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by
Cpt. Danny B. Catselas Burisch
LOTUS PROTOCOL OVERVIEW
In the early part of 2001, information was leaked concerning Dr. Dan
Burisch and his development of a new protocol for defining a "Genesis"
mechanism, which could have profound effects upon our future human
evolution. The protocol was broken into six parts - seven if you consider 4a
and 4b independently. Dr. Burisch gave a strong warning about the
potential dangers should this protocol be converted into an actual
experimental program.
Dr. Burisch’s Warning: Due to the potential for destruction of a fully
functional and conjoined L, it is my suggestion that any direct evaluation
be conducted in biocontainment levels normally associated with potentially
hazardous "foreign" materials (AKA: another name for a "Native American
baby").
The vitality of the L should not be underestimated given its ability to
conduct graded continuous creation/proliferative cytogenesis and the common
instances of ancient DNA (aDNA) revitalization.
Update - August 2001: From the recent events that have unfolded, I think
it's safe to say that Dr. Burisch is steadfastly refusing to help them bring
the halves together. His commanding officers are furious, as well as the 'defacto'
project leader, Debbie. As the project moved forward documents smuggled out
of the project show that Dan has risked his safety and his life by refusing
to provide the 'powers that be' with the keys uncovered in the Lotus
research necessary to alter the human DNA and RNA and move their project
forward. He lives and works under heavy security; and there is documented
evidence that they have orders to shoot him if he refuses to follow orders
or attempts to flee.
LOTUS PROTOCOL
- Sections 1 through 6
Contents:
Return to Burisch
Return to
Origen Vida
Subject: Protocol Section 1 of 6
Sent: Thu, 1 Mar 2001 21:13:01 -0800
To: mj01
The following is the first of six sections, in this protocol. The parts will
be sent at a rate of one a day and will be sent out of order for security
purposes......Debbie.......
SPECIAL MISSION RECITATION #01-04
To my anticipated readers, the Platonic Academy Admonition:
"Only He Who is
Familiar With Geometry Shall Be Admitted Here!"
If I know little, as a man upon this earth, I realize that the
Ani papyrus
speaks truth to each of us when reflecting that we are "...soul(s)
inside of
light, appareled in flesh, designed and created by divine forces." You may
have expected, by now, to be (dutifully with me) chanting a neo-Darwinian
mantra, to written words only surviving an allegation of plagiarism through
our little scientific society of self pleasuring. Rather than boring you
with a "premature" outcome (pun unfortunately intended), we are instead to
travel back to the earth's first age, once called the time of Ocelotonatiuh.
What will we see when we gaze into the smoking mirror of Tezcatlipoca, when
we are face-to-face with Quetzalcoatl? Will we see the beauty and grace of
the introspective mermaid or the slowly wasted form of Narcissus? I assert
the we will each see our unique reflection under the duality of nature,
either of our light or of our vanity, while experiencing the bold truth. To
the one true God, I bow in reverence and humbly announce that I come in
peace.
DARWIN COULD NOT HAVE FORETOLD THAT WE ARE DESCENDED FROM VIRUSES AS WELL
AS APES (Patience, C., et al., Review, Trends in Genetics, March 1997) And
so this discourse begins, save the contention that we are beholden to a
heritage with the genetic sequence to 'monkey around', well...okay...the
readers all know about "1+1=1plus", but that is another story, more meant
for the "land of dreams."
Many of us have taken refuge in the RNA paradigm from a "prebiotic soup",
mushroomed from raw material, and stand that RNA replication must have been
the second phase in the development of a so called "RNA world" (Annotation
from Reference, and used to follow: de Duve, Christian, "The Beginnings of
Life on Earth", American Scientist, 09-10/1995). From thence,
DNA is
theorized to have been put in order and that it announced the refinement of
a cell's information system. DNA was mystically birthed from the interaction
of a myriad of protein enzymes communicating with RNA, which in turn both
resulted from and was dependent on a number of random mutations. Also as a
result, and at the same time dependent upon, the protometabolism of the
early cell began its dance of life. The plasma membrane's constituents are
factored into this mechanism, factored even in those instances where
theorists regard cell membrane construction from the standpoint of
consecutive phospholipid integration by rotational augmentation. The
tautology implicit within the abhorrent attempts to justify these beliefs
through thioester logic and the explicit teleological import of the argument
itself (begging for an autogenetic pocket-watch with autotelic expression)
has been an object of snickering within the chamber of our quiet group for
some time. It's just technical enough to believed 'qualified' for public
scientific debate and just referential enough to meet the criteria of
weights and measures.
[Excuse my subtle plug for SI - I felt the hard working people at
IP needed
something after that little "Gallo"-phile arrangement, relative that
IP (ah,
I meant LTCB) isolate! Good God, something flies through their window and we
still get part of the patent! Bernadine, Varmus, juice, perks, and star
chambers! I love it!]
This atheistic approach allows the conceited to continue to devalue
the complexity of the life-system. Pocket-watch parts have been found, and
cellular membranes have been inferred. (Astronomical indication of
preliminary cellular membranes inferred from icy mixtures of water,
methanol, ammonia, and carbon monoxide, et al; Quick Reference Example:
http://www.cnn.com/2001/TECH/space/02/20/chemistry.of.life.ap/index.html
.)
So, where do we go? Have we attempted every solution to the riddle, short of
applying religion? No. We are nearing the attempt to apply other ones, but
you'll have to keep reading.
As a matter of REQUIRED reference, the origins of life in the form of
bacterial cells (publicly) currently dates to a little prior to 3.9 Billion
Years Ago (BYA), quite an event for the early Archaean Eon, with promitochondrial endosymbionts seemingly entrenching to become
mitochondria
(proper) by 2 BYA, terrestrial cyanobacteria appearing near 1.4 BYA, and a
significant taxa diversification of photosynthetic protoctists close to 1.3
BYA (correlated to the acquisition of symbiotic photosynthetic plastids).
