Toward racial transcendence

About anything we could talk about, is linked to genetics: Evolution, racism, health, sex, etc. To really make a change in the future, will require a solid understanding of heredity and evolution, of the kind even most specialists (part because of their overspecializing, part due their intellectual cowardice) is an extreme rarity.
We must also draw the consequences of the cause of racial transcendence, and be ready to do anything for it. Whatever the personal sacrifices and how society and other countries will see it. Ultimately, we abide by entirely different sets of morals - beyond good and evil - that we give ourselves.
At last, to bring back our species to the past biological perfection of our ancestors and continue existing indefinitely in the future, a plan needs be drawn: learning from the failure of last century’s eugenic policies of all kinds and go further beyond.




The debate between nature and nurture has raged throughout this century in the fields of genetics and psychology. For fifty years, it was believed that genes, as the presumed factors of heredity were called even before the discovery of the double helix structure of DNA, amounted to no more than to protein recipes. This is still in essence the summary fed to children in elementary and middle school.
Since Darwin, it has been taught that all new information, all diversity is due to mutations accumulating at random and then sorted by natural selection, the blind process of the survival of the fittest. These notions fit perfectly with the belief in a materialist world, purposeless and careless, truly Lovecraftian. The idea of an extrasensory influence in matter itself (pantheism), of the action of a spiritual principle that Ancients used to personify as gods or God with a capital D, immediately goes out the window.

Except that Lamarck was totally right with his idea of an active intelligent adaption by one’s body, contributing to the genepool as seen below. The central dogma of genetics Definition: The central dogma of molecular biology is an explanation of the flow of genetic information within a biological system, from DNA to RNA to protein. has been invalidated. Incidentally Darwin who explicitly endorsed inheritance of acquired characteristics, would not see eye to eye with the current darwinist religion1. At that time no modern notion of mutation (nor even of nucleic acids) existed. So if the mechanism of natural selection was not denied by anyone - not even (decent) creationists - the theoretical question revolved mainly around the source of variations, and an obvious hypothesis was in Darwin’s eyes, an internal origin of the change species underwent in the direct moment of confrontation with the environment (compounded by habits) seeping into the germplasm, what we would call today a true evolutionary feedback system.
He also realized how mixing species led to dissolution of their respective qualities, while crossing an animal with its own preserves its special characteristics acquired with difficulty. Then comes August Weismann. Him (a German biologist and physician) and Francis Dalton are responsible at the turn of the 18th century for initiating the idea (which would flourish latter for psychoanalytic reasons we will analyze another time), that the physical vectors of heredity could not possibly be directly altered by lifetime experiences, or only pathologically, through degeneration.

Before any knowledge of this process or the molecular basis on genetics could be attained the monk Gregor Mendel determined purely through experiments and statistics that traits were programmed by a number of genes, distinct units of heredity of which each organism had to carry two instances (alleles Definition: Refers to a variant of a gene, resulting from a mutation and hereditary, ensuring the same function as the initial gene but according to its own terms. Any gene can have several alleles, which often determine the appearance of different hereditary characters ) - because peas, his model species, appear to be diploid, but some other plants aren’t. Also, each gene was supposed to segregate independently as if being their own separate molecule. The laws are summarized thus:

Mendel’s laws of inheritance:
Law of dominance and uniformity Definition: Some alleles are dominant while others are recessive; an organism with at least one dominant allele will display the effect of the dominant allele.
Law of segregation Definition: During gamete formation, the alleles for each gene segregate from each other so that each gamete carries only one allele for each gene.
Law of independent assortment Definition: Genes of different traits can segregate independently during the formation of gametes.

Of these three laws, only second has stood the test of time, aneuploidy (failures of chromosome pairs to segregate correctly) most often leading to catastrophic failures in development, whatever the organism. The first and third laws are wrong at the molecular level, the phenotype Definition: Ensemble des caractères apparents d'un individu (opposé au *génotype*). depending on the precise concentration of gene products. The definition of genes changed, as any change on particular sequence along all chromosomes can have an effect… meaning that genes never were separate units. But Mendel could only study the genetic systems that lent themselves to study the most, mostly protein-producing loci Definition: A locus, as related to genomics, is a physical site or location within a genome, such as a gene or another DNA segment of interest. The plural of locus is loci with mutations causing different colors, sizes, aspects or obvious failure2.

Most laws concerning heredity have to do with the formation of gametes, its gene load and the cell body. Our whole DNA is packaged in a set number (23 for humans) of chromosomes, independent molecules going in pairs of homologues sharing the same structure. During meiosis Definition: Special type of cell division of germ cells in sexually-reproducing organisms that produces the gametes, such as sperm or egg cells. It involves two rounds of division that ultimately result in four cells with only one copy of each chromosome. Additionally, prior to the division, genetic material from the paternal and maternal copies of each chromosome is crossed over, creating new combinations of code on each chromosome , those homologous chromosomes physically bond, exchanging strands along the chromosome’s length. Such crossing-overs happen at 7 places on average (over a varying length of DNA and distance from each others) and are responsible for a reshuffling of alleles, their redistribution, leading to the same sequence of genes along the molecules but a different combination of alleles between the two homologues.

Then the pair separates and migrate to opposite ends of the nucleus, forming two different gametes whose total DNA is the same as the original cell, but pairs broke up, so each cell keeps only one chromosome thusly one version of each gene. In humans a full haplotype complement (that of a gamete, spermatozoid or ovule) makes for 23 chromosomes, and fecundation restores the pairs. But genes on different chromosomes have no reason to segregate together as they are on physically separate molecules. When on the same molecule in general the farther the pair of genes from one another the more likely crossing-over will take place and separate them. Inversely the closer a pair of genes the less frequently the combination of alleles of a given chromosome will be disrupted for any gamete (said genes are linked).
Independent assortment has been invalidated since 1910, with the study of linkage by Morgan: the proximity (or even superposition) on the physical chromosome would make them behave as one unit as seen below. Furthermore, early 1950s the study of TRD Transmission Ratio Distortion systems (or just drives) showed that physical linkage did not explain everything: some haplotypes Definition: Group of specific alleles bundled on the same or different chromosomes, in a single organism could bias transmission in its favor, either by causing the death of gametes with different combinations during sperm or ova formation (meiotic drive Definition: Phenomenon wherein unequal segregation of chromosomes or alleles during meiosis allow for the overrepresentation of that element within a population or species. Drivers or selfish elements arise as a means to increase the presence of that selfish element within the next generation , or increasing its chances at fecondation.

Quantal Genetics

Our DNA has been built over millions of years, forming sets of genes made to work together (epistasy) for an optimal result in a given natural environment. But how could these sets be conserved, if at each meiosis everything is mixed up ?
It’s been believed until now that statistics sufficed to account for this: by reproducing within your original population (a fortiori within your own family), you will find partners having necessarily in common a large part of your own patrimoine, therefore reproducing the allelic combinations… and we could postulate that natural selection would have over time put genes functionally interdependent close to each other, maximizing their linkage and minimizing the frequency of unfit recombinant [phenotypes][phenotype]. Population genetics teaches, that free recombination should prevent such packaging of [polymorphisms], some even considere this feature the main advantage of sex as mentioned earlier.

Quantal genomics, on the contrary emphasizes the natural clustering and conservation of [polymorphism], on a much wider scale and frequency than entailed by distance only. Ancestral haplotypes (later, [AH]) are specific sequences of up to 1 million base pairs in length conserved identical across hundreds to thousands of generations, counting sometimes in millions of years of age3.

They represent alternative versions of Polymorphic Frozen Blocks (PFB Polymorphic Frozen Blocks), continuous sets of genes in which mutations and recombinations (often less than 1% of recombinants within a population) are effectively suppressed. Multiple unrelated families display the same identical AHs, hinting at an extremely remote origin. These blocks often regulate genes expressed by cis (on the same chromosome) trans or epistatic interaction, as one super-gene. But not always, thence natural selection alone (nature killing recombinant mutants) can not explain such conservation:

Through their studies of diseases, the Alper–Yunis group discovered that the B-DR haplotypes contained specific alleles at duplicated loci which had no structural or functional relevance to HLA [ - a major component of antibodies- ] (i.e. complement and 21 hydroxylase loci) but which happen to be located within the major histocompatibility complex. Thus, cis interaction alone could be rejected as the sole explanation.
Further, the data imply that most, if not all, current SNPs [ - most frequent type of mutation, on a single amino-acid- ] occurring at reasonable frequencies already exist in close LD within a known AH or PFB fragment. Finally, when recombination occurs, it takes place between frozen blocks and it is not random.
Lloyd, Steel, Dawkins, Analysis of Haplotype Sequences

Linkage disequilibrium (non-independence of genes) when it occurs is simply a reflection of this conservation with some alleles relatively common in one haplotype compared to others. But each is ancestral. Only active preservation as an innate active cellular mechanism can account for this, a protection whose efficacy exceeds by several orders of magnitude (thousands of times) what we know of. And it appears the vast majority of genes lie in such blocks.

