Einstein was desperate for a career break. He had a 50/50 shot – and he took it. The necessary alternative he selected, fixed c, was one which was both purposely neglected by science, and yet offered the only viable alternative to standing and celebrated club dogma. Dogma which had for the most part, gone unchallenged. Developing mechanism for such an alternative is the antithesis of religious activity. Maturing the necessary alternative into hypothesis, is the heart and soul of science.

Mr. Einstein You’ll Never Amount to Anything You Lazy Dog

Albert Einstein introduced in a 1905 scientific paper, the relationship proposed inside the equation e = mc² : the concept that the system energy of a body (e) is equal to the mass (m) of that body times the speed of light squared (c²). That same year he also introduced a scientific paper outlining his theory of special relativity. Most of the development work (observation, intelligence, necessity, hypothesis formulation) entailed in these papers was conducted during his employment as a technical expert – class III (aka clerk) at the Federal Office for Intellectual Property in Bern, Switzerland; colloquially known as the Swiss patent office.¹ There, bouncing his ideas off a cubicle-mate (si vis) and former classmate, Michele Angelo Besso, an Italian Engineer, Einstein found the time to further explore ideas that had taken hold during his studies at the Swiss Federal Polytechnic School. He had been a fan of his instructor, physicist Heinrich Friedrich Weber – the most notable of his two top-engaged professors at Swiss Federal Polytechnic. Weber had stated two things which struck an impression on the budding physicist.²

“Unthinking respect for authority is the enemy of truth.” ~ physicist Heinrich Friedrich Weber

As well, “You are a smart boy, Einstein, a very smart boy. But you have one great fault; you do not let yourself be told anything.” quipped Weber as he scolded Einstein. His mathematics professor, Hermann Minkowski scoffed to his peers about Einstein, relating that he found Einstein to be a “lazy dog.” In similar vein, his instructor physicist Jean Pernet, admonished the C-average (82% or 4.91 of 6.00 GPA) student “[I would advise that you change major to] medicine, law or philosophy rather than physics. You can do what you like. I only wish to warn you in your own interest.” Pernet’s assessment was an implication to Einstein that he did not face a bright future, should he continue his career in pursuit of physics. His resulting mild ostracizing from science was of such extent that Einstein’s father later had to petition in an April 1901 letter, for a university to hire Einstein as an instructor’s assistant. His father wrote “…his idea that he has gone off tracks with his career & is now out of touch gets more and more entrenched each day.” Unfortunately for the younger Einstein, his father’s appeal fell upon deaf ears. Or perhaps fortuitously, as Einstein finally found employment at the Swiss patent office in 1902.³

However, it was precisely this penchant for bucking standing authority, which served to produce fruit in Einstein’s eventual physics career. In particular, Einstein’s youthful foible of examining anew the traditions of physical mechanics, combined with perhaps a dose of edginess from being rejected by the institutions of physics, were brought to bear effectively in his re-assessment of absolute time – absolute space Newtonian mechanics.

Einstein was not ‘doubting’ per se, which is not enough in itself. Rather he executed the discipline of going back and looking – proposing an alternative to a ruling dogma based upon hard nosed critical path induction work, and not through an agency desire to lazily pan an entire realm of developing ideas through abduction (panduction) – no social skeptics, Einstein did not practice your form of authority-enforcing ‘doubt’. Rather it was the opposite.

He was not doubting, rather executing work under a philosophical value-based principle called necessity (see Ethical Skepticism – Part 5 – The Real Ockham’s Razor). Einstein was by practice, an ethical skeptic.

Einstein was not lazy after all, and this was a miscall on the part of his rote-habituated instructors (one common still today). Einstein was a value economist. He applied resources into those channels for which they would provide the greatest beneficial effect. He chose to not waste his time upon repetition, memorization, rote procedure and exercises in compliance. He was the ethical C student – the person I hire before hiring any form of cheating/memorizing/imitating A or B student. And in keeping with such an ethic, Einstein proposed in 1905, 3 years into his fateful exile at the Swiss patent office, several unprecedented ideas which were subsequently experimentally verified in the ensuing years. Those included the physical basis of 3 dimensional contraction, speed and gravitational time dilation, relativistic mass, mass–energy equivalence, a universal speed limit (for matter and energy but not information or intelligence) and relativity of simultaneity.⁴ There has never been a time wherein I reflect upon this amazing accomplishment and lack profound wonder over its irony and requital in Einstein’s career.

