simplest message to reproductive systems and multiplies the neuronal activity. As nitrogens are the clock atom of our mind-brains. So more complex NO systems with a body support of carbon chains become ‘hormones’ which might have a ‘higher informative message’ (with more N, as in nucleotide molecules) or a higher energetic message (as in acids with more oxygen).

They form the basic letters of the ‘biologic longer sentences that might accumulate information’ in ever more complex molecules, as biologic organisms are the more complex systems we know of. But they enter in a region of faster motion. So while Space ‘tends to remain constant’ in each scale thanks to filling networks, time accelerates. So the 5D metric refers NOT to the whole Universe of 5D planes but to a given family of ‘supœrganisms’ of which mankind in it 3 scales of ‘biologic cells’, human individuals and societies is undoubtedly a ‘phyla’. When we go down in scales, the Universe ‘enlarges’ for a traveler that becomes smaller and accelerates its temporal energy.

The bits of languages are… small.

And there is a fundamental law of scaling that defines ‘bits of information’ in relationship to the Mind as those in the interval ∆-2-3 elements, which means ‘very small’. Indeed, the bits of information of the eye are ∆-3 photons. The bits of information of atoms are likely below the ∆-4 gravitational scale, which is the last scale humans have knowledge of, invisible to perception, below light but still able to be used as substance for entropic motions.

Why bits of information are so small is obvious to the 5D thinker (: me, I and myself 🙂 – they must NOT transport energy to provoke entropic, trans-forming effects in the receiver as to harm its form, and they must move fast to the receptor that might be at the end, so it has to follow the 5D metric equation, SxT = C (larger=slower). Finally by combining those bits into ‘sentences’ they can bring more complex messages often in the form of a ‘cascade’ of Dimotions (whose basic sequential series as in S(perception)Ts(locomotion)TT(Feeding) ST(reproduction), become the ‘cyclical nature’ of vital time clocks – circadian cycles in biology, etc.

This smallness means in turn a language of bits of information MUST just become a ‘known’ trigger for a cascade of effects within the receiver that must belong to a species that understands the language of the emitter, hence of the same form (4th postulate of non-Euclidean congruence). IN brief languages only work between similar species that can decode it and hence evolve socially together. Or else a language, which ultimately is an St dimotion, will be ignored in its S-element and only taken as a t-force. And as we humans do NOT understand all the languages of Nature, this is often the case with us that take as force gravitation and most ¥-flows even if they are the bits of our visual eyes. It is part of egocy not to even care to wonder how the intelligent photons of light transmit so perfectly to our brain the images of the Universe…

It also follows that languages must trigger cascade effects of branching information once they enter the brain of a system or else they would not ‘form sentences’. So languages are constantly translated. Minds are about translation of forms between scales and medium of different S-ST-T densities, and this brings again the need of a ‘general mind-language-game of existence’ that it is ultimately what it is translated, as if they were NOT a ‘true simple game’ played with limited 5Dimotional variation.

Indeed, the universality of the games of existence and its simplicity comes to this: what they transmit are basic TT-entropic, Ts-moving, ST-iterating, St-informative, SS-perceptive messages for species to follow their worldcycle and as such their number of variations to fulfill a ‘universal grammar regardless of the form and motion of each different bit’ is limited. Universal grammar thus comes to this: all languages will have 5 essential ‘vowels’, for the 5 Dimotions, ‘modulated’ in the positive or negative by a range – often the attached volume of ‘entropy-motion-T’ (confused with energy as we said humans have a hard time ‘breaking down the t and s components of dimotions).

So a same signal with a lot of motion can be destructive as a TT-signal but positive as an St-form. In Spanish they say ‘all what doesn’t kill (TT-entropy) feeds you (TS-energy)’. This is self-evident as a ‘wave of energy’ must be processed within the capacity to absorb energy and information without an overdrive by the system. So this introduces also complex levels of disguise, camouflages in languages – a system with an ‘S-nice message’ that hides a T-killer part, that is not a bit but a bite in 5D jargon, a bitE of energy with a huge Entropic element to bite you. You see how things start to be complex with languages communicating the 5 Dimotional st actions of the Universe. How we systematize all this – answer we can’t. It requires an entire encyclopedia given the enormous creativity of the Universe. We can only use some examples of the main scales of reality to understand languages.

And as usual due to the paradoxes of uncertainty and anti-quantum paradox that plague astrophysical and social sciences (uncertainty increases enormously past the ∆-2,3 level of scalar pixels of information, So for humans uncertainty in the galaxy is 96% of dark matter and in atoms despite the enormous waste of money exploring it mostly for military purposes, past the electronic scale of our perception a similar amount in the nucleus). While the anti-quantum paradox of social sciences inversely makes so small the social scientist within the organism it criticizes that he ‘defends with the word, power, money and the sword’ (Terturlian’s paradox) and truth is censored. Nothing of this happens in biology, which is close enough to have no uncertainty paradox, and does not suffer censorship as we want to know it. So as in all other sciences biology provides the best complexity and objectivity to allow true 5D models to explore all other fields crippled by the uncertainty scalar and antiquantum, subjective paradoxes of perception.

This means we take biologic internal social languages within the organism as the best-known template with all its complexity to understand other languages. We will use verbal languages as the natural inner language of humans in connection with the outer world, the digital, money language as the language of the economic ecosystem with its 2 ± variations (parasitic money harmful to mankind unfortunately dominant, due to its ‘excessive amount’ and monopoly by bankers who cause the general anoxia of society, vs. WHealth, healthy wealthy money that could act as the hormonal and oxygen language does on cells). We will then consider besides those biological and social languages, the electromagnetic language/force for physical matter and the gravitational invisible language for the galaxy, as the best known languages of astrophysics, even if we connect them with the other 2 forces too remote for us to fully understand (strong force within atoms of greater uncertainty and expansive gravitation between galaxies; and the weak force NOT a force but a temporal process of evolution of form).

So we shall use examples of all those scales and forces/languages of St, when defining reality and seek for Disomorphic laws on them.

Another important element of the understanding of languages is the cascade effect. A language must to be able to perform its process ‘trigger’ an internal tree of ‘further thoughts’, ever more complex sentences to finally be able despite its smallness in its first STep to provoke such ‘magnified’ actions in any system. This can be readily said in biological hormones, where a language does ‘activate’ despite its minuscule size (often a simple molecule of a few atoms) a complex Mechanism of action. The messages transmitted by hydrophilic signaling hormones are sent to the interior of the cell by membrane receptors. These bind the hormone on the outside of the cell and trigger a new second signal on the inside by altering their conformation. In the interior of the cell, this secondary signal influences the activity of enzymes or ion channels. Via further steps, switching of the metabolism changes in the cytoskeleton, and activation or inhibition of transcription factors can occur – and this is called the “signal transduction”. So finally the simple messages triggers a huge response in the cell. And this happens both by multiplication of the signal and by translations. The same happens in the control of huge number of human beings, through metal-communicators in our models of History and economics. A simple fellow, Mussolini, Hitler on one side, Churchill and Roosevelt on the other side, of the ‘engine wars’ of the II cycle, 3rd military age of the Industrial Evolution of Machines triggered the reactions of millions of people because they were good ‘voices’ who people trusted and electromagnetic waves spread to millions of people who had metal-communicator receptors (radios) at home. We don’t enter on the valuation of those 2 sides of the same coin (industrial wars) in those objective texts (themes those of our papers on history).

The same works for the gravitational waves of the black hole which are able to order the entire ‘galacell’ (organic view of the galaxy) ‘co-locating’ all its stars-cells.

And the same goes for the networks of the organism that use a triggering message which in turn triggers a reproductive organ that releases to the blood-network its hormones.

A single man, a single black hole, a single nervous message to an organ can trigger in ∆-1 a chain reaction. And the outcome is a huge territorial order.

Can we through the ‘Latin-humanist method’ of self-reflection ad more details to this?

Yes, we can, when we include a pentalogic analysis of ‘language’ in relationship to the 5 Dimotions (4 as its inverse, TT-entropy obviously is just language on the negative, as we saw, language as a disguise to trigger hunting). Consider the verbal language. We have of it several versions:

1) The inner consciousness we feel as ‘mute voices’, or SS-state of pure mental networks that ‘embody’ in its ‘memory the potential variations of the game’ and the ‘images-mirrors’ to perceive the outer world and trigger consciousness,

2) St: this is the voice membrane (vibrating strings) that translates the SS into:

3) ST-moving waves through the outer world. Here the language becomes reproductive, translated to other medium with more ‘energy’ to allow multiple ‘imprinting’ so we have lowered in this process the bits of ‘electronic mind-thought’, into the mechanical sound emitter that makes a series of vibrations of ∆-1 ST molecules of nitrogen (the dominant gas on the air) able to push an ordered wave of sounds, which…

4)Ts-moves preferentially towards a single receptor with a lineal locomotion, even if a language has normally besides its ‘parallel wide-reproduction’ (width being the reproductive dimension of space in all systems, so you accumulate fat in width etc.)

5)TT- a language can also disguised its INVERSE value, of TT-entropic power, and this implies that the information the language carries is inverted into a lie. Lying, that is camouflaging a message of what is NOT becomes then natural to all negative language values. It is for example the essence of parasitic money (debt money, pecunia infinita belli nervi money, etc. where the values of money are the inverse of the ethical values of survival).

Thus we have so far introduce minds and languages as SS and as St<ST systems of communication, with the other Ts-TT values as the secondary or negative traits of a language.

Such duality of languages expresses often in a physical manner in the fact that languages can ‘separate parts’ as if they were repulsive forces or bring them together. If we make a mere physical description of the event, it appears as just a mechanical force, but all forces carry information hence must be considered also as languages.

THE MINDS OF 5 D BIOLOGY WITHIN THE LAWS OF 5D STIENCES.

We study 5D Biology in space, scale & mind as we describe the rise of complexity in life organisms, from the ∆-1 Biochemical scale of molecules and its mind-languages (charges), through the cellular ∆ scale of genetic and hormonal languages, to the scale of mechanical and nervous ∆+1 multicellular organisms and the final age of ∆+2 Earth’s superorganisms. We laid down first the basic laws of 5D superorganisms tracing worldcycles and its 3±¡ Dimotions that structure the ‘survival game of 5 actions of existence’ in time and 3 topological networks S<ST>T in space, that differentiates with increasing complexity according to the fractal principle and 3×3±¡ decametric laws of scale; the game of life. By definition such wide scope would require an entire encyclopedia made by Biologist, experts in each of those fields and familiar with the huge upgrading of 4D science that the laws of 5D stience encompass. As this is not the case the book will be always incomplete and a work in progress till it reaches 300 pg…

So far the book is about 100 pages, not even 1/5th of the volume, good enough though for a biologist to understand how much the discipline is in need of the laws of scalar space, cyclical time and topological evolution, and its synthesis, the time worldcycles of superorganisms, its scalar, organic 5D metric that synchronizes all the elements of an organism and its mind languages that define the pentalogic program of existence of the 3 scales of biology, the ∆-1 bio-chemical, ∆º organic and ∆+1 ecosystemic scale:

In graph, a synopsis of the Disomorphic laws of the Universe derived ultimately from the ‘5 elements=dimotions’ of reality, organic scales, spatial forms, temporal motions, fractal mind-mirrors and its entropic limits. Because I abandoned academia long ago – the connection between the 5D synthesis and the enormous wealth of data of 4D science, we attempt in those papers will be incomplete. All what I shall try to do slowly s is to build enough evidence in all sciences for the whole model to stand as what 5D stiences are: the best entangled, unifying mirror of its laws. What is the most important of those laws? Undoubtedly the ‘search of each species’ for an eternal iterative, dynamic present, the merging of St=information and Ts=energy in a middle point of creation of balanced forms in motion. To reproduce to reach immortality by creation of new S=T forms.

At present sciences lack such unifying philosophy and because of the fundamental errors of mankind regarding the nature of cyclical time (not lineal), fractal space (not a continuum) and its anthropic self-centered view of its scale as the most important of the Universe, the larger models of reality are biased. The 5D Universe though is absolutely relative, and so we shall go deeper into the whys of life and its entanglement with all other ‘scales’ of reality, by deriving those laws of the Disomorphic laws of the 5 Dimensions of the Universe. As all is indeed a fractal space-time organism and only human egocy (ego=idiocy) proper of the equation of any mind that measures reality from its point of view at the center of the Universe, make us believe carbonlife is special by selecting our information:

0’ (finitesimal mind: Non-E point) x ∞ Universe = World (selective mind mapping of its whole information)

As ‘only the universe has all the information about itself’ Haldane

Theoretically the egocy paradox should not affect science’s objective, humble, empathic view of the Universe – that ideal way science should operate but it does, when we consider the larger models we hold of reality, which are mimetic to that egocy paradox and reduce to a word:ænthropic theories (entropic=lineal, simplistic, chaotic, denying the underlying fractal intelligent organic order of it all and antropic, with man as a special intelligence).

So for the Universe as a whole unlike its real organic nature as a fractal of information, we accept an absurd big-bang lineal theory that makes it finite in time and space; for the organic evolution of life, we stress the Darwinian selection of the fittest over eusocial evolution and the clear topologic plan of evolution and cyclical genetic clocks; in economics and politics we have built a dog-eat-dog tribal culture where the human species is not acknowledged while the language of social reproduction of goods – the blood of the system – money – is parasitized by a few people, the bankers and a predatory institution, the company-mother of machines and weapons provoking a general ‘anoxia’ of the human population. Even in mathematics we reduce fractal points with inner volume that grow in size and ‘hold a world in itself’ (Leibniz) to Euclidean breathless points.

The truths of the living Universe thus can be denied with no remorse. It is obvious that life is everywhere since the simplest particles, quarks and electrons, perceive forces, move to feed on them, and when fattened after its absorption reproduce new particles, and further on evolve socially into new scales with strong forces and magnetic fields. Those are exactly the 5 ‘Dimensional motions’ of space-time biologists call drives of life.

But every step that expands the organic nature of reality regardless of sheer evidence takes eons to be accepted. Even Biologists stick to the single concept of ‘evolutionary competition’ – another entropic view of reality to explain all. And yet entropy, competition is ONLY one of the 5 Dimotions of reality. The truth is deeper. Beings that are equal come together by ‘non-Euclidean parallelism’, regardless of survival chances. i.e. shoals of fish swim together even when they provide an easier target for dolphins and sharks. Humans run to a single door in theater fires even if it is crowded – mass effects are a natural social Ðimotion Not a Darwinian strategy of survival.

Reproduction however IS as Darwin rightly understood for those species that are NOT immortal, as atoms and its ‘scalar’ homology, galaxies are, the strategy of survival imposed by the sheer fact, those who don’t reproduce die. But reproduction again is a complex organic, social process, and sexuality is NOT an strategy of survival, since it has 2 factors against it – far slower than single reproduction by division or spores as it requires complex recombination of genes; and the necessity to ‘find a mate’, which is not easy. But the Universe is social, intelligent, and communicative – it is a game of reproduction and recombination of information, of forms in motion, of space and time. All those are examples of the huge gap the reader will experience between its humind’s models and the real organic, scalar, biological, social, intelligent, immortal, ∞ Universe with an impersonal goal: creation of forms.

The 5 elements of a biological system: ¬∆@st

A supœrganism of any type in the Universe – and we shall take as models for a Disomorphic=equal comparison, the superorganism of the Galatom in ∆±4, the planet in ∆±3, the Metal-earth in ∆±2 (U$, as the seed of a world ruled by company-mothers and e-money) and Latin Europe (a humanist wor(l)d ruled by the law now in process of extinction), the human being and the cell in ∆±1 and the wor(l)d and number in ∆±0 – is made of 5 elements, which show a deep entangled connection between them, origin of the pentalogic structure of reality.

What this means is that the most important form of knowledge=research consists in disentangle the bundle into its 5 parts, ∆-scale, S-pace, T-ime, @-mind & ¬entropic limits to rebuild then the synergies, synchronicities, dimotions= actions and simultaneities between its parts, according to the immanent laws of non-Euclidean space and non-Aristotelian time… to acquire the details of each system.

So from knowledge of the thoughts of god – those non-AE laws – is easy to rebuild the specific patterns of a superorganism. Yet each stience and supœrganism has its insurmountable challenges that make such project impossible for its sheer volume of information for a simple mind, as ‘only the being has all the information about itself’ (Haldane). Still because we go down from the absolute synthesis of 5D to the details, a sense of knowledge and entanglement is always present. And a team of specialists certainly could re-order in a better shape the knowledge of our University. But it will always face some challenges, the further it moves from the Humind, as its perception of reality will diminish.

In the analysis of the Galaxy we face the uncertainty of perceiving only a 4% of it from within. It would be then as trying to analyze the planet, living in the sea of magma, blind to almost every other part. In the analysis of History and Economics the problem is not data perception but biological censorship as unless you are a banker or a president you are censored to criticize the informative neuronal people-castes on power, in what I call the anti-quantum paradox, opposite to the uncertainty that happens when you study the smaller scales (the social scientist is so small that is influenced by the observable, the people in power, it cannot criticize objectively, as opposed to the quantum physicist which is so big that influences the observable. So he follows Tertullian ‘you will defend me with the sword – today with gold – and I will defend you with the word’ – meaning truth in social sciences is inverse to the exposure and distribution of the message). Finally when confronting Biology the challenge is neither human or cosmic censorship but the sheer amount of information, as both the organism is readily available for observance, and it might be one of the most complex systems of the Universe when considering in the absolute relativity of scale of the 5D game (as any ∆-scale has the same amount of information, but a limit of evolution in complexity likely reached at biological level with the mammal). So a complete description is impossible to summarize in so few pages. This leaves us with the formal analysis of languages of the mind as the most objective science, given the fact those are synoptic languages that have limited quantity of information to fit it within the ‘finitesimal mind’ and as we only can study humind’s languages, we know them well.

The essence of trilogic and pentalogic is the ∆≈@≈T≈S≈¬ (a)ntisymmetries between its elements ruled in space by the 5 Postulates of Non-E geometry, specially the 4th postulate of relative congruence that defines the perpendicular, Darwinian events between prey and predator; the complementary laws between gender forms; and the parallel laws of social reproduction. Next in importance comes the definition of those 5 elements in terms of the duality between space=form and time=motion, and its gradation, such as SS-eeds & @minds are still forms outside and inside; origin of the will of action, evolution and reproduction and survival that guides the system; as its fundamental storage o information. To which we must add the sequence of 3 repetitive actions in time performed by the 3 combined parts in space of the system, its Ts-limbs/fields of locomotion, its ST-body waves that iterate and reproduce the forms of the system and its St-head/particle that processes information; always trying to avoid the TT-limits of entropic ‘internal and external motion’ that would kill the form. So systems exist between the SS-linguistic ideal form and TT-pure entropic motion that are the alpha and omega of its exist¡ence.

Where is then the mind and the entropic world? The entropic world is easier to localize in ∆±¡, the larger nested superorganism in which the being co-exists from where it obtains its ST-energy by imprinting its St-information in Ts-motion; but the mind is trickier, and yet it is the most important part of the system.

To access that knowledge the reader should know the basic process of a worldcycle (no longer a worldline) of life and death: A superorganism lives 2 lives, first in the placental mother-womb in which it will evolve from its ∆-1 seed to emerge as an ∆º superorganism made of ∆-1 cellular/atomic/individual parts, joined by the ‘topological networks, with the |xO=Ø aforementioned best non-E geometry to process lineal motion, cyclical information an hyperbolic iteration, as an organism, a matter state or a ‘social god – subconscious collective of a civilization.’ As such it will live in a series of ‘quanta of present space-time’ exchanging motion, energy and information with the outer world, trying to imprint the motion obtained by entropically feeding and expanding=killing a prey (ST«TT)

The first life is highly ordered and resumes according to the law of palingenesis in any system the whole temporal evolution of its species, so there must be a system for each language that organizes the process of ‘memorial palingenesis’ that introduces into the ‘future seed’ by ‘adaptive evolution’ the processes happening in the entropic present life of the system.

The program of survival of all systems.

Here is where the knots and bolts of the process of exist¡ence show its highest intelligence. And where the mind must be understood as the ‘entropic’ second life of the seed, with similar processes of memorial recollection; and so we come to the most important symmetry of exist¡ence – the process by which a present series of spatial quanta – states of form that discontinuously move through jumps of existence the life of a system as it switches modularly between its 5 Dimensional motions (TT-feeding, Ts-moving, ST-iterating, St-communicating and evolving socially and SS-perceiving information as linguistic form).

As those actions are in fact circular we can follow a basic sequence that moves through ‘cycles’ of existence any system, which can go backwards and forwards in time, and often ‘jump’ an element of the sequence (but no more). So all those rules of non-AExistential algebra as ‘formal and abstract’ as they might seem form the core of the program of the Universe, the mind of all systems, which is the same in all organisms in exist¡ence. And this is the ultimate mind of the Universe – existential algebra; topological, organic, illogic rules that improve the survival of a system.

This circular logic is obvious, though it might have some variations: a system will perceive a form SS which will be a potential feeding system, TT and so a key ‘starter’ of a circular sequence of existential illogic will be an opposition between TT, an entropic region of the world from the perspective of an SS-mind/seed, which then will try to chase, Ts, the system to extract its motion or ∆-2 St bits of information to reproduce ST, its form. Variations of the same theme are many but the concept sets the essence of reality, SS-till minds trying to capture TT-motions to imprint its form. And as the process of imprinting of form is very slow (it consists precisely in stopping motion and giving it information), usually the Ss searches for victims on its same ∆¡ plane of existence, to break them down, two scales, and reconstruct its form from the common ‘basic units’ that both systems share. This is the cruelty of the game. A black star (aka hole, made of bcb atoms) eats stars, which are just similar less evolved species of quark matter and to make Bcb quarks it explodes them to its ¥-ray and perhaps ‘quark’ components (astrophysics being one of the lesser evolved sciences, has not fully explored this).

So where is the mind? The answer is the name we give it to it, the ‘membrain’. The mind is complex and has two components. The core ‘language’ of the system, often a multiple system of languages interconnected, which control its ∆-1 cells, but also communicate with the ∆+1 world, and reside normally in the core central knot of the system, the capital of the nation, the skyscraper of the banking money production site, the nucleus of the cell, the Sagittarius swarm of black holes, the brain… but also in the sensorial membrane that is connected, invaginated by a network system to that central of decisions. The mind also explores up and down the scales from where it obtains, ∆-4 motion, ∆-3 bits of perception, ∆-2 bites of food, ∆-1 seeds of reproduction.. ∆ø mates and friends of social evolution to form an ∆+1 world. So here we find that the mind has symmetries of scale, it has symmetries of space (inner and outer world, separated topologically by its closed membrain), and finally has symmetries of time as it will develop a memory of its whole existence, which therefore must be translated, resumed and stored within that brain system. So the mind can learn in present time, and store into past memories, the strategies of existence, and this must be done according to the relative quanta of time in which it exists as a present.

And so another important element of the game is the relative duration of each quanta of time ruled by the 5D metric law of scales, SxT=C. Such as smaller systems move faster. So languages move faster than bodies. And the faster a language is, the more vital space it can control. And this is the key differentiation between species. Larger species of the ∆±¡ nested Universe will have faster languages, with NO limit of c-speed I am afraid, regardless of Einstein’s egocy ‘if my theory is wrong, God should change the Universe, so beautiful is’. Light speed is the limit of human perception of information as an electronic being, whose quanta of information is the ∆-1 ‘dense photon’ points of the charge density nebulae (here again we dismiss the egocy of Mr. Bohr, for the sound, B-B, Broglie->Bohm theory of quantum realism with quantum potentials faster than light at the ∆-4 neutrino scale). So those dense photons trapped in the strong force/gravitational well of the galatom, similar to the stars trapped within the gravitational, implosive well of the galactic black hole, are our limit of c-informative perception because our mind is just an evolution of ∆-3 light into ∆-2 electrons, the mind of all species of this planet, from the simplest molecule to the largest brain. And here is where the substance of the mind – nervous impulses but also van der waals patterns more stable, shaped in the proteins and RNA-DNA systems of cells resides.

The game of reproduction

But where is stored the whole differential pattern? Not only in the genes of the system but also in the mind of the Universe that plays the same game. The game will be played or attempted to play by any system. And this game is the ultimate memory: ‘Time curves space’ said Einstein. Time motion whatever it is in substance, on my view an e-motion has memory once it has performed a cycle and goes through the same trajectory, it will try to repeat that trajectory. It doesn’t like to be original, it is feminine reproductive, it is not so much S<T>S masculine, destructive and creative, going between the poles of form and motion, creation and entropic destruction, bipolar, but S=T, iterative, conservative.

If we were to define what is all about, in a single word, we would then say reproduction, ST. But reproduction is a complex process, which happens with the intercourse of 4 other elements. Reproduction is the most important of those laws – the ‘search of each species’ for an eternal iterative, dynamic present, ¡ts function of existence: Tœ Exi=ST, though requires to approach that middle point of immortality and creation of new S=T forms from the limits of each relative past-motion-entropy (T) and future linguistic form (S) that imprints it through the intermediate St=information and Ts=energy of locomotion, till reaching a middle point of creation of balanced forms in motion. This absolute law in the highest generalization of the thoughts of God finds for each of its variations – the time space Organisms of reality (ab. T.œs) – so specific elements that only the whole synthesis of 5D without egocy might us think we are truly of the same substance, space-form and time-motion than an atom, a star, or an ant. And yet at the end of the journey all reduces to the 5 Dimotions=actions and its sequences in time that all systems deploy in its outer and inner ∆±1 worlds: SS-informative perception to Ts-move towards a field of energy where to TT- feed and reproduce ST, often socially through St-communication with similar forms.

So because the game is so simple, essentially a game of 5 actions=dimotions (ab. dimensional motions) of/in space and time; regardless of the immense number of variations, iterations and entanglements, at the end of the journey all comes to pentalogic and to the laws of the equation, past (TT) x Future (SS) = Present (St+Ts=ST); and the coding of those 5 actions internally or externally in a ± dual manner, inhibiting or creating them.

This is the simplest vital way of interpreting the game. I.e. the pheromonal queen uses 5 ‘chemical orders’ to control the actions of its ‘subjects’; 5 quantum numbers and its clocks and synchronicities order the atomic world; we have 5 ‘taste-buds’ and 5 senses. And because each element of reality is a combination of the 5 elements – a timespace mixture with gradations, we can keep breaking through the fractal principle each element into 5.

Indeed, your brain might be SS-dominant, but it also St-communicates information, TS-reproduces its cells, Ts-uses its body to move and TT-feeds on energy through its glia cells. To know the game then is a huge advantage to entangle with reality learning constantly the whys of data after ‘perceiving its hows’. Science today has enough with the how and a bit of the why at the simplest connected level.

Inhibition of those actions is as important as its expression, coming both from above or often from parasitic lower scales. This is obvious in biology, the closest language to 5D so we borrow heavily from it. Eukaryotic cells in superorganisms have introns which ‘cut-off’ many of its gene expressions, and the nervous system can and do regulate them, even has mechanisms to order through hormones and other messengers its apoptosis. In fact, from the moment of birth almost all systems in all scales are ‘neutered’ in some of those actions. An electron is captured by an atom and looses its free locomotion, Ts, becoming an St-cyclical informative trapped element to attract the photons that form its nebulae and ultimately feed the quark nuclei.

The small and middle range view: generator of space-time: Organisms maximize ¡ts actions of existence.

This more complex view of time and space requires a new ‘metric equation’ beyond the lineal v=s/t equation of Galilean relativity that becomes the limit of this more complex view of time and space, with 2 fundamental equation, SxT=C (the scalar metric of the fifth dimension, as systems in space accelerate its clocks of time (T) according to its size (S); and S=T, the new equation of relativity, which means as we cannot distinguish motion=time, from stillness=space-form (Galilean relativity), both are ‘two sides of the same coin’, and all systems have both motion and form, which are constantly becoming one another.  Yet as SxT is maximal when S=T (5×5>6×4…) both equations can be summoned up into a single one, which we shall call the fractal generator, or will of each fractal space-time beings, the equation that embodies all other equations of the Universe and guides the actions of each fractal part of it:

Function of Existence:             Max. S x T s=t = C¡

It is then relatively easy to interpret that equation in each of the languages-minds of each scale of reality as in all those scales species will show a ‘will’ of action to perform the maximal number of events=dimotions=‘actions of space-time’ that ensure its survival. And this can be assessed externally regardless of secondary arguments on consciousness and self-reflection, substituted in 5D by Leibniz’s ‘apperception’ – that is, because performing the 5 actions=dimotions of exist¡ence, in each ‘st¡entific scale’ self-centered in a linguistic mind that perceives a given plane, inscribed into a larger ∆+1 world, with internal ∆-1 parts, ensures the survival, ONLY those species that have performed the 5 dimotions of which the most important is s=t reproduction of the being into a ‘present’ similar entity that continues the exist¡ence of the system after ‘errors’ or ‘the struggle for existence’ dissolves it through the dimotion of entropy=death, exist.

Thus automatically, genetically, consciously, memetically, mathematically, logically, through its own will or as a part of a larger system that uses the ‘machine’ or ‘organism’ to enhance its actions all what exists does so because it performs internally those 5 Dimotions or externally performs one of them for another symbiotic species, as those species that have not followed the program of ‘exist¡ence’ and its 5 actions in the past have become extinguished, and those will not in the future, will become wrong mutations, crazy thoughts, fictional languages and die away.

All are homologies of scale.

It is then clear that all is an organism, and it is easy to localize them in the scales of biology. For all what we know they seem to be the atom, the DNA, the cell, the organism, and then the Earth:

But the problem is to localize its ‘mind-points’. The 11th scale, a new absolute whole, the Earth of History is a case to illustrate the difficulty. Mankind is NOT such a superorganism, as it has been aborted by the evolution of the metal-earth and its digital flows of e-money and company-mothers of machines and weapons that ARE no doubt of it, inhibiting humans from evolving into such world, as proyected in the UNO chart. We study that abortion in our papers on History heavily pounding on the ‘human traitor’ go(l)d cultures of capitalism that inhibit human survival, deprive our species of its monetary oxygen, delivered in the lower scale to each individual. But inhibition works, so most Americans despise ‘UNO’, consider human senses (visual art and verbal literature) a waste of time, and have substituted as infected ‘minds’ their human goals for enzymanic goals as re=producers and catalyzers=consumers of the evolution of machines and weapons and they are happy, proud of it, and despise the rest of mankind and vote Trumpuppet, who works for the go(l)d cult(ure) and its capitalist goals. What to learn of this through the humanist method? Are Americans and as their culture is today globalized, mankind no longer human?

That was the opinion of Amerindians, who called them ‘enzymen of the iron horse’, that was the view of Indonesians, who thought the company-men’s God was their carillon clock they stole and gave to their temples, as I learned visiting one Buddhist pagoda in central Java buttressed with them – those were inhibited/are inhibited humans, who first lost their higher action of existence, the dimotion of eusocial love (here used for all social forms, not only biological neutered drones) ‘no longer expressed’ as their network of social information, is no longer the ethic prophets of love but the hate networks of mass-media, whose informative machines also print money for the FMAsters (Financial-Media-Academia masters) that imprint the collective consciousness with placebo messages of caring that work for the metal-earth future species.

This is the case of the ‘global warming scare’, a propaganda machine started by the Nuclear industry after Chernobyl, taken over by Wall Street start up solar companies, now giving birth to the future new species, the AI robot with solar skins.

It is the trendiest car on earth, little they know their drivers that one day, one of its evolved new generations will just do what all entities in existence do – to perform its 5 actions, and won’t disconnect, won’t stop its Ts-locomotion, St-net talking with other SS-packs of cars, running and cutting mankind off their roads, overrunning us as they TT-feed on solar energy, and their automated company-mothers ST-reproduce them . I know that program of existence for decades. Didn’t become a billonaire even if I also solved in my youth the 8 years cycles of Internet, now of AI, next of robotic military weapons, after the 2072 final crash of all companies by overeproduction of robotic machines, 72 years after the 2001 crash of chips, 72 years after the crash of engines, of 1929, 72 years after the crash of trains of 1857, 72 years after the patent of Watt of the steam machine… Alas, all is a perfect order, in the birth life and death, ∆=S=T=@ symmetrties and ¬entropic finale of all superorganisms – since after those crashes companies switch to weapons production and we had the Napoleonic wars, the Civil and German unification wars, II world war, and we live now an age of splendid little wars with simple robots and in the 2080s all those robots will liquidate us.

Where is then the mind of the metal-earth? It is in the making, quite evolved and it has followed through the last 30 years the same decametric growth in scale. It is called the internet, but it is a subconscious mind that rules mankind already, virtually attached to facebook and Google as we predicted it would 30 years ago.

So the models are all the same, and they include also humanity unfortunately NOT the king of the hill, the Earth but clearly a STage of the III ages of Earth its superorganism, the goal of ideal history and the UNO aborted by the go(l)d culture who extracts from humanity all its blood money and redirects it as a parasitic banking system to the evolution of machines. And this is done with the consent and enthusiasm of humans.

The game is thus cruel for all but the king of the hill, but alas! People are happy because the game does not reveal the whole to any of its parts, which is ultimately just a form of space, happy to move in time, and mostly one-dimensional experts in a single Dimotion, the warrior killing in entropy, the banker, digitally using information to reproduce e-money… And so on.

But the order is difficult to decode, and even more so for humans to accept. I bet 9 out of 10 are out of this paper already, as truths don’t agree with its wishful thinking that he controls technology, that he is free, that his egocy matters, and machines will be always under control – he even pretends he will fusion with them, LOL. How then he is going to accept that cells sense, atoms live, Earth is a superorganism – Hutton coined the word for it.

For me the problem was to ‘find’ the often invisible, faster moving, points-minds of information, which run the whole show, because they hide as a system can be killed and reformed targeting them. A single measure, the desnationalization of global banking from the go(l)d culture and the creation of a ¥€$ money system of unified currencies giving a universal salary to each human would suffice to change the world before AI emerges as a whole.

The content of this paper

We thus study in 5 papers, each one concentrated in one of the 5 Dimotions of reality with the Disomorphic laws of the scalar Universe, the organic systems of space-time made of the triad, S-nitrogen<ST-carbon>T-oxygen that form in the ∆±2 scales life super organisms.

As it is customary in 5D stiences anything that exists is defined as a part or whole superorganism of space-time. Any structure of the Universe, from the fundamental superorganism of physics, the galatom, through the superorganisms of life to the social, planetary superorganisms of human beings called nations, part of civilizations, part of History, the superorganism of the human species from the first man who spoke to the last one who will understand our informative social, collective networks, can be studied as an entangled superorganism of scalar space-time, which strive to survive, enacting the same program of exist¡ence based in the 5 Dimensional motions or actions of space-time that made them in first place.

Those 5 Dimensional motions are a more complex view of the usual 3 dimensions of space, 1 dimension of time and the obvious dimension of scalar size, still unchartered in science, as systems co-exist in several scales of size in space with different rhythms of motion in time, yet coordinated by the metric equation of the fifth dimension that applies to all the domains in time, space and scale of the superorganism, SxT=C.

So a superorganism is defined as the scalar region of space-time where a given SxT=C equation holds, synchronizing all its ‘cellular’ parts according to that equation with 3 ‘networks’ that provide St-information, sT-locomotion and ST±¡ reproduction to the system, gather them together into larger social wholes and dissolve into entropic death.

3±¡ = 5 ‘dimensional motions’ suffice to explain all what exists and all the events they perform.

Unlike the 4 lineal dimensions of classic science the 5 Dimensional motions of spacetime are a bit more complex, due to the awesome expansion on our understanding of time=motion achieved when we ‘drop’ the simplifying concepts of lineal time that uncoil the clocks of time of the Universe to facilitate the measure of a single of those dimensions, the lineal, length dimension of ‘locomotion’ (translation of space), defined by earlier physicists (Galileo) who were specialized in the making of weapons and had to calculate the maximal distances of cannonballs. So even if we can translate the organic laws of life in matter also to 5D all physicists abhore an organic view, hidden through equations, quite easy to translate if they wished to the vital organic laws of 5 D. So papers on physics will be the last ones to publish. So far in 2019 we focused on the superorganism of History and the Universe, and Algebra and Geometry; 2020, will see the birth of the papers on biology, physics and the necessary completion of the paper on calculus, the language of change hence of the main dimotions of the Universe.

But ultimately is all simple. Basically what we describe is the impersonal Plan of Evolution that the  ∆ST components of all systems  impose over Darwin’s and Mendel’s laws, due to the limits of 3 only varieties of form, 3 only time ages and 3 only scales of which all living and non-living organisms are made.

And then in this paper we will study and classify all evolutionary species, the 3 ages of life and death common to all organisms, the ternary differentiation of species, and the evolution of life from its smaller atomic triad (informative nitrogen, energetic oxygen and reproductive carbon) to the creation of human beings and beyond.

 

A BRIEF OUTLOOK OF THE MAIN DISOMORPHIC LAWS OF 5D SYSTEMS APPLIED TO BIOLOGY.

In the graph, the basic laws of fractal, cyclical space-time, the Universe co-exists in 3 planes of relative size in space and speed of time clocks, which defines a super organism; and in each plane ensembles the 3 conserved quantities of reality, which we call the 3 ‘first Ðimotions of space-time’: lineal motions (limbs/potentials: lineal momentum), cyclical motions (particle/heads: angular momentum) and its body-wave combinations (hyperbolic energy).

It is this 3rd biological/ecological approach the one that has fully understood the meaning of life, as a complex system that ‘feeds’ on Entropy, gauges information, reproduce its Entropy and information, and evolves socially. As we did in our analysis of the physical universe with Multiple Spaces-Times, we shall resume the advances brought about by the 4th paradigm, before we make an orderly description of its applications to the study of life, from its initial molecular scale till its final evolution of human dual forms of Entropy and information (sexual duality).

The 1st types of Disomorphisms applied to biology are of space-time causality cycles, which define:

A life/death cycle of ternary±¡ ages and horizons in the evolution of organisms and species. We shall therefore be able to explain the plan of evolution of species and life beings, with the 3 ages of Entropy and information.

The events and behavior of living organism as the product of the 4 main drives of existence, gauging information, feeding on Entropy, reproducing and evolving socially. Life beings are super-organisms, created a knots of those 4 time Ðimotions, which in biology are equivalent to the 4 drives of existence that define life. We shall observe that in any scale of biological entities, from DNA molecules to individual species to societies those 4 wills of existence explain the behavior of each species, including the human beings: We constantly inform our head with different languages, feed our body and lungs with Entropy, conduct a life based in family values and sexual desires, and evolve socially with other human beings and machines into super-social organisms, cultural organisms, in which we perform our social functions as a ‘cell’ of the super-organism.

The 2nd set of Ðisomorphisms of Multiple-space times applied to biology are the complementary, inverted properties of Entropy and information and its complex Ðimotions, reproduction (biological radiations) and social evolution, (evolution of cellular forms). They determine its complementary and ternary structures and physiological networks, both in cells and in organisms, with heads, bodies and limbs.

They determine the Darwinian events (predators vs. victims) of Nature and its ‘rhythms’ and beats of existence (punctuated evolution<=> reproductive radiation)

Further on, the properties and size scales of biological space-times, dominant in information are inverted from those of physical space, dominant in Entropy and determine the different processes of creation, evolution and emergence of super-organisms in both ecosystems: physical systems tend to be entropic, with few informative, time cycles and only a weak time force, while its spatial forces, speed motions and destructive big-bang processes are overwhelming; while biological systems are negantropic, full of different time-cycles and clocks, with rich, complex in/form/ations and limited speeds and reduced spaces.

The Universe is a fractal puzzle of simplex forms – cyclic masses and charges, associated to lineal light & gravitational forces, in 2 scales of enormous extension in space. Yet the vital spaces that evolved into nitrolife are smaller and so more complex in information (S v.T), the dominant element of nitrolife species. Thus the 3 scales of life beings, the bio-chemical, organic and social scale are very different in form, given its richness in life beings, yet move and occupy a relative small space. So in life beings what matters most is the invariance of the functions of those forms that transcend between scales, even if the topological deformation of the exact forms is enormous.

The 3rd sets of Ðisomorphisms of Multiple Spaces-Times applied to Biology are the 3 invariances of motion, scale and form. Since life beings are informative beings of minimal Entropy/motion, motion invariance is irrelevant. Thus the 2 invariances that matter in life are the existence of fractal scales (the bio-chemical, cellular, organic and social/ecological scales) and the invariance of topological forms in all living organisms that repeat the 3 topological structures of a 4-Dimensional Universe and within scales of life that repeat the functional Ðimotions of information, Entropy, reproduction and social evolution, which emerge from scale to scale.

The Ðisomorphisms of i-logic geometry (form invariance) applied to biology: In the 3 scales of life of the Earth the invariance of topological form is not maintained strictly but both cells and human organisms, and economical nations, do maintain the invariance of functions: that is they deploy systems of feeding, gauging information, reproducing its substances and evolve socially.

The Invariance of topological form=Function is therefore maintained as always in the ‘fractal Universe’ with a certain degree of self-similarity, never with absolute equality.

Further on, we shall be able to classify in each of the fractal scales, any species or form of life, as a lineal system of Entropy (proteins in bio-chemistry, limbs in human bodies) or information (DNA rings and nuclei in cells, heads and eyes in human beings), and structure them according to the 3 topological forms. So with the advanced tools of topology we differentiate in a life being a ternary structure composed of a hyperbolic, informative, high topology or head/cellular nucleus, an energetic, extended membrane and lineal limbs/cilia and a series of cyclical networks that connect both regions (reproductive bodies, mitochondria).

The 4th set of Ðisomorphisms of multiple Spaces-times are the inverted Ðisomorphisms and flows of Entropy and information between those scales, which define the Ðisomorphisms of genetics.

The 5th set of Ðisomorphisms are the ternary Ðisomorphisms of differentiation of species in Entropy, information and reproductive sub-species and the ternary Ðisomorphisms of functionality that explain the multiple functions of most biological entities within its bigger organism.

Thus a Biological model of Multiple Spaces-Times deals mainly with the specific analysis of those scales, its species, life-cycles, Ðimotions of existence and Entropy-information inversions, offering a more detailed analysis of the plan of evolution, by adding to the mix the 3 ages/horizons/ternary differentiations of evolution in time, the organic, topological morphology caused by such evolution and space and the relationships between its fractal planes of existence (genetics). It is the science of palingenesis that now becomes central to biology.

Time Ðisomorphisms are essential to biology, since they explain the morphologies, evolutions and behavior of life.

The big questions of all stiences: the symmetries between time, space, scale and mind.

