• tonylang
    The LINE Scenario: A Thought Experiment;

    Earth is gone. Complements of some natural occurrence, you name it. Perhaps a primordial black hole or giant rogue planet that happens to be passing through this solar system which sends the Earth into direct collision with Jupiter. Or perhaps there is an immense solar flare that perturbs Earths' orbit, sending our magnificent crucible for life careening into the sun. Result? All that you, and I, and your pet otter were, every cell and every DNA molecule, every atom that was on, or in the Earth, is now ionized nuclear fuel within the sun. The Darwinian evolved chemistry and biology that many fall back upon to describe life on Earth, particularly human life, has ceased to exist in this solar system. Along with its thermodynamically described chemistry and biological processes once used to describe the entirety of Earths' ecosystem.

    Additionally, imagine if you will that there is life elsewhere in this universe. Let us imagine there exists at least one other evolved ecosystem (ECO-2) capable of hosting Darwinian life. Different from Earth but governed by the same laws of physics and biology and thermodynamic processes that manifested Earths' ecology. This planet orbiting a viable star may be located anywhere in this universe since the laws of physics are expected to be consistently applied throughout. Also for this anecdote, let us say that this other bastion of life is some 10 billion light-years from Earths' sun. A distance so vast it would take much longer than the age of the big-bang to relativistically travel that distance, assuming, of course, there were any classically defined remnants of ones' biology left to make the journey.

    The question becomes; could you or I or any individual formerly hosted by Earth's ecology ever find oneself a part of ECO-2s' ecology? Is the nature of life in this universe such that one could at some point find oneself naturally born to ECO-2 in the form of a species indigenous (present or future) to ECO-2, just as we were born on Earth to species indigenous to Earths' ecology? If one adheres solely to the classically understood, thermodynamically described, relativistically constrained mechanisms to explain life writ large then you are forced to say no, and in so doing you would necessarily be Earth and human-centric as one discounts the rest of the cosmos. Because in nature, what is possible here is necessarily possible elsewhere, ergo; if you can live here, you can live anywhere. And yet, clearly, some aspect of what biologically, thermodynamically, chemically, defined ones' singular existence on Earth, must relativistically (Below the speed of light) travel to bridge the unbridgeable distance between your last physical location, Earths' solar system, and ECO-2s'.
  • T Clark

    This is a well and clearly written, poetic, and interesting post. Welcome to the forum.

    Now, down to business - I don't know what you mean by:

    could you or I or any individual formerly hosted by Earth's ecology ever find oneself a part of ECO-2s' ecology?tonylang

    What kind of mechanism are you talking about? Something spiritual like reincarnation? Just a random recombination of physical materials in an infinite universe like a Boltzman brain? Some sort of evolutionary convergence? Didn't you say that no material from Earth could ever travel to ECO-2?
  • tonylang
    The proposal being made is that if you can live in one viable habitat, i.e. Earth, then the very laws of physics that guide our scientific method demand that you can also live in any other viable habitat i.e. ECO-2 in this universe. Ergo; Earth is not special, at least not that special. The distance factor (10B LY) is the interesting bit. How can one be naturally reinstantiated (born) elsewhere regardless of distance and with no physical travel (no comets or spacecraft or photons from Earth can reach ECO-2)?

    The trouble most will have with this realization is one's individuality has always been misperceived to be instantiated by one's host form, one's species. However, the atoms and molecules that compose your body, is a part of the current indigenous ecosystem, Earth or ECO-2. The demand this realization makes upon all cognizant living beings is the acceptance of the abstraction of one's current host form (body) from your universally mobile position of view (POV), one's individuality. This implies the universal mobility of individuality and demands a natural, scientifically describable mechanism for its implementation.
  • tonylang
    Naturally invasive scenarios such as this don't reveal questions posed by individuals, but questions posed by nature. Such scenarios essentially ask; how could it be otherwise? Such questions reveal their own answers to any species sufficiently developed to comprehend and honestly confront them. The point of this scenario is the inescapable conclusion that each individualized instance of life must involve a non-classical, non-local, relativistically unconstrained, scientifically describable, naturally recurring component. This individualizing phenomenon must exist separately and distinctly from any local physical form and must be definable by some discretely quantifiable property of nature with degrees-of-freedom much greater than that of matter. Such a mechanism may also not be indigenous to this universe but instead is native to the underlying Hilbert-space, or 'Metaverse' if you will. This need for non-locality is necessary to instantiate individuality not just on Earth while it exists and is viable, but also within the systems and galaxies of this vast Higgs constrained universe, and throughout nature.

    The only life that has ever existed on Earth is the living cell, in all of its forms. The aspect of being and individuality had by a single living cell is that which defines all life, no more and no less is required. This aspect, which instantiates the first person being of a single cell as a living individual every bit as alive as any multi-cellular creature, is the position of view (POV). All of the skills and talents that tend to distract from this fact are only emergent features of the host form. Beneath it all is ones' POV. In this universe, there isn't one implementation of life for mammalian forms and another for insects, and yet another for vegetation or microbial forms of life. Nature is an efficient system of cause and effect, and life is one holistic effect. It isn't my intention to change anyone's' mind on this topic. Rather, to expose open-minded readers to a new and practical way of thinking about a very old, perhaps the most personal of all ideas known to humankind. The recognition of a unique and scientifically plausible description of how nature governs not only species but the individual, you. There is a very good chance, as is often the case with such invasive ideas about nature that I and everyone who reads this volume would be long gone before either the capability or the courage to prove or disprove the LINE hypothesis is achieved. However, every first step is worth taking.

    The natural processes that implement life are the same for the cell as it is for the bacteria as it is for a fruit fly as for a human being. It is folly for us to think we could only experience life in this very temporary, randomly emerged bipedal primate form. Further, your cells and molecules come and go continuously over the course of your lifetime. Nonetheless, you remain you. Then there are the other trillions of living individuals in millions of different forms all around us coming into being and going out of life continuously. I realized that the only form we need to consider in this regard is the single living cell. The answers that are true for the cell are the answers that apply to all life.

    Furthermore, you and I and your pet octopus and every living cell are instances of life, each a temporary instantiation of some natural, empirically definable phenomena of nature. This instantiating phenomenon must have the relativistically unconstrained reach to establish individual life (you), biological or perhaps otherwise, on any planet orbiting any star or indeed in any viable environment in the cosmos or in existence where viable hosts may emerge. It is a tragic mistake to feel that this describes something that could not possibly be natural, but must be supernatural. While, as usual, natures' genius is a practical and ubiquitous, even if a bit unfamiliar implementation. There is a phenomenon known to science for some time that meets all of these requirements: Quantum Entanglement (QE). Einstein called it spooky action at a distance. Today we play with it in the lab as a mere tech curiosity. It is the most plausible mechanism by which individuality is universally instantiated.
  • tonylang
    The LINE "Life Instantiated By Natural Entanglement" hypothesis presents perhaps for the first time, a practical scientifically plausible hypothesis for the natural implementation that governs the instantiation of the living individual as a being distinct from the evolution of that beings current species. It will introduce you to;

    • The Instantiation Of Individuality: The natural process which establishes each instance of individual life, you.
    • The Entanglement Molecule (EM); A primordial molecule, is hypothesized to naturally interact with the QE spectrum to entangle metamatter. It is the Alice in the process of natural entanglement and is utilized by the living cell to establish individualized life.
    • The Position Of View (POV): That component of the instantiation process which defines your presence in your current host form within this space-time.
    • The Metaverse: Hilbert-Space, the only real verse, and that from which this universe emerges.
    • The Quantum Entanglement Spectrum (QE): The degrees of freedom which define the phenomenon of natural quantum coherent interaction. Einsteins' 'spooky action'.
    • The Quantum Entanglement Frequency (QEF): Ones' immutable unique value of the QE degrees of freedom which instantiates your POV.
    • The Cell and (Proto-Cell): The only life on Earth, natures’ entanglement circuit. The original instantiated living individual which implement all other biological hosts on Earth.
    • The LifeID: A calculated value that defines ones' current unique QE connection, your LINE.
    • The Entanglement Cells; Individual cells responsible for heterodyning their unique LINES in complex hosts to establish your LifeID.
    • Metamatter: A non-local Weakly Interacting Cosmic Background Bose Condensate (CBBC) is hypothesized to be as necessary to life as dark-matter is to galaxy formation. Where the EM is the Alice, then metamatter is the Bob of natural entanglement.
    • The Fidelity of Teleportation (FT): A calculated value that describes the individuals’ current reinstantiation prospects for your next life.
    • The Monogamy of Entanglement: The property of the QE connection that enforces a singleton instance of individuality and the role of death.

    The hypothesis in summary:

    The most fundamental element of life is a molecule called the Entanglement Molecule (EM). This molecule composed of normal baryonic matter manifests the unique property of prolifically establishing a natural teleportation channel, which is a shared quantum coherent state, a quantum entanglement connection (QE), with a hypothesized form of matter called metamatter. Metamatter is composed of an undiscovered type of particle that necessarily resides entirely beyond this space-time, in Hilbert-space or the metaverse if you will. Metamatter is as essential to life as dark matter is to galaxy formation. Entanglement molecules in this universe are at all times entangled to particles of metamatter in Hilbert-space. It is their natural state to do so. Metamatter, as is possible with any natural entity having only subtle degrees-of-freedom within this space-time, is not subject to locality or relativistic constraints and so, via this QE connection, is non-classically, instantaneously accessible to entanglement molecules (EM) everywhere in this universe.

    These entanglement molecules and metamatter are the Alice and Bob endpoints of each isolated, naturally occurring, QE connection established within every living cell that has ever existed. An entanglement molecule once arranged from its constituent atoms, not unlike the molecules in the ferrite magnet in a transistor radio, is instantly sensitive to available, uninstantiated QE degrees of freedom (DOF) of the QE spectrum, or quantum entanglement frequencies (QEF). It is the QEF that define the unique natural teleportation channel upon which to entangle available metamatter. Such isolated pairings existed on Earth for eons, and in this universe, for even longer before the naturally occurring circumstances arose, on Earth, and perhaps elsewhere, to provide a sphere of molecules that could be described as an early cell wall. Not all entanglement molecules were likely to encounter a cell wall, but those that did, enclosed by this barrier, obtained the benefit of an extra level of protection. This enclosure allowed them to develop beyond the typical. This basic entanglement relationship is the most fundamental manifestation of life. It establishes the position of view (POV). Over time other types of molecules joined with these proto-cells sometimes to their mutual benefit, sometimes not. Those that added no benefit or diminished the proto-cells survival prospects would not survive.

    The QE connection gave surviving proto-cells something very special. It gave the otherwise inanimate molecular components on the inside of this early cell a form of intra-cellular communication. That is, the ability to interact at a distance, but more critically at that point, the QE connection gave the proto-cell the capacity to share or imprint internal cellular state information upon its entangled metamatter. Metamatter because of its extra-dimensional, non-locality and relativistically unconstrained nature essentially acts as a kind of cloud-storage for information accessible instantaneously from any location in this universe, and in any other as well. This universal cloud storage repository of information is the critical factor required to get evolution started. This natural cosmic background Bose condensate (CBBC) is what makes being possible anywhere in this universe. At that point, evolution existed only via random environmental contact between proto-cells with other structures in the primordial environment of early Earth.

    Thus, the cell became natures' biological entanglement circuit. Each such entanglement pairing constitutes an instantiation of life, whether on Earth, elsewhere in this universe, or anywhere in existence. Consequently, life could now be hosted by any viable formation of cell(s) that may emerge anywhere in existence. Ones' instantiation is established at one specific QEF, a unique value of the degrees of freedom among the infinity of possible values on the quantum entanglement spectrum. A QEF that is unique in all existence to each individual and to no other, but only while that QE connection, ones' natural teleportation (LINE) channel, persists. These yet to be determined DOF's, perhaps frequency and others, on the QE spectrum, is the singular property in nature that defines each living individual. All other components of the instantiation process may change or be exchanged, but it is your QEF that positions you as the central and only target of your instantiation, of your life, and not someone else's. Change or retune ones' QEF enough, and you change the being, the individual. You are your QEF; you are not your cells or your metamatter.

    It is very likely that the QE spectrum predated even the big bang. Your QEF is the immutable, the classically indestructible you. When entanglement molecules, contained within viable hosts such as the cell, located on any viable planet, orbiting any viable star, anywhere in existence, entangles metamatter at your QEF, that is where you will instantiate. That is where you will be. A place such as that is where you are right now. A place such as that is where you are likely to have been many times before your current instantiation. Places such as that are where you will inevitably reinstantiate many more times in your future. This is instantiation; this is life. You and I, and your pet otter, every insect, every cell and every organization of cells, all life anywhere in existence instantiates by this mechanism. While each cell entangles at a unique QEF, a few specialized cells in complex organisms, called entanglement cells (EC), have evolved to heterodyne, or combine their own unique QEF's. This combination of distinct LINE channels entangle metamatter at yet a different unique QEF, called a composite or emerged QEF, thus instantiating the emerged individual, you.