The Necessary Alternative

If the antithesis of your alternative can in one observation, serve to falsify your preferred alternative or the null, then that antithesis is then, the necessary alternative.

But was the particular irony inside this overthrow of Newtonian mechanics all that unexpected or unreasonable? I contend that it was not only needed, but the cascade of implications leveraged by c-invariant physics was the only pathway left for physics at that time. It was the inevitable, and necessary, alternative. The leading physicists, as a very symptom of their institutionalization, had descended into a singular dogma. That dogma held as its centerpoint, the idea that space-time was the fixed reference for all reality. Every physical event which occurred inside our realm hinged around this principle. Einstein, in addressing anew such authority based thinking, was faced with a finite and small set of alternative ideas which were intrinsically available for consideration. That is to say – the set of ideas only included around 4 primary elements, which could alternately or in combination, be assumed as fixed, dependent, or independently variable. Let’s examine the permutation potential of these four ideas: fixed space, fixed time, fixed gravity and/or fixed speed of light. Four elements. The combinations available for such a set are 14, as related by the summation of three combination functions:

What reasoned conjecture offered, and given that combinations of 4 or 3 were highly unlikely to unstable, was to serve in bounding the set of viable alternative considerations to even a lesser set than 14 – maybe 6 very logical alternatives at most (the second C(4,2) function above). However, even more reductive, essentially Einstein would only need start by selecting from one of the four base choices, as represented by the first combination function above, C(4,1). Thereafter, if he chose correctly, he could proceed onward to address the other 3 factors depending upon where the critical path led. But the first choice was critical to this process. One of the following four had to be chosen, and two were already in deontological doubt, in Einstein’s mind.

•  Fixed 3 dimensional space (x, y, z)
•  Fixed time (t)
•  Fixed gravitation relative to mass (g-mass)
•  Fixed speed of light (c)

Ultimately then, only two choices existed if one is to suppose a maximum of two fixed elements as possible per below. Indeed this ended up being the plausal-set for Einstein. The necessary alternatives, one of which had been essentially embargoed by the science authorities at the time, were a combination of two of the above four combining elements. Another combination of two was currently in force (fixed space and time).

In other words, now we have reduced the suspect set to two murder suspects – Colonel Mustard and Professor Plum, and standing dogma was dictating that only Colonel Mustard could possibly be considered as the murderer. To Einstein this was at worst, an even bet.

This is the reason why we have ethical skepticism. This condition, an oft repeated condition wherein false skepticism is applied to underpin authority based denial in an a priori context, in order to enforce one mandatory conclusion at the expense of another or all others, is a situation ripe for deposing. Einstein grasped this. The idea that space and time were fixed references was an enforced dogma on the part of those wishing to strengthen their careers in a social club called physics. Everyone was imitating everyone else, and trying to improve club ranking through such rote activity. The first two element selection, stemming of course from strong inductive work by Newton and others, was a mechanism of control called an Einfach Mechanism (see The Tower of Wrong) or

Omega Hypothesis H_Ω – the answer which has become more important to protect than science itself.

•  Fixed 3 dimensional space (x, y, z)
•  Fixed time (t)

Essentially, Einstein’s most logical alternative was to assume the speed of light as fixed first. By choosing first, a fixed reference of the speed of light, Einstein had journeyed down both a necessary, as well as inevitable hypothesis reduction pathway. It was the other murder suspect in the room, and as well stood as the rebellious Embargo Hypothesis option.

Embargo Hypothesis H_ξ– the option which must be forbidden at all costs and before science even begins.

•  Fixed gravitation relative to mass (g-mass)
•  Fixed speed of light (c)

But this Embargo Hypothesis was also the necessary alternative, and Einstein knew this. One can argue both sides of the contention that the ’embargo’ of these two ideas was one of agency versus mere bias. In this context and for purposes of this example, both agency and bias are to be considered the same embargo principle. In many/most arguments however, they are not the same thing.

The Necessary Alternative

/philosophy : Ockham’s Razor : Necessity/ : an alternative which has become necessary for study under Ockham’s Razor because it is one of a finite, constrained and very small set of alternative ideas intrinsically available to provide explanatory causality or criticality inside a domain of sufficient unknown. This alternative does not necessarily require inductive development, nor proof and can still serve as a placeholder construct, even under a condition of pseudo-theory. In order to mandate its introduction, all that is necessary is a reduction pathway in which mechanism can be developed as a core facet of a viable and testable hypothesis based upon its tenets.