(Annotation from Reference, and used to follow: See: Margulis, Lynn,
"Symbiotic Planet" [2000] and "Five Kingdoms..." [1988]). Is it not
interesting that the issue of the possible polyphyletic origins of those
plastids remains open, yet dogma is pronouncing near certainty for the
predecessor of mitochondria, or is it, really? Let's take a close look at
the contentions of Dr. Margulis. In the search for mitochondrial origins,
the varieties to look toward for guidance (according to Margulis,
"Symbiotic...") would be either bdellovibrio (a small 0.3 micrometer
pseudomonad that is aggressive to larger bacteria and even burrows into
them, which respires its food sources and releases carbon dioxide) or
paracoccus (an oxygen respiring micrococcus of diameter 1 micrometer
[individual sphere]).
The problem, here, is this:
As late as 1981, citations of Margulis' work carried statements that a
likely category of mitochondrial precursor was an anaerobic phototrophic bacteium (purple nonsulfur
bacteria, that synthesize organic compounds by
direct incorporation of carbon dioxide). A big difference? You bet your
life! A crack in her theory? It is certainly a problem. The crack is not
found in the relevance of the new biochemical findings, alone. In the time
from 1981 (really somewhere before and it was then cited in texts such as by
Wallace, King, and Sanders in "Biology: the Science of Life", before fourth
edition) until now, research has been progressing on the contents of
mitochondria, and a striking resemblance has been found between those
contents and those of bdellovibrio. So, it appears that Margulis has moved
her "chip of support" from the basic biochemistry of the purple nonsulfurs
to the pseudomonads. This is the mistake! (Not that the purple nonsulfurs
were the end-all in the debate! You will soon see, quite the contrary!)
Under the current line of thinking, as the mutualistic symbiosis progressed
between endosymbiont and host, redundancy was screened out of the
endosymbiont.
The endosymbiont no longer used a large portion of its
biochemistry (and conversely its genomic components), as independent
existence allegedly became a thing of the past. Does this mean, necessarily,
that the remaining "left over" biochemistry correlations (no matter how
integral to the functioning of both the mitochondrion and that of the
counterpart under question) must posit a singular direct taxonomic linkage
between the two? Nope, not under serial endosymbiotic theory. Can this be
akin to "cell apoptosis" for the theory? No. Not just yet. Is the
correlation between the two (that is diminution of redundancy) correct?
Probably so. The complementary behavior between mitochondrion and nucleus
would infer as much. Is the origin of the relationship, a macroevolution
from a pair of independent organisms necessitated for us to now see the
refinement from redundancy? No. What say you of evolution? Are the first
acts of progressing organismic metabolism (a shared dance of catabolism and
anabolism) one imbued with a negotiated hyperbolic peace between predator
and prey (See: Margulis, Lynn, "Microcosmos", 1997) or does life follow the
apparent path of the Universe, a series of transparently stoic acts of
Cosmos from Chaos? (Pick up a text of a creation myth.) In defense of one or
the other, I would reference to "
http://unisci.com/stories/19992/0621995.htm"
for hierarchy through "productivity" (Drossel, Barbara, University of
Manchester in England), conservation of gene clusters (Andersson, Siv G.E.
and Eriksson, Kimmo "Dynamcis of Gene Order Structures and
Genome Architectures", Department of Molecular Evolution, Evolutionary
Biology Centre, Uppsala University, Sweden; as published on the internet in
http://www.ima.mdh.se/personal/keo/Forskning/Gene
,
http://www.ima.mdh.se/personal/keo/Forskning/Orders0410.htm ), and a refutation to the
Dawkin's "Selfish Gene Theory" as
published by Unisci "Daily University Science News" (Efros, David R., [New
England Complex Systems Institute], with an opinion defense by Dr. Bar-Yam, Yaneer,
04/25/2000). I remain prepared (and would encourage) to debate the issuance
of my opinions, relative the relevance between the aforementioned orders of
magnitude.
Cpt. Danny B Catselas Burisch, Ph.D. (U.S.M.C., Ret.)
END PROTOCOL SECTION 1
Subject: Protocol Section 2 of 6
Section 2 for your enjoyment........ :)
To: mj01
Debbie........
"I believe that the scientists, including Margulis (but no mistake I have
great admiration for her work), are too busy focusing on the newer
biochemistry, then jumping from one foot to another in the search for the
closest present biochemical counterpart, all the while praying that Gregor
Mendel will justify their beliefs with results of Polymerase Chain Reaction.
I have been guilty of the same.
As little as two years ago I would have presented the following, in reaction
to the above allegation:
"I would posit that it remains entirely possible that a completely different
variety of eubacteria may have been the precursor (of mitochondria) and that
the present likeness in biochemistry is the result of elimination of
redundancy: that we are presently looking at the vestigial biochemistry of a
variety completely different than what we would associate to present
examples; that the present physiology of the mitochondrion has no present
counterpart, or perhaps it (the unknown organism) may be the precursor of
more than one of today's phyla (and the mitochondrion).
To make matters worse, the
protocists envisioned for study may have a more
complicated history than the promitochondria. What their past incorporation
of endosymbionts will mean to their present behavior is largely unknown. For
these reasons, various bacterial types will be tested against various
protocists, and we'll look for patterns in their responses. As we were able
to find patterns involving the oxygen and salinity content and selective
incorporation of either a cyanobacteria or a respiring one, we may indeed
find such patterns involving the retention of such varieties. Should such
patterns develop (and they may do so over a wide span of bacterial and
protoctist types), we would then correlate to the known paleobiology. At the
end of the day, we'll relate back to the biochemical sequencing and use it
with a purpose that doesn't put the cart before the horse: verification of
relation and redundancy elimination. Some scientists are still trying to
build a cell from an at! om (their biochemistry), and are unable to do so.
