with the naked eye
of the aqueous humor specimens
and microscope slides
Instructions, Experiments and Process
It is possible there exist human emanations|
that are still unknown to us.
Do you remember how electrical currents and 'unseen waves' were laughed at?
The knowledge about man is still in infancy.
MICROSCOPIC VISION INSTRUCTIONS|
MICROSCOPIC VISION EXPERIMENTS
Microscopic vision requres a monocular right (or left) eye absolutely steady gaze at the 100W lightbulb to create higher frequency waves and a greater number of photons in the 500 to 1,000 nanometer range. Speedy reaction occurs at the iris's spincter muscle decreasing the iris/pupil aperture to a pin point size creating one to squint.
Squinting decreases the amount of high intensity incoherent light entering the eye. The eyelid squint point needed will obliterate the observed light bulb view and a perfect circle of bright light comes into focus. The light beam squeezes through the eyelid opening and tear fluid with photons concentrated at the exact center of the cornea called the stroma. Light coherence begins as incoherent waves travel through the stroma.
Light coherence is a decisive aspect in creating microscopic vision. Incoherent energy waves diverge chaotically in every direction, and coherent waves have an ordered definite relationship in each other. "Daylight is usually 'unpolarized' - its waves move up and down at all angles to its direction of movement. Reflected light is partially 'polarized' - its waves move mainly on one plane" (Burne, Light. P. 48). Therefore, light from the light bulb is not reflected, thus, unpolarized.
The stroma bands of well-aligned collagen fibers act as an energy-polarizing filter #1, allowing waves that vibrate in only one direction to pass through changing incoherent or scattered energy to coherent or parallel energy. No refraction occurs at the stroma as energy waves cross their wavefronts and convert phase differences, the shape of the light wave, into intensity differences, thereby permitting phase effects to be recorded. Coherent energy then enters the aqueous humor as plane waves.
The aqueous humor slightly slows the coherent energy waves and shortens the wavelengths. Coherent energy waves enhance the photon's ability to now encode holographically, like separate photographs, the signals for size and shape of the transparent microscopic specimens contained within the aqueous humor of the whole specimen, as well as an enlarged section of the whole. Coherent energy then reaches its focus point at the tiny iris/pupil aperture where the pigment in the surrounding iris absorbs stray energy.
The coherent waves continue through the infinitesimal iris/pupil oval aperture, which creates the observed bright circle of light, then passes through the exact center of the lens along the visual axis. The tiny aperture reduces energy intensity and continues to create shorter wavelengths. The coherent light beam now encounters the acellular elastic lens capsule also with no refraction, beneath which lies the lens cellular epithelieal layers.
The lens epithelial worn-out cell layers density is greatest at the lens center forming a hardened core. These cell layers are like an onion built to allow light to pass through without scattering. Each cell layer bends light differently, but the overall effect is smooth and gradual. The lens epithelial cell layers function as polarizing filter #2 and keep light coherent passing through the lens mass.
The lens mass is filled with long refractible fibers, whose transmission axis is parallel to the stroma and acts as polarizing filter #3. The energy waves begin to spread outward, diverging on their path through the lens mass, the greatest slowing of energy and therefore further shortening the wavelength. Due to no refraction, the eye's left visual field signals remain on the retina's left side and the right visual field and fovea signals remain on the retina's right side as energy enters the vitreous humor.
Light energy now passes through the vitreous humor, a colloidal gel created by the accumulation of protein fibers, further reduces the speed of light waves and wavelength shortening. These protein fibers function as polarizing filter #4 keeping the energy coherent on its diverging path to the retina.
The aqueous humor, the lens mass, and the vitreous humor slowed and shortened energy's wavelength altering energy to its particle-like characteristics as energy passed through four polarizing filters keeping the waves coherent. The minute pupil aperture diverged the energy onto a larger fovea-macula area. Coherent high frequency energy then passes unabsorbed through the retina layers of ganglion cells and bipolar cells to be absorbed at the rod and cone tips located at the rear of the retina.
The fovea-macula cones receive the diverged signals for the brilliant circle of light energy. Localized neural excitation inhibits surrounding neural activity, sharpening the constrast between the excited neurons (the brilliant circle of light) and nonexcited neurons (the surrounding dark peripheral area).
The fovea-macula cones begin the chemical and elecrical aspects. The cones contain three pigments or opsins, which vary in molecular structure. Each pigment reflects most wavelengths and absorbs only certain ones. The red-sensitive pigment erythrolade reacts to short wavelengths. A medium wavelength triggers the blue and greens pigment called calorolade. The pigment cyanolade absorbs long waves such as yellows and oranges.
