Native Martian Anatomy and Physiology

Botany and Biology Consortium Précis
Submission for consideration, addendum to the subchapter, “Native Martian Anatomy and Physiology.”
Submitter, Evan Mickal, Ph.D., VSD investigator.
Methodology: Magnetic Resonance Physiology at the Quark-focus Level
Date: Sol 28, 942

Focus of addendum: Locomotion in the absence of an endoskeleton and the Central Nervous System (CNS)

• Locomotion in the absence of an endoskeleton

Very much analogous to octopi, other cephalopods, and numerous non-skeletonized animals on Earth, the Martian’s posture and stance, erect stature, and functions of ambulation and usage of appendages depend on elastofluidics. Their bodies contain innumerable patterns of muscular tubes which are fiber-reinforced elastomeric enclosures that contain a pressurized fluid. The fibers surrounding them have angles of orientation that can be changed at will, which determines the direction in which the limbs/appendages move when the fluid within is pressurized of depressurized. The external plates (“feathered scales”)finalize the maintenance of a particular position or stance, and when in motion, louver and “unlouver” sequentially to effect smoothness of motion. Therefore, there is no endoskeleton nor one needed.

• Central Nervous System (CNS)

The shape of the Martian head is governed by the necessity of design that accommodates the complexity of the multi-oropharynx and the brain structures that innervate them and a tripartite trachea. Thus it has an elongated face—or a “long” face—reminiscent of a horse, that likeness furthered by a remarkably coincidental aspect of pigmentation: down the face is a vertical patch or pattern of depigmentation, creating a long irregular splash of white, which on a horse is called a blaze. Such a blaze, individualized for each Martian, could represent a way of telling each apart, although recognition may involve many factors other than merely how the Martian appears. The blaze seems to have embedded in it innumerable olfactory cells, making this an organ for smell.

To appreciate the Martian CNS it is first important to understand aspects of breathing and ingestion that also impact the shape of the head.

There are six bilateral sets of mouths and throats that funnel together such that they can effect a steady single intake of ingestion along a single esophagus no matter how many mouths are ingesting. This coalescing requires distance and is a major determinant of the distinctively long face. (The main mouth goes its separate way—SEE BELOW.)
Each throat has two posterior openings:

1. One leading into a separate esophagus that distally fuses with the other esophagi into a central one; and

2. the other leading into a “reverse” trachea [SEE BELOW] that is the source of the blasted air from the central air bladder used in vocalization.

These two posterior pharyngeal openings at the back of each throat are separated from each other by a glottis—an opening guarded by a septation that can flap closed against the reverse trachea so that food can be diverted properly downward into the central alimentary tract and not into the central air sac [SEE BELOW]. In this way, choking is prevented.

The esophagus related to the primary mouth and pharynx does not lead to the location where the six ancillary esophagi fuse, but instead enter the distal alimentary tract farther caudad. Although the primary mouth appears externally as two joined together at the midline, this is misleading, as it is single-chambered just beyond the lips. What was initially thought of as two separate tongues, one on each side, is in fact a single tongue for the single chamber, but with its terminal portion forked.

There are smaller but completely functional tongues for each of the separate ancillary mouths. There also appear to be taste buds for different discriminations among the numerous ancillary tongues, prompting the Martian to use specific mouths for specific tastes and textures of food and liquids ingested. Each mouth has teeth, clear but in the shadows appearing dark. Each tooth has a single fiberoptic tract.

The external proboscis-like cetaceous “blowhole” (main air intake) and its tract does not cohabitate with any of the pharyngeal area. Its trachea is a dedicated one-way route for air from the blowhole that distally trifurcates into the one central and two bilateral air sacs. The bilateral air sacs also exhale back out toward the blowhole, whereas the central air bladder has a valve such that it only exhales through its separate reverse tracheae when speech occurs.