We'll take a little more humble approach: ask the cell questions and maybe
it'll tell us a little about why it is the way it is.
It is also entirely likely that we may find that the selectivity under the
aforementioned criteria (salinity variance and oxygen infusion) breaks down
when studying potential endosymbionts. There may be no such defined patterns
under that criteria. This may mean that our selection criteria was off, that
the current endosymbionts somehow preclude further relationships, or that
the precursor(s) of mitochondria (and possibly chloroplasts) are something
totally different, something completely (forgive the term) "alien" to
today's world."
In this 1999 quote, taken from my personal diary, I argue with myself (while
committed to the evidence of endosymbiosis) about the next phase in research
from Fresh-Brackish-Marine (FBM), results from which have been previously
communicated and will be moderately restated in a few moments. The thought
begins with the idea that similarity between mitochondria and eubacteria may
be a function of an elimination of redundancy between the endosymbiont and
host, then ends (after an overly verbose passage...nothin' unusual there!)
with the notion that a present day counterpart to the original endosymbiont
may not exist. The idea stream was built upon the mistaken thought that
there existed nothing special at the point of apparent random food
selection, 0.031% marine salinity at +/- oxygen infusion. "Mission Genesis"
was to follow, carefully noting retention times and parameters altering phagocytic responses.
Did the 0.031% data mean nothing more than a cold number solute divided by
100? No. It turns out that there exists a relationship between 0.031
(conversely as the fractional solute equivalent 0.00031) and the
Sequence of Fibonacci (Reference to mathematical theory:
http://www.ee.surrey.ac.uk/Personal/R.Knott/Fibonacci/Fibnat.html
with associated links). That is 0.031 is 5.0161812% (notice 5.0"1618"12) of
the 0.618 "phi" (lower case "p") number (i.e. nearly exact 1/20). Of course,
we know that "Phi" (the geometric golden section; Phi exp2=Phi + 1) is
related to Fibonacci "phi" as {(sqrt 5 + 1) / 2} is to {(sqrt 5 -1) /2.
Further, the geometric import extends to "pi" via James Gregory's work
(extension from Euler). As we are all students of the sciences here, I need
to proceed no further (yet) having to do with the natural import of this
relationship. Is there a "real relationship" between the FBM findings and
the natural sequence to geometric convergence, you may ask? Well, as you
have read this far, there had better be, right? Become VERY RESTLESS, as the
relationship does exist! A very careful scrutiny of the FBM (0.091%-1.001%
marine salt salinity, inclusive) demonstrated some interesting points of
data dispersion, each worth expressing in an assigned category.
(As this is a proposal for furtherance of study, and as the original FBM
results are in front of you, no need here to rehash the standard deviations,
"t", "chi square" and "F" scores.)
With this description, the standard "hour-glass" plot shape should be kept
in mind. In addition to the point of selection randomness, found at 0.031%,
areas of high data-plot dispersion are found in the results. These areas
demonstrate high scatter plot dispersion (away from the smooth plot lines
and pulling the curve fits toward 100% and 0 % option selection). They (the
dispersion points) appear as circular foci of data, with the density of same
decreasing as the distance from the foci centers increase. The foci plot
bilaterally symmetric to the centerline (point of randomness). The points of
salinity, independent of oxygen regimen (Also important!) are at 0.019%,
0.024%, 0.030%, 0.040%, 0.047%, 0.058%, 0.060%, 0.069%, and 0.076%. Further
data dispersion is found after 0.091%, however; I believe that once the
aforementioned numbers are interpreted, it will suffice for the purposes of
this protocol. Statistical significance of the dispersions were verified.
(See the FBM results under "Errant Data".) A cursory
inspection of the percentages revealed nothing. It was not until the
percentages were grouped, that meaning developed. Additionally, as
statistical significance is demonstrated both within and between groups (but
see the 0.076% analysis of foci differential), the ultimate
interrelationship (found after group "Descriptions"
and before the "Predictions"
section) is easily observed.
Cpt. Danny B Catselas Burisch, Ph.D. (U.S.M.C., Ret.)
END PROTOCOL SECTION 2
Subject: Protocol Section 3 of 6
Sent: Fri, 2 Mar 2001 07:16:56 -0800
To: mj01
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Group One (The Golden Mean Group): 0.019%, 0.040%, 0.058%, and 0.076%
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Group Two (The Viral Code Group): 0.030% and 0.060%
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Group Three (The "Hypersea" or Geologic Timeline Group): 0.024%, 0.047%, and
0.069%
DESCRIPTIONS:
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Group One
(The Golden Mean Group)
Each of these points has a direct relationship to the
Golden Mean and the
Ratio Convergence Sequence of Fibonacci as we see that the point of
randomness (0.031) multiplied times that convergence sequence (0.618) equals
0.019 (1st. Percentage in this group, with rounding). Extending: 2 times
(0.031 times 0.618) = 2 times 0.019 = 0.038 (2nd. Percentage in this group
was 0.040). 3 times (0.031 times 0.618) = 3 times 0.019 = 0.057 (3rd.
Percentage in this group). 4 times (0.031 times 0.618) = 4 times 0.019 =
0.076 (4th. Percentage in this group).
