Making Sense of Orthodox Judaism: Understanding the Scientific Basis of the Oral Torah
In an earlier article titled, “The Extraterrestrials Who Evolved Billions of Years Earlier Than Humans, And Their Attempts To Communicate A Vital Scientific Information To Humanity”, we discussed how aliens had contacted the Sumerians and the Hebrews in ancient times and had strived to leave a lasting cultural impact on human civilizations. Today, we have discovered the scientific nature of this culture and why it is necessary. These findings cut across several disciplines: Evolutionary Biology, Cytogenetics and Quantum Physics.
Introduction
Before natural selection can take place, there must exist organisms within a population with a new beneficial trait. And as such kind of traits accumulate with time, they would distinguish the group from others. Sometimes, as postulated by Charles Darwin, two groups of organisms within a population might evolve different beneficial traits (This is what Darwin called the Principle of Divergence), which would confer on the two groups a competitive advantage against a third group that did not evolve any beneficial trait.
There is always this third group that is left behind— this is the group of organisms that did not evolve any beneficial trait, yet they lived in the same environment as other groups and they all constituted the same species, once upon a time.
The beneficial traits would emerge as a result of genetic variation, and with this new trait, some organisms are furnished by nature with the capability to adapt and survive better than their peers. But why would certain organisms evolve a new beneficial trait; while during the same course of time, there are other organisms that could not evolve a new beneficial trait, not even a different beneficial trait, which is in accordance with Darwinian Principle of Divergence. Yet all the organisms lived together as a population in the same environment and constitute the same species, before they became completely different from one another over evolutionary time.
After many generations, the group without any beneficial trait disappears. This is natural selection.
The big question is why did two groups developed beneficial traits, when, during the same course of time, the third group did not?
An organism would develop a new beneficial trait by genetic variation. But how exactly is the nuclear genome uttered to give rise to genetic variation?
The brilliance of Darwin’s work lies in the fact that it describes how beneficial traits accumulate with time to distinguish descendant organisms from their ancestors, branching out as a new species; not why the traits are able to develop in some descendants and not in other descendants, yet they all belong to the same species.
Yet this is a condition that must be met before adaptation and natural selection can take place, conferring favor on those organisms that have evolved new beneficial traits, and condemning to extinction those organisms that do not evolve beneficial traits.
After years of experimentation and research, we have finally obtained the answer to this very important question. In the evolutionary timeline, we can safely say that asexual reproduction came first. The earliest organisms reproduced asexually. This was the norm for billions of years until some organisms evolved sexual reproductive capabilities. Ever since this happened, there are two basic principles that govern evolution— that is, the onward evolution of sexually reproducing organisms. We discovered two basic principles of evolution, and we summarized them below:
The First Basic Principle of Evolution: The DNA Unitarity Principle (the Acquired Mitochondrial DNA Unitarity Condition)
This principle reminds us of Schrödinger’s Quantum Unitarity Principle, which is one of the principles that make up the foundation of Quantum Mechanics. As we stated earlier, this principle is essential for the continuation of evolution in sexually reproducing organisms. The story is similar from one species of sexually reproducing organisms to another. But let us see how it applies particularly to humans.
In humans, the female egg cell, called primary oocyte, stops all development and becomes dormant in female fetus several months before the female child is born. Then at puberty, the egg cell resumes development, after receiving stimulation from hormones. But during the dormant or arrested period, many of the mitochondria of the egg cells (primary oocytes) do lose their mitochondrial DNA to natural decay . And this decay process leaves compromised mitochondrial wall inside the cytoplasm of the egg cell.
With many damaged mitochondria, the affected primary oocytes cannot grow into secondary oocytes during puberty.
Nature fixes this problem by making use of mitochondrial DNA that are acquired from immature sperm cells in the semen donated by a male sex partner or several male sex partners.
The semen contains both mature and immature sperm cells.
A mature sperm cell has mitochondria with no mitochondrial DNA. But it is a mature sperm cell that fertilizes a mature egg cell. An immature sperm cell has mitochondria with mitochondrial DNA, and cannot fertilize a mature egg cell. That is why male infertility is linked to sperm cells with abundance of mitochondrial DNA. As immature sperm cells develop into maturity, they lose their mitochondrial DNA, and the mitochondria of a mature sperm is as good as dead. This is because a mitochondria without mitochondrial DNA cannot manufacture energy—it can only store it. Sperm becomes mature with an intact storage of energy located within its mitochondria. This energy was produced during the immature stage, when the sperm still possessed a mitochondrial DNA.