Lamarckism and the Weismann Barrier

If what I described above is a very controversial view (though very valid!), questioning can go much further. The generations of your ancestors did not give birth to you by chance, a happy (I hope) series of uninterrupted copy errors.

The Central Dogma of molecular biology states that biological systems can not modify their own heredity purposely, the information (including the body itself) cannot flow back to its source. Because it is lost, the converse must also hold true: it ensues that change to the germline could never originate from the environment nor the body can cause mutations. This belief took hold in 1958, with Francis Crick. It entailed that change to the germline must occur randomly.
Even mainstream science now acknowledges the fluidity of DNA and its considerable sensitivity to environmental variations. Experiments gradually undermined Weismann’s tale especially with the likes of Ted J. Steele, uncovering the molecular basis of the mechanisms for the heredity of acquired traits, revealing an information structure or plan deep within the DNA molecule itself. And a plan implies an intelligence… that of the brain or higher forces, no real difference as far as we should concern ourselves.

Among other papiers4, the most conclusive evidence is the paper by Cossetti et al demonstrating the transport of massive amount of injected RNA into spermatozoa, strongly suggesting that exosomes5 are the carriers of a flow of information from somatic cells to gametes6.

Image Cosetti article dna transfer cells to sperm

The reason was that hereditary information was before supposed immortal, fixed, and thus protected from any tempering by the environment by a purely hypothetical barrier around the gonads as the Weismann barrier, akin to the blood-brain barrier.
This belief became dogma in total absence of any evidence. However one chooses to dissect this strange, aberrant cultural shift, as a result our understanding of heredity and biology in general suffered a massive sterilization, and a dearth of researchers for the debunked Lamarckian perspective. Yet a sum of inconvenient data piled up… and faced silence.

The first (and rather immediate) dent into this dogma was epigenetics.
Taking only the narrow definition, it refers to potentially hereditary adaptations or changes which do not involve the DNA sequence but instead reversible chemical modifications on it7, for humans mostly cytidine methylation.

Explanation epigenetics

Such modifications can to the offspring either through RNA molecules distributed in a stochastic (random) non-[2ian manner, with no fixed transmission ratio as they multiply or not in various body parts and influence early development.
Studies showed that our lives - metabolic stress of all kinds (drugs, tobacco, starvation, diet), emotional traumas also - do leave clear methylation profiles on our DNA, regulating genetic expression through a whole range of specialized enzymes readers and writers, probably to better cope with a repeating situation and giving a head start to one’s descendants.

Integrated lamarckian inheritance schema

We commonly suspect an epigenetic origin in features with certain heritability but imperfect penetration and above all not respecting Mendelian segregation from one generation to the other.

Epigenetics has been all the rage since the 2000s, and much effort has been devoted, demonstration the complexity of a body bursting with somehow conflicting yet harmonious regulatory pathways operating at varying scales, deeply interdependent… And those fine transient chemical tunings can remain stable over dozens of generations in animals.
However, after a time methylated cytosines do tend to mutate, making the attemptive adaptation definitive, breaching the gap between accepted soft epigenetics and neo-lamarckism. Science had greatly underestimated the intelligence of the living, and its beauty. Studies and experiments showed how our body both represses and stimulates mutations, in a directed, designful manner.

Direct exchanges of brain genetic material to sperm (ovules too, certainly) have been observed, and gametes themselves are especially sensitive to any surrounding material, featuring an important retro transcriptional activity. Your seed spontaneously really absorbs part of the experiences you collect throughout your life, as in the Dune novels, though obviously there is not nearly enough place in DNA for entire memories… although the novels themselves (Chapterhouse) alluded to genetic memories taking place in another dimension, just like we think.

But the most critical rebuking of the Central Dogma (as well of the notion of chaotic mutations) took place in the early 1990s when the phenomenon of somatic hypermutation was discovered, in which immune system cells (lymphocytes B), to produce an exponential variety of antibodies out of proportion to the smallness of the genetic repertoire inherited from the parents (the V repertoire) routinely undergo localized and controlled rounds of mutations (for those with some background see the references in footnotes8). Steele thought in the context of immunology and fighting against pathogens so he immediately assimilated

Steele has shown that [2the new combinations produced were sometimes returned to the germ lines to be inherited. It was not taken well by the scientific community, retorting that however we always catch polio, flu etc. But with principles of instinctonutrition the contradiction disappears9.

The variations known as Single Nucleotide [Polymorphisms][polymorphism] (SNPs, pronounced as snips) which are the bulk of genetic variation world-wide, show for lots of them if not most, a mutational signature typical of deaminase activity, the main means of DNA/RNA edition at our disposal. That means a significant part of all changes considered so far as random (usually hazardous) could be adaptive innovations, either through the the aforementioned very slow, unreliable change of methylated cytosines, or the fast potent way featured by the somatic hypermutation:

Genes transcribed into RNA get holes punched into them with deaminases, holes then filled with faulty polymerases, then the result is retrotranscribed into DNA like viruses do, to replace the old version, with the new mutations. Data suggest, that the totality of the genome functional genes RNAs pseudogenes and repeated sequences alike have at some point or another, been subjected to hypermutation.

Incidentally, we have known for a long time embryos and gametes, though in theory the most guarded against retrotransposition/integration of foreign genetic material, actually demonstrates the opposite: Mature spermatozoa and early embryos are extremly permeable to foreign DNA and RNA molecules, by design.

Retrotransposon-encoded RT is stored in mature gametes, is highly expressed in early embryos and undifferentiated cells, and becomes downregulated in differentiated cells. In turn, RT plays a role in developmental control, as its inhibition arrests developmental progression of early embryos with globally altered transcriptomic profiles. Thus, sperm cells act as recipients, and transgenerational vectors of somatically derived genetic information which they pass to the next generation with the potential to modify the fate of the developing embryos.
Corrado Spadafora, Soma to germline inheritance of extrachromosomal genetic information via a LINE-1 reverse transcriptase-based mechanism

These mutations would thus affect all organs, the muscles, ears, eyes. Not unlike what Frank Herbert described. In this conception of evolution currently work-in-progress, selection still does matter, but its role is limited to sorting out endogenous ordered adaptations, putting to test the product of lives and intelligences.

Evolution of this type gives a satisfactory explanation to the enormous complexity of behavioral instincts: Such traits would be lost by mixing with other groups bearing adaptations of their own to wholly different selective pressures, born of different ecologies, social environment and pre-existing racial background. Mating within your family which in all likelihood experienced the same things under the same cognitive constraints, leads also in all likelihood to the same solutions, because your genetics are therefore compatible, essentially doubling down on your adaptation. Thus justifying the ancient practice of hereditary monarchies and noble marriages.

Despite the relative lack of diversity, such a model not only would not suffer from debilitating mutations nigh absent in a raw setting, but would allow an explosion of true genetic diversity with numerous small consanguineous lineages developping independently. However one should probably forget the whole spiel about muh diversity entirely, as it likely derived entirely from the irrational fear of insect treated in the homonymous article. On the theoretical the notion doesn’t hold well to criticism either10.

Exemples of immediate Lamarck transmissions of relatively complex adaptations of the most impressive kind do exist however:

The parathyroid gland helps maintain calcium levels in the blood. When the gland is removed (a parathyroidectomy), calcium levels decline. Fujii (1978) carried out parathyroidectomies on pregnant rats. Their newborn offspring experienced little decline in calcium during the first 24 hours of life even though parathyroidectomies had been carried out on them at birth.
In other words, parathyroid removal from the mother rat protected the newborn from the effects of a similar operation. In a control experiment, mothers were not subjected to the operation whereas the offspring were. None of these offspring showed the protection evident in the previous experiment. In the final and most informative experiment, a brother and sister with a parathyroidectomized mother, but who were allowed to keep their thyroids, were mated.
The progeny of such unions produced newborn rats with a protective response upon having their parathyroids removed
. The effect persisted for four generations, the obvious implication being that an acquired trait, namely protection against parathyroid removal, is inheritable.
Menger, ibid

We can see the potency of mating relatives who shared the same experience at play. One should absolutely replicate these experience, and evaluating statistically the strength of the protection shared depending on the level of consanguinity of matings. As a conclusion, science teaches us today that working to improve and live most intensely and precisely up to the limit of human potential is not a right but a duty to your species.

Yet today those same biological abberations and walking genetic depravities we denounce are increasingly recognized the same rights.

Image of Down syndrom wannabe politician

A woman with Down’s syndrome who is challenging abortion law’s stance on babies with the condition says the legislation doesn’t respect my life. As law stands, foetuses with Down’s syndrome may be terminated up to birth. Claimant Máire Lea-Wilson believes it is morally and ethically wrong to destroy a life on the grounds of a disability. But what we will try and establish is that it is legally wrong.

Two of the claimants are in the minority of foetuses who were diagnosed with the condition and not aborted and they live happy and fulfilling lives, as evidence shows the majority of people with Down’s syndrome do.