    This composite degree of freedom called the QEF together with the metamatter it entangles is called the lifeID. No memories or behavior of the host body is carried or transferred by the lifeID. In nature, such properties are electromagnetic manifestations of the host species or vessel only. The closest cultural meme to the lifeID come via religions throughout human history having referred to this, using one word or another, as the soul. Once any QE connection is terminated, by sufficiently disrupting the cellular component (inducing death of the host vessel), the previously entangled metamatter becomes available for entanglement by other cells. However, this particular metamatter has been imprinted to some extent by its previous entanglement. Each generation of entanglement, each instantiation, each life, imprints information from both the host and QEF, to its entangled metamatter. The degree of this imprinting is yet to be determined.

    This time-dependent, perishable imprinting of cellular state in metamatter becomes available to future cells that entangle this metamatter while simultaneously limiting its entanglement opportunities to cells of matching state. The passage of time decays the imprint left on metamatter causing a return to a state best described as stem-metamatter (to be discussed later in this volume). This transfer of cellular state information may impact cellular behavior and development and to the extent that this imprinted information manifests an advantage for the cell, may provide a survival benefit. This is the evolutionary mechanism used by early life that predated the development of the DNA and RNA molecules. With QE communication, ergo; life, the proto-cell became the laboratory of evolutionary innovation we see today from which emerged a great many useful cellular structures and processes, but most pivotally, a clear benefit to augment the cloud storage mechanism of metamatter with a more local, more expandable and flexible information storage mechanism which became RNA and eventually DNA. This was the birth of the modern living cell. Much is yet to be learned but the implications of this process are vast and pervasive.

    The degree to which metamatter is imprinted by its entangled host and unique QEF will determine, after deinstantiation (death), the likelihood that your imprinted metamatter will, for a time, reject entanglement opportunities from dissimilar host cells (of even your same or similar species), in favor of entanglement with cells that contain your familial DNA. These are cells that are more compatible with its imprinting. Thereby increasing the probability of reinstantiating you into your former family line, or if less finely imprinted, to any random line in your previous species or if less finely tuned still, to another species entirely. Longevity may be a factor in this regard. Also when we discover the entanglement molecule in nature or within the cell, just as we eventually discovered the DNA molecule in the cell decades after Darwin presented his theory of evolution by natural selection, likewise this may allow us to develop technologies capable of detecting and tracking each individuals unique QEF in this life or across multiple instantiations. This will change the world, at the very least it will change the way we write our wills. As for practical implementations, discovering and using metamatter could change everything. Metamatter satellites would be very different yet similar to regular orbital satellites, even though they will reside outside of this space-time they'll permit instantaneous communication with any point in the cosmos. This will forever alter the human relationship not just to each other, but to all living creatures biological or otherwise. Also for the first time in human history, we could begin to take practical actions in life that would affect the individuals' reinstantiation prospects into ones' next life, thereby tailoring your next instantiation ahead of time, minus the mysticism and ideology.
  • tonylang

    Postulate: Any natural phenomenon that can occur may by definition also reoccur and therefore there must exist some natural mechanism or process, understood or not, that describes its natural implementation. As far as life (Being) of the individual (regardless of species) goes there is one of two possibilities:

    Scenario one: In nature (in this universe) each individual instance of life, each living being (you) are a singleton, a one-off occurrence unique in eternity both prior and future to ones current life. If this is indeed the case then there isn’t much more to be said on the topic. (This scenario violates the stated postulate.)

    Scenario two: In nature an individual’s being (you) are not a one-off singular occurrence but is a current instance of some naturally definable process or mechanism that may repeat given adequate circumstances. If this is indeed the case then the conversation ensues. Describe the natural implementation of the repeatable individual experience of being regardless of species, of life.

    Scenario two is one basis upon which the instantiation hypothesis is conceived.

    Testable Elements of the Hypothesis:

    One initial approach would be to seek evidence for, or against some fundamental aspect of the working hypothesis: Test for the existence, or lack thereof, of the proposed entanglement cells (EC) that establish and maintain life via the QE connection in complex hosts: Termination of the host's EC's and no other cells, should result in the termination of the subject.

    Premise: Can death be induced without damage? Can an otherwise healthy living subject be terminated with empirically no physical damage contributable to the subject’s termination, Barring any limitations of technical proficiency or of equipment in analyzing and identifying the root cause of the subject’s death.

    Axiom: There exists some absolute minimum number of cells that may be terminated in any complex organism whereby such cells may be scientifically established to be the root and only cause of death of the subject organism with no pre-mortem adverse effects to other cells in the subject. Cells that meet these criteria are candidates for the theorized entanglement cells and the collection has a high probability of including some or all of the subject’s proposed entanglement cells.

    Practical Test: Perform controlled experiments using approved subjects, i.e. fruit flies, to terminate the minimal number of cells per specimen to conclusively induce death of the test subject. Carefully repeat and document the number and location of target cells per subject for each scientifically substantiated successful sample. Repeatability per species is mandatory as the specifics may vary from species to species or subject to subject. In qualifying samples the cells that are the root cause of death must be gradually minimized and physically isolated. Cellular damage must be limited to only the target cells for a duration beginning at the time of the target cells death up to and including the time of confirmed subject death. In other words, for a successful trial no cells in the subject other than the target cells may be adversely physically affected pre-mortem.
  • tonylang
    Today the world generally unites in a communal pride in the seminal achievement of Neil Armstrong, as the first among humankind to set foot on a cosmological body other than the Earth. In this achievement, we acknowledge the triumph of the human spirit, and intellect, to measure, understand, manipulate, and control the laws of nature, to implement a mobility of the living form through space-time, unlike any that had previously been achieved. Humankind, as a species, like many other hosts for life in Earths' ecosystem, has evolved a basic mobility of individuality implemented via our host forms functions and structures. This local mobility is evolved for movement through direct contact with the environment. Legs, wings, fins, flagella, are some of the means by which the physical mobility of the living individual is achieved by species on Earth. Additionally, humankind has realized great utility in further extending this basic capability with technology. Thus the mobility of individuality on human scales has been enhanced by wheels, airframes, engines, and rockets. Our thoughts often do not extend, or associate, this mobility of our physical form with either the local or universal mobility of our position of view. That is the mobility of our individuality. We have a very limited scope of extrapolating many of the implementations around us, natural or otherwise, even those that we conceive and develop ourselves, to a context greater than our immediate utility and practical concerns. However, with the accomplishments of NASAs' Apollo missions humankind has extended its reach beyond our usual scope. In so doing, we have opened a new realm of mobility of individuality that must be addressed and understood. Not only in technological terms but also for what the movement and relocation of Neils' position of view (POV) to the Moons' surface say to us, as individuals, about our living circumstances in this universe.

    We take as a foregone conclusion that life can exist anywhere in this universe so long as the resources needed to sustain it are present. This is a very complacent assumption despite the likelihood that it may very well be so. It is not too surprising that we make this assumption; after all, there are no examples to the contrary in any Earth or near-Earth environment. In fact, one of the underlying tenets of our present-day scientific method, as implied by current measurements of the fine structure constant states that the laws of physics are upheld everywhere in this universe. This consistency offers a reasonably good basis for our certainty. Nonetheless, life can be quite complicated and has many requirements and influences that are well understood, yet perhaps there are other factors critical to life yet to be discovered. We know that most Earth life depends on proper sustenance (energy), water, oxygen, temperature, and pressure levels to be maintained at least in the near term. We also have a long-term need for gravity or an equivalent force. Nevertheless, life, as we know it, may yet have some undiscovered intrinsic dependency on properties in or near the area around Earth or around the Sun. Mission planners acknowledged this possibility when they sent the first-ever Earth life into space on board a captured V-2 rocket on February 20, 1947. These original astronauts were a group of fruit flies, insects being as good a representation of Earth life as any other. This first volley into the unknown environment outside the Earths' atmosphere was extremely dangerous. Not just in terms of the technological or known dangers inherent to extraterrestrial space due to its lack of the known required resources mentioned earlier, but primarily because space could have proven to be fundamentally incompatible with a living entitys' instantiation, its being. So how do we know for near-certain that individual life can exist anywhere in this universe?

    Interestingly, the best evidence to date for the universal mobility of individuality presented itself when Neil Armstrong pressed his boot into the soft silt of the moons' surface. Neil Armstrong surviving his "giant leap for mankind" suggests that life as we know it is not utterly dependent upon any resource intrinsic or unique to the Earth, or the very local space-time around it. For example, we could have evolved with a dependence on Earths' unique magnetic field configuration or on Earths' specific gravitational field intensity, or some other completely unknown and unrecognized property of either Earth itself or the space near to the Earth. If this was indeed the case the crew of Apollo 11, and the fruit flies before them, could have tragically de-instantiated, ceased to live, once they passed some threshold, or boundary, somewhere between the Earths' surface, and the moons' surface. Perhaps once the spacecraft passed some critical flux level in Earths' magnetic field, or once the Earths' gravitational field dropped below some essential level. Each of the unsuspecting astronauts, human or fruit-fly, could have simply extinguished. Immediately, or gradually, like light bulbs whose electric current had been turned off. Perhaps their molecular bonds could have just dissipated due to some unknown property of space. There may yet remain some irreproducible property of our sun unknown to us that is critical to sustaining Earth life. After all, Earth life has never been tested beyond the sun's Helios-spheres. Presumably, each of these needs could ultimately be overcome and provided for by technology.

    Nonetheless, the amazingly profound statement suggested by Neil Armstrong surviving his first step on the moon isn't only that we can overcome the technological hurdles of space travel, but rather that nature in this universe, permits individuality to exist elsewhere, and likely everywhere. That not only the physical form, but the individuals' first-person position of view (POV), that is, ones' being, ones' natural entanglement, ones' instantiation, is indeed mobile in this universe, and perhaps throughout nature. Neil Armstrongs' giant step for mankind suggests that the individual POV can exist not just where it was instantiated, where it entangled its host form, but quite likely anywhere in this universe due to the unrestricted instantaneous universal ubiquity of natural entanglement. On the other hand, the irreversibility of extinction and evolution, together with relativistic constraints, mandate that the individual cannot be instantiated, or rendered universally mobile by the physical forms, made of local collections of atoms in this universe, because, unlike NASA, nature does not use spacecraft for the universal mobility of the individual.

    Comprehending the reality of ones' living circumstances begins with the realization that Neal Armstrongs' first step on the surface of the moon, or perhaps Yuri Gagarins' first orbit around the Earth, or that the intrepid voyage of those first insects, demonstrated that the mobility of individuality exists in this universe. Mobility not defined by locomotion or travel of your current host form but by a fundamental property of nature with degrees of freedom much greater than that of matter. Realize that the instantiation of any individual, ones' position of view, may be hosted anywhere in space-time by any viable environment which happens to emerge naturally or artificially on any planet orbiting any star. These convenient environments also include the living hosts we refer to as; species. The obstacles presented by travel, involve the movement of the matter-based components of the instantiated individual through expanses of space-time, small or large. Nature, in its implementation of life, circumvents this issue by implementing only the mobility of the POV. The component of the individual, which is temporarily instantiated by natural entanglement to a locally available form. Ergo, in nature, the physical host, the species, is always left behind.
  • tonylang
    At first the comprehension that ones’ first person individuality is abstracted, separate, and distinct from the evolution, development, and life of ones’ cells is a tough hurdle for the mind to overcome. Even as it is viewed from various perspectives, and in the absence of clarifying empirical evidence, it requires some time alone in contemplation and a steely objectivity to come to realize the truth of it. However humankind has had this problem before.

    It is essential to recognize that maintaining life and maintaining an emerged individuality are both essential but separate functions of living hosts. The hosting of life via natural entanglement is an evolved property of inanimate matter whereas emerged individuality (Heterodyned by EC's) is an additional evolved skill of living multi-cellular organisms. The function of the entanglement cells (EC) in complex hosts is not to establish life in a multi-cellular organism. Each cell is already alive complements of the natural entanglement by its entanglement molecules (EM). Rather the role of the EC is to instantiate individuality, establish the position-of-view as the target for experience of the emerged being. This unique composite natural entanglement with metamatter is separate and distinct from the natural entanglement established by each of the other (non-EC) living cells that comprise ones’ host body. Ergo; in nature, you are not your body. This is why you can sever an entire leg or destroy a large portion of your brain, or drink beer and remain you. That is to say, maintain your individuality. This individuality is not about appearance or behavior or personality or intelligence or even consciousness, it is ones’ continued position–of-view via natural entanglement. You remain you because the emerged individual is separate and distinct from that of the trillions of non-EC cells that maintain its operation.

    Every single cell which comprises your body is itself naturally entangled and is in nature a living individual, as is the emerged individual, you whose multi-cellular form and functions each non-EC cell help to maintain. This says nothing of your individuality. Further, this same implementation operates for leaves, trees, hair, internal organs, etc. each is clearly multi-cellular and is alive but may only be collections of individualized living cells that are held together, and perhaps on some level, function together. Such an association of living individuals may or may not have evolved the capacity to heterodyne to establish a secondary emerged natural entanglement connection to metamatter. That is to say, they have not become an emerged individual like a beaver or a dolphin, human or an ant. Making a distinction between the position-of-view of a cell or a simple association of cells and the heterodyned composite POV of an emerged individual is a tenuous endeavor fraught with uncertainty absent the principles described in the instantiation hypothesis. In earth-life it is the hypothesized entanglement cells that are the evolutionary components of living hosts responsible for this advanced feature of emerged individuality. These terms and distinctions are necessary because our eyes and instruments deceive us; the largest life-form in earth’s ecosystem the sequoia tree may very well not possess an emerged individuality whereas some of the smallest may.