The incoming energy waves for microscopic vision become coherent on passing through the eye and so have only one wavelength of energy. The yellow tones of the specimens within the brilliant circle of light suggest that this one wavelength is a long wavelength absorbed by the pigment cyanolade. It is also known that brighter luminace gives everything yellow hues. But light squeezing through a tiny aperture creates a short wavelength therefore, a reaction must be occurring at the red-sensitive pigment erythrolade, which reacts only to short wavelengths.
Rods need less energy to break away vitamin A from rhodopsin and cones need more incoming energy intensity to snap the bonds that hold the cone's vitamin A to opsin and creates a chemical and electrical impulse, which disrupts the cell's electrical field and possibly the area that alters energy to its negative form. These increased frequency impulses travel up the rods and cones and cross the synapse for more chemical altering into the bipolar cells, then jumps across the bipolar cell synapses to the ganglion cells for further chemical alteration.
Ganglion cell impulses gather together on the inner surface of the retina. The thinner cones of the fovea-macula area have single line pathways (one cone, one bipolar cell, and one ganglion cell) and make up one-half of the optic nerve. Impulses then travels down the optic nerve to the thalamus.
The right eye's left visual field impulses go to the left thalamus, and the right visual field and fovea-macula impulses proceed to the right thalamus.
Thalamus cell differences lie in their discharge patterns and handle signals separately for V3 shape and movement, V4 color and form, and V5 movement. These signals appear selectively innervated by different aspects of the ganglion cells. Impulses from the thalamus continue on to the laternal geniculate body where further reorganization of signals occur and send impulses into the occipal lobe visual cortex.
Traffic patterns for impulses from the lateral geniculate bodies go to the primary visual cortexs V1 and V2 areas where they are sorted and routed to V3, V4, and V5 areas.
The fovea-macula single line impulse pathway diverges at the right hemisphere's visual center to thirty-five times the space occupied on the retina and give the fovea-macula area the most acute visual acuity of any area. An increase in area copies the effects of an increase in intensity, since the quantity of energy increases as the area is enlarged.
The corpus callosum uses the "off" response because of the absence of left eye incoming waves. Impulses are then reflected back in reverse through the lateral geniculate bodies and thalamus. The impulse signals converge to 8% of the optic nerve back to the right eye's retinal cells to the innermost retina passing through the vitreous humor, lens, and aqueous humor.
Negative energy exits the cornea with no reverse refraction and diverges the aqueous microscopic specimen signals to the light bulb backdrop three feet in front of the eyes. Microscopic aqueous specimens are never in the same position due to continual movement, therefore cannot be used as the original backdrop to create a positive afterimage.
The outgoing negative energy strikes the 100W light bulb backdrop emitting incoherent unpolarized energy waves and creates an interference pattern resulting in a hologram. The observer's mind receives the sensation of sight.
The first sight sensation the observer's mind becomes aware of is the large illuminated circle created by the pupil's shape. Within the circle will be seen the detailed, magnified, vivid aqueous humor specimens floating towards the Canal of Schlemm. Sporadic larger target-like circles or live cornea cells will be observed stationary behind the floating aqueous particles because they are on a different level in front of the aqueous humor. Placing one's awareness in the darkness surrounding the illuminated circle, all the external objects in the peripheral visual range become apparent.
With further experimentation of viewing the microscopic specimens and with the highest degree of concentration and focus of attention, the observer can increase energy's vibratory level, which increases the negative energy's wavelengths to further enlarge a specific point of the whole image and receive a greatly enlarged view. The target-looking live cornea cell is used as an example.
Decreasing energy's vibratory level with a relaxed concentration state, decreases the negative energy's vibratory level and wavelengths. The observer then receives an opposite perspection --a whole image of the aqueous specimens.
For the honeycomb view of live cornea cells instead of only sporadic target-type cornea cells scattered within the illuminated circle, an even higher intensity light source is needed. In addition, the backdrop used needs to be much farther away to greatly increase the negative afterimage size of the cornea cells due to the ratio of cornea cell distant to image distant. In this case, the higher frequency sunlight, using the sun as a backdrop, obliterates the view of the aqueous specimens and brings into view a full and detailed picture of the live cornea cells.
Enlarged Cornea Cells
MICROSCOPIC VISION QUESTIONS & ANSWERS|
Why has not Man a Microscopic eye?
Man's perceptions change as centuries go by.
How did discovery of microscopic vision ability occur?