BBC, Down’s syndrome abortion law doesn’t respect my life
Image of the pope embracing a Downie

While poor victims of parents’ crimes can not be blamed (unless they promote their disability) and sterilization is preferable in most cases religious people preaching the degradation of life however, ironically calling their stance pro-life, deserve death.

The Morality of the Eugenic Imperative

The Most Sacred Tenet

When talking to people, it becomes apparent that purity spiral is never suddenly as bothersome, as when applied to oneself. People are often eager to endorse racism, only so long as they can be counted among the übermensch: very few accept their imperfection and its consequences. This raises a few questions which deserve some considerations:

If, throughout a period of not more than six hundred years, all physically degenerate or mentally defective persons were sterilized, humanity would not only be delivered from an immense misfortune, but also restored to a state of general health such as we at present hardly imagine.
Adolf Hitler, Mein Kampf

Except genetically defective people actually represent the overwhelming majority.

The objective understanding of the evolution of Man teaches us most of our degeneration was caused by cooking, with aberrant mutations induced by a loss of selection and autodomestication. Not mixing. Before cooking and Neolithic, mixing has been exceedingly rare as though one could make a case for our ancestors being quite capable of building boats and crossing continents as they please. As far as fossils can tell Asians (Denisova) and Europeans would interbreed very rarely and said individuals would not propagate their genome. Backcrossing Definition: Backcrossing is a crossing of a hybrid with one of its parents or an individual genetically similar to its parent, to achieve offspring with a genetic identity closer to that of the parent. and introgression Definition: Introgressive hybridization (introgression) is genetic modification of one species by another through hybridization and repeated backcrossing. would occur very, very slowly if at all, hybrids (if hybrids there were before cooking) staying confined in the vast expanses of Eurasian steppes.

Global exchanges in the Roman Empire

Not until the advent of widespread colonial empires starting from the 15th century causing big and quick migration flux did mixing with other continents become a thing. Some migrations did occur before though, through lands. In the South of France with Spaniards for instance, enough to change France’s phenotype completely. Or through Mongol invasions or the turmoil at the end of the bronze age or Italians from the Roman Empire mixing with Celts.


But coastal locations were more mixed already, being the places of much inter-cultural and commercial exchanges and population too. Modern means of transportation, in a way, merely accelerated (exponentially) what would already happen slowly but surely. This shows how the origin of all the issues has been the Neolithic with its technological improvements, and even more so, its drive to develop into degenerate complex societies. Hence the root and origin of mixing, was the diet change in the Neolithic, without which none of that could have happened, as indeed none of it had happened for hundreds of thousands of years prior, despite much intellectual capabilities to do so.

Knowing this, what is the moral action to take, what is the most ethical and rational behavior ?
It is not to simply reproduce the brightest, with the biggest brains or whatnot. Race-blind IQ eugenics is nonsensical. Lineages separated for tens to hundreds of millennia, can not blend qualities in such a simplistic way: our mind qualities and tendencies originate from separate factors, separate pathways, adaptive complexes of genes which individually have little value.

Instead of standing currently at the peak of evolution, we current Europeans are mere shadows of ourselves. Once you’re white there’s no upgrade, and it is proved too that statistical outliers tend to breed toward the average of their race, not all genetic traits are hereditary, assuming they are indeed genetic.

And more importantly, once we understand what happened in history and prehistory and what kind of unimaginably majestic otherworldly beings we once were, our objective can not be to simply select the best: no intellectual criteria can approach the wisdom of age, the selective pressures that create our (three) races. We can not substitute our intellect for evolution, and we do not know what evolution had in store for any race, because evolution was stopped dead in its tracks by cooking or the indirect effects of it.

Mixed Africans have bigger brains, but on average they tend to design smarter and more cruel ways to eat and massacre each other, while the character of blacker (or purer) Blacks, such as the Nilotic, Negrito, San or Pygmy people, is usually more temperate. Mixed Blacks are agitated morons just smart enough to think too much of themselves, while isolated pure Black ethnies stayed the more respectable and amenable animals moving peacefully along their evolutionary path. Perhaps climbing it or falling, but according to nature’s dictate and it is not our role to intervene.

Just as we should not suffer mixed people to breed, especially among ourselves. It is not that brown-haired Europeans are inferior to others, though statistical truth holds (the purer the bigger the brain and more intelligent), but their breeding is undesirable and its consequence unfathomable.

Perfection (relative to our current state) lies in the past, not the future. We were perfect and fell, but that means everything is still there, as seeds.
As long as we don’t mix.

Said otherwise, traits lost to cooking might be temporary losses only, such as a bigger brain or those [classical old-age Neanderthal facial traits]. Those traits are developmental rather than genetic, though the notions overlap in the sense that genetic degeneracy caused our inability to grow that old. The point is, the information that made us is not gone so much as we can’t access it anymore, hence any regenerative process is much easier with purer people as subjects, preserving more of the original perfect racial scheme.

Destiny of Mixed Races

On the opposite a mixed people can never go back in and of itself: adding incompatible data destroys forever the integrity of this genetic scheme. This is why interbreeding is the worst crime imaginable, from God’s perspective.

Hitler (among others) had no liking for evolutionary reasonings, instead mentioning God’s will to create races separate, to not dilute their essences through mixing. He had an excellent intuition: each race should follow its evolutionary path and by continuing to breed obviously mixed people we further our Neolithic forebears’ mistakes. Each passing decade considering today’s rate, sees more and more sullying of the pure Nordic race.

I did mention God, but this is not a mere turn of phrase: a mere scientific point of view leads to these conclusions, but stepping outside into mysticism or religion strengthens them significantly. God and evolution are one and the same, in the sense that extrasensory intervention be it through luck having a hand in which species survive and which don’t, or through direct genetic weird quantum effects or extraordinary unlikely events allowing for impossible qualitative jumps.

We don’t know what the gods or destiny had intended for any wild animal species we killed off, and we’ll never know because they’re dead. We simply can not fathom what direction destiny intended each race to go along, because cooking happened, messing with genetics with an onslaught of chaotic mutations and shunting the natural barriers against mixing that existed, first and foremost Europeans’ unfathomable wide gap in intelligence and robustness with Blacks, now limited to just a very big one. So the only meaningful policy is to focus on purity compared Neanderthals’ phenotype, rejecting any and all manifest element of admixture.

Logic dictates that non-Nordic Whites or anyone identifying with Europeans, putting their lots with them and suffering with them, should get sterilized - voluntarily - and adopt or nurture Nordic children: in a word cuck for Nords, while breeding is left to the experts. Purifying the race by correcting those thousands of years or straying away from nature and instincts being the most sacred task imaginable, it entails that it could not possibly be left to individual choices… Breeding should be the privilege of the few, according to a collective decision.

The needs of the many outweigh the needs of the of the few, as classical utilitarianism tells: with the sole difference that my many includes the infinity of all future generations. In front of that, no amount of imagined or real suffering of a few individuals - or entire generations worth of strife and efforts - can even begin to compare.

why don’t all people cuck for their betters with abnegation and joy like many Germans did, an attitude considered of the highest nobility and worthy of the utmost praise ? Because like Plato taught, Most people since the Fall have not been breeding out of love nor congruence with a sense of providence announcing an important destiny to fulfill for the incoming soul like in all myths about virgin births (common around the world).

This question is at the center of metapsychoanalysis: people have always projected the transcendence herring to the metapsychic instinctive program on to the breeding program, so investing much libido (both in the nervous enery sense or the narrow sexual one) into breeding, seeking to achieve a kind of immortality through making one’s own kids, looking like ourselves, regardless of our objective qualities.

Despite the fact we should value the qualities within ourselves in and of themselves, without always egotistically relating everything two ourselves as the point of reference, as I mentioned at the beginning of this article.
Most people can’t think otherwise, and women (or females of any species) by far the least easily (while funnily enough having less issue catering for others’ kids), owing to their accentuated biological wiring toward breeding.

We should desire the White (or East-Asian) race to prosper and improve, not because it’s us but because it’s the best or at least has a unique set of qualities, and its evolutionary potential is much greater than Africans or any mixed groups, as anthropology and biology taught us. So whoever is part of the folk should work in favor of the whitest of whites, meaning, Nords.
To work in hope of some personal reward is a dishonest fallacious motivation and quickly runs out as our misguided desires reveal to oppose the greater good of all, eventually of all life on Earth. If killing your whole family plus a million white children could set every back in time and save billions upon billions of future life, would you do it ?

About Non-Reproductive Racemixing

I must clarify here an apparent contradiction between eugenics and the metasexuality, which holds any and all barriers to the free exchange of energy as spiritually destructive, diabolical. It must be said that we do not hate other races as groups just because we wish for their disparition, just like we do not hate or reject or deny their rights to individuals, Whites or otherwise, deemed not fit for reproduction.
Along with the metasexual instinctive program, evolved an increasing separation of reproduction and sexuality. Both within coitus, by a conscious or unconscious control of fertility (that we already see in lower animals) and outside, by expanding the range and frequency of polymorphic, non-coital contacts.

Now let us answer precisely the following question:
why do we really object interracial relationships ?

