Documente Academic
Documente Profesional
Documente Cultură
Contents
Contents
1. Introduction
1
2
3
4
General Readership
Humans in the Universe
Design of our Anatomy
Predetermined Anatomy
2. Environmental Adaptation
12
13
16
16
17
18
20
21
23
23
24
24
25
27
5. The Design
30
iii
Contents
iv
34
34
35
36
53
Definitions in Science
Discreteness & Continuity
Continual Physics
Continual Biology
63
63
64
65
66
Isaac Newton
Immanuel Kant
Charles Darwin
Albert Einstein
68
8. Organ Substructure
68
84
87
89
90
91
91
92
93
9. Appendage Superstructure
101
103
107
108
115
Contents
117
118
122
126
128
Contents
192 14. Heat Loss in Physics & Biology
194
197
vi
1. Introduction
Predetermined Anatomy
I explain how the Design may apply to the universe generally
within an overall Scheme for existence. If the Design applies
to all of nature, then our anatomy may be the final product
of evolution in the universe. Nature may evolve according to
the Design across physics and then across biology.
Evolutions are by heat loss after an explosion at a Big Bang,
explained later, for atoms and compounds by more heat loss.
A universe drives to economy after a Big Bang.
In physics, the universe is in uniform expansion and evolves
according to fundamental capacities of mass prescribed and
reconciled by the Design. Particles and their fields would
reconcile their capacities by the creation of a gravitationally
neutralized universe in which they evolve cosmological
structures to the extent of solar systems and Earth-type
planetary surfaces for human-type evolution. Evolution of the
entire universe, from a state of containment before a Big
Bang event of expansion, may be led by the Design to
inevitably evolve Earth-type planetary surfaces. In evolution
of forces, the synthesis of the range of atoms on Earth is
essential. Then anatomies evolve by biology in environmental
landscapes of chemicals under an epicycle of Earth orbiting
the Sun, and the Moon orbiting Earth, to shape landscapes.
In biology, evolution by adaptation to an environment is
necessary, but evolution may not be undirected. Structured
layering of the chemical capacities of Earths surface may
predetermine the structures of anatomies. It may be inevitable
that anatomies will literally resemble their landscapes if DNA
constructs them using the chemicals of the landscape. In my
theory, DNA is not a selfish replicator. It is a replicator
serving an environment that shapes it. Our landscape has a
specific arrangement of layered compounds under an
epicycle, from given affinities between atoms to bond into
those compounds under the epicycle. Those affinities also
2. Environmental Adaptation
I will now draw a line to separate our anatomy and the world
around us. On one side of the line may be a landscape of
rivers, lakes, hills, and valleys. Our anatomy has evolved
from a single microscopic cell within a landscape. We have
evolved over several billion years by adaptation. This means
all our systems, senses, and appendages need to be suited
to our environment and maintained by our environment.
Usually, adaptation is understood by looking at what has
already survived. We can find correlations to environmental
conditions to which it may have adapted. However, I consider
preexisting chemical layers and construct creatures based
upon how they may be used to construct anatomies. Never
spout narratives that a species has its features because it is
environmentally Selected, working with what looks successful
to the narrator. That is the work of an inventive artist, not a
scientist. You start at lower levels of chemistry and physics,
not up to a Selection filter by a mantra if it works, that is why it
evolved. That is so shallow, it is ridiculous to rely on it.
Population Genetics is shallow math from random mutation or
duplication, for random shuffling. As with most of science
explored here, it is so inadequate as an explanation as to be a
sad joke. In fact, DNA engineers chemicals to be anatomies in
environments. Chemicals stand between DNA and Selection.
They are in pre-existing layers as constituents for engineering
by DNA. I do not simply put endlessly labeled anatomical parts
on a savannah to explain them by narratives around a 100%
blind, purely accidental, mutation of our three billion sequence.
Our anatomies are constructed using the chemicals of our
environment, and this has been overlooked by science to date.
I will show our anatomy may be a perfect embodiment of
chemicals at Earths surface. My removal of biologys pillar is
probably the most obvious original idea ever presented, sadly.
Gas Lifting
Lungs
Liquid Flowing
Heart
Solid Light
Nose
Back
Front
Spine
Mineral Tightening
Eye
Gas Pocket
Ear
Liquid Well
Gut
Solid Heavy
Right
10
Gas Lifting
Lungs
Liquid Flowing
Heart
Solid Light
Nose
Horizon
Spine
Mineral Tightening
Eye
Gas Pocket
Ear
Liquid Well
Gut
Solid Heavy
Internal
11
12
13
14
15
16
17
18
19
4. Layered Chemicals
20
Horizon
(Front)
(Spine)
Mineral Tightening
(Gut)
Solid Heavy
(Right)
Internal
Passive Chemicals
I will double the number of categories. There is also a
resting state, for their passive sensitivities. External to the
surface are minerals loosened in pools, and solids settling
as dust; and internal to the surface are gasses contained in
pockets, and liquids sunken in drains. Passive chemicals
would not move as they do in their active states. In
passive states, they also have alternative positions in the
landscape, higher or lower than active positions. Later, I
explain our anatomy is formed by gas bubbles (eye & alveoli)
and liquid canals (cochlea & heart) stretching; solid piles (nose
& gut) and mineral seams (spine & tongue) stacking. I include
all muscles to stretch and all receptors-effectors to stack, later.
