User:Quvez/Late-life mortality plateau

Mortalty late-life expectancies current stats globally to filter down genome survivals curve in cohort to add a chart asistaning extimate corosponding solor revolutional evolutions. Each Solor revolutions includes studies from calulated tools in facilities to allow this accuracies to broden the stopage vs the increases of holocene events that may or may not change current biodiversity that allows ethic demographic biospaning growth to increase validations of mortality rates early in predictable measurements pretaining to a mortality life expectancy table.

Early rates concurrent to survival curves are documented and stored to anylize to formulate the changes that due calulate a risk factor in curve change increases due part in longtivity measures. The Risk factors due play part to table back gentic genomes cohort first born formulation scene. This is my studies as it is biblicle as well. Today's match for intellegence regarding longtivity would seperate a host of holocene creations to slow or to monitor the longtivity Late-life mortality plateau occurance flow. This could be catorgorized by event, chance imprinted developments of cohort generations to other factors that biologic diversity may have played the rate of ageing less or aging faster or mortality rates increased or mortality decreased.

Each Rate of mortality has a chart to element cohort rates. This is not new, it has just been dormant like the vallicilla zorvex virus that lays dead in the nerve ending of a ganglion Axon waitng to communicat its awaking or "trip up" starts the complexes in gravitational polorized by human events that nerve stimulus can trigger a bout of dormant releasing this in the nerve endings. So any the same as rates of any enegy fatal decay process, it can accumilate to complie informations on viewing molecualr counts and reviewing cell divisions regarding the abilities to be able to do so. This may play to significant roles as chemicals balance out since the eariest rates of birth occured. Chemicals that parent rely and child dependencies on cell life divivsion factors is another part of longtivity.

The faster we process protiens the faster we endure the aging track to decay it is simple math in words and recognizing chemistry in anatomy and environments of course our entire makeup DNA and the ancectory cohort gene profile.

So chemicals that secrete after long uses of protien photosynthic naturally can become dependance on this id loss of parent divisions that rely on this process can effect the less likey to keep its ability to the prime actions as at one time early in life. Each chemical in our bodies has a atmoic weight life. It carries a significant role to what chemicals on the environments have and what our cohort tree has been given as cell reproductions to concievements and conceptions.

This is sharing the elements of chemistry. Each and every tissue is made up of a chemical process. From extrernal to internal. Each has a atomic life expectancy in bonding divided anatomy of cell divisions that make up are DNA chains given the placement of the very beginning to strucural building blocks such as our chains of human events occurred, the gravitations, the pools of demographic water bodies earlier, the decay mechanisms that thrived to become a curve attraction it later carries the gene needed to be passed on as imprinting occurs in atomic chemistry.

Like the Sun's Solar beginning, a gas mother spiraled to spin and spin on the rotaions of gravitonal mangnetic make up of our planets.

This too occurs in our behaviours to conclude the most abundant mineral closet to mom is the atomic mineral that each is divided by rotaional birth, the break aways of creation, the cores of hot plasma enriched atomic ore it is called after it has cooled.

Our planetary birth rights our decided on the amounts to balance the child dependencies that require the counter atomic mineral and weight decay process and thus it then evolutions occur upon cooled plasma to core a magnetic rotation spin down and decided by rotations weight, given plasma distribution in each planets quantities.

So the values are the same in reviving dead end nervlings that store vallcili Zorvex virus the chicken pox families. Can our existance communicate with the elements besides talking languages to understand sculptured squals to pefected tones of indications to absorb exterternal receptions of human speech? Yes were are the last to be given this, if is disputed no answer shall lie on this tool, why? mortality rates late in life concludes we our the only spcies on this planet to absob all chemical specifications to our storage cells A Axon drive i call it, it is only us and only we as human beings can decode what it is that lays ahead, presence pretense past and later on. Why? we imprinted all the nessisary binary codes in chemistry throught out our humanstart up existances, we were made to decode all life forms in our surounding Solar system. Basically our own. Other chains of Solar mineral make up is a task to be careful when space travel occurs as well. Mars has a slow rate of less mineral abundances it has a molecular mineral weight in atomic life shelf rate. Much less than ours. Why? Therory questions the make up of our selfs, were do we come from? and so on. It is no differant to put proper formulations to ensure the magnetic porizations and chemical balances given on Earth in what was given to us by reproductions of Solar rotations to evolve to evolutions on this clock rate. I hope my decoding skills is worth your time as well.Lauren J. Hendry Selkirk MB.