The answers among racists are either/or the disgust it inspires them (hardly a scientific answer), or the production of mixed-race babies. It is hard to argue against feelings of disgust, except that they shouldn’t be forced upon those who don’t share it. Policies require rational bases. So we oughto forbid mixed-race offsprings.

Hence, homosexual or pedophilic relations (with a prebuscent partner at least) are therefore an absolute non-issue, and being the prevalent kinds of unions in natural humans, it is easy to conclude that racemixing, as far as sex is concerned, only became an issue when humanity fell into the breeding instinctive program. Additionally, non-coital contacts either should not be forbidden. The Reich will enforce the sterilization of individuals of inferior blood, let alone inferior race, hence the genetic pollution of Negro females by White men is of no concern, their reproductive future being null, in particular in Europe. If the presence of racial strangers can be tolerated on a case by case basis, their reproduction won’t.

Similarly, a dutifully sterilized man emits no sperm, regular examinations will make sure of it. So racemixing even in the dreaded Black man on White woman, regardless of practice, should not an issue in Europe… Although the number of Black men allowed in the Reich will never be a concern. The same can not be said in the case of women visiting Africa or the rest of the world. Here precautions and testing would suffice to attest of her purity. As long as it is the case, the utter metasexual freedom of the White Race and its dominion over inferior races, should not suffer contestation.

Neonazis may seethe

MEME pedophilia white on black

And obviously, because the Reich will monitor tightly births, biological cycles and possibly the presence of microchimerism at least for populations of high genetic value, any infringement of the prohibition of coital racemixing by a White woman will be noticed and the offender sterilized, exiled or executed.

It must be said, that White nationalists love races, even when they wish their disparition. The absence of further pollution (or eugenic danger) does not correlate with aesthetic beautyor individual worth. A truly enlightened racist shouldn’t reject interracial sex, at least not the point of killing people. We should only hate making racemixed reproduction and eventual telegonic pollution.

It must be said that eugenics and the exchange of energy have little to nothing in common with one another.

To sum it up: racemixing should only be forbidden in case of White women having relationships with unsterilized Black men in absence of a white to ascertain the contacts’ purely metasexual character.

And so, the superior race will be free to roam the world, knows it beauty and savor its racial and infinite sexual diversity, until we no longer see fit for them or some of these races, to share the planet with us, engaging thus their global sterilization, at the rate we see fit. In the meanwhile, races all over the world, thanks to the military suppression of cooking, will enjoy a peace, freedom and love the like only the domination by the Nordic master race can offer.
Thus, in the meanwhile sexual diplomacy, the sterile intermiggling of different races, shall ensure a peace and understanding between every human and beyond, every species capable of metasexuality, apes, dolphins, some birds, octopuses, goats, as long as the aesthetic appeal is present and our anatomies proved compatible in some way for an erotic approach of some kind, with no coercion or violence involved.

IQ Nationalism

Since over generations children’ IQ align on racial averages and not their parents’ IQ, it makes sense if we have plenty of candidates, to select only aryans. For a lot of physical traits such as health and (some form) of intelligence the parents’ traits matter less than their genetic potential, and the latter is more clearly indicated by their extended family, as nurture plays a big role.

Also complex traits often depend on what is called non-additive genetics, which is the effect of precise sets of alleles hardly heritable because of the disruption of their unity through gametic segregation regardless of how much alleles are passed down because their effects comes from (epistatic) interaction. Individual alleles’ effects do not stack up.

The best way to preserve those traits depending precise combinations, is group or family selection: one gets a much better idea of a person’ hereditary potential by looking at its family and breeding the family as a whole. That way gene complexes are preserved as such, the same way we want to preserve the whole race.
Otherwise, breeding high IQ people whose family is only sub-average, would not help at all, you would choose an outlier unable to pass on its qualities.

It’s safer to base your criteria on the most genetically-determined traits, skull shape first and foremost. Therefore the SS valued physical beauty and strength and conformity with aryan measurements over intelligence, because the SS was meant to be a RACIAL elite, the new nobility seeding Europe with their offspring. In short, we’d better breed a group of stupid but pure, clumsy faggoty weak aryans which suffered from a terrible diet education and lifestyle than from intelligent and strong niggers assuming you can provide a good education and diet to these kids, because their offsrpings’ qualitty will align on racial averages.

The definition of a good trait isn’t always straightforward, including a subjective element. However things like reaction time or nerve transmission speed are universally adaptive, their value is intrinsic. One could also owe his big skull to either mutations, or a wholly different racial ancestry, Asian for instance. A good skull ideally isn’t just about size, it gets shaped like a Neanderthal’s, something on which a specialist would deliberate on better than the average joe.

It’s also difficult to measure intrinsic intelligence.
School results are an indicator only as many tests and educational opportunities are standardized, which imply control for parental influences (and reform the entirety of the school system !) so that everyone gets the same training.
Discaring IQ tests completely would be preferable as they are rather mechanical, hardly involving any efforts, unlike actual school work. This is shown by psychological studies. Yet it’s about the most trustworthy indicator in all of psychology…

Hence no effort should be spared, to develop the science of psychometry and neurology to an extreme degree: the scientific, objective measurement of acultural and mostly physical traits indicative of intelligence, brain efficiency or development. More on this at a later point, but clearly any idea of a multi-centuries breeding effort requires in order to assess progress, a reliable - non-invasive ! - means to define then quantify qualities by discovering physical measurements unambiguously and strongly correlated with them, limiting the interpretative, subjective work.

A Need for fanaticism

We need that fanaticism and sense of self-sacrifice in service of the community. The book Iron Dream from Norman Spinrad expressed that abnegation perfectly:

The fellow hesitated a moment; Feric spied tears in his eyes. Then suddenly Feric’s presence was noted and everyone—SS men and sour-faced inmates alike—snapped out Party salutes and shouted Hail Jaggar! with a vigor and enthusiasm that left nothing to be desired. Feric was deeply touched by such a demonstration of racial solidarity, coming as it did from those called upon to sacrifice their hope of future progeny for the good of the Fatherland.

A moment later, the Holder at the front of the line squared his shoulders, clicked his heels, came to attention and replied to the SS major clearly and firmly:

He then gave a letter-perfect Party salute and marched resolutely through the right-hand doorway.

Then, after the most powerful and twisted stand-in for Jews (the Doms, for dominators, hell-bent on destroying true humans to lord over an universe of enslaved genetic abominations bred for their own purpose)

Famous caricature of the Eternal Jew

Though SS scientists are close to perfecting his technique, much heroic effort is still called for on the part of the SS before the production of a master race of SS clones becomes assured. Therefore I have decided as your Supreme Commander that every last Helder must involve himself in a truly heroic act that will inspire superhuman fanaticism on the part of these scientists by making the price of failure the total extinction of sapience on this planet and the prize to be won by success the creation of a purebred master race capable and worthy of inheriting the entire universe for all time.

Within the next three months every Helder will be processed through the Classification Camps. There, we will all be sterilized, rendered permanently incapable of succumbing to any foul temptation to reproduce our damaged genes by conventional sexual means. Either Heldon will produce a posterity of purebred SS clones, or no posterity at all! Racial transcendence or racial death!

As a personal demonstration of my own total loyalty to the sacred cause of the Swastika and the production of an SS master race, I myself will be the first to undergo sterilization, followed by my High Commanders, the entire SS, and then the Helder people.
Hail Heldon! Hail Final Victory! Hail the Master Race!

Racial transcendence, the purpose for anyone human’s existence is to ascend to a new state of existence and repair the damage cooking imparted on our history and life on Earth in general. Which is increasingly quicker and better achieved as purification and cultural conditioning are both more intense, pushed to the brink of biological and psychological capacity. The more we suffer in this endeavor, the more divine next generations will be.

Eugenic Plan

Why Eugenics Failed

Germans and other eugenicists of that time were utterly impotent, because they lacked everything:

While classical breeding methods proved efficient enough with animal husbandry for centuries, the time they take is not one human beings could ever have the luxury of spending. People live longer lives than rats, fortunately or unfortunately depending on said human or said people. Ergo what does work to create pure races of hundreds of rats or cows from a select few individuals - while already taking its fair share of time - would take centuries in humans. Or rather millennia, taking into account millions of people. We imperatively need genetic engineering to accomplish that goal.

This is also way the early efforts, when such molecular methods were simply nonexistent, could never achieve anything. Moreover, while the Nazi emphasis on Nordic phenotypes was commendable, these early anthropological classifications appear today worthless. One had to understand the process of degeneration first, before drawing any conclusion. We do not advocate for gassing all imperfect people, first off because it’s not necessarily quick nor practical, then the moral outcry… What a bother. Sterilizing the unfits but convincing them to help the society in which they’ll have no genetic legacy has so much more benefits. I will lay out a plan to enact in order to purify Europeans’ DNA of all flaws brought about by cooking, both gross and subtle, in order to get back the Neandertals perfect phenotype.