Interpretation: With the understanding that salinity oscillation occurs even
under the most rigorous laboratory conditions that involve dynamic systems,
we can eliminate criticism of the small within-group variance. As one of the
main data target points was 0.076%, one needs to address the density of the
dispersion versus the density of the data that pulled the curve fit to the
smooth hour-glass plot. Analysis of this issue revealed that the dispersion
foci (above and below the curve fits - depending upon whether you are
speaking to the photosynthetic or the respiratory foodstuffs) were only
0.05% as dense as the other dispersion foci. (You have the early data in
front of you.) The difference between 0.076% and 0.031% (the point of
randomness) is 0.045%. I understand that I am in hazard of your opinions
with the statement that follows, however, may I remind the readers to
evaluate
sacred geometry issues, as
presented in
http://www.danwinter.com/orion/orionheart.html In that article,
Mr. Winter directs attention to the Golden Spiral and
Orion. Please look past the spurious references and to the issues at hand,
including the presentation of "wratcheted dodecahedra and the DNA
double helix." In relation to same,
http://www.meru.org should be
evaluated in regard to the issue of "Continuous Creation". The information
that follows will further the connection between those issues and this
document.
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Group Two (The Viral Code Group)
Recent research has shown that the human
genome may contain as much as 30% from retrotransposon action. (See:
http://www.panspermia.org/whatsne6.htm and
Moran, John V., et al,
"Exon Shuffling by L1 Retrotransposition," p 1530-1534 v 283 Science, 5
March 1999.)
[A note: Please accept my disgust at the presentation of ALH84001,0 resident
on the same web page. For those that claim such non-faith-based foundations
to their work, they certainly seem to be interested in the concept of
"resurrection." Now other SNC's have what they (our
Masonic Champions of
Truth and the American Way, NASA) earlier praised as special to ALH84001,0.
Hey, guys, remember your math identities? Any Real Number multiplied by zero
= zero. 1996: 1(0)=0...time passes...2001: 3(0)=0. See? It product remained
the same, "0", didn't it? They ought to be bent over a knee and spanked!]
The original span of the FBM salinity tests ranged from 0.001% to 0.091%.
30% of the range (0.091-0.001 = 0.090) is 0.027, very near to 0.030, or
0.031%. Is this enough to firm up an opinion of definite relationship? Of
course not! Let's, however, take a close look at the percentages assigned to
this group and the substrate control regimen applied in the FBM. Both 0.030%
and 0.060% are multiples of 30% of the data range, when the data range is
set at 0.100. Extrapolation fit to Brackish Low results. (See results you
already have.)
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Intepretation: The evolution of new genes may have their origin in the
action of Long Interspersed Nuclear Elements (L1s) as "...they insert into
transcribed genes and retrotranspose sequences derived from their 3'flanks
to new genomic locations...", thereby promoting the movement of non-L1
sequences. As a corollary, retroviruses are noted as having possible origin
as retrotransposons. The logical movement from the argument that places
retroviruses as possible evolutionary outcasts to the plausible creation of
the eukaryote genome by a retrovirus (or multiples of same) is not
difficult. Of course, if one has an argument for the exclusivity of the
direction of retrovirus creation or an effective discourse could be made
against the idea as teleology, in the wake of this study, please present it.
It is well defined that the eukaryote genome can carry endogenous
retroviruses, given its intrinsic structure (Sverdlov, Eugene, "Perpetually
Mobile Footprints of Ancient Infection's in Human Genome", p 1-6 v 428,
Federation of European Biochemical Societies - Letters, 22 May 1998). This
issue received further treatment in "Our Retroviral Heritage" by
Clive
Patience, et al (p. 116-120 v 13 n 3, Trends in Genetics, March 1977), and
opens the possibility that the current genomic complement from such may
contain as much as 40% (for mammals only; Wilkins, John, 8 March 1999, FEBS
Letters). The differential of 10% may be accounted for by more recent retrotranspositions. Given the readers, it would be improper to present
basic virology.
Substrate controls were placed on the groups under
evaluation, in the FBM (Please review your copy!), by applying various
synthetic substrata (such as microcrystalline spheres) as well as washed
natural alluvium to which the protoctists were normally accustomed. Results
were NOT reproducible with any synthetic substrate or natural items (such as
leaves). Only the natural substrate (independent of washing with solvents
such as distilled water, saline, etc.) produced the precise behaviors. This
leads us, by the nose, to an exclusive interaction between the protoctists,
the foodstuff selection under salinity, and the resident substrate. Therein
may lie a new paradigm of speciation.
Cpt. Danny B Catselas Burisch, Ph.D. (U.S.M.C., Ret.)
END PROTOCOL SECTION 3
Subject: Protocol Section 4A of 6
A continuation of your enjoyment:
Debbie :)
You are taking the next cognitive step without need of my further leading
this dance. I am postulating the interaction between a viroid-like (possibly
intracisternal) particle or integrated provirus and an activating particle
from natural substrate with the observed behavioral component. The extent to
which the behavioral component may also be mediated by localized metabiosis
remains an object for study. The high reaction cell liquid replacement,
during FBM, should have precluded protoctist-protoctist chemotaxis as the
source of data dispersion. Virusoids employing RNA-dependent RNA polymerase
may account for some intermediate biochemistry involving object(s) in
question (should the behavior not be a direct repercussion of a DNA or
RNA
artifact).
Another possibility may rest in the behavior being directed by an
A-type Retrovirus. If the linkage exists between viral origin of the
genome,
the observed periodic behavior, and an A-type retrovirus; I would posit same
to be mobilized and hiding as a retrotransposon within the "active" regions
of the genome, with such retrotransposon having relation to ultimate species
diversification (see available literature on 16S rRNA divergence). All 22
varieties of holozoic protoctists demonstrated like data dispersion. Given
control results of randomized food intake by the engulfers, within their
normal microhabitat, genomic complement (together with some type of
substrate interaction) is believed responsible for reaction to marine
salinity pressures. No studies have been found, relating to reactions to
salts present in marine water, that will accommodate the data. Studies of
grazing data versus prey size are available, but none would account for the
responses given the size parity of foodstuffs. The combination of salts, in
toto, seem to be the triggering factor at the percentages deployed. As you
have already seen in the data in front of you, subcontrols using variant
fractional combinations of salts did not elicit the same responses. If the
periodic and reproduced results can be attributed to other factors, outside
of anomalous genetic control, I would encourage response. Given the like
data, across species, we appear to be looking at something generic to these
eukaryotes. Should the potential of retrovirus expression be
discounted, in relation to this data, you are invited to visit and subsume
the data at
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?CMD=Display&DB=PubMed
impeach the FBM experimental design, then challenge the postulation with
vigor.