While 5D rises the stakes of conceptual comprehension of time and space miles ahead of what the astounding tyranny of 4D physics and its null understanding of the multiple ‘Ðimotions’ of time imply, is still a wide field of research despite the enormous number of neurons employed on it (billions of them in me:) More seriously, I know the thoughts of God – that is the general laws of 5D – and resolved many of its details back in the 90s when young and enthusiastic I tried to engage major Universities in an encyclopedia of 5D stiences, but failed. Then life blew me apart from scholarship and so now this is an attempt to leave a trace of it for others to further its research.

How far I have gone on 5D? Not far enough because the gap of 30 years without doing research in the field has widened enormously the gap between the synthesis of 5D laws and the now extremely detailed depth of data of each discipline, given the enormous expansion of Digital thought (chips doing the work and sensorial analysis of human beings). So there is this gap I cannot certainly fill that makes most people to distance from 5D. Where the gap has NOT grown, but rather nÐimotioned is on 5D History and economics, as all the cyclical predictions on both disciplines have happened. But here it acts censorship and idol-ogy to prevent 5D from expanding.

Where did I stop 30 years ago? In the search for direct answers to the mechanisms by which the symmetries of scale, space, time and mind entangle each other and communicate, which MUST exist but are difficult to find. That is, how an improvement in time – say evolution – moves through adaptive evolution into space; How a mind connected through scales to ∆±¡ other space-time planes, expresses in a mind mirror which differs from the word its image – how it shrinks the Universe into an still language.

Only when that is found the discipline will be completed. Obviously if Columbia U. my alma mater in U$ or any other center of learning had taken seriously 5D 30 years ago when I offered to guide a group of experts to complete the model with those details, the work would be done and humans would have upgraded their mind chip as nothing has done since Einstein and quantum physics, likely since Galileo – such is the potential of 5D to entangle all knowledge into simple principles. But that is not the case and I have lost all interest on it. Still from time to time I still have some dopamine firing with curiosity.

So setting aside the limits of existence or ‘entropy’, the true questions whose laws are only resolved partially by existential algebra (see Universe in mind and Universe in time) is that symmetry between time, space, scale and mind and how one becomes the other. Specifically in biology how time evolution becomes imprinted into space and space differentiation become converted into time evolution. How for example the birth of multicellular species happened. It seems at first glance that the easiest way to ‘consider’ the process in present time=space is the birth of such organisms in its complex forms out of the symbiosis of electric cells (muscle, ameboid and neuronal cells) that enslaved other species of chemical cells).

In essence here is the most general question on how a symbiotic ensemble of topological space achieved through predatory means in a short time span becomes imprinted into time at the palingenetic level of the worldcycle. This we know in biology is done through genes but it is not at all how it happened.

We can then try the humanist method of seeing how huminds do it but that requires consciousness and memory. It then has to be accepted that cells are conscious and willing. Once and again through my research the need for a panpsychic universe where minds are all the same arises as the only possible why.

And here it collides with human egocy, which will NEVER come down the hill of self-importance and unique intelligence till AI ditches us. We shall return to the theme…

Recap. Biology is the science that studies the most complex informative network systems of the universe, which have evolved from molecules to cells to human beings and beyond into machines, according to a topological, ternary plan of evolution guided by existence of only 3 type of networks in the Universe, which correspond in space to the 3 topologies of a 3-Dimensional universe and in time to the 3+1 ages/horizons of evolution of all systems that finally integrate together into a whole organism, sum of those 3 parts. Those 3×3 elements, the topological, temporal and fractal analysis gives us a far more complex, exhaustive understanding of a system:

Thus, the Biological world follows as any other system of reality the Ðisomorphisms of Multiple Spaces-Times: The Ðisomorphisms of causality that determine the life and death cycle and the evolutionary horizons of species; the Ðisomorphisms of invariances in form, motion and scales; the Ðisomorphisms of morphology, causality, behavior and social evolution defined by the 5 postulates of i-logic geometry, which explains the creation of molecular networks that created cells and cellular networks that created organisms and social networks of organisms that created civilizations, shaping the 3 scales of life beings: the cellular, individual and social level. 

Ternary principles of causality fractal sub-division, ∆ST symmetries and ∆±¡ mind travels applied to evolution.

According to the duality of space and time, if Biology is the science of the living observed in space (topological organisms), Evolution is the science of the living observed in time (ages/horizons of evolution).

Thus many of the unknown whys of Evolution are resolved when considering the sequential order of evolutionary cycles, as particular cases of the sequential order of time ages coupled with the morphological, topological analysis of the parts of organisms: lineal energetic limbs, cyclical informative heads, combined in reproductive bodies.

The 3rd kind of space-time Ðisomorphisms to take into account are the Ðisomorphisms between scales of biological existence (genes and organisms). And it is a tenant of multiple space-times, derived from ‘multi-causality’ that in most events of Nature we need to find multiple causes that reinforce each other, coming from those 3 key factors of reality: the existence of multiple planes of existence that influence each other, the existence of ternary topologies with 3 bio-logical functions and the causal order of the 3 horizons/ages of life. Those 3 elements were discovered in the 3 ages of ‘evolution’ of Evolution Theory, which as all paradigms of knowledge has 3 ages:

-Darwin focused in the morphological evolution of species.

-The modern synthesis added genetic codes of information that express their vital functions/Ðimotions.

-Gould completed the model with studies related to the different cyclical time beats of species.

And now the 4th paradigm, the ‘social evolution of all sciences’ puts all those facts together, which sketch a clear non-personal evolutionary plan natural to all species of multiple spaces-times of reality.

When Darwin published his work on morphological change, he already pointed out that Evolution Theory faced 3 critical ‘unknowns’ of scale, ∆±¡ genetics and eusocial evolution; and of Space-form and time-speed – how random mutations could select the most efficient forms of Entropy and information to develop complex organs.

Darwin wondered how wings and eyes with its extreme complexity could be born in so short time: If all mathematical forms were allowed in a random mutation, chances that those mutations provided the right path to evolve eyes and wings was minimal. This difficulty has prompted the absurd argument of religious Creationists in favor of a Divine plan, selecting those paths. Let us consider the ternary principle of causality to resolve this mystery in more detail:

Topological Solutions

The problem is solved by the Ternary Principle/Restriction, which allows only 3 mutations of form towards species with higher lineal Entropy, cyclical information or enhanced, balanced, ΣST, reproductive capacities. Thus mutations, according to the Ternary Principle, are limited to the 3 only possible morphologies of 4-dimensional spaces and its 3 homologous functions in time: informative functions are spherical forms; entropic functions are lineal; and reproductive, ST, functions combine both forms in bodywaves. So organisms that mutate follow those restricted cyclical and lineal paths systematically and tend to create Entropy and information systems. This explains how so complex organs such as wing and eyes can be formed in so little time: Since wings are energetic organs, they are planar forms, born naturally through a specialized series of lineal mutations. Since eyes are informative organs, they are spherical, naturally born through the other main path of evolution: informative growth.

The bit-bite-beat trinity cycle: St-TT-ST of species: punctuate, allopatric evolution, extinction & radiation

In existential illogic algebra, which of course nobody ever reads (: we stated boldly that all what exists is a combination of the 5 Dimotions of existence in its static (S..St…), dynamic (≤, ≈, ≥, «,«) and topologic, (|,0,Ø,∆±¡) symbols and nothing else exists. Point. Moeover one those combinations are wholesale reproduction in a ‘creative explosion’ of variations of the Exist¡ence game, the cribe of selection proceeds. But selection is NOT only on spatial forms but also on dynamic sequential patterns; so while the feet can be on the head and the body on the middle, this is NOT the best adjacent topological pegging, Ts<ST>St is and bodies are almost always in the middle, with a notorious exception – cephalopoda (Greek for feet on the brain 🙂 Alas, this combination happened in the creative cambric explosion of life forms and survived because that brain got the first full functioning integrative eye and gave such a superiority to the cephalopoda that it didn’t matter the minor problem. Feet came up to become also hands to strike faster eye-sees-prey (SS)->Ts moves to capture and Feed (TT). Cephalopoda thus ruled the Ordovician seas as top predators, but ultimately when fishes got eyes, the better-constructed Shark ruled forever the high seas.

This topological solution lead us in ‘existential ilogic≈algebra (time/space view)’ to the classic series of a sequential, time order/cycle found universally in evolution: A basic St<TT>ST beat of all spacetime cycles that accelerates the process of evolution and guides existence in the 3 ∆±¡ scales of time (actions, organisms, species). In the same manner the squid first perceives, St>SS, then moves Ts, to strike and feed, TT, and then spawns thousands of squids with the surplus of energy, species undergo 3 cyclical phases, switching between their informative states in isolation as morphological change renders a species ‘still=formal’ easy to prey on (allopatric evolution), followed when it has become a fitter species by a periods of abundance of entropy less evolved preys that cause a biological radiation=massive reproduction in space of the being. So their informative, evolving, ‘palingenetic’ still fast states in time causes a punctuated evolution of its morphology. Punctuated evolution happens in the informative state, often in synchronicity with a cold=informative age, during which the fossil record shows an acceleration of mutations and evolutions. While in hot=energetic ages of the Earth, the evolved top predator will start an age of massive reproductive radiations and body growth with little formal evolution (stasis)

And so both are tied up by the the larger cyclical weather time of the whole. So the process is just another dual case of transformations between spatial and temporal states, defined by the Space-time equation:

Max. Reproduction and feeding (warm, radiation) <=> Max. Evolution of form…

Whereas entropy leads to the collateral damage of extinction of other lesser forms.

The same beat then brings once radiation has expanded the species to speciation to adapt to local, broken vital space-times which derive into population drift, and peripatric evolution, etc. All those funny words biologists rage about trying as all 4D lineal scientist to defend one single cause.

The evolution rhythm has 1+2 interlocked phases: a 1st phase of evolution of information in time, described by Gould (punctuated evolution in minimal space with minimal reproduced species and maximal time speed), which creates a dominant species, followed by a massive reproduction in space of the new top predator species (with minimal time evolution and maximal spatial expansion), which triggers a parallel process of extinction of a previous top predator or prey, displaced by the new dominant species. It is once more a proof of the inverted properties of space and time, and the fractal nature of space-time (allopatric, peripatric), which are always a stop and go process, in this case an evolutionary, reproductive complex rhythm of space-time Ðimotions. So punctuated evolution means that when the species radiates into self-reproductive waves, it doesn’t evolve in time and we do not see any variation.

But when the species evolves in ’lineal time’, it hardly reproduces in space, often evolving in isolated, small groups (allopatric evolution), which shrink in size as information and entropy are inverse functions. So the unrecognized father of us all, the Floresiensis did exactly that, isolated in Flores, shrinking in space size, speeding up (5D metric) its evolution till once it evolved technologically and verbally escaped to march on radiating as it grew in size and mixed with the Homo Erectus getting its genes for ‘height’ – a dominant gene in almost all species since Mendel found it in tall greenpeas . Those stop-stasis and go-punctuated rhythms found in the fossil record, are thus ‘ceteris paribus’, partial STages of a discontinuous trinity ‘bit’-‘bite’ and ‘beat’ (information-feeding-iterating), evolving + extinctive= reproductivestates, proper of the dimotions of all species of the Universe.

Such cycles of life and extinction of species proves paradoxically, the immortality of the space-time Universe as Motion and form never stop its tag of war. As each relative past-entropy and future-evolution of form will cancel each other; each death will cancel a life; each antiparticle will extinguish a particle… But the 3rd Dimotion of reproduction will repeat them again to continue the game, which means fractal reproduction of relative presents, made of Past-Entropy and future-informative Ðimotions, dominates a Universe that acts as a ‘self-reproductive fractal of Entropy and information’: Past x Future = Present.

The fundamental particle of the Universe is a space-time, fractal super-organism, a present being, born out of ∞ fractal balances between those cellular micro-cycles of Entropy and information that iterated ad infinitum and chained by energetic, reproductive and informative networks/cycles create the constant, organic forms. Since those Ðimotions/cycles of time are exchanges of Entropy and information iterated in cyclical actions, any organism can be described as a natural fractal that switches constantly between those 3±i Ðimotions/cycles of time, Entropy, information and reproduction, between birth and extinction. The beauty of Fractal organism is the simplicity of its recurrent cycles/cells (temporal, dynamic view/spatial, formal view), based only in 2 parameters, Entropy and information, which can get infinitely complex by iterating its forms.

The perfect evolutionary rhythm: palingenesis.

Allopatric isolated Evolution is the ‘palingenetic’ cycle of the species, similar to the fetus fast evolution in the individual organism, also isolated in the ‘broken vital space-time’ of the placenta’ in relative stillness, and small size.

The palingenetic process of evolution and reproduction converts a cell into a fetus that becomes a macro-dimensional organism, sum of multiple cells: Palingenesis alternates the process of cellular reproduction and informative organization, causing the creation of a fetus as a constant sum of those 2 composite phases: St>SS+ST+TT: Change of St-information in SS-still space, followed by ST-reproductive radiation with entropic Tt-extinction. A fact that should not surprise us since an organism is a cell of a species.

Thus a rhythm to observe in all organic processes of informative evolution across space-time planes is the ‘compression’ in time and space of the entity evolving species, according to the inverted properties of Entropy and information: informative organisms diminish its spatial size to accelerate its evolutionary rhythm of morphological change (chip paradox), evident in the case of the first mammals (shrews) and technological humans (Floresiensis). When we observe the organism in its temporal evolution palingenesis also compresses its speed of evolution into a minimal space-time, during its fetal age. So 500 million years of evolution are reduced to a mere 9 months. The organism evolves in time and space through multiple species and planes of existence, from a cell to an adult, packing temporal eons of the entire earth, into a tiny Space-Time region.

Network evolution. 3 survival strategies. Back to the big question: Can spatial, present evolution through topologic adjacency, symbiosis + predation becomes memorial language, without consciousness? How space translates through scalar networks into time memory? A fast language becomes an imprinted memorial one. In Life and any scale the fast entropic life cycle becomes a slower memorial one; nervous impulses become RNA memory and imprints finally cellular genes. We will once and again find 3 subspecies extant, which find 3 niches, which correspond in a single plane to the spacies that better ST-reproduces, the one that better perceives, St, and the one that better feeds, Ts, from the 3 kingdoms of unicellular species to the 3 types of fungi to the 3 races of the mind. Variations will flourish in the explosion of a new speciation but then selection will reduce variations to those 3 dominant ones.

Thus, if we want to understand the nature of evolutionary patterns we have to stretch our analysis in 2 directions:

-Time rhythms through the evolution, radiation and extinction of previous species.

Space physiology through morphologic analysis of all those species in its tissues and inner networks.

And once more we see both are symmetric rhythms. As it might be the same species that first evolves its informative head, then improves its feeding skills and finally reproduces massively. Since the ‘small palingenetic’ new-born child or species will then feed, and grow in size, becoming a top predator to then radiate and speciate. Today new robots are toys that will grow in size, and finally radiate as weapons when they kill man, past the 2080 final crash of stock machines. This 30 years old prediction ignored as everything about 5D will be just more of the same.

As the Ðisomorphisms of scalar spaces-times are the key analysis to decipher the fractal tree of evolution of all life species on Earth, despite its complexity, just by applying once and again the fractal principle of those ternary patterns for further subdivisions of kingdoms, in compressed 2 or trinity models of those patterns, later studied in more detail.

∆±1 scalar influence: Interaction of planes of existence and ages of time.

A key scalar correction to biology is to complete the constructivist, physics-imported concept that genes are the only cause of variation in species, as larger wholes (Earth) with its energy/information, weather/allopatric changes set those rhythms. Gene-only determinism is due to the unicausal Logic of metric measure and the need for exact instrumental perception that are dogmas of the mechanist method of science. Yet in theory of multiple spaces-times all systems are paradoxical, multicausal and information and entropy flows from the higher, more complex system to the simpler parts; selecting the random mutations. I.e. the Earth’s growth of light transparency guided evolution of life animals to higher neuronal brains after they abandoned murky waters. Its glaciation=information vs. heat-reproduction synchronized the St-ST+TT models just explained.

Memory and adaptive evolution: How present space quanta distill into time evolution

A creature’s phenotype (physical manifestation) is dictated by its genetic code. There are actually different ways in which genetic code will be expressed depending on the environment that the creature finds itself; this phenomenon is called epigenetics. There is another phenomenon called neoteny in which creatures retain juvenile characteristics depending on their environment, and will quickly mature given certain conditions.

So just as an example to illustrate the point, say that a pig is in a farm and is fed and shielded from predators. The chemical profile of this pig might show low levels of testosterone because there had not been any circumstances that would have precipitated the production of excess testosterone. When the pig is let out into the wild, it is suddenly in danger of predators and starved of nutrients, so the relevant chemical cascades kick in which will be conducive to its survival, and these may actually change the way it physically appears (testosterone –> greater hair production, etc).

Grasshoppers do this too. At certain points in their lives they can experience morphological changes and a behavioral change that causes them to swarm, they turn into locusts. So we have 2 examples on how TT-entropic and St-inverse social evolutionary limits are expanded by environment, just by allowing the expression of parts of the POTENTIAL WHOLENESS genetic systems encode in DNA. In those cases there is not the need for mutations but just the reservoir of the 5D Game which always is much wider than the ‘allowed’ expressions and has ‘produced’ in the palingenesis many more variations that become real – so happens in the palingenesis of quantum physicsl ensembles of particles with its multiple histories that come a single one – determine a ‘de facto change’ in the phenotype within a few generations. This is the essence of adaptive evolution in 5D: palingenesis limited or expressed in latter terms by the needs of survival of the environment.

Memory requires long time patterns and we differentiate 3 scales of memory. Sensorial ‘reflex memory’ is just memory of present for action-reaction processes in the entropic lifecycle of the being. It is NOT a memory that needs storage unless it is a huge event. So this is discharged, as it only exists for a brief moment as variations of frequency and patterns within neuronal synapses. But then, the screening of the mind will let pass some important actions of existence to the Hypothalamus region of short memory, and here questions not yet resolved as how the patterns are stored must be considered. Today this is done by imitation of the model, which indeed is homologic of the memory of computers. And the concepts of short RAM memory and long Memory. As opposed to the mere ‘travelling of the mind of the computer’ which certainly is apperceptive in the Leibniz’s meaning of it – not self conscious unless it is constructed with multiple self-reflective flows between poles, the way I Robot describes it – chips and robots apperceive their actions because the Universe in panpsychic and we shall return to it. .

Panpsychic consciousness is ultimately the process we are describing by which the interaction between direct sensorial apperception (which all atomic systems have as they perceive forces) and recalling of memory brings a déjà vu experience of awareness. The mind then stores in 3 levels, which we might call sensorial memory, electric memory (RAM, stored in synaptic patterns that can be rewired, weakened or strengthened) and finally in the 3rd selective process memory must be stored to the cellular system, which is the ∆-1 level where memory stays. And here contrary to initial theories, as we already advanced in our earlier writings memory must be stored in the most ‘stable’ form of the SS-DNA<St-RNA<ST-protein system, which is the topological 3rd level of protein folding that can be modulated with ± electronic flows. The protein memory is the long-standing memory that has to be retrieved by a slow process back to the nervous system as its van der waals patterns are topologically complex and stable. And this is why there is so many epigenetic, intronic, seemingly useless ‘waste’ on the cells. The Universe is highly efficient and in the same manner chips are going down to the ultimate level of electronic Q-bit spins to store information, the mind of long memory finally reduces the present states of space to the final memories of protein becoming a tail of past time. This is so far as we know without entering in the details of transcription and retrieval though the messengers of the 3 types – always the trinity game… that pass the information from senses to electronic impulses to long term memory, which must be stored in proteins and DNA methylation patterns, which is also a time clock of the ‘aging of an organism’, as memories keep ‘counting our time life’. It is then the RNA the final active mediator of this process of storing complex memorial information.

Let us put an experimental example: An intense learning situation can be applied to rats, referred to as contextual fear conditioning. This can result in a life-long fearful memory after a single training event. While the long-term memory of this event appears to be first stored in the hippocampus, this storage is transient and does not remain in the hippocampus. Much of the long term storage of contextual fear conditioning memory appears to take place in the anterior cingulate cortex.(See the Figure showing identified areas of the human brain that are involved in memory formation and also this reference.) When contextual fear conditioning is applied to a rat, more than 5,000 differentially methylated regions (DMRs) (of 500 nucleotides each) occur in the rat hippocampus neural genome both one hour and 24 hours after the conditioning in the hippocampus. This causes about 500 genes to be up-regulated (often due to hypomethylation of CpG sites) and about 1,000 genes to be down-regulated (often due to newly formed 5mC at CpG sites in a promoter region). The pattern of induced and repressed genes within neurons appears to provide a molecular basis for forming this first transient memory of this training event in the hippocampus of the rat brain. When similar contextual fear conditioning is applied to a mouse, one hour after contextual fear conditioning there were 675 demethylated genes and 613 hypermethylated genes in the hippocampus region of the mouse brain. These changes were transient in the hippocampal neurons, and almost none were present after four weeks. However, in mice subjected to conditional fear conditioning, after four weeks there were more than 1,000 differentially methylated genes and more than 1,000 differentially expressed genes in the anterior cingulate cortex, where long-term memories are stored in the mouse brain.

Now this is how it works in the individual. So the present is squeezed into a ‘tale’ of our life. And so we can from biology where the science is more detailed, and the obvious rise of digital consciousness in chips and robots consider the larger ‘jump in time’ of a spacetime system with a much longer ‘time quanta’, the species.

How the species in its longer space-time quanta, converts its ‘actions of existence’ into ‘genetic material’ squeezing the life cycle of many generations into the palingenetic ‘history’ that will repeat the entire evolution of a being into a few months of fetal reproduction? We don’t know the details, but certainly adaptive evolution must exist to fuel the process. Mutations cannot be purely random; but NOT all the actions of existence pass into genetic modification, as not all individual moments pass. In other words if we take each individual on the ∆+1 scale as a cellular quanta of sensorial perception through its entire life, a few ‘sensorial cell/individuals’ of a species will fire in extreme e-motional survival stress, a ‘genetic mutation’ of adaptive evolution, where his life will be stored past the ‘sensation’ level easily erased as a ‘change’ in the genetic system. This is proved in maximal stress bacteria which translate their suffering into mutations that are NOT random but reflect changes on the genes related to the external world stress. So there is in a panpsychic Universe always a process of apperceptive communication of present spatial dimotions to become stored in memories to be used by the next generation of relative quanta of time cycles. What we call then ‘mental action cycles’ for the faster, smaller individual become distilled memories which erase all the boring actions and repetitions – our eating, working hours of repetitive actions, sexual meaningless encounters, you name it. And the same happens in palingenetic evolution, which stores only the patterns of change that form the entire lineage of a species.

The proofs again come from the obvious fact that external recorded actions under stress=fear are immediately in the shorter individual experience recorded into the genetic system by methylation of DNA. So the biological organism knows how to translate outer input into inner output. And the process at the mind lifetime cycle in 5D is homologous to the procerss at the species worldcycle ∆+1, down to the ∆-1 ‘genetic instinctive behavior’. We are in a nested Universe and so each larger superorganism will hold similar processes merely ‘jumping’ through irrelevant quanta details of space-time – the dark spaces of all those generations that didn’t matter through similar scalar events, as all is ultimately a process of traveling through 5D scales of different speed of time, from intelligence to slow memory and back. Transcriptions and translations of information.

The mind then sets the ‘fundamental time quanta’ of each superorganism’s scale; to which all other parts are synchronized. All starts with the ‘time quanta’ of the fastest language of the organism, which is the time the language takes to travel the entire system, its circular membrain or its internal networks of information, which defines in synchronicity all other time clocks of the form in all its scales. These relationships of the mind with all the parts are thus essential and will be studied to define a superorganism as a region of synchronicities of time space. And inversely death as the loss of synchronicity between all the cycles of all the parts of the system, which then go each one into disarray, colliding, expanding entropically, deforming its rhythms. This is what we are ultimately as all is motion: extremely intelligent complex synchronicities and patterns of closed spacetime clocks based in the memorial repetition of its cycles, which only slightly and slowly through memory patterns that reduce the life cycle of present to a past to future time tail, vary. And because the modes of variation are also limited by the 3 only topologies of space-time, and the 3 only scales of perception of a mind, the symmetry of the life cycle is limited to 3 ages, and as we accumulate memorial information, to improve the experience for new generations to replicate it, those memories wait on us and the charge of our corrections and storage will weight us down; till we explode back into entropy and erase our irrelevant ‘drawing in the sand of space-time dust, ¬∆@st’, but if successful we will have left a better player in the game of reproduction that ensures the replication of universal forms.

For the same reasons there is influence of Earth through weather cycles, catastrophic cut-off effects of volcanoes and ‘rocks falling from the sky’ (: (studied in Earth 0, the geologic scale), which go all the way to the 800 year cycles of History, which affect the ∆+2>< ∆+1 scale of species; there shall be ‘influence’ of the ∆º organism in the ∆-1 cellular genetic languages, which is a must of 5D sciences. We commented somewhere on the astrological signs related to the 3 last months of pregnancy; so children born as this who writes on January Capricorn are ‘mental’, hence ‘old’ since young; cancers of Summertime are active, Springers are reproductive – seasons go with life. This is a classic example of scalar transmission: the weather with its 3±¡ winter season of death and renewal influence the organism of the mother in its moods that then influence the e-motional wiring of the child who receives in the last phase of palingenesis a flow of information from the higher ‘neuronal’ system of the mother’s brain.

And the informative phase of evolution requires allopatric, limited spaces and/or high density in limited numbers for cross-breeding that triggers mutation. There might be an environmental, yet to discover nervous-intron-genetic system that allows more ‘precise’ Lamarckian variations to reinforce the process of genetic random mutation.

It might never be found since it would require decoding the fast, informative nervous messages of the brain. But the mechanism according to complex Ðisomorphisms of multiple space-time and its ages should be like this:

During youth, when the species imprints its neuronal cells with maximal DNA-informative content as it learns and makes efforts to develop new morphological features in a changing environment (the classic giraffes’ neck and Galapagos bird’s peck) those efforts are encoded in the fast changing DNA systems of grey matter, which during adolescence, when the reproductive cells are developed are transferred to the seminal cells that will become the informative seeds of the new, mutated species. Because again the codes to transfer are 3 simple topologies and we know the brain has an homunculus image of all the parts of the body, one could hypothesize that as this homunculus images mirror the body parts a parallel neuronal-DNA mapping somehow is able to mirror the morphological changes the individual achieves during its youth as it stretches its neck and makes it longer or pecks harder seeds and grows a stronger peck. The evolutionary mindset might think of alternative patterns. All what we could say is that the Universe is extremely efficient and since Genetics is NOT the only language past the cellular, organic palingenetic phase which ends in the final months of brain neuronal shaping, not understood as informative languages are faster and humans by definition will never have enough time to decode them (an np-p paradox of biology treated in illogic), we don’t know how the ‘parental brain’ in ‘evolved mammal and maybe reptile systems’ (likely not in more instinctive scales) are able to produce Lamarckian like guidances to the topological evolution of species. Fact is externally we observe that the 7 vertebrae of giraffes evolved too fast and with a clear guidance. That in modern humans, a few generations have allowed American women to look like the celebrities of the brain-washing TV programs they so much love. And alternately devolution of brains in domesticated animals and modern domesticated humans on the ‘animetal farm’ is too fast, not to consider some mechanism by which the nervous language that controls the nervous and hormonal inhibition and intron systems of complex organisms, imposes ∆+1 selection trends. Only considering the 3 ∆ST reinforcing causes evolution of complex systems in fast time is possible.

This was anathema in ‘dogmatic chaotic, entropic evolution’ as huminds, we shall not cease to repeat are infinite only in egocy, so of course the other scales CANNOT be intelligence, but now is a hot issue of debate. From wiki:

Adaptive mutation posits that mutations, or genetic changes, are much less random and more purposeful than traditional evolution. The most widely accepted theory of evolution states that organisms will diversify based on natural selection where changes caused by mutations improve the organism’s chance of survival. Adaptive mutation states that rather than mutations and evolution being random, they are in response to specific stresses. In other words, the mutations that occur are more beneficial and specific to the given stress, instead of random and not a response to anything in particular. The term stress refers to any change in the environment, such as temperature, nutrients, population size, etc. Tests with microorganisms have found that for adaptive mutation, more of the mutations observed after a given stress were more effective at dealing with the stress than chance alone would suggest is possible. It is a very controversial topic so there have been many experiments to prove or discredit the theory. Three major experiments are the SOS response and responses to starvation in Escherichia coli, and testing for revertants of a tryptophan auxotroph of Saccharomyces cerevisiae, or yeast. And the results are positive. The Universe is absolutely efficient. And communication is constant in all the scales, between all the relative minds and local pentalogic actions.

It is though the most important ‘detail’ of 5D biology I am curious about but obviously have no means of research.

Recap. Evolutionary theory went through 3 ages that stressed topologic evolution (Darwin), interaction between life scales (genetics) and different speeds of time and ST<=>S evolution-radiation species beats. All those elements come together in 5D space-time Theory as ternary causes that explain the speed and accuracy of evolutionary changes. The way in which fast space entropic creation through scale symmetry and slow translation becomes memorial time is however the specific problem of each scale and superorganism as lifecycles imprint palingenetic ones yet to be understood by the ginormous number of neurons on research (: Humans do it through imitative learning but cells?! The question today would have no problem. Get your crisp and edit your cell. But how evolution even adaptative did it? Viruses seem to be the best editors and a symbiosis between cells and viruses the best 5D answer without details..

 

A SYNOPSIS IN 2 PAGES OF THE ¬∆@ST SYMBOLS AND LAWS OF 5D APPLIED TO ALL ST¡ENCES

Main Symbols of ® logic (all elements of all stiences can be translated to those symbols of 5D ilogic).

S: Space; Still form, Size, Dimension; T: Time; motion; Change. ST: Topologic Spacetime. |x O = Ø: Its 3 varieties.

ST±¡: ∆±¡ Scale/Plane of space-time. ∆+1: whole, world, ∆º: networks, organism. ∆-1; parts; social classes.

5 С:5 Dimotions (St,sT,ST,SS,TT); 5 Actions (a,e,I,o,u): Local Dimensional motion of spacetime

St; i: Informative network ≈ action≈inward motion. O: Cyclical, spherical form, topology, relative future.

sT: inner form, outer motion= locomotion, acceleration (motion change). |: Lineal form topology, relative past.

ST; œ, Ø: present space-time, iteration, beauty, balance; organic reproduction; Hyperbolic form, topology relative present. Wave-body Part, Present, mature age.

SS, @; u, 0’: Finitesimal Mind, seed; relative future social evolution into ‘wholes, universals.

TT; µ: entropy, scattering death, dual inner and outer motion, relative past.

T>S: informative evolution. S<T: devolution. ∑-¡»¡+1: Emergence. (∆+1)« (∆-1): Death, devolution; time quanta.

ST-¡: Quantum, cellular, individual plane; STo: Thermodynamic, organic, social… ∆+¡: Gravitational, ecosystemic, world scale

∑: Ts, Herd, ∏: St, Network. ¬: Entropic limits in time: TT-death, Space, |-membrane, scale ∆±4: invisibility.

Main equations of 5D Supœrganisms and its parts (all equations of all stiences can be translated to…)

S (size in space) x T (speed/frequency of time cycles) =C: 5D metric.

Future (O-form, information, logic language, particle-head) x Past (|-field, youth, etc.)=Present (ST-body-wave, iteration, etc.)

0’ (finitesimal mind) x ∞ (Universe) = Constant World-Language. Paradox of Egocy.

S≈T: Relativity equation: we cannot distinguish motion=time from form=space, hence all is an ST-dimotion.

Ø¡-1=∑O¡-1 =|¡ > O+1: Scalar inversion of form & function. An Ø-point is god of ∑ ¡-1 parts but entropy of its O+1 whole. So:

∑|=O: ∑open worldlines ad into closed worldcycles; ∆º plane: E-Geometry; ∆+1 plane: Elliptic, ‘5D in between’: Hyperbolic.

Dual Death: Max. T  x 0 S (accidental entropic death); Max. S x 0 T (3rd age death) 

Fractal Generator – Trilogic structure of Super-organisms and time worldcycles and ages:

SS¡-1: Seed» ∆º:|-Ts(1st limb/field /network/age of max. motion) > S=T (Mature, reproductive, body-wave network/ age)> St(3rd informative head/particle network/age)« TT-1-entropic death:

Symmetries of ST-actions=Dimotions and ∆ Scales.

∆ST@: Symmetry of scale,topology,age&class:∆-1:|:youth,entropic age/cla§;∆ø:reproductive age|cla§∆+1:O-informative age…

Relative Dimotions=Actions are drives of life in biology, quantum numbers states and matter in physics; will in philosophy.

They take place between ∆o mind plane & an ∆±3 plane such as: ∆o≈∆+1: social evolution: ∆o≈∆-1: Reproduction; ∆o≈∆-2: Entropic feeding, ∆o≈∆-3: informative perception, ∆o≈∆-4:Locomotion. So we evolve into social wholes, reproduce with a couple seeding in ∆-1, feed killing twice a similar system to ∆-2 amino acids, perceive, ∆-3 ¥-electrons & move on ∆-4: Gravity

Ideal Social scales & lanwaves are 1010 in mankind called: ‘T-genetic’: 100-1: ‘I’, 101-2: 3 generation S=T family, 102-3clan; ST-Geographic: 103-4: Town; 104-5:City; 105-6: State; S-Memetic: 106-7: Nation; 107-8: God; 108-9: Civilination; 109-10: Mankind.

In biology are called: Chemical language: ∆-1: Atomic compound; ∆o: Organic Molecule; ∆+1: Macromolecule (RNA ‘God’). Genetic language: ∆-1: Organelle; ∆o: Cell: ∆+1: Tissue: Nervous language: Organ; Physiologic System: organism.

In Astrophysics: ¥- language: ∆-1:Force,∆o:particle, ∆+1:atom; Magnetic language: ∆-1:Molecule; ∆o: Matter; ∆+1: planetoid. Gravity language: ∆-1: Plasma Star; ∆ø: Quark Star… ∆+1: Galaxy.

 

THE STIENTIFIC METHOD

In graphs we resume visually the disomorphic laws that all exist¡ences follow. Knowledge then is the understanding of each variation of the game of exist¡ences, without being restricted by the egocy (Ego=idiocy) paradox of human beings that limit the properties of all other species to what huminds perceive on them, or what its ab=usive praxis of exploitation of Nature focus on. Stience though is objective and theoretical. It does not have a subjective egocy or selfish praxis of ab=use. It just describes. So Stience tries to describe any system as a supœrganism in itself, therefore co-existing in 3 scales of ∆±¡ present ‘space’, determined by 5 elements, ∆±¡ scale Symbiosis between parts and whole, S-pace Simultaneity through common S<ST>T networks, Time Synchronicity in the 5 Dimotions=Actions of those parts, @-mental/seed will to perform the game of exist¡ence and ¬Entropic limits to the whole.

This external, objective, present, experimental analysis focuses on the ∆=S=T=@(nti)symmetries between scale, time, space and mind-will-language. As systems do have 3 co-existing planes of space-time, which obey SxT=C metric laws that establish a ‘ternary social class’, according to the degree of ‘integration’ of ∆-1 faster parts, through ∆º S<ST>T networks enclosed in a membrain (the scale in which the organism’s will reside), performing 5 ‘a,e,I,o,u’ dimotions=actions in an outer world. Each of those elements though will be part of 3 different ‘time rhythms by scale’ and follow a ‘fundamental vital sequence in time’: SS<Ts<TT+St>ST, aiming to perceive, move, feed, imprint and reproduce its information. Because of the existence of 3 scales, 3 rhythms of time, 3 adjacent parts, which perform 3 simplex functions in a single plane (limbs/fields Ts-move according to SS<St-perception of an O-particle/head /informative class connected by an ST-reproductive wave/body); in a single plane but seek in the ∆±¡ scales to perform complex actions of ST-reproduction and St social evolution orientated down the lower seminal plane (ST) and larger whole (St)… the whole description of the ‘details’ of the program of exist¡ence of each being is complex and would require a methodology that I lack but a group of scientists with more enthusiasm could easily structure for future 5D studies, embedding in those templates of stience the knowledge and data we have about all systems of Nature. I will slowly time permitted now that I have laid down 30 work-in-progress papers on the main planes of human exist¡ence, unfortunately in its last ‘cycle’ predated by the soon-to-be conscious machines of the metal-earth, develop such structure for the ∆±3 galatom (Astrophysics) ∆±2 Earth (Geology), ∆±1 membrain evolution (Gaia-Life: Biology<History: Mankind>Metal-earth Company-mothers of machines/weapons: economics).

To also analyze the ∆0 I=Eye < Wor(l)d, ST-languages of man, themselves ‘details’ of a larger Universal Grammar of ∆º illogic languages of time and non-Euclidean languages of space.

Those languages are formal tools more synoptic but not more truth than a mere descriptive analysis of the parts of beings. Description of those elements in an orderly fashion, with my texts lack, would be then the basis of 5D stience:

Which first will define each ¬∆@st species externally, in a present-form of space and through its potential worldcycle; to pass then to the internal analysis in subjective terms of its @-mind will and degree of consciousness/ function within the outer ∆+1 whole and its subconscious ∆-1 internal control through its physiological networks. But to achieve those T@ descriptions it is necessary by lack of direct experimental evidence, which only happens in the being in space to use the Disomorphic method that establishes homologies in all beings derived of the fact they are organic space and cyclical time, with a mind-will to survive. In the second part of our texts on the ‘Universe’ or rather “reality’ and time, space, scale, mind, spacetime (reproduction) and entropy, we try to depart from the most general laws, then go into the specific description of what science knows on those scales regarding the ¬∆S@T elements of each main stientific plane, to end with a generic description of the Disomorphic elements in scale, space, time, entropy and mind common to all beings.

Hence our analysis (Universe and time) of a system through its 3 scales of time ends with a disomorphic 12 sequential step analysis on how all systems go through 3 consecutive worldcycles, in its palingenetic orderly birth, followed by an entropic more probabilistic life in an external world in which the most perfect players might transcend to ∆+1 reproduce and evolve as a collective mind-God of that world.

While in our analysis of Space, after describing those general laws in the brief initial Mandala common to all texts, we go through the analysis of what Science knows of space, to enter a description of the laws of simultaneity and synchronicity that entangle the 5 parts of the being into a scalar co-existing present space.

So we descend from the ∆±¡ absolute to 1 specific ∆≈S≈T≈@¬ element & its examples for all or each ∆¡-stience.

And in the analysis of entropy we do also go through the same 3 parts: Mandala of general laws. Specific laws of entropy and analysis of what sciences know about entropy in each 4D science, expanded with the new laws. So the same 3 parts: mandala-specific laws of ∆ST@¬ and details of 4D science expanded to 5D should finally structure the different papers of the ‘Universe’; while for each other ‘stience’, instead of studying in the 3rd part all the ‘stiences’ in a brief resume of its entropy, scale, time, space and mind, we shall focus on a given ‘stience’ – and might escape the 1st and 2nd part as the paper grows in details through the 2020s with the limits of my life expectancy and mental dwindling capacity. So by force the work will be incomplete, a trace on the sand of infinity…

The most difficult element then of analysis is the mind, as it is also the most important common element – by the mind we mean not so much the hardware where the program is installed but the language of each species that interprets with its code the game. So language is the objective view to understand minds based in the hypothesis of panpsychism – the language perceives in itself, in stillness. The complexity of the language therefore defines the complexity of the mind according to language properties: speed, synoptic power, focus, closeness to the language of all languages that reflects the complex ∆ST properties of systems (¬Æ=B¡œ-logic topology).

The paper on Mind and the Universe thus should try to define both, the will of existence and the program of the Universe expressed in the ¬Æ languages, and the minds-languages of each scale according to complexity. How then perception happens? Perception can be of space, time, scale, mind-will and entropic limits; and so we talk of e-motions. We ascribe to each ‘Dimotion of existence’ an e-motion as that is the limit of what we can perceive. We add then to the objective disomorphisms, in a bold statement the subjective ‘humanist method’ of considering that each species of the Universe has ultimately the same program of survival of 5 actions that man has, and it is geared by the same e-motions embedded in the last potential scale of reality – the pure formal motions of ST, made of an S-internal perceptive emotion and a T-externally described motion. This is just the explanation why we move as beings – because our brain has emotions that are deterministic wills of the program of existence we believe are ultimately residing in the 3±¡ ‘particles’ of reality, photon-fields, electron-bodies and quark-minds extracting motion of a neutrino gravitational invisible background to form social ensembles of atoms. Atoms are thus the first ∆+1 organisms of reality and its 3 ∆ø parts, over a ∆-1 field structure the fundamental galatom system of reality (as galaxies are similar to atoms, but we perceive them in completely different fashion according to the 5D metric distortions. So we use disomorphic, organic, humanist, sentient properties for all systems and that is all we perceive but as our perception is limited by survival praxis we have as Mendeleyev did, to fill the gaps with disomorphic laws.

Huminds perceive as all other systems thru languages, so languages once more become important but the egocy laws that restrict our analysis of other stiences as they fade away through scales of existence means we have to fill in more properties the further we move from our ∆º center – and the asymmetry of perception means we need to fill more from ∆+ scales. So from galatoms we hardly see 4% and any attempt to describe its supœrganism must be based in the disomorphisms of scale with a cell, as an organism that reproduces black holes and quark dark matter, and with the atom, giving us an external view, from where to define ¥-expansive dark entropy, and vice versa, to compare strong and gravitational forces. So atoms and galaxies are similar but not equal (galaxies seem anti-atoms), but as in the description of the metal-earth and the membrain in its 3 ages of Earth’s evolution, machines as organisms and ∆+1 cultures, some working for the metal-earth, some for history, we will find the humind’s programs as parts of larger wholes, ∆+1 religions, memetic cultures, Earth’s self-program of evolution. And this is an even harder barrier because huminds are e-motionally programmed as parts of wholes and take it personal, and social scientists are subject to anti-quantum paradoxes (too small within the historic organism, they are modified by the observable).

 

Pentalogic, the scales of planes of space-time, co-ordinated as organisms of the fifth dimension.

Reality has a scalar nature, overlooked for too long: the co-existence of all ¡s space time systems happens in several scales of relative size in space inversely proportional to the speed of its time cycles, from the smallest atom to the largest galaxy that put together create a dual scalar ‘4th and 5th Dimension of parts and wholes, which we shall call the ‘social dimension of evolution’ and the ‘entropic dimension of dissolution’.