This would only apply to Nordic Europeans matching satisfying criteria, the rest of mixed Europeans should be morally obliged (in time) to get sterilized and help society, enjoying the exact same rights as pure Nordics except for breeding, which is not a right but a duty for those necessitate by the eugenic program. Adoption should be generalized and seen as a noble sacrifice or not a sacrifice at all, given than loving a child is so much more important emotionally, erotically and spiritually speaking, than begetting them. Furthermore the term of “purity” is relative, and shouldn’t go much further than simply acknowledging the presence of all three major recessive traits such as fair skin, hair and eye color. High brain volume and later high score in the psychometric tests yet to be designed, are of course to consider these won’t be genuine indices of hereditary value before the educative conditions have been optimized and normalized in the whole (breeding) population otherwise we can not tell apart nurture from nature.

On the other hand, those recessive traits can not be influenced by the environment. Purity is only relative since the Neanderthal phenotype faded from this world, and our goal is to recreate it. So between pure and impure, Aryans and non-Aryans, the difference is just quantitative, not qualitative, and even a seemingly high-quality individual should consider this matter-of-factly, in the eventuality of even purer candidates available.

This endeavor will take multiple steps and probably at least a few centuries, probably millennia.

  1. The first will be to remove from the gene pools all gross genetic flaws, and by that I mean recessive (or dominant for the matter) genes whose full expression require both parents to provide the same defective version. This defect would show up and in most cases stop development early dead it in its track, leading to miscarriages in the overwhelming majority of cases.
  2. Studies on those cases would lead to an increased knowledge of said mutations present in common haplotypes (sets of genes inherited as a bloc in the population.
  3. Then through genetic engineering, it will be possible to correct them in the current generation, by copying over the same haplotypes still existing in the population.

Once all ancestral alleles still present in the population will gathered into pure bloodlines, the next step is to improve ourselves through training and a hardening of our lifestyle, while trusting Lamarck mechanisms to bring out the rest of Neanderthal traits.

However without a definitive change of diet none of this would make any sense as it has been up until now virtually the only source of chaotic mutations.

Place of Inbreeding

Beside de novo chromosomal anomalies such as trisomies which always result either in stillbirths, early death or sterility (hence can’t propagate), the grossest genetic flaws consist in recessive alleles who presence in the heterozygotic state (one allele flawed over two) does not cause death or a major trouble. It has been established that more than 70 % of the genetic load is made up of these alleles. When an allele is fixated – meaning all chromosomes in an entire population include it – there is no possible selection or improvement – save for new mutations to arise – as there is no possible variation between individuals, over which to select.

To select the healthy from the flawed, there needs to be a difference between the two ! Hence, to remove defects, one needs to either isolate them by amplifying their detriment in the homozygous state (then weeding out those bloodlines), or generate variation by concentrating their overall proportion (in the whole genome) in a select number of lines.

In fact, both endeavours cross and find achievement through consanguinity, as stated in the incest article. Among the same average genepool mating close kin has the automatic effect of heightening variance, depending on the existing allelic diversity.
Clearly, according to fossil remains we ought to be a fairly consanguineous species, with a fairly high degree of homozygosity or individual uniformity on a chromosomal level, hence while a few heterozygous recessives do not necessarily constitute defects (the resulting trait could be advantageous… theoretically!) our species is not meant to carry a lot of them and most likely not to profit from them either: within a natural mating framework, with the small effective population number that was ours, they could not remain heterozygous for long.

So with consanguinity degenerate bloodlines die out (mostly in embryo, or through predation, natural or artificial selection) whereas other survive and become much healthier, purged from the genetic load, minus some loss of diversity and « bad » but not lethal alleles which got fixated.

Meme about centuries of incest among Pharaohs

Hence once those purified bloodlines have been obtained, it is advantageous to mix them with each others, to increase variance and diversity again, and remove those other bad alleles as well, as each consanguineous line is susceptible to fixate by chance (or genetic drift) a different set of unwanted traits, not present in others.
Three factors determines the efficiency of this protocol:

It entails that the ultimate unmasking of alleles would be selfing, as a (very) low number of animals (mostly invertebrates) though a fair proportion of plants do. Selfing is different from cloning. We won’t consider forms of vegetative reproduction but only sexual reproduction without genetic input from another partner. From a vertebrate-minded genetic perspective, we can sort them in three types, depending on their relation to “normal” meiosis followed by fecundation:

a perfect preservation of the parental (maternal) sequence without formation of haploid gametes nor crossing over is very rare in vertebrates, and theoretically difficult to induce in superior ones as suppressing the very formation of the first polar body is not possible. Instead cloning requires a stupidly costly lab procedure, while all the others mentioned in this document can be done in batch. Breeders would find interest in multiplying a prolific specimen ad libitum to maximize production or ease in practicing line-breeding (keeping the same sire over generations), but we don’t, instead we mind the improvement of traits. This requires shuffling existing materials, sexuality.
Is the development of embryos from sexual tissues without adjunction from male material. Virgin births. It typically is automictic: diploidy is restored through fusion of a polar body with the ovocyte’s haploid nucleus. Fusion of the first polar body avoiding a loss of material happens in some lower vertebrates (such as mole salamanders, which incidentally prefaces the process with a doubling of chromosomes and sees close to no crossing-overs, making it almost identical to cloning) but typically birds and other facultative parthenogenetic vertebrates perform automictic parthenogenesis, in which the early state of meiosis eggs do go through chromosome reduction, then diploidy is restored through either fusion with the second polar body (known as terminal fusion automixis) or the suppression of the first mitotic division (fusion of the first two blastomere).

As shown in the diagram, the haploid complement of the second polar body is not exactly identical, since on average one sister chromatid has undergone crossing-overs prior (while the other not), so reuniting them produce (on average) 50% homozygous pairs, not 100%, while the first generation maintains 75% of the maternal information. Also allelic recombination (hence the heterozygous state) is more frequent for some chromosomes than others, and the closer to the centromere. o compare, the offspring of normal sibling (or parent-child) incest is 25% homozygote. Fusing the blastomere on the other hand, guarantees total 100% homozygotes or double haploids.

Selfing on the other hand
It implies the production of gametes of both sexes within oneself, followed by fertilization. The result of this seemingly counter-intuitive method is the exact same as automictic parthenogenesis though the ensuing genetic structure is different, as for each chromosome pair it is possible for both or no chromosome to be recombined while in the aforementioned model, one is always recombinant and the other not.

Hence selfing produces more varieties to pick from. This, would be the ultimate form of natural incest. One impossible to emulate per se since we cannot produce both gamete types, we are not hermaphrodite snails. Or are we not ?
Producing ovules out of a man yet (or sperm out of a female, though that would be much easier) is out of the question and with the current craze about transsexuals I hope will stay that way, but inducing gynogenesis (a synonymous of parthenogenesis) is possible through two kinds of chromosomal manipulation, which precipitates in respectively 3-4 generations or just one the genetic result of 12 generations of sibling matings. Gynogenesis is a common feature of reptiles, amphibians and fish, mostly associated with external fertilization.

Gynogenesis is useful for rapid improvement of genetic characters, producing inbred (clonal) lines compared with the traditional methods of sib-mating for up to 10 to 20 generations. Clonal lines are supposed to be very valuable products for improvement of fish stocks. In view of this, meiotic gynogenesis have been produced in many species of fish but are not completely homozygous due to recombination between non-sister chromatids. This occurrence is undoubtedly absent in case of the production of mitotic gynogenotes induced by the suppression of first mitotic cleavage and thereby the progeny are homozygous at every gene locus. Therefore, it is very advantageous for producing clonal lines in the subsequent generation(s) with unique gene combination.
1997, Induction of mitotic and meiotic gynogenesis and production of genetic clones in rohu, Labeo rohita Ham

Since the species of interest always require a fake fecundation (without syngamy) to initiate development, gynogenesis always requires sperm sterilized through UV rays. Suppressing the ejection of the second polar body is done through either/or osmotic shock (temporary pressurization) or heat shock.

All ectotherms (vertebrates beside mammals) can be treated like this fairly easily, and do so naturally on a regular basis owning to the frequency of external fertilization as those shocks aren’t uncommon and easily disturb meiosis (which is not finished until the very moment of fecundation), though there are genetic factors too. Also such species are often much more labile with surprising physiological resilience to polyploidy (plus sex change) and hybridization, as shown by fish and amphibians in particular.

On the other hand, mammals are notably more complicated with polyploidy being extremely infrequent and aberrant, and hybridization as rare as detrimental. Medical conditions in which one or more pairs of chromosomes come from the same parent are called uniparental disomy, and are nearly always lethal, very early… Even sharing fragments of chromosomes has the same effect, because of a phenomenon called parental imprinting which we won’t detail here. Progress on mastering this phenomena (erasing it to be precise, to fool the cell into thinking the chromosome comes from someone else) on mammals (after decades of failures) just started to show up in 202211.

Without a doubt, testing our ambitious eugenic program on rats will soon be a reality.