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Group Three (The "Hypersea"
or Geologic Timeline Group)
If the top two groups did not promote concern for significance, the like
responses at 0.024%, 0.047%, and 0.069% I hope may. Public timelines place
the age of earth between 4.56 to 4.60 BYA. Some other timelines exist.
{A treatment of those other timelines and issues such as the
COSMIC "D. of
the C.T.P." requires a degree of control over this document that may not
exist within the passage of electronic mail. So, should you wish me to play
the position of advocacy against my hypothesis for the sake of argument, we
would require another method of communication. Should the control authority
decide that this medium is acceptable, I am prepared to proceed along that
line.}
I have wondered, within the context of a possible viral genomic origin to
the responses, whether some of the data may have relationship with geologic
time. If, in fact, the data are representative of a complex code being
projected into the present, could not the code be bound to its origin?
Numerous factor combinations were tabulated against the percentages assigned
to this group. 4.56 and 4.60 were multiplied against 0.618, that pesky
number from above (double-entendre suggested). The result: 0.228 and 0.230.
I, therefore, noted a discrete range of 0.228-0.230, with 0.229 as the mean
(0.230 rounded). A view of the data dispersion points within this group
reveals the foci at 0.024, 0.047, and 0.069. The FBM range is rounded to
0.100%. 0.100(0.230)= 0.023, 2(0.023)=0.046, and 3(0.023)=0.069. Set against
each other in a Product vs. Data format, we have:
-
Interpretation: In a word:
Hypersea! (See: McMenamin, Mark and Diana, "Hypersea -
Life on Land", Columbia University Press, 1996.) The Hypersea hypothesis
(now possibly a theory with this document) treats the up swelling of minerals
from the ocean, a goddess-like extension of the ocean to new vistas. The
relationship between the precise mineral components found in marine water,
the behavior of the organisms under scrutiny, and the periodic response to
factors involving the predicted age of the earth and natural sequences
points a strong finger. Not since the binding between a creation myth and
the society within which it may dwell, has such a strong nexus been
attributed to life and the (eternal) ocean (our mother). This gives reason
to pause. Are we hearing an echo of an evanescence of the darkness that was
upon the face of the deep, or seeing the waters swarm-forth living souls?
We see, in this data, a clear artifact/demonstration of the connection
between modern eukarya and the origin of the earth. Is the connection a
direct function of the genomic programming to the timeline, or is it derived
as a reaction of the eukaryote to other factors (relating to the age of the
earth, environment, etc.) that we have not yet seen?
Cpt. Danny B Catselas Burisch, Ph.D. (U.S.M.C., Ret.)
END PROTOCOL SECTION 4A
Subject: Protocol Section 4B of 6
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<SECTION 4B HAS BEEN EMBARGOED FOR TRANSMISSION DUE TO THE AUTHOR'S
SUBMISSION OF TEXT THAT REFERS TO DETAILS OF A RESEARCH PROJECT THAT IS
HIGHLY CLASSIFIED. HE HAS BEEN REQUESTED TO PROVIDE A REDACTED REFERENCE,
EXCLUDING THE DIRECT INFORMATION. HE HAS AGREED TO DO SO, PROVIDING THE
REFERENCE IN THE FORMAT OF A "PUN". TRANSMISSION OF THIS SEGMENT IS DUE
WITHIN 24 HOURS. JM:rt Routed from ts/cjcs number confirm 18992> |
Sent: Mon, 5 Mar 2001 00:09:13 -0800
To: mj01
> >Once again: Deb
PREDICTIONS (my
humble discourse):
It is at this point that I must sue with apologetics!
This is not a publication meant for the modern journals. Rather, it is
something that we are encountering that requires more than the recounting of
previously published material, and is to be viewed within the context of the
quiet truths with which we, of the Maji, are entrusted. This is new ground,
or perhaps it is a loud demonstration of very old ground. Continued
confirmation of the FBM results will require a four-tier design, two levels
of which can be performed by this writer, two by more restrictive laboratory
facilities.
The Experimental Design is in your possession. (Reference:
Mission Genesis Design 1999, as filed and amended to the
Maji, January 1999. *Please note: The generalized design
shall be sequentially repeated over the various geologic strata, with
retention codes used.) The Frenchman Mountain Complex (FMC)
will supply six geologic segments (http://datawebman.bizland.com/rainbowgardens/StrataDesc.html in order that we may test somewhere between (public data) +/- 1/15 to +/-
1/16 of earth history.