Is there any scientific data regarding Man's microscopic sight ability?
What is the importance of Frithof Capra's conclusion regarding self-organizing systems? Physicist Frithof Capra's conclusion affirms man's microscopic vision abilities when he states: "Self-organizing systems...show the opposite, yet complementary, tendency to transcend themselves to reach out creatively beyond their boundaries and generate new structures and new forms of organization.... Forces inherent in every living organism can work in two different directions" (Capra, Uncommon Wisdom, p. 203-4). Thus, the human eye can work as "normal vision" or the opposite direction for "microscopic vision."
Can any individual acquire the microscopic vision ability?
Why does microscopic vision need higher intensity light than that for normal vision?
Visual signals for microscopic vision follow the optic/visual axis through the exact cornea center (stroma), and lens center. The minute pupil aperature causes the energy signals to diverge onto a larger fovea area.
Is the eyelid nonpermeable to light?
Why is it necessary to squint the eyelids for microscopic vision?
How does energy coherence occur in order for microscopic vision to be possible?
Normal vision's focus of attention whose signals fall along the visual axis where the stroma allows waves that vibrate in only one direction to pass through. The lens center, lens mass, and vitreous humor continues to keeps light coherence on its journey to the retina for the most acute vision.
What occurs as coherent energy enters the aqueous humor?
Where does the slowing of visual energy occur?
What is the advantage of darker colored irises when using microscopic vision?
Where is the focus point reached when using microscopic vision?
What is a unique feature of energy entering the eye along the optic/visual axis?
How is microscopic vision opposite from normal vision?
Incoming visual energy affects the retina by energy absorption, which then produces chemical changes and electrical impulses.
Why must incoming visual energy first pass through the retina cell layers before reaching the outermost rods and cones to be absorbed?
With microscopic vision, does action occur at the rods?
What clues do the rod's action present?
What is the cones role in microscopic vision?
Incoming microscopic vision energy is coherent after passing through the tiny eyelid and pupil aperature, and coherent energy has only one wavelength. The aqueous microscopic specimens yellow tones within the brilliant circle of light suggest the "one" wavelength is a "long" wavelength. But brighter luminance gives everything yellow hues and energy squeezing through a tiny eyelid and pupil aperture creates "small" wavelengths. Therefore, assumption is made that the action is placed upon the red-sensitive pigment erythrolade, which reacts only to short wavelengths.
When viewing microscope slides with colored specimens, and if decreasing the eyelid/pupil aperture creating short wavelengths, why can color be observed?
What affects the train of chemical and electrical aspects?
How is the right and left visual fields within the microscopic vision path in opposition to that of normal vision?
What is a main aspect of the thinner fovea/macula cones?
What occurs at the optic chiasm, thalamus, lateral geniculate bodies?
What occurs as the single line fovea/macula pathways leave the lateral geniulate bodies?
What occurs with the sorted and rearranged microscopic visual cortex signals at the corpus callosum?
Is microscopic vision observed with depth perception?
What are the steps for microscopic vision observations?
When a different view grabs ones undivided attention and using a high degree of concentration, a magnified, vivid, and closer view of that specific point of attention is observed. Speculation for this occurrence is that the machinery (concentration) used shifts the vibratory level of consciousness into a higher vibration and also possibly increases that visual energy's wavelength and gives the observer the ability to view the image closer from a different perspective (an aspect of holography).
Does this aspect of holography also apply to observation of a single cornea cell greatly magnified showing color?
The sun used as the backdrop with the minute eyelid/pupil aperture creating short wavelengths cause the red-sensitive pigment erythrolade reaction. How is the greatly magnified cornea cell seen in other wavelength colors for black and green?
What is another holography aspect when using microscopic vision?
The prevailing theory is that sight occurs within the brain! This new theory shows vision as holograms, a sensation detected by the mind outside the brain! Can this new theory be proven?
Furthermore, two Soviet psychologists, Dr. Alexander P. Dubrove and Dr. Veniamin N. Pushkin, have written extensively that the frequency processing brain capabilities do not in and of themselves prove the holographic nature of images and thoughts in the human mind. They have suggested what might constitute such proof would be an example where the brain projected an image outside of itself, then the holographic nature of the mind would be convincingly demonstrated. Or, to use their own words, "Records of ejection of psychophysical structures outside the brain would provide direct evidence of brain holograms" 65 (Quoted in Talbot, Holographic Universe, P. 110).
© Copyright Mary Coffin Johnston
ALL RIGHTS RESERVED
Mary Coffin Johnston