The assertion ‘there is a God’, does not stand as the necessary alternative to the assertion ‘there is no God’. Even though the argument domain constraints are similar, these constructs cannot be developed into mechanism and testable hypothesis. So, neither of those statements stand as the necessary alternative. I am sorry but neither of those statements are ones of science. They are Wittgenstein bedeutungslos – meaningless. A proposition or question which resides upon a lack of definition, or presumed definition which contains no meaning other than in and of its self.

However in exemplary contrast, the dilemma of whether or not life originated on Earth (abiogenesis), or off Earth (panspermia) do stand as a set of necessary alternatives. Even though both ideas are in their infancy, they can both ultimately be developed into mechanism and a testing critical path. The third letter of the DNA codon (see Exhibit II below) is one such test of the necessary alternatives, abiogenesis and panspermia. There is actually a third alternative as well, another Embargo Hypothesis (in addition to panspermia) in this case example – that of Intervention theory. But we shall leave that (in actuality necessary as well) alternative discussion for another day, as it comes with too much baggage to be of utility inside this particular discourse.

Einstein chose well from the set of two necessary alternatives, as history proved out. But the impetus which drove the paradigm change from that of the standing dogma and to Einstein’s favored Embargo Hypothesis, might not have been as astounding a happenstance as it might appear at first blush. Einstein chose red, when everyone and their teaching assistant, was of the awesome insistence that one need choose blue. All the ramifications of fixed speed of light (and fixed gravitation, relative only to mass), unfolded thereafter.

Einstein was desperate for a break. He had a 50/50 shot – and he took it.

Example of Necessity: Panspermia versus Abiogenesis

An example of this condition wherein the highly constrained set of alternatives (two in this case) inside a sufficient domain of unknown, forces the condition of dual necessity, can be exemplified inside the controversy around the third letter (base) of the DNA codon. A DNA codon is the word, inside the sentence of DNA. A codon is a series of 3 nucleotides (XXX of A, C, T or G) which have a ‘definition’ corresponding to a specific protein-function to be transcripted from the nucleus and decoded by the cell in its process of assembling body tissues. It is an intersection on the map of the organism. Essentially, the null hypothesis stands that, the 3rd letter (nucleotide) digit of the codon, despite its complex and apparently systematic methodical assignment codex, is the result of natural stochastic-derivation chemical happenstance during the fist 300 million years of Earth’s existence (not a long time). The idea being that life existed on a 2 letter DNA codon (XX) basis for eons, before a 3 letter (XXX) basis evolved (shown in Exhibit II below). The inductive evidence that such an assignment codex based upon 3 letters derived from 2, is beyond plausibility given the lack of probability of its occurrence and lack of time and influencing mechanism during which that improbability could have happened – this evidence supports its also-necessary alternative.

In this circumstance, the idea that the DNA codon third digit based codex, was not a case of 300 million year fantastical and highly improbable happenstance, but rather existed inside the very first forms of life which were to evolve (arrive) on Earth, is called panspermia. The necessary alternative panspermia does not involve or hinge upon the presence of aliens planting DNA on Earth, rather that the 3 letter codon basis was ‘unprecedented by context, complex and exhibiting two additional symmetries (radial and block) on top of that’ at the beginning of life here on Earth, and therefore had to be derived from a source external to the Earth. Note, this is not the same as ‘irreducible complexity’, a weak syllogism employed to counter-argue evolution (not abiogenesis) – rather it is a case of unprecedentable complexity. A much stronger and more deductive argument. It is the necessary alternative to abiogenesis. It is science. Both alternatives are science.

The key in terms of Ockham’s Razor plurality is this:
In order to provide hypothesis which aligns abiogenesis as a sufficient explanatory basis for
what we see in the fossil record – we must dress it up so that it performs in artificial manipulation,
exactly as panspermia would perform with no manipulation at all.
This renders panspermia a legitimate and necessary hypothesis.

This circumstance elicits the contrathetic impasse, a deliberation wherein a conundrum exists solely because authority is seeking to enforce a single answer at the expense of all others, or forbid one answer at the expense of science itself. The enforced answer is the Omega Hypothesis and the forbidden alternative is the Embargo Hypothesis. And while of course abiogenesis must stand as the null hypothesis (it can be falsified but never really proven) – that does not serve to make it therefore true. Fake skeptics rarely grasp this.