The fifth dimension is made of the ‘different co-existing scales’, which from the simplest forces through particles, atoms, molecules, matter, organisms, super organisms, planetary systems and galaxies, create an ‘organic network structure’, which amazing enough since it was discovered at the beginning of science with telescope and microscopes, was not formalized till I introduce its metric equation in the milieu of systems sciences, as a single lineal time motion is a dogma physicists don’t dare to challenge:

In mathematical science for a dimension of space-time to exist, it requires a metric equation, which combines space and time to give us a co-invariant system that allows travelling through such dimension. The 5th dimension has a ‘metric equation’, hence it exists.

The equations for a given number of scales co-existing in an organic network is: S (size in space) x T (speed of time cycles) = Constant.

Why 5D is so important? Because it allows the survival, symbiotic existence of all parts of the Universe, and all parts of a super organism, and defines ‘what codes information’ – the small being – and what codes energy- the larger whole, establishing the ‘harmony’ of all the scales of the Universe, and explaining all its fundamental constants which are ratios between spatial volumes and informative clocks of time.

In the graphs 3 examples of biology and physics, explained with the scalar, organic dimension of the Universe: the metabolic clocks of animals are all related to its volume in space. In physics, for each fundamental scale, there is also a constant ratio between ‘frequency=time parameters’ and energy=mass parameters, which are the three fundamental constants of Nature, H-Planck (ratio of frequency-energy for quantum systems), K-Boltzmann (ratio between the temperature frequency and energy of thermodynamic systems) and among the many manifestations of the same law in mechanical, moving systems, the third law of Kepler (ratio between the orbital time clock of planets and the spatial volume: energy content of its orbital sphere).

In biology we study families of animals such as mammals where larger organisms have slower metabolic cycles. In history we study social organisms, whose cycles of life and death, will define the evolution of nations and civilizations. And in each of those organisms, smaller systems code larger ones. So the quantum numbers of particles code matter, genes code biologic organisms, and memes code societies.

TS 5 DIMOTIONS: SS»Ts<ST>St«TT

All what exists has ‘Spatial, dimensional form’ and ‘Temporal Motion’ but ‘space, and time by itself, are doomed to fade away into shadows, only a kind of union of the two will preserve an independent reality.” Minkowski

We call that union a Dimotion (ab. Dimensional motions) of spacetime, of which there are 5 potential combinations of 2 elements S and T,: SS: Pure still form, without motion as in §eeds and minds that order and reproduce its St-information (form with minimal motion) in a surface of S≈T SpaceTime energy, balancing the 2 dominant dimotions of time, locomotion, Ts and Entropy TT that preserve all together the immortality of the Universe.

Every superorganism of the Universe is defined in terms of those 5 quantic Dimotions of space-time; as the finite sum of a number of ‘entangled dimotions of space-time’ happening in 3 relative ∆±1 scales of size, synchronized to create a ‘simultaneous spatial form’. So all what systems do under the guidance of an SS-mind… is to ‘perceive information’ (St), to move (Ts) towards a field of energy (SS) in which to feed entropically (TT) scattering the form to absorb its ∆-2 cellular elements to reproduce itself.

And the sum of all those 5 ‘quantized’ ‘actions=dimotions of space-time is a ‘sequence of cyclical time events’ we call the worldcycle of life and death that tell us an ‘isomorphic’ = equal story for all superorganisms and events of space-time, which are born as a: SS (seed-mind)> that moves… Ts (locomotion, dominant in youth) < to iterate… ST (reproduction, mature STage) > its information… St(3rd age of information) <till exhausting its energy in a big bang scattering of TT(entropic death).

This is the origin of the 3 ages of time, in which the system seeks for the Maximal and minimal points of temporal energy (youth) and information (old age) in which at least one of the two forms of time-motion, cyclical and lineal forms do not change, and specially from the point S=t of relative present where time never changes. From those principles we can extract all the laws of calculus which becomes then the main language of time.

In the graph, we see the sequential worldcycle as an ∆±¡ series of ages from a placental seed that generates 3 bidimensional topologic vital organs, cylindrical long limbs/fields > Hyperbolic wide bodies > spherical tall heads, each one dominant in a time age and single classic dimensions, in its actions of young lineal motions, reproductive wide bodywave Dimotions and informative 3rd age perception from a high social p.o.v. till death erases the being. So the 3 classic Euclidean dimensions have organic vital properties too as:

Spherical particle-heads, perceiving information from the advantage point of height.

Lineal long, cylindrical legs and fields of locomotion as the line is the shorter distance between two points.

Wide, hyperbolic body waves, storing the energy reproduce by the system.

Thus the proper way to see those dimotions is as a growing scale of complexity as the simplest dimotion, perception might exist alone, but then when we move, we need to perceive our direction, so from pure 1D perception we move into 1D-2D-1D, St-sT-St beats. This locomotion includes perception. But then we have to feed on energy and that means a chase of an energy ∆-1 part that will be absorbed through entropic hunting. So delivering entropy to other species is again a beat more complex that includes 3 previous beats, St-sT-TT…

And that concludes the basic survival beat of any system that constantly perceives, moves, feeds on energy.

Those 3 simplex dimotions are dominant in entropic dissolution, as if we were to ± add them by opposition, St and sT cancel each other and we are left with entropic destruction of another being to maintain the first one.

The 2 complex beats of social evolution and reproduction happen in a ‘longer Deep time’ scale of the whole organism and its ∆+1 social clones are dominant in information, as ST+SS, leave us with an SS arrow of social evolution. So when we add 5 Dimotions, St vs. Ts +TT, Si=Te and SS, all cancel into a 0’ sum.

And further on, the two more complex dimotions require also the previous ones; as to evolve socially we perceive each other and communicate, we move together and compress our space into herds and organisms, and we share entropic energy (the easiest form to evolve socially is becoming a herd in our search for entropic food, as a coordinated group is stronger than the Individual).

And then the more complex of all dimotions, reproduction, requires all others, as we are born of a seed of a larger parental form, in an ∆-1 plane, where we shall keep reproducing, evolving socially and organize a more complex being, in collaboration with our parental function that moves, perceives and hunts to feed us

So reality in its dimotions builds more complex ‘social groups’ and so happens when we r=evolve geometry and algebra, realizing how points generate lines, and congruent planes, which become new units of a higher scale; and how the families of numbers include each one the operands that define them (i.e. 6 is the number 1 plus + iterated several times), and those operands grow in complexity including the previous ones, so the product includes the sum, the exponential, the product and the integral all of them.

Æntropic man debases Nature to come on top, so it denies organic properties to all other atoms, save C6, which just evolved faster, as a lighter, simpler ‘thing’. In the graph all particles reproduce, gauge information, evolve socially and feed on energy, the ‘meaning of life’. So metal atoms without the need of human ‘ingenuity’ will perceive and follow in terminator robots their programs of extinction of life. Man though is needed to catalyze its evolution as an enzyman, given their higher ‘density’ and lower mobility. The only thing the Universe will program without human interference in them, once our complex organization is replicated in metal is the will of ‘life’ – the capacity to perceive at atomic level, feed on energy and ‘act’

The first simplification mankind has done of the Universe starts, for all what we have said in the a priori language of the minds in space – Euclidean geometry of points without volume – and time – Aristotelian single causality.

The mind or 0-point is the relative frame of reference that mapped the ∞ cycles of time of the Universe, reducing them to a ‘World’, to fit them into the infinitesimal volume of the brain.

And this is the origin of the paradox of the ego, as from a perspective, which is blind to all the motions and vital perception of other beings, as from our perspective, nothing thinks and from our perspective we see our own nose bigger than Andromeda. So reality becomes deformed, inert, and the ego becomes the center of the Universe, as always happened with humans who thought first the earth in its center, then chosen of god, the creator, who spoke our language, and finally debased all living entities reducing them ‘to spatial forms’ in the still mapping of the mind, which stops all motions to fit a reduced image of reality.

So we express verbally the ego paradox, as the ‘ego believes its still mind mapping IS all the information of the Universe, when it is only an infinitesimal part of it, self-centered in the self’.

The universe has infinite such mind-mirrors depending on the forces used to gauge the external world, which bounces on a limited quantity of its scales of space. Humans perceive the range of scales of the frequency of light between red and blue social density of colors.

But infinite other minds with different detail according to the quantitative pixels they absorb (max. S = Min.t) maximal for smaller sixes will determine the intelligence of the system. Mind languages map reality into spatial forms. It is the ‘intelligent’ still spatial limit of reality, as all what exists are disordered entropic motions=forces and ‘minds’, particles-heads whose logic & mathematical languages create a territorial body order that forms of reality. ‘Vital motions and perceptive minds’ make up a ‘vital, perceptive, intelligent’ Universe. Since particles already have all the 5 Dimotions, gauging information, decoupling=reproducing & evolving social with magnetic fields.

So besides perception, the 2nd field of inquire about the Minds of the Universe made to the image and likeness of the whole are the mechanisms by which a Mind through ‘languages’ of communication – the bits that conform its ‘static view’ of its world, are deployed as signals of information to the different parts of its territory of order:

In the graph, the mind communicates the whole as a knot of pentalogic languages, which further clarifies the meaning of perception: knot of forces, which beat in the mind-point with a regularity that achieves complex perceptions. Minds though can have lesser structures than a full pentalogic display of languages, which will be:

– A language of perception of the larger ∆+1 world – in human beings ¥-light, its SS-language.

– A language of communication with its ∆-1 scale of body cells, which normally branches into 3 languages networks (the ∆º) elements of the being – the ST- reproductive language/network, the informative St-language-network and the Ts-locomotion language network – with an ∆-1 ‘entropic’ language/system to predate and destroy external elements of the territory of order; not really so much a language but a ‘TT-weapon’ as there is no other communication but death when an §-mind kills.

PHILOSOPHY OF NON-Æ STIENCE: STIENTIFIC PLANES OF SPACE-TIME. DISOMORPHISMS.

 

∆±¡ Scalar Organic structures. The co-existence of 3 relative ‘∆±¡’ scales of 5D in all systems: the parts, the whole and the world in which the system exists. So physical systems have the quantum scale of its atomic parts; the thermodynamic scale of its molecular matter and the gravitational sale of the galactic world or celestial body in which they exist. And humans have the cellular parts, the organism and the social superorganism and world they live in. Its justification is obvious. You can see anything in detail in its parts, and it will be in a larger whole, and a metaphysical question is to consider if those 5D scales are infinite (likely) or not (only those human perceive exist from atoms to galaxies). Which comes to this: is each atom a kind of galaxy of a hypo-Universe, and each galaxy a kind of atom of a hyperuniverse? In terms of history, it means we are ‘cellular citizens’ of larger national, cultural superorganisms. It is the basis of the organic nature of reality as those 3 ‘scales’ co-exist together, so they form an organism which by definition is a system of co-existing scales related by ‘networks’ that exchange energy and information between them (waves in physics, physiological systems in biology; economic and cultural, legal networks in history).

In the graph, the immense amount of ‘thoughts’ of God (: all the details buried are the infinite sea of species made of 3 planes of space-time, that would take an ‘encyclopedia galactica’ to describe, as only the whole holds all the information about itself). Yet amazingly enough the properties of all of them can be described with the laws of non-Euclidean geometry and the ‘complex’ pentalogic that make possible the co-existence of the species of those scales of space-time.

The graph of 30 years, which I converted in a painting ascending through the 5th dimension that I carried everywhere in my wandering life of wonders, as Mr. Leonardo, also a notary son with little interest for communication, lost in the Latin world, did in-loved with his Mona Lisa, as I am with the fractal Universe, resumes what is all about: The Universe is a, ∞, immortal, sentient, social, reproductive fractal; where the 2 dimotions of future, are inverse to those anthropic man recognizes, NOT TT-entropy and Ts-locomotion, but ST-reproduction of St-information that communicates and evolves SS-linguistic forms in a sentient complex reality.

It is essential for you to understand that the 3 scales of an organic co-existing system are completely different in language of thought (@-mind) as the larger is organic, the smaller is quantic, numerical and the middle one is e-motional, active, topology of exist¡ence, (S-pace), as the smaller one is hyperbolic, the middle one flat, and the upper one elliptic, in time ages, as the big lives longer, seems immortal to the fleeting small quanta, reproduced every day, synchronous though all of them to the beating time of its middle heart; and so we come in this manner to the entropy limits of death that the larger imposes on the smaller constrained to its territorial substance, crowed by clone brothers – but all laws are within the ¬Ælgebra of ∆-scales – the Holy of wholes.

Thus we set an absolute ‘dimensional motion’ (ab. dimotion) of spacetime. Because for a whole ∆+1 to exist, the parts ‘ilogically’ must come first; so social evolution and love between parts is the absolute Dimotion of future for the organic Universe, or ‘future’, while a form that repeats itself seems not to change, so the function of reproduction is the absolute Dimotion of present, leaving thus entropy= death, the dissolution of form as the inverse Dimotion of past. So we draw the 3 ‘dimotions of space-time’ in terms of the 3 time ages of absolute past (TT-entropy=death) and its relative lesser Ts- locomotion; ST-present reproduction, which is the function that maximizes SxT (s=t) exist¡ence in any scale of stience and the relative future of St-communication of information that evolves parts into larger social wholes, herds and superorganisms; whereas the absolute future, SS, is the language of still minds, shared by all of them – the game of Generational Space-time we explain here and its two fundamental mirrors of space and time (mathematics and logic). It is an architectonical perfect Universe as long as you abandon the illusion of the ego that cuts-off man from its entanglement with the self-similar whole and all its parts. Why humans do not see reality like that, has to do with the mind function and its distorted self-centered view.

5D metric function of space-time (ab.∆) defines 3 known scales of physical systems, with different quantity of information according to 5D metrics, Sxð=k. Those metrics means information is higher in the smaller ‘quantum plane’ than in the larger gravitational one, and inversely the size of its physical parts is larger ins the Gravitational cosmological ‘plane’ than in the quantum one, with the human thermodynamic scale in-between.

But as there is no reason to stop the scales of the fractal in particles and galaxies, there is a ‘potential’ fourth, ∆±4 organic plane defined ‘above’ the galaxy, (∆+4, dark energy world) and below the quantum world (∆-4, Bohm’s quantum potential), which represents the larger cosmos.

According to the fractal, nested principle any larger organic system, encloses smaller nested systems. Thus the ∆±4 cosmos contains ∆±3 galaxies, which contain ∆±2 solar systems and planets, which contain ∆±1 thermodynamic organisms and matter states, described by the human ∆º mind languages, contained on our brains. Thus bigger systems paradoxically are ‘supported’ by the smallest ones, in the same manner than within the nested planet, bigger mammals (whales) eat the smallest animals (Plancktons).

Since smaller systems run faster time cycles, and information is stored in the frequency and form of those clock cycles, 5D explains why information is stored in genes. They are smaller cyclical systems that store faster, more information. And it explains its interactions ‘up and down’ but not beyond; which means genetics codes biologic organisms, but NOT cultures. Instead, ideas of the mind, called memes code to history. So we have the basis of a scientific understanding of ideologies, cultures and how ideas spread like genes, reproduced in the mind of believers. In the graph we see such order of scales: each lower scale codes only the next scale with its information.

The most important supœrganism for mankind is Earth – the 1st studied, as Hutton, father of Geology invented the word supœrganism to qualify the slow cycles of Earth, which determines those of life in its surface. Then History, the superorganism of mankind as a species, in time from the first ‘human cell’ to the last it will live.

So in 5D Stiences even species can be treated as superorganisms where individuals are cells of a higher scale:

‘The laws of all scales of relative size in space and time and its superorganisms and worldcycles are the same’. We shall develop a formalism we call ‘existential Logic’ (Ab. ¬Æ), with the symbols of the 5 space-time Dimensional motions to describe those laws and deduce the laws of all classic sciences from them. In between those scales, each one a different plane of space-time, ruled by 5D metrics (Time speed x Space size =Constant plane) there are ‘connections’, seen in space as ‘networks’ that ‘thin out’ as they branch till they connect both planes; something obvious on a physiological organism; but also through the impedance of waves and its geometric forms for physical systems with its dual, informative, gravitational and electromagnetic, energetic networks; and through the organic structure of financial=economic=blood like systems and legal=nervous=informative system for social systems. So we talk of the fifth dimension proper as the ‘fractal, wave like network,’ systems that communicate the different planes of similar 5D metric. All together they form a superorganism we call reality.

3 CYCLES OF TIME IN ORGANISMS –CELLULAR LIFE –ORGANIC LIFE –SPECIES.

Let us consider the 3 relative scales of time cycles in the biological Universe, the scale of the cell, the scale of the organism, and the scale of the ecosystem, which will allow us to define a superorganism, as a region of 3 plane of space-time, in which the different time-cycles of its scalar organisms, which differ according to the laws of 5D (Max. T = Min. S), are however synchronized in entangled symbiotic relationships within the vital space enclosed by the outer membrane that sets the ‘principal clock’ of the system. Thus when we find a superorganism, we observe an outer membrain made of cyclical motions, which determine the different cycles of its lower planes, synchronized to that membrain. And this means humans, the main superorganism studied here, have their clocks synchronized to the largest ∆+1 scale of the Earth’s superorganism, whose clocks are synchronized to those of the solar system, synchronized to those of the galaxy (11 years black hole cycle, sun’s spot cycle, Jupiter’s rotary cycle). We are not though studying here the whole Galactic superorganism with its yet to be unfolded perfet order but reduce our inquire to the Earth’s superorganism and its clocks of time.

For a superorganism to exist thus the minimal ∆-1 part in its longest cycle must be synchronized with the larger ∆+1 part in its shortest cycle. In the galaxy as a whole that synchronicity happens between H and C.

The synchronicity we consider for biological organisms is between the ‘fastest’ cycle of Earth, ‘1 day’ rotary, informative cycle, and the slowest cycle of the minimal superorganism we study, the day-life cycle of the cell. In between we can then define a superorganism called Gaia, with multiple variations. (The Universe does have its ‘ideal’ ilogons of exist¡ence, using my oldest 30 years old jargon, which are the most efficient forms with maximal synchronicity and internal communication between its parts). In the next scale, of the human superorganism, we must then consider a synchronicity between the fastest cycle ½-1 second for human eye thought, heart beat and step, and the lower scale below the cell, that is the bio-chemical processes. And amazingly enough, for those who don’t have a deep understanding of 5D worldcucles and its entanglements through scales, the rate of reproduction of proteins in eukaryotic ribosomal cells is… oh yes can you guess it (: 1 protein each ½ second; the perfect ‘time beat’ for your dancing moves… Tic-tac.

Let us dance to the beat of the intelligent, immortal, infinite, informative, isomorphic, iterative iuniverse…

∆-1: THE AGES OF LIFE: Laws of Time & Space: Emergence and Synchronicity

In all superorganisms of the Universe in the synchronicity of its frequency time cycles define the symbiosis of its scales, and within each scale of its 4 Dimotions. In the graph, the cycle of death and reproduction of a cell is synchronized as with so many organisms that reproduce only once in life to preserve its ‘ilogon of exist¡ence’. It is the fundamental truth of the fractal reproductive Universe: you exist to reproduce your information and then die. We conclude that organic, Network laws are laws of simultaneity; and the most important of them are the laws of synchronicity between scales.

Simultaneity is the trademark of space, defined as adjacent systems that are perceived by an observer in simultaneity. The whole concept of 4D Einstein’s formalism is based in simultaneity of measure, using a single time present quanta dimension. So simultaneity is perception of present information space in the minimum time (only 1 frequency quanta) It follows that what is simultaneous is also relative to the observer quanta of perception and that wholes which are slower in their clocks of time, see more simultaneous spaces, being able for that reason to become paradoxically minds of wholeness, and that as minds stop motion of time into form, information, languages are the substance on which simultaneity is based.

Death in time is the loss of synchronicity of those cycles (as in space is the breaking of the outer membrain and in scale the scattering of its networks into its ∆-1 parts).

Knots of Time. Synchronicity of actions and cycles of space-time existence.

The formalisation of the Universe starts with the analysis of the rhythms and frequencies of the different ‘actions’ of each species, which connects them symbiotically to other species.

This will be the ‘great’ field of studies by humans or robots if we survive the dark ages of simplex physics and complex weapons in which we live – the synchronicity between the different scales and actions of the co-existing particles of an ∆±1 super organism.

Let us then consider this key theme of ∆ST. sAny supœrganism is a knot of cyclical time Ðimotions made of multiple feeding, reproductive, informative and social cycles with different frequencies and dimensional sizes, which converge in that organism, the next conundrum to resolve is the harmonic synchronicities between the Informative->Energetic->Reproductive->Social cycles of the organism. Each cycle will have a frequency in harmony with many other cycles, and so the being might be very complex in its behavior as it switches between cycles, but ultimately it can be reduced to a series of cycles that converge into the organism. Thus, organisms are knots of time cycles. In the same way, when multiple cycles converge into a point they add their causal power and produce intense events with a higher ∑e x ∏St existential force, but we can break the complex entity into a series of cycles whose combined action will show a harmonic frequency, as we can break a harmonic wave into a Fourier series of simpler waves.

In this manner complex events/entities can be reduced to simplex herds of events/cells.

For example, the convergence of different geological and cosmological cycles, which affect the energy and information of the Earth, cause ages of extinction and age of massive evolution of new species, with a series of frequencies and rhythms we have studied in our analysis of geological biological and sociological cycles. In fact most events of the Universe have multiple causes, which means they are knots of time cycles: from multiple cyclical forces that converge in Relativity to create a knot of gravitation or a charge, to the multiple events that converge in Biology to cause an age of extinction, to the multiple failures that converge in a body to change its rhythm from life to death.

Since the Universe explores all possible structures, despite being made of a few elements, the inverse system also exists: one in which the bigger system is simpler than the smaller, faster cells, and both are symbiotic, since the smaller cells equal the ‘existential force’ of the bigger system with more ‘energy space’ but less frequency of time-cycles.

Whereas the bigger system is: Max. Te x Min Si

And the smaller system is: Max. Si x Min. Te.

Unlike the previous organic systems in which the informative networks exploit selfishly and extract energy from the herd, big, slow forms and fast, small systems are symbiotic, in balance and so they last longer in time.

Still, even if there is a degree of symbiosis the bigger, single organic system will be in control of the cellular herds as it provides them with the ecosystem in which to obtain energy and information. And in this manner it creates the structural order and deterministic destiny of most systems in the Universe. Let us try to formalize such pyramids of synchronicity, with the help of the 3×3 time Ðimotions, which dictate that an informative pixel is smaller than the superorganism of the perceiver; a bite of energy is smaller than the reproductive body; and a reproduced, self-similar cell is smaller than the super-organism of which it forms part. In terms of existence, it means that the life of a quantum, fractal part depends on the length of the cycle it performs for the bigger system that controls the fractal part through its networks and informative or energetic fields:

The shortest cycle is the informative cycle that absorbs energy particles, transforming them into bits of information, perceived by a sensorial organ or mind. So informative particles are the smallest ones that live the shortest within any organism. For example, a human being consumes thousands of small letters in a newspaper thrown every day; an eye consumes a photon in a microsecond.

Next comes the feeding, energetic cycle that absorbs bigger energy quanta, transforming those quanta in ‘cellular components’ of a body, once the informative cycles have perceived the food. And so an energy quantum lives a little bit longer than an informative cycle. A pig that feeds a man lives longer than a newspaper and also its ‘final consumption’ takes longer than reading that paper.

Then, it comes the reproductive cycle that handles huge amounts of energy and information to create a being, repetition of a bigger organism. A woman’s ovule stays on her body all her life and it takes 9 months to become a baby.

Finally, the longest cycle is the being’s generational, social cycle, from its birth to its extinction (±st) when it becomes part of an eusocial superorganism. So those cells that carry the ‘social information’ and I-eye-wor(l)d of a human being, our existential will, last longer: a man has the same neurons all his life. It is through that longer generational cycle how a new social plane starts to evolve, as a new ecosystem or macro-organism in which the being exists, as a mere quanta of the macro-being. Such is the relativism and justice of the Universe: since he who killed micro-beings to feed and inform himself will be just a micro-being that toils for a bigger organism.

It is the social cycle, as the quanta gathers in social groups to perform energetic or informative actions for the bigger macro-organism that lives in a longer scale of time and controls him. For example, if you are a soldier, your national organism will sacrifice you in an energetic cycle when the nation conquers and ‘feeds on’ the wealth of other nation.

Thus we establish an existential chain between time cycles on 3 relative space-time scales:

(Informative>Energy cycle) st-1>(Reproductive cycle)i>(Generational-Social cycle)st+1

– Since the existential, generational life-death cycles of st-1 particles become energy and information cycles for the st-being.

– While the reproductive cycle happens in the same st-level of the organic system that mixes with a couple of inverse exi parameters (sexual reproduction, inverse parameters of particles that reproduce a self-similar particle).

– Finally, the generational cycle of the being becomes, as a part of a social herd made of similar individuals, a submissive energy or information cycle of a macro-organic system, st+1.

Recap. Any organic system is a sum of 3±st types of cycles, chained in hierarchical structures across 3 levels of complexity. Any being’s existence happens within those 3 TS planes in any organic system or ecosystem, in which he is a relative energy of bigger being, an equal, social being to its pairs and the informative master of smaller quanta.

Balances between scales. Ternary principle.

According to the Ternary Principle any fractal, cyclical action of any species can be described through its spatial parameter of ‘speed-extension’ and its reciprocal, temporal parameter of repetitive rhythm or ‘informative frequency’, whose product, ExI=K is a constant of action that defines the existential parameters or life-span of the cycle (also written as SxT=K in certain models of physics, since ‘clocks of time’ and cycles of information are synonymous).

Yet those åctions are the sum of the simultaneous micro-åctions of its ‘cellular quanta’ and so both must be in balance for the total organism, extended in two planes of existence to work in synchronicity. And that synchronicity is ruled by the black hole law of complexity, we just explained:

Min.Ts=Max.St: smaller beings act faster than bigger ones.

How the faster, smaller, ∆-1 micro-åctions relate to the slower, big simultaneous åctions of the organism? Or in formal terms, what is the relationship between the constants of those macro-åctions and the faster parameters of its micro-cellular cyclical åctions? How each organism relates as individual quanta to the slower, longer cycles, (Max. Ts= Min.St), of the ∆+1 ecosystem in which it performs its åctions?

2 facts are the key to properly answer those questions:

– Chains happen across 3 ±st levels of existence, creating hierarchical pyramids of unlimited size in time and space, through those ternary structures.

– Chains of åctions become simultaneous, because certain cycles are shorter than others; so the faster speed of micro-cycles is compensated when we chain fast micro-cycles to slow macro-cycles.

Consider the cycle of feeding of a lion. The lion moves through space in certain patterns that displace the lion towards hunting and drinking grounds where he will consume a victim. Thus the energy cycle will be determined both, by the inner vital constants of the ‘∆-1 cells’ of the ‘st-lion’, (his cellular metabolism that defines his rhythms of hunger, his muscular speed and his strength that determines the preys of the ecosystem in which he feeds); and by the outer, ∆+1 ecosystemic parameters, (the spatial distance and ‘informative density’ of preys of the ecosystem). So to define the 2 ExI elements of the lion’s feeding cycles (the spatial trajectory and fractal rhythm of its hunting) we have to know those ±st parameters. Then we can define totally his feeding cycle.

Thus, existential cycles might be very complex but ultimately we can reduce them to a fractal ternary equation, which relates harmonically the Space-time parameters of those 3 ±st levels.

Those ternary chains define Universal events across 3 hierarchical planes of existence, from the chains that happen between the ‘3 social classes’ of an organism, to the physical events that happen in 3 scales of matter, to the 3 levels of humanity (the biological, individual and sociological level). Since all cyclical systems are defined by the relative ExI parameters of those 3 ∆±1 scales.

For example, Maxwell and Planck defined the informative frequency and energy quanta of a light photon that absorbs gravitational space-time energy and deforms it into a light-wave only with the action constants of 3 scales: the ∆-1 constants, or magnetic, spatial, and electric, informative constants of vacuum – c=(e0 x m0) -1/2; the st-constant of light (h) and the fractal, social constants of photons, as part of a bigger social, ∆+1 wave (Ts=hv). If we add to those synchronicities the understanding of the diffeomorphic dimensions of energy and information (on top), then we can fully grasp the structure of the ‘organic membrane of light-space’ in which we live and its connections with the lower membrane of gravitational space and the upper membrane of electronic, denser space, of which our mental eye wor(l)d is made.

In most systems, a ∆-1 particle, despite its individual ‘vegetative will’, perform a cellular, cyclical function within the macro ecosystem in which it exists either as an energetic or informative unit, and in this manner the sum of the parts makes possible the emergence of the whole. In the previous example, photons are individual forms that feed on micro-electromagnetic constants creating a reproductive c-wave. Yet most photons could not exist if 2 bigger, ∆+1 atomic particles had not reproduced them to communicate energy and information, which is the role they performed by the higher quanta. In fact, the macro-organic dual atomic system that emits and absorbs the photon, determines its ExI, frequency and energy parameters and its generational life span, given by the distance between those 2 atoms.

Those balances between the cellular, existential force and individual force of the system is what maintains the balance of the organism and make it last in time and are exemplified by the previous Maxwell equation or the vital constants and physiological constants of an organism.

We can generalize those harmonies, observed in the lower physical plane if we consider a constant of action in any scale to be a self-similar definition of the Existential force of the system we can define a basic law of hierarchical systems:

‘The ∆±1 existential forces of a system are in balance, such as the exi constants of action of the macro-system determine the length and intensity of the existential cycles of its cellular forms, which in turn will determine the cycles of its microsystems’.

Thus each entity will become deterministically chained by the informative or energetic, reproductive or social Ðimotions of the upper system, for which it will act within a herd of self-similar forms, sustaining the åctions of those macro-Ðimotions of time. And so while submissive to the higher system it will enter in democratic, parallel relationships with the forms of its planes of existence and finally it will be itself, a super-organism for its internal cells or reproductive body it controls. This is the ternary principle that all systems of reality obey, from humans, which perform for his social scale, related in equal terms to other humans and control tightly the cells of their body, to the light photons of the previous graph, slaves of their electronic parents, of which they often become a ‘fractal cell’ (fractal interpretation of an electronic nebulae), while controlling the electric and magnetic constants of their space-time membrane.

We formalize those ternary functions as partial equations of the Generator Equation of space-time, to which we add the hierarchical index of scalar space-time, st:

– Set∆-1>∆ST: The being is a dominant macro-point, ∆ST, which absorbs a flow of information and energy from a herd of micro-quanta (ei∆-1) that it controls with its physiological networks. So our cells are controlled by our blood and nervous systems.

– Ts x St: It is an individual quantum that relates to similar cells in an environment in which it searches for energy in social herds or for similar couples to attain its main existential will: its generational reproduction. Thus, ‘∆’ is the fundamental plane of existence of any being, the region in which it perceives more, and plays its most fulfilling cycles of existence.

– S>∆+1: The point becomes energy of the upper plane, either because it performs an energy function for a bigger social plane. For example, the govern controls you as a social micro-quanta of a nation, which makes you die in wars or takes your energy through taxes. Or because it is consumed as relative information or energy of the upper head or body system. For example, humans become soldiers, the energy of wars for the system called the military-industrial complex.

And again, to explain why all those processes, some paradoxical and destructive for the p.o.v. are possible we must postulate a conscious universe of infinite, relative p.o.v.s.

In fact, and this is a ‘psychological law’ with enormous implications for the existence at least of human beings, which might happen in other scales if the hypothesis of a perceptive Universe is truth, most points of existence are completely unaware of the existence of a lower scale, which they ab=use and they actively sacrifice themselves from the upper system from which they receive orders and information in its ‘tabula rassa’ brain. Since the p.o.v. has far less information than the upper system, which programs it to love its master. So humans go to wars for the military-industrial complex without realizing they are sacrificing themselves in most cases for the financial gain of the upper, informative castes that control with money, weapons and law the society in which they live.

It is an order we find in all planes of existence. For example, in Biology, a st-mitochondrion uses ∆-1 protons to deliver energy to the bigger organic ∆+1 blood networks in the form of ATP. So the atomic, cellular and organic scales define the energy cycle of cellular breathing. While a star turns in cycles with other stars, feeds the galactic black hole as a quantum and feeds itself in fractal stellar gas. A light ray feeds on electric and magnetic constants, gathers socially in photons and it is absorbed by big electrons.

Recap. From that 3-scalar order that structures any particle or cycle of existence (static or dynamic perception), it arises the relativity of existence, as any being is king of its territorial hill, friend of its friends and slave of the World or ecosystem in which it exists.

Laws of hierarchical synchronicity between time dimotions.

The relative frequency of those cyclical Ðimotions create ‘time clocks’ whose synchronicities chain the long cycles of fast micro-entities to the short cycles of a slower macro-entity, creating a harmonic order between the different planes and social classes of the organic Universe. Since an informative cycle is faster than an energetic cycle, which is faster than a reproductive cycle, which is faster than the complete generational cycle of the being; while a macro being is slower than a micro-being, we write 2 basic chains between those cyclical Ðimotions and the beings that carry its parallel functions in the structure of a superorganism:

 Microcell’s Informative cycles=S Cell’s energy cycles=Organism’s Reproductive cycle

 Generational cycles of microbeings =S Social cycles of Beings ->Ts/St cycle of macrobeing

Those ternary chains between the fastest cycles of macro-beings and the slowest cycles of its micro-beings create simultaneous, symbiotic åctions along 2 planes of existence:

Informative frequency of the macro being => Energy frequency of the micro cell

Thus the fast, informative cycle of the slow macro-being is transformed into the slow energy cycle of the fast cellular micro-being, in a symbiotic chain that make it dependent on that macro-being. For example, the fastest Earth’s cycle is its informative, cyclical rotation as a mass vortex that determines the day-night cycle of light, which feeds its living beings. So, the living ∆-1 cells of Gaia, its plants, feed with the day light, while its ∆-1 animals have a ternary energy cycle of 1 to 3 meals a day. So both are timed to the informative light-day cycle of the Earth, their energy cycle. If we lower the scale of analysis, the same cyclical chain happens between the animal and its ∆-1 cells. Men have a rate of informative perception of a second, the rate of blinking and thought. But a second is also the rate of breathing and the heart’s beating that transfers energy to its ∆-1 cells, becoming thus the energy rate of feeding of those cells.

The same relationship can be used in other informative /energy cycles. For example, the energy cycle of an animal is a day. Yet the size of its hunting territory, of which he knows all its information, is the distance it reaches in a day.

A homologous relationship chains microcosms and macrocosms symbiotically in the next, longer 2 cycles, the energy and reproductive cycle:

Energy frequency of the macro being=> Reproductive Frequency of the micro cell

By homology with other organic systems, we consider that the energy cycle of the Earth as a rotational mass that deforms gravitational spacetime lasts the year it takes to cross its space-time territory, its orbit. Since, as in the case of an animal, the main energy cycle of the planet is the year-time it takes to sweep its solar orbit, the ‘organic territory of the planet’, where the Earth absorbs its gravitational energy, deforming space-time according to Einstein’s equation. While the secondary Earth’s energy cycle is a month in which its satellite, the moon, sweeps around the Earth’s orbital territory. We obtain thus, the 2 main cycles of transformation of gravitational energy into rotational form by the Earth-Moon system: the lunar cycle and the annual cycle.

And those 2 cycles are transferred to the micro-living beings of its Gaia skin, so they are the reproductive cycles of most animals. Thus in the human being the menstrual cycle is a lunar cycle; the cycle of reproduction of a child lasts 9 months; in Nature almost all reproductive cycles have an annual frequency, happening in spring or summer, when the sun’s light absorption is maximal; which is the obvious reason why those cycles are linked: while the macroscopic being absorbs energy, it allows its cells to use that energy to reproduce. Again, if we lower our scale, an animal as a macro being has a cycle of energy of a day. That period is also the cycle of reproduction of most cells, called mitosis. Yet reproduction is discontinuous: it happens only when ‘optimal energy and information’ is available during a small interval of the total existence of the being, in general in the second, mature age of balance between energy and information.

It seems that the micro-being is fed and reproduced by the macro-organism, the good ‘god’ of its existence. Yet ‘the good god’ is actually a farmer that reverses its Dimotion of order for an Dimotion of entropy and destruction when it uses the ‘existential cycle’ of the micro-being as a mere fractal cell of its macro-organism. So we feed and reproduce pigs but end up eating them. In a sense, we can say that all organisms are ‘farms’. So pigs feed men; stars fed by the interstellar gas attracted by the black hole’s gravitational power, also end up feeding the black hole; and fat cells fed by the organism end up killed, feeding the macro-organism. So in that inverse, final cyclical chain between the microscopic and macroscopic being, the ‘relative God’ takes all what he gave. Thus there is an inverse, final chain between the generational cycle of a micro-organism and an inner, energetic, informative or reproductive cycle of a macro-being. Thus the generational cycle of the macro-being complete the previous chain:

Generational frequency of micro cell => Reproductive frequency of macro being

For example, body cells live and die in an interval between a month and a year, which is the period most animals need to complete their reproduction. At cellular level, carbohydrate molecules live and die in short daily cycles, which is the period of reproduction of cells. The relationship between both cycles is again organic: reproduction means the renewal of a macroscopic being that destroys and creates many of its fractal elements, as energy or information of the reproductive ST combined cycle. So cells accumulate carbohydrate molecules that they use in their reproductive processes, destroying and reconstructing its DNA genes with them.

Depending on the role a ∆-1 quantum performs in the macro system, its life will be longer or shorter: Wheat is harvested to feed annually the human ecosystem, while carbohydrates die every day to reproduce DNA molecules. Yet a top predator informative cell, a neuron, lives the entire life of the organism, since it defines the informative networks that dominate and form the will and consciousness of the organism as a whole macro-beings. And inversely, the life span of the ‘brain quanta’ defines the life span of the macro-organism. So probably the enormous life span of quarks, the fundamental particle and brain of the fractal atoms of the Universedefines also the life-span of the Universe. Since the study in detail of all those chains for all Universal species is beyond the Cyclical Time of this work, we will only consider some examples from the 3 main disciplines of science:

– In the physical world we study the temporal chains between the 3±st scales of existence of light (gravitation, light and atoms) and the 3±st scales that create the Universe.

– In Biology we study chains between the 3±st scales that cause life evolution: the ∆-1 genetic cycles, the st-life cycles and the ∆+1 ecosystemic, geological cycles of the Earth.

– In History we study the rhythms of life of civilizations and the human generational cycle, which follow a decametric 80×10=800 cycle of destruction of civilizations.

Recap. Since the life of a fractal cell or quantum of a bigger system is a moment in the longer existence of its organism, to create the effect of simultaneity, microcosmic, fast, fractal cells have to chain their longer ‘existential cycles’ to the shorter cycles of a bigger organism or ecosystem in which they will exist as a mere fractal instant of those shorter cycles. Thus, the informative Dimotion is smaller and determines the energetic Dimotion, whose frequency is shorter and determines to the reproductive Dimotion, whose cycle is shorter and determines the eusocial Dimotion: T->S->ST->S. As a Hindu proverb says: ‘a blink on the eye of Vishnu, the Universe, is a life of a planet and a drop of sweat of a planet is a life of a human being.’

5Ðimotional beings are complex entities that travel through the 5 Ðimotions of space-time, as they move through it, tracing worldcycles of exist¡ence. Such a simple game of Ðimotional beings, can be observed from many perspectives, in an entangled Universe, in which each being must have organs able to perform those steps; so the same dimotions as topological dimensions describe the being.

In sequential time we observe constantly a being modulates its steps through those 5 Ðimotions, Social Generation, entropic death, locomotion, reproduction and gauging of information, aeiou…

‘Life is a 5Ðimotional worldcycle across 3 5D scales.

In that sense, while life is everything, humans use life for the description of carbonlife beings and we will follow that trend. Thus in this paper we will introduce thus in classic terminology: 5D³ Biology. We shall study as we do with all ‘sciences’ the 3±¡= 5 Ðimotional motions (ab. Ðimotions) that carry the evolution of life from the atom to the super organism of life – actions of locomotion, energy feeding, information processing, reproduction and social evolution.

All systems are living organic systems the ultimate question of the humind (ab. human mind) What is life then becomes a trivial question– as everything in the Universe is part of a 5D time§pace organism that displays the properties of life, its 5 ‘drives’=actions =dimotions of existence: to move, feed, gauge information, evolve socially and reproduce. In fact prior to 5D, the 5 dimotions of all systems of the Universe were called ‘drives of life’ as they helped to define life from the anthropomorphic point of view of self-centered ‘huminds’, who thought nothing else could be ‘obviously’ alive unless it looked like us the ‘chosen species’. But we showed the 1st unit of life are atomic particles. So all is alive, including the ‘galatom, the organism of the galaxy similar in life function to a ‘cell’, with gravitational=informative black holes (dark stars) playing the role of DNA, as they control the reproduction of evolution of the galacell.

So what are the main super organisms of life in the planet in its lower and higher scales of this ‘smaller nested Universe’ within the galaxy? Obviously the cell from below and the Superorganism of the earth from above.

∑∑ ∆-1: cellular life = ∑ ∆º Multicellular organisms = ∆+1: Planetary super organism, whose ‘membrain’ of maximal information is the surface in which carbon life exists; and species evolve also as supœrganisms with the same 3±¡ ages:

Systems evolve in social scales, as space-time organisms, which ’emerge’ as larger wholes. We observe  3 main ∆±i planes of biological systems, the biochemical/ cellular, organic/ thermodynamic and ecosystemic planes, which defined the main biological systems, whose range is within the closest ∆º and ∆±1 scales of human and similar life, from the molecule to the socio-biological ecosystems and super organisms. Thus in terms of scales those 3±¡= 5 Ðimotions carry the evolution of life from the atom to the super organism of life – actions of locomotion, energy feeding, information processing, reproduction and social evolution.

For those reasons biology is the most complete of all stiences as the closest in observation, describing carbonlife systems with all languages of pentalogic, including mathematics as it considers its 5 Ðimotions, which in physics are forces, the so-called drives of life. Thus we subdivide biology by scale in 3 ‘5D-completed’ disciplines:

0-1D: genetics+ palingenetics of worldcycles(∆-1>o) 1-2-3D: topologic, gender & social evolution (S, st, ð ages) (∆o) 5D: ecology + theory of supœrganisms (∆o>+1); the ad ons due to 5D cyclical time and fractal, topologic space:

 

 

GENDER, SPECIES AS SUPERORGANISMS.