21
Horizon
(Front)
(Eye)
Gas Pocket
(Ear)
Liquid Well
(Right)
Internal
22
23
24
Sunshine
Arc
Earths Spin
(2) Gravitational Arc
Moons Drag
Arc
Earths Pull
25
Gas Lift
Tongue
Lungs
Moons Drag
Liquid Flow
Solid Light
Heart
Nose
Horizon
Spine
Eye
Mineral Tight
Gas Pocket
Earths Spin
Ear
Gut
Liquid Well
Solid Heavy
Earths Pull
Earth-Based Causes
26
27
5. The Design
Gas Lift
Active, Levity
Liquid Flow
Active, Gravity
Solid Light
Passive, Gravity
Time
Space
Mineral Tight
Active, Levity
Gas Contained
Passive, Levity
Liquid Sink
Passive, Gravity
Solid Heavy
Active, Gravity
Cause
28
Space
(Where)
(Compression To Me)
Electromagnetism . Gravitation
(To)
(From)
Rest Mass
(Stop)
Energy
(Go)
29
30
31
32
33
34
35
Discrete
Complement
Forces
Life
Substance
& its Form
Design
as Product
Design
as Product
Continuous
Form
Substance
36
37
Time
Space
Cause
Ionic
Levity
Covalent
Gravity
Positive
Rest
Negative
Energy
38
39
40
41
42
43
44
45
46
Light Speed
Low Ends
Front
High Ends
Front
Light Speed
Left Spin Up
High End Low End
Decay to Electron
View From Below Backward Rotation
Electron Hill at One Pole (Body)
(2) Standard Right Spin of Gravitons Counter-Shearing
Sets a Right Spin, But Neutral to Poles
.
Resting String Reels
Right Hand Spin
(Spine)
(Hearts)
(Spine)
Left Shear Points
to Widen & Densify
47
48
49
Diagram 12, Accretion Disc Spring-Shift (Piston Line across Cog Line)
One Contour
Cog Line
Zoom View
Higher
Piston Line
Lower
50
51
42
53
Continual Biology
In biology, form and substance as an anatomy are cellular, by
pure discrete binary form of DNA in Diagram 9, with its own
substantive nucleotides & chromosomes interfacing open and
closed substantive continuities. It is comprised of substance to
interface, but with pure form. DNA encodes a use for those
interfaces by coding for growth from sexual reproduction. DNA
is intact as chromosomes lined with nucleotides. It uses
continuities and adapts sequences to make best use of them
by coding to grow from a single cell under nurturing of parents
encoded with sex. That is complete use of interface, as
seamless in creating cells as use of continuities in physics.
DNA is a formal strand of four substantive nucleotides of
adenine, cytosine, g uanine, and thymine to initiate bonding for
cell growth. All nucleotides have exactly two open protons, and
two open electrons, as hydrogen bonds interfacing a chemical
continuum. Open continuity is represented in Diagram 10 (2)
by resting proton & energetic electron as equal triangles, with
continuity to their open bonding into chemical compounds for
all cells, initiated by DNA through mechanisms and proteins.
Open charges of hydrogen bonds interface other atoms,
tending continually to lower energy orbital bonding, for DNAs
mechanisms to extend bonding continually from the digital
strand itself. It is substantive continuity used for continual DNA
purposes. All atoms beyond the strand are subject to pure
formal coding by DNA, including its mechanisms, proteins, and
those from the landscape permeating a cell membrane.
Biology has a closed continuum, with restriction to the freedom
of bonding. DNA has substantive chromosomes, to use a
chemical continuum for blending compounds between ionic
and covalent limits. Ionic bonds conduct electromagnetic
charge, while covalent bonds do not. Ionic compounds rise
with levity, and covalent fall by gravity. Chromosomes carry
genes for DNA to encode reproductive blending between
54
55
56
57
58
59
60
61
62
63
64
65
Kant took the bold step of saying that we cannot know if those
forms exist in the world. We have them unified under a soul
to work with what we can sense from the world. We impose
ordered forms upon sense datum for an experience of entity
in relation to sense datum as objects perceived by a soul. The
experience is not from finalized neural activity, known today but
not to Kant, it is from a soul perceiving entity and a world as
objects in one experience. He unified entity & world necessarily
in the experience but not clearly by interface of self-stimulation
with a world of stimulation for capture of both by neurons in a
contained neural representation of entity within a world.
Neural activity for both entity and world equate to the word I.
I am a subjective experience of a representation of both, by
the interactive capacities of I to cause effects on others or be
effected by cause of others. I use the word I here, but I could
use oneself as equally causal and effected in Diagram 8.
We have experiences representing an interactive interface, and
using the experience at all times, we consider its objective
reality. I think, therefore, I assume I am an object thinking about
its interfaces after delay, by Descartes. A subjective experience
is just that, and it assumes things are out there, as necessary,
in the locked-in experience itself. We only experience after
delay for processing. We are always immersed in a world of
objects, from one cell, and never separate. We assume things
are out there, including entity as an object, as entity in world,
in what appear in experiences to be objects in interface. I is a
pure point of reference in experiences. The world is mine, but
it owns me in reality. I explore interfaces with my world to
differentiate them as objects, to attain my goals in my world.
Charles Darwin
Next in time, immediately following Kant, is Charles Darwin
(1809-1882). He said in his theory of Natural Selection that
life evolves by absolutes of growth and reproduction, and by
adaptation to the environment. Viewing from universal
66
67
68
8. Organ Substructure
69
Effect Left
Mineral Loose
Gas Lift
8 Tongue
1 Lungs
Liquid Flow
Heart 7
Solid Light
2 Nose
Time
Back
Space
Front
Spine 6
Mineral Tight
3 Eye
Gas Contained
5 Ear
4 Gut
Liquid Well
Solid Heavy
Cause Right
Merged across both sides
70
2 Nose
Upright Levity Organ
3 Eye
Right
Front
Back
Left
8 Tongue
5 Ear
Broad Trough
Back
Right
Left
Front
4 Gut
Broad Front
1 Lungs
71
72
73
Solid
Fovea
Tilt Down
Olfact
Slice
Gas
Down
Optic
Ear
Up
Vestib.