Therefore, the necessary alternative – that the DNA (XXX) codex did not originate on Earth, is supported by the below petition for plurality, comprising five elements of objective inference (A – E below). This systematic codex is one which cannot possibly be influenced (as is evolution) by chemical, charge, handedness, use of employment, epigenetic or culling factors (we cannot cull XX codex organisms to make the survival group more compatible for speciating into XXX codex organisms). Nor do we possess influences which can serve to evolve the protein based start, and silence based stop codons. It can only happen by accident or deliberation. This is an Einstein moment.

Omega Hypothesis H_Ω – the third letter of the DNA codex evolved as a semi-useless appendage, in a single occurrence, from a 2 letter codex basis, featuring radial symmetry, featuring block assignment symmetry and molecule complexity to 2nd base synchrony, only upon Earth, in a 1.6 x 10^-15 (1 of 6 chance across a series of 31 pairings, across the potential permutations of (n – 1) proteins which could be assigned) chance, during the first 300 million years of Earth’s existence. Further the codex is exceptionally optimized for maximizing effect inside proteomic evolution. Then evolution of the codex stopped for an unknown reason and has never happened again for 3.8 billion years.

Stacking of Entities = 10 stacked critical path elements. Risk = Very High.

Embargo Hypothesis H_ξ– the three letter codex basis of the DNA codon, pre-existed the origination of life on Earth, arrived here preserved by a mechanism via a natural celestial means, and did not/has not evolved for the most part, save for slight third base degeneracy. Further the codex is exceptionally optimized for maximizing effect inside proteomic evolution.

Stacking of Entities = 4 stacked critical path elements. Risk = Moderate.

Note: By the terms ‘deliberacy’ and ‘prejudice’ used within this article, I mean the ergodicity which is incumbent with the structure of the codex itself. Both how it originated and what its result was in terms of the compatibility with amino acids converting into life. There is no question of ergodicity here. The idea of ‘contrived’ on the other hand, involves a principle called agency. I am not implying agency here in this petition. A system can feature ergodicity, but not necessarily as a result of agency. To contend agency, is the essence of intervention hypotheses. To add agency would constitute stacking of entities (a lot of them too – rendering that hypothesis weaker than even abiogenesis). This according to Ockham’s Razor (the real one).

The contention that panspermia merely shifts the challenges addressed by abiogenesis ‘off-planet’ is valid; however those challenges are not salient to the critical path and incremental question at hand. It is a red herring at this point. With an ethical skeptic now understanding that abiogenesis involves a relatively high-stacked alternative versus panspermia, let’s examine the objective basis for such inference in addition to this subjective ‘stacking of entities’ skepticism surrounding the comparison.

The Case for Off-Earth Codex Condensation

Did our DNA codex originate its structure and progressions first-and-only upon Earth, or was it inherited from another external mechanism? A first problem exists of course in maintaining the code once extant. However, upon observation, a more pressing problem exists in establishing just how the code came into being in the first place. Evolved or pre-existed? ‘Pre-existed by what method of origination then?’ one who enforces an Omega Hypothesis may disdainfully pontificate. I do not have to possess an answer to that question in order to legitimize the status of this necessary alternative. To pretend an answer to that question would constitute entity stacking. To block this necessary alternative (pre-existing codex) however, based upon the rationality that it serves to imply something your club has embargoed or which you do not like personally – even if you have mild inductive support for abiogenesis – is a religion. Given that life most probably existed in the universe and in our galaxy, already well before us – it would appear to me that panspermia, The Embargo Hypothesis, is the simplest explanation, and not abiogenesis. However, five sets of more objective inference serve to make this alternative a very strong one, arguably deductive in nature, versus abiogenesis’ relative paltry battery of evidence.

As you read Elements A – E below, ask yourself the critical path question:
~ ~ ~
‘If the precise, improbable and sophisticated Elements A – E below were required
as the functional basis of evolution before evolution could even happen, then how did they then evolve?’