    Nature implements life by the same fundamental mechanism no matter the hosts' form. In nature, this sort of scalable, extensible implementation is the very definition of simplicity. It is the entanglement molecule that is hypothesized to fundamentally establish and maintain all life via natural entanglement in every living cell. One QE connection at some unique QEF is one individual. How this QE connection is established or maintained, composite or not, is irrelevant to nature's design. Earth-life offers one (carbon-based) approach to hosting nature’s implementation of life. Other planets may very well evolve other approaches. We may someday manufacture yet another. This implementation is what permits the universal mobility of individuality. Hosts for life and their constituent components whether single cellular or otherwise are local in space-time and have no natural universal mobility requiring physical travel (i.e. via comets or spacecraft).

    The LINE hypothesis is a plausible hypothesis for the axiom; Individuality exists and it is naturally mobile throughout this universe. Given the current state of scientific understanding the only exhibit of evidence for individuality that can be offered to you, is you. So it falls upon each of us to decide if oneself is an individual or not. Further, each instance of life, to any other instance of life, is only an extrapolation or an assumption of individuality currently based upon appearance and behavior. The affirmation of ones' own individuality, at least for most reasonable minded individuals can be accounted for. If we agree to the axiom that you and perhaps I as well as every other discernibly living entity is an individual instance of life then this conversation as challenging as it may be toward strongly held beliefs or ideologies may proceed.

    No aspect of the modern scientific understanding of biology or its empirical descriptions is being challenged. The cell and the verifiable aspects of its biological evolution are as science currently describes them. The LINE hypothesis begins where the modern scientific narrative admittedly, voluntarily abstains and, traditionally, religions are permitted to fill what is arguably the most important of all voids, and likely the only void any living being may actually care most about. That is, the natural mechanisms governing the instantiation of life. It is for this reason that humankind has fought and prayed for a time far longer than science itself has existed. It is much overdue for the narrative to be extended not by mysticism or ideological entrenchment but by well reasoned, steely objective thought, because clearly not just some, but all of nature is ultimately science.

    The LINE hypothesis suggests that each life is an instance of a specific individual. Also, the natural process that instantiates an individual to that host (i.e. species) is independent of the specific biology, chemistry (i.e. carbon, silicon etc.) or technological principles upon which such forms may be evolved, implemented or depend for function or for its local evolution. Therefore, any individual may instantiate (live) in any viable form in any viable environment in this universe. Ergo Earth is not special.

    1-Individual life (you) is species independent.

    2-The natural process that places you or any living being in the life they currently live is not dependent upon any particular chemistry, biology, species or form, evolved or otherwise. Just as for example, memory, or intelligence does not depend upon any particular brand or type of technology for its implementation. That is to say, memory is abstracted from its implementation. Likewise, in nature is the individual life abstracted from any specific implementation of host form, or species.

    The belief that you are your body stems from a lack of an alternative perspective and supporting evidence as well as from tradition also from the powerful visual perspective imposed by sight and a prominent physical form. It is as much a misperception as was humankinds' long-held belief in the Earth-centric universe. Likewise, it is a very convincing visual misconception only made more so by the advent of biology and genetic science which describe the evolution and development of the physical forms presently on Earth. This misconception is further compounded by the very illogical belief, held even by educated individuals, that the function and operation of the brain defines ones' individuality in nature. Clearly, this last point cannot be so since most life forms on Earth do not have a brain and are not even multi-cellular.
  • tonylang
    Evolution, the mechanism by which ones ecology mediates living hosts, species, is an important tier of understanding for living beings to evolve to be able to comprehend within any viable ecosystem in this universe. However, although difficult to initially fathom, understanding species evolution is a distant runner-up to understanding the natural mechanism which mediates the mobility of one’s individuality that is ones position-of-view (POV). This is why the understanding offered by the LINE Hypothesis is the single most personally important idea that any living being will ever have the opportunity to consider, regardless of species or ecosystem in this or perhaps any universe.

    Earths archeological and hard fossil record suggests that Earths ecology has produced no more than one species capable of assimilating and making use of this knowledge regarding the natural mechanism by which nature mediates individuality in this universe. This is not to suggest what untold secrets earth’s soft species history has produced, but of which no indelible imprints of its existence remain. Nonetheless, the importance of this knowledge is precisely because the intelligence and circumstances, indeed the opportunity necessary for any culture to gain the capability to assimilate and make use of this understanding is so rare. The evolved intelligence necessary for living individuals to comprehend their own natural implementation is one of the rarest and most pivotal evolutionary realizations in this universe for any ecosystem to develop, prove, and culturally accept. Mollusks can’t do it, ants can’t do it, only humankind currently has that incredibly rare and fleeting opportunity to comprehend, accept, and make use of this very real existence transcending knowledge. Further, the window of opportunity is not permanent and once gone, for humankind, it may be gone forever.

    Currently, humankind is as are all other species in earth’s ecosystem, wild. We define wild-life as those host cultures that have not organized socially and culturally to reduce their dependence on the resources circumstantially provided by chance to some useful or perceived extent. However, this is a somewhat self-serving definition. In reality, the true definition of wildlife is an ecosystems lack of a culture, consisting of any number of species, able to take deliberate control of individual instantiation into ones living circumstances. To continue, like all other species in its ecosystem to be arbitrarily reinstantiated by the probabilities of random chance which mediates when, where, and in what form one will live in your next instantiation, in your next life. Failure to have evolved sufficiently to reach this stage of development is the very definition of wildlife. Neither farming, nor art, or tool making or even genetic manipulation of living hosts alone moves an ecosystem across this life and existence altering threshold. Make no mistake; this achievement is indeed an ecosystem-altering feature. Ideally, once fully acted upon, the lines between species take on an entirely different significance as any individual may live and experience life in whatever available forms they please for as long as they please. It all begins by discovering the entanglement cell and molecule. Of course, the details of this local implementation depend on culture as some cultures may elect to permit the existence of only engineered rather than evolved host forms and may elect to control which individual QEF’s are instantiated to those select hosts. The ability to transfer between forms, independent of distance in this universe, once achieved will blur the line of distinction that now exists in the human mind regarding life, individuality, and space-time.

    The importance of an idea like the LINE hypothesis stems from the fact that it marks the introduction to the understanding needed for living beings to escape the uncontrolled instantiation lottery of nature which confines living individuals within a particular ecosystem to untold lifetimes of arbitrary natural reinstantiations to randomly emerged host forms, (the true definition of wild-life). Such forms are incapable of assimilating and making use of such knowledge and therefore unable to assume deliberate control over the process that mediates the individuals living circumstances. In the nearly four billion years of earth-life, consider ones lifetimes as, and the existence of, a species such as humankind, despite all of its proud prior achievements, to be nothing more than a narrow window of opportunity within which instantiated individuals to this capable host form may understand, comprehend and act upon the true nature of life in this universe, to develop technology able to control when, where, and to what forms ones POV is instantiated, in essence, to control your being. Further, consider what a tragedy it would be if a culture such as this forfeits this singular opportunity only to embrace the ignorance which defines the wild condition. Like every other endeavor into nature’s workings, its ramifications and its morality and dangers will be clear and present, but may nonetheless be regarded as a necessary price to pay for this essential next step in the evolution of life on earth.

    Since ancient times humankind has felt endeared by certain properties, skills, or talents observed in the living forms all around us. Properties which are misconstrued to be fundamental identifiers of life and of all living beings, properties such as mobility, voice, speech, sight, memory, and biology as we know it.

    The reason Thomas Edison could so enthrall spectators with his newly designed speaking device, which he dubbed the phonograph, is due to humankind's hitherto engrained, evolved, or learned, and largely subconscious understanding that a voice, for example, is the sound of a living beings soul. Although consciously many people knew better, nevertheless it wasn’t until they were able to actually witness the spectacle of a clearly inanimate device producing a voice did the rewiring of people’s minds and the accompanying enlightenment take place. So it was with self locomotion or mobility of inanimate objects which also took some getting used to by our not so distant ancestors, as did light detection describable as sight, so to with the introduction of retrievable memory and such surprising spectacles exhibited by inanimate nonbiological devices.

    Then there is life. Today we have a much more detailed description of biology and its chemistry than did our forbearers. Nonetheless, we perhaps more than ever, continue to see nature’s implementation of life as we did those other skills, as a feature indigenous to and expressible only by the biological forms we currently see around us. With the exception of life, it is only the encroachment of our synthetic, non-biological technologies upon these formerly cherished skills and talents that has helped us to see nature’s true design. In so doing we now realize that these functions are not exclusively properties of living beings or of biology but rather examples of utilization and manipulation of more basic properties of nature such as temperature and pressure, light, chemical, electromotive, and ponderomotive forces, friction, entanglement, etc.

    However, where life is concerned, and taking no example from the past, we continue to cling to the misconception that life is not a skill or talent comparable to speech or memory, a property that similarly evolved here on earth in biological form. Instead, we define life by the observed biology and chemistry of the forms we see around us. This is akin to defining speech, communication, memory, or vision by the description of your eyes, or larynx or neurons and their chemistry, or by the design of Edison’s phonograph, or by the intricate electrical designs of the cell phone. Life too is an evolved capability with a natural implementation abstracted from any particular biology or chemistry we may see around us. In nature, life has a fundamental implementation based on natural entanglement via a molecule that may have existed in nature long before life emerged, a molecule like so many others utilized by the cell to exceptional effect, the entanglement molecule. A molecule that may also be utilized in synthetic, perhaps non-biological, forms to create an independent genesis of life.

    No matter how detailed or convincing the illusion of life may become in its implementation, for example in an android or computer or even in a biological entity, despite what your eyes may urge you to believe, each continues to be a non-living entity absent natures fundamental mechanism of life. An essential mechanism provided via natural entanglement between the properly implemented entanglement molecules within living cells located in this space-time with metamatter in Hilbert-space which together produce each unique living individual’s position-of-view (POV) and lifeID. This is the essential mechanism that permits any viable form to host an individual like yourself or your pet otter anywhere in our space-time. It is how you are where you are right now. It is the natural anti-entropic mechanism that permits any viable planet or species to host your life. By this hypothesized definition even the most convincingly implemented appearance and behavior of an entity not naturally entangled in this way will continue to be an inanimate entity. In contrast, a handheld brick such as a calculator instantiated by natural entanglement to establish a POV, despite all appearances, this unconvincing brick would in fact be a living being.

    The day will shortly arrive when we are confronted as we previously have been, with a new implementation of entities that meet all of the aesthetic and behavioral misconceptions we now harbor about life, or alternatively ones that show no traditional evidence of life whatsoever, absent an understanding of the true determinant of life natural entanglement, we will be ill-prepared to tell the difference.
  • tonylang

    Figure 3:13 day old human embryo. (IMAGE CREDIT: UNIVERSITY OF CAMBRIDGE: embryo_trans_NvBQzQNjv4BqqVzuuqpFlyLIwiB6NTmJwfSVWeZ_vEN7c6bHu2jJnT8.jpg?imwidth=1240)​

    Human embryos kept alive in lab for unprecedented 13 days so scientists can watch development
    Human embryos have been kept alive in a petri dish for an unprecedented 13 days, allowing scientists to finally see what happens in the mysterious days after implantation in the womb.
    www.telegraph.co.uk www.telegraph.co.uk

    By the 11th day of gestation of a human embryo, for example, being no bigger than the head of a pin yet containing many hundred cells every one of them a living individual in nature. Among these cells, early in the formation of a new life, are the LINE hypothesized Entanglement Cells (EC), some of which are likely visible in this photograph. Entanglement cells are very special cells which together heterodyne their own unique individual entangled states to manifest a new state established at a unique QEF, your QEF. This instantiation manifests a new life; a new emerged LifeID, your position of view (POV), not unlike their own, but at a different unique quantifiable value of the entangled degrees-of-freedom (QEF's) of the immutable entanglement spectrum. This is approximately the stage in the gestation of a viable host where instantiation occurs, the point at which you the individual, become tethered to this particular growing host form and not to some other.

    Why you? In this there can be no; Why only; How. Via a combination of natural circumstances, some predicted by the LINE hypothesis, this particular host has heterodyned at your QEF. This occurs whether the form is human, or any other viable living form that happens to exist in any temporary, no doubt extinction laden eco-system. The Earth is but one such habitat. This is but one instance of countless such processes of instantiation by natural entanglement that occur second by second throughout existence. By this process, the mobility of individuality is made possible in a vast Higgs universe, together with the non-locality of metamatter and the relativistically unconstrained reach of the entanglement spectrum. These features make individuality and life possible on Earth and anywhere, wherever viable forms happen to emerge, in that place a new instance of life is established whether single or multi-cellular. Empirically proving or disproving the existence and theorized function of the EC and identifying the ubiquitous entanglement molecule which makes this all possible will be greatly facilitated by using subjects that are at this early pivotal stage of development.

    This initial two-week stage in human gestation, for example, marks the point where the embryo may form one or more hosts (i.e., twins, etc.). Also at this stage, the characteristic central structure of the host form begins to emerge. It is very likely that the EC are present but have not yet heterodyned at this juncture. At this stage, the embryo remains a collection of distinct individual cells each with a specific or soon to be determined mission. Once the EC combine their individual entangled states to establish the one or more new emerged entangled states and the POV's defined therein, an equal number of new instances of individuality come into existence perhaps for the first time, or perhaps not for the first time. The one certainty in this process is that this particular host has never before existed and never will again.

