What is a living individual and is it naturally universally mobile?

[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]

The UMI-LINE Framework Publication; https://doi.org/10.5281/zenodo.19193894

[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]

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 next fertile undiscovered frontier of science is the study of how the individual (you) naturally inhabit this universe. This topic speaks to the really interesting question of how any life, you, came to be where you are in the form that you are. Consciousness, self-awareness, sentience are evolved attributes had by very few forms of life in earth’s ecosystem, yet all are just as alive in nature. Such attributes cannot be relevant to either nature’s fundamental implementation of life, to being alive, or to experience. Experience may be enhanced by these attributes as they evolve in more complex hosts or species, but the phenomena which establish an instance of life likely brings no experience at all.


The position-of-view (POV) as described by the instantiation hypothesis is implemented by a fundamental property of nature called natural entanglement. This process produces the POV which localizes you in your space-time, whether you have five, one, twenty or no senses. Regardless of what or where ones living form may be in this universe. Effectively ones POV is the target for all of the sensory information we call experience. Any beings lifeID is temporarily localized to its host body by the naturally occurring entanglement between its physical host such as ones cell(s) together with a non-relativistic form of matter called metamatter (in Hilbert-space). The POV of each individual life can be represented mathematically by its unique wave function. This wave function is a unique solution of state for the individual in space-time and is the term missing from many of our quantum mechanical solutions. The POV is nothing less than the mathematical representation of a living being.


In life the POV brings no experience but only that which may have an experience. In nature a POV is the mathematical representation of a lifeID established either by entanglement of a single cell to metamatter, or alternatively by the heterodyning of multiple entanglement cells (EC) to metamatter. If you are in fact alive then your composite lifeID and its position-of-view together constitutes your being regardless of your physical state, form, condition or location in space-time. If the entanglement hypothesis accurately depicts the reality in this universe and the entanglement molecule exists, then it represents the most fundamental physical component of life as we know it. Like the Top-Quark, or the Higgs, the Ether or DNA, the entanglement molecule may someday be isolated and identified either in the cell or in the environment. or not. Either way we may learn something along the way.


However rare or ubiquitous host species for life may actually be in this universe, they nonetheless likely emerge via countless varied means and circumstances throughout this universe or throughout existence. Most can never be imagined by us. The implementation of host species in any particular environment in this universe is only one component of a much larger, grander implementation, that of individuality. We have become too accustomed to, and somewhat tunnel-visioned in, our understanding of life as being only the classical functional chemistry of the physical hosts that emerge here and there on this planet or in this universe. Individuality however is the original, the indigenous component of life. Like snowflakes, living hosts transiently come and go as they assume forms too varied and randomly influenced to predict or to repeat. With humankind being the very visual species that we are, we are once again confounded by the visible and captivating facade of life that reflects visible light, namely the physical, electromagnetically congealed component of the living individual, the species. The ongoing cognitive immaturity of humankind is engendered by this limited or flawed understanding of life.


The only life on Earth is the living cell. The lesser point being submitted for your collective consideration is that such attributes as consciousness, self-awareness, sentience, intelligence, etc., concepts already defined by others, are emergent skills or capabilities arbitrarily ascribed by observers to particular emerged composite hosts (with EC) and therefore cannot be fundamental to natures’ basic implementation of life. Currently and for billions of years on earth %99.99… of living hosts for life were and continue to be either single-cell individuals or non-emerged (no EC) collections thereof. To truly understand what life is and the mobility of its fundamental component; individuality, and the natural principles that govern and influence its instantiation, we need to consider only the single living cell. Viewed as an individual, a property traditionally ascribed only to human beings, the single living cell forces us to come to conclusions we never would with our usual limited perspective.