A.  The most early use amino acids and critical functions hold the fewest coding slots, and are exclusively dependent upon only the three letter codon form. Conjecture is made that life first developed upon a 2 letter codon basis and then added a third over time. The problem with this is that our first forms of life use essentially the full array of 3 letter dependent codex, to wit: Aspartate 2 (XXX), Lysine 2 (XXX), Asparagine 2 (XXX), Stop 3 (XXX), Methionine-Start 1 (XXX), Glutamine 2 (XXX). Glutamic Acid and Aspartic Acid, which synthesize in the absolute earliest forms of thermophiles in particular would have had to fight for the same 2 digit code, GA – which would have precluded the emergence of even the earliest thermal vent forms of life – under a 2 letter dependent codex (XX). These amino acids or codes were mandatory for the first life under any digit size context – and should hold the most two digit slots accordingly – they do not. As well, in the case where multiple codons are assigned to a single amino acid, the multiple codons are usually related. Even the most remote members of archaea, thermophilic archaea, use not only a full 3 letter codon dependent codex, but as well use proteins which reach well into both the adenine position 2 variants (XAX) and thymidine position 2 variants (XTX) groupings; ostensibly the most late-appearing sets of amino acids (see graphic in C. below and Table III at the end).⁵

It is interesting to also note that the three stop codons TAA-TAG-TGA, all match into codex boxing with later appearing/more complex amino acid molecules, and as members of the adenine position 2 variants (XAX) group. They box with the more complex and ‘later appearing’ amino acids tyrosine and tryptophan. The stop codes needed to be a GG, CC, GC, or at the very least a CT/TC XX codon basis at the very least, in order to support an extended evolutionary period under a two letter codon basis (XX). This was not the situation as you can see in Exhibit III at the end. This would suggest that the stop codes appeared later to last under a classic abiogenetic evolutionary construct. Life would have had to evolve up until thermophilic archaea without stop codes in their current form. Then suddenly, life would have had to adopt a new stop codon basis (and then never make another change again in 3.6 billion years), changing horses in mid stream. This XX codon previous form of life should be observable in our paleo record. But it is not.

Moreover, the use of the two digit codex is regarded by much of genomics as a degeneracy, ‘third base degeneracy’, and not an artifact of evolution.⁶ Finally, the codon ATA should in a certain number of instances, equate to a start code, since it would have an evolutionary two digit legacy – yet it is never used to encode for Methionine – this is incompatible with the idea that methionine used to employ a two digit AT code. Likewise, Tyrosine and the non-amino stop code, TA would have been in conflict under the two digit codex. In fact, overall there should exist a relationship between arrival of an amino acid use in Earth life, and the number of slots it occupies in the codex, and there is not. Neither to the positive slope, nor negative slope.⁷

One can broach the fact that protein reassignments were very possible and could explain away the apparent introduction of a XXX codon dependency of all observable life, midstream. But then one must explain why it never ‘speciated’ again over 3.6 billion years, along with the apparent absence of XX codon life in the paleo record. This chasm in such a construct is critical and must be accommodated before abiogenesis can be fully developed as a hypothesis. In comparison, panspermia possess no such critical obstacle (note, this is not a ‘gap’ as it relates to the critical path of the alternative and not merely circumstantial inductive inference).

Codon Radial Symmetry

B.  Evolution of the codex would necessarily occur from amino absences rather than positives. Of particular note is the secondary map function of the start and stop codons. Notice that the start of a DNA sentence begins with a specific protein (the polar charge molecule methionine-ATG). The end of a DNA sequence however, consists of no protein coding whatsoever (see TAA, TAG and TGA). In other words the DNA sentence begins with the same note every time, and ends with protein silence. tRNA evolved a way to accommodate the need for a positive, through the employment of proline-CCA during the protein assembly process. This is how a musical score works – it starts with a note, say an A440 tuning one, and ends with the silence dictated by the conductor’s wand. Deliberacy of an empty set, as opposed to the stochasticity of positive notes, as another appearance of a start code methionine could have sufficed for a positive stop and start code instead. This positive stop mechanism would succeed inside an evolution context much better. Why would an absence evolve into a stop code for transfer RNA? It could not, as ‘absence’ contains too much noise. It occurs at points other than simply a stop condition. The problem exists in that there is no way for an organism to survive, adapt, cull or evolve, based upon its use of an empty set (protein silence). Mistakes would be amplified under such an environment,  Evolution depends intrinsically upon logical positives only (nucleotides, mutations, death) – not empty sets.