Tilt Up
Vomer.
Decompress Tongue
Tilt Up
Edges
Splay
Liquid
Down
N Cords
Periphery Middle
Body Symmetry
N Cloth
Liquid
Middle Periphery
Med .
Bulge Down
Atrium
Slice
Mineral
Down
Cord
Gut
Up
Liver
Bulge Up
Decompress
Ventr.
Lungs
Bulge Up
Chest
Splay
Solid
Down
Horizontal: Convex & Concave with Spread & Sandwiched Rings & Links
Splay
Gut
Nose
Slice
Lung
Splay
Slice
Heart
Splay Tongue
Spine
Slice
Ear Splay
Slice
Eye
74
The correct side for links is seen in Diagram 13, as eight relative
positions that are also absolute from a landscapes using color
by numbers. A correct level for rings is also absolute, by causal
rings below their links, and effected rings above their links for
cause and effect in a landscape. Those levels have correct
relative positions, but you will see in Diagrams 16 & 17, upper
organs have almost complete overlap of ring & link levels of two
organs together, slicing. Lower organs have almost complete
distancing of ring & link levels of two organs apart, splaying.
Upper organs slice inwards by links from ring compression to
decompression. Lower organs splay outward by their links from
ring compression to decompression. Links slice or splay at
transition, but rings conform by fixing for a slice or freeing for a
splay, so slice or splay is by both links & rings. Links counter to
rings are like twists between action & reaction of inertial rings,
75
which change their inertia by links, and this may apply also in
general to physics, including collisions for anti-state formation.
Respectively, slice or splay are concave or convex, upper or
lower. Concave-convex have opposite depths back-front. Slice &
splay have opposite widths in-out. Upper & lower have opposite
heights up-down. A present moment of pulse mirrors left-right
sides. Gas has depth, liquid has width, solid has height, and
mineral has pulse. Two charged axes of depth & pulse seen
from above flat on the surface for forward traction, combine with
two pivots by width using height seen from the side to wind a
mound around axes for circular momentum for that traction.
Charge unifies flat, by axes to four sides laterally. Mass unifies
pivotally around the axes, as width extending to or from height
for momentum around crossways charged axes that are flat on
the surface for forward traction by momentum. This enables
charge to be causal back & effected front for traction, while
mass can be causal down & effect up for momentum cycles.
There is complete inversion of slice versus splay on each side,
and unity between both sides by two axes and two pivots. All
moves match between two organs in each of four layers, to
provide perfect traction to momentum across an entire system.
The lines for rings and dashed lines for links in Diagrams 15 &
16 each have moves by arrows. Moves of each organ match for
both in layers. Time flows or ebbs by waves, and space
converges or diverges by planes. The moves are achieved by
tilts at a head or bulges at a body by rings & links from set
positions, in a legend at right in Diagram 16, as root moves.
Upper organs overlap by compression in shared layers by
waves or planes. Lower organs disperse by decompression. The
legend of root moves underlies the apparent symmetrical
moves in the diagram, which are moves from Diagram 15.
Liquid flows down from up at an atrium and up from down at a
ventricle in overlap to make a flow direct from sites to an atrium
that can be modulated by a ventricle at transition to pump back
76
77
78
79
M Link, its nodes to the N Cloth. It uses a gut link in the right
atrium cooperating with spinal logistics via the sinoatrial to
favor a gut & spinal logistics before flow to lungs, coordinating
atrioventricular nodes to modulate ventricle flow for both gut
and lungs. The rings are Full Cones above and right at a heart,
and I prioritize the ventricles to slice, but using a sinoatrial to
settle atria for a gut & spinal logistics. The nodes adjust ring
flow for supply of oxygen and nutrients by blood at sites for
logistics. Modulation controls filling out & down and beating in
& up to get the blood out, as counter cycles extending a ring to
sites. Its location at left sets locations for other body organ
links. A full cone is right & above, and links tend left & below.
Muscles at sites are integral as the effected periphery driving
regularly to enable a heart to compress blood flow back to it.
A first spinal ring move is at front of back in & up. A first link is
at back of back out & up in a deep brain with sensory at back
in Diagram 26, later. A second link for motor moves is front of
front in & down in a brain, slicing back to front. A second ring
move is back of front out & down to move, behind to forward.
A medulla braces a brain deeper back and front than a spine.
To match a spine, a heart sends a blood flow from SVC & IVC
blasted front of front by atria in & down, then a ventricle stops
it to fill back of front out & down, then it flows front of back by
slicing in & up from that fill, to then flow back of back out & up
behind the SVC & IVC by an aorta or pulmonary. Later, an arm
& hand throw objects using the same sequence. All moves of
two organs sharing each layer are synchronized for front,
back, left, right, in, out, up, and down moves. This extends
clearly to appendages they share in Diagram 21, later. Each
organ has a different starting move by ring compression from
its layer partner, but all moves are matched, despite starting
and finishing differently in a shared cycle.
At lower body, a liver links rings of a gut to a heart to extend
beyond its stomach & large intestine, for nutrition to sites by
blood vessels. Link moves are counter to ring, using a portal to
80
81
82
central & shallow below fovea from a deep & wide arc of light
above, to etch. A solid eyeball shudder tends downwards in
pressure, as saccades tend to read down a page and not up,
in all languages except a few ancient religious ones. This
sends light cones in an eyeball upwards as a levity cone to a
fovea. It benefits from a half link oscillating centrally to a
vestibular from the optic nerve, but an eye has a blind spot at
the optic nerve when light comes from bright sources above.