A mature sperm, the sperm that fertilizes the mature egg cell, does not pass its mitochondria to the egg. During fertilization, only the region of the sperm that contains the nuclear area joins up with the mature egg. The region that contains the mitochondria is left behind. Therefore, Mitochondria are passed only from mother to offspring. However, this is not the case for mitochondrial DNA from immature sperm. They reach the immature egg cells. And they are used by nature to repair damaged mitochondria. Hence, the scientifically proven cases of paternally inherited mitochondrial DNA in embryos.
There are two problems:
1.) This mitochondria repair process does not occur one after the other amongst the affected primary oocytes. Mitochondrial DNAs from immature sperm do not fix up one primary oocyte completely before it fixes another. There is no mechanism as such. Rather, the repair occurs in a zig-zag manner, as mitochondrial DNAs are distributed randomly among all the affected primary oocytes by chance. Therefore, for a given affected oocyte, it could take up to about 45-50 years (just before the age of menopause).
Until the repair is completed, a primary oocyte cannot graduate into a viable secondary oocyte. Therefore a primary oocyte can be in the repair process for 45 to 50 years.
2.) The second problem is that a mitochondrial DNA is best called a mitochondrial DNA bundle because it consists of the DNA itself ( the backbone structure, which always carry a negative charge) and protein sequences called genetic codes that are attached to the DNA. Each of these proteins may carry a positive charge or a negative charge or a neutral charge. The charge of each protein depends on the PH level in the mitochondria. This means that, together, all the proteins have a Net Charge. In the same vein, the DNA which is negatively charged, and all the proteins that are attached to it, will, collectively, generate a Gross Net Charge. Therefore, we conclude that the mitochondrial DNA bundle has a Gross Net Charge.
The following holds true:
a.) The Gross Net Charge of a mitochondrial DNA bundle may be positive, negative or neutral.
b.) Every mitochondrial DNA bundle from the same source, that is from the same male sex partner, has the same Gross Net Charge. But a pool of mitochondrial DNA bundles from different sex partners will consist of mitochondrial DNA bundles of varying Gross Net Charges.
Electrostatic Interactions
(a) When damaged mitochondria are repaired with mitochondrial DNA acquired from the same source, that is, the same sex partner, electrostatic repulsions occur inside the cytoplasm of the egg cell, as the acquired mitochondrial DNA bundles repel themselves. Electrostatic repulsion takes place because all the acquired mitochondrial DNA bundles inside the cytoplasm contain the same Gross Net Charge.
This electrostatic repulsion maintains order in the cytoplasm. From our careful consideration, we conclude that an orderly cellular environment promotes constructive cellular behavior. Order is required for evolution to proceed constructively inside the cell—not disorder.
The result is that evolution will proceed constructively inside the cells of an organism eventually produced from such an egg cell after it gets mature and fertilized.
(b) When the repair process is furnished with mitochondrial DNA acquired from different sources, that is, from different sex partners, electrostatic attractions may occur inside the cytoplasm of the egg cell, as acquired mitochondrial DNA bundles do attract themselves inside the cytoplasm of the egg cell when they have opposite Gross Net Charges.
This leads to disorder in the cell. As we have carefully observed, such disruptive environment hinders the constructive process of cellular innovation and evolution.
The result is that evolution will not proceed constructively inside the cells of an organism eventually produced from such an egg cell after it gets mature and fertilized.
These electrostatic attractions produce “mobile” genetic materials within the cytoplasm, otherwise called transposable elements or transposons.
It is important to note that, although all Mitochondria in the offspring are maternally inherited, not all Mitochondrial DNA inside the Mitochondria are originally maternal.
In summary, mitochondrial DNA from semen of male sex partners are used to fix damaged primary oocytes (damaged as a result of degradation during the arrested stage of egg cycle) so that they can become viable secondary oocytes. When the mitochondrial DNA used for this purpose come from several male donors, it is most likely that a problem will arise. Electrostatic attractions of opposite charges that emanate from the acquired Mitochondrial DNA bundles inside the acquired mitochondria within the cell lead to genetic instability and disruptions in the egg cell, and this will continue to occur throughout the lifespan of the organism that is reproduced from that egg cell, after maturity and fertilization, and it is the cause of abnormal genetic conditions and diseases.
Mitochondrial DNA bundle in undamaged mitochondria in the primary oocytes are shielded from all electrostatic activities within the cytoplasm by the mitochondrial wall. However, electrostatic attraction and repulsion occur amongst the acquired mitochondrial DNA in the cytoplasm because, prior to their arrival in the mitochondria of the cell, these mitochondria are damaged and their walls are already compromised.