C.  Features triple-symmetrical assignment, linear robustness, ergodicity along with a lack of both evolution and deconstructive chaos. This is NOT the same set of conditions as exist inside evolution, even though it may appear as such to a layman. This set of codex assignments, features six principle challenges (C., and C. 1, 2a, 2b, 3, and 4 below). Specifically,

• radial assignment symmetry (B. Codon Radial Symmetry chart above),
• thymidine and adenine (XTX, XAX) second base preference for specific chemistries,
• synchrony with molecule complexity (C. Codon versus Molecule Complexity 64 Slots graphic to the right),
• block symmetry (C. Codon Second Base Block Symmetry table below) around the second digit (base), and
• ergodicity, despite a lack of chemical feedback proximity nor ability for a codon base to attract a specific molecule chemical profile or moiety.
• lack of precedent from which to leverage.

These oddities could not ‘evolve’ as they have no basis to evolve from. The structure and assignment logic of the codex itself precludes the viability of a two base XX codex. Evolution by definition, is a precedent entity progressing gradually (or sporadically) into another new entity. It thrives upon deconstructive chaos and culling to produce speciation. There was no precedent entity in the case of the DNA stop codon nor its XXX codex. As well, at any time, the stop codons could have been adopted under the umbrella of a valid protein, rendering two SuperKingdoms of life extant on Earth – and that should have happened. Should have happened many times over and at any time in our early history (in Archaea). Yet it did not.⁸ An asteroid strike and extinction event would not serve to explain the linearity. Evolution is not linear. We should have a number of DNA stop and start based variants of life available (just as we have with evolution based mechanisms) to examine. But we do not. In fact, as you can see in the chart to the right (derived from Exhibit III at the end), there exist four challenges to a purely abiogenetic classic evolution construct:

1. An original symmetry to the assignment of codon hierarchies (codex), such that each quadrant of the assignment chart of 64 slots, mirrors the opposing quadrant in an ordinal discipline (see Codon Radial Symmetry charts in B. above to the right – click to get a larger image).

Codon Second Base Block Symmetry

2. The second character in the codon dictates (see chart in B. Codon Radial Symmetry chart above) what was possible with the third character. In other words

a. all the thymidine position 2 variants (XTX) had only nitrite molecules (NO₂) assigned to them (marked in blue in the chart in C. Codon versus Molecule Complexity 64 Slots to the upper right and in Exhibit III at the end – from where the graph is derived). While the more complex nitrous amino acids were all assigned to more complex oversteps in codex groups (denoted by the # Oversteps line in the Codon versus Molecule Complexity 64 Slots chart to the upper right).

In addition,

b. all adenine position 2 variants (XAX) were designated for multi-use 3rd character codons, all cytidine position 2 variants (XCX) were designated for single use 3rd character codons, while guanine (XGX) and thymidine (XTX) both were split 50/50 and in the same symmetrical patterning (see Codon Second Base Block Symmetry table to the right).

3.  There exists a solid relationship, methodical in its application, between amino acid molecule nucleon count and assignment grouping by the second digit of the DNA codon in rank of increasing degeneracy. Second letter codon usages were apportioned to amino acids as they became more and more complex, until T and A had to be used because the naming convention was being exceeded (see chart in C., Codon versus Molecule Complexity 64 Slots above to the right as well as Exhibit III at the end). After this was completed, then one more use of G was required to add 6 slots for arginine, and then the table of 60 amino acids was appended by one more, tryptophan (the most complex of all the amino acid molecules – top right of chart in C. Codon versus Molecule Complexity 64 Slots above or the end slots in Exhibit III at the end) and the 3 stop codes thereafter. Very simple. Very methodical. Much akin to a IT developer’s subroutine log – which matures over the course of discovery inside its master application.

4.  Ergodicity. Prejudice… Order, featuring radial symmetry (B. Codon Radial Symmetry chart), synchrony with molecule complexity (C. Codon versus Molecule Complexity 64 Slots graphic) and and block symmetry (C. last image Codon Second Base Block Symmetry table) around the second digit. The problem is that there is no way a natural process could detect the name/features of the base/molecule/sequence as means to supplant such order and symmetry into the codex, three times – much less evolve is such short order, without speciation, in the first place.