1.7BYA, 570-510 MYA, 409-330 MYA, 330-245 MYA,
245-200 MYA, and less than 20 MYA. As I am inclined to accept the clues
given from the FBM, I would expect that the responses of the modern
organisms to the substrate may change, as the general age of the substrate
changes. To wit, I predict that responses will be revealed over the
predictable range, with the oldest strata mediating behavior at a closer
distance to marine salinity, moving toward a mathematical limit between
3.000% and 4.000% salinity (marine salts mixture). Using easy extrapolation,
and dividing the predictions between Low, Medium, and High groups; random
foodstuff selection is expected at the following salinities (in
percents): > >BYA: LOW EXPECTANCY MEDIUM EXPECTANCY HIGH EXPECTANCY > >1.840
0.194 0.206 0.217 >1.610 0.154 0.162 0.171 >0.690 0.062 0.063 0.064 >0.460
0.050 0.050 0.050 >0.230 0.040 0.040 0.040 >0.000 0.031 0.031 0.031 >
>Original interpolation was conducted at 0.230 B.Y. increments with the mean
salinities factoring to the 3.000% and 4.000% with the use of original
factors, Low End: 1.255 and 1.260, and High End: 1.275 adn 1.276. (Complete
Interpolation Available Upon Request.) > >
As we are discussing a two-piece puzzle with evidenced predictable periods,
we can postulate the devaluation of the genomic component in a similar
manner. Taking the argued 30% retrotransposition as the current internal
artifact (or secreted provirus particle), and accepting a predictable period
(evidenced Hypersea) as an intelligent movement from marine salinity to
fresh water (ultimately a movement from ocean to land), the point of
randomness may be defined in relation to viral component. Yes, I am
postulating that a multivariant viral structure seeded the earth (in
agreement with the now understood "unnerving details" VERY DEEP PUN
INTENDED!) encapsulating the mobius-like reality of Adam {'the' Red Earth}
within Eve {Life}, and that such viral structure purposively motivated its
totipotency to produce an exemplar cellular structure, the same requiring
further phagocytic behavior, as time passed, to maintain sufficient genetic
diversity to mobilize the internally consistent biosphere humanity now
perturbs. For purposes of further identification, the cellular component of
the LOTUS (abbreviated as "L") will henceforth be termed "V" for "the
VISHNU " in historical respect, after the tradition of
"...the great maintainer and preserver." (See internet citation:
http://skipper.gseis.ucla.edu/students/rroberto/208/Vishnu7.html
The lithospheric component (natural state unknown) of the L will be termed
"S" for "the SHIVA" in historical respect, after the tradition of "...a
reproductive power which restores what has been dissolved." (See internet
citation:
http://www.gurjari.net/ico/mystica/html/shiva.htm ) The
communication medium (or particle{s}) will be called "G(s)" for "the
GANESH " in historical respect, after the tradition of
"The remover of obstacles". (See internet citation:
http://www.hindu-gods.com
The functions and natures of that hypothesized virus-seed is the subject of
Tier-2.
Cpt. Danny B Catselas Burisch, Ph.D. (U.S.M.C., Ret.)
END PROTOCOL SECTION 4B
Subject: Protocol Section 5 of 6
Sent: Fri, 2 Mar 2001 00:14:29 -0800
To: mj01
Section 5 of 6, a little ahead of schedule......Debbie.
In essence, Mission Genesis, as originally envisioned in 1999 is reborn.
Please review the Bacillus subtilis/Spirulina platensis sequencing compendia
and see the quote of previous pages, then add to it the opportunity to
substrate with numerous geologic strata. Should predictable periodic
progression be plausible (as with Hypersea), the percent at which random
foodstuff selection is made (with original random percent being postulated
at 3.500) may be hypothesized at a reduction of +/- 20 % joined viral
component (L) for every +/- 1% decrease at the point which random selection
is maximized. A short interpolation follows. Should the complete
mathematical scheme be required, please request same.
L COMPONENT IN %:
% RANDOMNESS MAXIMUM:
100.000 3.500
80.313 2.524
60.625 1.549
39.844 0.519
30.000 0.031
Confirmation of the L component and the primary through quarternary
structures of the V, the S, and the G(s) are the aims of
Tiers 3 & 4. I
leave the experimental methodology and design parameters in your hands.
[Due to the potential for destruction of a fully functional and conjoined
L,
it is my suggestion that any direct evaluation be conducted in biocontainment levels normally associated with potentially hazardous
"foreign" materials (AKA: another name for a "Native American baby"). The
vitality of the L should not be underestimated given its ability to conduct
graded continuous creation/proliferative cytogenesis and the common
instances of ancient DNA (aDNA) revitalization. (See: Joint Symposium
Details: Cano, R., et al., "Beyond Jurassic Park: Assessing Genetic
Information Hidden in Herbaria and Archival Plant, Microbe, and Insect
Specimens," American Phytopathological Society and the
Entomological Society of America, November 8-12, 1998. Further results
may be located at
http://www.comic.sbg.ac.at/staff/jan/ancient/aDNA
library.html
This protocol would not be complete without a short presentation of an idea
stream concerning the nature of the original L. Until confirmation/isolation
occurs, please maintain my hypothetical stream as "straight-away guesses."
After it (the L) is verified - you are invited to change my position as
having stated I was 100% sure! (A little joke! Yes,...I know,...VERY
LITTLE!)
A believed central role for the L would be its original ability to not only
promote the first viable cellular structure, but also maintain its own
internally consistent vitality (fit expression mechanisms) through the
expanse of time. Should the search bear out this triumvirate vehicle of
genesis, it is anticipated that a key to its role (over geologic time) is
that it can orient a cells' ability to adjust under varying conditions. We
know that energy-dependent proteolytic systems involving multicatalytic
proteases (ex. steps in ubiquitination) are central to this notion. (See:
Maupin-Furlow, Julie A., et al., "Proteosomes in the Archaea: From Structure
to Function," Frontiers of Bioscience, 5, d837-865, September 1, 2000.)
Further, high turnover proteins are directly related to metabolic nodes.
Such proteolytic systems are based upon "ring" structures that unfold
proteins and facilitate their insertion into the appropriate catabolic
processes. (Relate this also to attached scissor mechanisms on a synthetic
helix.) It is this ring-associated structural basis, relating to both
eukarya (now) and prokarya (now and in the Archaean) that gives us a few
more clues to L structure, and possibly an originally non-endosymbiotically-based
origin for mitochondrial cDNA. Viroids, usually described as naked circular
pieces of infectious RNA that fold back and anneal to form stable
structures, are not affected by proteases or DNAse treatment. It is only
with RNAse that viroids are destroyed. What could be a better progenitor
system for the aforementioned proteosomal mechanisms? You may have
ascertained, by now, that we are slowly reconstructing a theoretical
L, from
constituent parts: the V, the S, and the G(s).
