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.
