Enumerated Similarity States - 4: Quessivity

Daerthropes can contain a number of base activant settings. Some of these have an Enumerated Similarity State Index Value (ESSIV) that determines how one daerthrope may be compared against another. The fourth of five settings under consideration here is:

Quessivity

Daerthropes that have this ESS activated are only affected if they are within an embropheme in contact with a vasque. The ESS does not have an effect in the globinscular region itself.

Where two particular daerthropes are within an embropheme for the purpose of undergoing a daerthropic reaction, the one with the superior ESSIV will take precedence.

For example, chysanthrone synthetase is superquessive to gylon concentrate within the corlex region, so if both daerthropes are present, chysanthrone synthesis would take place rather than xebosynthesis. Ebulons from the pendiphlabatic neulones are able to reach the corlex region as there is an enclosing vasque defined by a plauric attractor zone.

Enumerated Similarity States - 3: Triessivity

Daerthropes can contain a number of base activant settings. Some of these have an Enumerated Similarity State Index Value (ESSIV) that determines how one daerthrope may be compared against another. The third of five settings under consideration here is:

Triessivity

When a phlabaglobic daerthrope is awaiting issue from an embropheme, they use pectlions to communicate this state to the nearest unencumbered Generalised Phlaba (geph).

The pectlions will assign a geph to the daerthrope and the geph will seek out the daerthrope. Normally, each daerthrope will then be processed according to the order the gephs present themselves, until all phlabaglobic daerthropes in the same pectlionic group are processed.

However, when these daerthropes have this ESS activated, those with the most significant Index Value will take precedence over others. The relevant phlaba will pick up the daerthrope with the specific ESSIV, and leave the pectlion behind. (Note that any phlabaglobic daerthropes that do not have this ESS activated will not be affected by this ordering.)

Only when all daerthropes of this ESSIV have been processed will daerthropes with ESSIVs of lower significance be considered. This will continue until all daerthropes have been processed. Pectlions will then be able to react to new arrivals.

Note that the phlabaglobic daerthropes will all be processed in either situation. As such, triessivity is more significant where timing is an issue. Timing plays more of a part within chronomodular fenduments.

Enumerated Similarity States - 2: Diessivity

Daerthropes can contain a number of base activant settings. Some of these have an Enumerated Similarity State Index Value (ESSIV) that determines how one daerthrope may be compared against another. The second of five settings under consideration here is:

Diessivity

Daerthropes that have this ESS activated are only affected if they are within an embropheme in contact with a vasque. The ESS does not have an effect in the globinscular region itself.

Groups of daerthropes with the same or complementary ESSIV take precedence over those with an inferior Index Value.

To assist in understanding the concept of complementary ESSIVs,  one may think of a diessive pair of daerthropes having negative and positive Index Values. If a daerthrope with index values of -2 and +2 are within a relevant embropheme, those with indexes of +/-3, +/-4 would be excluded from the embropheme. Also a single daerthrope with an index value of 1 would be excluded provided that no daerthrope with an index of -1 was present, and vice versa.

Enumerated Similarity States - 1: Unessivity

Daerthropes can contain a number of base activant settings. Some of these have an Enumerated Similarity State Index Value (ESSIV) that determines how one daerthrope may be compared against another. The first of the five settings under consideration is:

Unessivity

Within a vasque, daerthropes that have an activated primary ESS are ranked so that only those with a superior Index Value may remain within that part of the globinscular region affected by the vasque. Note that this restriction only applies to autoglobic and phlabaglobic daerthropes within the globinscular region, not to daerthropes found within embrophemes.

Such daerthropes are superunessive to those with an inferior ESSIV.

All daerthropes encountered to date have this ESS.

The most obvious example of unessivity is within the nidroment. The nidroment is a vasque defined by the nidegral orb, which is an ebaschulent embropheme. Within the nidroment, part of the globinscular region extends into the nolar chain, and it is here the daerthrope nolarin is found. Nolarin is superunessive to all other daerthropes, so they are excluded from the nidroment.

Sub Namli

Pectlions

Examination of the irregular indentations upon the surface of pendiphlabatic neulones confirmed that these were a major source of generalised phlaba.

These were issued via a trumpet shaped bezet at the bottom of the indentation. Around this bezet, a series of tubular openings were found, these periodically issuing what originally appeared to be another type of namli. These were named pectlions, and the indentations became known as pectlionic gaps.

It was subsequently discovered that, rather than a type of namli, these were a cluster of even smaller embrophemes.  This class of embrophemes were named sub-namli, and it was agreed that the term pectlion should be redefined to refer to these particular sub namli, and the cluster should be redefined as a pectlionic cluster.

Pectlionic clusters had no problem in traversing the globinscular region, and have been observed all around the periclentious fendument. Upon encountering an embropheme, they appear to split and the individual pectlions will penetrate the embropheme.

The choice of embropheme does not appear to be random, and investigations continue into the driving factor.

With the discovery of this particular sub-namli, investigations were made to see if further sub-namli could be found.