    Further, we may inquire; at what stage in its evolution does an emerged species gain its EC and go from being a colony of individual cells, to become an emerged form hosting a position of view with a unique emerged QEF? To understand this, it would help to seek living forms representative of each evolutionary stage of development. Species that straddle the evolutionary line between a colony of living individual cells and an emerged living being with a POV distinct from its other non-EC's. Such species no doubt exist but are not easily categorized. For some reason, evolution seems to favor full emergence once a colony develops the EC, like a switch being flipped. This is not to suggest that such recently emerged species would immediately possess highly integrated systems like a central nervous system which links its disparate regions of specialization. Such complex features would take time to evolve but the QE connection to metamatter had by all living forms requires no such embellishments.

    Also, how might a species respond evolutionarily to developing a newly established POV as compared to being a colony of living individuals? This would be a truly fascinating study to undertake. The LINE hypothesis suggests that imprinted metamatter influences evolution throughout this universe in ways that should not be underestimated and may very well play a crucial role in disseminating this amazing capability to eco-systems separated by distances that are otherwise physically unbridgeable. Thus, like all other features of the cell, the capability to combine the natural entangled state first evolves in cells which then further specialize. Thereby passing on their newly acquired talents to offspring. Together these new EC perform the initial combination of their individual QE connections to establish the new emerged individuals position of view thereby marking the emergence of a new host form for emerged individual life, a new species.

    From an evolutionary standpoint, one may be tempted to expect a dramatic transformation to accompany the transition from the collection to the emerged host, but this is unlikely to be the case. More probable is a slow evolution out of the hitherto normal behavior of that particular colony as new possibilities slowly take hold of its evolutionary trajectory. Thus the cloud-storage repository of newly entangled metamatter further shapes the destiny of a new species. The science which describes POV evolution will, like all aspects of living biology, be deep and complex in its own right. The evolution of a species has many influences and likely goes stepwise with the evolution of its POV as both number and complexity of EC may evolve.

    So if you, whatever your species, are impressed and proud of the evolved capabilities of your living form, it is well and good that you should be, but also realize that none of those known features can be considered to be more impressive than the feature of natural entanglement heterodyning evolved in the EC. This remarkable feature permits nothing less than the establishment of complex emerged beings, like you, in this universe. If not for this amazing feature of the cell only individual cells and colonies thereof would populate the Earth. This is not to suggest what forms such colonies might take, but the distinction between a colony of individual cells and an emerged being such as a human or a millipede or a finch is significant and important. Today science defines no clear basis for such a distinction, the LINE hypothesis does.
  • tonylang
    So, I have a position of view (POV), how then does my POV interact with my body? The LINE hypothesis suggests that in all living entities the hosting form has evolved to establish, maintain, and protect the delicate quantum state that is the position of view (POV) from intrusion, or specific violation. Failure of the host in this basic responsibility is the very definition of death. In this endeavor, the body and POV have coevolved to have the POV as the target, the kernel of certain host-specific processes and functions. In any given instance of life, these functions establish your presence and other evolved manifestations of the host, broadly describable as experiences. This interaction between the POV and the host form, sufficiently evolved, is the manifestation described in human cultures for generations, using one word or another, as the mind.

    The mind is one tier of implementation above the actual instantiation of the POV. While the POV will exist in every living entity, even in the absence of evolved systems that may manifest a recognizable mind, a mind cannot exist in the absence of the POV. The mind is the interaction of the POV with the living form. The mind functions as an antenna, or a receiver for whatever workings, and telemetry, and other evolved manifestations the host, such as it is, is capable of producing. i.e. memory, consciousness, self-awareness, intelligence, thought etc., or the lack thereof. The POV brings none of these features, but only that which may experience these features. The classically measurable implementation of the POV is as a standing quantum wave, established at the individual’s unique QEF, one’s own unique values of the degrees of freedom (DOF) of the QE spectrum. The POV is maintained by the entanglement molecules (EM) within all cells, and in emerged species by the entanglement cells (EC). Further, the physical host establishes a very real bond with the POV. This POV-host bond (POVH) is not unlike the standing waves shared between the valence shells of atoms which establish and maintain covalent bonds that join molecules in this universe. It is the POVH bond which naturally provides the foundation of the mind upon which the individual’s first person sense of presence may evolve in all living beings, within you.

    The POV is implemented, in biological hosts, during gestation at the point where instantiation occurs in the growing host form by the EM and EC. However, in sufficiently evolved complex host forms, the mind is established when the nervous system (i.e. Brain) form the unique infrastructure which may interface with the POV. This interface of the nervous system with the POV also takes the form of a standing quantum wave maintained by other specialized cells of the host which maintains the coupling which describes the POVH bond between these two, critical natural implementations. This joining provides the antenna state which becomes the basis for experience we call the mind. This temporary, but crucial link lasts a lifetime and naturally manifests the collapsed reality as well as the possibility to evolve perception and experience for one living individual. Because the POVH bond is essentially a molecular bond, it also may be represented by a mathematical equation or Hamiltonian. This Hamiltonian has its roots based on the Schrödinger wave equation. This is the quantum mechanical equation that very powerfully represents the complex standing probability waves of electrons in shells around atomic nuclei observed in atoms and molecules. However, this similarity will have very definite limits because, unlike molecules, the interactions and DOF that produce the POV are not derived exclusively from interactions between standard-model entities, but between matter with metamatter. Metamatter is hypothesized to be a non-local particle that very weakly interacts in this space-time. Therefore, to formulate the proper wave equations for the POV, the DOF which permits the EM within living cells to share a coherent quantum channel with metamatter, will have to be well defined through intensive research. This research will begin with the discovery of the EC and the EM.

    An apt analogy for the role of the POV within living hosts is to consider an individual in the middle of an atmospheric storm. A storm may take on many forms, and have a number of features such as winds, tornados, rain, snow, hail, lightening, thunder, clouds etc. all described by certain degrees of freedom, temperature, pressure, humidity, surface absorption and radiation coefficients etc. which inform varying storm intensities. As a storm circumstantially manifests, it may be given various categorizations, akin to species of storm, and may evolve to a form that may even be given a proper name, an identity. Consider if we placed a living being, a human being for example, at the center of our imagined storm. This individual does not add to, and takes nothing away from the storms manifestations and activities. This individual does however bring, in the case of a human being, one individual’s singular perspective within the storm. This individual has its own capabilities and functions which define it as such. Additionally, if this person has a communications device with an open channel, they may transfer information from within the storm to the outside world. This individual only very weakly interacts with the storm itself. This individual presents both a conduit and a target for information and experience from the storm, but in one direction only.

    Likewise, the instantiated POV bonded to a living host form is metaphorically similar to this in that the POV brings no effect or effect of its own, but is essentially a teleportation channel bonded to a host, able to receive telemetry and imprint information manifested by its living host. This interaction, this POVH bond in human beings, for example, which receives telemetry manifested by the human brain-centered upon the individual POV, is the very definition of the mind. The mind can be described as being composed of two primary components, the POV, and the rest. On earth, the rest may be anything from; not much at all, as in a single cell, to the complex workings of a fully functional complex nervous system and brain of the human host. Whether in a human, in an eagle, a mantis, or an octopus, the POVH bond is the bond that builds upon the standing wave of the POV which manifests the QE connection to metamatter in all life. Further, in sufficiently evolved forms, the POVH bond becomes the mind. The description of the mind in various species is subject to cultural definition and perceptions, accurate or not, regarding a particular host forms observed behavior and nervous system function, or the lack thereof. However, to be accurate any definition of the mind must include the QE connection and POV as an essential prerequisite of individuality in any living presence in this space-time.
  • tonylang
    As you look into the eyes of your newborn daughter and wonder; who are you? Who is in there? You, I expect, understand that every last atom that now, and will ever, compose her little body were each forged in a long expired star and has been here on Earth, for example, for billions of years, and in this solar system for even longer. The rational part of your thoughts understands that the property which uniquely instantiates her, here, now, cannot be those same anonymous atoms or molecules. Evidence; if they did, that would demand that conjoined siblings, sharing the same host form, the same body, composed of the same group of atoms and molecules and DNA, are one individual. However, we know empirically, in as much as any scientific evidence has ever validated anything, that this is not so.

    Conjoined siblings are in nature often two distinct, although not physically separate, individuals. Not unlike two different isotopes of water poured into the same vase may seem to become one entity. Nonetheless, at the deepest levels, in conjoined siblings, as in the vase of water, nature recognizes their distinction, their individuality. It is just a matter of understanding their fundamental, natural, eventually scientifically describable, implementation. Although conjoined twins may share the same DNA and even the same host form and thereby any number of organs, including at times portions of the same brain, they nonetheless are two distinct instances of life. No matter based component or classically defined property of these anonymous atoms and molecules can assign this distinction. The LINE hypothesis suggests in such cases (i.e., conjoined twins) there are fundamentally two positions-of-view (POV's) instantiated by two separate sets of entanglement cells which maintain two separate quantum coherent states at two unique QEF. Those QEF are, as is your daughters QEF, immutable and indestructible. All QEF are a permanent fixture of the metaverse (Hilbert-Space) currently hosted here on Earth.

    In conjoined siblings, the host form, the body, described and mediated by its local genetics, goes terribly wrong. In this situation, DNA exposes its severe limitations as the possible mechanism by which individuality is instantiated in living beings. If ever there was evidence of a claim, in this regard conjoined siblings qualify. The unique degrees of freedom (DOF) of the entanglement spectrum, manifested by the hypothesized entanglement molecules contained within all cells and in the entanglement cells of every living host, is as abstracted from the existence of ones' DNA, and its anonymous atoms, molecules, and local evolutionary process, as is the tuning of a radio or TV channel abstracted from the anonymous polymers, rare Earth molecules, manufacturing process, and general physical designs, of your radio or TV set.

    It is hypothesized that upon the successful separation of conjoined siblings if you were then so situated as to empirically compare, with both sufficient resolution and understanding, their DNA currently believed to define each siblings individuality, you will discover no classically identifiable difference between the now separate host forms. Further, for a time the siblings will remain genetically 100% identical. This is because the body in the case of conjoined siblings, as in all living beings, does not establish individuality whether genetically diverse, or identical down to the deepest recesses of their DNA. Therefore genetic sequence (ATCG, etc.) must be empirically ruled out as the most fundamental defining feature of individuality.

    The individual that is your daughter, or my daughter, indeed all life is instantiated in their respective habitats by virtue of natural laws and circumstances. You and her other parent donated local evolutionary genetic information, as does trillions of other hosts in and perhaps beyond Earths' ecosystem, to create a new living form of its kind evolved to host individual life. More significantly, your daughter donated her own uniquely tuned metamatter, tuned via her QEF's lifetimes of past instantiations in Earths' ecosystem. This enables the establishment of her unique natural teleportation, her LINE channel. This is a shared coherent state established between metamatter with her gestating entanglement cells some 11 days into human gestation.

    This natural entanglement is established at her unique QEF to establish her position of view (POV). This standing quantum wave once bonded to her new human host establishes a new POV-host bond (POVH). The POVH bond is the antenna state that establishes the mind of the individual that you will come to know as your daughter. With this POVH bond to a human form, all things human become possible. However, her specific features, her capacities, depend entirely on the specifics of her particular growing host form. Not only her physicality, but her sentience, consciousness, self-awareness, cognition, creativity, joy, sorrow, or the lack thereof, all will manifest from her new host form and its path through life. This occurred and can reoccur because re-occurrence is scientifically observed to be the way of nature in all things. It is only the collection of anonymous atoms and molecules that will necessarily establish a new facade as they come and go even now as you watch her grow into what is essentially a new form, an adult. Certainly, a true joy to observe, but don't let the visuals confuse your understanding unless of course, you want it to. The details of this implementation may be unfamiliar, nonetheless, like the deep details of genetic science today, such details do not now, nor have they ever required our understanding, or acceptance to nonetheless define individual life throughout this universe.
  • tonylang
    Where is everyone? As we probe the depths of the known universe with increasingly majestic instruments based upon the detection of electromagnetism, and as of very recently, gravity waves, it becomes increasingly apparent that the proliferation and distribution of living ecosystems in this universe is curiously low. Today we refer to this absence of detectable extraterrestrial living contact in the cosmos, as the great silence. What could account for this apparent barrenness in a universe known to host at least one prolific, remarkably diverse, extremely long lived habitat for individualized life?

    Historically, humankinds search for extraterrestrial life has been based upon a premise that may be false. We consider the prospects for life beyond the earth to be loosely based on the Drake equation (N = R * fp * ne * fl * fi * fc * L). This formula, conceived by Frank Drake in 1961, considers the quantity of possible extraterrestrial civilizations to be dependent upon a number of factors all of which considers only the presence and duration of classical matter based entities and conditions. However, nature has never proven to be as simplistic as humankind may first imagine. The LINE hypothesis suggests that individual life throughout this universe is instantiated and mediated by the entanglement spectrum and it is this pervasive non-local natural medium which ultimately determines the quantity of simultaneous living individuals that is possible in this universe.