The blind spot gives range to find bright edges for a fovea with
less harm, and the link extends eye function to balance a
whole head for it. An eye can voluntarily move on its own, and
also oscillate into a vestibular for static balance. An optic nerve
enables a mirror between eyes for width & depth, to level at a
fovea more centrally focused, by etching over its tight images
below using arcs of light from above & sides.
An eye has a pure light cone captured in its ball as a recreated
environment for light to excite gasses in pressurized solid
pockets. In Diagram 15 (2,) a cone is made by a lens from a
saccade tending down from X, in & up to compress dim light to a
fovea, which is not preferred. Saccades move all ways, but tend
down. This literally drains light from the eye out & up as a link, to
then seek light at the upper edge of X, towards Y, to saccade an
edge to X using light above it. The pupil closes from edging at Y,
to return to X and open for a clear view of the object revealed by
edging, taking in light by opening for dim light. In my current
model, edging reveals objects for ring examination in a relation
of pupil moves for light levels, and saccade moves for edges that
excite from above but favor cooler objects below in doing so.
Saccades are our fastest anatomical moves, and at lower
head we use our smallest anatomical muscle to reflex by an
ossicles pedal at a middle ear. The cone of an ear is set from
auricle out with helix as an apex, down a canal to a drum
angled down, and then down to a cochlea. Ossicles intercede
that cone to amplify waves at the drum and to speak using a
reflexive sensitivity. The drum is a cone angled down to the
83
helix and cochlea cone, and the middle ear link creates a
leveraged reflex, so that waves externally tighten to increase
hearing. A cochlea is liquid in a well with mineral hairs, to
detect sound waves, below added canals for vestibular
balance. Ossicles are between the cochlea and drum and
below the vestibular. A cochlea uses a vestibular to reflex
balance, for turns to hear from the leverage of ossicles with a
helix as an apex. Cochlea reception of internal waves from
vocal folds can loosen by a Vocalization-Induced Stapedius
Reflex. We can favor external over the internal. A bird uses it
to sing, and a bat blocks its cry to hear its echo.
A heart is subject to sinoatrial logistics for supply to sites, while
a tongue and its use of vocal cords is subject to a high level of
supply by ears to replicate by tones. An ear helix stop waves
out & up as a reservoir to canal down to a drum angled for an
M Link to go in & up by pressure from ossicles to an oval
window at a cochlea to intensify drum waves. A helix tilts for
any waves in any direction. With a face lowered, ears go up at
back for the helix to be an apex for favored waves from below,
to go down a canal to the drum. However, ossicles can release
the pressure pedal out & down as a reflex for internal waves,
to favor the external and continue in & down to a cochlea,
which swings to relate external & internal. In Diagram 15 (2)
the swing up to speak to unfix ossicles is tolerance to still go in
& down to a cochlea. It compares to a gut as a lower gravity
organ by collection wide to channel down, then up by link and
down by link, and then down with nothing left to digest or hear.
A tongue can move on its own like an eye, in tilts up and down
alternating to hear and speak. Its link is also muscular, and it
also goes to vocal folds, by a gutter crossing over ring tongue
edges to shape waves blown from vocal folds. The ring edges
make a mineral cone level, barely above its own gutter as a
counter cone tending back and down relative to ring up and
front. The gutter collects waves to blow and cross over in a
mouth chamber, in wave formation. It wets continually, and its
84
85
86
87
88
89
90
91
92
93
9. Appendage Superstructure
94
Gas Lift
Length
1
Liquid Flow
7 Length
Solid Light
2 Joint
Time
(Horizon)
Space
6 Length
Mineral Tight
3 Joint
Gas Contained
5
Joint
Liquid Sink
Edges
4
Length
Solid Heavy
Cause
Bases
Relative View
Out
Organ 6
Organ 4
Out
In
95
3 orbit 8 duct
In
Slice
2 sinus
7 lower arm
6 lower lid
Fix
Out
5 shoulder
In
2 elbow
Out Fix
4 cheek
4 upper arm
Slice
2 knee
In
Free
Out
Splay
4 palate
5 hip
Out
7 calf
2 lips
6 toes
Free
In
8 sole
3 ankle
Out
Free
1 big toe
Splay
8 gums 3 hinge
Splay
Out
In
1 lower teeth
7 chin
5 arch
96
Lever
Slice In
Down
Back
D
A
Cause Rings
(From the Front, Slice Follows Diagram 15)
6
4
Splay Out
Lever
Back
1
7
Down
B
C
Cause Rings
(From the Front, Splay Follows Diagram 15)
A
Out & Down
B
In & Down
C
Out & Up
D
In & Up
97
Gate Slice & Splay from Above, Inversion Each Side to Mirror Between
Right Front Spatial Gates
Right Back Temporal Gates
Center
Center
Splay
Hip
Wrist
Orbit
Slice Splay Arch
Slice
Slice
Slice
Sinus
Gape
Splay
Sole
Splay
Elbow
Cycle Down
Ride Out
Dark Branch
Ride Back
Cycle Up
Low
One Contour
Cog Line
(Adapted from Wikipedia)
98
99
100
101
102
103
104
105
below level to bounce, even if land does not give way. Then still
below level at C, a foot angles to open the instep for a big toe
open out & up using hip and thigh extended again to support
and lever us forward. Then at D, above level ankle and toes
close and instep opens again in & up to for a next step, using
knee and calf closure upright in & up behind to swing ahead.