Since the DNA chemistry itself is separated by two chemical critical path interventions, how would the chemistry of thymine for instance (the blue block in Exhibit III below) exclusively attract the nitric acid isomer of each amino acid? And why only the nitric acid isomers with more complex molecule bases? First, the DNA base 2 is no where physically near the chemical in question, as it is only a LOGICAL association, not a chemical one so it cannot contain a feedback or association loop. Second, there is no difference chemically, between C2H5NO2 and C5H11NO2. The NO2 is the active moiety. So there should have not been a synchrony progression (C.3. above), even if there were a direct chemical contact between the amino acid and the second base of the codon. So the patterns happen as a result of name only. One would have to know the name of the codon by its second digit (base), or the chemical formula for the amino acid, and employ that higher knowledge to make these assignments.

Finally, this order/symmetry has not changed since the code was first ‘introduced’ and certainly has not been the product of stochastic arrival – as a sufficiently functional-but-less-orderly code would have evolved many times over (as is the practice of evolution) and been struck into an alternative codice well before (several billion years) this beautiful symmetry could ever be attained.

We claim that evolution served to produce the codex, yet the codex bears the absolute signs of having had no evolution in its structure. We cannot selectively apply evolution to the codex – it must either feature evolutionary earmarks, or not be an evolved code. The mechanisms of evolution cannot become a special pleading football applied only when we need it, to enforce conformance – because in that case we will only ever find out, what we already know. It becomes no better argument philosophically than ‘God did it’.

D.  Related codons represent related amino acids. For example, a mutation of CTT to ATT (see table in C. above) results in a relatively benign replacement of leucine with isoleucine. So the selection of the CT and AT prefixes between leucine and isoleucine was done early, deliberately and in finality – based upon a rational constraint set (in the example case, two nitrite molecule suffixed proteins) and not eons of trail and error.⁹ Since the assignment of proteins below, is not partitioned based upon any physical characteristic of the involved molecule, there is no mechanism but deliberacy which could dictate a correspondence between codon relationships and amino acid relationships.¹⁰

E.  Statistically impossible codex, not just improbable. Finally, it is not simply the elegant symmetry to the codex which is perplexing, but as well, items A. – D. usage contexts identified above, allow one to infer (deductive?) that the codex, its precedent, provenance and structure are difficult to impossible to accommodate in even the most contorted construct of abiogenesis. Observe the A-G vs C-T tandem relationship between Lysine and Asparagine for instance. This elegant pattern of discipline repeats through the entire codex. This is the question asked by Eugene V. Koonin and Artem S. Novozhilov at the National Center for Biotechnology in Bethesda, Maryland in their study Origin and Evolution of the Genetic Code: The Universal Enigma (see graphic to the right, extracted from that study).¹¹ This serious challenge is near to falsifying in nature, and cannot be dismissed by simple hand waving. Take some time (weeks or months, not just seconds) to examine the DNA codex in Exhibits I thru III below, the three tables and charts in B. and C. above, as well as the study from which the graphic to the right is extracted, and see if you do not agree. This argument does not suffer the vulnerability of ‘creationist’ arguments, so don’t play that memorized card – as Ockham’s Razor has been surpassed for this necessary alternative.

The hypothesis that the codex for DNA originated elsewhere bears specificity, definition and testable mechanism.
It bears less stacking, gapping and risk as compared to abiogenesis.
It is science. It is the necessary alternative.

Assuming that life just won the 1 in 1.6 x 10 to the 15th power lottery (the Omega Hypothesis), again, and quickly, near to the first time it even bought a lottery ticket – has become the old-hat fallback explanation inside evolution. One which taxes a skeptic’s tolerance for explanations which begin to sound a lot like pseudo-theory (one idea used to explain every problem at first broach). However this paradox of what we observe to be the nature of the codex, and its incompatibility with abiogenesis, involves an impossibly highly stacked assumption set to attempt to explain away based solely upon an appeal to plenitude error. A fallback similar in employment of the appeal to God for the creationist. The chance that the codex evolved a LUCA (Last Universal Common Ancestor) by culled stochastics alone in the first 300 million years of Earth’s existence,¹² is remote from both the perspective of time involved (it happened very quickly) and statistical unlikelihood – but as well from the perspective that the codex is also ‘an optimal of optimates’ – in other words, it is not only functional, but smart too. Several million merely functional-but-uglier code variants would have sufficed to do the job for evolution. So this begs the question, why did we get a smart/organized codex (see Table II below and the radial codon graphic in B. above) and not simply a sufficiently functional but chaotic one (which would also be unlikely itself)? Many social skeptics wishing to enforce a nihilistic religious view of life, miss that we are stacking deliberacy on top of a remote infinitesimally small chance happenstance. Their habit is to ignore such risk chains and then point their finger at creationists as being ‘irrational’ as a distraction.