The mechanism for viroid replication is poorly understood. Known viroids
need no helper function and create havoc through cellular damage. A viroid,
presented to the cytosol, via the action of a retroviral provirus may
constitute the postulated V. Direct therapeutical advantages
have been demonstrated, in experiment, with the use of retroviruses,
that assimilate into the host genome and modulate mRNA's.
As a matter of stating the required information: viral-based gene
therapy is commonly practiced with retrovirus vectors as a gene
induction system. (See:
http://www.bioscience.org/1999/v4/d/Klimach/fulltext.htm.)
Should the V be a combination of such a provirus and a viroid devoid of
cytopathological aspirations (pardon the personalization), Defective
Interfering Particles (DIPs) may be assayed in response to cells undergoing
a simultaneous environmental stressor and a coinfection by a
well-established viral gene replacement vector, such as an amphotrophic or
polytrophic murine retrovirus. The possible association between the
resultant DIPs and the mitochondrial cDNA may still be out of reach due to
packaging capacity. The produced DIPs would have to closely scrutinized.
(Forgive my intervention into your Tiers.)"
Cpt. Danny B Catselas Burisch, Ph.D. (U.S.M.C., Ret.)
END PROTOCOL SECTION 5
Subject: Protocol Section 6 of 6
Sent: Mon, 5 Mar 2001 00:02:51 -0800
To: mj01
Here's the last one.......just as you asked.........Debbie. :)
"The conjecture of the lithospheric component, the S, leads us into the
discussion of the selected respiratory foodstuff: Bacillus subtilis. This
unique bacterium has had a long and very interesting relationship with human
beings. (No. It was not by chance that it was picked for the original
FBM study, some years ago. Yes. I had a "heads-up" on what I
might find. I must, however keep that information a "Captive" of my mind and
soul. You must understand, some things shared between "friends" that respect
each other should remain in confidence until the "future" time is right.)
Yes, what an interesting relationship! May I refer the readers to the
1941 Nazi German medical corps' interactions with, and their
subsequent approval of the gobbling of warm camel dung? (See:
http://upwardquest.com/crit1.html
for some light cell-mediated immune response and humoral activation
folklore.) Should that not suffice for reference, call JPL, they know just
about "everything" concerning the Nazi's, yes they do!. Why, where else do
you think they obtained the policy to feed faeces to people?
The biological
point here is this: Bacillus subtilis relates in some special manner to
normal human-involved ecosystem biology. The critter has the ability to
positively interact with human cytophysiology (while being taken
internally), but is nominally only resident in soil. Further, I have
previously theorized an association between research conducted on the
YER057c/YjgF protein family (involving Bacillus subtilis
biosynthetic PurA)
and modulation of polycationic histone proteins binding to exterior
phosphate groups on DNA (a communicating membrane transduction device, a key
to extracellular control over nDNA, m/cDNA, and
RNA synthesis...we're a-talkin'
with cells! Please take a look at the theoretical transcriptions I produced
at the "site". I believe the nexus here is enough, now. If they say anything
interesting involving the collective unconscious, ask them to tell my brain
to let me know, okay? :) Isn't the holographic Universe a beautiful place to
be! See, also: Mission Genesis Discourse, June 2000, R4808) If we are to
postulate a Bacillus subtilis type bacteria, within the strata, we would
need to justify its residence. As I am sure that a dissertation on desert
soil microbial community chemistry or viral absorption standards would bore
you, I will continue. I would submit negative chemotaxis to ozone for the
promotion of the niche, and a graded niche size relating to geophysical
history. (See: Kim, J.G., Department of Food Science and Technology, The
Ohio State University, "Inactivation of Bacillus subtilis Spores by Ozone in
Combination with Heat or Pulsed Electric Field", 2000 IFT Annual Meeting,
78F-3.)
Although spores of Bacillus subtilis are
resistant to physical and
chemical assaults, the addition of ozone appeared to sensitize the spores to
heat. This is relevant as we understand that the unfolding of life's
progress demonstrates the procession from the thickest blanket of protection
from ultraviolet radiation (deep ocean and deep geology) to a thinner one (euphotic,
land, limnology, shallow geology, free-atmosphere and cloud-borne). Simply
put, this may be an artifact of the constraint of life to its proper place
at proper times. Lest we forget: the public placement of the first
mutualistic endosymbiosis of that which we call mitochondria is set only 100
M.Y. after our regarding the ozone shield sufficiently thickening, and the
fossil record of such as Gunflintia, Huronospora, and Leptoteichus golubicii
becoming a reality. Putting all of this together, we seem to be looking at a
variety of bacteria that remains a candidate for the vehicle of the S,
whether it acts as a mediator from an imbedded crystal protein, or directs
relevant membrane transduction with the S being a resident item. The
G(s)
are to be the greatest isolation difficulty and may only be realized
indirectly, by the affirmative identification of the V, the
S, and the
behavior between the two. It may be as simple as a shuttle system, involving
an organism such as Bacillus subtilis, Bdellovibrio bacterivorus, a
Wolbachia-like type, or the like. It could also be as elusive as a phantom's
whisper.
READ CAREFULLY AND SAVOR THE BUTTERY TASTE OF YOUR "BISCUITS":
With this information on our minds, what may have the original L have been?