One must wonder though: in practice, assuming total access to the purest Aryan sample, how many defects would we observe in humans with such a drastic method ? Hard to gauge. While normal incest with sound parents is usually very safe, these protocols we discuss entail from twice to four times the amount of consanguinity of sibling incest in one go, making dead certain to reveal whatever might be hiding in the recesses of your genome. Fish species throughout evolution went through several rounds of entire genome duplications, and some species - like trouts - more recently than others, producing highly redundant gene families, acting in effect as multiple extra alleles, hence in these cases the resilience to higher degrees of homozygosity than customary for us.

Even then, fishes respond in a variety of way:

Consequently, to obtain the sufficient DH genetic materials without reducing reproductivity for many fish species is still an important challenge. In this study, all six gynogenetic fish were successfully induced to produce DH offspring, whereas only one common fish did. In addition, both the CHR and the CNR of the common fish were lower than those of the gynogenetic fish. Induction rates of DH increased with Parental fish homozygosity rising, and a very significant correlation was found. Meiotic gynogenesis could provide an effective means to rapidly obtain homozygotes in fish. As indicated earlier, meiotic gynogenesis is easier to conduct than mitotic gynogenesis.
The mean survival rate of offspring produced by mitotic gynogenesis was very poor (4.1%) when compared to meiotic gynogenesis (19.3%) in loach (Arai 2001). Goudie, Simco, Davis and Liu (1995) tried meiotic and mitotic gynogenesis in channel catfish. They documented survival rates at 1.5 months of 2% for meiotic and 0.2% for mitotic gynogenesis. We observed a similar result: the CNRs of C1 and G3 for mitotic gynogenesis were 10.34% and 20.40%, respectively, compared to 48.42% and 57.25% for meiotic gynogenesis.

In this study, CHR increased from 0% to 20.00% in outbred females **to 21.74% to 44.59% in the first generation of meiotic gynogenesis. This phenomenon could be due to a decrease in the number of recessive lethal alleles (Nagy, Rajki, Horvath & Csanyi 1978), because deleterious genes should be eliminated from proximal regions of chromosomes by consecutive meiotic gynogenesis. Therefore, this may be a feasible method to obtain DH genetic materials for flounder.

This shows the efficacy of the method. The more inbred the stock, the more intense inbreeding it can tolerate without failure, purging bloodlines even faster. The wild brown trout12 show a survival rate up to the hatching stage though, was hatching stage 42.1 ± 3.17 %, against 91.9 ± 1.30 % for normal heterozygous brow truta fishes.


The probability of two alleles to be identical by descent for brother/sister matings is 25%. We established that the actual risk for first generation incest offspring of unhealthiness (not even proper birth defects) in a subpopulation with no obvious hereditary issues (though no thorough tests have been made) is no higher than 12.4% and if we exclude troubles most likely of dietary origin, than 6.2%.
Extrapolating for a 100% chance of identity by descent (basically what they did with fish) would give hypothetically a maximum of 12.4✕(100/6,25) = 49.6% risk assuming all diseases are congenital and genetic, and a minimum of 24.8%, figures framing those of the fish experiments.
Although we have to keep in mind that fish in general and the brown trout in particular differ from us in many ways, with both higher mutation rates but also higher survivability due to a genome13 more robust and redundant than ours due to successive rounds of genome duplication over the eons, so direct analogy provides only a rough estimation. But on the other hand extrapolated probabilities for inbreeding morbidity in humans have proven wrong.

The fastest method will undoubtedly be the creation of Opposite Sex Clones by inducing twinning then exchanging one X chromosome for a Y from an external source in one of the twin, thereby producing a pair of embryos of opposite sex sharing 98% of their DNA, or more if we take the Y from a male in the maternal line.
This would be the ultimate form of incest, with minimal manipulation. Such individuals would not be inbred at all but rather error-free copies of one another, beside hormonal differences. However their offspring would be as close as selfing as can be for mammals, with very little manipulation.

But most of all their offspring’s heterozygosity would halve immediately, and again each generation. Compared to usual breeding practices the time saved would be tremendous, considering that one human generation canonically takes 20 years and fish take 6 months or less. With such couples one could dial the speed up to eleven.

Robert Heinlein popularized the trope14 for titillation’s sake but in all seriousness, this is a very good argument: not only would this expedite any and all genetic purification endeavour, this would also provide essentially the level of Genetic Sexual Attraction and psychic link true twins possess, but on the heteresexual mode. Producing a female from a male is easier, but then produces an identity of the two X, which despite lyonization or X-inactivation would still produce some issues due to recessive lethals (the inactivation is not total). So the success rate would be impredictably low.

There is one reason it has never been seen except in lab mice clonal lines, taking at least ten generations to make: parental epigenetic imprinting. This is a system where DNA is loaded with transient chemical marks altering the expression of genes, and are recognized as Self, so that fecundations or later fetal development is automatically aborted for a single pair of chromosomes inherited from the same parent as a bloc, whether it be a duplicate chromosome or the two homologs. Even for a short piece of a chromosome. As mentioned before11 these issues might not wait long before their resolution.

Genetic Modification

For the moment, beside the we lack one technology in particular, that hasn’t shown much development is the ability to cut and paste pieces or whole chromosomes from a cell or egg to another, seamlessly, as the epigenetic programming of any cell is a pretty annoying hindrance to any such manipulation past a number of genes

For a long time I’ve been against genetic engineering (of any form), because the way we usually do it. Our case would chiefly qualify as knock-in procedures that substitute a sequence provided from the outside to an existing one. Changing an allele or haplotype for a designer one. But efficient manipulations on a large scale (hundreds of genes) would require perfect reading, digitization and synthesis of millions of base pair, follow by their integration into a cell without side effects. And sadly enough, none of this is possible yet, not even the reading part.

To enable modifications at the nucleotide (single base pair) level, we employ sets of enzymes basically acting as scissors, cutting then pasting or calling the cell’s gluer. The issue with this technology (CRISPR-Cas9 among some others) is its unavoidable imprecision: the cutting place is hardly controlled and the pasting no more, while multiple instances of the gene often integrate the genome. This doesn’t bother plants or bacteria, and fish DNA (for purpose of commercila exploitation), being so polyploid, can take a lot of punishment, but it is another story altogether for mammals. Yet we do not mind a lot of waste in order to get a viable product in industrial husbandry though, and it easy to overlook the whole lot of detrimental health effects on animals fed processed food regardless: they are already closer to machines than living being anyway.

Horrible picture of industrial ducklings

But such awful results are unimaginable on humans, and edition on human germlines are banned internationally, rightfully so. For once that convention has been enforced quite effectively world-wide, until that ridiculous Chinese anti-HIV supersoldier experience which will probably get those poor kids killed by cancer.

On the other hand, the very first method we used for genetic edition (beside dumb blind irradiation) to use constrasts a lot, and called homologous recombination. The idea was simply to inject and propose an alternative DNA strand, with which the cell will substitute to the one it already has, based on their overall similarity and/or a prior double-strand breaking of two boundary-limiting motifs.
The reason better methods were sought out is the inherent slowness and random nature of this one, in the sense that such phenomena would normally occur under control of interrelated sequences underpinned by complex protein scaffoldings, specific to meiosis. Without direction, the success rate of insertions at the right place has historically been around the percentage level.

Beside the sometime considerable time and money aside needed historically for genetic experiments, it has served research well. However such rfailure rate will not cut it for genetic therapies on fragile genetically ill poor Jewish children.
The same holds regards to gamete manipulation considering the limiting rarity of ovules plus ethical regulations. Yet this way has the advantage of inserting only once the modification, and more precisely as well. Artificial scissors are an external aggression on a complicated machinery that evolved for tens of millions of years, one we will never master.

Homologous recombination or its variant, gene conversion, are in vivo highly directed and controlled, animal cells have been capable of autonomous complex genetic edition as part of Lamarckian processes forever15. The majority being die-hard reductionists, has considerably stunted the progress of science in this direction until now. Progresses have been made though, thanks to which techniques for minute efficient inducing of gene conversion wherever needed will undoubtedly be available in a matter of years.16

I particularly endorse the following rationale:

One approach to gene therapy is to replace defective genes with wild-type functional genes at a targeted site in the genome. This approach has the advantage of ensuring gene expression at endogenous levels under the physiological control of normal gene regulatory elements.

If we could learn to collaborate with cells like with an intelligent system with its own rationale, we could profit from their own innate capabilities. I am ferociously against against a human reproductive use of artificial molecular tools.

The solution is to stop wanting just about anywhere in the genome at our discretion, but study quantal genetics that we discussed prior.

We must learn to see genes not as a continuous stream of base pairs but as the cells themselves understand them, as a network of isolated yet interconnected atoms of information of many different kinds, inside a predictable yet open-ended system, A living entity qualitatively different from a machine as it is its own designer, evolving its own rules and purposes as it goes.

Evidences abounds17 that cells do not see individual genes but entire PFBs at once, separated by efficient though fluid boundaries, mainly driven by the PRDM9 gene family. Steele18 showed experimentally the deeply intricate relationship between the quantal structure and acquired inheritance mechanisms. Mastery of directed gene conversion respectful of this structure would allow seamless and efficient manipulations without size limit.

