What's new in

Magnetospheric Consciousness

Note: Newest contributions are at the top!

Year 2007

Quantum version of Expanding Earth theory

TGD predicts that cosmic expansion at the level of individual astrophysical systems does not take place continuously as in classical gravitation but through discrete quantum phase transitions increasing gravitational Planck constant and thus various quantum length and time scales. The reason would be that stationary quantum states for dark matter in astrophysical length scales cannot expand. One would have the analog of atomic physics in cosmic scales. Increases of hbar by a power of two are favored in these transitions but also other scalings are possible.

This has quite far reaching implications.

  1. These periods have a highly unique description in terms of a critical cosmology for the expanding space-time sheet. The expansion is accelerating. The accelerating cosmic expansion can be assigned to this kind of phase transition in some length scale (TGD Universe is fractal). There is no need to introduce cosmological constant and dark energy would be actually dark matter.

  2. The recently observed void which has same size of about 108 light years as large voids having galaxies near their boundaries but having an age which is much higher than that of the large voids, would represent one example of jerk-wise expansion.

  3. This picture applies also to solar system and planets might be perhaps seen as having once been parts of a more or less connected system, the primordial Sun. The Bohr orbits for inner and outer planets correspond to gravitational Planck constant which is 5 times larger for outer planets. This suggests that the space-time sheet of outer planets has suffered a phase transition increasing the size scale by a factor of 5. Earth can be regarded either as n=1 orbit for Planck constant associated with outer planets or n= 5 orbit for inner planetary system. This might have something to do with the very special position of Earth in planetary system. One could even consider the possibility that both orbits are present as dark matter structures. The phase transition would also explain why n=1 and n=2 Bohr orbits are absent and one only n=3,4, and 5 are present.

  4. Also planets should have experienced this kind of phase transitions increasing the radius: the increase by a factor two would be the simplest situation.

The obvious question - that I did not ask - is whether this kind of phase transition might have occurred for Earth and led from a completely granite covered Earth -Pangeia without seas- to the recent Earth. Neither it did not occur to me to check whether there is any support for a rapid expansion of Earth during some period of its history.

Situation changed when my son Paavo visited me last Saturday and told me about a Youtube video by Neal Adams, an American comic book and commercial artist who has also produced animations for geologists. We looked the amazing video a couple of times and I looked it again yesterday. The video is very impressive (no wonder!) but in the lack of references skeptic probably cannot avoid the feeling that Neal Adams might use his highly developed animation skills to cheat you. I found also a polemic article of Adams but again the references were lacking. Perhaps the reason of polemic tone was that the concrete animation models make the expanding Earth hypothesis very convincing but geologists dare not consider seriously arguments by a layman without a formal academic background.

1. The claims of Adams

The basic claims of Adams were following.

  1. The radius of Earth has increased during last 185 million years (dinosaurs appeared for about 230 million years ago) by about factor 2. If this is assumed all continents have formed at that time a single super-continent, Pangeia, filling the entire Earth surface rather than only 1/4 of it since the total area would have grown by a factor of 4. The basic argument was that it is very difficult to imagine Earth with 1/4 of surface containing granite and 3/4 covered by basalt. If the initial situation was covering by mere granite -as would look natural- it is very difficult for a believer in thermodynamics to imagine how the granite would have gathered to a single connected continent.

  2. Adams claims that Earth has grown by keeping its density constant, rather than expanded, so that the mass of Earth has grown linearly with radius. Gravitational acceleration would have thus doubled and could provide a partial explanation for the disappearance of dinosaurs: it is difficult to cope in evolving environment when you get slower all the time.

  3. Most of the sea floor is very young and the areas covered by the youngest basalt are the largest ones. This Adams interprets this by saying that the expansion of Earth is accelerating. The alternative interpretation is that the flow rate of the magma slows down as it recedes from the ridge where it erupts. The upper bound of 185 million years for the age of sea floor requires that the expansion period - if it is already over - lasted about 185 million years after which the flow increasing the area of the sea floor transformed to a convective flow with subduction so that the area is not increasing anymore.

  4. The fact that the continents fit together -not only at the Atlantic side - but also at the Pacific side gives strong support for the idea that the entire planet was once covered by the super-continent. After the emergence of subduction theory this evidence as been dismissed: sounds very odd to me. It seems that geologists are doing "Wegeners" again.

  5. I am not sure whether Adams mentions this objection. Subduction only occurs on the other side of the subduction zone so that the other side should show evidence of being much older in the case that oceanic subduction zones are in question. This is definitely not the case. This is explained in plate tectonics as a change of the subduction direction. My explanation would be that by the symmetry of the situation both oceanic plates bend down so that this would represent new type of boundary not assumed in the tectonic plate theory.