The codex exhibits unprecedentable, empty set as a positive logical entity, static, patterned codex format, exposed to deconstructive vulnerability which happens in everything else, but which chose to not happen in this one instance. In other words, evolution actually chose to NOT happen in the DNA codex – i.e. deliberacy. The codex, and quod erat demonstrandum, the code itself, came from elsewhere. I do not have to explain the elsewhere, but merely provide the basis for understanding that the code did not originate here. That is the only question on our scientific plate at the moment.

Exhibits I II and III

Exhibit I below shows the compressed 64 slot utilization and it efficiency and symmetry. 61 slots are coded for proteins and three are not – they are used as stop codes (highlighted in yellow). There are eight synonym based code groups (proteins), and twelve non-synonym code groups (proteins). Note that at any given time, small evolutionary fluctuations overlapping into the stop codes would render the code useless as the basis for life. So, the code had to be frozen from the very start, or never work at all. Either that or assign tryptophan as a dedicated stop code and mirror to methionine and make the 5th code group a synonym for Glutamine or Aspartic Acid.

Exhibit I – Tandem Symmetry Table

Exhibit II below expands upon the breakout of this symmetry by coded protein, chemical characteristics and secondary mapping if applicable.

Exhibit II – Expanded Tandem Symmetry and Mapping

Finally, below we relate the 64 codon slot assignments, along with the coded amino acid, the complexity of that molecule and then the use in thermophilic archaea. Here one can see that it is clear that even our first forms of life, constrained to environments in which they had the greatest possibility of even occurring, employed the full XXX codex (three letter codon). While it is reasonable to propose alternative conjecture (and indeed plurality exists here) that the chart suggests a two letter basis as the original codex, life’s critical dependency upon the full codon here is very apparent.

Exhibit III – 61 + 3 Stop Codon Assignment versus Molecule Complexity and
Use in Thermophilic Archaea (see chart in C. above)

Recognizing the legitimacy of the necessary alternative – one which was both purposely neglected by science, and yet offers the only viable alternative to standing and celebrated club dogma – this is a process of real science. Developing mechanism for such an alternative is the antithesis of religious activity. Maturing the necessary alternative into hypothesis, is the heart and soul of science.

Blocking such activity is the charter and role of social skepticism. Holding such obfuscating agency accountable is the function of ethical skepticism.

The Ethical Skeptic, “Embargo of The Necessary Alternative is Not Science” The Ethical Skeptic, WordPress, 24 Nov 2018; Web, https://wp.me/p17q0e-8Ob

1. Biography.com: Physicist, Scientist (1879–1955); web, https://www.biography.com/people/albert-einstein-9285408
2. Thorne, Kip S.; Black Holes & Time Warps: Einstein’s Outrageous Legacy; Norton & Company, New York, 1994; pp. 59 – 86.
3. Thorne, Kip S.; Black Holes & Time Warps: Einstein’s Outrageous Legacy; Norton & Company, New York, 1994; pp. 59 – 86.
4. Wikipedia: Special relativity; web, https://en.wikipedia.org/wiki/Special_relativity
5. Cleber C. Ouverney and Jed A. Fuhrman; Marine Planktonic Archaea Take Up Amino Acids; Applied and Environmental Microbiology; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC92387/
6. Lewin, Benjamin; Genes IX, Graduate Text; Jones and Bartlett; Boston, 2008, p. 190
7. Lewin, Benjamin; Genes IX, Graduate Text; Jones and Bartlett; Boston, 2008, p. 191
8. Lewin, Benjamin; Genes IX, Graduate Text; Jones and Bartlett; Boston, 2008, p. 190
9. Lewin, Benjamin; Genes IX, Graduate Text; Jones and Bartlett; Boston, 2008, p. 191
10. Lewin, Benjamin; Genes IX, Graduate Text; Jones and Bartlett; Boston, 2008, p. 191
11. Eugene V. Koonin and Artem S. Novozhilov; Origin and Evolution of the Genetic Code: The Universal Enigma; National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, MD; IUBMB Life, 61(2): 99–111, February 2009.
12. Betts, et al.; Integrated genomic and fossil evidence illuminates life’s early evolution and eukaryote origin; Nature Ecology & Evolutionvolume 2, pages1556–1562 (2018); https://www.nature.com/articles/s41559-018-0644-x