My second criticism of current genetic manipulation and arguably a much more fundamental one is our incapacity to predict the consequences of our modifications.
Like this Chinese madman: even assuming he did inserted his knocked-out gene exactly where intended and nowhere else (he apparently couldn’t…). No one has any clue what a virus is, so who the hell can predict what knocking out an important receptor whose functions beside viral entry we don’t anything about ?

The same goes for most designer sequences. Our gene plan, either God-given or a result of (a not quite blind) evolution, can’t be cut in pieces without dire repercussions…

But said plan can be entered.
My suggestion amounts to letting the tried and true natural selection pit the clean natural haplotypes against their flawed versions, incapable to sustain life under homozygous expression as revealed through the many proposed methods some theoretical (artificial selfing), some common and starting to work on mammals after decades of failure. Then more artificial methods (in vivo through implants for instance and/or widespread retroviruses, or in vitro) could inhibit or reject the gametes featuring defectuous haplotypes, stacking the odds considerably towards increasingly better offspring. Or possibly cause a population-wide correction. Possibilities are endless.

At last, the truly limiting factor in any of these kinds of research is, alas, the low number of mature eggs in women, compounded by the rarity of very pure Nordic women, foreclosing anything close to what we do with fish, cutting down the practical degree of consanguinity allowed or speed of selection by a factor 10 to 20.

Obviously if your mating scheme generates, say, only 5% (for argument’s sake, as it would be significantly worse in practice) of embryos (that we assume infinitely superior) while all other get crippled and die, you would need at least twenty attempts (with at least 20 mature eggs) to statistically get one success. Hardly a number conducive to any eugenics purpose. No hormonal treatments can change that. Hence an incredibly desirable scientific progress would consist in the ability to produce ovules de novo (from DNA samples) or duplicate them in cell cultures, in order to remove this limitation.

And after decades of researchs of dreaming, it is now almost certain to become a reality in the next decade or two19:

Scientists have created mice with two biologically male parents for the first time - a significant milestone in reproductive biology.
The team, led by Katsuhiko Hayashi, a professor of genome biology at Osaka University in Japan, generated eggs from the skin cells of male mice that, when implanted in female mice, went on to produce healthy pups, according to research published March 15 in the peer-reviewed journal Nature.
However, scientists warn there’s still much to learn before cultured cells can be used to make human eggs in a lab dish.
It is expected that application into humans takes a long time, maybe 10 years or more. Even if it is applied, we never know whether the eggs are safe enough to produce (a) baby, Hayashi said.

A truly eugenicist State will extend a Lebensborn project to the totality of the population, and collect all this DNA for study or breeding purpose. It would provide unlimited resources along with millions upon millions of Nordic candidates.
This is our dream.

There is another reason why genetic modification the way it is done today is problematic. In the natural case according to litterature20, natural conceptions include a 40% to 60% (within a 5% error margin) of embryo loss, hence a 5/3 (or 1.2) attempts per success for the lowest success rate to 2.2 attempts per success for the highest success rate.
Whereas the average overall pregnancy rate from IVF using fresh embryo transfers reached 29% in 2021, with the highest rate peaking at 41% for the age range 18-34 accoding to official British sources. So in the best of case the loss post fertilization is 59%, compared to 40% in the natural case, mostly because the techniques have improved considerably and both ovas and embryos are selected thoroughly on morphological criteria. Yet the failure rate is still higher, or maybe much so (but the level of precision of a clinical IVF study is for the moment technically challenging for the natural case21). It is estimated that most of the implantation or pre-implantation losses(pre-clinical spontaneous abortions Definition: Loss that occurs before the ultrasound is able to detect an embryo, so before 5 weeks usually. ) alike are due to chromosomal instabilities, evidences indicating a higher rate for IVFs embryos than live ones.

It is believed that the failure of the culture medium to stand in accurately for the maternal environment even for the first few days: the same environment that we know now is reponsible for the selective nurturing or termination of embryos depending on their genetic health, as mentioned when we treated the role it played in weeding out rejects of consanguineous unions, making them much safer than expected with statistics. The dialog between the mother and the child, from the moment of conception, exceeds by far what machines could simulate, dooming any risk of ectogenesis Definition: Ectogenesis is the growth of an organism in an artificial environment outside the body in which it would normally be found, such as the growth of an embryo or fetus outside the mother's body, or the growth of bacteria outside the body of a host in higher animals without getting cripples in mass.

It is highly suspected that children born from artification insemination alone, are more susceptible to diseases because of the those artificial conditions in a critical moment, leading to epigenetic abberations22. Because we discovered how much more efficient the human body is in selecting good sperm23, tests improved that screen for morphological difformities (hinting at DNA fragmentation), leading to higher and higher success results. Yet these artificial methods still leave late life health issues, because something as gross as a morphological anomaly most only would cause failure at fecundation and early development. It can not screen for trits impacting the whole life. But the maternal body as well as gamete selection, do.
Evolution has found many ways to expediate the tedious and wasteful process of natural selection, by displacing the sieve onto the haploid phase, meaning the gametes, making a lot of them, applying high stress and competition on many levels leading to the apoptosis or failure of more than 99% of all gametes produced, before even fecundation. Science is starting to consider the crucial importance of that phenomena and its wide-ranging implications. Sperm selection24 and competition[^sperm-competition] go way beyond

Beyond Selection

Lastly, I must straighten out that not every objectively undesirable trait can be singled out this way, even in the best case scenario. It is because I specifically mention flaws borne from cooking accumulated throughout millennia. These are chaotic mutations of a rather gross nature, typically so much so they do not sustain homozygous expression at least not in number.

They constitute the mutational load as commonly defined.

But a lot of what separates us from Neanderthal, are rather misadaptations, divergent mutations fixating and changing our whole ontogenesis (development along species-specific morphological lines), without reduced lethality or even sublethality. Just gearing us toward different though objectively inferior courses of development, weaker more fragile bodies and brains. Once we reach total purification down to the ground level of chaotic errors (infinitely small in raw primates, compared to insects or bacteria), how to go further toward full recovery of the Neanderthal phenotype ?

Motoo Kimura, a leader of the synthetic theory of evolution and later the neutral theory of molecular evolution (stating that most mutations are synonymous hence neutral and random drift being the principal driver of change) said very well:

Even if in the distant future it will become possible to freely replace DNA base pairs in the nucleus, it is premature to think that the genetic qualities of the human can be freely improved. This is comparable to the notion that the blueprint for any splendid machine can be drawn provided paper and a pencil are available, and ignores the higher dimensional problem of information. Moreover, the conundrum exists of how far the human can improve its brain by using its brain.

Regardless of computers, what does the comprehension in last analysis is always the brain, and nothing ensures our brain can outdo millions of years of evolution nor is designed to understand itself totally. The intellect can not exceed itself by its own means. What Kimura couldn’t know is that we don’t evolve but devolve, so one simply needs to amplify the ancestral part of us:
we don’t know why molecularly speaking the past was better, we just know it was from reasoning and looking at bones. And then Lamarckian mechanisms do not require our understanding either, we just need to set up the good conditions for their application.

Lastly, the brain does not only possess intellect but also the extrasensory, infinite in scope and depth and superseding everything material. Hence it open the path for a possible conscious genetic improvement under divine guidance, such as that Teilhard De Chardin would have called for.
Here the heredity of acquired characters starts to play. Through a comprehensive physical, physiological and cognitive conditioning, fully integrated into a totalitarian culture pervading every aspect of our lives, we’ll bring out the total potential of the genetic gifts of all children. As well as induce the self-evolution of our species through the feedback mechanisms shown by Sally S. Lloyd, Edward J. Steele, Roger L. Dawkins and others, by exposing ourselves willfully and systematically, to the very limit of human experiences, stress tolerance while our mind also reaches its very spiritual limit.

In order to recreate, in a directed manner, the outer (environment) and inner (the mind) evolutionary pressures which brought forth our species in its state of biological, evolutionary near-perfection. In this dream, you are welcome to participate.