  6. As a master visualizer Adams notices that Africa and South-America do not actually fit together in absence of expansion unless one assumes that these continents have suffered a deformation. Continents are not easily deformable stuff. The assumption of expansion implies a perfect fit of all continents without deformation.

Knowing that the devil is in the details, I must admit that some of these arguments look rather convincing to me and what I learned from Wikipedia "../articles/ supports this picture.

2. The critic of Adams of the subduction mechanism

The prevailing tectonic plate theory has been compared to the Copernican revolution in geology. The theory explains the young age of the seafloor in terms of the decomposition of the litosphere to tectonic plates and the convective flow of magma to which oceanic tectonic plates participate. The magma emerges from the crests of the mid ocean ridges representing a boundary of two plates and leads to the expansion of sea floor. The variations of the polarity of Earth's magnetic field coded in sea floor provide a strong support for the hypothesis that magma emerges from the crests.

The flow back to would take place at so called oceanic trenches near continents which represent the deepest parts of ocean. This process is known as subduction. In subduction oceanic tectonic plate bends and penetrates below the continental tectonic plate, the material in the oceanic plate gets denser and sinks into the magma. In this manner the oceanic tectonic plate suffers a metamorphosis returning back to the magma: everything which comes from Earth's interior returns back. Subduction mechanism explains elegantly formation of mountains (orogeny), earth quake zones, and associated zones of volcanic activity.

Adams is very polemic about the notion of subduction, in particular about the assumption that it generates steady convective cycle. The basic objections of Adams against subduction are following.

  1. There are not enough subduction zones to allow a steady situation. According to Adams, the situation resembles that for a flow in a tube which becomes narrower. In a steady situation the flow should accelerate as it approaches subduction zones rather than slow down. Subduction zones should be surrounded by large areas of sea floor with constant age. Just the opposite is suggested by the fact that the youngest portion of sea-floor near the ridges is largest. The presence of zones at which both ocean plates bend down could improve the situation. Also jamming of the flow could occur so that the thickness of oceanic plate increases with the distance from the eruption ridge. Jamming could increase also the density of the oceanic plate and thus the effectiveness of subduction.

  2. There is no clear evidence that subduction has occurred at other planets. The usual defense is that the presence of sea is essential for the subduction mechanism.

  3. One can also wonder what is the mechanism that led to the formation of single super continent Pangeia covering 1/4 of Earth's surface. How probable the gathering of all separate continents to form single cluster is? The later events would suggest that just the opposite should have occurred from the beginning.

3. Expanding Earth theories are not new

After I had decided to check the claims of Adams, the first thing that I learned is that Expanding Earth theory, whose existence Adams actually mentions, is by no means new. There are actually many of them.

The general reason why these theories were rejected by the main stream community was the absence of a convincing physical mechanism of expansion or of growth in which the density of Earth remains constant.

  1. 1888 Yarkovski postulated some sort of aether absorbed by Earth and transforming to chemical elements (TGD version of aether could be dark matter). 1909 Mantovani postulated thermal expansion but no growth of the Earth's mass.

  2. Paul Dirac's idea about changing Planck constant led Pascual Jordan in 1964 to a modification of general relativity predicting slow expansion of planets. The recent measurement of the gravitational constant imply that the upper bound for the relative change of gravitational constant is 10 time too small to produce large enough rate of expansion. Also many other theories have been proposed but they are in general conflict with modern physics.

  3. The most modern version of Expanding Earth theory is by Australian geologist Samuel W. Carey. He calculated that in Cambrian period (about 500 million years ago) all continents were stuck together and covered the entire Earth. Deep seas began to evolve then.

4. Summary of TGD based theory of Expanding Earth

TGD based model differs from the tectonic plate model but allows subduction which cannot imply considerable back flow of magma. Let us sum up the basic assumptions and implications.

  1. The expansion is due to a quantum phase transition increasing the value of gravitational Planck constant and forced by the cosmic expansion in the average sense.

  2. Tectonic plates do not participate to the expansion and therefore new plate must be formed and the flow of magma from the crests of mid ocean ridges is needed. The decomposition of a single plate covering the entire planet to plates to create the mid ocean ridges is necessary for the generation of new tectonic plate. The decomposition into tectonic plates is thus prediction rather than assumption.

  3. The expansion forced the decomposition of Pangeia super-continent covering entire Earth for about 530 million years ago to split into tectonic plates which began to recede as new non-expanding tectonic plate was generated at the ridges creating expanding sea floor. The initiation of the phase transition generated formation of deep seas.