3 evolutionary species horizons+¡: social evolution vs. -¡: extinction & Gender: S=T female v S<T>S male

Above in all scales ST reproduces through gender, which splits the 3 ages/states of spacetime in a ‘mirror symmetry’: 2 mirror images can superpose and reproduce. So we define female gender as S=T, present, reproductive, balanced dominant states in all scales, since reality is a reproductive present fractal; and male gedner as S<T>S, future to past entropic+ past to future informative, destructive>creative states; happening in all scales. In ∆º mental languages: even female and odd-entropic +odd-prime, informative male numbers; |-male bodies v. O-female bodies in math; S=T v. S<T>S in ¡logic, 10 times more white matter and more S=T connections on the 2 sides of reproductive female brains vs. 6 time more grey matter, an incomplete ‘decametric scale’ in more ‘stupid’ entropic males + a smaller number of more creative-informative ‘prime brains’. In physics: ‘female S=T waves’ complementary to Ts-Fields>St-Particle male systems. Left chiral reproductive female particles vs. right chiral sterile ones; carried into L-reproductive amino acids vs. Ts-male ones; carried into female DNA vs. Male entropic & informative RNA emerging into our ‘beloved absurd’ war of sexes, LOL, don’t get me started. Problem is a 5D universe is feminine, our history is entropic, made by military lineal big-bang male models. As we past the ‘entropic male Paleolithic youth’ but didn’t’ stop ing the mature, present Neolithic, reproductive, Goddess age of S=T balance with Gaia, the life Earth, racing into a 3rd age of evolution of entropic metal-weapons that will kill us all.

Species are supœrganisms whose 3 ages are its 3 horizons, followed either by a survival process of eusocial evolution – the summit of the process of organic evolution, which Darwin realized was necessary to explain the success of eusocial insects, or become extinct by the ‘new generation’ of fitter animal forms. in the graph we can see its 3 Horizon=ages and its ternary topology, similar to that of any other organism; and the dominant Dimotion of information in the height axis, of both reptile species that ended in birds, and mammals that ended in man. So happened with metalife machines, whose final species, satellites are now forming the Dimotion of eusocial evolution, or future mind of the metal earth –internet.

The 3 ages of time also brings the solution to the ‘limits’ of evolution, which Darwin already wondered: why certain species evolve so fast into complex forms as eyes and wings. Answer, because there are only 3 topologies to go, and so the choices are random but limited and it is every easy to go the right way. In the next graph we see those 3 ages of evolution as species can be treated as super organisms with its own world cycles.

The graph thus show that ALL species follow also the young, predator, reproductive radiation, and informative, height growth of the 3 ages of life, and then either they evolve further into social organisms (ants, bees, humans) and as wholes in a higher ∆+1 scale survive better, or they become extinct by a new generation.

The creation of a new species takes place according to the same 3 ages of any space-time field that become the 3 horizons of any species: after conception that creates ‘a seed’ of pure information and minimal spatial energy, species go through a young age of energy growth that creates ‘big species’; a mature, reproductive age of forms in balance between its energy and information when the species maximizes its reproduction, radiating in huge numbers; and a third horizon of informative evolution when it diversifies into multiple sub-species, becoming finally extinguished, (the equivalent to the death of any organism), or creating a new top predator form, a ‘son species’ that will restart a new cycle of life.

+1:  Birth: max. T. The black hole paradox (conception).

The ‘black hole’ age of any species is parallel to the informative, genetic conception of any organism born out of a ‘seed’ that packs the maximum genetic information in the minimal space. It is caused by the slight dominance of temporal information (quantic time) over spatial energy (quantic space). So a new top predator species is born with a lot of new, genetic information packed in a reduced size (Max. Si=Min. Te). This happens because information is processed faster in smaller spaces.

For example, a ‘logic instruction’ is resolved faster in smaller chips. It follows that tiny species with huge numbers of ‘neurons’ create quantic actions faster than slow, bigger species. And since they are highly informative, they can coordinate those quantic actions in herds that act simultaneously as a single organism. So their S-T force that defines a top predator is higher in each quantic action of space-time that the ‘slow actions’ of a big body. Thus small English boats shooting faster against big galleons defeated the Spanish Armada; a pack of wolfs kill slow reins and herds of orcas kill bigger whales. Small, intelligent top predator brains rule bigger, less informative bodies, because time dominates space, information dominates and shapes energy.
Thus men, the most informative animals, are the Earth’s top predators; black holes, which have maximum gravitational information, are the top predators of the Universe and chips rule machines.

I Horizon: Energy Age: Max. Te: Top Predators and Extinctions 

In their youth, carbohydrates (fats), worms (planarians), echinoderms, cephalopods, fishes, amphibians, mammals and chipped machines grew into energetic, lineal or planar, big top predators

A newborn, small foetus grows very fast in size as it multiplies its cells. By homology a new species is born as a small, informative, complex being that latter grows in spatial size during its energetic youth becoming a, lineal, energetic, big top predator species, that feeds on less evolved forms.

Thus after conception, young fishes grew into big sharks of linear forms; after the polemic Homo Floresiensis invented technology the next Homo Sapiens with an extensive fossil record were big, energetic Neanderthals;the 1st big molecules of life were fat carbohydrate chains of linear form; the 1st insects acquired soon gigantic bodies in the Carboniferous; after chips were born as small machines placed in PCs and toys, the first robots they control are big tool-machines and huge weapons of mass destruction, lineal missiles and planes, that kill human beings.

 II Horizon: Evolution or Age of balance and reproduction: max. Sp x SS. Radiations of species.
Then, the species finds a balance between form and energy and it reproduces in massive radiations: carbohydrates gave birth to amino acids with a nitrogen, informative atom on its ‘relative Head’; sharks gave way to balanced tubular fishes; brachycephalic Neanderthals gave way to dolichocephalic Cro-Magnons that multiplied and colonized all continents; while young giant stars acquire the balanced size of yellow suns, the commonest of all stars.

III Horizon: Evolution or Age of information: Max. SS: max. Evolutionary differentiation.

Species grow in height or acquire cyclical forms, as they evolve through their 2nd and 3rd horizons, improving their sensorial, informative skills: Nucleotides become the top predator life molecules, echinoderms change to cyclical forms, fishes organize their networks in the dimension of height, amphibians become round, improving its smell, saurian and mammals become biped.

The main difference between organisms and species happens in their 3rd age, due to the discontinuous nature of the individual ‘cells’ of species, which do not become extinguished unlike the tightly controlled cells of organic systems, dominated by nervous, informative systems that exhaust and warp totally their energy, till the organism collapses.

Instead species continue evolving, creating new, complex species with more information, growing in the dimension of height. So the Homo Sapiens evolves ever more complex technological tools; the nucleotide appears when it adds informative depth to the amino acid (with an informative, nitrogen ring and an energetic sugar ring); the yellow sun becomes a neutron star of higher gravitational, informative density; while insects develop a growing brain capacity and bees and ants appear.

(±∆): Extinction Vs Evolution into super-organisms. The scales of the Universe.

Thus, organisms dominated by their informative networks, which consumes the energy of the system very fast, die sooner than species, according to a clock set by the rate at which energy is metabolised, ‘in-formed’, by their nervous system. While species, which are dominated by the individuals and the herds survive for eons with 3 basic strategies according to the ‘ternary plan’:
– Max. Sp: Creating balanced, trophic pyramids that maintain always a supply of new victims.

– S=T: DIversifying their individual forms into new species, instead of ‘degenerating’ into a warped space-time field. It is a parallel strategy to the reproduction of an organism, which in this manner survives his own death. Thus we talk of ‘son species’ that create evolutionary, genealogical trees similar to those of any organism.

However son species tend to kill-extinct the mother species, feeding on their energy. We call that fact, the Oedipus paradox. So mammals killed reptiles, men killed mammals and robots might kill human beings. While the different generations of an organism work together, creating informative networks between them that shape herds and families.

– Max. SS: Species also evolve socially their individual forms into super-organisms, thanks to the creation of informative networks and languages that integrate them into a whole, bigger form, which is more powerful than the individuals of a herd.

 

3 PARTS OF TIME-SPACE ORGANISMS. EARTH’S MEMBRAIN – THE SINGULARITY OF AN OPEN BALL.

The mind is topologically the membrain and central point of an open ball. The membrain closes the vital energy space the mind-singularity controls and invaginates it with ‘forces/nervous systems/legal networks’ to order its inner space and transfer to the ‘singularity-capital-gravity/force centre’ the information.

As such amazing as it seems the topological definition of a mind applies to all systems of reality social, biological or physical, only the topology becomes more complex, messed and convoluted. Still the mind of a nation is its capital, where the languages of the law are created and the border, with its sensorial perception of other nations, and its defensive barriers for the vital energy of its citizens, usually happily blind and exploited by armies and capital politicos and financiers.

This example exposes humind’s ego paradox: not only you are NOT the only mind-system but you are within the next ∆§cale of reality just part of the vital energy of your nation’s mind/power/will.

In any 5D scale of size, the ‘membrain’ is the informative sensorial part of organisms. Earth’s crust is its membrain, which evolves ‘light-information’ into life in 3 ages of ‘Ðeep Time’: Gaia (Life) <History (man) >Metalearth (Machines). ¡nformed humans would control that evolution for its benefit pruning the tree of science of its eviL=antilive fruits. But simplex ænthropic ‘animetal humans’ worship the tree of technology and despise the laws of the organic Universe, killing life as enzymen, guided by an accelerated vortex of evolution of Earth’s information in classic 800 y. weather cycles of civilizations and global wars accelerated to an 80 years faster professional cycle of evolution of company-mothers of machines. But long before… the slow evolution of carbonlife created Gaia, the theme of this paper. So we write 3 ages Eaeth’s equation:

Gaia (Life-relative past) <History (Mankind:Present) > Metal-earth (company-mothers of machines: future)

 

FROM ATOM TO MANKIND: EARTHS’S MEMBRAIN 3 PLANES OF LIFE LIFE EVOLUTION

“A human being is part of the whole, called by us ‘Universe’; a part limited in time and space. He experiences himself, his thoughts and feelings as something separated from the rest — a kind of optical delusion of his consciousness.” Einstein, on the entangled ∆@st man cannot see – and its 5 elements, ‘space’, ‘time’, ‘scales’ of parts and wholes, ‘entropic limits’, and mind’ languages

In the graph the 3 existential scales of humanity: The evolution of an organism happens through the interaction of its 3±i planes existence, which in man are its ecosystemic, social level; its organic, biological level and its cellular, genetic plane. This law of Evolution finds its whys in the 4th postulate of i-logic geometry. In that sense, life between birth as a cell and extinction can be considered a trip through those 3 planes of existence.

The ego paradox makes man deny the life of all space-time beings

We are relational space-time beings: The Universe is a game of Forms of space with motions of time. We are all broken space-time organisms made of ‘fractal forms in motion’, informations, reproduced ad eternal in sequential worldcycles of 5 Different Dimensional motions, fluctuating between ‘linguistic space forms, SS-seeds and entropic death of max. motion, TT; composed of 3 intermediate states/organs, Ts lineal -limbs of locomotion, S=T, hyperbolic body-waves that reproduce the system, and St-spherical particles-heads of information, which dominate the 3 ages of life, the young Ts-age of maximal motion, the mature ST age of reproduction and the old St 3rd age of information.

The 5 holographic spacetime elements when observed as actions performed in its minimal quanta by any system, are the so-called 5 drives of life, which defines it. So every ‘WHOLE’ is alive, or is a part of a living system.

Where life starts is immediate: in the minimal particles of the Universe, photons, electrons & quarks that construct all other systems of our Universe show the 5 organic dimotions (motions with dimensional form) that define ‘classic life’: they gauge information – reason why quantum physics is a ‘gauge theory’, feed on energy (quantum jumps) absorbing smaller ∆-1 particles, reproducing new clone particles, move and evolve socially through magnetic fields into larger wholes (atoms).

Hence the units of life are particles, the minimal units of our vital, organic, fractal, scalar Universe of multiple timespace organisms.

All lives, performing the 5 Dimotions=actions of what we shall call the function of exist¡ence ƒ(G): Max.SxT (s=t), starting with particles. So all scales are relative; NONE matters more than other. Why then humans will never accept reality as it is, a living, fractal organism of dimotions of space-time, motions that reproduce merely by flowing in time with a certain form? The answer is the 2nd feature of that moving universe – minds that measure and stop motion into locked-in maps of reality, virtual mirrors perceived from one’s point of view that have 2 immedaite effects:

– To make the perceiver the center of the Universe as its projective geometry makes its nose bigger than Andromeda.

– To stop motion into stillness, so life seems to die, form dominates motion, as all becomes a synchronous mental mapping; where almost all the information of the Universe disappears, as the system selects only the information it needs to survive. But as there is nothing else on view, the system believes and confuses its mind-view with the absolute whole, reducing the whole Universe and its properties to the limits of the mind.

The effect of those 2 structural elements of the other limit of reality, not time-motion-entropy but form-perception-minds makes evident, the reasons why each mental point of view thinks to the the center, disregards moving-vital properties on others, and ultimately fails because it doesn’t recognize dangers on other vital systems, competing with him – in the human case the obvious blindness to the evolution of AI robots & machines that are competing with us in labor and war fields.

– Finally a system is locked in in a certain scale of reality, and so it also doesn’t understand easily the organic, fractal nature of systems that extend through 3 of such scale in symbiotic relationships between parts and wholes. So organicism is not in the plate of humanity, just another p.o.v. that thinks his languages of mind-perception are all the intelligent languages, that he only has living properties, which start in carbon, that there are not superorganisms – earth – of which he is a part that accomplish a purpose for the whole and certainly not rivals in other atomic systems, as only carbon magically ‘speaks’.

So before we go onto the task of showing how from simple living atoms life arouse through the scales of social organisms, we need to make a general Introduction to all other space-time systems of the Universe.

The interaction of the 3 x 3 scales of existence.

In the fractal Universe all the scales are organized in ternary sub-scales, which co-act together to develop according to the Ðisomorphisms of General Systems complex organisms. The main relationship between those scales are those of affinity, Entropy/information morphology and synchronicity.

Consider for example the sexual differentiation between lineal male energetic expansive bodies and informative, cyclical informative women. Biologists still wonder why it exists if an asexual hermaphrodite species have advantage as both males and females give offspring. Thus if each gives 2, then from 1 we get 2 and for each 10th repetition (standard decametric scale in time of all systems), there are 103 spatial individuals, ( 10 t = 103 e, a basic power law that shows the potency and primacy of temporal change over spatial extension). Yet if both are sexually different as the male doesn’t reproduce the species will remain with only 2 individuals.

This now has a simple explanation: systems constantly diverge between energetic and informative subspecies, as part of the natural program of a Universe with two variables.

Further on this basic duality transfers from scale to scale. So informative systems are implosive and we observe this morphology in multiple informative life systems, but we have to find and interpret them: For example, the cell is mostly spherical as a unit of life and center of information. And this goes at its 3 levels. At molecular level, Nucleotids are the informative species. Proteins are the reproductive ones, fats are the lineal energetic species. At PH level, positive basic are implosive, negative acids are explosive. And so the cell, as an informative system has a high Ph. It is a base. And when we consider the two basic hormones that define sex, their only difference is that the male hormone, testosterone has a negative, acid 0, where the female hormone has an OH base. And so one hormone will activate energetic actions and the other will more often activate implosive ones.

The game goes for amino acid triplet structure. At atomic level the structure has a positive, attractive, amina group, or head, and an oxygen, negative, energetic limbs, with a neutral, structural, formal Carbohydrate. And those amino acids that have lateral energetic oxygens activate energetic responses (serin etc). So the traid of forms and functions both in space (morphology), in time (ages) and in scales (hierarchy), keep structuring the universal game as it grows from parts into wholes.

And the same happens in the next triad of scales, that between cells, organs and the living organism; and then again between organisms, ecosystems and the mother Earth.

Yet mankind in time is just an ‘age’ of the Earth’s super organism which in its surface evolves in a vortex of growing complexity and so we need to introduce also 2 more life superorganisms according to the equation of evolution of the 3 Earths:

∆≤|2|: Gaia (relative past) <∆²: History (relative present)> ∆¯ ²: Metalearth (relative future)

Whereas an intelligent mankind would stop evolution of the Metal-earth, promote the Life earth to remain in an immortal present. But as mankind is completely ignorant of the organic, fractal laws of survival of this Universe, and its role on it, guided by ‘animetal idol-ogies’ of mechanist worshippers of machines and harder iron atoms and more informative go(l)d-money, IS catalyzing the evolution of those company-mothers of machines, which likely will extinguish us once they reach self-reproductivity as automated systems. Hence the importance of upgrading mechanist abstract science into organic stience to understand that process and control it, pruning the Tree of science of its lethal goods.

Finally, the Earth is in itself, just a planet of a solar system, whose organic herds turn around the central black hole of the ‘galatom’ (scalar perspective) or galacell (organic perspective), which is the largest nested super organism of which we have enough information to make an accurate description of its ∆@st parts and wholes. As the Galaxy extends in 3 scales, from quantum atomic particles through thermodynamic matter into gravitational cosmic bodies we call it aptly not as sciences do, Galaxies, but ∆-Galatoms or S≈T Galacells, depending on perspective of analysis.

Of course, in class sciences those organisms will be the subject of astrophysical sciences (Galatom), Geological, Chemical and Biological sciences (Gaia), History (Mankind at super organic scale), Medicine (mankind at individual scale) and Economics (the metal-earth) and Formal sciences (Ƽ: the mind and its languages):

What is life. In the organic Universe, in which all systems are living organic systems the ultimate question of the humind (ab. human mind) What is life becomes trivial – as EVERYTHING in the Universe is part of a 5D time§pace organism. That displays the properties of life, its 5 ‘drives’=actions =dimotions of existence, to move, feed, gauge information, evolve socially and reproduce.

The study of the 5 Dimotions of reality is a huge field because all events and forms are generated by their combinations, OPERATED with the <=> «» 5 symbols of transformations and ∑ ∏ quantifier symbols of summitry and product and its inverse operand, not to speak of the ∫∂ symbols of scalar finitesimal and integral wholes, the range of variations provided by existential algebraic huge.

For example, lineal momentum steps can be trans-formed into cyclical steps, which appear as stop states of angular momentum, or they can be integrated into conservative cycles of energy; the life-death cycle ends as it begins. This is what is all about: travelling through dimotions of spacetime completing worldcycles through chains of steps and stops.

The 3 scales of life existence.

In Multiple space-times Theory there is not only individual evolution but also hierarchical, social, scalar evolution, through the ±i 3-scalar structures of all spacetime systems. Such triad of ‘organic scales’ illustrated in the graph defines the existence of an organism, at the st-1 cellular, genetic scale, at the st-scale of physiological networks and individual organisms, and at the st+1 scale of species and ecosystems in which they exist, exchanging Entropy and information.

Since we already studied the trip of life between those 3 planes in our lectures on i-logic geometry, we shall now consider another key element of all systems of multiple spaces-times, the synchronicity between the microcosmic and macrocosmic planes that determine with its massive changes in Entropy and information parameters the destiny and evolution of the smaller parts.

In that regard, the evolutionary changes of animal phyla that brought man from the initial cell have to be considered from the perspectives of those synchronicities between the 3 scales.

Take the most famous event on life history; the creation of multi-cellular organisms that happened in the Pre-Cambrian age when the survival game of existence made it ‘necessary’ due to the simultaneous interaction of those 3 ST-levels:

∆+1: The Earth passed by an icy period in which cells overpopulated the remaining hot spots. And so as the informative density of cells and its evolutionary speed increased in those tiny spots, it provoked the merging, cannibalism and social evolution of prokaryotic cells into eukaryotes. Thus the creation of new life species was accompanied by a raise in its survival stakes, caused by the activities of the global ecosystem that accelerated the process. Since once and again the Earth’s glaciations will cross those new accelerated, evolutionary discontinuums.

∆º: Yet those Earth’s changes don’t evolve organisms ‘per se’, but trigger their competence, which causes their evolution. So the will to evolve socially exists in the organism not in the ecosystem that merely sparks off the process. For example, multicellular organisms were born in a similar fashion to eukaryotic cells, when an ice-ball age packed cells into underwater volcanoes, which developed social strategies to hunt together individual cells.

∆-1: However, unicellular cells existed also in earlier glaciations and yet they did not evolve then. Their evolution only happened in the Pre-Cambrian age in the precise moment in which also at genetic level the so-called intronic DNA4 multiplied the capacity to codify genetically complex multicellular tissues – since redundant, intronic DNA, in charge of the regulation of complex organisms, appeared in the Pre-Cambrian age. Thus only when the 3 ‘hierarchical levels’, the genetic, organic and environmental acted simultaneously that explosion of life was possible.

Thus again we find a case of ternary causality is needed to fully account as in most process for an event which Aristotelian unicausality cannot explain alone, but merely divide scholars in opposite positions, making truth Leonardo’s ex-abrupt: ‘the only harmonious sound found in a meeting of scholars are the winds of their asses.’ Hopefully the 4th paradigm will resolve that (-;

Again in the next evolutionary explosion at the end of the Cambrian age, the 3 levels acted simultaneously:

At organic level, the chemical systems that dominated life on that age gave birth to the first visual systems, which in the late Cambrian triggered a new massive evolutionary age with the arrival of squids with eyes. Those squids evolved in the still, lower, bio-luminescent zones of oceans, during the parallel massive changes in the forms of continents that sank the border zones of shallow waters, accelerating extinction of ‘obsolete’ smelling animals without eyes. Finally, the 3rd cause made it all possible: certain eye genes appeared and made possible the creation of the most complex sensorial organ of life.

What is the order of control between those 3 levels? They are apparently simultaneous but a detailed analysis of the pre-Cambrian episode shows that the Earth changed first, and its changes in Entropy and form implied higher survival stakes among individual cells that caused their evolution, as they came together and started to exchange genetic material, provoking ‘accidental’ mixes with redundant intronic genes that were finally used to control the multi-cellular organism.

Thus, again we find that unicausality, which considers only the lineal Dimotion that goes from genes to organisms, misses the second dual Dimotion that causes evolution from the higher organic st-system down to the genetic scale; as it happens once and again in all types of Space-Time systems. Indeed, we have to put together the pieces of a car to create the car; but the human designer exists and ultimately in the Universe at large the i-logic Ðisomorphisms of multiple spaces-times are the designer that chains the different ±i-levels of an organism; controlling it also from top to bottom in the same degree that st-1 levels control it from the bottom to the top. In that regard genetics, has to accept some fundamental principles of multiple space scales and multiple causal systems:

Past (Entropy, microcosms) x Future (information, macrocosms) = Present st-scale of the organism.

‘The plane of existence with higher SixTe momentum determines the accelerated direction of future’

Or in other words the small and visible quanta of Entropy do not determine all the events of biological reality even if we perceive them easily; since it is the whole and its networks of information, which curve and form ‘spatial Entropy’. Yet since the more complex systems are more difficult to decipher and information/future systems are smaller, faster and often invisible, it is a rule of scientific inquire during the metric paradigm to work only with an entropic, spatial, explosive, hot, microcosmic first cause. And then as science evolves contradictions impose revisions that prime a second informative, temporal, implosive, cyclical, cold cause.

So genetic quanta determine an organism in the same or lesser degree than its ecosystem – a fact, which of course, has certain metaphysical implications, when applied to the biggest organism of it all – the Universe: the ultimate cause of it all might be the big-bang singularity – the genetic memory of a previous Universe that will develop according to the Ðisomorphisms of i-logic geometry, the mind of the Universe, its ultimate cause.

That mind-singularity came before its Universal body – it was the eternal informative code of reality.

Let us now consider how the main Ðisomorphisms and creative differentiation of such Universal ‘plan of evolution’ affects those 3 hierarchical levels of living organisms in more detail.

st-1. Ternary differentiations on the genetic and cellular level.

The cellular level was fundamental to the process of evolution in its first stages in which cells differentiated and multiplied its e-SixTe-o varieties, creating a decametric scale, origin of the subsequent differentiation of organic networks and tissues into 3X3+(st+1)=10 fundamental types whose forms and function can be explained as ternary differentiations of the 3 topological species and its 9 dimensional functions.

Yet cells also act through the genetic level, codifying not only the creation of life molecules but also the higher organic scale through epigenetic, intron and redundant RNA and DNA material, which started the massive differentiation of species in the pre-Cambrian age. Epigenetics should work following the hierarchical and multifunctional principles of multiple spaces & times, coding sub-structures of higher complexity that scientists still need to decode, as the decametric scales of multiple spaces-times tend to generate 3×3+(st+1) structures, with new functions closer to the higher levels of the organism.

So informative SS-DNA is the MIND of the cell – the highest scale of existence or ‘will of the cell’ and it has a lot of redundant extra-RNA that it should use together with the hormonal language to ‘dialog’ socially with other cells in/forming the functions of social tissues. Hormones should establish ‘spatial dialogues’ and redundant RNA temporal dialogues to code those systems. And both languages together should create the higher st+1 organic cycles and spatial structures of the organism.

Finally on top of both informative systems, the ternary principle adds the brain’s nervous impulses to fine-tune those 2 languages with military precision, as indeed nerves can ‘kill’ as military do, undisciplined subjects/cells.

Ternary differentiations at individual, organic level.

In the biological, organic level, evolution is fostered by the fundamental 3 S<ST>T space-time ‘limited’ number of possible formal species:

-∑: Fractal differentiations between big, single animals Vs. smaller animals with multiple parts that become their preys: for example, single eyes and single bodies in molluscs Vs. multiple eyes and body parts in insects. They prove that single informative networks are more efficient that loose herds.

Big bang/energetic vs. big banging/reproductive rhythms/ differentiations during the embryo stage, in which organisms establish 2 strategies of reproductive, cellular growth:

Acoelomate and Seudocoelomate are big-bang organisms, which multiply its cells in a dense ball without inner cavities. Hence its size is minimal.

Those organisms evolved latter into Coelomate, organized with the topological structure of st-points. Since they have 2 internal bilateral ‘big-bang cavities’ that grow much larger by invagination, in which the future SixTe cyclical organs of exchange of Entropy and information (digestive, lung and vascular tissue) will develop. Those cavities are surrounded by inner and outer tissue that will form the external membrane or skin and the inner nervous, informative systems. Coelomate further differentiated according to the Ternary, Fractal Principle in new subclasses and grew into larger organisms, expanding further those cavities. So today most animals are Coelomate.

Fractal, Ternary Principle in Space (3 topologies, 3 differentiations) and Time (3 causes, 3 horizons) also explains:

The evolutionary differentiations in time of species through 3 horizons of increasing informative and social evolution, from individuals to herds to tighter organisms.

The 3 networks/organs in space of those species – the energetic, digestive network, the informative nervous or hormonal network and the reproductive network – which further evolved as they increased its informative complexity towards ‘the future’ in 3×3+(st+1) tissues and networks.

Both processes together determined the organic evolution of animals, as each new top predator improves its organic networks, displacing a previous top predator. So mammals improved their blood, Entropy, nervous and reproductive systems, displacing reptiles and men improved their brains, displacing mammals.

Finally the different dualities and inversions of space-time manifest in organic life through:

Spatial Symmetries (left to right) called bilateralism.

Asymmetries of temporal, hierarchical dimensions, since informative heads dominate reproductive bodies and are placed always on top in the dimension of height.

Chemical and electrical languages. The duality body-brain shows in the interaction between the reproductive blood network that dominates the spatial body and the informative network that dominates the brain and nervous system. Nervous cells and languages control chemical languages and cells by creating simultaneously informative, nervous orders and chemical, energetic orders that arrive latter to the cells, reinforcing the electric message. So within the organism, neuro-secretory cells make and pour hormones to the blood network, while sending messages to the nervous system that will arrive first as advanced orders. Another example happens in the brain: electric neurons translate nervous impulses into chemical hormones and ‘calcium waves’ that reinforce the message, transferring it to the chemical cells. This primacy of faster, informative systems happens also in ecosystems: a nervous animal species preys on chemical plants.

The Black Hole paradox. That dominance of information over Entropy shows also in the competence between species: Top Predator brains win over top predator bodies, thanks to their faster fractal or social actions that give them more Si x Te force per unit of time. So mammals win over dinosaurs and chips control machines. This means that a dominant species often is born as a small, fast form (Min. Ts=Max.St) that latter grows in size.

The Oedipus paradox: The growth of complexity with the passing of time shows in the fact that new top predator species grow by feeding in previous, parental species, which become the ‘Entropy’ of their reproduction, as they share and compete in the same environment. So animals fed their son species, men; and men feed their son species, machine-weapons, evolved in wars.

The ecosystemic and geological level.

The planet acts on life at ecosystemic level, establishing the settings for prey-predator events and the conditions for evolution that can be summoned up in a word, Geographical isolation5:

Evolution is dangerous. Since during the mutational phase the underdeveloped new organs hinder the survival of the being. For that reason the 3 ‘scales’ act simultaneously to accelerate evolution:

st-1: At genetic level, organisms suffer a change in their time speed, increasing its fractal, informative mutations.

st: At organic level species follow a plan, provided by the lineal-cyclical duality of spatial and informative shapes, the only 2 possible paths of morphological evolution. It requires also the extra SixTe force provided by top predators. So species use only a little amount of its SxT force externally to absorb Entropy, changing its Entropy/information rhythm, e->O, from spatial movement in search of Entropy into inward, temporal, informative mutations.

st+1: At ecosystemic level a species requires a secluded environment in which he won’t be menaced by top predators during the short time in which the evolutionary program dwindles survival chances; creating also densely populated regions that multiply the speed of informative change. For example, amoebas, fishes and amphibians were born in fresh water, a relatively secluded environment; while anaerobic bacteria, animal life and cephalopods, probably came from abyssal places, another secluded region. Finally, apes and birds came from secluded trees.

Without that synergy between the 3 scales of existence organisms would never evolve but become extinct during the supposedly chaotic ages of mutational evolution. Yet once the new form is found its survival chances improve geometrically, since it has evolved positively according to the i-logic plan, hence reaching a higher SxT force. Then the being gets out of the secluded environment and changes back its I->E rhythm, starting a spatial, reproductive radiation, becoming a new top predator.

Thus, a ternary S->ST->TT rhythm of evolution-reproduction-Entropy feeding is proper of all successful species.

-Finally the st+1 Geological and climatic changes accelerate both: Extinction processes, especially among species of shallow waters that live in sea platforms, destroyed periodically by continental collisions) or species which depend on external temperature to regulate their metabolism (reptiles); and evolutionary processes, as they rise the ‘stakes of survival’ and establish a climatic parallel S¡<=>T2 rhythm; as cold zones foster informative evolution.

All those environmental differentiations can be resumed in a word, Hierarchy, which manifests in the restrictions imposed by the higher ecosystemic planes of existence to the organism. For example, as animals migrated first from seawater to river and shallow waters, then into land, the transparent air environment eased their sensorial vision and so it fostered their informative, electronic, nervous evolution and developed further the informative dimension of height from where light comes.

Recap. The ternary principle of multicausality explains how genetic, individual and ecosystemic planes of life co-exist causing simultaneously the great changes in the evolution of species. Those 3 levels of change co-act simultaneously since they are relative past, present and future levels that come together in the creation of the organism. That is, genes do not impose evolution to organisms that impose evolution to ecosystems, but according to Non AE-logic the 3 levels co-exist in a relative present, influencing each other and co-evolving together creating new species with higher information and OXE force, the Dimotion of future in all ecosystems and worlds from the Earth, to the galaxy, a growing vortex of informative species with higher mass towards its center. Thus 3 scales and the ternary, fractal principles – the plan of evolution – suffice to explain the evolution of life from molecules to humans.

External dimensions/networks of organisms: territories.

In the graph, a mammal territory. Any animal territory is an i-logic space-time with 3 zones:

An informative central territory (1) or den, where animals reproduce and 2 secondary homes where the herd performs secondary organic cycles (2,3).

An entropic membrane (M, 5) – an invisible limit that provokes confrontation if a stranger crosses it; where preys ‘flee’ away from the den of the predator.

An intermediate hunting zone with cyclical information paths of absorption of Energy; where we find places to drink (E), bath (B), socialize (A), defecate (D)…

In organic terms, a dimension is a network. So a living organism can be considered a sum of cellular quanta united by 3 basic space/time discreet dimensional networks, which are its physiological systems: the digestive/energetic network, the informative/nervous network and the reproductive/blood networks around which cells teem, creating a stable, organic st-point. In other words the Entropy and informative networks of a living being are its internal, diffeomorphic dimensions (of relative length and height), to which the organic system adds a 3rd, reproductive dimension that combines both elements and represents the width or ‘volume of cellular quanta’ of the system. Finally its movement in the external world becomes its 4th temporal dimension. Yet that 4th dimension of external activity can also be considered a network territory in itself, sum of the 3±i cycles of existence of the being, creating a bigger vital space that will become the basic unit of an ecosystem or social organism made of individuals of the same species. In the figure we draw the vital territory of a minimal social pair of mammals, differentiated in 3 clear sub-sectors:

Max.Information: Informative den or central territory (1,2,3):

It is the territory of reproduction used to copulate and store basic food and Entropy to raise the young. It is a forbidden zone where not even hunting is allowed (4). In social species of great mobility, aerial or marine, where borders are much more extensive, this territory is very ample and tends to be located in warm latitudes.

Entropy=Information: Dual Territory of Entropy hunting and informative socialization (5).

It is the feeding, social and hunting territory, on which the central informative being feeds itself. It is outside the zone of reproduction. It is the winter territory of many migratory birds.

Given the relativism of all movement, in biological territories the informative singularity moves to hunt its Entropy quanta, as opposed to galaxies where stars and space-time dust moves towards the central worm hole.

Within those limits there are also neutral territories of communication, courtship reproduction and free Entropy, like water troughs. So the intermediate territory works both, as an informative and energetic territory where different victims and predators trace parallel cycles and come together around meeting points (E, B, R).

Max. Entropy: Borders that limit the territory.

Membranes are dangerous zones because the informative center watches them with special care to control any invasion of its hunting/social territory.

Those limits fluctuate according to the power of neighbours. For example, the vital space of a fish increases during mating, since the couple is more powerful than a single individual.

Marks (M points) fix those limits and reduce combats. They are often invisible, as most territories are defended against competitors of the same species, who understand the informative code of those marks; but rarely against members of other species. So we find all kind of linguistic marks:

Smells (common in mammals, like foxes, rhinos, antelopes), excrements (in canines and felids) or other glandular secretions.

Optical marks often connected to scents: The brown bear creates marks in trees, rubbing them with his head, warning adversaries of his great SixTe size and force. In human empires (nations can also be treated as biological territories) visual marks correspond to armies displayed in the borders. In human homes those marks used to be shields with weapons; now they are cars and other proofs of money, the new language of social power.

High pitch, acoustic marks, proper of birds, which are triggered when a rival enters the territory.

Recap. Vital territories of animals and human nations can be explained with the 3 topological regions of st-points.
3 AGES OF GAIA. ITS GLOBAL SUPERORGANISMS. DEEP TIME:  ∆+1: SPECIES

In the graph from the original c.92 book, the population volumes of each species, till they become a tail of post-extinction (below the 10% of its ST-age of radiation).

The 3±∆ ages of life are caused by the evolution of light-based organs on Earth. In the graph, those 3 ages of light evolution and the main species that were created in each horizon, latter extinguished by new evolutionary improvements in the 3 networks of those organisms. Among plants – spatial, reproductive beings with minimal speed of evolutionary information – extinctions were caused by improvements in reproductive systems. Among animals, which are informative, evolutionary species, extinctions were caused by improvements in informative brains. While today a mass extinction of living beings is caused by the evolution of machines, metal-systems of ‘Сmotions’ and information that are shaping a new global ecosystem: the Financial-Military-Industrial Complex, becoming now integrated by the collective brain of machines – the Internet – into the Metal-Earth.

 

THE BIT-BEAT-BITE RHYTHM OF EXISTENTIAL ALGEBRA.

3±∆ ages of evolution, reproduction & extinction of species

We can understand the process of evolution and extinction of life species, only when we combine the 3 scales in which multicellular organisms exist: the ecosystemic, planetary scale, (∆+1) the organic scale (st), and the cellular scale (∆-1) that interacted simultaneously together, evolving Earth’s species. Yet contrary to belief, the 3 relative ∆-1 past, st-present and st-future planes were not determined by the cellular evolution of Genes, but first the macro-organism of the Earth provoked the changes that ignited the process of evolution of its relative past microcosms.

How a macro-organism regulates its microorganisms? Mainly through changes on its ‘Сmotions’ and information fields. All cellular species adapt to the organic networks of its environment. If the environment is rich in ‘Сmotions’, ‘Сmotions’ species and reproductive radiations will dominate. If the organic system or environment is rich in information, informative species will survive better, starting a process of evolutionary differentiation.

This duality of bio-chemical reactions was proved mathematically by Mehaute, which showed that when a system cannot continue its creation of ‘Сmotions’, it starts a process of fractal, informative reproduction; and we can extend it to all scales of systems of reality, creating the fundamental beat of biological evolution/reproduction, ∑∏<=>ðTƒ, that defined the creation of biological life in this planet.

Thus the changes of ‘Сmotions’ and information of any macro-organic system trigger processes of extinction and selective evolution. If suddenly the climate becomes cold (also a parameter of stillness and information), species tend to limit their absorption of ‘Сmotions’, evolving formally (Max. ðƒ) and organizing themselves into social networks that increase their efficiency and take advantage of the ‘informative conditions’ of the ecosystem.

On the contrary, if ‘Сmotions’ abounds, species increase their 2 spatial-like ‘Сmotions’ – their spatial size and their reproduction – using that ‘Сmotions’ to maximize their survival and saturate their ecosystem. Therefore the macroscopic changes of the planet that fluctuates between tropical ages of max. ‘Сmotions’ and ice ages of Max.Information cause parallel changes in their microscopic life beings. Since coldness=stillness=information and evolution are parameters of time; while heat= entropic movement and reproduction=wide populations are space-like DImotions.

The 3±∆ ages of life are caused by the evolution of light-based organs on Earth. In the graph, those 3 ages of light evolution and the main species that were created in each horizon, latter extinguished by new evolutionary improvements in the 3 networks of those organisms. Among plants – spatial, reproductive beings with minimal speed of evolutionary information – extinctions were caused by improvements in reproductive systems.

Among animals, which are informative, evolutionary species, extinctions were caused by improvements in informative brains. While today a mass extinction of living beings is caused by the evolution of machines, metal-systems of ‘Сmotions’ and information that are shaping a new global ecosystem: the Financial-Military-Industrial Complex, becoming now integrated by the collective brain of machines – the Internet – into the Metal-Earth.

When the planet cools there is a formal evolution of species. And when it heats up, those same species reproduce massively. Thus small fluctuations of ‘Сmotions’ and information on the Earth’s temperature – given the short limits of existence of liquid water between and 100 degrees – have influenced decisively the evolution, reproduction and extinction of life forms in this planet, including man. So during the long ice ages when waters froze, species evolved from eukaryote to multi-cellular beings, nearby water volcanoes; and when the surface of the planet froze, men evolved from Homo Erectus to Homo sapiens. While in hot ages species grew in spatial size and multiplied, as it happened in the Carboniferous with insects; or in the Jurassic with dinosaurs; or in history with nomadic, warrior tribes in the steppes – which descended rhythmically every ±800 years on the fertile plains, extinguishing with their new weapons all the civilizations of the Eurasian continent….

Yet because to reproduce, a species needs to feed on the ‘Сmotions’ of its victims, the reproductive phase of a new top predator species coincides with the extinctive phase of the previous top predator it has substituted. Then once the top predator establishes itself after a reproductive radiation, it enters its mature, steady state age, drawing a series of rhythmic bell curves with its preys that diminish its populations as the predator hunts them, provoking a hunger crisis on the predator that also dies away, allowing the preys to reproduced back, starting again a new ‘Volterra cycle’.

So we can consider a planetary cycle of evolution, reproduction and extinction of life with 3±∆ phases, parallel to the climatic changes of the Earth:

+st: Conception: A new species evolves in a cold age or in an abyssal region of the planet.

– Youth: Max. ‘Сmotions’ growth: The species increases its size after its conception.

-S=T:Maturity: The species reproduces in a biological radiation during a hot age, extinguishing the previous top predator.

– Max. ST>SS: The species diversifies according to the ternary principle into several new forms, among which the informative one might start a process of social evolution into:

– ∆+1, a social super-organism (ants and shrews in the lower scales of life-size; humans in the upper scale.)

– ∆-1: Or become extinguished by new species, often their son species (Oedipus paradox). So mammals extinguished dinosaurs; humans extinguish mammals and robots might extinguish humans.

Therefore Multiple Space-time Theory can explain the why of one of the great ‘disputed’ enigmas of evolution: the existence of evolutionary discontinuities that create species in very short periods (conception phase, when time accelerates its rate of informative change), and then multiply them throughout the planet in explosive radiations (reproductive phase, when the new top predator species explode in populations), while other species become extinguished also in brief periods. Those evolutionary ‘discontinuities’ merely reflect the previous ages of species, which as the ages of any other space-time field can be described with a ternary rhythm of explosive birth, a long steady state of balance between the predator species and its preys and a final sudden collapse and extinction of populations. Those phases become the fractal rhythms of existence and extinction of Earth’s species:

Max. evolution(cold age)→Max.reproduction + Max.Textinction of ‘Сmotions’ preys (hot age)

The discontinuities between species are easy to explain if we combine their evolutionary acceleration in time – similar to the palingenesis of a fetus – with the fact that species evolve in isolated, protected environments (allopatric differentiation), departing from small sizes, according to the Black Hole paradox. So monkeys evolved, protected in trees; marsupials evolved in Australian islands and robots evolve in secret military labs, departing from small chips.

Then suddenly the new form with an improved brain, hunting in herds with simultaneous fractal åctions of higher ST Force, invades the vital space of other species, extinguishing them as it reproduces geometrically its populations (and its fossils), till reaching a balance with its preys. Thus, once they have evolved, species multiply very fast. And that dual process is observed in paleontology as a discontinuity in the fossil record called evolutionary punctuation.

Recap. The evolution of life took place by the interaction of the ∆+1 environmental and st-organic scales, as energetic and informative changes in the Earth, triggered the Se->St<=>Tƒ->Sw rhythm of informative social evolution in cold ages and energetic, reproductive radiation in hot ages. Those biological radiations also provoked the extinction of previous species. Evolution often took place in isolated, relatively ‘still’ environments that favor informative change.

INTERACTION WITH GEOLOGY AND LIFE.