Feet open and close ahead and behind to complete a sequence
of inhale to exhale. Leg pivots have an alternative sequence of
eat to excrete, starting at C to eat at a stomach.
At lower head, sequencing forward from stage A to favor levity
(C starts gravity), a mouth is above level, but lowers its lower
teeth & gums to open out & down to be level, gaping with a
palate & arches hovering open as a sound dish. Then at B,
upper teeth & hinge close by biting to make a mouth lever down
below level in & down, with a chin & lips hovering with them, in
& down, to bite and cradle solids, to pack by a tongue. Then at
C, palate & arches open out & up from packing solids by tongue
edges & gutter, with lower teeth and gums hovering open out &
up by a swallow moving to level. Then, moving from level to
above it again at D, chin and lips close in & up to use edges &
gutter, with upper teeth & hinge hovering in & up to open up.
Gas waves are collected below like solids and projected above
like liquids in speech. These moves harmonize for collection of
waves at N Cords, begun by a ring opening above level for a
tongue to drop out & down to speak, continuing to a stage of
listening in & down for an opportunity, to readiness to speak out
& up, to projecting outwards in & up. A mineral tongue may
have solidity below and liquidity above for gas shaping as it
nods with pauses between speaking and listening using the
ears vestibular for balanced nodding. That nodding can be very
subtle across a level of harmony shared with ears, like surf on
an undulating sea level gathering tones to utter. It would go
round & round like surf over undertow rolling back as surf.
Balance is maintained by a vestibular, while a tongue also
reflexes at a cerebellum for pulses over waves rolling forward.
106
107
108
109
Functioning
Retain
Release
Manual
- Automatism -
Delineation
Delineation
Input
Output
Awareness
- Automatic -
Sensory
Motor
Identifying
Anticipating
Brain
110
Diagram 24, Gravity & Levity Differ in Scale, but Accrete Together
Synapse
Bulbous
Hormone Transmitters
Hormone Flow
Hormone Hook-joins
Receptors
Hormone Ends to Join
Dendrite
Nerve Cup-join
111
Back
Cerebrum
Corpus Callosum
Thalamus
Hypothalamus
Network
Hippocampus
Amygdala
Pituitary
Preserve
Cerebellum
Medulla
Neurons
112
113
anatomy, but words may have that basis for that purpose as
familiar rote cues. Neurons preserve by hormone and network
by nerve, with components networked for rapid exchange of
words in speech by cerebrum & cerebellum to commons.
As noted on pages 82-85 on levels & goals, interface of moves
and world are automatically regulated. Neuroscience is well set
in its view of a literal back-check of our own moves, to avoid
being in a reflexive loop to our own moves when levelling to a
world. In my model, there is no back-check from motor to
sensory, for each sequential levelling move, to continually
attenuate. All species are chemically level, with automatic
adjustment to maintain levels in a flow that is one-way in each
neuron, although it falls like dominoes within overall pivotal &
lateral flow. I value forward momentum, but allow cycling stalls,
as a hormonal stall to edge experiences to and from it by
current. Back-checks are hypothesized in all papers, dealing
with species including birds, insects, fish, and primates.
Although we need to manually differentiate our moves and a
world in one impact at interface, our moves are our own. They
are sent delimited for levelling. Attenuation for automatic levels
means we have goals in a world that are un-attenuated, but we
condition by nerves for comfort, like our own automatic levels
for comfort. In my model, mass stalls, and charge bounces. By
partitioning of influences, hormonal stalls preserve extant
states for attenuated levels felt by inputs, while bounces to &
from stalls preempt to condition levels to goals in a world. A
medulla allows stable talk across hemispheres and a vestibular
is a more tidal pivot, and there might be some tidal aspect to
stalls in processing, while bounces condition around.
I note awareness is a continual present moment that does not
favor past or future. It represents past-to-future sites in chapter
8 equably. Sensory input is action preceding motor output as
reaction, even though cause is past and effect is future, and
even though cause is action by levity and cause is reaction by
114
115
116
117
118
119
120
121
122
123
Back
Motor Sensory
Leg Leg
Trunk Trunk
Arm Arm
Associations Hand Hand
Face Face
Tongue Tongue
Vision
Taste
Effect Exposed
Hearing
Causal Brace
Smell
Medulla
Neurons
124
125
126
127
Apex Motor
Options
Apex Sensory
Goals
Sensory Builds
Old Motor Level
Input
Readiness Potential
Milliseconds
350
Thought
470
550
Feeling Move
The chart does not show other sites instigating for a flex. Prior
functions include any subtle poise before a flex. Subtle rise & fall
in support becomes obvious as needed, as the subject will flex
eventually. Scans invade privacy to reveal that we are entitled to
be confident in anticipations, but scans reveal subtleties that are
not important enough to be obvious. We can leave the subtle to
rise and fall. Privacy is always the issue during automatism,
because we are fractionally open to being read by others before
we read ourselves anyway. We feel our self-stimulation and
world stimulus after processing in a brain builds to finalization.
128
129
before they are felt, and build to send moves to site effectors
before they are sent. In Diagram 29, three sensory & motor
cerebral-apex cortices are separated, but they in fact lateralize
in layers by different patterns, rather than by clear borders.
Splitting of components into commons is intricate. In Diagram
29, plastic processing might work with the merest relation of a
thing and thingness. Automatic outputs from inputs, as
reaction from action, using matching apex cortices for motor
and sensory, should always be functionally direct while subject
to intricate continual adjustment to appear controlled. We learn
about our evolved potential for connection of sensory action
and motor reaction by taking them both for workouts.