  4. The eruption of plasma from the crests of ocean ridges generated oceanic tectonic plates which did not participate to the expansion by density reduction but by growing in size. This led to a reduction of density in the interior of the Earth roughly by a factor 1/8. From the upper bound for the age of the seafloor one can conclude that the period lasted for about 185 million years after which it transformed to convective flow in which the material returned back to the Earth interior. Subduction at continent-ocean floor boundaries and downwards double bending of tectonic plates at the boundaries between two ocean floors were the mechanisms. Thus tectonic plate theory would be more or less the correct description for the recent situation.

  5. One can consider the possibility that the subducted tectonic plate does not transform to magma but is fused to the tectonic layer below continent so that it grows to an iceberg like structure. This need not lead to a loss of the successful predictions of plate tectonics explaining the generation of mountains, earthquake zones, zones of volcanic activity, etc...

  6. From the video of Adams it becomes clear that the tectonic flow is East-West asymmetric in the sense that the western side is more irregular at large distances from the ocean ridge at the western side. If the magma rotates with a slightly lower velocity than the surface of Earth (like liquid in a rotating vessel), the erupting magma would rotate slightly slower than the tectonic plate and asymmetry would be generated.

  7. If the planet has not experienced a phase transition increasing the value of Planck constant, there is no need for the decomposition to tectonic plates and one can understand why there is no clear evidence for tectonic plates and subduction in other planets. The conductive flow of magma could occur below this plate and remain invisible.

The biological implications might provide a possibility to test the hypothesis.
  1. Great steps of progress in biological evolution are associated with catastrophic geological events generating new evolutionary pressures forcing new solutions to cope in the new situation. Cambrian explosion indeed occurred about 530 years ago (the book Wonderful Life of Stephen Gould explains this revolution in detail) and led to the emergence of multicellular creatures, and generated huge number of new life forms living in seas. Later most of them suffered extinction: large number of phylae and groups emerged which are not present nowadays.

    Thus Cambrian explosion is completely exceptional as compared to all other dramatic events in the evolution in the sense that it created something totally new rather than only making more complex something which already existed. Gould also emphasizes the failure to identify any great change in the environment as a fundamental puzzle of Cambrian explosion. Cambrian explosion is also regarded in many quantum theories of consciousness (including TGD) as a revolution in the evolution of consciousness: for instance, micro-tubuli emerged at this time. The periods of expansion might be necessary for the emergence of multicellular life forms on planets and the fact that they unavoidably occur sooner or later suggests that also life develops unavoidably.

  2. TGD predicts a decrease of the surface gravity by a factor 1/4 during this period. The reduction of the surface gravity would have naturally led to the emergence of dinosaurs 230 million years ago as a response coming 45 million years after the accelerated expansion ceased. Other reasons led then to the decline and eventual catastrophic disappearance of the dinosaurs. The reduction of gravity might have had some gradually increasing effects on the shape of organisms also at microscopic level and manifest itself in the evolution of genome during expansion period.

  3. A possibly testable prediction following from angular momentum conservation (ωR2= constant) is that the duration of day has increased gradually and was four times shorter during the Cambrian era. For instance, genetically coded bio-clocks of simple organisms during the expansion period could have followed the increase of the length of day with certain lag or failed to follow it completely. The simplest known circadian clock is that of the prokaryotic cyanobacteria. Recent research has demonstrated that the circadian clock of Synechococcus elongatus can be reconstituted in vitro with just the three proteins of their central oscillator. This clock has been shown to sustain a 22 hour rhythm over several days upon the addition of ATP: the rhythm is indeed faster than the circadian rhythm. For humans the average innate circadian rhythm is however 24 hours 11 minutes and thus conforms with the fact that human genome has evolved much later than the expansion ceased.

  4. Addition: My son told that scientists have found a fossil of a sea scorpion with size of 2.5 meters which has lived for about 10 million years for 400 million years ago in Germany (see also the article in Biology Letters). The finding would conform nicely with the much smaller value of surface gravity at that time. Also the emergence of trees could be understood in terms of a gradual growth of the maximum plant size as the surface gravity was reduced. The fact that the oldest known tree fossil is 385 million years old conforms with this picture.

5. Did intra-terrestrial life burst to the surface of Earth during Cambrian expansion?

Intra-terrestrial hypothesis is one of the craziest TGD inspired ideas about the evolution of life and it is quite possible that in its strongest form the hypothesis is unrealistic. One can however try to find what one obtains from the combination of the IT hypothesis with the idea of pre-Cambrian granite Earth. Could the harsh pre-Cambrian conditions have allowed only intra-terrestrial multicellular life? Could the Cambrian explosion correspond to the moment of birth for this life in the very concrete sense that the magma flow brought it into the day-light?