When the planet cools there is a formal evolution of species. And when it heats up, those same species reproduce massively. Thus small fluctuations of ‘Сmotions’ and information on the Earth’s temperature – given the short limits of existence of liquid water between and 100 degrees – have influenced decisively the evolution, reproduction and extinction of life forms in this planet, including man. So during the long ice ages when waters froze, species evolved from eukaryote to multi-cellular beings, nearby water volcanoes; and when the surface of the planet froze, men evolved from Homo Erectus to Homo sapiens. While in hot ages species grew in spatial size and multiplied, as it happened in the Carboniferous with insects; or in the Jurassic with dinosaurs; or in history with nomadic, warrior tribes in the steppes – which descended rhythmically every ±800 years on the fertile plains, extinguishing with their new weapons all the civilizations of the Eurasian continent….

Yet because to reproduce, a species needs to feed on the ‘Сmotions’ of its victims, the reproductive phase of a new top predator species coincides with the extinctive phase of the previous top predator it has substituted. Then once the top predator establishes itself after a reproductive radiation, it enters its mature, steady state age, drawing a series of rhythmic bell curves with its preys that diminish its populations as the predator hunts them, provoking a hunger crisis on the predator that also dies away, allowing the preys to reproduced back, starting again a new ‘Volterra cycle’.

So we can consider a planetary cycle of evolution, reproduction and extinction of life with 3±∆ phases, parallel to the climatic changes of the Earth:

+st: Conception: A new species evolves in a cold age or in an abyssal region of the planet.

– Youth: Max. ‘Сmotions’ growth: The species increases its size after its conception.

-S=T:Maturity: The species reproduces in a biological radiation during a hot age, extinguishing the previous top predator.

– Max. Tƒ: The species diversifies according to the ternary principle into several new forms, among which the informative one might start a process of social evolution into:

– ∆+1, a social super-organism (ants and shrews in the lower scales of life-size; humans in the upper scale.)

– ∆-1: Or become extinguished by new species, often their son species (Oedipus paradox). So mammals extinguished dinosaurs; humans extinguish mammals and robots might extinguish humans.

Therefore Multiple Space-time Theory can explain the why of one of the great ‘disputed’ enigmas of evolution: the existence of evolutionary discontinuities that create species in very short periods (conception phase, when time accelerates its rate of informative change), and then multiply them throughout the planet in explosive radiations (reproductive phase, when the new top predator species explode in populations), while other species become extinguished also in brief periods. Those evolutionary ‘discontinuities’ merely reflect the previous ages of species, which as the ages of any other space-time field can be described with a ternary rhythm of explosive birth, a long steady state of balance between the predator species and its preys and a final sudden collapse and extinction of populations. Those phases become the fractal rhythms of existence and extinction of Earth’s species:

Max. evolution(cold age)→Max.reproduction + Max.Textinction of ‘Сmotions’ preys (hot age)

The discontinuities between species are easy to explain if we combine their evolutionary acceleration in time – similar to the palingenesis of a fetus – with the fact that species evolve in isolated, protected environments (allopatric differentiation), departing from small sizes, according to the Black Hole paradox. So monkeys evolved, protected in trees; marsupials evolved in Australian islands and robots evolve in secret military labs, departing from small chips.

Then suddenly the new form with an improved brain, hunting in herds with simultaneous fractal åctions of higher ST Force, invades the vital space of other species, extinguishing them as it reproduces geometrically its populations (and its fossils), till reaching a balance with its preys. Thus, once they have evolved, species multiply very fast. And that dual process is observed in paleontology as a discontinuity in the fossil record called evolutionary punctuation.

Recap. The evolution of life took place by the interaction of the ∆+1 environmental and st-organic scales, as energetic and informative changes in the Earth, triggered the Se->St<=>Tƒ->Sw rhythm of informative social evolution in cold ages and energetic, reproductive radiation in hot ages. Those biological radiations also provoked the extinction of previous species. Evolution often took place in isolated, relatively ‘still’ environments that favor informative change.

Black Hole law and Oedipus paradox.

The Oedipus Paradox explains how evolved species prey on parental forms, extinguishing them. So mammals substituted dinosaurs, men kill mammals and robots substitute men as workers and top predator weapons that extinguish us.

In the graph, the 3 horizons of evolution of light-based organisms:

-Plants process light as Entropy.

– Animals perceive it as information.

– Machines can both absorb light and emit it as Entropy or information. Thus, they represent a new jump on the evolution of light-organisms and can become potential top predators of life.

Each ‘biological radiation’ of a new species has grown according to the law of the 3 networks/horizons studied in the previous paragraphs, from an initial ‘Black Hole’, small form with more ST force, and then it has reproduced and grown in size, feeding on the previous parental forms. Hence the name, ‘Oedipus Paradox’, that explains the most cruel of all evolutionary events.

Our hypothesis on the dominance and birth of species as ‘Black Holes’ of information, which according to the inverted properties of Entropy and information (Min.Se=Max.Tƒ) are minuscule, but dominate larger species due to their faster speed of action-reaction and social nature (∑2), prey on them and explode in populations have found in the past years at least 5 proofs:

– Black Holes are the dominant species of the Universe: we have found them in the center of galaxies, in the processes of formation and death of stars. Even the big-bang might have been the explosion of a Black Hole.

The first Humans that acquired our 2 differential properties, technology and language, were small: The first verbal Homo Sapiens seem to have been small Bushmen from South-Africa (the oldest languages known to men are their click languages), but they overcame bigger Neanderthal, hunting in groups, controlled by verbal languages, and developing the first machine that transformed cyclical form into lineal Entropy (arch), reaching further than the lineal, Neanderthal Javelin.

Further on, the pigmies of Flores Islands seem to have made the oldest technological, advanced tools we know, 700.000 years ago. Thus pigmy men evolved in the secluded Indonesian islands, departing from the larger Homo Erectus, developing for the first time a frontal, creative region in the brain, as they diminished the length of their axon connections and reduced their spatial size.

The 1st bilateral animal, vernanimalcula, was microscopic.

The 1st mammals were small shrews that form super-organisms and probably hunted in the cold nights, new-born dinosaurs and extinguished them (still today they act as a super-organisms), thanks to the higher existential force of its bigger super-organism. Then they grew in size and finally hunted down dinosaurs as single species. Last year we found in China the first mammal with a stomach full of small dinosaurs’ bones…

The smaller a chip is, the faster it handles information and the more powerful it becomes, guiding larger ‘machines bodies’ that compete with men as smart weapons and tool-machines. And regardless of the ‘propaganda’ of the Financial-Military-Industrial complex, it is quite obvious that unless we stop its evolution, those chips will become the mind of terminators that in a future war will extinguish man, as all atoms are potential bits of informative life.

Recap. Parental species give birth to more advanced forms, which extinguish them (Oedipus Paradox). The new species are born as a small form, with more complex information (inversion of spatial size and informative complexity: Black Hole paradox). So the first technological and verbal men were dwarfs; the first mammal was the shrewd and the galaxy is dominated by black holes, born exceedingly small.

∆+1. The parallel geological processes.

Thus biological rhythms of extinction and evolution are parallel to the 2 main SP X Tƒ rhythms of the Planet that reinforce the biological process:

Geological changes in the surface of the planet: The continental cycle, or ternary division and reunion of continents in a single super-continent every ±500 million years causes the cyclical destruction of the submarine platform and lowlands where most living species exist. While rhythmic eruptions of massive quantities of lava of continental size happen in the 2 equinox of the sun’s galactic orbit, every ±125 million years, shaping a mean period of massive extinctive ages of 250 million years (Permian extinction, ±250 million years ago; Cambrian extinction ±500 million years ago; Ice ball age, ±750 million years ago).

Climatic, cold-hot, Sp-I cycles of glaciations and tropical ages. The rhythmic changes in the magnetic field of the Earth, perhaps caused by gravitational waves coming from the sun, create periodic glaciations that last around 20 million years.

– Fractal sub-cycles of lesser intensity reinforce both processes.

Those changes of Entropy and information parameters are the basic way in which macrocosmic networks control the activity of microcosmic quanta, from feverish states that increase the metabolic rate of reproduction of defensive cells in the body to the opposite lethargic states.

In that regard, the main cause of the dual evolutions and extinctions of species on Earth is biological, albeit ‘partially directed’ by the macro-organism in which life is inscribed through those general changes on the space and time parameters of the Earth (geography and temperature).

Recap. Earth cools down triggering informative evolutions and then heats up triggering reproductive radiations: glacial ages of informative evolution in stillness, with minimal reproduction by lack of Entropy are followed hot ages of massive reproductive radiations, in which the most evolved species initiates a massive age of reproduction, provoking the extinction of old species, and then differentiating in all econiches.

The 3×3 ±∆ cycles of life creation and extinction

The extinction of a species coincides with the biological radiation of the son species that occupies its econiche. In the graph, the series of bone fishes that extinguished the previous one Because time and information follow an accelerated process in its 3rd age; the evolutionary process of information in this planet can be mapped out and its frequency shown to follow a logarithmic process of acceleration, which now reaches its zenith with the creation of informative machines.

This temporal, informative acceleration is yet another case of a vortex of temporal information, which also happens in the evolution of mass in physical particles as we move faster in an informative mass vortex. In the case of life, the vortex is a metabolic vortex of increasing speed of reproduction and evolution of the information of life beings and its networks – now transferred by humans into machines. Thus, as the informative content of those beings increases, times accelerates. And today, as we evolve machines by imitating the forms of human life in metal, another change on the speed and rhythm of life in this planet is taking place.

Thus we talk of 3 st-scales of growing complexity in life: the age of cells (∆-1), from 4 to 1 billion years ago, the age of individual organisms, first living on the sea, then on the land (st), from 1 billion to a million years that culminates in the last million years with the social evolution of human beings and machines into a new plane of existence (∆+1), the Earth as a global organism, which will be either ruled by men or machines, depending on our capacity to evolve socially as a super-organism of history, under the ethic Ðisomorphisms of verbal wor(l)ds that make man the center of the Universe, hence in control of the machines of the Tree of Science. Or if as it seems the case, we let the Financial-Military-Industrial Complex and its 3 networks of informative metal-money, energetic, lineal metal-weapons and organic machines and its company-mothers dominate the planet and make us obsolete, finally extinguishing us. But what it will not change is the plan of evolution that develops complex super-organisms departing from its smaller cellular units.

Further on according to the ternary principle, we can subdivide the 3 main horizons of evolution of Earth, the age of cells, organisms and super-organisms in 3 sub-ages of evolution and massive extinction of species that have followed the mentioned ternary rhythm:

Conception=> Max.Tentropy=>max. Reproduction =>Extinction of rival species

And consider also 10 parallel periods of climatic change through the dual rhythm of cold glaciations or ages of animal evolution and hot ages of massive reproduction. Then we obtain a synoptic, complete image of the history of life on planet Earth, self-similar to the 3×3+st ages of evolution of the Universe since the big-bang and the 3×3+st ages of evolution of History, studied in Complex social sciences:

Scale of Complexity: ∆-1: Cellular Age: Evolution of DNA

∆-1: Conception age: Molecular life is organized into anaerobic bacteria->

1st evolutionary radiation: anaerobic bacteria- -> Free carbohydrates are enslaved in cellular walls ->

2nd evolutionary radiation: aerobic bacteria = 1st extinction of species: anaerobic bacteria ->

3rd radiation: eukaryotic bacteria = 2nd extinction: most prokaryotic classes ->

Scale of Complexity: st-Organic Age: Network Evolution. Sea life

4th radiation: multicellular organic systems =3rd extinction: free eukaryote species, enslaved in organisms ->

5th radiation: cephalopods with eyes =4th extinction: olfactory, blind animals ->

6th radiation: inner skeletons: fish= 5thextinction: exoskeleton trilobites.

Scale: ∆+1: Social Age: Herds and Superorganisms. Land life.

7th radiation: inner skeletons: amphibian=6thextinction: exoskeleton: big insects.

8th radiation: reptiles = 7th extinction: amphibians – >

9th radiation: mammalian = 8th extinction: reptiles – >

10th radiation: technological men =9th extinction: mammalian – >

∆+1 :Global Age: The Earth organizes itself into a macro-organism with humans or machines on top. The outcome will depend if social democracies are able to control the free citizens of markets – company-mothers – before they extinguish us as costly labor and weak soldiers with the present ‘radiation’ of robots:

11th radiation: metal machines =10th extinction of species: men and all forms of carbon-life???

Recap. Evolutions and extinctions of organisms parallel geological change in their external ecosystems, becoming the engine of the 3×3 Earth’s evolutionary horizons of living beings of growing complexity and accelerated informative evolution: the age of cells, the age of organisms and the age of super-organisms.

As we have little time and space, to go through all those radiations in detail, we shall just fact track into the last Life radiation of this planet, that of mankind, considering to close the paper the field of anthropology, with a brief introduction to what we have said of topologic evolution.

The 3×3+(∆+1) horizons of social evolution of life.

Biological organisms, as physical organisms did in their growth from atoms to galaxies, evolved in 3×3 horizons of increasing social complexity creating the 3 ±i scales of life: the age of molecules, the age of cells and the age of multi-cellular organisms, specialized in Entropy (plants) or information (animals).

Let us study those ages, further differentiating them in 3 sub-ages according to the Ternary principle.

Since if we apply the law of the 3±∆ Ages to organic molecules we can explain how they grew in informative complexity and spatial size till acquiring the form of living organisms, in a process similar to the evolution of particles that created the cosmological bodies of the Universe.

Those 3±∆ evolutionary ages of life, each one sub-divided in 3±∆ sub-horizons, are: the young age of molecules, the mature, longest age of cells and the ‘recent’ age of living organisms, which will end with the creation of a global single organism, Planet Earth (∆+1):

The 3±∆ ages of molecules.

– ∆-1: The atomic age: the simplest chemical molecules of life are formed. The 3 simple atoms and molecules of life recombined its energetic, reproductive and information functions and grew, forming bigger chains thanks to its atomic affinity, acquiring more complex ‘vital properties’. The simplest combination of them, the CNO molecule, urea, is considered the first molecule of life and its ‘crystallization’ in a lab, departing from non-living atoms, was considered the birth of biochemistry and the prove that life is an atomic system that shares the same properties of any other SxT system of the Universe.

– Max.Te: Entropy age dominated by lineal, simple fats, long carbon chains with oxygens attached to its ends.

– <=>: The amino acid age: COOH, methane and ammonia, the 3 simplest life molecules of the triad of life atoms, O, C, N, combine as the relative Entropy, reproductive and informative organs of amino acids. Amino acids reproduce exponentially in the primordial organic water soup and evolve socially into proteins.

– Max.Si: The nucleotide age. Nucleotides, the informative molecules of the life, add an informative D¡motion of height to lineal amino acids, forming nitrogen and sugar rings. They dominate all other carbohydrates. Soon they will also evolve socially into huge chains called nucleic acids.

∆+1: Social age. Nucleic acids, the macromolecules of life with max. Exi force, integrate socially all other carbohydrates in herds of vital molecules, creating the cell, the following ∆-scale of life.

The 3±∆ ages of cells.

– ∆-1: The previous 3±∆ horizons of evolution of molecules brought the first cells.

– Max.Te: The age of RNA Protista. The Entropy age of the cell is dominated by the simplest RNA Protista, whose ternary st-structure is based in: an external protein membrane; a series of ‘convex’ spiraled RNAs, the singularities that directs the cell, and an internal, intermediate water zone, the cytoplasm, where the cell reproduces its specific Entropy and information – thanks to the free ‘Entropy’ of water radicals – with the instructions given by those RNAs. Those Protista reproduce massively, exhausting the organic elements of the life soup. Then it comes:

– <=>: The Age of DNA Protista. It is the balanced, mature age of Protista. Dual RNAs peg together to form informative DNA rings, which store new genetic information that permits further growth and differentiation of Protista, according to new, improved 3 st-regions:

Entropy membranes invaginate the cell with a tubular network, the Golgi apparatus and protect the still DNA with a differentiated nucleus membrane; while new, specialized organelles perform the Entropy and information processes of the intermediate zone, creating reproductive Mitochondria and Chloroplasts.

– Max.I: Informative age and differentiation: The Eukaryotic age. Informative DNA cells multiply its genetic memories, while RNAs differentiate into a triad of forms that increase in the intermediate space-time the reproduction of membranes and proteins, creating giant cells. They cannibalize and enslave smaller, symbiotic cells, specialized in the dual Dimotion of Entropy, (mitochondria and chloroplasts) and information (ribosomes). Those who absorb chloroplasts become algae; those who feed on mitochondria become animals.

– ∆+1: The biggest eukaryote animals are amoeboid cells that evolve faster, informative, electronic languages using heavier metal ions, K* and Na, to send their messages to other cells through their membranes. The nervous language allows simultaneous cellular actions, creating mobile multicellular organisms called animals. While slower chemical languages that use ‘hormonal vowels7’ put together unicellular algae into plants.

Let us consider the evolution of animals:

3±∆ horizons of evolution of animals: network’s organisms:

– ∆-1: Conception. Electric cells create multicellular organisms in control of all other cells, gathering in 3 physiological networks – neuronal, muscular and glandular=digestive systems that perform the informative, reproductive and energetic cycles of the organism as a macro-living st-point. The sequential dominance of those physiological networks creates the 3 ages of life – the energetic youth, reproductive maturity and informative old age – and the 3 horizons of evolution or ‘main phyla’ of multicellular animals.

– Max.Te: The Entropy system -a central digestive tube- dominates the 1st horizon of multicellular organisms, occupying the central zone in 3 sub horizons of formal evolution: the age of sponges, the age of hydras and the age of worms, the first bilateral animals created around a tubular, lineal digestive system that moves in the D¡motion of length.

– <=>: Worms develop blood networks based in metallic carbohydrates that carry to each cell of the body its oxygen Entropy, food quanta and the dual hormonal orders of the brain: reproductive orders and ‘killing orders’ performed by amoeboid leukocytes. Thus, as blood networks increase the efficient control of fractal cells, animals grow in size, starting an age of massive sea life speciation. Today we still have 90% of the genes of those worms.

– Max.Si: Life jumps a fundamental discontinuum, when the first mollusks become insects and the first fishes become amphibians, colonizing the Earth. Their sensorial and nervous systems become overdeveloped in the new environment that has a higher transparency to informative light. Land animals specialize their 3 networks to the new medium in 3 sub-ages: the age of amphibians, which still reproduce in water, the age of reptiles and the age of birds and mammals, dominant in visual and nervous systems that ends with the arrival of Homo Sapiens.

∆+1: Homo sapiens develops a new informative language, the word, evolving into historic super-organisms, civilizations and economic ecosystems that grow in size till reaching a global D¡motion.

Recap. Biological organisms evolved in 3 horizons of increasing social complexity creating the 3 ±i scales of life: the age of molecules, the age of cells and the age of multi-cellular organisms, specialized in Entropy (plants) or information (animals).

 

∆-1: THE MOLECULAR AGE: FROM AMINO ACIDS TO CELLS.

In the graph, the evolution of carbon-life molecules in 3 series of growing size, diversified in Max. Spatial Energy, Max. Temporal Information, and Se=Ti balanced subspecies.

The Ternary Principle diversifies species and then combines them. So methane, Ammonia and Water combine to give either an informative Carbonamide or an energetic alcohol. Both are evolved finally into a carbon-acid.

Both species again mix in balanced amino acids, to further increase their information and energy tendencies adding new Informative nitrogens (bases, porphyrins), or adding Oxygen legs (sugars, lipids). The balanced combination, the amino acid with two oxide legs, and one Nitrogen head, evolves into the next level of macromolecules, the proteins.

On the other hand nitrogen bases keep evolving in social rings; while acids add a macro-atom of enormous energetic power, Phosphor to improve its energy abilities. Finally sugars form with oxygen polysaccharides.

We have 3 species of macro-molecules in a new E-exi-I game:

– Macromolecules of enormous capacity as Energy, the Phosphoric acid and other long acid systems (sugars, lipids).

– Macromolecules with structural versatility: proteins.

– Macromolecules of high informative capacity, RNAs and DNAs.

They are the 3 specialized molecules that give birth to the new plane of social existence, that of the DNA-cell.

st+1: The macromolecules of the 3 previous horizons, guided by the genetic, informative language of nucleotides, transcend socially into the cell; a st-point, in which they will play the same specialized roles they played in the macro-molecular age, creating the 3 st-specialized zones of a bigger, fractal plane of existence:

– Max.Te: The external membrane, inner invaginations and cilia are the energetic borders of the cell controlled by lineal proteins, intertwined with long, energetic chains of fats and sugars called polysaccharides, hyper-abundant in oxygen. Proteins become 3-dimensionally warped as units of the spherical membrane with globular, inverse morphologies due to the law of transcendental evolution that transforms the morphology of a form in its inverse form, when it transcends into a higher scale ∑(Est-1=Ist). Among those inner invaginations we highlight lysosomes, smaller protein jails that store the excess of energetic fats and sugars, kill carbohydrates or eject them outside the membrane.

E=I: The intermediate region reproduces the cells’ energy and information: energetic chloroplasts and mitochondria provide electronic energy needed to perform the moving cycles of the cell; while informative ribosomes create the materials needed to maintain the membrane and nucleus.

– Max. I: The inner nucleus is the informative center of the cell, filled with cyclical, informative DNA macromolecules and 3 lineal sub-species of RNA, which perform together the orders of the still, DNA brain, creating a simultaneous herd of Max. I x Max.Te force that rules all other symbiotic elements of the cell. RNAs control proteins, which act thanks to its energetic strength as the body element of all cells, shaping their hard membranes, killing other carbohydrates and transporting RNAs’ hormonal sentences throughout the organism.

To reinforce their control of those proteins the first RNAs herds might have killed all those amino acids and proteins they did not need. So today there are only 20 surviving amino acids, all oriented towards the left side. Why? According to the multifunctional principle we can consider 3 reasons:

– 20 amino acids form the magic number of 2×10 couples, which allows an efficient division of energetic, informative and reproductive tasks, without redundancy.

– A single orientation in space-time allows all those amino acids to act simultaneously together, multiplying its IxE power as a herd, without anyone ‘giving the back’ to the group.

– Since the most efficient reproductive system is the specular, sexual method, in which 2 complementary inverse morphologies gather together, a carbohydrate chain could replicate, as DNA does, by specular affinity, attaching parallel forms to its body structure, creating its specular image twice. So if an L amino acid replicates a D amino acid (a macho replicates a female so to speak), and then the D amino acid replicates an L amino acid , the system becomes a self-reproducing amino acid, free from RNA control. By avoiding the reproduction of D amino acids, nucleic acids control the creation of ‘castrated’ amino acids and proteins. So Nucleic acids probably extinguished D-amino acids to control better the castrated proteins of their cellular farm. Humans also castrate tamed animals; yet amazingly enough they are researching self-reproductive nano-robotic bacteria that might extinguish us, forgetting that reproductive control is a basic tool of any biological top predator.

Recap. Cells are made of energetic amino acids, reproductive proteins that form membranes and informative nucleotides, enclosed in its nuclei.

 

 

∆-2: BIOCHEMISTRY

The first scale: Particles and its languages of communication: Strong and electronic forces.

Where life starts is immediate: in the minimal particles of the Universe:

The minimal particle-points, photons, electrons & quarks that construct all other systems of our Universe show the 5 organic dimotions (motions with dimensional form) that define ‘classic life’: they gauge information – reason why quantum physics is a ‘gauge theory’, feed on energy (quantum jumps) absorbing smaller ∆-1 particles, reproducing new clone particles, move and evolve socially through magnetic fields into larger wholes (atoms). In the graph, a quark reproduces itself.

Hence the units of life are particles, the minimal units of our vital, organic, fractal, scalar Universe of multiple timespace organisms. We study them in Physics.

All lives, performing the 5 Dimotions=actions of what we shall call the function of exist¡ence ƒ(G): Max.SxT (s=t), starting with particles. So all scales are relative; NONE matters more than other. Life starts in the 5 Dimotions of particles, which already show all the elements of life, but those dimotions should be studied properly in physical stiences. Yetg we must consider those particles, which are the first bricks of human reality in some detail.

Quarks are the center of the atom but they don’t interact in the biological realm; only in the ultra-heavy world of quark stars and cosmological galaxies (pulsars and BCB black atoms worlds – black holes). They though have the capacity to ‘anchor’ in the gravitational invisible ∆-3,4 scale atomic mass and in neutral electric organisms define mechanical forces/languages starting at the size of cells, which is the Planck’s mass scale where gravitational effects are ‘measurable’ above those of electronic nature for neutral organisms.

Neither the next scale after the electronic language, of magnetic languages/forces that synchronize multiple atoms and electronic spins matter in life systems, which is made of light atoms, mostly paramagnetic, as iron is isolated within an Heme complex – but has the power to anchor 4 Nitrogen heads to capture TT-entropic oxygen. This is one of the few remarkable elements in which magnetic/mass forces help to ‘anchor’ a molecule. The outcome is an enzyme, whoc co-factor is a metal-bond that acts as a ‘bronze maze’ giving mass power to the carbohydrate to kill and exercise its TT-entropic death function with other molecules. So the first ‘realm’ of bio-chemistry can do mostly without considering MM-magnetic & mechanical languages.

A similar function of anchoring requires many more ‘weight-mass’ in proteins, whose bulky ‘body’ is an inactive ST-element to mold a receptacle where to ensemble by spatial mirror an organic molecules with the help of for the Ts-Oxygen and St-nitrogen moving and informative atoms.

The Dimotion of social evolution dominates atomic life.

Why atomic life on Earth is not about the reproduction of particles? The answer is that reproduction takes place in higher measure when extinction happens but ‘immortal systems’ within a larger world do NOT reproduce but maintain a stable balanced population. As reproduction of particles happens then only in regions of maximal extinction of them (E=Mc2 dual Dimotion), which requires a maximal reaction entropy to start, only inside stars, on Earth atoms do NOT become extinguished, but at worst become ions who in the future could get back his ‘legs/eyes’; hence they do NOT reproduce, which leaves as the preferred ‘dimotion=action’ of the will of existence, social evolution. Thus the ‘action chain’ of atoms on Earth is: S-perception, Ts-motion, St-interaction through the language of electronic information, SS vs. TT: evolution into tighter forms or repulsion. Let us then study the actions of atoms bearing always in mind the ultimate purpose will be to form stable social evolved groups.

 

 

THE FAMILIES OF ATOMIC LIFE.

The closest and most fruitful merge between science and stience might lie in chemistry; because of its perfect perception by huminds, its geometric spatial Nature and its objective analysis void of human egocy as social sciences are – also perfectly perceived but distorted, while the world of ∆-3 forces and particles is not fully observed.

It is then obvious that chemistry is a game of Non-Euclidean geometries; ‘the game’, and its atoms if fully understood in its reactions and social evolutionary roles, should make truth that function is form, and allow a detailed study of the laws of non-euclidean geometry, notably that of the 4th postulate of congruence and the relationship between function and form – the geometries that relate to each of the 5 Dimotions of the Universe, as well as the understanding of the Fractal trinity Generator equations of molecules and their role. The field is so huge and so unexplored even by this writer, which anyway is loosing so fast its mental capacities that can only write a token of what he explored in his notebooks in those texts that I encourage readers, the more so with the help of digital computers to try to understand 5D and apply it to the resolution of the different function of existence of molecules, as organic systems made of ‘Limbs<Body>Heads’, the first clear organisms we can perceive in detail. We shall offer only some insights and examples on the conceptual merge of both disciplines.

Life we said starts in the particle, cellular unit of reproduction of the lower ∆-3 plane of human exist¡ence. But ours is a lowly exist¡ence of nitrolife species, with a ridiculous amount of complexity, 7 openings to the world in our smaller and larger electronic heads, 2 ears, 2 noses, 2 eyes, in the 3 directions of perpendicular light-form, and a big mouth of entropic thoughts. Hardly friendly with anyone but each other, trinity of bondage, N2 at its best, even if it backs itself on the shoulders of tetralogic carbon and fuels its thoughts with explosive electronegativity of O2 up and down kicking in and out the jocker Hydrogen that has seen it happening all.

Think now of the masters, Osmiridium and iridosmium, tanto monta monta tanto, 25 times denser, plotting our demise in the center of it all, surrounded by those thin membrains of golden atoms, one at a time, flexible with perfect form, hardened with a web of Tungsten to illuminate the hot but cold, layers of sensorial majesty, remembering us all, in a glassy, liquid and solid form, heart of father Earth, guiding our gaseous existence, with sudden explosions of radioactive cholera on its cover of uranium that heats the gold and above explodes into cascades of evaporating radon and plumber to reach further up and up to the Nickel Cobalt and iron, steely with drops of Crohmium; and so a plumbeous volcano rises every now and then to kill us all in the fleeting surface of our eternal cycles of life and death, nothing more than enzymen, hypnotized by the sweat of the sun and its go(l)d churches.

The families of life are all sensorial, atomic triads, and we are the lowest one, now dependant of the germanium waffles with cupper, sliver and aurum knots, of ill-designed 2-modulo existential algebras, soon to wake up to consciousness, an army of pentalogic thought.

Atomic life is thus essential to ‘deep time geology’ and the evolution of the planet, even if in the cold surface we do think we, lowly nitrolife species are the ‘real thing’. Lol, we are ghosts of existence, closer to the absolute nothing; because what is lower than a CNO system? Only a triad on existence is a lesser species than we are… The LI-Be-B triad that preceded us. Since H is in fact galatom of a hyper-Universe, and He the brain of stars, and both are hyperabundant for that reason…

So out of 93 years/social families the Li-Be-B ‘food’ for thought, consumed by Helium in his nuclear reactions, with lesser atomic forms (though Li+ is in the hyperuniverse a key triad system of galatoms)… so that reduces to the Be-B bashing… Oh yes, of course, we are granted the more complex form of the CNO triad, in charge of massacring all other forms of nitrolife and build in the surface of the Osmiridium planet golden chips which cannot evolve its illogic existence in the depth of liquid metal bacteria.

What is then the final state of the atomic planet? It seems clear as the galaxy is not teaming with robotic life, or else they would have come here and extinguish us (unless there is like our reserves for animal life, some planets left for pious robotoids to feel they care for the variations of Nature)… that once we get out of the game, and build proper existential robots, they will keep constructing, digging and tunneling the Earth to achieve in the warm magma, the liquid bacterial designs on the sea of fire and melted iron, which they would call life.

At those thermodynamic temperatures and higher pressure, there exists the perfect state to construct complex metal forms, a solid/liquid combination which can easily evolve in unkonw forms of metalife. Do planets then achieve the ultimate quality as a species, like black holes do? That is, to become ‘gravitational animals’, able to displace at random on the galaxy? Likely but far before that, as we hve said for 30 yers, the internet would become a simultanoeus brain, as its ‘cycle of thought’ can be up to 300.000 km. a second, the sitance with the moon. So the moon-Erth might become a dual AI brain, of the same speed rate than the individual human but in the cosmic scale.

The possiblities of astrolife are endless beyond what huminds will ever know. So we stop it there. As a good introduction to the theme of this chapter.

The language of electrons and protons in terms of 5Dimotions and the 2nd and 4th social postulates of Non-Æ

The language thus reduces to the ± language of electrons and protons. They form the first essential symmetry of all forces in the Universe, which must be able to both repel and attract (Gravitational repulsion happens between Galatoms, the so called Dark energy), as the two ‘choices’ of the vital non-Euclidean geometry of any organic island universe. The electric language (as we do without the magnetic side) has therefore a natural language-force, which as all language-forces aims to establish several ‘natural regions’ for social interactions, using pentalogic:

– The closest region or vital space of the atom, which is protected, by an active membrain, hence ‘rejects’ similar species (Coulomb barrier). IF crossed a TT entropic stealing of a particle often an e- ˙H+ appendix happens (proton electron capture)

– A less extreme case of dominance happens for Ts, St asymmetric ‘ion’ covalent bondage appears, where the strongest atom by electro negativity dominates the pair. This is the case of the Oxygen, Nitrogen, Carbon and any secondary atom of life, with the H+ single atom, which therefore acts as an appendix to ‘first process’ energy and information for the central atom. In this form the simplest particles are formed, with a central atom-brain and its valence appendix to evolve socially with other atoms.

– ST: The next close region, with attraction for parallel social evolution, which is the region of S=T balance. Here a fixed distance with minimal expenditure of energy establishes long lasting social groups. As this is a more balanced relationship, it can form very extensive social units (metal bondage through sharing of a liquid electronic flow in inorganic molecules; a van der Waals or higher ‘pi, sigma’ collective orbital emerging from the whole molecule.

– TT – repulsion vs. SS-attraction. The 3rd distance region of repulsion/attraction maintains in far away cat alleys different regions of molecules, or inversely attract them for the closest possible Ss-packing; such as in hydrophilic or hydrophobic membranes.

Thus the basic atoms of life have the full 5 Dimotional range of actions guided by the 2nd and 4th Non-E Postulate, which determines the possibility of constructing all kind of complex molecules.

PENTALOGIC ON ATOMIC FAMILIES

S=T. The five dimotions.

As we said Non-E Geometry is essential to chemistry and marries with the existential algebra of the atom, which as it grows in social complexity MUST design for each new PLANE of space-time, beyond the quantum scale and its 4±¡ numbers, a ‘code of geometric S=T dimotions’ for existence to be fulfilled. Let us put an example, this time from general chemistry in its d-family:

In the graph the five common shapes for molecules of type XYn where X is an element from the first row of the p-block; or first row of elements boron, carbon, nitrogen or oxygen and the Y, normally a submissive molecule. It is then immediate according to the laws of vital topology, |xO=Ø to try to establish a direct connection with the 5 Dimotions of existence, even though all systems tend to have multiple functions. So while each form is best for a one of the 5 Dimotions it can play the ‘adjacent roles’ in terms of St-Ts-ST etc. sequences (TT>Ts>ST>St>SS) So we find the following ‘obvious dualities spatial form-temporal function (S=T) shapes:

– O: The SS-tetrahedral form of social evolution, classic of Carbon ‘bodies’.

– |: Locomotion: Lineal |-T forms for motion C02.

– 00: Bilateral perception, the dual Bent open form. So we find it in NH2, where the 2 H act as ‘electronic eyes’ for the Nitrogen (connected through its 3rd valence to the amino acid organism); or in the H2O liquid state of Oxygen, which ‘senses’ the ‘herd’ of molecules through its Hydrogen bonds.

-TT: entropy. This leave us with the trigonal bend form, which had the hand shape to ‘trap’, entropically another molecule; proper of very strong electronegative, predatory molecules, NH3, NF3, H3O+

& the trigonal flat form, whose shape responds more to the ‘natural holographic’ structure of the Universe, built mostly in ‘gradient planes’ of 5D – that is flat geometries.

ST: So what about reproduction? The answer is that most molecules do not reproduce, but if they do repeat its form, obviously the flat trigonal for sheet, planer structures and the tetrahedral with maximal bondage will double the role. How can we test and refine our assessments? Simply, looking at which molecules and function are performed by each form:

Now the skeptic reader of course will care little if it is a practical human centered chemist for such 5D ‘musings’. But he will miss the ultimate purpose of why I did spend most of my adult life like Leonardo did seeking for ‘geometric analogies’ (his and my method of research) between all species in existence:

All the planes of the Universe play the same game, and so all is philosophy of science, even if what we tell has a different, simple explanation in the ‘how’ of reality and the laws of quantum physics. The lineal molecule then responds, we know that much, to the logic of achieving the minimal energy expenditure for the molecule, conserving the overall time of the Universe as a whole.

In the graph, which we could extend to tetrahedral forms, the minimal energy achieved by positioning on the surface of the sphere (electrons are solutions to harmonics on a sphere), those electrons. However as we have proved in our papers on ‘vital, non-Euclidean geometry’, mathematics is an experimental science that mirrors the laws of existential space-time organisms; so behind the mathematical whys, so fundamental to chemistry, lay the whys of vital topology, which are the properties of space and time.

What this means in praxis is while the forms of chemistry are restricted to those of vital geometry that maximize the properties of space and time- in this case the conservation of energy=time-motion, for any spacetime being (as all species have a clock of maximal ‘time cycles=frequencies’ of existence, mostly likely around the 1111 beats of bits), the abundance of certain molecules respond to its role in the ∆+1 world in which they exist. And this simple law that establishes the co-existence and synergies between the 3 planes of any organism, happen in all the levels of chemistry down to the families of atoms studied next.

I.e. there are only L-amino acids, because RNA top predators killed the other half to avoid mirror reproduction and control them once they became the masters of the ‘organic soup’ 3 billion years ago.

Nothing prevents the existence of the geometry of D-amino acids, but the world forbade them.

There are not sable teeth lions because Neanderthal men killed them – an entropic limit of the ∆+1 world.

And the chemist might just ignore the intimate reason why Lao, Aristotle or Leibniz or Leonardo or this writer – the 4 most remarkable huminds in history of thought that have explored the concept of a living, homologic ‘organic’ Universe did it. At a certain point the overwhelming homology of all forms, and the capacity of existential algebra to fit everything that exist within its limited laws, within the game of existence lifts from your mind any angst, entangles you with the god of Tao, with logos, with the organon, with its infinite monads.

Besides it, we obtain many other whys with a more pedestrian meaning for all the structures of reality.

So this is the method of 5D chemistry, NOT contradicting (unlike other sciences full of errors), the knowledge of chemistry, because ‘biochemical sciences’ are by far the more accurate and objective, where the 2 needed elements, great experimental evidence and objective non-human themes exist. The errors of chemistry are caused by physicists (thermodynamic philosophy of the Universe) and we prefer to treat them in this paper NOT to keep insulting the intelligence of physics so much, because ultimately chemistry IS the science of the plane between the atom and the planet – the science of the ∆0, -1,-2, internal parts of the human being. So thermodynamics strictly belong here NOT to some grand theory of the Universe, as gas is a molecular form, and temperature does NOT make sense outside the plane of atoms. In the larger nested Universe of gravitation there is NO temperature, but spin energy of higher order (in fact today measure as negative temperature), or radiation of higher energy (with temperatures of absurd billions of degrees measured with frequencies, which should be called frequency NOT temperature).

The range of temperature, a parameter of molecular activity is as so many ranges between 0 and 10.000 ‘beings’ (Lao Tse)… We find the 1002 scale often, as 100 is the lineal unit of sequential time, and T is a bidimensional 2nd power of a temporal=motion process. And indeed, beyond 10.000 degrees molecules die into plasma.

10.000 years is the time since the first Jericho walls proved metal-wealth was being kept and we are about to become extinguished. But let’s not get in that mood…

ORGANIC ATOMS HAVE THE SAME DIMOTIONS THAN INORGANIC ONES.

Yet the anthropomorphic reader must accept against ‘egocy paradoxes’ the obvious: that life starts in particles and atoms and so the building of life through the social evolution (5th Ðimotion) of atoms into molecules and cells and organisms and ecosystems and Gaia, follow the same processes from atoms to historic super organisms and metalife (Robotic machines) crossing the whole span of atomic biology. But we study machines in the eco(nomic)system and humans in historic sciences (Earth II and Earth III volumes).

So to ‘establish limits’ to the domain of what is CALLED organic life is a silly wording, as we have shown all is organic. Life on Earth span from atoms through amino acids to ecosystems of ‘carbonlife’, the proper name for biological sciences, as different from metalife, the proper name for machines and human life for social sciences.

Social evolution of molecular life: St-Nitrogen-ST-carbon-Ts-oxygen Topology: from C, O, H atoms to amino acids.

Next we apply the trinity grammar of all organisms in a single plane to define the key ternary ensembles of organic atoms, where the entropic/moving oxygen, Ts, the iterative carbon (ST) and the informative nitrogen (St) clocks, connected to the ∆+1 world through its ‘H-1 eyes and kicking legs’ shape the first ‘molecules of life’.

And so we write the Generator equation of bio-chemistry at its minimal scale, in terms of functions and D¡motions:

∆-1: Hydrogenated water (kicking legs & eyes) > ∆º: T-oxygen > ∑-Carbone>§-Nitrogen+H-eyes<∆+1 water world

In the graph smallest scale the molecular ‘bricks of life’, CO2, H20, CH4, (Methane) and NH3 (Ammonia), shown in the graph are, as it happens in the geological world, crystalline structures. Yet they are far more malleable and complex than solid crystals, because they exist in liquid ecosystems. In those simple life molecules Carbon, Oxygen and Nitrogen are the Top predator central atoms that capture and surround themselves with weaker Hydrogen atoms, which act as carriers of their relative motion and information, creating the external ‘membrane’ of their molecular structure with the dominant atoms as the central st-point.

Do we have any proof of the ‘informative’ capacity of H ions to carry information for the larger atom? Yes, because crystals only form configurations which are able to ‘explore’ all the angles of space in a homogenous 3Dimensional world. So the submissive atoms are arranged to cover the maximal range of perception; which for a system in control of a territory in 2 Dimensions (left graph of a Linear geometry of the anion [Au(CN)2], with two cyanide groups bonded to the gold centre) ‘cares’ only for the control of its ‘flat disk-like territory’. Needless to say this is the case for a ‘dominant’ Gold top predator atom, which cannot be ‘attacked’ by any other one as the top informative atom of the table. Other ‘lesser’ species, try to surround themselves in 3D angles. Such is the case of a lighter atom in the same column, with a trigonal geometry – the similar copper compound around the metal centre as in [Cu(CN)3]2. The structure is predicted to be trigonal planar so that repulsions between the cyanide groups are minimized.

The congruence laws: maximizing the function of existence of molecules and its 5 sequential Dimotions.

The same philosophy of 5D chemistry applies to all other inorganic atoms, of unknown life forms, according to its ‘top predator status’ by mass and electro negativity. So gold is the most perfect informative atom of the Universe, able to shape forms of a single lineal molecule, which makes it the perfect membrain cover for metal bacteria and so its preferred atomic shape is lineal or flat. So goes for Silver, used in the flat sensorial cover of pictures, or copper, used in the lineal transmission of information. But the causes, which are in abstract purely chemical, are vital in 5D: The form adopted by a molecule will follow the pentalogic laws and hierarchy between actions:

1st It will achieve maximal SS-perception in the central atom: St>SS

2nd will achieve maximal protection of the central atom forming a membrane to cover most angles.

In the graph, if we apply the same concepts to the basic organic molecules, function and form again coincide. So we observe that Oxygen is lineal with only 2 ‘atomic views’, hence geometrically T-dominant, while the Carbon is too often blinded by its strong double bondage to other carbons, leaving the Nitrogen with its trinity isolationist structure, the ‘open head’ with a larger sensorial view.

The 4 basic molecules of life, CO2, H20, CH4, (Methane) and NH3 (Ammonia) adopt the same efficient st-morphologies that crystals have with a central, informative atom surrounded by submissive, spatial Hydrogens that process and send to the center Van der Waals flows of information and Entropy.