  1. In The Origin of Species, Darwin developed a theory about how this might happen: he theorized that if changes in the soma occur as a result of physiological adaptation, something would be transmitted to the germ cells to carry the information. He invented the idea of gemmules, small particles that he assumed would travel (presumably through the blood) to carry the relevant influences.
    This theory (called pangenesis) is found in the 1868 book The Variation of Animals and Plants under Domestication. Darwin forsaw exosomes and retroviruses↩︎

  2. Despite that in reality most mutations are completely silent, and that effects can arise at many levels, which might or not change the protein, its expression or regulation in any numbers of ways, which might or not impact the phenotype. But of all genes, only a fraction produce proteins, while the overwhelming majority of mutant alleles. Early geneticians suffered from selective perception, often (still now…) rejecting unconclusive data they had no means to make sense of yet, in the name of dogmas born from those very limitations. Scientifics often prefer nice consistent theories to unclear facts, at the price of falsity. ↩︎

  3. By 1987, it was clearly established that each ancestral haplotype has a specific content of genomic features such as duplications and indels. These too are actively conserved and can themselves be used as signatures for haplotypes of hundreds of kilobases and even megabases. These observations were very difficult to explain in terms of any form of neo-Darwinism, natural selection, random errors or population genetics as taught then and today. Rather, we realised, the genome is not actually homogeneous but partitioned into protected quanta or PFB
  4. Steele, E.J et al.: Lamarck and Panspermia - On the Efficient Spread of Living Systems Throughout the Cosmos, The evidence for Larmarck ↩︎

  5. I also summarizes the similarity between viruses and exosomes and what hitherto unknown extended identical roles they may have in evolution.
    [polymorphism]: DFN “In genetics, a single-nucleotide polymorphism (SNP /snɪp/; plural SNPs /snɪps/) is a germline substitution of a single nucleotide at a specific position in the genome and is present in a sufficiently large fraction of the population (1% or more). They come from mutations, old or new, and their presence identifies haplotypes (aka, alternative versions of a gene within a person or population). Single nucleotide substitutions with an allele frequency of less than 1% are called single-nucleotide variants, not SNPs.” ↩︎

  6. To address these issues, we have now generated a mouse model xenografted with human melanoma cells stably expressing EGFP-encoding plasmid.
    We find that EGFP RNA is released from the xenografted human cells into the bloodstream and eventually in spermatozoa of the mice. Tumor-released EGFP RNA is associated with an extracellular fraction processed for exosome purification and expressing exosomal markers, in all steps of the process, from the xenografted cancer cells to the spermatozoa of the recipient animals, strongly suggesting that exosomes are the carriers of a flow of information from somatic cells to gametes.
  7. Histones Definition: Histones are the key parts of DNA compaction into chromatin and play a major role in regulating genome functions. They are the targets of multiple post-translational modifications which provide epigenetic information. and many other molecules (carbohydrates, fatty acids, RNA, everything) also modified in mass but as part of the normal cellular functioning, and this is not inheritable.
    really part of the experien Youu collect throughout your life, as in the Dune nov, though obviously there is not nearly enough place in DNA for entire memories… although the novels themselves alluded to genetic memories taking most critical rebuking of., just like we think, so who knows ? ↩︎

  8. General papers:

  9. The body does not adapt to fight viruses, but on the contrary to get sick more efficiently and use these pathogens in the context of endogenous processes of elimination of denatured molecules, mostly cooking-originating molecules nowadays. The error is simply to project the parasitic-hote model on the virus instead of blaming the environment, meaning the lifestyle. ↩︎

  10. It is customary to think that it would be necessary to maintain a great heterozygosity (both alleles of a pair of chromosomes differing), the greatest genetic variety, to stay adaptable to a changing environment. It is also believed that a consanguineous species would become uniformly homozygous and vulnerable to environmental changes. These two assumptions are false. In addition, adaptation to a changing environment is not necessarily based on a heterozygous population.
    Evolution acted on our genetic system, precluding the need for any more insane sieve culling 90% of each generations, something tadpoles rats or mosquitoes know something about.

    Adaptation to ecological conditions should not be limited to the allelic substitution in response to each fluctuation in the environment. A current alternative seems to be the fixing of complex epigenetic systems which respond adaptively to environmental flows in a phenotypic rather than genetic way. Characters such as developmental and genetic homeostasis, switching genes controlling phenotypic expression in heterogeneous environments, pipes and experiential modification of behavior (learning), all allow and promote the development of favored phenotypes in the face of considerable environmental disturbance. The fact that human populations are, and were largely dispersed geographically, assured the heterozygoty of the species even when local isolates are highly homozygous. This ensured the survival of the species even in the event of local extinction.
    Shields (1982: 266)
  11. Viable offspring derived from single unfertilized mammalian oocytes ↩︎ ↩︎

  12. the wild Salmo trutta m. fario (the brown trout), a diploid species like us ↩︎

  13. The genome sequence of the brown trout, Salmo trutta Linnaeus 1758 - PMC ↩︎

  14. I am not speaking of monsters, Lazarus. A true change in sex A single cell is selected for cloning. Before cloning is started, the Y chromosome is removed and an X chromosome from a second cell of the same zygote is supplied, thus creating a female cell of the same genetic pattern as the zygote save that the X chromosome is replicated while the Y chromosome is eliminated. The modified cell is then cloned. The result is a true female clone-zygote derived from a male original.
    Robert Heinlein, Time Enough For Love
  15. Haplotype structures and polymorphisms of dog leukocyte antigen (DLA) class I loci shaped by intralocus and interlocus recombination events ↩︎

  16. Methods to trigger seemless secure genetic modifications:

    Genetic elements that are inherited at super-Mendelian frequencies could be used in a gene drive to spread an allele to high prevalence in a population with the goal of eliminating invasive species [ - such as subhuman genes- ] or disease vectors.

    Using multiple approaches, we provide evidence for an endogenous IHR mechanism in the early embryo that can be enhanced by RAD51. This process can be harnessed to generate homozygotes from wild-type zygotes using exogenous donors and to convert heterozygous alleles into homozygous alleles without exogenous templates.

  17. In many eukaryotes, sites of meiotic recombination, also called hotspots, are regions of accessible chromatin, but in many vertebrates, their location follows a distinct pattern and is specified by PR domain-containing protein 9 (PRDM9). The specification of meiotic recombination hotspots is achieved by the different activities of PRDM9: DNA binding, histone methyltrans-ferase, and interaction with other proteins. Remarkably, PRDM9 activity leads to the erosion of its own binding sites and the rapid evolution of its DNA-binding domain. PRDM9 may also contribute to reproductive isolation, as it is involved in hybrid sterility potentially due to a reduction of its activity in specific heterozygous contexts.

  18. Genesis of ancestral haplotypes: RNA modifications and reverse transcription–mediated polymorphisms
    The broad mechanism is explained as follows:

    To be more specific, a large RNA recombinant string is formed . The RT- priming step would be as envisaged for Somatic HyperMutation such that the nicked transcribed strand (TS) DNA with a free 3=-OH end anneals to the long modified RNA thus allowing extension of the cDNA to produce a long newly synthesized transcribed strand with all the RNA mutations now embodied within the DNA strand 287 as SNPs (or indels, etc). The last steps would involve strand invasion, endonuclease action to remove the displaced resident strand “flap” and then integration to seal the gap on the TS (via ligation). These events could happen during gametogenesis and meiosis and manifest as a biased or directional DNA conversion tract from one parental chromosome to another. It may involve alterations of the structure and position of recombination hotspot motifs, such as the PRDM9 gene, and their reallocation to the boundaries of the PFB and thus minimize recombination within the newly formed PFB Polymorphic Frozen Block. That is, the donor strand low in PRDM9 motifs would invade and convert the target strand to create a tract of low density PRDM9 motifs.

  19.  ↩︎
  20. Estimates of embryonic death in most mammals, including swine, sheep, cattle, and humans, ranges from 20% to 40%, with two-thirds of the losses occurring during the peri-implantation period of pregnancy.
    During that stage of pregnancy, the dialog between the mammalian conceptus (embryo/fetus and associated membranes) and maternal uterus involves signaling for pregnancy recognition and maintenance of pregnancy as the stage is set for implantation and placentation that precedes fetal development. Uterine epithelial cells secrete and/or transport a wide range of molecules, including nutrients, collectively referred to as histotroph, that are transported into the fetal–placental vascular system to support growth and development of the conceptus.
    Molecules to Medicine with mTOR, 2016
    A recent re-analysis of hCG study data concluded that approximately 40-60% of embryos may be lost between fertilisation and birth, although this will vary substantially between individual women. In conclusion, natural human embryo mortality is lower than often claimed and widely accepted. Estimates for total prenatal mortality of 70% or higher are exaggerated and not supported by the available data.
    Early embryo mortality in natural human reproduction: What the data say, 2016
  21. Early embryo mortality in natural human reproduction: What the data say, Gavin E. Jarvis, 2016 ↩︎

  22. If maternal nutrition during the periconceptional period has effects on life-long health risks, it is reasonable to assume that this also applies to various IVF treatments. In embryo cultures, the culture medium replaces maternal nutrition. Both periconceptual deficiency and overabundance of nutrients seem to increase the risk of disease in later life to a similar extent.
  23. One interpretation of this situation is that females have developed sophisticated mechanisms to screen the spermatozoa that enter the reproductive tract, eliminating most of them but providing protection for the selected and privileged few that reach the oviducts. This mechanism implies that the female reproductive tract applies stringent selection criteria to the sperm population. Given the context of this review, if we could eventually find out how these selection mechanisms operate, we should be able to mimic them in vitro and thus develop objective tests that predict the likelihood of spermatozoa reaching and being able to fertilize the oocytes
    Is semen analysis useful to predict the odds that the sperm will meet the egg?, 2009
  24. Within-Ejaculate Sperm Selection and Its Implications for Assisted Reproduction Technologies, 2021 ↩︎