  1. Gould emphasizes the mysterious fact that very many life forms of Cambrian explosion looked like final products of a long evolutionary process. Could the eruption of magma from the Earth interior have induced a burst of intra-terrestrial life forms to the Earth's surface? This might make sense: the life forms living at the bottom of sea do not need direct solar light so that they could have had intra-terrestrial origin. It is quite possible that Earth's mantle contained low temperature water pockets, where the complex life forms might have evolved in an environment shielded from meteoric bombardment and UV radiation.

  2. Sea water is salty (for why this is the case see this). It is often claimed that the average salt concentration inside cell is that of the primordial sea: I do not know whether this claim can be really justified. If the claim is true, the cellular salt concentration should reflect the salt concentration of the water inside the pockets. The water inside water pockets could have been salty due to the diffusion of the salt from ground but need not have been same as that for the ocean water (higher than for cell interior and for obvious reasons). Indeed, the water in the underground reservoirs in arid regions such as Sahara is salty, which is the reason for why agriculture is absent in these regions. Note also that the cells of marine invertebrates are osmoconformers able to cope with the changing salinity of the environment so that the Cambrian revolutionaries could have survived the change in the salt concentration of environment.

  3. What applies to Earth should apply also to other similar planets and Mars is very similar to Earth. The radius is .533 times that for Earth so that after quantum leap doubling the radius and thus Schumann frequency scale (7.8 Hz would be the lowest Schumann frequency) would be essentially same as for Earth now. Mass is .131 times that for Earth so that surface gravity would be .532 of that for Earth now and would be reduced to .131 meaning quite big dinosaurs! We have learned that Mars probably contains large water reservoirs in it's interior and that there is an un-identified source of methane gas usually assigned with the presence of life. Could it be that Mother Mars is pregnant and just waiting for the great quantum leap when it starts to expand and gives rise to a birth of multicellular life forms. Or expressing freely how Bible describes the moment of birth: in the beginning there was only darkness and water and then God said: Let the light come!

To sum up, TGD would provide only the long sought mechanism of expansion and a possible connection with the biological evolution. It would be indeed fascinating if Planck constant changing quantum phase transitions in planetary scale would have profoundly affected the biosphere.

For more details see the chapter Pre-biotic Evolution in Many-Sheeted Space-Time.

DNA as a topological quantum computer

For years ago I developed a model of topological quantum computation combining TGD based view about space-time with basic ideas about topological quantum computation and ended up with the proposal that DNA might act as a topological quantum computer.

The first guess (see this) was that parallel DNA or RNA strands could form braids. The problem is that the number of braid strands is limited and the computations are restricted within single cell nucleus. The need to establish the hardware for each computation separately can be also seen as a restriction.

One can imagine also other manners in which DNA or RNA could act as a topological quantum computer and it good to try to state clearly what one wants.

  1. Natural requirements are that the topological quantum computer programs can be naturally combined to larger programs and evolution means this kind of process; that the programs have a natural modular structure inherited from the previous stages of evolution; and that the computation is not restricted inside single nucleus.

  2. DNA and/or RNA defines the hardware of topological computation and at least for more advanced topological quantum computers this hardware should be static so that only programs would be dynamical. This leaves only DNA in consideration and the entangled initial and quantum states at the ends of braids quantum states would be assignable to static DNA structures.

  3. The program would be determined by different braidings connecting the states of DNA in time direction or in spatial direction. Since the genomes are identical in different nuclei, the strands could connect different nuclei or conjugate strands of double DNA strand.

1. The recent progress in quantum TGD and TGD inspired quantum biology

After the advent of the first model for topological quantum computation in TGD Universe (see this), the mathematical and physical understanding of TGD has developed dramatically and the earlier quite speculative picture can be replaced with a framework which leads to a rather unique view about topological quantum computations by DNA.

1.1 Universe as a topological quantum computer

One can say that the recent formulation of quantum TGD states that the entire Universe behaves like a topological quantum computer. This notion of topological quantum computer differs however from the standard one in many respects.

  1. The emergence of hierarchy of Planck constants realized as a generalization of the notion of imbedding space is now a basic piece of TGD allowing an elegant formulation of quantum TGD (see this and this). The phases of matter with large Planck constant are interpreted as dark matter. Large values of Planck constant make possible topological quantum computations in arbitrary long time scales so that the most fundamental objection against quantum computation can be circumvented.

  2. Zero energy ontology forces to unify S-matrix and density matrix to M-matrix - the product of the square root of density matrix and S-matrix- defined as time-like (or rather light-like) entanglement coefficients between positive and negative energy parts of zero energy state (see this and this). Connes tensor product emerging naturally from the notion of finite measurement resolution described in terms of inclusions of hyperfinite factors of type II1 defines highly uniquely the M-matrix. M-matrix would be natural candidate for defining topological quantum computation in light-like direction. Connes tensor product makes sense also in space-like direction and would define quantum storage of functions represented as entanglement coefficients.