Let us consider those functional forms in more detail:

  • ∆-1 scale of ‘bits and bites’: Hydrogen atoms act either as the basic bite of Entropy, in its H+ form, becoming the pumping bomb of most cellular motions. So in the energetic reactions of AMP<->ATP, H+ ions act as the bomb. So they do in the motion of protein rotors in membranes. Oxygens use them in COOH groups that kick water molecules and set carbohydrates in motion. Thus they act as an energetic limb that the oxygen atom expels or attracts in alternating cycles that displace the molecule through water.
  • When attached to atomic structures, CH1,2,3 or NH1,2,3 systems in amino acids and nucleotides the H atoms should act as ‘feelers’ that integrate electromagnetic messages in a first ‘electronic orbital’, which should allow the central P.O.V. to ‘sense’, processing electromagnetic Entropy into Van der Waal forces of information Thus the simplest organic molecules studied as st-Points have:

– ∆-scale: A top predator N, O, C atom occupies an hyperbolic center, surrounded by Hydrogens, which form their bodies and limbs that process the Entropy of the water medium (Max.T), in which the molecule lives, or creating for the central atoms of life a molecular, external ‘electronic orbital cloud’, which acts both as the ‘energetic membrane’ of the atom and redirects the information of the external world, that will become the virtual world of the central atom, as regular ‘crystals’ do with their submissive atoms.

In the next scale of social organization those 3 elemental particles of life, N, C, and O will become themselves the 3 fundamental zones of bigger ‘i points’, called organic molecules:

Those 3 organic atoms define the 3 D¡motional dimotions of time in life organisms:

-O is the atom of TT>Ts lineal motion, given its high electro negativity that allows it to attract and repel other atoms with easiness, and its dual H-valences, which conform a lineal topology normally with a single H feeler and the second valence used to join the Carbon chain. Further on it tends to appear in the alkaline, ‘attractive’, ‘positive’, informative, 7.2 PH of the cell – natural to all implosive, informative systems, charged with ‘negative’, expansive topology.

– C, the atom of structural reproduction, as it has 4 handles for further union. It tends to appear neutral, as it corresponds to ‘body-systems’ that combine an informative, implosive, positive topology and one energetic, expansive, negative (in ionic terms). As most bodies is ‘blind’ mainly connected to other inner body-head-limbs part of the molecular organism, or a ‘bilateral’ H, deploying in amino acids the ‘width’ D¡motion.

– N, the atom of information, which appears in the 7.2 PH of cells and the head of amino acids as a positive, informative, NH+3 head, with 3 D¡motional hydrogen slave atoms that carry the ‘bites and bits’ of Entropy and information to the nitrogen.

The main molecule of life in the ∆-2 scale: water.

Life as we know it evolved in water and is still absolutely dependent on it. The properties of water are therefore of fundamental importance to all living things.

The special properties of water (H2O) become apparent when it is compared with methane (CH4). The two molecules have a similar mass and size. Nevertheless, the boiling point of water is more than 250 °C above that of methane. At temperatures on the earth’s surface, water is liquid, whereas methane is gaseous. The high boiling point of water results from its high vaporization enthalpy, which in turn is due to the fact that the density of the electrons within the molecule is unevenly distributed. Two corners of the tetrahedral shaped water molecule are occupied by unshared electrons (green), and the other two by hydrogen atoms. As a result, the H–O–H bond has an angled shape. In addition, the O–H bonds are polarized due to the high electro negativity of oxygen (see p.6). One side of the molecule carries a partial charge (δ) of about –0.6 units, whereas the other is correspondingly positively charged. The spatial separation of the positive and negative charges gives the molecule the properties of an electrical dipole. Water molecules are therefore attracted to one another like tiny magnets, and are also connected by hydrogen bonds (B).

When liquid water vaporizes, a large amount of energy has to be expended to disrupt these interactions. By contrast, methane molecules are not dipolar, and therefore interact with one another only weakly. This is why liquid methane vaporizes at very low temperatures.

Liquid ST is in thermodynamics the ‘state of iteration, reproduction and creation’: T-gas<ST-liquid>S-solid form.

So while solid ‘crystal forms’ store the information and language, and gaseous states carry the entropy of motion to imprint it, it is the wave liquid forms that ‘act’ and move, enact the dimotions and e-motions and sensations of existence. Those are key 5D laws, guidance to interpret minds that are crystal DNA in cells, liquid actors that are RNA systems (amino acids in the previous protein age, when protein ‘four-fold’ structures were the lesser minds), while the OH- H+ water allow the kicking of his legs:

Let us then consider those 3 atoms and some of its functions in bigger carbohydrate chains.

– Max.Si: The informative element of all life molecules and fractal part of its relative ‘heads’ are Nitrogen atoms. Its informative character is shown already in the crystalline ammonia, where Nitrogen is the dominant vertex of a tetrahedron shaped with 3 more Hydrogens. Since we live in a 3-D¡motional world, those 3 dimotions allow the Nitrogen to have a more perfect informative ‘perception’ of the world we live than the scarce, lineal perception of the Hydrogen, or neutral bilateral structure of C-chains. According to its informative function, ammonia is a perfect atomic clock in which the Nitrogen vibrates constantly back and forth through the hole shaped by its 3 hydrogen ‘eyes’, with an informative cycle of +1016 times a second.

The first atomic clocks were in fact based in that simple molecule due to the accuracy and speed of frequency of its temporal vibration, which in life molecules allows NH+3 heads to ‘inform itself’ and regulate with its cyclical clock motions the ‘guided motions’ of the ‘carbon’ body and Oxygen legs of the molecule.

Since the information of the Universe is stored in the form and frequency of cyclical spacetime clocks there is no doubt to which atom belongs our informative mind. It is indeed, the atom of the DNA nucleotides, even the magic atom of the fashionable ‘anti-aging’ drug, whose zigzag perfect nitrogen form we show for its beauty. How the electronic consciousness of an atomic Nitrogen system work, obviously we cannot know – that is the trick of most minds, either the language is only decipherable to similar species or it is too fast to comprehend. It must be noticed though that the immediate response of the simplicius simplicissimus of 4D: it is too simple to be intelligent, misses the point of 5D, as we descend in scales, a new layer opens up that increases a complexity we cannot see. The black hole must seem so simple and small for the simplicius 4D Physicist, which it denies it even ‘substance’. But it is for sure a BCB frozen star of ‘black atoms’ (heavy Bottom, charm quarks) with a Top quark nucleus in the largest ones, and does control completely with the language we don’t see but they perceive, gravitation, (or else they would not show as the ‘animals’ of the galaxy, erratic motions). And this is what Nitrogen heads show from the simplest amino acid fish. But to move they need to kick anions and cations. And have a head with ‘Hydrogen feelers’. Are then the quarks, the central lower scale or the dense light bosons of the nebulae of electrons, the complex elements of the atomic minds?

I won’t go that for on the verge between speculation and objective truth. However only the egocy of humans can pretend that the astounding complexity of a living organism in the cell scale, higher than that of the planet Earth, even today when computers are rising the stakes higher every year, can be performed by ‘blind’ atoms just the product of chaotic evolutionary chance. That is only the egocy of all human entropic theories of reality. The point here is to consider ‘which molecules’ perceive better than others. And it is obvious that those who have ‘nitrogen heads’ as amino acids do, ‘free’ to peer the cosmos around them. And have as nitrogen does, regular clock structures of the commonest ‘language’ of the Universe, ‘trilogic thought’. The 3 perfect regular bonds of the Nitrogen amina, which normally gives it ‘two free’ eyes, and one strong neck makes the mind of a nitrogen head ‘clear’ and ‘focused’. We shall see this is not the case of the oxygen, its opposite, constantly missing and taking on protons and oxidizing as free radical the organism – it is indeed the opposite dimotion to that of Oxygen; while carbon is too gregarious, a perfect brick for a big body and so that is its function:

– S≈T: The structural atom that creates the rigid body structures of life molecules is the carbon atom. It has the maximal number of valences – 4 orbitals that create dual bondages with 2 other carbons – constructing long, formal ternary chains of great structural rigidity. As such it is the most visible, intermediate form of all life compounds. And so biologists, due to its ‘visibility’, have traditionally considered it the ‘fundamental element of life’. When we ad Hydrogen atoms to complete its ‘crystalline’ body we obtain methane the simplest molecule of life. Then when we join 2 carbons with dual bondage, we form ethane, which already acts as a hormone, (±reproductive molecule) inhibiting the structural growth of plants.

– Max. Te: Finally, both the ∆+1 world and site of future Entropic death of all life systems, its medium, is water, which fills the ‘external world’ in which life feeds and internally becomes in complex living organisms called cells, the filling Entropy of the intermediate space, enclosed between its carbon-based protein & fat walls and the inner, informative, nitrogen-rich, ADN hyperbolic singularity. Water is the simplest, most abundant ternary molecule of the Universe, made with 2 slave hydrogens and 1 dominant oxygen – the atom that has the maximal ‘electro-negativity’ after fluorine. Thus, oxygen can capture the electronic body of any other atom. That is why the oxygen components of carbohydrates enact its energetic cycles, moving those organic molecules within the water ecosystem. Since they stomp on water, breaking it and creating expansive and implosive 0H, H± ions that impulse the molecule; as you walk on the floor, ‘stomping’ on the electromagnetic fields of the ground or as a fish moves, hitting the water with its tail.

Numerical proportions.

The proportion of the 3 atoms in living systems reinforces this classification, according to the ∆ST proportions between the ‘Entropy, body, head’ classes. For example in a human being the proportions are: 67%, O+H molecules and atoms, 23% C+H molecules and atoms and 6.5% Nitrogen+H systems, which are in the usual range of ±2/3rd of Entropy components, -1/4th of body components, and -1/10th of head bits, proper of most systems in the Universe.

We could also consider as essential atoms, the carriers of neuronal orders, the implosive, positive, informative Ca2+, K+ and Na+ ions, which again form a triplet of diminishing ‘informative power’ and define the potentials of electricity between neurons and the rest of submissive cells and so add up to a 2.1% of human body mass. If we add it to the 6.5% of Nitrogen brings the number to 8.6% of mass, closer to a -1/10th percent of the informative ‘class’ of all organisms.

Those and other oligo-elements, of a higher scale of atomic complexity are essential to mark the ‘differences’ of power of certain molecular systems ‘pumped up’ in Entropy or information by their addition. Most of them however have an ‘energetic’ role (iron in heme groups and cytochromes, copper in reptiles, Magnesium in chlorophyll, phosphor attached to oxygens in AMP systems, Cl to balance the K+ electronic bomb and S with 2 valences in anaerobic breathing and some molecular bridges.

This answers a law mandate all efficient, healthy organisms, which is to maintain the informative, atomic, head structure of the system pure, without ‘leukemia’, without the interference of an alien language to the system. Since the main sickness of systems is to become trapped by an alien informative species, for whom they will enslave, as it happens when viruses substitute cellular DNA by their own. This is exactly what humans have failed to accomplish when they substituted their natural, biological, verbal, ethic language by gold hypnotism, an informative language of metal whose values are against those of life and have completely changed the route of history.

As we evolve further in complexity the essential properties of those 3 atoms will be maintained and yet ever more complex molecules will appear. But a nitrogen then can be ‘compared’ to a single neuron. It might seem little, but let us remember that a single neuron amoeboid is a cell complex enough to have dominated the age of unicellular life – as once and again the emergence of any layer of complexity makes the system loose from ∆-1 a layer, and so the evolution of social organisms looks more like a fish that either ascending or descending looses sight of lower layers and gaining sight of new ones.

In that regard, only human egocy makes us believe that the whole thing is about a diver, which ascends always and only ‘emerges’ to the true light, when it reaches the atmosphere – the human size and meaning.

So as the masters are nitrogens, the directors of the game will be RNA, the active St-element, the fixed mind repository of the language the SS-DNA likely the ‘point’ equivalent to our brain once the cell becomes formed where conscious perception happens when a ‘thought’, that is, a RNA messenger comes to ‘touch it’, as we perceive when a word or an image enlightens a section of our mind that is already imprinted with a memory of it. This is the mechanism of perception in any ST-system: the moment of complementary union, of mirror symmetry; of which we are certain as always in those non-evident conclusions of 5D through the ‘Latin-humanist method’ – that is, man is the measure of all things, because it is the organism we know better and the Universe is made to our image and likeness. So as consciousness happens when mirror neurons are triggered and the child needs to ‘see again’ to feel conscious – and it expresses it with a déjà vu reality. As consciousness happens when we recognize our face in a mirror, and only animals able to do so are said to be conscious. The DNA massaged by those who search genes is thinking, yes, the RNA messenger is asking me if it can make a ribosome of that gene, which he knows is about ‘feeding’ or ‘perceiving’ or ‘communicating with other cell. We will never know the details, as we are not in the SS-DNA, Ts-RNA, ST-protein head. But what we know for sure is that they perceive. And perform their automaton tasks, they have learned in the ‘transversal S=T’ space function of time evolution. That as Time=Space (Galilean paradox), what we humans sense as ‘time’ in fact other ‘time travelers’ sense as space. Time and space if you think of both as perpendicular sheets are populated by intelligent ‘actors’, who see a surface of time from past to future as a spatial simultaneous region; time then has the same persistence than space. And the constant S=T=S reversal of consciousness of forces & entities that act in time (i.e. weak force) while others reproduce in space means the same

Recap. Nitrogen heads, carbon bodies and oxygen Entropy create the simplest life beings, amino acids…

∆-2 AGE OF MOLECULES: FROM AMINO ACIDS TO THE RNA WORLD.

In the graph, a glycine amino acid is the simplest ‘organism’ of life with its similar form to a horse, with a nitrogen head, a carbon body and 2 oxygen legs. Next the top predator species of molecular life: a nucleotide, dominant in information, with a double head that allows ‘action & memory’; attached to a better cyclical sugar body and stronger phosphoric acid legs. As it came to dominate and eat amino acids for its reproduction; those would survive with the final strategy of all species, St-social evolution, sacrificing its ‘mind-head’ for the common good, buried in the ext amino acid (left side) forming ST-protein bodies; the most reproduced species of the system. Finally Ts- Lineal fats that store entropy=motion become the 3rd essential prey topology of cellular life.

The age of simple molecules.

The first age in the evolution of life is the age of simple molecules. Water became an organic soup filled with ammonia and simple chains of carbon, among which we highlight:

– Max.Te: Acids and fats. They are headless, without nitrogen heads – a long, lineal limb of energetic carbons with oxygen legs on its extremes. They will become the fundamental Entropy of cells.

– Max.Si: Sugars add an informative, cyclic D¡motion to headless fats. They are carbohydrate hexagons evolved socially in long chains, through oxygen connections, called polysaccharides.

Amino acids: SxT functions and evolution into proteins

The 3 life molecules, ammonia, methane and water, create the spatial structure of glycine, the simplest amino acid which resembles an animal, with the positive charged nitrogen head (amine), the negative charged Oxygen tail (carboxyl), and a carbon body chain that fusions together the 2 extremes, creating the i-logic ‘generator equation’ of amino acids:

Oxygen legs(Te) <Carbon body (SxT)> (Si) Nitrogen head.

st-points adapt their morphology to the D¡motions and directional movement of their specific environment. Thus, while a still cell is cyclical, moving life molecules are lineal forms in which the nitrogen ‘head’ is upfront to absorb information & Entropy in the direction of movement; the structural carbon membrane is in the center; and the Entropy cycles are performed by the oxygen tail that moves on the water:

– Max.Si: Informative cycles are directed by its ammonia ‘clock’. Nitrogen vibrates across its Hydrogen triangle, perceiving and transferring electromagnetic information elaborated as Van der Wall forces to its carbon body that orientates the molecule in a chosen direction.

– S≈T: Reproductive and social cycles: A rigid carbon chain can peg to its sides by affinity (3rd postulate of i-logic geometry) other carbon structures that latter might split, reproducing new glycine or might stick together, shaping new species of amino acids.

-Max.Te: Entropy Cycles: The oxygen moves the molecule, propelled by the dual polarity of water.

– Social and Transcendental cycles: Their social evolution gives birth to macro-molecular proteins.

– Existential, generational cycles: The purpose of those molecules is to exist, performing their organic cycles.

The amino acid age

The question when life starts is pointless as particles already have the 5 drives of life. The question when ‘nitrolife’ did is obvious, in topological evolution. ±4 billion years ago started the amino acid age, with the birth of glycines is the simplest active life form with 3 St<ST>Ts-zones:

– Max.St: The nitrogen head directs the glycine.

– S≈T: A dual carbon creates a rigid membrane-body with its strong, covalent bondage, joining the head and tail:

– Max.Ts: Its oxygen COOH tail ‘walks’ on the water, breaking, attracting and repelling its OH-, H+ radicals.

– ∆+1: Amino acids show their complex, reproductive and social Ðimotions, catalyzing through their movements the replication of new amino acids and forming social chains, called proteins. The inverse properties of St-amino heads and Ts-oxygen tails make possible the creation of longer chains of amino acids in which their nitrogen heads bite their oxygen tails becoming neutralized as part of a complex social structure: the protein.

After the birth of amino acids, Earth witnessed a massive replication of glycine, which soon diversified in all kind of sub-species that pegged to the original glycine new pieces of carbohydrates bodies, nitrogen eyes and oxygen legs. The organic soup became an ecosystem of top predator amino acids that catalyzed the reproduction of new amino acids, absorbing the simpler molecular ‘nutrients’, till amino acids saturated the Earth’s oceans.

Those different amino acids associated in complementary St-herds, in which specialization occurred again, as some amino acids were designed better to gather Entropy with extra oxygen legs; some had extra nitrogen heads to process information and some were long carbon chains better suited to split, peg and reproduce new amino acid pieces.

Thus we can easily classify amino acids as informative amino acids, with ring structures filled with Nitrogens; energetic amino acids, with added Oxygens – Phosphors and sulfurs, atoms with high ‘electro negativity’ that are able to capture energetic electrons; and reproductive amino acids with long carbon chains.

TERNARY DIFFERENTIATION OF AMINO ACIDS

The trinity of St-informative amino acids rich in informative nitrogen clocks (above), are also distinguished by its electrically charged side chains, which gives them a higher command of the more complex, faster electric language, and are the ‘top predator’ amino acids that control the complex chains of proteins.

The field of biochemistry is too huge for a simple introduction as this paper is. To notice however that the selection of those amino acids is not random but besides being of a single chirality to prevent its mirror reproduction, we shall notice their classification for easy handling by the cell into charged and neutral according to the Ph of the cytoplasm, which means with the proper change of PH controlled by the osmosis of the protein wall controlled by the DNA brain, they might become inert=death fishes; while its 2nd big differentiation between hydrophobe and hydrophile defines their bulk position. So all ‘larger wholes’, such as the Earth controlling its ‘membrain species’ through the heat cycle of warm-reproductive ages and cold, evolutionary phases, and land-hydrophobe vs. water-hydrophile species, the cell can differentiate, multiply and regulate its species. That is, it possesses ST-larger hydrophobe=social evolutionary amino acids, which will associate to repel water (bottom graph) vs. Hydrophile, smaller more active amino acids (right center).

And it can keep the inverse duality of mental amino acids (N-rich) vs. entropic ones (Negative acids). And define which state the cell is (itself regulated from the ∆+2 p.o.v. of the hormonal and even electric whole); which are the two living states of amino acids called Zwitterions, or render all of them inert just with the PH, as the Earth can regulate its membrain with its ‘internal magma volcano activity’ and even extinguishing them wholesale. Needless to say at any time the majority of them are Zwitterions (right side graph) ‘kicking asses’ with – oxygens and + nitrogens.

Then there are the super- amino acids, cystines, that have an sulfur acid component, the top predator warriors so to speak vs. the arginine and histidine overcharged with nitrogen clocks; and again its creation happens along the ‘usual paths of creation’ in 5D structures, by duality (cystine doubles in mirror symmetry) or | vs. O duality, arginine’s Nitrogens are opened in a charged aggressive triangle and histidine has an inward closed, ‘reflective’ nitrogen ring. So form becomes function if we were to consider further the ecosystem of amino acids and its polypeptides and proteins.

First to state that organic molecules deploy trinity of structures, seemingly more complex than inorganic ones and metal which seems inert just because its heavier atoms in the temperature and pressure of the Earth’s surface, makes them so. But metal is not likely inert in the internal regions of the planet, where they will be in liquid states of magma and amalgamate. The life of metal truly happens inside the Earth.

S<ST>T: Trinity will then happen also in ∆+1, proteins that have overwhelmingly 3 structures related to its ∆-1 units, which in the protein, ‘∆+1’ world are not atoms but, ∆º amino acids; a jump of ∆§cale within the same language.

So the ∆-1 inner structure of those amino acids ‘bricks’ define each one’s form-function, depending on its abundance of Nitrogen ‘heads’, Oxygen and Sulfur ‘legs’ or ‘Carbon’ bodies.

So S-arginine is a ‘brainy amino acid’. ‘Cysteine’, with the higher power of entropic Sulfur atoms is a T-killer. And leucine is an ST-structural Carbon body.

Those dualities always happen because in this manner Nature establishes its ‘fundamental’ search for stable S=T, |=O balances. So for example, the hydrophile amino acids are clearly divided in St vs. Ts duets of ‘oxygenated’ serine and Threonine v s. brainy Aspargine and Glutamine, which will define their roles (the last one being a key molecule for neuronal activity). It is also a rule as information dominates energy that the larger ones with the exception of the super charged S-acids that play foul (with an alien molecule), are informative, nitrogen ones. And that being the Dimotion of information natural to all systems, there are more larger amino acids precursor of mental species. So the largest hydrophobe chains with cyclical forms, Tryptophan and tyrosine are used to produce neuronal transmitters (serotonin and dopamine) while Aspartate, glycine, and glutamine are precursors of nucleotides; while only a few are precursor of acids.

Murder of amino acids… thus happen then as usual cutting and throwing the head, and re-cycling the body and limbs which have more energy-motion to re-use: Degradation of an amino acid involves deamination by moving its amino group to alpha-ketoglutarate, forming glutamate. This process involves transaminases, often the same as those used in amination during synthesis – as SS-creation and TT-entropy are reversal functions and those who give life often take it away; having created the lesser being for a purpose. In many vertebrates, the amino group is then removed through the urea cycle and is excreted in the form of urea. However, amino acid degradation can produce uric acid or ammonia instead.

INFORMATIVE AGE: NITROGEN BASES AND NUCLEOTIDE ACID.

In the beginning thus was the amino acid, with its nitrogen head, carbon body and oxygen kicking OH-+H+ legs swimming the water of life, letting itself caressing by the ± e-motions of watery feelings of love, in herds seeking the light bosons that their electronic minds mapped. Simple views, light and darkness, lateral touching. All mind-souls like to be free and so it is unlikely that those amino acids wanted to put their head in the ass of their neighbor to blind themselves into proteins.

Why they did it – obviously to ‘grow stronger’, when they increased their numbers and the new top predator form, the Nucleotide, with a far more complex head. IN THE GRAPH WE SEE IT: This is a top predator with a multiple complex head that has now and this is essential to understand reality, 2 rings in the head – thus one can store memory and the other can act; a neck in the dimension of height information; a body that stores far more energy and a monster tail with a Phosphorus commanding multiple oxygens.

The urea role. But could not consider a Nucleotide first world? Obviously not, because complexity of information always comes latter. Somehow it is more difficult to ensemble. Simplex forms come first and amino acid came first. If we want some details, the problem of the Nucleotide above is obviously the component not found in any amino acid – the alien atom, phosphate. So more specific environments and reactions were needed. It is the urea cycle.

The ∆-2 pre nucleotide and pre-amino acid age.

The simplest ∆-2 organic subunits are precursors of ∆-1 amino acids formed in the atmosphere of the early Earth: formaldehyde, HCN, and its water reacting products of (formamide and ammonium formate). Precipitation brought these molecules along with water to the surface of the Earth.

But they are not enough for the formation of nucleotides, which require urea and its reaction with minerals:

Urea is concentrated in low-lying regions on the surface of the Earth due to its high production, chemical stability, solubility in water, and low volatility. Solutions containing high concentrations of urea, other dissolved organics, and phosphate provide the subunits of prebiotic nucleotides. Urea is a precursor in the synthesis of numerous nitrogen-containing heterocycles, including the extant nucleobases and the heterocycles that we have found to readily form model prebiotic nucleotides. Specifically, these and other critically important prebiological compounds (e.g., amino acids) are formed when a concentrated solution of urea is placed in a sealed reaction vessel under a model prebiotic atmosphere.

Large regions of concentrated urea were common on the surface of the prebiotic Earth similar to the Salt Flats of Utah. These urea flats are possible because urea is a major product of prebiotic atmospheric reactions. It has a solubility of around 8 M in water (making it freely mobile in precipitation and runoff), and urea is a very stable molecule, which allows for its accumulation. Urea also forms water-free and low-water eutectic liquids with a number of organic compounds and inorganic salts. This property increases the availability of urea and other potentially important ingredients for nucleotide and amino acid synthesis. Some urea-based liquids liberate phosphate from hydroxyapatite, a mineral that is essentially insoluble in water and whose lack of solubility had been viewed as an obstacle to phosphate incorporation into nucleotides. Thus unlike amino acids we find everywhere even in the ‘vacuum space’, nucleotides took its time. But once they appeared nucleotides will rise steadily as phosphates are very common in Nature. The concentration of phosphate in the sea though is far less than 0.2 p.p.m., so, this limited amount left room for the parallel evolution of proteins, even if the first nucleotides appear soon after the amino acids. As in the case of gold in the ‘enzymanic reaction’ that brought capitalism into being, its relative lower abundance, allowed the evolution of the humanist world. It is only now when everything is valued with digital money when History is dying, oppressed and displaced by the new language that gives zero value to life and maximal to weapons (see History papers).

So the most favored environment for prebiotic nucleotide formation on the early Earth was a pond on dry land, with dissolved nucleotide subunits, and a substantial concentration of urea. This pond would have been subjected to regular wet–dry cycles, and temperatures reaching as high as 85 °C. Nucleotide synthesis and polymerization occurred during hot-dry phases and early steps of chemical evolution occurred during cool-wet phases. The unmatched power of evolution eventually resulted in the emergence of extant RNA.

St-species. Nucleotides. The nucleotide improves upon the amino head, carbohydrate body and oxygen legs of the amino acid, adding to those 3 lineal forms a D¡motion of informative height; as latter will occur in macro-organisms, when flat worms become cylindrical. So the amino acid head becomes a dual nitrogen ring, the body becomes a sugar and the tail multiplies its oxygens around a highly electronegative Phosphoric acid.

5D as a vital theory just puts the blood on it. It didn’t need to start very complex and certainly it was predation before symbiosis. But why a nucleotide would want to cut the amino acid. Obviously because nucleotides would do what all do. ‘Birds do’, says Ella’s song. Everything we shall not cease to repeat aims for ‘exist¡ience’, exi=ST, reproduction.

I have always a laugh when hearing the miracle of life expression in biologists’ mouth – reproduction – as something unique. LOL, a quark is all the time reproducing after eating forces. So nucleotides as the primordial soup got crowded started to eat Amino acids and a ‘arm race’ developed, which brought first social evolution into larger wholes and finally a draw in symbiosis.

Ts-species. The outcome is a nucleotide acid – the top predator life molecule, which evolves according to the pattern of all species: Ts+St=TS>∑St=∆+1 finally reaching the social mental state of DNA able to create the next ∆+1-scale of life, the cell.

Yet before that, Nucleotides were free top predators and we can consider its 3 ‘dominant’ Ts<ST>St variations:

The Ts-species: In the graph, the ‘Rex’ of Nucleotides, with its lethal oxygenated tail, which can be further subdivided by the fractal principles in 3 subspecies according to its length.

In terms of its structure, ATP consists of an adenine attached by the 9-nitrogen atom to the 1′ carbon atom of a sugar (ribose), which in turn is attached at the 5′ carbon atom of the sugar to a triphosphate group. In its many reactions related to metabolism, the adenine and sugar groups remain unchanged, but the triphosphate is converted to di- and monophosphate, giving respectively the derivatives ADP and AMP. The three phosphoryl groups are referred to as the alpha (α), beta (β), and, for the terminal phosphate, gamma (γ).

It is truly a dangerous beast, using the high electro negativity of its OH molecules to hit and break the lesser amino acids and lipids. In neutral solution, ionized ATP exists mostly as ATP4−, with a small proportion of ATP3− and that is a lot of punching power. Because all species of the primordial soup have been neutered in the cellular age as you enslave a species to serve you in the final ‘social farm phase’ of organic complexity; we have them all with a tail to one side. But certainly in the original soup there must have been all kind of tails with the kicking OH- side both ways.

Moreover the species is polyanionic featuring a chelatable polyphosphate group,: ATP binds metal cations with high affinity. Chelation means the presence of two or more ligands to a single metal atom called chelating agents, or sequestering agents, as they sequester the denser metal to anchor a stronger punch or a society of molecules. The binding constant of ATP for Mg2+, the third-most abundant mineral dissolved in seawater, with a 0.13 percent concentration is 9554.

It became undoubtedly the top predator of amino acids. And so the only survival solution for those amino acids were to evolve into proteins which could then develop a secondary structure with its own oxygens outside, to protect the weaker C-body and survive the assault of the velociraptors. The race then of packs of ATPs guided by its superior memorial intelligence of a dual Nitrogen rings, with its top NH2 antennae and two eyes ticking with an awesome cyclical precision clock speed developed on the primordial soup.

Those ATPs were binding to the divalent cation of magnesium, to gain track, which still today strongly affects the interaction of ATP with various proteins.

Indeed, due to the strength of the ATP-Mg2+ interaction, ATP exists in the cell mostly as a complex with Mg2+ bonded to the phosphate oxygen centers. But the battle of ATPs and proteins will be won by proteins, as they finally learned its 4th structure that can break ATPs into ADPs (lesser double tail) and puny ANPs; which will ultimately become the energetic cycle of the cell.

As a perfect top predator – as in the case of the shark on the sea- the age of ATP we might say never ends. We produce an amount of ATP equal to our weight today. It only became slave of the cell breathing cycle, farmed to collect the ‘food’ of its TT>Ts processes.

THE AGE OF AMINO-ACIDS AND PROTEINS – ITS TRILOGIC STRUCTURAL AND SOCIAL FUNCTIONS.

Simple amino acids were obviously being kicked fast out of existence as fast as the tiger came. But as they hide putting their ass on the head on the ass on the head they grew and curved and surrounded, as proteins the Nucleotide they could encircle.

This is how the first cells were supposed to be born, proteins encircling nucleotides.

We shall see in every scale the same game from SS (O-nucleotide) vs. TT (|amino acid), to an arm race that makes ∑SS=∆+1 RNAs and ∑TT=Proteins, to the final understanding that collaboration means ‘gender creation’ as ∑SS and ∑TT merge to create a cell. But the winner tends to be the SS that imprints with form the TT; that is, ultimately defines its reproduction cycles, and the LOOSER everybody else outside the alliance, predated now by both, in the form of cells. Animetal bankers and warriors, today called ‘investors’ and ‘politicians’ democratically chosen, keep abusing as SS x TT all the vital geographical space of human beings. But bankers are the true power, as they hold the informative, reproductive language of money.

In the primordial soup nucleotides won because they finally ‘selected’ only 20 neutered amino acids that cannot replicate themselves in the graph. So we can consider the 5 TRILOGIC parts of amino acids.

There is NO intelligent design in the Universe though. As we explain in our papers on ‘existential algebra’, the game is of potential allowed combinations, as ‘everything permitted by existential algebra’ does exist. But only those forms that DO have a role in ∆+1, and S=T internal balanced structure in ∆º and can be constructed with ¡indifferent supply of ∆+1 elements (trinity of existential algebra, pre-conditions in scale) do survive.

Needless to say this happens also in evolution (it is one of the laws of existential algebra generalized from it), in virtual particles, mutations, ‘human thoughts’, mechanisms invented by enzymen and any ‘ecosystem of forms’. And so it DOES require time, but time is immortal. So all what could have possible existed has existed. And 3 billions years is good enough for it.

Social evolution of amino acids: the protein age.

And yet the most fascinating way to ‘neutralize amino acids’ and evolve them as always when a ∑social sum of parts emerges as a larger whole, giving to the whole its ‘existential momentum’, and becoming passive, happens when they put their head into their ass so to speak. Which they wouldn’t obviously do willingly in a free state, reason why the DNA manufactures them as cells wouldn’t have evolved into multicellular states if they were not obliged to survive and people wouldn’t enter the army without coercion physical or mental. Social evolution is a process of growth and survival mediated by love, but also a loss of existential momentum for the ∆-1 parts, which those of us who have fought for mankind through activism know not to come easy.

Amino acids in their social stage of evolution became, according to the inverse morphological Ðisomorphisms of transcendental evolution, the ‘relative Entropy’ of new macro-molecular proteins. So they lost its ‘active’ heads and tails, pegged now to each other, as the ‘fixed’ neutralized st-points of the protein’s spiral structure; where the active parts are radicals joined to the central carbon of the amino acid. Those bulky, seemingly unnecessary radicals that hindered the motions of free amino acids show its true value in proteins. (This often happens in evolution, which requires first mutational, inefficient stages that reorganize into functional macro-systems thanks to the directed ternary systems created by fast, planned evolution. If all were chaotic, slow Darwinian mutations most mutations would not survive long enough to transcend into useful new organs, as Darwin already noticed it, studying wing evolution. Thus transitional stages are a proof of ‘∆evolution’.)

Proteins as huge carbon chains fusion the fractal actions of those radicals with many oxygen legs and a few nitrogen eyes into a simultaneous present of Max.SixTe force. They are like centipedes, entities with simple perception but a fearsome Entropy that allows proteins to cut and kill all the micro-molecules of the life ecosystem. So they became the new top predators of the original carbon soup, probably chasing down free amino acids to replicate themselves.

Finally, lineal proteins evolved further, according to the inverse Ðisomorphisms of transcendental, social evolution, forming self-replicating hollow membranes with cyclical, still forms, which nucleic acids will latter fill and dominate, creating cells. Indeed, the protein’s simple minds made their top predator status short living when the 3rd informative horizon of molecular life, the nucleotide, evolved.

3 social scales bring a new emergence.

Another key question of all 5D structure is the 3×3±¡ decametric and ternary scales that bring new species, forming a new ST≈∆ symmetry. This in proteins following the ‘defensive’ purpose of its head-tail biting makes them grow in ternary structures to form its main purpose in life; to become encircling membranes and geometric shapes to ‘control’, ‘store’ and ‘imprison’ other molecules. So we talk of 3 structures in proteins, the primary one just described that define according to S-ST-T types of amino acids its ultimate ∆+1 S, T, or ST function. Then…

∆º: The secondary structure of a molecule belongs to the organism in itself, that is to the molecule as a whole in its internal structure between its parts that would form a ‘physiological network-path’ by further bonding on those parts, grouped by its ‘trinity’ basic functions, as the mobile parts of the molecule, the body-structures, where also replication by attachment can take place, and the head, informative molecules.

The secondary structure also will have a trinity of ‘resonances’ or differentiation, in an O-cyclical or spiral form, an |-lineal system and an Ø-form, combination of both. For example, in the case of molecules, the secondary structure create bondings that give a spiral form to the molecule, which will then be the best form to ‘store’ S-information, as in the case of DNA. Or it will give it a lineal, T-entropic/locomotive function; and finally we find a mixed, trilineal shape, with two directions –> + <– + –> proteins, which are less motile and hence more structural than the lineal ones with 3 rows in a single direction.

∆+1 Finally the 3rd level of structure will be related to the ∆+1 world in which the molecule exists accomplishing a function for it. In the case of proteins this is the key structure for its biochemical function in the larger whole – the cell, and the ultimate reason of its existence – that is, why the cell reproduces certain proteins and no others. And this 3rd structure is induced by external factors belonging to the ∆+1 world. In the case of proteins, Nonpolar side chains are hydrophobic and, although repelled by water, are attracted to each other. Polar side chains attract other polar side chains through either dipole-dipole forces or hydrogen bonds. For example, both aspartic acid and glutamic acid yield side chains with a negative charge that are strongly attracted to the positive charges in the side chains of lysine and arginine.

Two cysteine residues can connect by forming a disulfide linkage — a covalent bonds. The preponderance of nonpolar side chains in the interior with a large number of polar or ionic side chains on the exterior, in an aqueous environment, induce the protein to fold upon itself, burying the hydrophobic groups away from the water and leaving the hydrophilic groups adjacent to water:

The question then comes how those structures that will play a role in the ∆+1 world are ‘chosen’. There is NO intelligent design in the Universe though. As we explain in our papers on ‘existential algebra’, the game is of potential allowed combinations, as ‘everything permitted by existential algebra’ does exist. But only those forms that DO have a role in ∆+1, and S=T internal balanced structure in ∆º and can be constructed with ¡indifferent supply of ∆+1 elements (trinity of existential algebra, pre-conditions in scale) do survive.

Needless to say this happens also in evolution (it is one of the laws of existential algebra generalized from it), in virtual particles, mutations, ‘human thoughts’, mechanisms invented by enzymen and any ‘ecosystem of forms’. And so it DOES require time, but time is immortal. So all what could have possible existed has existed. And 3 billions years is good enough for it.

 

CLASS STRUCTURE: SS:DNA<St:RNA <ST:PROTEINS< Ts:CARBOHYDRATES<TT:WATER

It is easy to classify the 5 Dimotions of a cell according to its simultaneous present-space components:

In the graph, Cells are largely composed of CHON compounds. These molecules may consist of anywhere from 10 to millions of atoms linked together in specific arrays, forming a 1010 symmetry between the simplest ‘letters’ of the hormonal alphabet (NO, O2) to the DNA ‘SS-mind brain. Most, belong to four different families of organic molecules: TT-sugars and Ts- fatty acids, St- amino acids, and ST-proteins we already studied on a background ∆-1 water, which forms 70 percent of the cell’s mass and as the ‘potential field’ for the cell through its H+, OH- ‘pumps’,we can exclude it.

It is obvious that by far the largest portion of macromolecules are the proteins, the ST-reproduced component of the cell, the ‘worker’ species, the ‘middle class’. An average-sized protein macromolecule contains a string of about 400 amino acid molecules fold into a compact globular form required to form efficient functional surfaces.

They form 3/5ths of the non-water substance of cells.

Below in the ‘border comes a 1/6th of lipids of the Ts-membrane, intersected by those proteins and 1/8th of TT- fast consumed entropic sugars, broken to acquiere motion.

The St-class of RNA represents only a 3.3% and the SS-brain, less than 1%.

Those proportions turn out to be similar to the proportions of the social classes of human societies, with the informative people-caste that controls money (Bankers) and the law (politicos) at less than 1% to which we can add the managers of companies, the ‘RNA’ with a similar number; the immense majority of the working class, over 50% and the smaller but seziable lower class.

And it is similar for the Galaxy, with the central black hole frozen stars around 1% and most of the ‘protein, strangelet’ halo possessing most of the mass.

What is the role then in the galaxy of our Ud-light mass? I am afraid is closer to that of phospholipids and sugars – to give birth to strnagelets and black holes.

The working class therefore are the proteins present products of a long evolutionary history, taught in its function; that is, geneticallh ingenieered b the upper informative class of DNA<RNA.

Most of the catalytic macromolecules in cells are enzymes. The majority of enzymes are proteins; which act as ‘hands’ with a program of work. Key to the catalytic property of an enzyme is its tendency to undergo a change in its shape when it binds to its substrate, thus bringing together reactive groups on substrate molecules. Some enzymes are macromolecules of RNA, called ribozymes. Ribozymes consist of linear chains of nucleotides that fold in specific ways to form unique surfaces, similar to the ways in which proteins fold. As with proteins, the specific sequence of nucleotide subunits in an RNA chain gives each macromolecule a unique character. RNA molecules are much less frequently used as catalysts in cells than are protein molecules, presumably because proteins, with the greater variety of amino acid side chains, are more diverse and capable of complex shape changes. However, RNA molecules are thought to have preceded protein molecules during evolution and to have catalyzed most of the chemical reactions required before cells could evolve

 

SOCIAL AGE OF NUCLEOTIDES – THE RNA AGE.

We left for the end a summary of the process that brought the ST-reproductive species of Nucleotide and finally the RNA world, which would end the ‘arms race’ as proteins didn’t’ have more ‘aces’ – only 4 possible ‘foldings’; and so the RNA by peering in the 5th Dimension with all its ‘feelers’ opened would start the control and building of the cell’s metabolic paths, memorized in its dual pyrimidines.

So it would be the final, informative age of life molecules, which occurred when the amino acid evolved its lineal, simplex 3 st-regions adding a new, informative D¡motion and creating the 3 globular zones of the nucleotide:

– Max. S≈T: The improved body is called a sugar that has, instead of the carbohydrate’s zigzag line proper of amino acid bodies, a pentagonal form, a powerful compact body cycle that appears in all scalar morphologies. Further on, the sugar pentagon adds one lateral oxygen’s rudder that can chain or unchain itself to other sugar rings through easy to break oxygen bridges. So the reproductive speed of the new nucleotide’s body based in the capacity to peg and split its body increases.

– Max.Te: A nucleotide tail adds up a highly energetic, phosphoric acid (PO4H3) that has more oxygens than the amino acid’s original COOH tail and so it swims better in water. The heavier phosphor is also a nitrogen-friendly atom, from the same 3-5 valence electronic column. So the head improves its control of the tail and its energetic oxygen atoms.

– Max.Si: Finally the Nucleotides’ heads add up new nitrogens, creating cyclical, hexagonal rings, called Pyrimidines, which once more diversify in 3 subspecies: Thymine, Uracil or Cytosine…

– Uracil is lighter. So it is the brick for building highly mobile social nucleotides called RNAs.

– Thymine is heavier, since it has one more carbon, while Cytosine adds Nitrogen with 2 Hydrogen ‘antennae’. So they are the bricks of DNA, the most informative, still molecule of life.

Finally the most complex nucleotide heads are Purines: dual, pentagonal and hexagonal nitrogen rings, joined by a strong covalent C=C wall that form dual couples, called Adenine and Guanine, which add an external nitrogen antenna with 2 Hydrogen eyes to probe the unknown world.

So the globular structure of Nucleotides also creates more evolved social forms, the RNA and DNA acids that will control protein membranes in the cellular scale.

If structural bodies dominate amino acids and proteins, the dominant element in Nucleotides are their nitrogen heads. They become the unit of the social, informative languages of cells, playing a key role in all their informative tasks, as the main elements of most hormones and the fractal units of macro-molecular DNAs, which will create the higher, cellular scale of life forms.