The blowhole entrance that trifurcates distally into three separate tracheae ultimately end in two bilateral primary bronchi and one secondary central bronchus, the bilateral ones ending in multilobular air sacs on either side of the large central unilobular air bladder the central bronchus supplies. The bilateral air sacs provide oxygen by passive diffusion into venous lakes surrounding them, much like the placental systems in Earth mammals.
While the bilateral air sacs are for oxygenation, the central bladder, alternately, provides two functions:

1. It serves as a storage depot of breathable air that, through spillover (passive diffusion)seeps through its semipermeable membrane into the adjacent primary multilobular air sacs [SEE ABOVE]; and

2. there is a collection of hundreds of sphinctered tubules emerging from its posterior that coalesce into seven separate “reverse” tracheae [SEE ABOVE] that provide the expulsive impetus for speech through each of the seven mouths. The seven reverse tracheae each house a set of vocal cords at varying distances from their eventual target mouths, the variation of distance contributing to a wide variation of different tonal qualities (pitch, timbre, resonance). The Martian, linguistically, uses these variations in conjunction with the number of mouths speaking or singing to express nuance and/or emphasis. Whereas in the human the glottis is relative to the vocal cords, in the Martian the sets of vocal cords and glottises are separate from each other for each of the reverse trachea (“air routes”); each glottis is at its junction to its respective pharynx, to preclude food aspiration, using a valve for closure in lieu of the cords themselves as in humans. Even though the sets of vocal cords are at varying distances for effecting unique phonation qualities, each glottis is at the same position, i.e., the glottopharyngeal junction.

In summary, the blowhole feeds air to two bilateral air sacs and one central air bladder. The bilateral air sacs exhale their breaths the way they came in, through the primary tracheae; the central air bladder eliminates excess air by diffusing into the adjacent air sacs, but its main function is to blow air through a set of unrelated “reverse” tracheae through vocal cords. The only possible site for choking would be between the pharynx of each mouth and the termination of each reverse trachea, but this is precluded by the flap of tissue over each glottis.


The Martian brain is made up of six lobes, or hexaspheres. Functional Magnetic Resonance Physiology has determined that each lobe (hexasphere) directs independent conversational thinking that results in vocalization from one (or more, simultaneously versus serially) of the six ancillary mouths. All six hexaspheres appear to contribute cogitation for conversing with the primary mouth, when articulating a “main message.” Although they can act separately, all of the hexaspheres also are interconnected by an infrastructure analogous to the human corpus callosum, which I theorize allows a consortium of unified awareness, thinking, and volition among the set of hexaspheres.

Hearing is via an acoustic apparatus that begins with four independently aimed calderas on each side of the head, all eight each contributing a neurotubule that terminates at a central ganglion in each hexasphere. Thereby, each hexasphere’s acoustic ganglion receives a bundle of eight neurotubules representing the gamut of the collective caldera perception of sound. The central acoustic ganglia appear on functional scans, at the electron level, to deal with filtering pitch and sonolocation.

Each caldera is associated with its own ganglion that surrounds its sound transport tubule (STT), more specifically, surrounds that portion of the SST that houses small osseous structures shaped like varying tiny tuning forks, 18-20 nm in size; each of these caldera ganglia have afferents from all of the hexasphere acoustic ganglia and efferents to the small muscles that comprise and aim the caldera rims. Consortium thinking of what is being heard focuses the directional pivots of the individual calderas. Externally, the calderas, which hold a small amount of fluid each, are each covered by a parabolic tympanic membrane.

For each eye there is a laminated neurotubule that is a coalescence of thousands of neuromusculotubular fibers that seem to both convey collected visual stimuli and move the globes.

The bilateral laminate optic neurotubules meet interiorly in the midline, as a “light basket,” positioned equidistant from the hexaspheres of the brain; this light basket appears to be a tightly spiraling structure that follows the Fibonacci path of the “golden rectangle,” i.e., the spiraling neurotubules are shaped like a nautilus. This nautilus-shaped light basket is surrounded by an iron-rich magnetic encasement, itself dynamic in that it can magnetically focus free electrons as an undulator, along the spiral. The neurotubules are highly reflective and at the central termination (innermost part of the nautilus) an escape channel allows egress of a potentiated lasered pulse that feeds all hexasphres as well as returns some light back to the eyes (for unknown reasons).

Essentially, the light basket is a free-electron laser that distributes, arboreally, synchrotron radiation to all hexaspheres and the eyes at the speed of light. Theoretically, because the undulator encasement can vary the parameters of the magnetic field, the intensity and wavelength of the radiation can be adjusted on the fly, i.e., are tunable from microwave through ultraviolet and even X-Ray spectra as well.