Variation to a regular flow might be revealed by Phantom
Limbs. Flows backtracking from, or invading across, cerebralapex cortices are theorized. V. S. Ramachandran suggests
invasion into a sensory apex. When a hand is missing and its
cortices are working, touching a cheek is reported by a
subject as if a missing hand is being touched. Instigations
could be by back flow or directly between apexes. Two-way
lines in Diagram 29 are for back or direct flow. In my model, a
cheek instigates to confirm a hand in a conditioned cycle
of cheek & hand, to mistake a touch as by a missing hand.
Perhaps a stump contributes feelings for plastic thoughts
of a hand. Invasion might be limited to creation of pain.
There is a brief delay before the subject starts to feel a missing
hand. There is priming, with a cheek anticipating a relation in
plastic processing. In my model, it is the hand touching the
cheek, and simultaneous. Touch a cheek and a hand is
identified, but insufficiently to align it to the face, which may
only deal in touch in this instigation of a hand relation. A cheek
instigates anticipation of the subjects own hand touching it as
usual, and both feel it. The subject was a smoker with an
intensified relation of hand and cheek. In Diagram 20, a
compressed arm and hand position has a hand to face, ready
for a shoulder, also felt by the subject. They are proximate.
130
Site
Limbic
Cerebral
Apex
Cerebral
Limbic
Accretion
Motor Sensory
Accretion
Front
(Hand)
Site
Back
Fill
Fire
Fill
Cheek
(Hand)
Cheek
Fill
Fire
Fill
Fill
Fire
Fill
Fire
Eye
Eye
Fire
131
132
133
134
135
Words in a World
Words are thoughts & feelings conditional with themselves,
using rigid hubs for assured construction and perhaps also for
their own attenuated levels by self-stimulation. Thoughts guide
feelings by networking them, to delimit them by commons
across components of feelings. Thoughts & feelings are
conditioned to a world, and words can be deconstructed using
key struts by commons across site components. Settled
languages should use struts effectively for conditioned use in a
world, and site analogies evidence struts by thoughts &
feelings, which deconstruct their own words for their struts.
The issue reduces now to responsibility for words. We are
given words from infancy, and we personally adopt them as
conditional thoughts & feelings. They are conditional on useful
analogy in choice of words, and that depends on whether our
words incorporate the worlds laws, which they generally do by
settled languages. Conditioning of conditionals enables action.
We can reinvent or reshape inadequate settled languages if
their conditioning of conditionals is poor, as judged by the
actions that accompany words. That is the shortcut answer to
the issue, giving personal adoption of words some freedom
from responsibility for settled errors, by invention to remove
them. However, it does not remove the ever-present dynamic
between social and personal reliance on words for action, and
responsibility by relying on them. A measure of responsibility is
reliance beyond conditionality, for felt action in a world in some
measure of conformity with the words we use. That dynamic is
relevant also to animals that are given words by human
conditioning for action, generally. Some species may have
invention to reshape words to suit their personal preferences,
but they might be less conditional by thought and more felt as
hormonal commands for habitual actions. We need to know
hormonal feelings to any conditional words in thought, by
humans & other species. Words may sometimes represent a
conditioned rather than a conditional state, important to know.
136
137
138
139
140
141
142
143
144
145
146
147
148
149
These are fine strings that shear each other for compression
fronts in a void radially around particles for adjustable linear
motion, while particles are anchored to those successive loops
by a back end providing adjustable angled direction. On pages
183-188, this is by a two-dimensional spatial plane as a string
with uniform height and distorted depth, to shear standard
heights to widen loops that are also uniform in their relation to
string by providing direct linear motion by loop widths. Height &
width are uniform relations of mass, and the depth & pulse
along string for a loop are distorted charged relations within a
graviton. A pulse distorts with depth in the direction of motion,
when loops shear to compress string to move it, or when a
particle is pushed to compress string in that direction, as loops
also compress in a void for a particle moved by an explosion.
Although loops will widen linearly with motion, a pulse thickens
& depth shortens to resting string as density inverse to motion
for momentum, summarized by a fundamental graph in
Diagram 30 for energy usage to accelerate motion linearly. A
Lorentz relation is by thickened pulse & less depth slowing the
loop rotation around string. The slower pulse around string
remains along string for widths of loops to be uniform at light
speed with uniform heights despite less depth & denser pulse.
Light speed loops continue to shear linearly for motion, but
thickening takes resting string, compressing it more directly
rather than by loops. And that direct compression is non-linear,
in Diagram 30, as an angled distortion to resting string.
Depth would allow that angling by lessening for it, consistent
with a slower temporal rate to resting string by slowed pulse,
as the well-known Lorentz relation of spatial contraction and
temporal dilation. At root, massive height paired with massive
width are for linear string motion, and they relate to a charged
pulse paired with charged depth as string distortions by a
curve when motion becomes more string by density. Less
depth takes up string to affect motion, but to a distorted curve
along with a thicker pulse to densify, while mass gives motion.