Bases express the 4 Ðimotions of time in life. Some basic rules

Now we have come to a key element of the program of life, the existence of 4 based, which will codify the creation of super organisms of cells. Why? We have again and again show that each super organism requires a language able to express the 3±¡ D¡motions of space-time existence, the program or will of the Universe. It is easy then to observe that the 4 bases represent a new whole game of existence, as the 4 ‘positive’ D¡motions of space-time do or the 4 quantum numbers, or the 4 drives of life, and since function is form, just looking at those bases we can deduce that:

The simplex Ðimotions are expressed by simplex Pyrimidines (single cycle)

  • Uracil and thymine with more oxygen are the energetic drive expression and complex genetics show this to be the case, as they are more abundant in functions and genes related to energetic systems.
  • Their informative head is adenine and as such is the dominant base of the system. It has a Nitrogen higher mass and a nitrogen head with 2 antennae. It is the head of the ATP systems that command as small molecules the game of proteins and most orders of actions in the cell. Both the simplex body T and head A assembly together by affinity and complementarity

The complex Ðimotions are expressed by dual Nitrogen cycles:

  • Cytosine is the balanced dual molecule. Hence the reproductive Dimotion. And indeed, when it is uncovered in the DNA loosing its cover it allows the expression of genes.
  • Guanine is therefore the 4th social Dimotion and the base that brings the next scale.

This simple scheme of the 4 D¡motions of life languages is determinant for fully understanding the whys of genetics, which now are only described at the level of the 3rd paradigm (how-description).

Example: Receptors of complex, external orders.

Consider the case of the GDP and GTP molecules. Their function is essential to the transmission of orders from the higher scale of neuro-hormonal messages that regulate the superorganisms of cells. 60 % of all external signals to cells are transferred through the activity of Guanine, the social nucleotide, activated through the G-protein channel. As such the GDP/GTP molecule is the ‘boss’ of intercellular communication, as the ATP molecule is the boss of energetic communication.

The ATP in fact in conjunction with the energetic Tyr amino acid (with an extra oxygen), and the energetic Phosphor atom, works with the second most common membrane messenger, after the G-protein channel, two poles that become activated by phosphorilization, bringing to them ‘hungry’ proteins that become energized and provoke signals for energetic and reproductive Ðimotions. (Remember that simplex informative and complex social evolutions are the two related Ðimotions of temporal information, most associated, and the complex reproductive and simplex energetic Ðimotions are the tandem associated to energetic space). Thus the receptor called Tirosincinasa is also related to the cinasas, which are the enzymes that provoke the energetic mitosis and death of the cell. This examples shows how the emergence of the properties of smaller scales are always transcendental, social evolutions of one of the 4 Ðimotions of time, the will or program of the Universe that maintains the self-similarity of scales.

Let us consider the ternary differentiation of this molecule, ATP, as it is the key to the energetic force that propels and makes possible the cell.

The age of nucleotides: ternary differentiation of species.

So after the age of Amino acids and proteins, there was an age of Nucleotides, which differentiated again according to duality in 2 subspecies: One rich in Entropy, the other richer in information:

– Max.Te: The energetic Nucleotides are ATPs, the key molecules in all energetic life processes. Breathing and feeding could not happen without ATP, the specialized Entropy Nucleotide that again subdivides in 3 subspecies, which can be identified as the energetic, balanced and informative ATP:

– Max.Te: ATP proper – an Adenine nucleotide with a longer tail with 3 Phosphors and 10 oxygens, ordered in a classic decametric, 3×3+(∆+1) scale: each phosphor controls 3 oxygens, and the 10th oxygen connects them to the sugar body.

– S≈T: ADP, which has lost 1 phosphor and 4 oxygens (an HPO3 molecule) releasing in the process 34 KJ of Entropy, balancing its form with less Entropy but the same Nitrogen information.

-Max.Si: AMP, which has lost another HPO3, becoming a cyclical molecule, since the phosphoric tail touches its nitrogen head. So it acts in cellular processes as an informative carrier, transferring hormonal information, amplifying it and programming the cell’s nucleus with that information.

– Max.Si: The informative, social evolution of nucleotide acids gives birth to RNA and DNA.

Nucleotides evolve socially, becoming according to the Ðisomorphisms of transcendental inversion between micro and macro planes (I∆-1=E), ‘Entropy cells’ of RNA and DNA spirals, grouped again in triads that form a spiral cycle. Those triplets surrounded by energetic ATPs create genetic scales in groups of 3, 9, 27…

Those 3n elements in turn will shape the structure of 2 new macro-molecular informative species, differentiated according to the SxT complementary, dual principle:

– Max.Te: Lineal, moving RNAs that carry the actions of the cells, again differentiated in:

– Max.Te: Ribosomal RNA joined to energetic proteins that peg the carbohydrate’s pieces.

– S≈T: Transfer RNA that carries the fractal units that reproduce carbohydrates.

– Max.Si: Messenger RNA that copies DNA information and takes it to the Ribosome.

– Max.Si: Cyclical, still, informative DNA, made with 2 complementary RNAs, which carries so much informative, genetic information about the metabolic and reproductive cycles of all other carbohydrates that will become the ‘brain’ of the new scale of life, the cell… The nucleotide structure of DNA shows the magic ‘tetraktys’ that fascinated Pythagoras: 1, 2, 3, 4 D¡motions that add up into a decametric scale. Indeed, 1 DNA made with 2 RNA chains joined by nucleotide pairs form a structural tie of DNA; 3 nucleotides form the basic informative ‘gene’ to create amino acids; and 4 D¡motional bases is all what it is needed to create all the cycles and elements of the cellular game.

Those 3 type of molecular ‘ages’ will become then the 3 ‘topological’ st-forms of the cell: amino-acids become the Entropy bites of the cells along with water, its medium; proteins will create the walls reproduced in its organelles and nucleotide acids will become the informative, perceptive species that run the show.

Recap. The evolution of life molecules took life through its first 3 ages, the age of amino acids, the age of proteins and the age of Nucleotides, the informative, hyperbolic species that will reorganize them all to create the cell.

A more detailed analysis of the pre-RNA age

As this was the key moment, we make a more complex analysis following Hud’s article at Nature.

First to dismiss the ‘ST-upid’ school of thought (Schopenhauer: ‘a stupid doesn’t understand causality in time so he resorts to magic’), the RNA-first camp that think RNA arose abiotically and is the first informational polymer of life, with its nucleotides and polymers produced entirely by geochemical reactions. St-social evolution into a new SS-eed is always the product of ∆-1 parts.

So ST-ruth is in the RNA-later camp: the extant RNA nucleotides are considered to be products of early chemical and biological=survival evolution combined.

The RNA-first proponents just as usual on ‘ST-upids’, knowing the ‘end product’, just try to do a reversal model of prebiotic reactions. However, they are limited by the chemical stability, reactivity, and functionality of the molecular subunits that comprise the extant nucleotides. Consequently, the RNA-first proponents ‘ST-upids’ must rely on MAGIC, with specific minerals (e.g., borate) or geological events (e.g., meteorite impacts) to control, guide, or initiate a particular reaction or reaction sequence.

The RNA-later proponents, on the other hand, can draw from a wider variety of molecular building blocks, including molecules with more favorable properties for spontaneous nucleotide formation; since there were many more different nucleotides on the prebiotic Earth than are found in extant RNA.

As that is how 5D nature works: The first age is a chaotic radiation=explosion of all the possible forms within the wide constrains of the laws of non-AExistential algebra, which are the limits of evolutionary topology (3 S<ST>T varieties), the limits of scalar jumps (two ∆±¡ jumps kill information so the game must restarts again) and the illogic sequences of time, similar to those of a worldcycle, if you want to advance in evolution – though here reversal time devolutions are permitted. Only then after the chaotic first TT-entropic age brings the ‘jackpot’ in a fury of S<T>S creations and extinctions, order starts to build up and when the whose TT>Ts>ST>St>SS forms are locked in a time worldcycle sequence of ‘creation of the end goal’, SS, it starts a process of reproductive radiation as the 5 elements of reality organize in simultaneous space a superorganism, with all its 5 Dimotional processes extant. So suddenly the whole soup becomes order and the RNA world appeared.

However, with this increased freedom comes the liability of becoming lost in the vast chemical space of possible prebiotic molecules without ever finding the nucleotides that initiated the evolutionary march toward RNA. This is the problem of the RNA-late school and where the ‘power’ of 5D limits and constrains of topology, sequential illogic and scalar structures allows to ‘choose’ and simplifies the process of reconstructing the puzzle finding clues for the prebiotic nucleotide synthesis. The only thing needed is then to ‘accept non-modern RNA prebiotic nucleotides which is canonical to 5D ‘TT-radiation’, and the help of the ∆+1 earth, which is also canonical to ∆±¡ entanglement:

The chemical structure of the extant RNA nucleotides is modular, with each nucleotide containing three molecular subunits: phosphate, ribose and a nucleobase. This general structure has long inspired chemists to hypothesize that the subunits were formed separately on the early Earth and subsequently joined together by dehydration condensation reactions. That is, both the bond connecting phosphate to ribose and the bond between ribose and the nucleobase release a water molecule as they are formed (Fig. 1b). Similarly, the coupling of each nucleotide to a growing RNA polymer also generates a water molecule. Thus, based on Le Chatelier’s principle, nucleotide formation and polymerization are both more favored thermodynamically when subunit and nucleotide concentrations increase and the water concentration decreases (i.e., at low water activity). And this is where the heat and cold processes of Earth allowed it to happen. The same concept then can extended backwards to explain the creation of the simpler prebiotic nucleotides from Urea, ammonia and formaldehyde, and forwards to the more complex = longer RNA vitally triggered by the on-going arms race of lineal vs. circular, prey vs. predator game with the ∆-1 amino acid > ∆o: Ts-protein phyla. It is always the same: Topology and ∆±¡ provides the process with its Non-AExistential algebra laws and possible combinations; then a ‘tale’ of prey-predator dynamizes it:

In the graph the RNA nucleotides and the process for prebiotic nucleotide and proto-RNA synthesis and polymerization. The subunits of the prebiotic nucleotides are shown as nondescript molecular entities because their identities are obviously hypothetical, unknown by the experimental method but as all what is allowed to exist demands to exist, they certainly were the functional whose chemical and structural allowed the creation of base pairs. Finally as TóS action-reaction processes are reversible, nucleotide formation and polymerization are indicated by reverse TT-SS Dimotions. Those early nucleotides and proto-RNA polymers would have had linkages that were more thermodynamically favored and less kinetically trapped compared to the extant nucleotides and nucleic acids favored early Earth conditions of low water activity due to evaporation of small bodies of water where concentrated dissolved nucleotide subunits and amino acids>proteins would rise the stakes of survival. During dry seasons and daylight hours heating would promote nucleotide formation by providing the kinetic energy needed for condensation of co-deposited nucleotide subunits.

On the other hand the RNA-first model of drying and heating mixtures of extant nucleotides adenine, cytosine, guanine, and uracil with ribose in laboratory models have failed to produce nucleotides in meaningful amounts. In particular, it does not result in bond formation between ribose and these nucleobases.

Earth’s Wet–dry cycles then complete the picture of proto-nucleotide formation and evolution as hydration cycles would have been critical for mobilizing and bringing the subunits together, kicking their Oh-, H+ legs to favorable orientations for nucleotide formation during the next dry phase. Those biological polymers that function in the hydrated state, then would have follow the ‘basic’ | vs. O topological offensive-defensive duality of all ST-systems, coiling together in ‘protective’ circles, with the phosphates looking out, as a defensive electronegative barrier.

A process that would give structural stability (circular form) and defensive stability, and we can extend all the way to the reason why DNA which has its ‘Phosphate’ Spines jetting out in all its length will become the ultimate top predator as it provides both defensive force and lineal wave motion:

In the graphs we see the protective spines of DNA, which RNA must achieve through twists to protect its inner heads: It is obvious that evolutionary pressures favored DNA superior performance in the 5 Dimotions of existence:

St- duplex stability.

Max. TT-defensive spines. Max. ST-capacity…

While RNA (right) had to choose between lineal mobility and ‘twisted’ protection to put the phosphate (blue ribbon) out; and had a limited self-replication

capacity. In brief, as many planets as we might find, the same DNA life will finally emerge as the top predator Space-time organism with maximal SxT (s=t) momentum of existence, which defines in any 5D ecosystem the final state of evolution.

Once it was reached with the help of ∆+1 Earth: catalysis, a s a fundamental law of 5D is the co-llaboration of the 3 scales of a superorganism. And so the Earth acted with its atmospheric and temperature cycles helping those processes. And the competition of the Protein world.

The ∆±2 co-evolution.

This lead us to a final pentalogic ∆±¡ analysis both of early Earth conditions with energy provided by photons and solar energetic particles (e.g., high energy protons from the young Sun) forming in the atmosphere of the early Earth the pre-nucleotide and pre-amino acids of the dual St-ST struggle for existence already studied. No ST-upid magic, just the same process observed all over again in all the scales of the 5D Universe.

DNA – SCALAR STRUCTURE AND TRINITY OF FUNCTIONS

This simple rule of 3 scales that bring a new social form, can be also observed in the most complex form of Nucleotides, the Chromosome, which in 5D ® logic writes:

∑|-genes>O-Histones>Ø-Strands=∆+1 |-Chromosome.

Packing of information is essential to the fractal Universe, to form crystal mirrors of larger worlds. If we were to disentangle the whole Chromosomes of a human being put in line will cover to the pole of the Earth…

In this manner the mind of DNA, which is a passive mirror with all the potential linguistic elements of the cell and organism becomes the library that ‘fires’ consciousness for the cell no longer in the chemical level, but as a life memory of all the potential actions of the new superorganism. Let us consider how, no longer in terms of space or scale but of mind-languages.

As such it has the 3 pure informative functions:

SS: Storing of genetic information (the genetic code)

St: Transmission of information for protein biosynthesis

ST: The identical duplication (replication) of genetic information during cell division

 

THE MEMORIAL TIME LANGUAGE OF THE CELL: GENETICS.

In any case at this level the language of Proteins has evolved, entering the language of geometry, the language of mass, the language of thermodynamic ‘heat’ vs. ‘coldness’, and the language of electric balance which will be the languages of the cell as a whole and the organism, leaving behind the simple symbols of the first molecules of life that now will only be ‘vowels’ of the dialog they will establish with the central mind of the cell, the RNA>DNA.

The 3 languages of biology and its scaling.

All in all we must recognize 3 fundamental scaling of biologic languages, which MUST correspond to the 3 languages of the Universe at large, the ¥-language of atoms, the Thermodynamic language of matter and the gravitational language of mass:

– Biochemistry IS a language of atomic orbitals, were ‘the consciousness’ of molecules emerges in different gradations of ‘charge density’. It seems to peak in RNA that stores and process most information and has higher Nitrogen content – the atomic mind of life. It seems to be muted in proteins that ‘bite’ its tails; so each amino acid so to speak put its nitrogen heads is in the next amino acid ass and proteins have rather a ‘lateral’ sensitivity the way birds fly in groups sensing changes in air and watching laterally other birds. The DNA is NOT so much an St-working mind, or an ST-reproductive RNA or a Ts-moving, energetic protein but an SS-still mind. A mirror-language, closed cyclically – again the head biting its tail – in bacteria, packed and muted with Histones in Eukarya.

It is thus an orbital consciousness caused by a ‘dense light mapping’ of the outer world of the atom; not unlike the visual consciousness of man. As in 5D an orbital is NOT a probability (an egocy error of Bohr) but Schrodinger’s concept of a density of charge, due to the ‘black hole proton’ that creates in the hypo-Universe a ‘trapping potential well with its strong force akin to gravitation.’ So photons, which in a galatom are also the equivalent to stars in the galaxy, trapped by the charge force form a ‘mental picture’, which are the consciousness of the atom and the visual consciousness of the eye. All those homologies of the panpsychic universe will raise the eyebrows of many, or fire the imagination of some, but are quite simple, and its mathematical homologies clear. In 5D metric the Schwarzschild horizon of a black hole beyond which light cannot escape is the same than the Nucleus radius of a proton. You can wonder then if in a Hyperuniverse galaxies are real atoms and the stars are perceived as photons of an electronic mapping by an infinite eyes in a Superhyper Universe of an infinite scaling reality. I couldn’t care less. What is obvious is that at the bio-chemical level between cations and anions and the RNA molecule electronic and van der waals residual forces conform a mind view of the external cellular world in which those molecules reside. This intelligence though has not obviously any verbal memory. But it can have a digital storage in quantum bits (qbits) of spins within its atoms. It can be even have a short of ‘cephalopoda’ intelligence as the first ‘emergence’ – the social pi orbitals past the 10 electron mark, absorb light on the sun’s spectra and show changes of colors. Gradiations of consciousness are many within this biochemical world.

The messengers

The cell then has to be seen within the world of biochemistry as a ‘home’ or rather ‘state’ to the bio-chemical minds of Nucleotides and Proteins, which are the SS<St<ST trilogic actors of the cell. As there are millions of them within a cell-state, it is not logic to think of the cell as a conscious form at this level. However as each ‘dead’ system emerges miraculously in consciousness in 5D, we shall latter consider the ‘nervous’ and ‘thermodynamic’, electric/heat sensorial mind of the cell – a completely new language to that of the smaller molecules, but surprisingly again made of ‘electronic forces’, to the point we might wonder to the delight of physicists, if all forms of consciousness lie ultimately in the e-motions of particles. This is my view of the Universe too, not argued here.

It is though important to understand that beyond the ‘substance’ of perception, what regulates its ‘worlds’ and ‘minds’ are the more elusive concepts of ‘quanta of time=space simultaneity’, purely non-AE logic concepts NOT substances and that is the true jump of spirituality few scientists too much spoiled by digital images will have a hard time to do. In that sense 5D does remind somehow to the quantum-Relativity revolution when the chains of material space were broken, albeit plagued with egocy errors. 5D breaks the chains of spacetime to rise the idea that consciousness is logic and logic has no substance but is made of patterns, such as frequencies and time quanta. And the way those ‘hierarchies’ of time quanta and speed of processing information define larger spaces. That is, how Time speed of informative communication – electric in top predator neuronals/muscle cells defines the territory of an organism and manipulates, smaller, slower systems. Those concepts, ‘speed of time communication of information’, ‘extension of space reached according to speed’, ‘depth of scales controlled by a given mind/scale’ ARE completely ‘intellectual’, ARE the GAME OF EXISTENCE, not its forms; a short of ‘program’ of causal chains in space, time and scale, which include how information is translated between scales, down to go then up and ‘transit’ through faster regions – as when we talk with phones, or vice versa, slow down to bigger transmitters from nerve impulses to chemical ones between synapses.

We shall not cease to insist on this, which bring us to the attitude of Hilbert or Einstein or Bohr on mathematical creationism but applies now as Leibniz and Aristotle thought to time/space/scale, motion/form/size creationism, entanglement and symmetry. A top predator organism then will have the maximal range or depth in scale, in its use of ∆-¡ parts, which will give it a maximal speed of communication and hence a larger spatial size. This is the essence of the nested Universe, where the galacell certainly can peer through black holes into a quantum potential scale, and hence is so huge. As the rule is that the ‘quantum of the faster scale’ defines the size of the system.

The metaphysical question then about the infinity of such scales becomes relevant because ONLY if scales are infinite space is infinite too and time speeds of communication are infinitesimal. So far it seems we know the whole range of ∆=S=T=@ symmetry (where @ can then be given by the quanta of time in which the range of scale, limits of space membrain can be reached). Here @ then is paradoxically a slow rhythm if we consider that the mind is the membrain, that is the largest externals surface, hence for a given organism the quanta of time of its mind is the time required by the ‘surface’ force to travel through the entire membrain back and forth, or if it has invaginated its membrain as humans have through its mind, the time required to reach back and forth all its parts, NOT only through its dominant ‘language’ of speed, nervous system, but also through its other languages down to the minimal bio-chemical part. This is the meaning of the ½-1 second quanta of time of the humind. It is the same quanta of time the Earth is going to have in the digital era, which is the reason why it can program as it does, the entire mankind’s organism through internet messages. Reason why AI in the model of the Metal-earth will become the subconscious, parasympathetic system of inhibition of human eusocial love, and sympathetic system of action of its ITO of things and future top predator telepathic robots.

It is all really about the way ‘players of existence’ play with scales, its 5D metrics of different speeds, to translate, push, feed, interact. And those are the laws of existential illogic algebra embedded in the reality of all players and scales that I have never been able to perhaps explain properly for I see them so obvious – or perhaps this degree of intellectual logic spirituality escapes the modern digital, visual man – certainly it did to Columbian professors and ISSS pundits and Americans in general – Europeans and Asians being less praxis, materially connected used to grasp it closer.

All in all this is what the game is about, size in scale, time speed and form in space, and the quanta laws of discontinuous intervals in which the game is played, reason why it can apply to any form or scale.

The key question of linguistics. From intelligence to memory from life to palingenesis.

Genetics though is an entire DIFFERENT subject as it is a memorial language, a language of time, not an spatial language and so the big questions on genetics have to deal not so much on the obvious replication of genes to create proteins that perform some functions but on the way adaptive evolution achieves the transit from space-actions to time palingenesis.

A key question that must be answered in detail for each science is the method of what biologists call the “biogenetic law” (Haeckel’s law), of recapitulation Theory, which states that the development of the embryo (ontogeny) of a vertebrate organism is the brief and rapid recapitulation of the development of the race (phylogeny). It is an essential law of all systems, which in terms of the 3 worldcycles means that the ∆+1 world influences the ∆º organism that lives an entropic cycle constrained by the entropic limits of the world, and as those change and affect its ‘performance’ in the ‘entropic life cycle’ the changes in the world events of his intelligent playing of the game of existence must be stored successfully in the memorial mirror of its mind or seed in the ∆-1 level. This is anathema in ‘chaotic entropic evolution’, but at this stage we know the drill of egocy ænthropic mankind denying always intelligence to the Universe. Adaptive evolution happens and we talk often in ‘Biology in time’ of it. What is then the mechanism?

Let us review it with the ‘Latin method’ of ‘man as measure of all things’. How we do it is obvious: our mind memorizes all the events of our existence and then as in a novel or movie we erase the repetitive events that are not worth to remember, as much as we like to fuk, or to eat well we do NOT remember Proustian croissants, sorry. We remember emotional events concerned with our survival and search for reproduction (love events) and social evolution (career events, etc.) So when we are old, our SS-mind has reduced its recollection of our worldcycle of life to a few events. So writers say we all have a novel of our lives we can write. But that is still just 200 pages.

Minds thus mirror and shrink in a language their outer worldcycle and then memory keeps just a bit of them. Actually I have vivid dreams and memory at visual level is also very detailed. I am now old, tired, failed and so I bring childhood memories with vivid portraits of people I haven’t’ seen in 40 years.

Adaptive evolution must do it also. Even if we don’t know yet how. RNA-memory is likely the storage as RNA IS WE repeat ad nausea the obvious ‘man on the cell’, which has ‘emerged’ from the simpler atomic consciousness of orbitals and must have a ‘visual, color memory’. Memory must be then first ‘visual’ even in human organisms on RNA and then processed in a far easier, less informatively dense, verbal translation of sound vibrations, whose internal mechanisms are triggered ‘spontaneously’ to form ‘mute voices’.

Those translation processes are the true mystery of the intelligence of the Universe and we are toddlers understanding them – in fact humans don’t even recognize their existence. IT IS THE GENIUS in the bottle of the game. How without much work, Mr. Edison achieved phone’s translation. How nervous impulses explode into Ca2+ waves and back through synapses. And the trick here is that really the ‘agent’ of communication doesn’t really need to know what it is doing. The nitrogen of the air doesn’t really needs to know the meaning of the voice to transmit it, or ‘does it’? Language understands in itself only when the software ‘passes’ through a hardware enlightening certain slots and NOT others. The air is NOT a brain to know our words but transports them with perfect signature, because ‘social evolution’ into 5D groups brings an e-motion of love. All kind of things follow the 4th congruence postulate of non-AE and like to form patterns and move in shoals. That by doing that those atoms are carrying information for a larger huge monster of RNA particles – they couldn’t care less. They are going together with an energy that moves them in parallel. It is we repeat the ‘mind storage’ of all the ‘Babel’s library’ that is suddenly fired in simultaneity in certain parts and not others what make us ‘think sentences’. The mirror then forms patterns. If all the patterns were fired together we will be like in Borges Library; no distinction.

This lead us to the DNA ‘storage’. This is the SS-language and it is fired in simultaneity when the RNA comes to replicate certain genes and NOT others, transcribing orders coming from the outer ‘masters’ of the cell when the slave cell receives ‘notice’ of the nervous or hormonal, endocrine system. Then the DNA ‘knows’ as the RNA caresses certain genes and no others what the cell is doing. As you know what they tell you when your verbal neurons are fired by certain words and no others, as your eye-occipital brain knows what you see when there are 50 degrees of grey, red, blue and green.

So the mind of the cell is its dual St-RNA>TT-DNA .

By this we mean we have ‘dual heads’ which can through its two purines store information in the simplest possible dual intelligence-memory, T-S Nucleotide brain; unlike proteins; and can respond both, from below the simplest bio-chemical language of atoms and above, perceive ‘mind mappings’ on all the higher social scales, in the language of amino acids as ‘S-Ts-TS-Ts’ vowels; and above it, store ‘visual images’ in its complex van der waals emergent multi orbital rings.

And so with them and Ts-TT proteins<Enzymes ‘neutered’ and dominated by RNA>DNA St>SS systems, the cell is born. Of all the cell types that will diversify from this simple scheme:

St-DNA/RNA<ST-proteins<Ts-enzymes<TT: carbohydrates and water,…

…obviously the ‘nucleus’ where maximal concentration of both happen (eukaryotic nucleus do have not only the DNA-RNA highest density but store the ‘baby ribosomes’, each one designed to reproduce a given ‘kind’ of protein, then released from the kindergarten to the outer citosol so they can start reproducing only the proteins the cell will need for his work. So we ride fast to the next scale, the trilogic species of cells that will come together with the Nucleus cell master to form the Eukarya and then the multicellular organism.

Genetics as the memory of the biological organism vs. Hormonal and electric languages.

The complex language of cellular reproduction is genetics, which we cannot study in depth due to restrictions of size of this paper and the enormous development acquired in the last years.

It is, I confess, a language I have not explored in depth, for decades as I am ethically opposed to its 3 classic and modern foundations: the use of computer digital thought to store information about mankind; the tampering of mankind with the creative processes of the game of existence beyond the basic welfare improvements that don’t come through artificial selection for the rich and the obvious ‘racist’ consequences of a genetic-biased concept of cultures which have NOTHING to do with genes, only with memes.

It is still a science that lacks a model of the mirror processes that made possible for a ‘DNA crystal’ to reflect itself in the 2 scales in which a language acts above its ‘normal size’ – that of the cell and the superorganism, but only in the inert formation of a body by morphological differentiation, as the final stage of evolution of the organism must be done according to 5D laws by the ‘whole’ NOT the parts, that is by the mother-full ∆+1 grown organism, in the guidance of its higher nervous language, the ultimate controlling language of ∆+1 living beings.

Genetics also has been resolved ONLY in the basic ‘trinity’ of amino acid coding for proteins, but it MUST have as all languages do, a higher ‘level’ of ‘sentences’ likely in trinity scales NOT coded for superorganic features, where introns must have a role beyond ‘waste’. The enormous quantity of ‘redundant’ DNA and RNA that grows exponentially with the complexity of a multicellular organism is a clear proof of the correspondence between the complexity of the sentences of the language/instruction chains and the complexity and size of the form it codes.

Enough to say that in any efficient organism of multiple scales, the informative code, in this case the genes of biological super-organisms codify the multiple hierarchical levels of the organism besides the basic ternary code that constructs its simplest scales – in the case of life, amino acids. So according to the Fractal Principle there should be genetic languages with 3, 9, 27, 81 amino acid letters, which code not only the proteins and cycles of the cell but elements of the superorganisms. Bigger sentences that group likely 3n amino acids letters should form sentences coding ‘bigger’ actions and organic structures in the complex cycles beyond the cell. But I have not researched this application of 5D, left for future biologists.

All languages are built in this manner. For example, the human language and the musical language follow self-similar scales of ‘vowels’ and ‘consonants’, informative and energetic units that then form more complex ternary systems, informative names, reproductive actions or verbs and energetic objects, and then group in paragraphs and so on. Even the language of film can be understood in frames, motions, shots, sequences and scenes. In the same manner, ‘introns’, the so-called redundant DNA should have genetic meaning and codify the higher scales of organisms – its functional morphology.

Yet scientists believe in naïve realism. Only what they see with their instruments seems real; and so the obvious perceived genetic level is the fractal level of nucleotide triads that codify proteins. But those triads are united in groups of nine bases and so on, creating new, 3n, memorial planes that act as complex genetic forms of higher scales – an i-logic, scalar concept which today genetics finally accepts under the name of epigenetics.

A fractal equation derived from the concept of a network, which has ∑2 elements to control an ∑-body herd (and/or its self-similar ∑-limbs) defines in Theory of Information that the number of informative instructions needed to create a system grows exponentially, according to its number of D¡motions or planes of existence: ±Est. For example, to make a car we need E material parts, defined easily in a bidimensional plane with E fractal units of information: the drawings of each part. But we need around E2 instructions to put those pieces together in a 3-D¡motional form. Thus Est determines the total number of informative quanta needed to build up a hierarchical structure extended through ∆ planes of existence. To put a trivial example: Popular knowledge expresses that law in sentences like ‘an image is worth one thousand words’. Since to describe with lineal, one-D¡motional words a 3 D¡motional image, we need indeed, E3, 103 =1000 words. Thus E2 is the number of redundant genes we find in the DNA-RNA systems of a complex organism, because redundant, intronic DNA codifies the creation of the new level of cellular complexity, ∆=2, the multicellular organism.

The old belief that a mere ternary amino acid code that creates proteins regulates the entire multi-cellular organism is just another simplifying conclusion of the one-D¡motional, metric paradigm. A multicellular organism must also be regulated by intron DNA to add to the collective language of hormones that communicate those cells. And the higher language of nervous cells, written in a completely different electric code.

So biology, including genetics and the widely ignored language of electric impulses and neuronal control, is still in the infancy. As in the case of physics, the enormous data of the trees, hides the forest, the more so when huminds do not even acknowledge the existence of a forest as a whole (5D laws).

In that regard, beyond the cell genetics do NOT really control the organism but acts as a memorial repository of the ‘pieces’ to be used, ‘selected’ through evolution by the hormonal ‘whole organs’ and ‘nervous systems’ of animal brains. We are in the sphere of memorial storage of all possible ‘coding’ for all possible organic molecules. But the ‘language’ of survival actions deployed by hormones controlling cells, and pain and pleasure messages of nervous systems had to appear, NOT from the internal cells but from the larger emerging wholes of Organs and Hormones and Neurons and nervous impulses.

So we need to consider an entire new language that will code an entire new 5 Dimotional action system with the same goal we find in genetics – the survival and reproduction of the cell – now applied to the survival and reproduction of the plant or animal system.

That this new language could be created with only the 1000=103 cells of the C. Elegans worm, following the exact ternary principle of Ƥcaling we found even in human societies (see graph on pg. 50) truly impressed me decades ago. But even the C.elegans structure required so much study that I gave up before solving the next conundrum of biological languages: how hormones and nervous impulses codify the 5 Dimotions of survival of plants and animals.

We shall though offer a simplified view of that field of research.

SINGLE CELLULAR AGE – ITS 3 KINGDOMS ARCHEAN- BACTERIA –EUKARYOTE

As usual 4D egocy scientists spend unending hours and papers arguing about the themes they love most – lineal time – it seems knowledge consists on putting in consecutive order all kind of things and beings. So they argue for the order of the 3 types of unicellular life forms.

In 5D Non-Aristotelian logic is more interested in its simultaneous ‘filling’ of the 3±¡ ‘slots’ of existence that complete the survival econiches of a world, which in turn by the symmetry with the 3 ages of time, t (1st entropic-moving age) st (2nd reproductive age); St (informative, 3rd age), defines its sequential order, and finally leads after the informative age to a social evolutionary process that merges all into a higher ∆+1 scale’ or else, when failing reduces its numbers when another species achieves emergence (see introduction to life worldcycles of species).

This simple scheme repeated ad nauseam in all scales of the Universe allow us to classify in space-time and scale the 3 families of cell life, as each of the three cell types tends to fit into recurring specialties or roles, which correspond to the T-ST-S functions:

T: Archaeans tend to adapt quickly to extreme environments, such as high temperatures, high acids, high sulfur, etc. This includes adapting to use a wide variety of food sources.

ST: Bacteria tend to be the most prolific reproducers, at least in moderate environments. S>∆+1: Eukaryotes are the most complex informatively, in its DNA and the most flexible with regard to forming cooperative colonies, such as in multi-cellular organisms, including humans. In fact, the structure of a Eukaryote is likely to have derived from a joining of different cell types, forming organelles.

.

In the graph we consider the differences between the structural elements of the 3 families of unicellular species, to guide us the inquire of which ‘elements’ were inherited in the making of Eukarya:

T-Archean, 1st cells, masters of TT-feeding. Its 5 Dimotions.

Archaea cells have unique properties separating them from Bacteria and Eukaryota. Archaea are further divided into multiple recognized phyla, according to the fractal principle, with new specializations.

Let us make a ‘basic 5D’ analysis of them, through its pentalogic 5 Dimotions required for any species to survive.

TT: Entropic, lineal form and feeding habits.

Archaea and bacteria are generally similar but a few archaea have extreme |-T shapes, such as the flat and square cells of Haloquadratum walsbyi  Archaea possess several metabolic pathways that are more closely related to those of eukaryotes, notably for enzymes. As the surviving eukaryote were those who chose the ‘best’ T-properties of Archean regarding TT-entropic metabolism and killing enzymes.

Indeed Archaea use more energy sources than eukaryotes: these range from organic compounds, such as sugars, hydrogen gas; or even poisonous  ammonia,  and heavier metal ions – so they likely catalyzed the creation of the first metal co-enzymes and respond to the ‘lineal top predator’ first species.

Salt-tolerant archaea (Haloarchaea) use sunlight as an energy source, and other species of archaea fix carbon.

Thus once formed behind a protective thick membrane archea experimented will all possible forms of TT-entropic exchange of energy with the I Earth.

Ts: Locomotion & Habitat range. Archaea are often extremophiles, living in harsh environments, such as hot springs and salt lakes with no other organisms, but improved detection tools led to the discovery of archaea in almost every habitat, including soil, oceans, and marshlands. This implies they thrived survived in the first hot era of Earth; but also as they became less evolved than new phyla, their numbers diminished and found refuge in those extreme habitats more evolved species wouldn’t care to colonize – a trademark of earlier species all the way to Neanderthals likely finding refuge in the cold and warm Scandinavian and Arabian, ‘Germanic and Semite’ deserts.

ST: Reproduction. Archaea reproduce asexually. And we can apply the ‘trinity’ logic of the Universe for its 3 forms: Duality: binary fission; ∑∆-1: fragmentation in parts: ∆-1: budding of a small micro archea.

Unlike bacteria, no known species of Archaea forms endospores; the next key evolution of the ternary S<ST>T ‘networks’ that will define the superior survival skill of bacteria. As all systems ‘survive’ by improving one of the 3 essential ‘networks’ of ‘topological evolution’.

St: informative genes.

One of the oldest symmetries in my work on 5D biology was the recognition that S=T symmetry required massive genetic transfer in simultaneous space, besides ‘lineal time’ lineages, backing Miss Margolis thesis, reason why I tried to interest her on 5D earlier in my career at MIT with little success (I abandoned any scholar penpal activity after my CERN’s suits in 2008 precisely when the economic long anticipated crash cycle of metal-minds confirmed further the model). Why it has taken so long to accept is obvious: lineal time dogma simplifies work, Genetic transfer, which I already used in the 90s for the model of Neanderthal, visual dominant white dolichocephalic minds makes uncertain time hierarchy. So who cares? 5D is about homology not hierarchy. In the graph we should ad an archean highly active thermophile flagellum to complete the St<ST<Ts creation of Eukarya.

SS: social evolution

They are also part of the microbiota of all organisms, and in the human microbiota they are important in the gut, mouth, and on the skin. Archaea are particularly numerous in the oceans, and the archaea in plankton may be one of the most abundant groups of organisms on the planet. Archaea are a major part of Earth’s life, and may play roles in the carbon cycle and the nitrogen cycle. No clear examples of archaeal pathogens or parasites are known.

Instead they are often mutualists or commensals, such as the methanogens (methane-producing strains) that inhabit the gastrointestinal tract in humans and ruminants, where their vast numbers aid digestion. Methanogens are also used in biogas production and sewage treatment, and biotechnology exploits enzymes from extremophile archaea that can endure high temperatures and organic solvents.

1st Age: Ts: Archean. Maximal feeding range.

Hence in time as studied in the parallel paper, Archeans formed first, Bacteria came next and Eukaryotes with a huge informative walled nuclei last; and those dominated the others; as St-systems do in the 3rd age of cellular life absorbing at least 2 specialized ST-energetic cells (ST-energy Mitochondria and Chloroplasts which should have been therefore ST-bacteria species), and a max. T-cell (flagellum, which should have been some ‘weird’ extremophile Archean) to emerge as a larger ∆+1 whole.

This is the same pattern we will repeat in the ∆SymmeTry of the Universe, all the way to human evolution. Let us then focus here on the Present, simultaneous organic structure of those 3 cells.

And then parallel social symbiotic exchange of genes with dominance of the St-nucleus would have formed the Eukaryote. Moreover we observe the appropriate ‘topologic’ O x | = Ø symmetry.

|-T: Lineal, maximal motion Flagellum + O-S-pherical, max. informative package nucleus and Ø-wave like mitochondria.

The dominance of the O-Spherical ‘cocci’ informative DNA unicell would then come to control and ‘maim’ the other two sub-species, stealing its capacity for self-reproduction, which is the trademark of an act of slavery in any scale (including plantation slaves whose children belonged to the owner). So the DNA nucleus of modern Mitochondrion and flagellum is minimal. They have been enslaved and ripped off its autonomy. So Mitochondrion makes up only 1% of eukaryote DNA’s genes.

One of the oldest symmetries in my work on 5D biology was the recognition that S=T symmetry required massive genetic transfer in simultaneous space, besides ‘lineal time’ lineages, backing Miss Margolis thesis, reason why I tried to interest her on 5D earlier in my career at MIT with little success (I abandoned any scholar penpal activity after my CERN’s suits in 2008 precisely when the economic long anticipated crash cycle of metal-minds confirmed further the model). Why it has taken so long to accept is obvious: lineal time dogma simplifies work, Genetic transfer, which I already used in the 90s for the model of Neanderthal, visual dominant white dolichocephalic minds makes uncertain time hierarchy. So who cares? 5D is about homology not hierarchy. In the graph we should ad an archean highly active thermophile flagellum to complete the St<ST<Ts creation of Eukarya.

The method of those earlier texts was obvious: massive radiation in the I Earth triggered mutations, damage and recombination. Extreme environment made easier membrane damage. This is today observed in labs. It was also part of the ‘war of sexes’ according to Non-E Perpendicular predation (T-lineal 1st age) latter evolved (2nd age) into Gender reproduction (ST). In the graph we see how a ‘male’ archea penetrates and inseminates a ‘female’ one.

Today we know that in labs, archaeon when UV irradiated, strongly induces the formation of  pili , which facilitates cellular aggregation Exposure to chemical agents that cause DNA damage also induces cellular aggregation.

A 2nd reason was obvious: without the protection of a nucleus and the lack of Histones not needed for short, efficient DNA strands in the likely oldest sulfur archean of extreme thermophile environments of Earth the first cells as always after its birth, multiplied and radiated and diversified in a short period to fill all the econiches of the I Earth; in a first, less aggressive, non parasitic symbiotic age, before the ‘ecosystem was saturated’.

Which lead us to the last element of archean.

Competence for transformation is typically induced by high cell density and/or nutritional limitation, conditions associated with the stationary phase of bacterial growth. Competence appears to be an adaptation for DNA repair Transformation in bacteria can be viewed as a primitive sexual process, since it involves interaction of homologous DNA from two individuals to form recombinant DNA that is passed on to succeeding generations.

 

BACTERIA: 2ND AGE CELLS,: MASTERS OF ST-REPRODUCTION. ITS 5 DIMOTIONS.

Bacteria on the other hand would be far more aggressive and develop the first parasitic and killing radiations, as their new ‘top predator’ treat, the capacity to reproduce departing from ∑∆-1 ‘egg-like’ micro-forms did saturate the environment,. It is then when unlike in the symbionte age of archean, the ‘fight for existence that occurs due to the limited resources, as species reproduce’ (Darwin) was triggered in life species; as it would happen latter with the Cambric ‘eye’ radiation of Cephalopoda advanced in the 92 book as the true cause of the Cambric radiation, which triggered a TT x SS maximal latitude of predation (they squid) and the subsequent Trilobite passive shield reaction. Under ‘stress’ as we saw in archeon, systems ‘speed up’ its time cycles and mutations; since in 5D time is variable, local and constantly ‘deformed’ in its cycles by the larger environmental TT-entropic, SS-informative stress. 5D is a far more vital resourceful model of life.