As a consequence, if we are to take the new direction of original viral totipotency,
prokaryote and eukaryote development may have had no need for
original endosymbiosis. Future, successive endosymbioses (possibly with
graded intracellular retention times) may then have acted (and still may do)
under a "natural law" of sorts that increases internal variation, as such
suppressing unfavorable or recessive traits. (Applaud for Darwin, here!) The
intracellular symbioses may also act, in some yet unknown way, to support
the protection the originally "planned" progression. As to the reproductive
strategy, we see it commonly, but may have been interpreting it from an
incorrect bias. In the framework being expounded, the L was seeded in that
mythic "time-before-time" as a "genesis egg" that provided the original
unicellular differentiation program, similar to the spore development
checkpoints in Bacillus subtilis; wherein the L's capsid evaginated (See,
also, meru.org on the
Flower of Life) and provided the necessary phospholipid and
proteinaceous materials to invaginate and compartmentalize
the contents of the L as a communicating membrane-bound cell (i.e. a
dual-ring heterochiral cDNA retrovirus absorption 'metamorphosis', based
with a reverse-transcriptase like functional unit). As the evagination
progressed, it is postulated that the two rings of cDNA became separated
through progressive intracellular invagination, each then becoming encased
within their own environment (organelle), the original D-type-cDNA becoming
the division driver of a new item, a mitochondrion, and the
L(laevorotary)-type-cDNA undergoing homochiral
transition as the driver of another organelle: the eukaryotic
nucleus. (See: Speculative Intermediate Biochemistry,
http://sciencedaily.com/releases/1998/06/980610082901.htm)
The almost frightening observation, implicit within this scenario (but
commonly found in pattern by the present day virion), is the creation of
prokaryotes from eukaryotes. Let your theoretical minds go wild under
punctuated equilibrium scenarios and frantic with new notions of phyletic
grandualism! This idea is heresy, so be it, and so the Sun no long spins
about the earth, and the spirits fall inward through the time of gnosis. You
have asked of me, so let it be. (For supportive concepts, look to the newer
constructs of dissipative/replicative structures,
http://users.viawest.net/~keirsey/pofdisstruct.html
and to this understandings' ability to confront ancient cell size
issues,
Special Creation? Intelligent design?
Concluding Notes:
This protocol was not intended as a step-by-step analysis within an
experimental design. That is not what was requested of the author. Rather,
the "offer" was made to present a global idea stream so that all the
"biscuits" were in plain view. The overall approach to the notions
elucidated within this discourse offers the possibility of a new paradigm
(albeit one that will NEVER see the halls of polite discussion). It may give
us clues as to why we see a Universe replete with structure conservation and
sacred pattern repetitions. Recent work has been conducted by the "Procloners
(as I like to call them)" on the back-engineering of stem cells from fully
differentiated ones --- their dedifferentiation into embryonic totipotency.
What totipotency is this, however? Not only mammalian, but human, not
generic eukarya. This constraint is demonstrative of a contention that the
L
is not present in fullness under the experimental design, yet sequencing
argues slight subunit differentiation between we and the chimps. (See Recent
Developments: PPL Therapeutics.) From thence, no other so-called "species"
can be made. In other words, we are still stuck in a macroevolution paradigm
that is not proved, in either direction.
If we have proved that:
A. We cannot assemble a logic string that requires 1 to 2 to 3 (ranging in
temporally increased complexity);
and
B. We cannot take the same reality of 1, 2, and 3, then dismantle them as 3
to 2 to 1 (ranging in decreased temporal complexity);
but
C. We CAN associate them as 3 to 2 to 1, as a "progressive" system (this
protocol);
then
D. Why are we kneeling at the altar of a
NeoDarwinian religion?
Does this ring old bells and light up old bulbs, guys? Sadly, it did with
me. Add to all of this the genetic potential being holographic resonance
between sequences of base pairs, and we have a case for a migraine, a case
within which we are all incompetent. So, then, I ask those of you "in the
know": why can't we solve our future "problem" by stepping back (in respect
for the Designer) and label our regard for the "problem" in terms of a
"warning" rather than an issue to be "wrestled into reality"? Illusion. Have
we not fallen from this before? Is this future, this "chimeric possibility",
not the true reason for imprisonment of truth-finders? Yes, I know the
reasons. They are written, they are foretold. It is sad that the "tear from
the eye" on the red sands teaches you nothing as you watch those underfoot
become awashed in the flood of history. I expect nothing as I cannot expect
one to conduct a search of the soul after consummation of a "bargain". I
will never give up, for my soul travels and is given to Christ. I hear the
screams of those yet unborn, in concert with the angels making indictment of
humanity for the crimes being conducted upon the innocent and "innocence" in
these, the "special" days. I must give a warning, concerning those that may
seek to rejoin the Lotus, once fully understood:
"And so He drove the man
out and posted at the east of the garden of Eden the cherubs and the flaming
blade of a sword that was turning itself continually to guard the way to the
tree of life. Gen. 3:24"
It's time for me to go digging and to once more peer with the
reticules of
artisans. I feel in this research both the dwelling peace of Christ and the
arrogance of that one who would aspire to place himself above the stars of
heaven. I do this research because my soul is driven to encounter truth, no
matter what "cell" into which I become "evolved". Should the
Lotus be confirmed, the power will exist to humbly ask for
forgiveness of our transgressions onto the boundary of Eden, and to wipe
away the stain we have so arrogantly placed upon our future. That is my
reason, my hope. Decide wisely. The one of avarice still seeks the Throne,
the unattainable, and would revel in our continued destruction. I am caught
between the need to help and a reason not to assist. I would be simply
honored beyond my worth to have a glimpse at its beauty, never to touch. The
Tree of Life is reserved for the hand of God.
Cpt. Danny B Catselas Burisch, Ph.D. (U.S.M.C., Ret.)
END PROTOCOL, ENTIRE
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