    The QE spectrum is hypothesized to naturally limit this universes capacity for life. Not unlike the electromagnetic spectrum which although also quantifiably infinite, is practically limited in its utility for simultaneous useful unique channels by classical technological devices. However, for the QE spectrum and life in this universe, this is not only a limitation of biology or even of technology, but is a limitation imposed by the topography between this verse and the underlying metaverse which define this universes local QE spectrum. If life and individuality are indeed dependent upon unique singleton teleportation channels of the QE spectrum, hence, it is hypothesized that there exists a maximum number of simultaneous living individuals possible in this universe, regardless of location or host form. This capacity is described by this universes laws of physics to be some finite, potentially calculable population regardless of the number of viable habitats for life that may exist. This capacity for life is called the LINE Capacity (LC) and is the number of instantiations of individual life that may exist simultaneously in this universe.

    This living population represents not only the number of POV’s had by emerged multi-cellular hosts like humans or whales or ants, but far more significantly, includes the number of instantiations of fundamental hosts, such as individual cells, currently in existence whether composing such emerged hosts or not. On earth this is a large number. In nature, each count as one instance of individual life. At any one time a human host consists of perhaps 100 trillion cellular instantiations and over a lifetime, many more than that, plus one additional. That additional instantiation is you. Ones POV heterodyned by the entanglement cells (EC) is one of nature’s pinnacle evolved invocations in Earths ecosystem. It is hypothesized that once a verses living population exceeds its LC, any additional viable ecosystems that emerge will only be perfectly habitable yet completely barren worlds, like so many well constructed houses with no one home. Near the LC, for the emergence of life to take hold, such habitats will need to remain viable for the emergence of life for a time during which the QE spectrum simultaneously has available bandwidth viable for the instantiation of living individuals, i.e. cells, to entangle at unique uninstantiated degrees of freedom (DOF) of the entanglement spectrum. Thereby initiating an indigenous genesis of life.

    Further, as any universes living population approach its LC, any ecosystems therein actively hosting life will begin to experience increasingly higher mitosis, gestation, and birth mortality rates. This occurs as the existing living hosts, unbeknownst, continue to procreate, to create new viable hosts for life which then fail to instantiate the crucial teleportation channel needed to establish the living individuals position-of-view (POV). In circumstances where the universal living population remains near its LC, like an establishment approaching its fire occupancy limit, the life and death cycle of living beings throughout the universe becomes increasingly influential as it essentially consumes and liberates QE bandwidth universally. Like occupants entering and leaving an establishment, this flux of instantiation increasingly informs the availability of unique QEF to instantiate new living beings. It is highly probable in most evolved ecosystems still possessing a robust micro-biome, that this outage of life will be largely absorbed first in the vast mortality rates of diminutive host forms such as single cell life and colonies thereof. Hence, primarily by mere attrition, this outage may only rarely effect the heterodyned QEF of more complex emerged multi-cellular hosts (with EC) such as mammals, birds, fish or insects.

    A universal LC potentially informs the local success rates of new life in wild ecosystems such as Earth. Further, if the LC of this universe is near some integer factor of the current population of life on earth, or even if the LC is several million times that population, nonetheless, such a finite capacity for living beings combined with this universes unfathomable vastness probabilistically infers that humankind may never detect extraterrestrial life. At least not by classical means, because where the QE spectrum reigns, neither distance nor time holds sway. In light of this possible upper limit to the natural instantiation of individuality, it should come as no great surprise that this universe appears to be so devoid of extraterrestrial life. Ergo, it is not simply a consideration of matter or of the habitability of worlds that dictate and mediate the proliferation of life in this universe. No wild ecosystem can know where its universes living population currently lies relative to its LC absent a deep command of the principles described by the LINE hypothesis.
  • tonylang
    The Cambrian explosion is one of the great mysteries of evolutionary science today. It marks the sudden emergence of complex species from a significantly microbial ecosystem with little evidence of corresponding intermediate evolution in the fossil record. To shed light on this conundrum, we need to view the Cambrian through the prism of the LINE hypothesis to understand what effect does living have on the individuals prospects for life after death. This will be a central question for all sufficiently developed, intelligent, self-aware beings throughout nature. For human life on earth it is also the question that many religions have sought to address throughout human history, via one mythological narrative or another. Through their doctrines, such belief systems suggest what are the rules to live by which will influence whatever it is those myths determine will become ones destiny after ones’ current life ends. These questions regarding living influences, as it turns out, are very good questions to ask. They, necessarily must have corresponding answers. Answers which can and must be founded in nature and accessible and describable by natural law and eventually by science, otherwise you couldn’t be alive. What natural, scientifically inclined basis can be used to make such determinations for ideas critical to science, yet long held close to the vest by religions throughout human history?

    The LINE hypothesis suggests that metamatter is imprinted via natural entanglement. This QE connection persists throughout the course of each individual’s lifetime, no matter ones living form. While instantiated to fundamental forms, such as hosts in earths micro-biome, such hosts necessarily imprint metamatter in low volumes, or densities, given that a microbe is composed of only a single cellular instantiation. This combined with the incredibly short life-cycle, and high reinstantiation rate of life in the micro-biome, given sufficient time, causes this low information throughput to accumulate, and aggregate to become immensely significant to evolution on earth. The information volume imprinted to metamatter by such fundamental forms is very low in content and therefore has a very low impact or influence on the individuals FT. As a result this renders such host forms very weakly tuned to the individuals’ QEF, and therefore for future instantiations, renders the individual more open to arbitrary natural entanglement with a wide range of compatible hosts, ergo other microbes. On Earth prior to the Cambrian, with no forms of greater complexity available at that time, this condition persisted for billions of years. Should it persist, this period in the evolution of life in any ecosystem, results in a vast accumulation of evolutionary potential which may result in an explosion of complexity. Such inflations in ecological complexity cannot be explained by bottom up, random mutation, and natural selection alone. Ergo, today the influence not considered in Darwinian evolutionary science, is the influence of the LINE process.

    An apt analogy for how the LINE process may lead to an explosion of complex life is with the printing of information by a computer printer. Consider the natural teleportation channel that is the LINE hypothesized QE connection to metamatter, established by the entanglement molecule within each single cell, as being like one element on a computer print-head. Each cell possesses the information transfer capability of just one such element per cellular instantiation in any host form. So, if your form is composed of just one cell, you have one print element with which to imprint metamatter in your ‘name’, that is to imprint metamatter at your QEF. In this analogy the more print elements there are in a print-head (living host), the more information can be transferred to the sheet of paper (metamatter), and the larger ones information bandwidth. The 100 trillion cells of a human host imprints that many times more than an ameba, bacteria, or a protozoa. Each cell of your host, whether one or many, are imbued similarly with some common degree of freedom (DOF) of your unique QEF and is therefore able, to some degree, to imprint, or otherwise contribute, to metamatter on your behalf. This metamatter ultimately informs one individuals fidelity of teleportation (FT) and ones future prospects for reinstantiation.

    In this analogy a microbe is metaphorically equivalent to one print element which imprints metamatter during a great many, very short life spans, due to the incredibly rapid life, mortality, and reinstantiation rate of the microbial world. In this way an individual’s QEF imprints small volumes of metamatter, but very frequently, with information from many iterations of simple living forms repeated over epochs of ecological time. On earth, such forms dominated the planet for billions of years before more complex forms became possible. This information stored in metamatter is theorized to influence the evolution of living hosts on earth and universally. Eventually this imprinting by fundamental living hosts became a huge volume of evolutionary information stored in this non-local universal repository. Together with local conditions and circumstances on the early earth, this lead to the emergence of the entanglement cell (EC). Once the entanglement cell came onto the scene, it brought with it the capability to heterodyne individual cellular QE connections to establish the earth’s first generations of secondary emerged QE connections to metamatter , the position-of-view (POV). A heterodyned POV establishes a secondary emerged individuality, you. With it, the evolution of vastly more complex host forms became possible. On earth, this essentially marked the emergence of life 2.0, if you will. The wide proliferation of the EC began the amazing period in earth history known as the Cambrian explosion.

    During the Cambrian, the newly emerged EC together with instantaneous universal access to a vast volume of imprinted metamatter, drove the unification and specialization of many formerly distinct living forms into complex communities, marshaled by new organelles able to distribute common aspects of the POV to all cells of the holistic host form, to propel the formation of new complex species. These new species quickly evolved due to the new emerged secondary entangled state, and the interaction at a distance resulting from the sharing of common degrees of freedom of the POV which describes this natural teleportation channel to metamatter. This metamatter imbued with evolutionary information from earths billions of years of fundamental life, as well as information from other life hosting ecosystems in this universe, gave the Earths new species a sudden and tremendous boost in complexity not possible by random mutation and natural selection alone. Hence, the QE connection soon evolved not only into the earth’s first POV’s, but eventually, into the earth’s first minds.

    Further, individual QEF, having participated in countless instances of microbial life, hosted by Earths local ecosystem, and with FT’s by then highly tuned by terrestrially imprinted metamatter, burgeoning to propel a great transition, that is the natural teleportation of those individuals from simpler forms to more complex forms, became eminent. This new innovation which permits the sharing of common degrees of freedom by all cells in an emerged complex host with EC, bonded to one POV via the POVH bond, permits the organism to evolve in sudden and remarkable ways previously unattainable absent the EC. These more complex evolved forms will consist of increasingly larger numbers of fundamental hosts, such as cells. Each a metaphorical print element for metamatter and also, by virtue of an evolved protective host form, may live longer life spans for imprinting matamatter. This accelerates the imprinting of matamatter at the individuals unique QEF and further probabilistically tunes the individuals FT for compatibility with even more complex and compatible host forms, whether such forms were evolved, or engineered. On Earth the human form, for example, may consist of 100 trillion individual instantiations and many more than that counting from the point of QEF instantiation in the womb, up until deinstantiation, death.

    The metamatter imprinted over the course of an increasingly longer lifespan, by any host, is potentially cumulatively significant to ones FT. For humankind this is not necessarily more so than the imprint made on metamatter by other, non-human, equally long lived host forms in earths ecosystem. In other words human beings may not be the undisputed champions of FT stability currently on earth. FT stability tuned by increasingly greater volumes of similarly imprinted metamatter describes the individuals chances of naturally entangling a particular host form, and perhaps of greater interest, reinstantiating to ones current host form. So, if sperm whales, having perhaps 1000 times more cells than the average human, and living equally long life spans on average, will imprint, at least by volume, orders of magnitude more cellular state information to metamatter than humans. This says, at least on its face, that whales may be a more stable, and more forecastable host for reinstantiation than the human form. That is to say, an individual QEF instantiated to a whale, all things being equal, may be more likely to reinstantiate to that same form than a QEF instantiated to a human form would likely be to reinstantiate to a human form in ones next life.

    However, reality may not be quite this simple. What other aspects of one’s QEF, of one’s host form, and of its circumstances in life might there be that are imprinted to metamatter, which may influence ones FT? What properties of the cell are conserved via natural entanglement after death? Which degrees of freedom of the QE spectrum imbue this conservation of local living information to the non-local, more permanent, more accessible universal medium of metamatter? For now, the LINE hypothesis suggests volume of imprinting per cell, per host, and lifespan, but what of the type, or the nature of information imprinted? What other factors might there be as we live life which may creep into ones metamatter and effect ones FT via a complex nervous system bonded to a unique teleportation channel that is the POV-host bond (POVH) which constitutes the mind? Whether in a human or a whale, the answers to this question essentially form the basis for a new list of commandments. Not unlike the commandments of religions which purport to influence what comes next for the individual. The natural, empirical information which actually, naturally influences ones FT does likewise. Species do undergo Darwinian type evolution, but it is also driven by natural entanglement and punctuated by the evolution of forms like the entanglement cell, the pivotal catalyst for the formation of complex hosts in this ecosystem. Due to the EC being a host form, the remains of which will never be found in any shale, the Cambrian appears to be a true mystery until viewed through the prism of the LINE hypothesis.
  • tonylang
    Presumably, there is a first time for everything. Consider then this earths first life, that is to say, the first time you or I or any individual is instantiated as a living being in any ecosystem, perhaps in this ecosystem, Earths ecosystem. This may seem like a strange notion to consider but realize that no matter what your current belief system one cannot deny there has to have been a first instantiation for each individual even if you think this life is that first time, the only time, the last time you will live. Further, let us call this first-ever host of life in earths ecosystem and perhaps first in this universe Cell-1. What individual was hosted by Cell-1? Who was it that came into being so many billions of years ago entangled by this first living host here on earth? Was it me? Was it you? Was it someone we now know? A single cell being in nature as much a living being as any other, how then could we identify this or any individual position-of-view including ones own? Since the natural process that populates this universe with living beings is as all natural processes are, ubiquitous, prolific, and may repeat whenever, wherever conditions are favorable, this first individual may very well be among the living today. If you are having trouble comprehending this notion it is likely because you are thinking of individuality from a second or third-person perspective, the visible tangible behavioral perspective. Instead, consider individuality from ones own first-person position-of-view. As with you or I, the form that any living being instantiates does not change the fundamental nature of ones position of view which is presence not experience. It is only ones form, placement, and time in this universe that vary. Make no mistake the POV is not to be confused with a point of view which if had by a given species or host is a function of that particular host and is nothing more than the skills manifested by that particular entangled form. Skills manifested perhaps by cognition of a complex brain and/or nervous system, or a lack thereof.