150
Light Speed
0.8
0.6
0.4
0.2
10
Linear Momentum
Low Density Loops Shear Fast Around at Constant Light Speed Along
151
Vestibular Cycle Begins at Ear, Right Spin Down all the Way
Cup-join
Lower End
Ear
Upper End
Tongue
Stretch
View from Crown
(Brain Direct)
Stack
Right
Eye
Left
Nose
Front
Medulla Corrects
Front
Gut
Lungs
View from Ground
(Brain Crossover) Stretch
Right
Left
Stack
Heart
Spine
Cup-join
Upper End
Lower End
Medulla Cycle Begins at Spine, Left Spin Up to Cross Half Way
152
Near
Destinations
Hook-join
Right
Far
Hook-join
Lefts
(Muscles)
Shearing
Hearts
(Nerves)
Spine
(Nerves)
Spine Right
Far
Sources
Near
153
154
155
156
157
158
159
160
161
162
& variable frame for blocks & fields, or strings & loops. This
frames a root relation of electrical & magnetic lines. The
magnetic slings equally to move the economical line in or out
for interactions with other atoms, ultimately for molecular
compounds, not the extremes of physics. Magnetism is also
responsible for vibration around surfaces for orbital rotations,
with either spin or anti-spin options inevitably by smooth or
angled photons tilting with momentum and polarizing to
opposite rotation at poles, positive north and negative south.
An electrical line has economy by quanta for orbitals, while
the magnetic line has variability by slinging both ways across
it, for a new orbital level, or vibrate it around the economical
line, as necessary. Momentum by atoms collectively creates
vibration to their orbitals, as both electrical & magnetic lines
align to any momentum of atoms. A surface vibration is from
excess & shortfall of momentum at a pole, from relative
momentum of particles in proximity. Any variation in relative
momentum will have the effect of orbital magnetic vibration
to resolve economy at pole and vibration across a surface for
momentum excess or shortfall in any photon exchanges.
Spin as Rotation & Vibration in Physics & Anatomy
Underlying these relations there is a fundamental choice of spin
made by a neutron for its proton on decay, and for an electron
to have a spin to match a proton automatically on decay. Antiparticles are no more than particles that spin the opposite way,
with poles reversed so that left-right becomes right-left. This
does not concern an angled photon loop, which already has
options of opposite spin between a proton & electron matching
each others spins. But it concerns the intact photons within a
neutron, as spin one way or the other will decay its two parts,
proton & electron, with opposite poles to align to matching
spins. A proton rotates backward left handed in my model, while
an electron rotates backward right handed, and a graviton
rotates forward right handed. Those simple oppositions and that
163
164
165
166
Time
(Back)
Lines of
Alternative Motions
Space
(Front)
(Right)
Cause
Lines of
Constant Directions
167
168
169
Energetic
In
Resting
In
Time
Space
In
Energetic
Lines of
Alternative Direction
In
Resting
Resting
Energetic
Out
Out
Cause
Lines of
Constant Motion
170
(2) Field:
Varying Rotations &
Constant Screw Tension
Decompress
Decompress
Neat Disc
.
Compress Photon
Compress
Fuzzy Atom
Compress Graviton
Decompress
171
Time
(Back)
Space
(Front)
Lines of
Alternative Tension
Lines of
Constant Rotation
(Right)
Cause
172
Rot. In
Rot. In
Time
Space
Rot. In
Lines of
Alternative Rotation
Lines of
Constant Tension
Rot. In
Rot. Out
Rot. Out
Cause
173
Fields
Motion
Variable
Constant
Direction
Constant
Tension
Variable
Rotation
Constant
Variable
Constant
Variable
174
175
176
Pulse & depth compress to twist graviton string away from its
strict position in the Design to merge as a neutron to become a
proton oppositely aligned to an electron. Decay decompresses
for free photon loops to twist to accrete in massive rotations.
String angles by mass create alternative spin around smooth
photons that tilt by graviton momentum, as their fundamental
relation by shearing for momentum. They reverse north &
south spontaneously on Earth in geomagnetism, neutral to any
preferred right hand rotation by gravitons. Gravitons require a
right handed rotation for a residue of particles to be created by
a Big Bang, but in geomagnetism, gravitons create poles and
saying whether they are right or left handed depends entirely
on a charged alignment to differentiate them. Gravitons care
nothing for polar choices, it cares only for a right handed
rotation. For its part, an original photon is neutral to rotation
either way, even though it can only detonate one way, but it
has one matching pole for each particle proton & electron after
neutron decay. How do we know if gravitation only rotates right
handed? It does not differentiate poles, even though it always
spins. Photons spin either way for poles as particles and fields,
but now merged as particles and accreting as their fields.
A proton relates to mass as a pivot, and when a neutron
decays, an electron is made and sent with Angular Momentum
from extant massive density of a neutron. Matched rotations,
whatever their spin, are built into the relation, and seen in
anatomy by a twist at a medulla. The same photons can have
the same spin for anti-spin particles, as angled loops
exchanged with opposite spin from particle exchanges. Antiprotons send the left hand photons that an electron would
send, and anti-electrons send the right hand photons that a
proton would send, by reversing the particle spin. A positive
charge of a proton becomes a negative charge of an antiproton, while a negative charge of an electron becomes a
positive charge of an anti-electron. It is well known that
particles and anti-particles are made in pairs. Even so, facing
equal alternatives, a photon string can be spun either way.
177
178
Pure Isotropy
I noted on page 43, a sphere has no knowable center. Pi used
to find it is endless. Eternality is from the self-consistency of
intactness. It need not change, being stable in rest-energy, but
unbalanced by favoring a compressed form. Balance by
neutralization keeps charged stability for decay to atoms.
Gravitons around Pi cannot center, but may center on the
shape of one photon as a discrete mechanism. All gravitons,
by contiguous shearing, use one photon as a detonator for a
mutual center with initial bounce for a wave, if a photon
vibrates evenly. There is a simple tilt to flatten by the charged
axes in Diagram 6, for merger upon detonation, aligning away
from buffeting by epicycle field loop momentum. A detonator
snuffs out from no energy at the center slot if aligns for antispin friction and the compression is permanent. It is no more
than an even chance to a given compression, as it existed
infinitely with that potential. Be thankful it did not snuff out.