Ebulons

It had been known for some time that some embrophemes, whilst otherwise unrelated, possessed an unusual bezet whose purpose was unclear. In appearance, the bezets are irregularly shaped patches whose surfaces gave the impression that they are subtly changing shape. As examples, these patches may be found around the sides of pectlionic gaps on the pendiphlabatic neulones, and randomly on the surface of the nidegral orb.

With the search for new sub-namli, these patches were examined in more detail. It emerged that the bezets comprised a host of small spherical extrusions which were continually growing, bursting, being reabsorbed and then being reformed. Each burst of a miniature bubble revealed an individual sub namli primed for issue into the globinscular region. These sub namli would eventually be named ebulons.

Ebulons could only venture into the globinscular region if that part of the region was a vasque formed by a cruomative force.

A theory had been expounded that these bezets were in some way related to the action of nearby daerthropes. The ebulon was the linking factor which led to the establishment of the Snedril Vasque Theorem

Embrophemes which possessed the patch were called ebaschulent. It was found that ebulons could traverse the vasque and enter any embropheme that encroached upon the vasque. Upon encountering daerthropes, they would enable the base activant settings of these daerthropes.

Namli

A namli is a generic term for a very small embropheme, usually of specialised and/or limited functionality. They tend to exist in comparatively large numbers (the plural of namli is also namli), and are found throughout the entire class of prelentic fenduments. As such, they are very much an integral part of our studies of the periclentious fendument.

Phlaba

Phlaba are namli that transport particular classes of daerthropes around the globinscular region. These are sometimes – but very rarely – referred to as daerphores. We will encounter generalised phlaba (sometimes abbreviated to gephs) and phlaba which are more prescriptive in their tasks. A umicrophene is an example of the latter class.

Generalised Phlaba

Within the periclentious fendument, generalised phlaba are produced by two types of neulones. Each phlabum may carry more than one type of daerthrope simultaneously.
Once a daerthrope has entered the globinscular region, borne by a generalised phlabum, it has an associated globinscular density.

Umicrophenes

(Unitising micro-phlaba; holdings enclosed non-evident)
These namli bring together specified daerthropic elements into a single type of daerthrope. They are comparatively small phlaba, and shield their payload from the globinscular region. As such, any daerthrope carried by a umicrophene does not have an associated globinscular density.

Within the periclentious fendument, umicrophenes are limited to the viscinity of the Khryban Cube and are essential for the continuity of Tridelic Exchanges. This will be discussed elsewhere in some detail.

Taebrites

Taebrites are produced by the Asceguum and are directed towards the canortic bodies. The canortic bodies use indexes on the taebrites to meniate them with the appropriate ethroceles, at which point they become indethrocelic taebrites that are directed to the other canortic body. In this manner, a canortic body becomes aware of the assorted properties of its counterpart. When the indexes are exhausted, the taebrites return to the Asceguum.

When they have a presence within the Khryban Cube, they affect the Obel Ristor Valve, preventing umicrophenes from leaving this node.

Gylons

These namli are only found within the gylonic body, so will be discussed in more detail as part of the Gylon Theory eliset.

It is sufficient to say that gylons are broken down within the gylonic body and form part of the autoglobic daerthrope gylon concentrate – a primary mover in the eliset of Corlex Theory.

Snedril Vasque Theorem

This theorem relates to a class of daerthropes within the periclentious fendument.

First, two definitions.

• Vasque is used to relate to a restricted area within the fendument.
• Snedril is an acronym - "sub-namli enabling daerthrope ranking in localised"

Sometimes "Snedril Vasque" is abbreviated further to SV.

Basic Theorem

Within a specified vasque, the presence of an ebaschulent embropheme ensures  that the quessivity property is enabled in all daerthropes within the same vasque.

N.B. The adjective ebaschulent itself is a partial acronym - "Enabling a  Base Activant Setting Creating a Hierarchy Under Limits".

Example
The volume bounded by the concave part of the plaurioa, containing the corlex region and egloberal strands, is an example of such a vasque to which the Snedril Vasque Theorem applies. Within this vasque, the pendiphlabatic neulones are ebaschulent.

Two daerthropes compete to react within the corlex squamata. These are

• Gylon Concentrate
• Chysanthrone Synthetase.

Chysanthrone Synthetase is superquessive to Gylon Concentrate, which means that chysanthrone synthesis occurs in preference to xebosynthesis.

Corollary to the Snedril Vasque Theorem (in relation to the corlex region)

If the ebaschulent embropheme is endocyclonous, egloberin will be restricted making its superquessivity to gylon concentrate an irrelevance.

This is the original wording of the corollary. Egloberin is another term for chysanthrone synthetase, reflecting the source of the daerthrope (i.e. the egloberal nodes). Whilst still accurate, the term is rarely used these days. as fendumentologists usually wish to stress the before/after relationship between the daerthropes involved in chysanthrone synthesis.

Endocyclon affects the permeability of the hystelcium layer to chysanthrone synthetase, so the latter is unable to enter the corlex squamata. Consequently, gylon concentrate may be processed without any quessivity issues. In other words, Xebofactor Precursor (XFP) can be formed, providing the trigger for xebosynthesis.