  3. The notion of number theoretic braid (see this and this) is now well-understood and has become a basic element of the formulation of quantum TGD based on the requirement of number theoretical universality. As a matter fact, the notion of braid is generalized in the sense that braid strands can fuse and decay. The physical interpretation is as motion of minima of the generalization eigenvalue of the modified Dirac operator which is function of transversal coordinates of light-like partonic 3-surface and has interpretation as vacuum expectation of Higgs field. Fusion of braid strands corresponds to fusion of minima.

    For generalized Feynman diagrams partonic light-like 3-surfaces meet at 2-dimensional vertices defined by partonic 2-surfaces (see this). This implies that braids replicate at vertices: the interpretation is as a copying of classical information. Quantum information is not copied faithfully. The exchange of partonic 2-surfaces in turn corresponds to quantum communications. Hence quantum communication and quantum copying emerge naturally as additional elements. Space-like Connes tensor product in turn defines quantum memory storage.

  4. Computation time is a fundamental restriction in both ordinary and quantum computation. Zero energy ontology makes possible communications in both directions of geometric time, which suggests the possibility of geometric time loops in topological quantum computations. Could this mean that computation time ceases to be a restriction and ordinary computations lasting for infinite amount of geometric time could be performed in a finite time interval of observer's time? This is perhaps too much to hope. The subjective time taken by the computation would be infinite if each step in the iteration corresponds to single quantum jump. If this is the case and if each quantum jump of observer corresponds to a finite increment of geometric time perceived by the observer, time loops would not allow miracles.

1.2 The notion of magnetic body and the generalization of the notion of genome

The evolution of ideas related to quantum biology provides also new valuable insights. In particular, the notion of magnetic body leads to a model of living system in which dark matter at magnetic flux quanta of the field body of biological system uses biological body as a motor instrument and sensory receptor (see this). Quantum control would be naturally via the genome and sensory input would be from cell membrane containing all kinds of receptors. This would suggest that magnetic flux sheets traverse through DNA strands and cell membranes.

The quantization of magnetic flux with unit defined by Planck constant having arbitrarily large values leads naturally to the notions of super-genome and hyper-genome (see this). Super-genome would consists of DNA strands of separate nuclei belonging to single magnetic flux sheet and these sequences of genomes would be like lines of text at the page of book. Super-genomes in turn can combine to form text lines at the pages of a bigger book, I have used the term hyper-genome. This hierarchy of genomes would give rise to a collective gene expression at the level of organs, individuals of a species, and at the collective level consisting of populations containing several species. Even biosphere could express itself coherently via all the genomes of the bio-sphere. The model of topological quantum computation performed by DNA should be consistent with this general picture.

2. Model for DNA based topological quantum computation

The most promising model of DNA as topological quantum computer relies on the hierarchy of genomes. The flux sheets or collections of parallel flux tubes assignable to a magnetic body would traverse the DNA strands of several nuclei so that strands would be analogous to lines of text on the page of a book.

DNA strands would define the intersections of magnetic or number theoretic braids with plane and braiding would be associated with with the magnetic field lines or flux tubes transversal to DNA. The M-matrix defining topological quantum computation would act on quantum states assignable to nucleotides.

2.1 The interpretation of nucleotides

The interpretation of the A,T,C,G degree of freedom is not obvious and one can consider several options.

1) The quantum numbers entangled by braids having nothing to do with (A,T,C,G) assignable to nucleotides and the braiding does not affect nucleotides.

2) The nucleotides (A,T,C,G) correspond to four different colors (a,t,c,g) for braid strands with conjugate nucleotides defining conjugate colors. The subgroup of allowed braidings would preserve the color patterns. The minimal assumption is that braid strands connect only identical nucleotides. A stronger - probably unrealistic - assumption is that braiding permutes nucleotides physically.

3) The entangled quantum numbers are in 1-1 correspondence with states A, T, C, G of nucleotide. In zero energy ontology this would be possible without breaking of fundamental conservation laws. One can even consider the possibility that A,T,C,G are these quantum numbers. Topological quantum computation in time direction would thus make it possible to replace the DNA strands with new ones and provide a purely quantal mechanism of genetic evolution. Only introns could be involved with topological quantum computations in this sense since they would not induce mutations visible at the level of amino-acids. The intronic portions of genome would not be evolutionary invariants: whether or not this is the case should be easily testable.

4) The combination of options 2) and 3) might make sense for topological quantum computations in time like direction. One would have superposition of topological quantum computations associated with various color patterns and the halting of the computation would mean in general the occurrence of a mutation.