Caveat: Primary oocytes that do not undergo damage during the arrested stage will develop into secondary oocytes during puberty. Since the mitochondria within the oocytes are all walled (undamaged), electrostatic activity is null within the cytoplasm of the cells of the offspring produced from such oocytes. Therefore, evolution will proceed constructively throughout the lifetime of the offspring.
The First Instruction of the Oral Torah
There was a time in ancient Sumer when people practiced what could be described as Reproductive Fidelity. It is one of the three cultural practices that constitute the culture we could call “semitism”, traceable to the early Sumerians. It is a cultural practice that required a female to keep to only one male for all sexual activities from the age of virginity until she decided not to bear offspring any longer. This practice was inherited by the Hebrew women, most particularly the women of the Levitical tribe, because this teaching was incorporated into the original Oral Torah handed down to the Hebrews from Abraham who originated from Sumer. Particularly, it was emphasized in the Written Torah for the priesthood tribe, that is, the tribe of Levi. [Read Leviticus chapter 21 verses 13,14 and 15; Hosea chapter 1 verses 2 to 6.] However, it was meant for all the tribes [Matthew chapter 19 verses 8 and 9].
Reproductive Fidelity, a term quite distinguishable from monogamy, is one of the instructions of the Oral Torah. Like we stated before, we deduce that it was a cultural practice among the early Sumerians. However, it was rejected by the latter Sumerians because they considered it too much of a burden to bear, and they despised their predecessors for procreating in line with such a stringent rule.
So they revolted against it. This revolt was well documented—albeit, as an allegory—in Sumerian writings discovered in contemporary times. According to the legend, the latter Sumerians rebelled against “forced labor” which was being enforced by the Annunakis, those “who from heaven came”.
What the latter Sumerians did not understand is that the Annunakis were trying to fast-track human biological evolution through certain cultural practices like the one mentioned above—reproductive fidelity.
The Second Basic Principle of Evolution: The DNA Metamorphic Principle
There are two types of DNA bundles —the nuclear DNA bundle, which is found in the nucleus of the cell; and the mitochondrial DNA bundle, which is found in the mitochondria. Also, the nuclear DNA bundle has both coding and non-coding parts. The coding part determines the nature of the species, and it changes to give rise to new species.
The big question is how?
We discovered that there are two types of nuclear DNA metamorphosis:
a.) the Exclusive Nuclear Metamorphosis, which governs epigenetic evolution; and
b.) the Mitochondrial-Dependent Nuclear Metamorphosis, which governs genetic evolution.
Firs of all, let us remember that the DNA is the skeletal structure or backbone of the DNA bundle. Usually, when people talk of the DNA, they are referring to the skeletal structure and the proteins that attach themselves to it. For us, that is not the DNA but the DNA bundle. There occurs other attachments to the DNA apart from the proteins, vis-a-vis biochemical structures like methyl that attach themselves to the proteins. These biochemical materials that attach themselves to the proteins alter the ways the genes express themselves, resulting in the emergence of a new class of traits—epigenetic traits.
Just as there are two types of traits, genetic and epigenetic, there are two types of biological evolution: genetic and epigenetic. Traits from these two types of evolution accumulate over evolutionary time to distinguish a set of organisms from their ancestors.
However, the two types of evolution do not occur the same way. For example, epigenetic evolution occurs when new biochemical structures attach themselves to the proteins, which themselves are attached to the nuclear DNA—which is the backbone structure. This process can take place in a lifetime such that the result is not only expressed in the organism, but also inheritable and expressed in the next offspring generation. This is because epigenetic evolution takes place exclusively within the coding part of the Nuclear DNA bundle in the nucleus. That is why we call it Exclusive Nuclear Metamorphosis—these changes occur exclusively inside the nucleus.
Genetic evolution is another story. Genetic evolution takes place when new protein chains are generated within the nuclear DNA bundle. And when it happens, a slight change in the protein sequence can result in a significant observable characteristic.
But unlike epigenetic evolution, genetic evolution does not occur within a generation. For example, monkeys have remained genetically the same for more than one million years and humans have remained genetically the same for more than 300, 000 years. Modern humans of African descents are not genetically different from humans who lived in Africa 300,000 years ago.
Genetic evolution begins in the mitochondria of female organisms and continues there for hundreds or even thousands of generations, with no result to show as an observable character or trait. Afterwards, it emerges as an expressed trait within one offspring generation down the line, within which the mitochondria communicates changes in the protein sequences to the nucleus. Therefore, we call it Mitochondria-Dependent Nuclear Metamorphosis.
In summary, unlike epigenetic evolution, genetic evolution occurs in two phases:
(a) the hidden phase (which lasts for hundreds or thousands of generations), and
(b) the emergent phase, in which the genetic trait becomes expressed.
