A possible explanation that seems to fit all the experiments
on magnetosphotophoresis, which is the collateral effect induced
by the rapidly shifting NMR magnetic field, due to pulse chirp-
ing the magnetofluxgate near the NMR frequency, which splits up
the flow of magnetic monopoles and causes single monopoles to
get trapped in blood plasma, esp. for the magnetosome particles,
has been researched.

A fluorescing light source such as provided by fluorescing
quantum dots, would be necessary to keep them from escaping. The
effect doesn’t show up when using an external source of magnetism
or in a slow varying magnetic field, and it doesn’t show up
(either externally or internally) without a light source.

Labeling blood plasma cells with inorganic cellular probe
'quantum dots' that fluoresce when energized by specific
frequencies can help to de-luminate the harmful inten-
sities of Cherenkov radiation during hypertranslation and
restore the lightbody health contained in memory water.
The glow intensity component mentioned in the link,

http://home.comcast.net/~samuel_rans...ron_states.htm

contains a spectral region of radiation requiring some
frequencies to be filtered while others, such as the 'interband'
types, require enhancement and/or filtering by each 'occupant'.
For such a 'filter' to be designed, it is recognized that
the spin of the electron is only weakly coupled to its
"charge degree of freedom", and must be "tuned" in order
to limit the phenomenon of dephasing of noise in the
surrounding and programmed VR environment.

The definition of a "qubit" would be the "information that
is contained" by the light source or quantum dot that gets
"fluoresced", thereby destroying the "qubit" in luminessence
when the quantum dot becomes activated by an RF signal. These
signals comprise part of the information contained in memory
water that gets erased by the fluorescing quantum dot.

Bandwidth of the fluorescing quantum dot variety can thus allow
the further investigation of what some particular infolded
harmonics can lead to the discovery of dormant DNA w/degenerate
Goldstone Boson variety, in terms of both secondary spectral
thermoluminessence and radiative amplitude (temperature dependent).

While the REAL part of memory might be contained in dephased
memory water, the VIRTUAL part of memory becomes the new
"working part" or "erasable" part of memory that would
be required by the dephasing of white noise within the
VR environment. Some kind of model architecture for a human-
type "VR assistant memory", that features the most important
aspects of growth and self-organization in the human biogene
would be in order here, while a zero-time reference point,
used to establish the occupant in REAL space-time, preserves
the DNA imprint of the occupant across 4-space.

The part of the negative or "unexposed" DNA imprint is also the
part that can be used for artificially exposing or VR programming
the conscious environment in projecting one's VR assistant memory
into the field space, using the same zero-time reference point
as the memory water. This is accomplished by INFOLDING the
fractal-pulse-chirped quadrupolarized positronium beam with
an artificial phonon/multiplexed version of the VR "memory",
external to the near field, yet giving the human the ability
to become a "more fully exposed negative DNA imprint" within
the "supra-conscious environment of parallel worldlines".


American

"A fair field and no favor"
-Toasts and Declamations