The eyes themselves are not sufficient to contribute enough light to power the light basket’s ultimate output. Besides the laminar afferent optic nerves, the light basket also receives another afferent trunk of laminated neurotubules from the lux-cap, the area on the external head analogous to the scalp portion of the human head.

The lux-cap is very much like a scalp in that fiberoptic projections emerge from it in a hair-like fashion. These are sparse, otherwise they would pose interfering shadows for the miraculous nature of this head covering. Louvered parabolas, layered down to a depth of approximately one centimeter, collect light and an entire subscalp cranium receives coalescing bundles of phototubules that ultimately end intracranially at the light basket. Thus, the light basket has a dual source of light—from the eyes secondarily but from the lux-cap primarily.

The fiberoptic, sparse “hair” appears to be efferent only, varying colors and intensity, possibly indicating mood as a fiberoptic, lighted version of “body language.” I can discern a reverse polarization along these “efferents only,” indicating they should be able to receive input as well, like the lux-cap.

Light collected by the lux-cap, defying current wave physics until a logical explanation ensues, experiences no loss of photon energy. When the electromagnetic spectrum was applied to the lux-cap, it was evident that, besides the visible human spectra, IR and UV were collected without loss as well.

The light basket is quite large, about five centimeters in diameter, and with its iron-rich magnetic encasement, almost ten. Below it is a five-cm ventricle, but unlike human brain ventricles that have circulatory cerebrospinal fluid, it is filled with an unknown gas, the spectroscopic identification of which failed due to the interference from the overlying light basket magnetic encasement.

From the center egress of light and radiation of the light basket, branching of neurotubules swirl in complexity to become the actual six hexaspheres. It appears the light basket is the innermost origination of the entire Martian central nervous system.
The hexaspheres also accommodate the afferents and efferents that appear to either receive information from or innervate, respectively, the rest of the body.

There is no analogue to the human or mammalian cerebellum, all autonomic processes, i.e., breathing, pulsatile cardiovascular system, proprioception, distributed along a decentralized scheme among the respective organs or joints.

There is no spine, per se. Bundles of tracts find their way along two main lateral bands at the Martian’s sides, distributing from or coalescing toward them.

Crucial to the evaluation of the CNS is the nature of the neurotubules and larger neurotubes, themselves.

(There have been observed similar, although rudimentary, structures in the few humans with indwelling ferropods, suggesting divergent evolution of species as distantly related as Martians and ferropods, from a common ancestor. In humans harboring ferropods, the interaction of two xenospecies will no doubt prove informative, but to date the chapter on this interaction remains unwritten. This will undoubtedly cross-reference with the official findings yet to be written as a subchapter of the Cultural Psychology Committee Précis.)

The arboreal cascade of the CNS from hexasphere to neurotubes to neurotubules and vice versa demonstrates a consistency of structure. Whether such structures effect muscular, glandular, or neuroinformative processes, it is clear that they constitute a fiberoptic system.

Although a simplification, it is also a truism that light plays an important part in Martian cognition. Its complete absence renders a Martian not only unconscious, but barely alive, its light basket engaging in a secondary backup system of phosphorescing to maintain at least a baseline level of minimal survivability. It is unknown how long the light basket backup can last, but it is apparent that once exhausted, death would be imminent.
The neurotubes and neurotubules are multichambered along their neurotubular lengths by septations. Each septated chamber is able to polarize the as-of-yet unidentified rarefied gas within, which can then propagate an electrical potential across subsequent septa, propagating subsequent polarizations en route. This appears analogous to action potentials causing propagations of neurosignaling along dendritic/axonic paths in the human brain. The result of these propagations, whether Martian or human is the same:

Cognition, intention, autonomic and voluntary actions; viable function; volition; self-awareness and sentience; perhaps a conscience.

A soul?
At quark focus, the MRP showed Cooper pairs, entangled photons on either side of each septum. Such Cooper pairs, seen in superconductivity across membranes, the phenomenon in physics—called a Josephson effect—was a thing of beauty. And it was in each Martian head.

It was fast. The simple reality is this: Martians think at the speed of light!