Continual Spacetime expansion in physics has Symmetry
Breaking for particles to bridge separation conveniently as if it
is not happening in our solar system. It requires a relation of
mass and expanding Spacetime, which must relate anyway by
tying ad hoc to an Inflation to disperse particles. Particles keep
original proximities and velocities, and continue as if coasting
in a void, consistent with my model. Einstein uses three
spatial dimensions and time, and we should be able to wind
back and see shape to expansion, but this is not possible in
Relativity, which views from mass and not from a void at
mass. Einsteins Spacetime could be placed entirely within a
void to view it, but an absolute Gods Eye view from a void is
replaced by an absolute analogous to Expanding Rubber with
pure Isotropy. It is two-dimensional rubber that is flat locally,
and flat or curved as one universe. There is only a rubber
surface, with all observers seeing pure Isotropic recession.
This is uses one fact, Earths view of approximate Isotropy,
and more approximate as we try to measure outwards.
179
180
181
182
183
184
185
186
187
188
189
190
191
192
193
Dynamic
Static
Static
Time
Space
Static
Static
Dynamic
Dynamic
Cause
(2) Biology
Dynamic
Dynamic
Static
Static
Static
Static
Dynamic
Ionic
Levity
Covalent
Gravity
Dynamic
Positive
Rest
Negative
Energy
194
195
dumb numbers are four forces & four nucleotide bases, and
twenty physical constants for forces & twenty amino acids for
nucleotide bases. Coding strands ride static-dynamic change,
when repeated replications are pulled by more stable bonding
as a functional or non-functional mutation growing. Plants tend
to gain heat for chemical energy, to lose heat from around
them. Warm mammals tend to lose heat to around them.
All cells are in complete immersion in environments, for heat
loss each way as a fundamental exchange. Forget terms
like entropy and track the economy of exchange, to lose heat
to a final human product still immersed in its environment. In
Diagram 41, there is sheathing in sex cells statically for
Recombination before fertilization, then dynamic release for
replication. Cells are a product of drawing down to economical
bonding, with mutation in leaps by momentum.
Diagram 41, Nucleotides of DNA Strand
(1) Static Offset
Code
Sheath
C
G
Sheath
196
197
198
199
200
The Scheme
Forces
Substance
Form
Discrete
Continuous
Life
Continuous
Discrete
Socrates
Aristotle
Einstein
Darwin
Plato
Newton
Kant
201
202
203
204
205
confidence. We also wildly cut off our noses to spite our faces
if we assume equality, and others get better access. Access is
by appendages on a conditioned level of freer momentum,
relative to others in gaining access, for relative confidence. A
binary gamble for usage is a waste, and not grounded by
biology. Equality of access is maintained by grounded biology.
We can recondition to reasonable levels of satisfaction. Social
aims must be restructured to avoid waste, both knowledgably
& openly. Reduce absolute use, and equalize relative access.
On the ground, just stay in trades for goods & services. Always
adequately service at a trade level and be open to the public for
enquiry. Spread a name, trade, extras, waste, and social aim,
as we determine nature now. Advertising creates ideas and
conditions you to them. Avoid being told who, or what, to love.
Here is a tip to avoid binary reflex from overload of bad info and
denial of good. Fill in the gaps yourself. Subjects overloaded
are tested, allowing a guess or tying them in futile analyses to
find an accurate answer so they end up tossing a coin. They
guess a bit more accurately than a toss by subtle trends
otherwise suppressed by futile analysis. Again, we do not know
how it works, but we know how it does not work. We draw
useful pops whose content we regulate to be regular, by
undistracted decisions. Always flatten a plate. Note, the worlds
leading brand is too limited. Hot air. Use Meccano to model.
Consequences of Predetermination
A consequence of predetermination is that we would be the
purpose of nature, and that purpose may have a purpose. Try
to define it. Predetermination refines to individual anatomical
structures regardless of sex, age, or race. We may range in
standard organ & appendage use in landscapes. Species are
Convergent, which challenges random mutation of types.
Australia has evolved marsupial species like cats, dogs, bears,
rats and others, separately from placentals. Hox Genes may
provide standard structures for niches.
206
207
208
17. Conclusion
I have shared my ideas about nature in my book, using new
terms for new ideas. The first part presents my theory; the
second details the human anatomy; and the third details
particles for human evolution. I used action-reaction on the
four rigors of physics, chemistry, biology, and psychology, as
intact rigors that build one upon the other. I used the mutuality
of electromagnetism and gravitation around an action-reaction
frame and within a space-time frame for rest mass and energy.
Science attempts to unify the forces of nature to a single
particle or field, when in fact the appropriate level of unification
may be to define the mass that constitutes all particles
according to the fundamental properties of mass reconciled by
the Design within its Scheme. We might simply have a logical
universe, and we may need to use the Design and its Scheme
like a Rosetta Stone. Our anatomy may be predetermined.
This may change many of our values, given that we might now
speculate about the purpose of our existence within nature.
Such speculations may be more useful than spirituality. My
book is literal, unlike confusing spiritual texts I have read.
Metaphysics is difficult, as a void is undetectable. Science
needs broad principles to encompass non-measurable facts
of nature, but science must study substantive and formal
definitional bases for measurement, which include a void as a
frame in my Scheme. I include the study of metaphysics
among the fundamental rigors. I like the classical definition of
science as a body of reliable knowledge, with philosophy
included in it. Science may have six rigors in foundational
order as metaphysics, physics, chemistry, biology, psychology,
and methodology. In reading science, I have found it difficult to
be methodical, as I must always question conformity to
definition, like our old friend Socrates.
209
210