    A unique position-of-view is what defines the individual regardless of form. It is very difficult for hosts such as humankind to imagine the being of other life forms. So how does one imagine a beings POV even ones own? It isn't easy, particularly since there has never been anything one could do to change ones instantiated form, apart from terminating ones own life. Even then, with no natural persistent memory of ones past instantiations, it is very difficult to comprehend this natural implementation. However, one first step may be to realize the natural entangled mechanism of life and to develop technologies for the detection of the living POV and record individual inter-longevous histories.

    If in fact the first host ever to exist in this universe had entangled your QEF, in nature, you would have been every bit as alive then as you ever were in any subsequently instantiated host including ones current form. When we ask; what individual was cell-1? What is it that is being identified if not cell-1's host form, its body the cell, and its functions and skills? The LINE hypothesis suggests it is ones unique value of some quantifiable degree-of-freedom of the entanglement spectrum the QEF, call it QEF-1 if you will. Whatever the actual value that QEF-1 turns out to be for an individual, let's say cell-1 for example, that unique value of the QE spectrum will always instantiate cell-1's POV its position-of-view, POV-1. no matter where, when, or what the design, biology, or technology of the available host. Long after that first host had decayed back into the anonymous atoms that had first contributed to its form its QEF, QEF-1 has likely reinstantiated on countless other occasions since then. With each instantiation, in each life, QEF-1 by entangling matter to metamatter brought the same first-person position-of-view into this universe, POV-1, by providing a place and a time to something that otherwise has neither. No second-person perspective would recognize the individual that is POV-1 from the outside, in fact as with current earth-life there is often no means by which any individual could recognize itself as a recurring entity. Particularly if it were a single cell. However, perhaps if billions of such individual POV'S came to entangle highly evolved hosts possessing sufficiently high intelligence and perhaps if a critical mass of such individuals were to become enlightened, no doubt kicking and screaming every step of the way, to the reality of their living circumstances to develop technologies adequate to the task of analyzing and detecting the entanglement spectrum and the standing entanglement wave it manifests in living beings, such a species could one day measure, quantify, and identify the unique living POV of the individual no matter ones physical form. With the identification and comprehension of naturally invasive ideas often comes an ever-increasing level of control. In this case, it is control over the instantiation of ones own being, which is ones’ form, placement, and time in this universe.

    Nature cannot be assigned the property of purpose. Nature doesn’t implement individuality in the manner in which a cognitive species such as a human might. However, the ubiquitous natural universal process of instantiating a living being in any given environment ought to be quantifiable and understandable and may be described in terms of natural cause and effect. So how does the natural process of instantiating a living being resolve which QEF, who’s QEF is entangled to cell-1? Whose first-person position-of-view, whose being, exists first, second, third, etc. Clearly, life doesn’t seem to us to be sequential but how can we know for certain?

    As a thought experiment, consider that Earths’ hypothetical Cell-1 undergoes mitosis and creates a cell-2. According to the LINE hypothesis, both must necessarily entangle stem-metamatter since at that time there can be no metamatter in existence which was imprinted by host species from Earths' virgin ecosystem as there would as yet have been no deinstantiation (Decoherence of an emerged individual), no death. Death is necessary to provide disentangled imprinted metamatter for future generations of life in any ecosystem. Further, if cell-2 later divides to create a new cell; cell-3 before cell-1 dies then cell-3 will, as did its two living relatives, also entangle any viable host to stem-metamatter to instantiate yet another original POV never before instantiated in this or perhaps any ecosystem in this universe. Why? Because Cell-1, if it is anything like a modern cell, likely has a mechanism like DNA to transfer its hosts' design information physically generationally and so each host offspring, each relative, be it familial, special, or ecological, imprints upon metamatter with a diverging degree of similarity. All of this coherent cellular and QEF state information stored in metamatter attracts future generations of genetically similar hosts to entangle this metamatter. Presumably, the individual is unaware of any of this as are even complex species such as present-day human beings.

    Alternatively, consider if cell-1 instead had disentangled, died before cell-2 divided to produce cell-3, then the LINE hypothesis suggests that this newly minted host (cell 3, grandchild of cell-1) would be more likely to reinstantiate its bygone relatives' QEF (QEF-1). Host cell-1 and 3 are in this scenario generationally, physically related due to their common DNA, and cell-1 over the course of its lifetime has imprinted metamatter, as do all living entities, with information from both their physical component (DNA, etc.) and also from its’ unique entangled degrees-of-freedom (QEF-1). The QEF is not part of the cell nor is it an aspect of metamatter it is of the entanglement spectrum. The entanglement spectrum exists as a distinct implementation of nature with properties, characteristics, and degrees-of-freedom which define it as such, not unlike the electromagnetic spectrum. These three elements of nature operate in concert to make individuality and life possible and mobile (teleportable) in this universe.

    QEF-1 now uninstantiated and unentangled, mediated by the monogamistic rules of quantum coherent interaction becomes available universally for future instantiation with viable hosts. So cell-3 (grandchild of deceased cell-1) with DNA more compatible with deceased cell-1's existing residual metamatter imprint than not, will more readily attract or enter into an entangled state at cell-1’s QEF-1 and its existing recently disentangled metamatter in lieu of widely available stem-metamatter. So the individual, the POV that instantiated previously to host cell-1 is now reinstantiated to its own offspring host cell-3. The possibility of familial reinstantiation is likely highly dependent upon the actual resolution of the theorized imprinting upon metamatter by the living cell. For familial reinstantiation ones fidelity of teleportation may need to be above some pivotal value (i.e. .75 or greater above the classical limit), any lower and only species and inter-species entanglement may become likely.

    Nonetheless, Cell-3 the individual the world sees as the grandchild of deceased cell-1 could once again host POV-1. Such is the nature of life. It is only when there is no compatible imprinted and simultaneously disentangled metamatter and compatible hosts available that a newly emerged host will entangle stem-metamatter to establish an original (to this ECO system) position-of-view. In nature the laws of conservation mandate that every interaction has an effect and induces a change in its participants. Whether or not we can sense, measure, or understand the interaction or the effect it produces. On human scales, the gentlest touch transfers heat induces friction, deformation, etc. Electromagnetism changes the atoms and electrons it interacts with or there would be no electronics. A subatomic particle entangled with another or with others interacts regardless of distance or time (even when in different temporal frames of reference). By this natural mechanism metamatter, ones non-corporeal life-matter if you will, is changed as it entangles with your cells over the course of each lifetime.

    By this process individuality emerges in otherwise inanimate matter and gives rise to a living being that has either never lived in this ecosystem before or may have never lived in this universe previously, The implications for individuals currently instantiated on Earth, as in any viable ecosystem, are that ones future place (reinstantiation) in this eco-system is all but guaranteed barring some global-scale catastrophe which erases all life on earth leaving only the possibility of reinstantiation elsewhere, barring such a catastrophe the entire DNA pool of earth-life will attract your QEF to available metamatter to host you once again.
  • tonylang
    How does a living being with the capacity to do so begin to determine ones' prospects for life after death? The LINE hypothesis suggests it is via the determination of ones' fidelity of teleportation (FT), a little-understood but very real property of quantum information transference which is one metric that governs the instantiation of a living individual. It is the mechanism that the LINE hypothesis describes as the natural process that distributes individuality throughout this universe and likely throughout nature. Estimates of ones' FT is perhaps the value most important to any living being capable of fathoming its importance, no doubt followed closely by the value of ones' QEF.

    The FT value describes the accumulated probabilities that will influence an individuals' next instantiation. There are always going to be uncertainties involved in determining ones' reinstantiation prospects, but generally, some of these influences can reasonably be assumed to be constant. Factors such as the assumed persistence of conditions for life within Earths' ecosystem, and thereby the likelihood of the continuation of ones' current species, ones' DNA line. Extinction being a fundamental aspect of host evolution is an eventuality that may be generally deferred for such a consideration. Factors such as the proliferation and similarity of ones' existing familial DNA as well as lifespan species and near-species population, also volume and resolution of imprinted metamatter may all be more dynamic factors relevant to ones' FT value and reinstantiation prospects. One's prospects for reinstantiation describe what host form, or species an individual might entangle in ones' next life. Where one entangles that form depends entirely on where such compatible hosts are located in this universe.

    Each currently living individual has more likely than not undergone numerous instantiations and lived many lives, many presumably may have entangled hosts right here on Earth. Earth is the only known ecosystem with hosts for life that are compatible with your current indigenous Earth form, whatever that form may be. Some day the Moon or Mars may become seeded, non-original bastions for Earth life. This makes Earth a factory of imprinted metamatter and therefore a powerful attractor, if not the only existing attractor, for the reinstantiation of any being currently alive on Earth. Given that ones' metamatter imprint is expected to lose its resolution over time spent uninstantiated, compatibility with hosts that emerge in extraterrestrial ecosystems becomes increasingly possible over time. Other ecosystems that emerge on other planets or in other viable environments in nature will host living forms with different indigenous designs. However, the one common mechanism for life is the entanglement molecule, responsible for the QE connection to and the imprinting of that unique design upon metamatter.

    Familial reinstantiation may be most desirable to the individual, whether consciously by enlightened consideration or only subconsciously by genetic evolution, but may nonetheless be a very high bar to expect of a pervasive universal natural process such as natural entanglement. Even if, in nature, familial reinstantiation is possible, the frequency of it occurring may be quite low, or tenuous absent synthetic intervention. Factors competing for the influence of the reinstantiation process are in nature likely to be quite aggressive and disruptive to the delicate resolution required for predictable, forecastable familial DNA entanglement. More frequent may be the occurrence of species and near species reinstantiation. This is particularly true for species with many large populations of close genetic variations simultaneously in existence such as beetles, finches, or cichlids.

    Further, in natural settings, distance although irrelevant to the coherent information teleportation of natural entanglement remains a very real obstacle to genetic proliferation across space-time. After all, in the entire history of Earth life, the number of viable hosts that have left Earth's ecosystem is negligible at best. Most may never even have left their landmass or lake of origin. Hence the LINE hypothesis predicts the probability of reinstantiating in ones' current planetary ecosystem to be quite high. This is due to the localization of corporeal genetic material that is tuned to ones' existing imprinted metamatter. It is possible for ones' QEF to entangle hosts indigenous to other original ecosystems in this universe. However, the probabilities involved with such stem-metamatter instantiations are comparatively very low, very unlikely, requiring the passage of relatively long spans of time. Of course, to the individual, any span of time spent uninstantiated is inconsequential. Since the uninstantiated individual QEF is removed from space-time, and devoid of experience.

    The specific implications for human culture and its survival and in understanding the actual natural mechanism for the mobility of individuality in this universe are unpredictable yet will be profound. Humankind up to now has essentially suffered from a form of existential dislocation syndrome. The result of appearing in a place, for a time, with the capacity to comprehend ones' existence, but with a deficit of ideas and information adequate for realizing the natural mechanism governing ones' presence, ones' being, ones' position of view. This deficit fosters erroneous ideas of life, species, and self, leading to destructive and unfulfilling self-actualization schemes such as intolerant religions, scientific over-extrapolation, bigotry, and speciesism, which corrode social and ecological cohesion necessary for the survival of a species such as humankind.
  • tonylang
    The search for the entanglement cell (EC) will require the isolation and identification of critical regions of cells that may be referred to as 'Follicle regions.' Follicle regions in this context describe isolated diminutive groups of cells which when sufficiently disrupted appear to cause the termination of the subject in a manner difficult to distinguish from genuine EC termination. EC (Entanglement cells) being the most fundamental physical implementation of individuality of an emerged composite being, disruption of EC exclusively is hypothesized to result in disentanglement to metamatter which is deinstantiation, individual death.

    Follicle regions may actually contain EC, or alternatively, only cells whose function is critical to systemic function not unlike cells of the heart or liver only whose role is much less obvious. Determining which of these two possibilities is the case will require the investigation to focus on each follicle group of cells by process of elimination to reduce the group to the barest minimum of effective follicle cells within the group and then to trace and definitively determine how those remaining follicle cells contribute to host termination.

    For each follicle group, this process should always lead either to the determination and identification of yet another indirect cause of death or the discovery of the presence of genuine EC within the follicle group. These EC will be those, one or more cells that contribute only and exclusively to the observed subject termination. This process requires the discounting (not subjected to disruption) of those cells which either cause intermediate damage to other host systems or do not directly cause host termination.
    Subject termination due to EC candidate cells within the follicle group must not result in any pre-mortem cellular disruption (non-necrotic) physically or functionally to any region outside of the follicle group, ergo; death without damage.

    Approved subjects (flies, nematodes, etc.) chosen for this process may need to be high-fidelity clones in order to provide the required consistent physical structure and predictable systemic cellular distribution. This is so the process of elimination may continue unabated with minimal loss of progress as subjects are terminated, and new test subjects are needed to continue the investigation. Further, subjects may not need to be fully formed individuals but may be sufficiently developed living embryonic forms. These are subjects viable for testing but not viable by current definitions, for independent growth.

    Probing for the entanglement cell (EC) does not require physical contact with candidate cells. On the contrary, the astute investigator will quickly realize that the less physically disruptive the probing mechanism, the more progress will result from the exercise. Since the task at hand is not to disrupt any internal cellular function that could kill the cell, but rather to disrupt only the heterodyning mechanism by which the EC maintains the emerged individual POV. The means of disrupting EC heterodyning are potentially numerous as the monogamy of this delicate state is unforgiving. Infiltration or only identification of the entangled state may occur by the use of appropriate entanglement witnesses such as properly tailored photonic, electronic, or other nonphysical mechanisms. Of course, there is a chance that every cell is an EC. This would require a slight modification of the predictions of the theory as in such a case the heterodyned state would be far more robust than currently predicted. This is because the entangled state of emerged POV would need to survive the massive changes in cell participation as cells of the holistic host are perpetually transient.