The first person position-of-view we refer to as individuality (Life) in this universe has emerged from a very basic natural phenomenon, namely natural quantum entanglement, a property of a naturally occurring molecule. Clearly like all other phenomena or processes or reactions involving groups of atoms and molecules these can also be categorized as being chemical in nature. Natural entanglement is the basis for individuality. When one is misguided into thinking that life is only the physical component of this natural entangled relationship a great amount of confusion and misconception will be the inevitable outcome. The first casualty is the dismissal of the mobility of individuality in this universe. As is usually the case we can live just fine with all of our misconceptions as life makes few demands on the intellectual awareness of its tenants. However, as we all know advancement requires enlightenment and the time for our further enlightenment in this regard grows near.

The classical ideas of thermodynamic entropy although essential in many practical technological applications, cease to exist at and below the atomic level. So attempting to describe the existence of life in these terms requires some implausible assumptions. Firstly one must accept that in nature individual life (you) is only defined at the cellular level where DNA is functionally implemented. In other words one must believe that nature does not have a mechanism or basis for distinguishing individual life once that individuals DNA has dissipated. This suggests that you and I and all instances of life begin and end with ones cellular DNA. This is logically and empirically inconsistent.


There are examples of living individuals with identical DNA, twins who are clearly not the same individual even when they are physically connected as are Siamese twins. More pointedly however, If any one or all of your trillions of cells were responsible for uniquely defining and distinguishing you from any other living being then separating even a single cell from your holistic body would cause you to lose your current identity (become someone else) or else terminate you as a living individual. However since all life in our ecosystem loses, replaces, transforms and exchanges our entire body mass daily over the course of a few short years, this also invalidates this belief.


Thirdly, this untenable notion violates the principle of re-occurrence of natural phenomena which states that for any natural phenomena to occur there must exist natural mechanisms which by their existence will also permit that phenomena to reoccur given appropriate circumstance. In other words whatever caused the big-bang can cause other big-bangs. Whatever causes nova and super-nova can cause other instances of both. Whatever caused and permits life here can and probably has caused life elsewhere. Further, whatever caused you can cause you again. The universal basis for this postulate of consistency in the laws of nature is the observed consistency of the fine structure constant in this universe.


Any individual life that can occur can reoccur. This last point mandates that you do not end with your DNA/RNA or with your thermodynamic, entropic biology. That nature must indeed have mechanisms known or unknown which serves to define or instantiate you from all other existing or possible instances of life, and such a mechanism must be an essentially immutable and reoccurring property of either this universe or of nature. This feature necessarily exists below the cellular and molecular level into the quantum realm.


To date the most promising structure yet discovered which displays some of the features and function consistent with those predicted by the instantiation hypothesis for the entanglement molecule (EM), while perhaps falling well shot of complete equivalence, is the Fenna-Matthews-Olson (FMO) complex. This photosynthetic antenna complex is the naturally occurring molecular structure responsible for the photosynthetic non-classical conduction observed in living plant cells via natural entanglement. In green algae it operates to overcome the otherwise inefficient latency of classical mechanisms which would result in a devastating loss of anti-entropic information needed from sunlight for the continued evolution of viable hosts on this planet.


Likewise, a similar natural entanglement antenna complex describes the predicted entanglement molecule which instantiate the living individual to available hosts wherever they may emerge in this universe. This Entanglement is between the living hosts (cells) and a form of matter (metamatter) in Hilbert-space made accessible only by the non-locality, non-relativistic reach of natural entanglement. It is indeed a true testament to the amazing ingenuity and flexibility of nature that such an implementation is not only possible, but naturally emerges, for life may not exist without it. This instantiation mechanism is the most plausible solution to the conundrum of individuality in this universe posed by the scenario of this thread.


If the entanglement molecule indeed predated the cell then, structurally if not functionally, it must be of a different design than the FMO complex. The FMO is a protein based structure assembled from complex amino acids and likely evolved within the cell here on earth or planets nearby. To predate the cell the EM must permit natural entanglement by utilizing a more fundamental elemental design. The entanglement molecule may be one with which we are already familiar.