The option 2) with braid strands connecting only identical nucleotides is rather attractive since it explains several facts about genome (as do also options 3) and 4)).

  1. The model requires that the genomes in different nuclei must be identical: otherwise it is not possible to realize braidings as symmetry transformations mapping portions of DNA to itself (as noticed, this map need not occur at the chemical level). An interesting question is whether also the permutations of nucleotides of different codons are allowed or whether only codons are permuted so that they would define fundamental sub-programs.

  2. One can understand why the minimum number of nucleotides in a codon is three. The point is that braid group is non-commutative only when the number of strands is larger than 2. The braidings acting as symmetries would correspond to a subgroup of ordinary braidings leaving the color pattern of braid invariant. Obviously the group is generated by some minimal number of combinations of ordinary braid generators. For instance, for two braid strands with different colors the generator is e12 rather than e1 (two exchange operations/full 2π twist). For codons one would have four different subgroups of full braid group corresponding to codons of type XXX, XYY, XXY, and XYZ. Each gene would be characterized by its own subgroup of braid group and thus by an M-matrix defining topological quantum computation.

  3. One could understand the "junk DNA" character of introns. Introns are the most natural candidates for the portions of genome participating topological quantum computations The transcription process would disturb topological quantum computation so that introns should be chemically passive. Since the portion of "junk DNA" increases with the evolutionary level of the species evolution would indeed correspond to an increase the amount of topological quantum computations performed.

2.2 Two realizations of topological quantum computation

One can imagine two basic realizations of topological quantum computation like processes- or to be more precise - entanglement by braiding. In TGD framework this entanglement could be interpreted in terms of Connes tensor product.

1. Space-like entanglement The first realization would rely space-like braids. Braid strands would connect identical lines of text at the page of book defined by sequences of genomes of different nuclei. Inside nucleus the strands would connect DNA and its conjugate. The braiding operation would take place between lines.

In this case it would be perhaps more appropriate to speak about quantum memory storage of a function realized as entanglement. These functions could represent various rules about the behavior of and survival in the physical world. For this option A,T,C,G cannot correspond to entangled quantum numbers and the interpretation as braid colors is natural. Braiding cannot correspond to a physical braiding of nucleotides so that (A,T,C,G) could correspond to braid color (strands would connect only identical nucleotides).

Strands would not connect strand and its conjugate like hydrogen bonds do but would be like long flux lines of dipole field starting from nucleotide and ending to its conjugate so that braiding would emerge naturally. Color magnetic flux tube structures of almost atom size appear in the TGD based model of nucleus and have light quarks and anti-quarks at their ends (see this). This could be the case also now since quarks and anti-quarks appear also in the model of high Tc superconductivity which should be present also in living matter (see this).

2. Light-like entanglement

Second realization would rely on light-like braids at the boundaries of light-like 3-surfaces connecting 2-surfaces assignable to single genome at different moments of time. Braiding would be dynamical and dance metaphor would apply. The light-like surface could intersect genomes only at initial and final moments and strands would connect only identical nucleotides. Light-likeness in the induced metric of course allows the partonic 3-surface to look static at the level of imbedding space. The fundamental number theoretic braids defined by the minima of the Higgs like field associated with the modified Dirac operator would be very natural in this case.

Genes would define only the hardware unless they code for the magnetic body of DNA too, which looks implausible. The presence of quantum memory and quantum programs would mean a breakdown of genetic determinism since the braidings representing memories and programs would develop quantum jump by quantum jump and distinguish between individuals with the same genome. Also the personal development of individual would take place at this level. It would be these programs (that is magnetic bodies) which would differentiate between us and our cousins with almost identical genome.

3. Biological evolution as an evolution of topological quantum computation

This framework allows to understand biological evolution as an evolution of topological quantum computation like processes in which already existing programs become building blocks of more complex programs.

  1. The transition from RNA era to DNA era (for TGD inspired model for pre-biotic evolution (see this) involving also the emergence of cell membrane bounded structures would mean the emergence of the topological quantum computation using a static hardware.

  2. For mono-cellulars double DNA strands define space-like topological quantum computations involving only single step if the braids connect the nucleotides of the two DNA strands: obviously a reason why for double DNA strands.

  3. For multicellular organisms more complex space-like topological quantum computations would emerge and could code rules about environment and multicellular survival in it. At this step also introns specialized to topological quantum computation would emerge.

  4. A further evolution as a generation of super-genomes in turn forming hyper-genomes and even higher structures would have a concrete counterpart as the organization of braids of lower level to form braids at higher level so that topological quantum computations would become increasingly complex and program module structure would emerge very naturally.

For details see the chapter Prebiotic Evolution in Many-Sheeted Space-time.