    Depending on the relative orientation and positioning of EC relative to other EC the probe will need to target individual candidate cells or very diminutive groups of the same. This is because it is possible that EC may have developed in close proximity or even in direct contact with each other during the gestation period of initial conception and engaged their heterodyning of their individual QEF to establish the emerged QEF and then later physically drift apart as the billions of new non-EC cells develop as the subject grows. Alternatively, the heterodyned EC may in all or some species remain in direct physical contact with other EC to maintain the heterodyning function required for emerged individuality to persist. Therefore the probe may need to be focused down to within the diameter of a single cell and be as noninvasive as possible yet highly maneuverable as to scan many cellular diameters in rapid succession.

    Given all of these requirements, the inventive investigator may imagine a probe not dissimilar from the polarized blue or UV laser found in a Blu-ray disc player and research labs around the world as a good foundation upon which to fashion the probe for this endeavor. The LINE hypothesis suggests that sufficient disruption of the heterodyned state of EC will deinstantiate the emerged individual even while the non-EC or even the actual EC remain instantiated, alive as individual, functional cells. With all cells of the host remaining fully functional, how is the deinstantiation of the emerged individual determined? There is expected to be a time-lapse between POV termination and the first signs of the shutting down of cellular function associated with postmortem necrosis of the host body. The more immediate symptom of deinstantiation will be an alteration in species or subject-specific nervous system and brain functions. Each of such symptoms may be used separately or together to identify POV termination of the subject.
  • tonylang
    To the environment, a living host entangled at one QEF is identical to that same host entangled at any different QEF. There is no classically detectable outward influence or behavior of the POV that can immediately affect one's surroundings which includes ones host. because the host, the species is a part of that local environment. No causal difference between one POV and another is available to the outside world, only to the individual is the difference rendered manifest by the isolation of individuality. It is only the isolation of individual instantiation and also of experience centered upon ones position-of view that affords a clear distinction of self, being, and individuality via the acquired skill of self-awareness in each being capable to fathoming the distinction. The isolation imposed upon the individual POV by a protective composite, and often disconnected host, is a solitary condition which the instantiated being strives to overcome. This is widely achieved through communication in all of its forms which includes mobility. From the single living cell to bacteria to vegetation to human beings, genetically all strive to break the isolation imposed by this fundamental living condition of life. This journey out of the isolation of the basic natural entangled state of life not only began but continues with the living cell in all of its forms and has evolved to become the prolific, diverse eco-system we see today.

    Communication requires the development, usually via evolution, of structures and functions that augment the basic implementation by which natural entanglement is hosted. Evolution no doubt favors the group, which also benefits from communication. This is not to suggest that the perception of individuality cannot be clouded perhaps by intimately integrated communication systems of both a technological and biological nature. Such augmentation could fade the experiential distinction between self and others. Even so, make no mistake, there can be no classical infiltration of the individual POV as there are strict natural monogamistic laws of quantum coherent interaction that guarantee the isolation (or forfeit) of the individual entangled state that is the position-of-view.

    Most often the information of self that is acquired during a lifetime is dissipated from the individual upon deinstantiation. Some information of ones past instantiations may persist in the memories of other instantiated beings for a time or within indelible works or, in the archival repositories of advanced societies. However, currently with no means by which any reinstantiated QEF can be identified, for now, the anonymity of the reinstantiated individual remains assured. It would require the development, evolutionary or technological, of persistent personal individual inter-longevous memory or the societal archiving of such information, coupled with the capability to identify and distinguish the unique individual QEF to then inform reinstantiated individuals of their past histories. Also with this capability would emerge the even more profound capability to influence ones future instantiations by manipulating aspects of ones’ fidelity of teleportation (FT), and further, to eventually develop controlled universal travel via targeted reinstantiation as advanced enlightened species in this universe already would. In so doing a threshold would have been crossed in the maturity of a species as the accompanying enlightenment transforms life as we know it.

    An understanding of ones’ living circumstances in this universe remains equally important even if there are actually no other life-hosting environments other than the Earth. This is because regardless of one's current location in this space-time the mobility of individuality described by the LINE hypothesis also describes how one instantiates not only throughout this universe but also within one's current local environment which is just as interesting and important as knowledge of life elsewhere. We too often expend our concerns on finding extraterrestrial life in lieu of understanding the natural implementation by which nature populates this universe with living individuals. This latter point does not negate the importance of seeking other life in this universe, quite to the contrary. However, it may alleviate the concern caused by never actually finding such life which is highly probable in a universe as vast as, and having the laws of physics of, this universe. The laws of physics that placed you in the ecosystem in which you currently live didn’t do so because there are fundamental laws of nature that are exclusive and unique to this planet, solar system, or even galaxy. The fundamental laws of nature are expected to operate equally at every point in this space-time, thus all phenomena are also possible at every point in this universe including the phenomenon that is you. It is only the circumstantial probabilities of state that vary from point to point and moment to moment that determines local outcomes. Hence, life and individuality are circumstantially possible everywhere in this space-time. More profoundly, we know without question that life and individuality are a fact and the principle of natural reoccurrence guarantees that anything that has occurred can reoccur.

    Viewed in this light concerns about the eventual expiration of the sun or the end of this universe when considered through the prism of the LINE hypothesis takes on a decidedly reduced urgency. As we realize that even as you read these words countless ecosystems, stars, galaxies, and perhaps even universes have come and gone in the eternal history of nature prior. So too has countless instances of individual life, some even your own. Yet here you are alive with precious little memory or consideration of the vast history of both nature and you that came before, and so it shall be again. With this enlightenment, the urgency of the fate of specific conditions and objects or collections thereof, small or large, becomes somewhat less significant as we realize our true place in the permanent structure of nature and that although all stars die and this universe may eventually become non-viable for life the immutability of the quantum entanglement spectrum and its underpinnings is fundamental in nature and the mobility of individuality ultimately sacrosanct.

    The realization of the science which describes the mobility of individuality in this universe, of the kind suggested by the LINE hypothesis, adds yet another layer of ethical concern to the already ethically laden endeavors of modern-day genetics. That is, the manipulation of existing, and the proposed resurrection of bygone species. Naturally evolved hosts, even those that were bread by us, are generally of sound evolutionary foundation. Humans, dogs, cats, pigeons, bacteria are made viable by natural selection even when deliberately bread by humankind. However, with the advent of genuine genetic manipulation of the sort made possible by the discovery of the Crisper CAS9 gene comes a new level of divergence or even a complete disassociation from the process of natural evolutionary selection.

    Further, in the presence of complete ignorance regarding the implementation by which nature distributes individuality in living beings throughout this universe these concerns today give rise only to relatively moderate levels of controversy and discussion. We consider the question of should we manipulate and create new species from a naively disassociated perspective which just barely rises to the level of personal concern. We may consider our distress in eating a genetically modified cow or chicken or feel some displeasure in seeing an unfamiliar host resulting from the more esoteric or misguided attempts at genetic manipulation or perhaps we worry about creating a species that could threaten our current life in some manner. This is largely because we do not see how we may one day be the direct recipient of a synthetically manipulated host.

    Most of humankind is prone to accept established ideas which we were thought or exposed to early in ones current instantiation. Most are ideas that were last exposed to the bright light of cognizant consideration many hundreds or even thousands of years ago. Careful rules of non-questioning tradition and the hierarchical consideration of new ideas have been erected to protect the status quo from the corrosive influence caused by the acquisition of factual scientific information over time. Ironically even specific scientific ideas regarding the possible nature of individuality is guilty of this protectionism. Or perhaps it's not at all deliberate but a natural evolutionary implementation meant to protect the self-aware mind, We may be largely ignorant by evolutionary design. A form of mental protection akin to the shell of an egg for the conscious intelligent self-aware mind. Perhaps some things are best left unknown.

    Nonetheless, the time to break through the shell of ignorance is upon us. Shortly it will become increasingly difficult to ignore the mechanism by which individuality is distributed throughout nature. With the discovery of thousands of planets, all evolved similarly to earth but with different specific circumstances, questions will arise in the scientifically alert nimble minds that are proliferating in today’s dynamic information culture. Questions like; What is the mechanism that places me here to experience life from this body which is a part of this particular planet as opposed to some other? Why are you in that body and not me and on this planet or on some other planet? These questions can be posed from the perspective of each of trillions of living beings alive on or off the Earth at any given moment in time. In dealing with these questions one is almost certainly either in scientific denial or you cling to some religious narrative. You see science doesn’t try to explain these questions because for most of its history there was insufficient information to address them. This is no longer quite the case. We know of the mechanisms and are beginning to develop the principles for understanding how nature universally mediates the mobility of individuality.

    Realize that the collection of species that exist on earth or on any viable planet at any time is the repository of living hosts from which nature will probabilistically naturally entangle a viable form to host ones next instantiation. This combined with the realization that there is a universal phenomenon mediated by the quantifying quantum measure described by ones unique QEF and fidelity of teleportation is what will define your existence in nature for perpetuity. As we are discovering more often than not, just about anything in nature is susceptible to some level of manipulation and with such influence is born control.
  • tonylang
    The ability to realize beyond ones species is a hard-earned capability. Would an ant, an earth species naturally equal to any other, consider importance, if it could, beyond the concerns of the nest? Could a bee realize concerns beyond the interests of the hive and if they could what might they ponder? In what do we, as equal tenants of life, find importance beyond our own immediate concerns, being perhaps the only species in the history of earth-life with the capability to entertain such considerations? What aspect of nature might all life share commonly with immediate local urgency beyond all of the interests of their respective cultures regardless of their location in space-time? Human religion has long invented such a universally shared entity in the form of various Gods. A god by its very description is considered to be a common cause a shared universal concern of all life and of every individual. That which transcends place as well as time. However, might there be a somewhat less mystical more empirical natural implementation which fits this description of common cause for life and individuality regardless of which star or planet or perhaps universe one may live?

    Of local interest for individuals on earth may be concern for the state of earths ecology as a viable habitat to sustain ones current host form, ones species. Also the stability and trajectory of the sun and indeed all matters relevant to our common star. Also our common planets’ fate would certainly top such a thoughtful list. Excluded may be internal strife and politics and such for such cultural local distractions are not often shared by other forms, at least prior to humankind. Testament to this is the fact that when any human, for example, is confronted with the inconvenience of say a thriving bee hive or ants nest or termite mound in ones vicinity no consideration is ever given to which individuals therein are deserving of benevolent consideration or are right minded. Nor is any consideration given by us to which termites can be considered above the fray, which individuals are good or bad hearted among its kind. No, we simply torch the entire culture. This is perhaps as it will be in all such encounters.

    Nonetheless, The LINE hypothesis suggests that there may yet exist universally immutable natural implementations, not unlike a common atmosphere or shared star or habitat. Natural implementations seen or unseen which may be of common importance to all living individuals regardless of form or location in this universe or indeed in existence. Such aspects of nature would be of common importance to individuality everywhere? For example, what might earth species hold in common regard with say indigenous mars-life if it existed? Perhaps matters concerning the condition and fate of the Sun since the survival of both depend on the state of our common star. Not on each list may be concerns for the state of the others eco-system since we are not affected by conditions on the surface of mars or Venus or any other planet. Also present on such a list may be the goings on in the asteroid belt and ort cloud as both could affect all life within their reach. Further, if we consider this same conundrum from the perspective of species separated by the vastness of interstellar space sharing no classically described resources or structures in common dependence what else then might there be to include on such a list? Perhaps the ultimate fate of the universe itself is about all that meets with our traditional misconceptions about life and individuality.

    This suggests that the internal goings on of any species is irrelevant to nature writ large. So then might there be something more? Could there exist in nature considerations of greater and common relevance and dependence? Is there a common list of concerns and implementations that can be made by members of any species no matter where they may be located in this or perhaps any universe no matter their form or local culture or circumstances ? A list of actual, no doubt natural, structures and considerations whatever their description whose existence or state will ultimately matter simultaneously indelibly to all life to every living being. What ideas or entities or phenomena might such a perennial list detail?

    The entanglement spectrum and the imprinting of cellular state information upon metamatter described by the LINE hypothesis during the instantiation period, the lifetime of any individual QEF is such a common cause. This information transfer may be compared to the formatting of a computer hard-drive by its electronic circuitry. In this analogy metamatter is akin to the unformatted ferrite coating of the HD disc surface. During the course of every lifetime the cell, natures entanglement circuit, writes or imprints information via its entanglement molecules to entangled metamatter. This information transferred to the universal repository of metamatter is essentially evolutionary formatting via natural entanglement and occurs during the course of each lifetime by every living hosts specific DNA and entangled degrees of freedom (QEF). As the ferrite particles of a HD are altered or formatted by the computers programmed circuitry via electromagnetism so too is matamatter by the host and its LifeID via the entanglement spectrum.