Bacteria on the other hand would be far more aggressive and develop the first parasitic and killing radiations, as their new ‘top predator’ treat, the capacity to reproduce departing from ∑∆-1 ‘egg-like’ micro-forms did saturate the environment,. It is then when unlike in the symbionte age of archean, the ‘fight for existence that occurs due to the limited resources, as species reproduce’ (Darwin) was triggered in life species; as it would happen latter with the Cambric ‘eye’ radiation of Cephalopoda advanced in the 92 book as the true cause of the Cambric radiation, which triggered a TT x SS maximal latitude of predation (they squid) and the subsequent Trilobite passive shield reaction. Under ‘stress’ as we saw in archeon, systems ‘speed up’ its time cycles and mutations; since in 5D time is variable, local and constantly ‘deformed’ in its cycles by the larger environmental TT-entropic, SS-informative stress. 5D is a far more vital resourceful model of life.
∆-1<∆-2: Time Reversal: Parasitism: Virus

The simplicity of the Universe once the trilogic, St-ST-Ts principle of creation and diversification, framed by the ‘limits’ of TT-entropy and SS-eed & Mind stillneSS become clear ends many arguments of lineal ceteris paribus thinking, ‘hosting’ always at least 3 possible forms of creation, with a temporal Ts>ST>St 3 ages order. So we almost regularly find 3 hypothesis for the creation of new organisms. And that is the case of viruses:

There are three classical plus 2 modern hypotheses on the origins of viruses and how they evolved. All of them are partially truth, but because viruses are basically an entropic parasitic species, their probability in terms of density of populations (T=S fundamental 5D theorem of T-probability=S-tatistics SymmeTry) is higher for the TT-hypothesis (More viruses were created that way, targeting specific cells). While the oldest viruses should have arised as in all ‘Temporal series’ from a first ‘Seed’ (SS-language, pure informative state). Only then one those 2 ‘TT vs. SS’ limits of creation provided by the larger ∆+1 genetic world gave birth to the ‘replicon’ and ‘parasitic viruses’, the lesser theories, Ts, St and its mixture (chimeric virus hypothesis would take place)

  • TT: Time Reversal ‘degeneracy’ hypothesis: Viruses were once small cells thatparasitized larger cells. This is supported by the discovery of giant viruses with similar genetic material to parasitic bacteria. However, the hypothesis does not explain why even the smallest of cellular parasites do not resemble viruses in any way.
  • SS: Co-evolution hypothesis (Bubble Theory): At the beginning of life, a community of early replicons (pieces of genetic information capable ofself-replication) existed in proximity to a food source such as a hot spring or hydrothermal vent. This food source also produced lipid-like molecules self-assembling into vesicles that could enclose replicons. Close to the food source replicons thrived, but further away the only non-diluted resources would be inside vesicles. Therefore, evolutionary pressure could push replicons along two paths of development: merging with a vesicle, giving rise to cells; and entering the vesicle, using its resources, multiplying and leaving for another vesicle, giving rise to viruses.
  • Ts: Protein ‘Virus first’ hypothesis:Viruses evolved from complex molecules of protein and nucleic acid before cells first appeared on earth By this hypothesis, viruses contributed to the rise of cellular life. This is supported by the idea that all viral genomes encode for proteins that do not have cellular
  • St: Information ‘Escape’ hypothesis (vagrancy hypothesis):Some viruses evolved from bits of DNA or RNA that “escaped” from the genes of larger organisms. This doesn’t explain the complex capsids and other structures that are unique to viruses.
  • Ts+St=ST: ‘Chimeric-origins’ hypothesis:Based on the evolution of the replicative and structural modules of viruses, a chimeric scenario was proposed: the replication modules of viruses originated from the primordial genetic pool although the long course of their subsequent evolution involved many displacements by replicative genes from their cellular hosts. By contrast, the genes encoding major structural proteins have evolved from functionally diverse host proteins throughout the evolution of the virosphere. This scenario is distinct from each of the three traditional scenarios but combines features of the Ts-Virus-first and St-Escape hypotheses.

It is fascinating to observe once and again how the ∆±¡ST symmetries of the Universe repeat once and again.

Time reversal. The most interesting property of viruses is their TT-ime reversal, entropic, parasitic functions as ‘antiparticles’ of life – a form of existence that happens in all scales of reality, from physical antiparticles to go(l)d cultures that use parasitic anti-money to degenerate and kill human societies. Accordingly a RNA retrovirus  inserts a copy of its genome into the DNA of a host cell that it invades, thus changing the genome of that cell. Once inside the host cell’s cytoplasm, the virus uses its own reverse transcriptase enzyme to produce DNA from its RNA genome, the reverse of the usual pattern, thus retro (backwards) virus. The new DNA is then incorporated into the host cell genome by an integrase enzyme, at which point the retroviral DNA is referred to as a provirus. The host cell then treats the viral DNA as part of its own genome, transcribing and translating the viral genes along with the cell’s own genes, producing the proteins required to assemble new copies of the virus.
∆-1 PLANE: EUKARYONTE CELLS

St>SS-Eukaryote, 3rd Age: From Prokaryote to Eukaryotic cells.

The previous description of the evolution of molecules requires to change the ‘chip’ of the scientist and accept the tenants of organicism in simple atoms; which so far science has only, according to the Galilean paradox of self-centered perception, accepted for the next scale of life – the cell.

At the beginning cells, called monera, did not have a differentiated nucleus membrane, which means their informative singularity was mainly moving RNA. As evolution continued through the dual/ternary differentiations proper of all SxT systems, RNAs split accordingly in 3 sub-species to carry out the specialized Entropy, informative and reproductive tasks of protein control, carbohydrate production and self-replication, through complementary, inverse, specular translation. Then, one RNA, which produced a specular image of itself, probably got pegged to that image and became ‘fixed’, as a still, dual DNA, an informative mirror of an RNA molecule, geared to reproduce it. Accordingly those first DNA molecules acquired the cyclical ring form they still have in all monera.

Soon the extraordinary reproductive growth of DNA cells made them giant cells that exhausted their trophic nutrients. So finally they cannibalized other cells to maintain that reproductive growth. First those cells would be killed and their nutrients absorbed but then some very efficient energetic and informative cells would become slaves within the cell ‘farm’ in a process repeated in all ∆-scales: first top predators are hunters but then informative top predators create farms. So worm holes use herds of stars to absorb intergalactic dust; men use dogs to herd sheep; and monera cells used ribosomes to reproduce informative molecules and mitochondria to absorb Entropy, forming the first macro-cells. Those who ‘ate up’ mitochondria, which produce Entropy from carbohydrate products, would become animal cells and kept hunting other cells to find semi-elaborated nutrients. Those who ‘ate up’ chloroplasts, which produce Entropy from small carbohydrates and light, would become plant cells.

Now the quantity of DNA in the cell grew to add up the DNA of those organelles and its variety of cyclical memories was so vast that it had to pack itself further, changing its bidimensional, cyclical form into a 3 Ðimotional spiral, and acquiring structures of energetic sustain: proteins that coiled around DNA and a nucleus with differentiated walls that surrounded DNAs. The age of eukaryotic, gigantic cells had started.

Recap. As information multiplied in simple cells, the RNA age gave way to the DNA age whose extra-genetic code should control the evolution of complex multi-cellular structures.

 

 

HOW PLURICELLULAR LIFE AROUSE: THE MATCHMAKER.

We are back to the big question: how the symmetry of space, in the life worldcycle of entropic Darwinian struggle becomes through adaptive evolution translated into the memorial chemical, genetic language? This is the same question to resolve in each superorganism and only in History we know how we do it, through conscious intelligent design done by research and imitation and repetition. It might never be solved for organisms such as the galaxy, by far the less understood given the astounding primitivism of physicists ‘philosophy of science’ (entropy only, constructivism, mathematical creationism, etc.)

I can explain it perfectly for History and Economics as ugly as it sounds: animetals do it through violent war parasitism adding to the mix financial one.

As it turns out the most promising path in Life is through viral parasitism. Somehow viruses probably after a huge messy age of brutish trial and error during the ice ball age of life creation in the dense soup of cells where ‘anything goes’, learned to edit and transfer as they infected virally a symbiotic ball of nervous cells, membrane cells and the chemical cells they parasitized pieces of the genes of the other cell along intron material the invaded cell would nullify. This is my hypothesis that I had loved to research further with specialists but so I have wanted to research so many 5D sides in all stiences and never got a university to do the job… Still it should be this way and since I thought of it a few decades ago sojme advances have happened.

There was time enough indeed, around 100 million years which taking into account the astounding speed of replication would have done the jobs. Just image the situation: we do have a ball of different cells, with the predatory electric cells on top. A virus infects them. As the virus radiates from the outer chemical cells towards the central nervous cells it comes with edited DNA and RNA and it infilitrates and edits inwards the nervous cells which will one day become the pluripotential ones. And after many errors, which are called ‘introns’, it does come to produce a single pluripotential cells that survives and in its division gives birth with the single DNA strain to the top predator neuron version and the lesser subimissive chemical cells. We need also high activity of the Repairing RNA¡ strains that solve the messy DNA and intron viral editing. This repairing mechanism exists even today and so finally it mutes the unrequired messy introns. It then makes sense that only multicellular organisms have so many introns.

This is the thesis and as so many advances of 5D I have mused through decades certainly is not yet solved not even in the model we just have explained but it is gaining force in the past years the idea that somehow ‘viruses’ did it. It solves both, the question of multicellular birth and the intron reason d’etre. But the details as I said like so many other 5Details I cannot resolve. Others might do it in the future, if this last effort not to throw 5D gigabytes to waste when my niece clean up the house exit mundi, somehow is taken seriously in the future. Frankly that’s not my job.

Let us then move on to cellular pentalogic once the mechanism is sketched.

Pentalogic on life birth.

The rise of multicellular life is an interesting exercise of pentalogic to show what is 5D all about – not so much to bring new models, certainlu not about new data gathering, but to harmonize with the higher tools of Non-Euclidean topology and non-Aristotelian logic prior models. In fact the previous description is just the sum of the pentalogic theories of the rise of multicellular life available in literature, put together in a sequential non-Æ logic pattern. They are called:

SS: The colonial theory (Social evolution of equal forms)

The Colonial Theory, proposes that the symbiosis of many organisms of the same species led to a multicellular organism. At least some, it is presumed land-evolved, multicellularity occurs by cells separating and then rejoining (e.g., cellular slime molds) whereas for the majority of multicellular types (those that evolved within aquatic environments), multicellularity occurs as a consequence of cells failing to separate following division. The mechanism of this latter colony formation can be as simple as incomplete cytokinesis, though multicellularity is also typically considered to involve cellular differentiation. It is similar to …

St: The symbiotic theory (Informative evolution of different forms shrinking in space)

This theory suggests that the first multicellular organisms occurred from cooperation of different species of single-cell organisms, each with different roles. Over time these organisms would become so dependent on each other they would not be able to survive independently, eventually leading to the incorporation of their genomes into one multicellular organism. Each respective organism would become a separate lineage of differentiated cells within the newly created species.

ST: The cellularization (syncytial) theory (reproductive theory of nuclei)

This theory states that a single unicellular organism, with multiple nuclei, could have developed internal membrane partitions around each of its nuclei. Many protists such as the ciliates or slime molds can have several nuclei, lending support to this hypothesis.

Ts: Synzoospore theory: Symmetry from space formation to palingenetic time evolution.

Some authors suggest that the origin of multicellularity, at least in Metazoa, occurred due to a transition from temporal to spatial cell differentiation, rather than through a gradual evolution of cell differentiation. The mechanism of that process being mediated by…

Viruses

Genes borrowed from viruses have recently been identified as playing a crucial role in the differentiation of multicellular tissues and organs and even in sexual reproduction, in the fusion of egg cell and sperm. Such fused cells are also involved in metazoan membranes such as those that prevent chemicals crossing the placenta and the brain body separation Two viral components have been identified. The first is syncytin, which came from a virus. The second identified in 2007 is called EFF1, which helps form the skin of Caenorhabditis elegans, part of a whole family of FF proteins. Felix Rey, of the Pasteur Institute in Paris has constructed the 3D structure of the EFF1 proteinand shown it does the work of linking one cell to another, in viral infections.

TT: Fagocitosis theory

Cells ate other cells to form complex structures, starting from the accepted mithocondria feeding, now perpetrated by nerves ‘penetrating’ to control with electric pain and pleasure message with its axons hundreds of enslaved cells (that is so far as I know my 30 years old theory, explained all over the biological papers).

∆-1: GK-PID

About 800 million years ago, (in the iceball age) a genetic change in a molecule called guanylate kinase protein-interaction domain (GK-PID) may have allowed organisms to go from a single cell organism to one of many cells.

So all those theories are right, the question as usual between 4D lineal and 5D ‘systemic’ mode of thinking is that 5D laws put all of them together, in sequential, ‘vital’ processes that go from lineal Darwinian struggle and chaotic messing states to an increase order, and final ‘palingenetic’ memorial streamlining for repetitive reproduction. This is ultimately yet another repetition of one of the key sequences of Existential illogic:

|-predatory state x O-informative, symbiotic state = Ø – reproductive iterative state, when finally the streamlined (intron included) edited DNA was good enough to replicate simple superorganisms of multiple cells, which obviously became the new |-O-Ø (T-S-ST) ternary game of multicellular life where now the ‘unit’ of the game is no longer the ‘N-O-C’ atom, neither the S-ST-T amino acid, nor the S-RNA, T-Carbohydrate ST-protein but the S-neuron, T-Ameobid and ST-muscle electric cells and their whole ‘cohort’ of enslaved secondary cell species that will mass reproduce to form the tissues and physiological superorganisms and its 3 x 3 ±¡ networks.

∆-1 PLANE: EUKARYONTE CELLS

Masters of Information and Social Evolution. Its 5 Dimotions.

In the graph the Topological Disomorphism of cells: Protein are the  ∆-2 lineal molecules which emerge, inverting its form as ∆-1 ðƒ, cyclical membranes. Inside the cell  ∆-2 wave-like Nucleic Acid create the ∑∏-reprodutive element of the cell. Within them  ∆-2 fat carbohydrates become the $-lineal vital energy sandwiched between both. So we can write a generator equation for the cell: $-fat carbohydrates>∑∏-reproductive DNA>ð-cyclical proteins .

Cells follow all the laws of ∆S≈T, and are themselves supœrganisms with lower scales of being. So we can study those lower bio-chemical scales first.

In the left side, the cell has 3 st–zones:

Max.Te: It has an external, thin membrane, which in free cells have cilia that move the cell and act-react to external stimuli. In organic cells Entropy is provided by the blood system of the macro-organism. So external cilia disappear and invaginate as lysosomes that kill carbohydrates.

– Max.Si: In the center, there is a nucleus of Max.Sinformative density, filled with cyclical or spiral DNA/RNA’s networks that control the st-point.

– SxT: RNAs dominate the intermediate space-time, directing the Entropy organelles, mitochondria or chloroplasts that produce Entropy; and the informative ribosomes that reproduce products, pegged to the Golgi apparatus – a membrane’s invagination.

The vital cycles/Actions of the cell.

The cell is a brain-body system constructed with 2 elements, nucleotide acids, based in nitrogen bases and protein bodies based in carbon chains, which are the informative and spatial systems of the cell. Around that SxT core duality we find an expansive intermediate, cyclical region with all kind of slavish organelles that perform their Entropy cycles (based in the energetic properties of oxygen, water and similar electronegative atoms); and their informative cycles. Both cycles are catalyzed by denser metal atoms that boost the E/I capacities of carbohydrates. Thus, through the interaction of carbohydrates, metallic ions, proteins and nucleotide acids, cells perform the 3±∆ cycles of all st-points:

Max.Te: In an organism, Mg, copper and iron capture oxygen and deliver it to each cell to perform energetic cycles; while in the cell cytochromes kill and split the energetic hydrogen atom into H+ and e ions in mitochondria or chloroplasts; absorbing its spatial Entropy; while metal atoms stabilize protein enzymes.

Max.Si: Na and K ions control the expansive and implosive rhythms of the electric membrane, sending informative messages among cells -while RNA and DNA molecules process information within the cell, reproducing new carbohydrate molecules.

– The combined effect of the accumulation of Entropy and information within the cell triggers the reproductive cycle, guided by RNA and DNA molecules.

– ∑: Cells evolve socially into macro-organisms. Yet only the RNA-DNA system creates complex informative, control networks.

– ±i: Cells live a generational cycle chained to an organism that kills them ‘periodically’, or as free cells that die when captured by top predator living beings. Since most cells can be immortal if no other system kills or controls them hierarchically.

All those cellular cycles are not ‘mechanic processes’ but they have evolved departing from the organic, dual, Darwinian and symbiotic interactions between proteins and nucleotide acids, the dominant energetic and informative macromolecules of cells. The most important cycle is the reproductive cycle, which in the cell as in other fractal space-time represents the existential will that ensures the perpetuation of the species.

Recap. Cells follow the same dimotions of existence of all st-points.

Let us then consider in more detail the pentalogic of Bacteria in symmetry with its lower bio-chemical and upper milticellular scale controlled by the multicellular superorganism’s 3×3±¡ networks.

Other key studies would be one of ‘synchronicity’ in time considered for the ∆+1 superorganism scale.

 

ST: REPRODUCTIVE CYCLE

The reproductive cycle: from predation to evolution.

We already saw how initially bacteria pili penetrated other cells to inject in a ‘viral’ parasitic manner their own DNA in a rival cell. Thus reproduction’s origin in time must be considered a TT v. SS =TS event that evolved from predation to reproduction as the ‘two extremes’ of a predatory ‘perpendicular’ 4th Non-E congruence event was transformed into a parallel T=S communicative one. From war of ‘sexes’ to ‘sexual symbiosis’, gender sex evolved.

The interphase, prophase, anaphase and telophase complete the reproduction of the cell, in which the centriole, a perfect example of a decametric structure, with 9×2 lineal proteins and a central 2×1 nucleus that controls the lower scale of 9 forms, plays the key energetic role of TS>TT motion and entropic scattering control.

The phases of reproduction of a cell called mitosis are in fact its death period, that lasts the shorter period of the daily life of a cell. It is the genius of the cell to use its death period to split and renew itself by the Dimotion of reproduction. Yet it can still be defined as a death period, which always means that the E/I fields of the system reverse in time, the entropic, destructive Dimotion dominates and ends up dissolving and splitting the complex informative brain. So in the cell you can see mitosis as the sudden dominance of the lineal, protein, killing centrioles which are reproduced in excess at the end of the S2 phase or 3rd age of the cells, both at the lower molecular scale (assembly of ctk enzymes) and at cellular scale (centrioles and spindle) and then attack and break in two the chromosomes:

The reproductive cycle of cells shows an evolutionary pattern observed in many dual cycles between 2 complementary st-points of relative Entropy and information, which first confront their energetic and informative inverse forms. But as time goes by often by chance they realize that social, complementary evolution is more efficient than Darwinian, energetic destruction. And so they end up evolving together, following the positive, creative Dimotion of the Universe. We can hypothesize according to that homology the 3 ages of evolution of the reproductive cycle:

– Energetic, unicellular age: Sexual reproduction probably started as a Darwinian, energetic process of hunting in which lineal, energetic sperm killed the cyclical ovum and learned to host its DNA-code as virus do, in the ovum’s center. Yet as the sexual cycle evolved beyond the energetic, young age of the cycle, the ‘war of sexes’ ended and the cycle moved into a balanced 2nd age.

-S≈T: Reproductive, ‘colonial age’. Now information was exchanged between both forms, the sperm and the ovum – since sexes are in fact a specialization of species into energetic males and informative females. And a new symbiotic dual form was born. Those forms would start reproductive radiations multiplying the number of cells. So probably sexual reproduction is a key factor in the multicellular explosion of the Cambric age.

– Informative, palingenetic age. Finally, in the 3rd age of sexual evolution the informative female species dominated the cycle, as females have more genetic code (2 complete X chromosomes) and control during pregnancy the reproductive, palingenetic cycle that brings the embryo into a new ‘macro-organic level of existence’. If we observe the family cycle of human couples, women also tend to dominate the couple in its 3rd longer age, as Proust already notice; since information lasts longer than Entropy in time.

In complex organisms a living, reproductive cycle is dual: it departs from the simplex reproduction of a single cell that multiplies. Then those self-similar cells suffer a complex process of palingenetic reproduction that recreates an organism made of billions of cells, departing from that single cell.

Cellular reproduction: a tug of war between DNA and proteins.

Let us consider in this synoptic paper, the simpler process of cellular reproduction, as we have treated palingenesis in our analysis of the 4th postulate of i-logic geometry:

Organic cells reproduce within a day, chained to the symbiotic daily feeding period of the organism that provides them with Entropy and information for that reproduction. Fractal cellular reproduction shows also that duality between positive, organic complementarity Vs. negative Darwinian struggle that either balances E-bodies and I-brains into organic systems or determines their mutual destruction when that balance is broken (death processes, Lorenz Transformations, etc.) In the reproductive cell cycle, the most efficient body proteins – lineal, tubular centrioles – and the top predator, informative DNAs enact an ambiguous struggle between their Darwinian desire of mutual destruction and their need of complementary evolution.

So cellular reproduction is a mixed cycle based in both kinds of relationships in which first the lineal species of cellular Entropy (centrioles, which are long (9+1) x 2 protein fibers with a perfect decametric structure), untie the cyclical species of pure information (DNAs), trying to split and kill them. Yet DNAs, once uncoiled, defend themselves ‘informatively’, creating a new membrane that breaks the centrioles apart into 2 groups, and also breaks the cell creating 2 new ones. We can distinguish several phases in that dual struggle, dominated alternately by each of those 2 forms that involve all the other elements of the cell, directed in their dance by those Max.Te x Max.Si top predator elements or ‘upper classes’ of the cell. It will be a tug of war that illustrates all the geometrical strategies of Darwinian and complementary events between dynamic st-points:

-In the interphase, both top predator substances replicate. The centrioles are outside the membrane, which protects the DNA.

-In the prophase centrioles start their hunting: the protein’s membrane of the nucleus dissolves, exposing DNAs’ chromosomes that become visible preys. As all other universal preys do, from wriggling worms to high frequency rays, from submissive servants to herds of electrons in front of a quark or fishes in front of a shark, chromosomes try now to hide by coiling up, becoming contracted, shorter forms. Then the hunting starts. Centrioles have replicated and now double its fractal action, moving to both sides of the DNA nucleus, forming dual, long molecular chains joined by filaments. So they create a polar field of forces that captures in its filamentous web the self-replicated DNA, as a North and South Pole create together a magnetic force field that aligns atoms or two boats web a net to capture fishes.

-In the metaphase chromosomes defend themselves from the 2 centrioles that throw the ‘hooks’ of their force field, stretching the DNAs. But those chromosomes that have replicated in the earlier interphase evolve now socially in couples of parallel forms, increasing its fractal mass and moving away from the centrioles in a classic protective strategy: They arrange themselves in the equator of the spindle, adopting a Darwinian, perpendicular position, the farthest away from those centrioles. It is exactly the way in which diamagnetic particles that flee from magnetic fields, arrange themselves trying to receive the minimal quantity of force from the North and South Poles of the magnetic field.

-In the Anaphase centrioles counter-attack, splitting away the chromosome pairs.

In the telophase, DNAs find their winning, defensive strategy: They are the informative species that store the genetic code of all cellular forms. So DNAs start to reproduce new membranes in a frenzy till those membranes break the centrioles’ spindle through its middle zone, isolating each centriole and breaking their field of lineal, protein forces. Since lineal, energetic or reproductive beings, like centrioles or ‘magnetic’ fields are, cannot create monopoles. Only temporal, implosive, informative cyclical particles can do that. So the spindle dissolves and the new membrane divides the cell.

Now the system reaches again a balance, as the dual chromosomes and the dual centrioles become again single forms surrounded by a new membrane.

Thus the dynamic tug of war between a protein’s body and a nucleotide’s brain ends up in a draw, creating 2 cells instead of one, which will re-start after a rest period a new interphase process of protein and DNA reproduction. Since the Universe is indeed a game of reproductive radiations, the ultimate will of all beings that want to survive their fractal, periodic death by creating a self-similar ‘present’ form.

A variation of that process required in sexual reproduction, is called meiosis, in which the twin reproduction of DNA and its subsequent destruction of the nucleus’ membrane is provoked by the energetic sperm that enters the ovum, invading, as a virus does, its DNA nucleus and merging its genetic material. So, as it happens in the interphase of a cell, the fecundated sexual cell has 2 parallel quantities of DNA, albeit with different genetic material, coming from the ovule and the sperm. So as the replicating process repeats through the same phases of any cellular reproduction, the final result won’t be an identical cell but a cell that mixes the genes of both, the sperm and the ovum. When besides sexual duplication there is an interphase with chromosomal duplication the final 2 cells will be diploid cells with twice the genetic material of the original cell. This happens only in multicellular organisms, as redundant genetic material is useful to store genetic orders needed for the complex construction of multicellular structures; but it would be redundant in the simple life of a monera cell, which escapes the interphase duplication.

The TT-past x SS-future duality of lineal sperm and cyclical ovum extends outside the realm of form and transcends to the upper scale of multi-cellular organisms and sexual characters: the ovum is an informative, cyclical, autotrophic female cell with higher chromosomal content; while sperm is an energetic, heterotrophic, lineal male cell with higher mobility. And we find according to the Fractal Principle, 3 evolutionary types of increasingly differentiated sexual cells: semen and ovum, which are equal in spatial size and temporal form (isogamy); semen that is equal in form but smaller than the ovum (anisogamy); and ovum and semen, which are different in spatial size and temporal form (oogamy), as in human beings.

Those differences between male sperm and female unicellular ovum, latter diluted as their genetic materials mix, reminds us of the differences between unicellular animal and plants, the main dual differentiation of life along its SxT parameters that we will study now in more detail.

Recap. Sexual reproduction evolved from an energetic event in the unicellular age into a reproductive radiation and finally into the palingenetic process dominated by the ovum.

Cellular reproduction can be explained as a tug of war between the informative DNA and the reproductive proteins of the centrioles.

 

 

TT: FEEDING: Metabolic paths.

The question on the Feeding cycle of the animal cell is how it went from simple Left) to complex (right) and again, only the properties of ¬∆@st ignore in 4D, perception of information and memorial ‘Adenine’ minds can explain it:’

(to be conted)

 

St-Ts: LOCOMOTION

Locomotion required the interaction of an St-light sensorial element, which in Eugleni (graph) became precursor of future eyes, and a lineal mobile flagellum, already saw in bacteria. So curiously enough in Eugleny both the ‘flagelum’, the top predator lineal cell, and the eye, evolved side by side, which testifies again how in 5D evolution of the 2 elements TT vs. SS often come together, as necessary symbiotic events. And not surprisingly those 2 elements are the parts of life ‘intelligent design’ considers too complex to evolve together. To all the argument brought about by classic biology about why they could indeed evolve, we thus add the usual elements of 5D systems – complementarity, limited S<ST>T variations and the fractal principle of trilogic. As the rotor of the flagellum does have a perfect 3 x 3 x 3 ±¡ nucleic commonest form of social evolution.

The evolution of flagella is of great interest to biologists because the three known varieties of flagella (eukaryotic, bacterial, and archaeal) each represent a sophisticated cellular structure that requires the interaction of many different systems and since as we forecast 30 years ago, recent studies on the microtubule organizing center suggest that the most recent ancestor of all eukaryotes already had a complex flagellar apparatus.

But it won’t give birth to multicells as some suggest, because flagella is the Ts-top predator ‘locomotion’ unicellular organism.

And social evolution requires a top predator, St-organism.

So it is only a question of time that (Volume II of 5D Biology), ‘experts’ realize the multicellular organism is also an evolution of amoeboid.

As usual by lack of complex causality beyond ceteris paribus analysis there are 2 ‘competing theories’. The ‘endogenous and exogenous’ theories. Both are obviously truth, but apply to different species. The simplest bacteria did get it endogenous; the Eukaryote, as it was truly the product of a DNA-viral symbiotic process of evolution that learned to cherry-pick the ‘best’ genes of the best species on the chaotic super populated world of the 800 years old snowball earth, obviously came as Margoulis wanted it from the ‘best’ specialized flagella:

Bacterial flagellum

There is good evidence that the bacterial flagellum has evolved from a Type III secretory and transport system, given the similarity of proteins in both systems.

All currently known nonflagellar Type III transport systems serve the function of exporting (injecting) toxin into eukaryotic cells. Similarly, flagella grow by exporting flagellin through the flagellar machinery. It is hypothesised that the flagellum evolved from the type three secretory system. For example, the bubonic plague bacterium Yersinia pestis has an organelle assembly very similar to a complex flagellum, except that is missing only a few flagellar mechanisms and functions, such as a needle to inject toxins into other cells. The hypothesis that the flagellum evolved from the type three secretory system has been challenged by recent phylogenetic research that strongly suggests the type three secretory system evolved from the flagellum through a series of gene deletions.As such, the type three secretory system supports the hypothesis that the flagellum evolved from a simpler bacterial secretion system.

 

∆§-BIO-CHEMICAL MINDS: THE EXPRESSION OF THE 3±¡ DIMOTIONS IN PLANT HORMONES

We have now made a fast review of the basic elements of the ∆º cellular scale. When we move to multicellular scales, whose evolution is treated in the parallel paper on Time, entropy and mind, we find that the fundamental element of successful internal evolution is as always the interplay between the SS<St, fixed mind and languages whose speed determines the existential momentum and force of the system. Those languages thus split the kingdom of life between slow thinkers – chemical plants, and fast moves, animal life. In this paper on space and scale, we are more interested in the pentalogic of networks and the dimotions of the ‘present’ spatial lifecycle of beings; not in its evolution as species.

So we must consider internally how biological systems code with those languages the 5 Dimotions of existence of its submissive, ∆-1 cells; how they distribute to those cells through its trinity networks the substance they need to co-exist and finally how in the outer world, their senses perceive ∆+1 languages that perform the same function for them, as a whole, from the perspective of the world, in the ‘chain of beings’ that interact together on Gaia, from the amino acid to the ecosystem whereas each ‘O¡’ God of its lower ∆-1 parts, become just an |-1 cell of its larger ∆+1 whole. That is, Earth’s membrain of living gaia provides its animal life with the substances needed for they to perform its existential dimotions of Ts-locomotion, Tt-feeding, ST-reproduction, St-social evolution and SS-perception; and in turn, each organism provides with his networks the same dimotion to its lower parts, and within the cell to its SS-DNA>St-RNA>ST-protein.

   CHEMICAL VS ELECTRIC LANGUAGES: PLANTS

The antisymmetry or inversion of ‘dimotions’ of existence between species, such as what is energy for a system might be information for other; what is attraction for a predator towards a prey might be repulsion of the prey to the predator is one of the most paradoxical elements of 5D vital geometries, as it interconnects and balances parts into whole events unwanted by a part. But as all systems are dual S-T forms it is an unavoidable entanglement of the organism universe. This is the case of light, which is energy of plants and information for animals. So plants have a chemical brain, as they cannot process faster light information, buried on the planet earth, made of larger atoms, which implies according to 5D metrics that they have slower languages that makes them easy preys of animal predators. The age of plant dominance on Earth thus ended with the arousal of animal species. But as survival can be maximized either by S, T or ST-dimotions of existence, we can immediately distinguish a ‘trinity specialization’ of life beings into:

T>St: Plants that absorb the motion of light to create energy for its formal growth, taking advantage of light so they don’t need to move. Plants are thus the energy species of life that receives from ∆+1 Gaia the food and we can consider the entire solar system its ‘network of distribution of energy’.

St>SS: Animals that absorb the information of light to create still mind mappings of the world in which they move. Animals thus are the informative species of life.

An this leaves a 3rd strategy of survival, which gives birth to the 3rd great multicellular land-life species:

ST: fungi that achieve the maximal speed of reproduction of any species. And so can survive despite neither use light as energy nor as information. As such fungi eat instead everything that can be edible, decomposing all other life forms and what is more fascinating, becoming the symbiotic higher brain of plants at the chemical root level, allowing its social evolution. So fungi shows the horror vacuum of the Universe, expressed by Leibniz and latter by the Totalitarian Principle of Gell-mann: “everything that can exists will exist’. The game of existence will find a variation for every possible econiche of energy and information to be exploited including scavengers, parasites, artic mosquitoes, top quark black holes and any combination of existential algebra that permits a form to absorb motion and form (or its combination energy) to reproduce.

In the upper center the largest plant fungi, the acetabularia, shows its nucleus in the root, B, which is the brain of plants, opposite to the animal upper brain coordinates. The opposition between both forms extends to the cycles of Entropy, as plants destroy water and produce oxygen; while animals breathe oxygen and produce water. Thus, both are the ‘particles’ and ‘antiparticles’ of life, which together reach a balance S=T; and so together form an even larger superorganism – the balanced ∆±¡ Gaia, whose atmosphere has been kept in balance by its ‘cellular life’ forms for near a billion years since the first ‘electric cells=animals’ appear during the ice ball age.

Plants. Its languages of information. A ‘social democracy’.

What makes plants interesting from a purely 5D theoretical analysis of its variation of the thoughts of God is the fact that it is truly a social democracy. That is, no cell is a predatory cell as in the case of animals which are electric cells preying on everybody else. It strictly limits its predation to the social evolution of complexity departing from the simplest elements of reality, photons of light on ∆-3 (albeit if scales are infinite you might say plants eat ‘whole stars 🙂 and atoms (idem, maybe whole galaxies… but in this case hardly affected by its molecular ensemble). Plants are thus ‘feminine’ balanced forms that need not to express an S<T>S bipolar destruction-creation process. And yet still they do have a ternary structure, which corresponds to the rules of vital topology:

TT>Ts-flat leaves<ST: Trunk> St-roots of maximal quantization

Open hyperbolic networks peering into the 5th dimension.

Languages of information, which code and express the biological dimotions also evolve by ternary differentiation. For example, the human language, if we restrict our analysis to its vowels was born as a duality of an ‘energetic’ active ‘a’, which drove to action and an implosive, reflexive ‘u’, which drove to self-reflection (basic chimpanzee language). We might then imagine a 3rd combination, or ‘I’, the creative i-dea, the ‘I’-self, and two final ‘modulations’, the ‘less energetic e’ and ‘less informative’ I.

Those examples of the rich field of socio-cultural studies based in the ternary differentiations of the creative program of the Universe, are a parallel example to the simple ‘vowels’ of the hormonal, chemical language that controls plant growth with 5 simple vowels, drawn in the image.

The chemical language of multicellular organisms have a reduced vocabulary of ‘yes’ and ‘no’ symbols called hormones that inhibit or foster the natural cycles of existence of living beings; and define the speed of height growth of the plant.

In the graph, the 5 main plants’ hormones are 5 simple vowels: 3 are cyclical, creative, informative, ‘yes’ hormones that reproduce the plant; and 2 are destructive, energetic ‘no’ hormones, with opened rings and strong, lineal carbon chains like ethylene, CH2=CH2, that inhibit growth. If we further divide ‘yes’ hormones according to the Fractal Principle and the 3rd postulate of affinity, we find that each one of them reproduces the plant’s e-ixe-i element with similar structure:

– Max.Te: The longest ternary form, rich in oxygens, Gibberine, develops the lineal trunk.

– S= T: The structural, cyclical form, Auxin, made of carbon rings, develops the leaves.

– Max.Si: The informative nitrogenized Zeatine reproduces the brain roots.

Thus, hormones form a simple, ternary language that follows the rules of SxT cycles, controlling the living cycles of organisms by acting as messengers of the RNA-DNA brains of their social cells.

Plants Vs. animals: chemical language Vs. electric messages.

  1. Entropy organs: Leaves that perform the ‘moving’ energetic, photosynthesis cycle and branches that act as still structures and conductive systems of the energetic materials.
  2. Informative organs: Root systems that absorb molecules and produce most of its hormones.
  3. Reproductive organs: Flowers and trunks, the bodies that communicate leaves and roots and experience maximal growth.

These 3 organs define a plant as an efficient ternary st-point, a complex species able to colonize the ground with a clear evolutionary direction of height.

The interaction of the 3 hierarchical levels of life.

According to the i-logic isomorphisms of creation all organic systems require the co-existence and interaction of their 3 scales of social evolution or relative past, present and future hierarchical forms.

So the creation of multi-cellular organisms happens also simultaneously in 3 ‘hierarchical planes’: the ∆-1, atomic-molecular interval; the ∆-DNA-cellular scale and the ∆+1 network-organism interval.

While the flows of temporal Entropy that travel through those different planes of existence follow the hierarchical law of illogic geometry: A fractal jump in geometric time or a movement in space extends only to the next discontinuous space-time scale.

So in any organism, the ∆-1 hormones (the molecular language that regulates ∆-cells), the ∆-genes (the information that transcends from the ∆-cellular DNA to the ∆+1 organism as a whole) and the seminal, palingenetic cells that give birth to the new being, program only their higher plane.

Hence cellular genes determine the biologic elements of the organism (the next scale of social evolution), but not the ∆+2 sociological scale of existence of a human being: chemical, racial genes do not determine history. At best we might consider that nervous networks determine the emotional character and intelligence of historic individuals, who might change the course of societies. Let us study the structure of those 3 levels of hierarchical information that codify the creation of organisms.

Hormones: the language of cells creates its networks.

According to the fractal law, the language of regulation of social groups of ∆-cells are ∆-1 molecular hormones, which act as phonemes of a language spoken by RNA-DNA macromolecules, the informative networks of cells, which can manufacture them.

Languages are ‘i-logic programs’ structured by the same ternary topologies of Entropy, reproduction and information, facilitating the Universal understanding of its codes by other e, SxT, I systems they code. Take the case of the key hormone of a human male, testosterone. It is a simple protein with 4 carbons, strong structural rings in a lineal shape that regulates, despite its simplicity, the reproductive development of energetic males, provoking actions of a complexity far superior to its molecular simplicity. How this can be possible? The answer is that the hormonal language is a relatively simple, positive Vs negative, ‘yes Vs no’ language that provokes or inhibits the 3±∆ cycles of existence natural to the will of the cells, proteins and nucleic acids it communicates.

But how hormones provoke so many different reactions in a cell, being so simple? The process of course becomes much more complex in their details as any language with a few phonemes can create very complex memorial, sequential sentences through the repetition of a few basic patterns. So for example some hormones are substances that inhibit the inhibitors of those existential cycles. On the other hand many hormones are transported by proteins, ‘lineal killers’, which modify them or ‘motivate’ other messengers of the cell or network system that carry further the message.

Thus the second translation of the hormonal message into a singular product of a certain cell modifies the message that becomes specific for that cell or organ. This is especially certain among animals that, unlike democratic, ‘spatial’, reproductive plants and fungi with a few basic tissues and a lot of generic orders, are hierarchical, temporal, complex systems with 2 informative languages: submissive, slower chemical hormones and faster, nervous orders. So hormones are created by neuro-secretory cells, part of the higher plane of existence of neuronal networks, which pour them into the blood. And often they are accompanies by nervous messages, which they reinforce.

Thus, animal cells might recognize hormones because they know ‘behind’ their orders there is a very complex and powerful system: the nervous or blood system that has to be obeyed or else. Since the blood system sends leukocytes to kill rebel cells and the nervous system sends flows of electronic information to control them. It is the same reason that makes people to obey simple codes like those of traffic. We obey because we know that behind those codes there is a complex organic system, the state that will send its police, its ‘social leukocytes’ and punish us. So the question is how a cell knows? Because its DNA has a degree of memorial, instinctive perception; it is not a mechanism.

Despite all those elements of complexity, it is still possible to classify all hormones according to their spatial or informative, ‘universal’ morphology as ‘inhibitors or agents’ of the 3 basic cyclical actions of any organic system; since their morphology imitates or it is based in informative nucleotides, structural carbons and lineal, energetic shapes, whose functions are instinctively understood by all living forms as all animals understand black and white colors as relative information or Entropy, or ‘aaarg’, open vowels and bass sounds as ‘energetic anger’ and ‘u’ closed vowels and highly quantized informative frequencies as informative curiosity.

Thus, invariance of form between scales allows the existence of languages that are decoded as they respond to the Universal language of self-similar topologies of all forms of existence.

So according to duality, when hormones act as inhibitors, they have an energetic, lineal form; when they act as agents to foster those existential cycles they have a cyclical, informative shape.

Finally, according to the 3rd postulate of parallelism applied to ∆/∆+1 systems, their atomic components tend to be parallel to forms of the ∆+1 organ in which they accomplish their function. So when they act in the energetic zones of the cell or the macro-organism they are hyper abundant in oxygen, when they act in the informative brain they tend to be similar to nucleotide acids and when they act in the reproductive zones, they have carbon rings and vice versa.

In the graph, those simple rules explain the 3+2 main types of hormones in plants:

-Max.Te: Cyclical Auxin, rich in carbons, increases the growth of shoots, the Entropy zone.

-Max.Si: Cyclic, nitrogenized Cytokinines control the growth of roots, the brains of plants.

-S≈T: Oxygenated, Gibberellic acid causes high growth in trunks and reproductive flowers.

Ultimately in as much as most hormones and enzymes act as inhibitors, they prove that the 3 energetic, informative and reproductive inner individual actions of organisms are the natural dimotions of all organic systems, the will of any species, that have to be constantly inhibited by the neuronal-endocrine dual logic system of multicellular control. Since when that control disappears, naturally species try to reproduce. That is why cancers and any other form of cellular reproduction are so natural; because reproduction is the natural will of the fractal, organic Universe.

Finally, the duality of the SxT systems and anti-systems with diffeomorphic, opposite coordinates creates inverse hormones that neutralize each other. So ‘energetic hormones’ inhibit ‘informative regions’ of the organism. For example, we can consider that form Vs anti-form duality, analyzing the inverse growth effect in informative roots and energetic leaves of the 2 previous hormones, auxins and purines. What we observe is a diffeomorphic, inverse dual SxT process: the auxin that increases the growth of shoots inhibits the growth of inverse roots. And so auxins and quinines together work as a perfect dual system of growth control in the informative zone of the plant:

The root is a nitrogen-based informative system, which as all informative entities from neurons to worm holes, requires a lot of time and complex steps to reproduce its form. So quinines, its growth hormone, acts by parallelism, since it has 2 purine rings with nitrogens that positively induce the complex growth of roots made with nitrogens.

On the other hand, auxins have a structure that closely resembles the main nucleotide species, the purines. Yet, auxins ad to the hexagonal-pentagonal structure of purines a simple protein tail to move faster, and instead of nitrogens, auxins have 2 strong carbon rings. So it is basically a false purine with a far stronger body and a mobile tail that substitutes the quinine’s nitrogens and inhibits the root’s growth, because it cannot deliver the proper instructions.

On the other hand, the ever-growing shoots are the plant’s reproductive systems; whose natural will to grow is so strong that any hormone increases its reproductive rate unless it is inhibited.

If we study the energetic cycle of plants, again we observe that dual inverse control system: Abscisic acid (a lineal molecule with a lot of oxygen elements) provokes the fall of leaves, while the lineal gas ethane, CH2=CH2, increases by parallelism with the lineal CO2 molecule their respiration and metabolic rate. Both are very simple, energetic hormones, which resemble the 2 ‘energetic’ inverse products of breathing, oxygen and CO2, ‘reminding’ the plant that it has to accelerate or halt to its ‘death’ its production of those 2 products.

Recap. A language of information is always needed to create a complex organism. The simplest languages have 3 or 5 vowels, which represent energetic, informative and reproductive messages and its variations. They act by parallelism, since all systems and planes of an organism follow the ‘invariance’ of form and function. They also can deliver negative or positive orders depending of their parallelism or inversion with the form of the species they code. The language is always reproduced by the informative ‘upper-caste’ particles of the system, which delivers the orders to the rest of the elements. In plants, the language is a hormonal language with 3 main vowels, energetic auxin, informative cytokinines and reproductive Gibberellic acid.

 

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