Fractional Quantum Hall effect in TGD framework

The generalization of the imbedding space discussed in previous posting allows to understand fractional quantum Hall effect (see this and this).

The formula for the quantized Hall conductance is given by

σ= ν× e2/h,ν=m/n.

Series of fractions in ν=1/3, 2/5 3/7, 4/9, 5/11, 6/13, 7/15..., 2/3, 3/5, 4/7 5/9, 6/11, 7/13..., 5/3, 8/5, 11/7, 14/9... 4/3 7/5, 10/7, 13/9... , 1/5, 2/9, 3/13..., 2/7 3/11..., 1/7.. with odd denominator have bee observed as are also ν=1/2 and ν=5/2 state with even denominator.

The model of Laughlin [Laughlin] cannot explain all aspects of FQHE. The best existing model proposed originally by Jain [Jain] is based on composite fermions resulting as bound states of electron and even number of magnetic flux quanta. Electrons remain integer charged but due to the effective magnetic field electrons appear to have fractional charges. Composite fermion picture predicts all the observed fractions and also their relative intensities and the order in which they appear as the quality of sample improves.

I have considered earlier a possible TGD based model of FQHE not involving hierarchy of Planck constants. The generalization of the notion of imbedding space suggests the interpretation of these states in terms of fractionized charge and electron number.

  1. The easiest manner to understand the observed fractions is by assuming that both M4 an CP2 correspond to covering spaces so that both spin and electric charge and fermion number are quantized. With this assumption the expression for the Planck constant becomes hbar/hbar0 =nb/na and charge and spin units are equal to 1/nb and 1/na respectively. This gives ν =nna/nb2. The values n=2,3,5,7,.. are observed. Planck constant can have arbitrarily large values. There are general arguments stating that also spin is fractionized in FQHE and for na=knb required by the observed values of ν charge fractionization occurs in units of k/nb and forces also spin fractionization. For factor space option in M4 degrees of freedom one would have ν= n/nanb2.

  2. The appearance of nb=2 would suggest that also Z2 appears as the homotopy group of the covering space: filling fraction 1/2 corresponds in the composite fermion model and also experimentally to the limit of zero magnetic fiel [Jain]. Also ν=5/2 has been observed.

  3. A possible problematic aspect of the TGD based model is the experimental absence of even values of nb except nb=2. A possible explanation is that by some symmetry condition possibly related to fermionic statistics kn/nb must reduce to a rational with an odd denominator for nb>2. In other words, one has k propto 2r, where 2r the largest power of 2 divisor of nb smaller than nb.

  4. Large values of nb emerge as B increases. This can be understood from flux quantization. One has eBS= nhbar= n(nb/na)hbar0. The interpretation is that each of the nb sheets contributes n/na units to the flux. As nb increases also the flux increases for a fixed value of na and area S: note that magnetic field strength remains more or less constant so that kind of saturation effect for magnetic field strength would be in question. For na=knb one obtains eBS/hbar0= n/k so that a fractionization of magnetic flux results and each sheet contributes 1/knb units to the flux. ν=1/2 correspond to k=1,nb=2 and to a non-vanishing magnetic flux unlike in the case of composite fermion model.

  5. The understanding of the thermal stability is not trivial. The original FQHE was observed in 80 mK temperature corresponding roughly to a thermal energy of T≈ 10-5 eV. For graphene the effect is observed at room temperature. Cyclotron energy for electron is (from fe= 6× 105 Hz at B=.2 Gauss) of order thermal energy at room temperature in a magnetic field varying in the range 1-10 Tesla. This raises the question why the original FQHE requires so low a temperature? The magnetic energy of a flux tube of length L is by flux quantization roughly e2B2S≈ Ec(e)meL(hbar0=c=1) and exceeds cyclotron energy roughly by factor L/Le, Le electron Compton length so that thermal stability of magnetic flux quanta is not the explanation.

    A possible explanation is that since FQHE involves several values of Planck constant, it is quantum critical phenomenon and is characterized by a critical temperature. The differences of the energies associated with the phase with ordinary Planck constant and phases with different Planck constant would characterize the transition temperature. Saturation of magnetic field strength would be energetically favored.


[Laughlin] R. B. Laughlin (1983), Phys. Rev. Lett. 50, 1395.
[Jain] J. K. Jain (1989), Phys. Rev. Lett. 63, 199.

For more details see the chapter Pre-biotic Evolution in Many-Sheeted Space-Time.

Intronic portions of genome code for RNA: for what purpose?