The emergent phase takes place within one generation down the line. In other words, the hidden phase occurs over hundreds or thousands of generations in the female mitochondria. But the emergent phase occurs within one generation in the nucleus, with materials generated in the mitochondria and transported from the mitochondria to the nucleus.
This leads us to the second basic principle of evolution: Genetic evolution (changes within the protein chain itself) chiefly takes place in the mitochondria of female organisms for hundreds or thousands of generations, after which these changes are communicated to the coding part of the Nuclear DNA (the nuclear DNA bundle have both a coding part and a non-coding part); it does not take place exclusively in the coding part of the Nuclear DNA. In fact, only the emergent phase of genetic evolution takes place in the nucleus.
Genetic evolution, which leads to upgraded or novel protein chains, called genes, takes place over hundreds or thousands of generations hidden or unexpressed in organisms because they occur chiefly within the mitochondria of female organisms.
During the emergent phase, materials transported from the mitochondria are used to generate new exon (coding) layers that displace the old ones into intron (non-coding) layers within the protein chain in the nuclei of cells of the emerging organisms. These materials have been in the making over hundreds or thousands of generations—a timeline we call “the hidden phase”. This is why we refer to genetic evolution as Mitochondrial-Dependent Nuclear Metamorphosis.
And it explains a formerly unknown process of evolution; we call it “Evolutionary Replacement Via Sexual Reproductive Regeneration”—the process by which a new species “suddenly” emerged from an earlier one by sexual reproduction, after hundreds and thousands of generations of evolutionary development within the mitochondria—what we call the “hidden phase”. For instance, it explains how modern humans appeared “suddenly” from Neanderthal lineages across Europe and Asia ; and within 6000 years, they have completely replaced their Neanderthal parents.
The Second And Third Instructions of the Oral Torah
Jewish Law, called Halacha, emphasizes the importance of matrilineal descents. In fact, according to the Halacha, a Jew is one who is born by a Jewish mother. But we show in our other articles how such a definition is not a complete list of all possible definitions of a Jew.
One of the instruction of the Oral Torah is called the Kashrut. It is incorporated into the Written Torah by Moses [Read Leviticus chapter 11]. This principle explains the scientific basis of the Kashrut because it answers the question:“Why are there Kosher (dietary) Laws ?”
The third instruction of the Oral Torah is what we call Matrilineal Preservation. This principle guarantees the steady progress of evolution within the hidden phase by ensuring that all female offspring are kept within the community from one generation to another. Males are allowed to marry from outside the society, provided that the women being married into the society are virgins. But daughters are forbidden to marry from outside the community.
This is because the hidden phase of evolution progresses steadily along the matrilineal line, that is from mother to daughter. And a loss of a matrilineal lineage to the outside community must be considered a great waste of efforts and time. This is so because evolutionary developments in the hidden phase, which takes place exclusively within the mitochondria of female offspring, would be disrupted indefinitely, if violation of the DNA Unitarity principle kicks in. In other to ensure that this doesn’t happen, women are not allowed to marry anyone outside the community.
Jews are instructed to observe what is best described as the Matrilineal Preservation. The written Torah contains several verses that allude to this, and critics have used these verses to label Jews as racist for generations (Deuteronomy chapter 7 verse 3; Nehemiah chapter 13 verses 23 to 25) . Moses was only putting emphasis on an instruction that was originally part of the Oral Torah.
The importance of this instruction is now obvious: it was given to act as a guaranty or insurance against the loss of constructive evolutionary developments already achieved but hidden within female mitochondria.
Today, it is imperative that the non-orthodox factions of Judaism come to know this scientific fact and adjust their stance with respect to inter-marriage and conversion. The essence of Matrilineal Preservation is to preserve progresses made over so many generations that are hidden in the old matrilineal generations—the mitochondria remains chiefly maternally inherited.
The good news is that we can do so, while, at the same time, allow new matrilineal generations to start from ground zero by creating new Jewish societies, with individuals not only from Israeli populations without Jewish matrilineal history, but also with individuals from diverse Gentile populations who are ready to uphold the three instructions of the Oral Torah, and ready to dedicate their offspring to this cause. Learn more [here].
Matrilineal Preservation is one of the three doctrines of semitism and one of the three instructions of the Oral Torah.
This science was well understood by the aliens that interacted with the Sumerians and the Hebrews in the past. Therefore, we refer to our findings as a “rediscovery” rather than a “discovery”. And throughout human history, aliens have sought to communicate this information to humanity. This is because in order to evolve beyond the present human class of Homo sapiens, it is mandatory to put this science to work.
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