    As any individual POV establishes yet another place and time in any universe this conservation of information transfer or imprinting upon meta matter occurs and in so doing this universal cloud storage repository of state information stored in metamatter becomes the major driver behind evolution and the emergence of initial or existing host forms throughout nature. Neither distance nor time nor the persistence of any particular matter structure be it species, planet, star, galaxy or perhaps even universe is essential for the continuation or proliferation of this mechanism because the viability of such forms to host life are all that is required. These matter based components are one means by which a POV may be hosted but are not necessary for the instantiation of the individual thus are properly transient and temporary. The instantiation of life by natural entanglement occurs with equal persistence regardless of the location or proliferation of living hosts in the immensity of the cosmos. The only mechanism which possesses the natural description to implement such an amazing feat is a natural immutable universal quantum entanglement spectrum.

    Why should any living being love or care for its offspring, or about its family, about ones species, for ones village and country, or about your eco-system and planet, or even your local Star? How does any individual assign concern to these locally interdependent physical forms? Any assignment of concern in this regard depends on ones species and culture. The sea tortoise lays her eggs in a carefully excavated hole on a particular beach then gently covers them over with sand then leaves them forever to the not often tender graces of circumstance. The bald eagle pairs with a mate for a time to prepare a nest for her eggs and together they care and rare their young to a viable state of readiness for its new life. Human beings have taken the raring of familial members to an extreme mostly as a cultural demand. With adequate enlightenment we begin to extend our concern to other members of our and other defined species and the communities they form and the environment which makes it all possible? All this occurs in the absence of any certainty about the true nature of one’s living circumstances. How are we here? Where were we before? What or where comes next. For some, abject denial offers occasional respite from the unknown, however, eventually no human escapes the wonderment endemic to the conundrum of life.

    The layers of concern we manifest for the various structures that form our existence and upon which we depend for survival and well being at this emergent macroscopic level can be described as a sphere or bubble of concern. This bubble describes all of the cultural and instinctual notions which form an individual’s concerns for its surroundings. For humankind this bubble may be manifested by particularly rich narratives based on instinct, imagination, fear, ambition, perceptions, and as of relatively recently on empirical data. Each host form or species and the individuals instantiated therein may be circumstantially free to define its own unique bubble of concerns which describe the day to day trajectory of the individual’s current life. The stresses intrinsic to being alive for any living being able to fathom such notions are significant and unavoidable. The bubble of concern comes from an evolved need to survive not just physically but also cognitively. Ones bubble of concern contributes to the definition of one’s living reality.

    The evolution of experience which defines the sphere of concern in living hosts often fosters a progressive increase of sensitivity to the environment. Being overly sensitive or overly sensory in an entropic universe may not be the best condition for a living being. Humans have five major senses but this by no means defines a limit for viable hosts. We need not think about all which we cannot sense just as do other creatures that share this ecosystem with us. What of the world might a being with more than five senses glean? Are there host forms possessing sensory implementations that permit a being to sense the state or condition of its ecosystem perhaps as a kind of emotion? Or sense the presence of a POV, the presence of life itself? It is difficult to imagine what experiences there can be which you can't, however, the fundamental natural implementation of life in this universe, natural entanglement, which brings no experience of its own, does indeed accommodate an untold diversity of living forms and their emergent skills and accompanying spheres of concern limited only by the metaphorical imagination of nature herself.

    However, Just beyond the proverbial skin of this sphere are the natural laws of cause and effect that determine when where and how any living being is located in space-time, ones position-of-view (POV). A POV, instantiated by natural entanglement, is the rigid framework which defines and drives the presence of individuality throughout this universe. With distance being no barrier to this teleportation channel, as living hosts emerge and evolve out of the isolation of initial living forms, biological or otherwise, and as living hosts evolve to permit survival of the entangled state and experience, these also define ones unique sphere of concern centered upon ones the POV, upon you. The POV is the naturally teleportable definition, the instantiation, the kernel, of one’s individuality in this universe.

    This behavior of concern or caring, whether instinctual or cognitive, although mostly culturally defined at the emerged host level, fundamentally derives from the basic natural cause and effect implementation of life itself, an implementation about which most life on earth today is utterly unaware including humankind. The imprinting of metamatter caused by the instantiation by natural entanglement that defines you, the individual, your position-of-view, is the source of this perceived concern. For offspring of basic hosts, like a single cell that divides to create new cells, it is only the cause manifested from the imprinting or tuning of metamatter by similar genetic progeny that renders apparent attachment to offspring. For a cell or microbe it is nothing more than the evolved tendency of like to seek like.

    Metamatter imprinted by a newly available host’s progeny enters more easily into an entangled state with that new host, thereby increasing the value or scalar magnitude of the individuals’ (QEF) fidelity of teleportation (FT) and thereby ones reinstantiation prospects with similar species. Species evolution simply selects for this similarity by genetic variation as it does for many other properties. It gives the species an evolutionary benefit via access to non-local cellular state information stored in more similarly imprinted metamatter. The drive to proliferate ones’ own similarly imprinted matamatter is advanced by spreading ones current genetics (DNA), however, genetics are local to ones current position in space-time. Whereas the coherent state information stored in metamatter during the course of each lifetime, made accessible to living hosts throughout nature via ones uniquely defined natural teleportation channel, is one major driver of evolution throughout the cosmos even when the viability of local circumstances catastrophically cease to exist. Today most understand the drive to procreate only as the individual’s dedication to host offspring or to species. Seen from humankind’s evolved cognitive vantage point we narrate this effect as love and caring described by a lexicon of emotional terms, from these perceptions emerge community, religion, politics and culture.

    In what order does the instantiation of life by natural entanglement select, and assign, any individual QEF to ones next host form, among the great diversity of genetic lineages on Earth, and perhaps elsewhere in this universe? As we live, we fixate on our current host species and its genetically related ancestry, and its future prospects, not realizing that one’s current defined species may be only one of many viable forms that have hosted your POV in past instantiations. In the short term, this diversity of lineages that has played host to you, to your position-of-view, may very well include a few different species and near-species. However, in the longer term history of earth-life, for any individual, ones host history may include a great many, often very different host forms. Further, Parents and ancestors are current and bygone individuals (QEF’s) that were also hosted by Earths tree of life.

    The degrees-of-freedom (DOF), of the QE spectrum, and their implementation in the LINE process, may reveal underlying complexities which defines categories of QEF types which determines which host forms are able to instantiate certain QEF types. Ergo, not all QEF can immediately be hosted by all forms. A single cell may not be capable of hosting your QEF. Metaphorically speaking, as your FM radio cannot tune a TV signal. Not because your QEF is in any way dedicated specifically to the human form, but due to the underlying defining structure of the QE spectrum, and the underlying metaverse (Hilbert-space), and the topographies of their interface with this universe. Such a determination will require invasive research to discover the truth of it. Because this is a nuanced, and not at all as simple a thing as it may at first seem. Further, the LINE hypothesis suggests that QEF are described by the DOF’s of the QE spectrum, which are governed by nuances of the underlying metaverse. Consequentially, only a certain range of the entanglement spectrum may be exposed to any particular universe. Ergo, the QE spectrum may be essentially pre-filtered by overriding conditions, and circumstances, to expose this universe to only a certain band of QEF. That is, of potential individuals, which is then further filtered, or tuned, by more local circumstances described by ones fidelity of teleportation (FT), which instantiate these available QEF to compatible viable hosts. All of this contributes to the natural description of how you came to be what you are, where you are, and what comes next.

    Like you, each ancestor, via their instantiated hosts, have participated in the local dissemination-of genetic information through various processes of procreation. More significantly, however, also by storing its cellular state to entangled metamatter over the course of each lifetime. Ones ancestors are bygone lives of individual QEF’s that, like you, were temporarily instantiated to hosts that contributed genetically to yours, in any given instance of life. However, more influentially, also by contributing to the universal repository of evolutionary information. This tuning influences ones FT value, and future prospects for reinstantiation. Each of those individual QEF’s are also on their own trajectory through the universal network of life. Via this mutual, cellular-QEF tuning of universal evolutionary information, individuals of ancestral QEF’s, could cross paths with your trajectory again. Realizing and comparing the DNA mediated tree of host forms on Earth, with the natural teleportation network that governs the assignment of individuality to those forms, will no doubt be a new and unfamiliar cognitive hurdle for humankind. If you feel evolution has been rough going, then buckle-up.
  • tonylang
    The LINE hypothesis suggests that there is no multiverse, however, there is a metaverse (aka Hilbert-space). In a metaverse, universes evolve by a process of Darwinian evolutionary natural selection, not unlike the evolutionary process we see in viable ecosystems for life in this universe. The universe or verse in which one finds one’s self is but one viable species of verse on this tree, or complex of verses, which has evolved to host individual life by its unique laws of physics. Many verses will not have this fortune of circumstance. A verse with no evolved mechanism by which to instantiate individual life may nonetheless inherit this capability from the evolutionary information imprinted in metamatter by other compatible verses which in turn inherited likewise from others. This is different from a multiverse in that, within the metaverse, verses may actually evolve, inherit, and in a sense compete, and even consume one another for existence, not unlike the way galaxies do, all on a time scale which makes the age of one's universe seem infinitesimal by comparison. Within the metaverse complex, the state or health if you will, of a verse is indicated by whether it is contracting or expanding and the rate of each. So where does the big bang fit in?

    The metaverse is essentially an ecosystem where verses are the evolving species. However, resist the temptation to over extend this analogy with life as we know it. The goings on in the metaverse is governed by physics that are necessarily unfamiliar to the physics within any universe that it may produce. What we refer to as a big bang is but one of many metaverse phenomena which only hints at the goings on in this unfamiliar realm of nature. The appearance of the big bang to us as some kind of an explosion is as nondescript as the way a rain drop falling from the clouds may appear to a microbe caught therein, attempting to describe the hurricane, planet and solar system from which the drop emerged. In this, the microbe is just along for the ride. The degrees of freedom at work in the metaverse are far from fathomable by humankind. This is not a limitation of intellectual capacity, but rather a limitation of the type of intellect that is possible in ones universe.

    The unique laws of physics of different verses manifest not just fundamentally different types of host forms, but also their very own unique type of position of view (POV). This is due to the unique degrees of freedom and topographies which define a particular verse and its laws of physics. Further, as in our universe, all life in each unique verse can only instantiate that same unique type of POV to become the kernels, the seeds of evolution for any living individual hosted by that universe regardless of the specifics of the indigenous ecosystems therein. Each viable verse is a different realm for instantiation and produces living individuals which can evolve to fathom its own living circumstances in that verse as humankind may in this universe while finding the nature of other verses impenetrable. You see, intellect is but one tier of an inverted pyramid of capability which evolves from the seed that is the instantiated POV. However, in the rich pallet of possibilities for life described by the metaverse, there are no doubt verses which evolve living beings which can transcend some of these limitations. This may ultimately prove to be such a verse.

    A Metaverse by its hypothesized nature permits universes like ours to evolve with uniquely tuned degrees of freedom that seem too specific to be randomly emerged, this is because they are not, they are evolved. Like species verses do not lose evolutionary information like inanimate entities do. As in living beings, via the entanglement spectrum, each verse can store and inherit evolutionary information imprinted by its living tenants to metamatter. This imprinted cloud-storage repository of intra, and inter-universal evolutionary information mediated by natural laws of conservation of information, such as the monogamy of natural entanglement, not only guides the evolution of species, but also influences the evolution of verses to become finely tuned, unique habitats for life in the Darwinian complex of the metaverse.

    Ones’ gene pool defines a region on the Darwinian tree of earth-life. The LINE hypothesis suggests that this region encompasses all of those host forms which have contributed genetically to your current form, and also to the metamatter imprinted by those forms during each instantiation. During each lifetime imprinted metamatter defines, or tunes, the individuals' fidelity of teleportation (FT). Ones’ gene pool encompasses all hosts possessing similarly converging genetic underpinnings to your current host form, because you did not instantiate your current form entirely by random accident. Each individual QEF, alive in its current host, has empirically earned its right to occupy that host.

    A species may have wide and relatively secure genetic foundations and circumstances in its current ecosystem, or not. For example, the individuals in a newly founded Mars colony will clearly have no genetic roots in that habitat such as it is. Even if we terraform Mars with the nonbiological conditions need to sustain earth-life, air, water, temperature, pressure etc., the probability of a colonists' position-of-view (POV) re-instantiating, being naturally born into this Mars ecosystem will be very low. However, if we managed to seed the newly established Mars ecosystem with earth-life, whether human or not, then this will slowly but progressively increase the chances, over time, of hosting similarly tuned individual LIFEID's to local hosts.

    The FT of any host for life within one's gene pool is not reduced by travel, or relocation in space-time, because, the mechanism of instantiation, natural entanglement, is distance agnostic. Of course species as a group are defined by their population, and as reinstantiation is a statistical mechanism, not unlike a lottery, likewise each host which comes into existence, whether on earth or on Mars, like a lottery ticket, has some chance, in this case defined by its calculated FT, to host a particular LIFEID, even if that LIFEID was last instantiated, living, at a location whether inches, miles, millions of miles, billions of light years, or even universes away.

    Ergo, if a new Mars colonist died on Mars, or even in the space between these, or indeed any, two habitats for life, that individuals FT remains unaffected by its location. That individuals LIFEID remains highly likely to re-instantiate, establish a new POV, on Earth simply because that is where the most opportunities for similar genetic natural entanglement for any indigenous earth-being currently exists in this universe. Ergo, genetic home, while it remains viable, always calls to the individual.
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