The last issue of New Scientist contains an article about the discovery that only roughly one half of DNA expresses itself as aminoacid sequences. The article is published in Nature. The Encyclopedia of DNA Elements (ENCODE) project has quantified RNA transcription patterns and found that while the "standard" RNA copy of a gene gets translated into a protein as expected, for each copy of a gene cells also make RNA copies of many other sections of DNA. In particular, intron portions ("junk DNA", the portion of which increases as one climbs up in evolutionary hierarchy) are transcribed to RNA in large amounts. What is also interesting that the RNA fragments correspond to pieces from several genes which raises the question whether there is some fundamental unit smaller than gene.

In particular, intron portions ("junk DNA", the portion of which increases as one climbs up in evolutionary hierarchy) are transcribed to RNA in large amounts. What is also interesting that the RNA fragments correspond to pieces from several genes which raises the question whether there is some fundamental unit smaller than gene.

None of the extra RNA fragments gets translated into proteins, so the race is on to discover just what their function is. TGD proposal is that it gets braided and performs a lot of topological quantum computation (see this). Topologically quantum computing RNA fits nicely with replicating number theoretic braids associated with light-like orbits of partonic 2-surfaces and with their spatial "printed text" representations as linked and knotted partonic 2-surfaces giving braids as a special case (see this). An interesting question is how printing and reading could take place. Is it something comparable to what occurs when we read consciously? Is the biological portion of our conscious life identifiable with this reading process accompanied by copying by cell replication and as secondary printing using aminoacid sequences?

This picture conforms with TGD view about pre-biotic evolution. Plasmoids [1], which are known to share many basic characteristics assigned with life, came first: high temperatures are not a problem in TGD Universe since given frequency corresponds to energy above thermal energy for large enough value of hbar. Plasmoids were followed by RNA, and DNA and aminoacid sequences emerged only after the fusion of 1- and 2-letter codes fusing to the recent 3-letter code. The cross like structure of tRNA molecules carries clear signatures supporting this vision. RNA would be still responsible for roughly half of intracellular life and perhaps for the core of "intelligent life".

I have also proposed that this expression uses memetic code which would correspond to Mersenne M127=2127-1 with 2126 codons whereas ordinary genetic code would correspond to M7=27-1 with 26 codons. Memetic codons in DNA representations would consist of sequences of 21 ordinary codons. Also representations in terms of field patterns with duration of .1 seconds (secondary p-adic time scale associated with M127 defining a fundamental biorhythm) can be considered.

A hypothesis worth of killing would be that the DNA coding for RNA has memetic codons scattered around genome as basic units. It is interesting to see whether the structure of DNA could give any hints that memetic codon appears as a basic unit.

  1. In a "relaxed" double-helical segment of DNA, the two strands twist around the helical axis once every 10.4 base pairs of sequence. 21 genetic codons correspond 63 base pairs whereas 6 full twists would correspond to 62.4 base pairs.

  2. Nucleosomes are fundamental repeating units in eukaryotic chromatin possessing what is known as 10 nm beads-on-string structure. They repeat roughly every 200 base pairs: integer number of genetic codons would suggest 201 base pairs. 3 memetic codons makes 189 base pairs. Could this mean that only a fraction p≈ 12/201, which happens to be of same order of magnitude as the portion of introns in human genome, consists of ordinary codons? Inside nucleosomes the distance between neighboring contacts between histone and DNA is about 10 nm, the p-adic length scale L(151) associated with the Gaussian Mersenne (1+i)151-1 characterizing also cell membrane thickness and the size of nucleosomes. This length corresponds to 10 codons so that there would be two contacts per single memetic codon in a reasonable approximation. In the example of Wikipedia nucleosome corresponds to about 146=126+20 base pairs: 147 base pairs would make 2 memetic codons and 7 genetic codons.

    The remaining 54 base pairs between histone units + 3 ordinary codons from histone unit would make single memetic codon. That only single memetic codon is between histone units and part of the memetic codon overlaps with histone containing unit conforms with the finding that chromatin accessibility and histone modification patterns are highly predictive of both the presence and activity of transcription start sites. This would leave 4 genetic codons and 201 base pairs could decompose as memetic codon+2 genetic codons+memetic codon+2 genetic codons. The simplest possibility is however that memetic codons are between histone units and histone units consist of genetic codons. Note that memetic codons could be transcribed without the straightening of histone unit occurring during the transcription leading to protein coding. Note that prokaryote genome lacks the histone units so that the transition from prokaryotes to eukaryotes would mean the emergence of memetic code.

[1] E. Lozneanu and M. Sanduloviciu (2003), Minimal-cell system created in laboratory by self-organization, Chaos, Solitons and Fractals, Volume 18, Issue 2, October, p. 335. See also Plasma blobs hint at new form of life, New Scientist vol. 179 issue 2413 - 20 September 2003, page 16.

For details see the chapter Pre-biotic Evolution in Many-Sheeted Space-Time.

To the index page