An Overview of Daerthropes (Part One)

This post is intended to provides high level documentation of information regarding daerthropes.

1. Daerthropes are a class of activants - something that causes a change within an embropheme.
   
2. Daerthropes have numerous properties which have a bearing on their functionality and their range of influence.
   
3.  One such property is the globic property, also known as the caenic property. There are three mutually exclusive globic properties as follows.
   
   (a) An autoglobic (autocaenic) daerthrope is capable of traversing the globinscular region unaided.
   (b) A phlabaglobic (phlabacaenic) daerthrope requires a phlaba to transport it about the globinscular region. A phlabum (also known as a daerphore) is a namli (small embropheme) that is dedicated to this task.
   (c) An aglobic (negacaenic) daerthrope is incapable of entering the globinscular region so must remain in the embropheme in which they are located.
   
4. Some daerthropes neeed to physically contact their destination embropheme(s) in order for the associated reaction to take place.
   
5. Some daerthropes only need to have a particular quota within the globinscular region for the target embrophemes to react to their presence. No physical contact need take place. These are sarpoidal daerthropes.
   
6. Globinscular Density is the proportion of a particular daerthrope within the globinscujlar region. The amount of a particular daerthrope as a fraction of all daerthropes within the region. This is symbolically shown as γ(x) where x is a unique symbol representing the daerthrope under consideration.
   
7. Quotal daerthropes is a term sometimes used for particular daerthrope that needs to fill a quota. Such daerthropes only register a presence in the globinscular region over a prescribed interval. These are usually ones which are issued by a particular embropheme, continuing until a fixed amount has been issued (prior to this, the globinscular density will be zero). The target embropheme(s) will then accept the quotal daerthrope until the globinscular density is again zero. This implies that the target embropheme(s) need a fixed quota of that daerthrope in order for a reaction to occur.
   
8. Some phlabaglobic daerthropes do not register a presence within the globinscular region. The common explanation is that the phlaba isolate the daerthrope the carry until they relese the activant into the target embropheme. The umicrophene is such a phlabum. This property of the phlabum differentiates it from the generalised phlaba (gephs) as issued by the neulones.
   
9. Some daerthropes are categorised by the daerthropic elements (dels) that define their structure. Once such example is the class of daerthropes known as tridelics. Three types of dels are combines in different ways to form different tridelic daerthropes. The elements comprising such daerthropes are given the designation h-type, r-type and y-type - the daerthrope being referred to by the numerical amount of each element. For example, T241 is a tridelic daerthrope with 2 h-types, 4 r-types and 1 y-type dels.
   
10. Tridelic daerthropes with less than 4 h-types, less than 4 r-types and less than 4 y-types need to be carried by umicrophenes. In other words, they are classed amongst the phlabaglobic daerthropes. If any del is ranked 4 or more, then the daerthrope is autoglobic. The interaction between a number of these tridelic daerthropes is almost an eliset by itself, so will not be detailed here.
    
11. Daerthropes can contain a number of Base Activant Settings. Some of these have been mentioned in previous Notes. In particular, please refer to the discussion of Enumerated Similarity States and their Index Values (ESSIV) - that is, the concepts of uniessivity, diessivity, triessivity, quessivity and quinessivity.

The Globinscular Region

The globinscular region is a diffusional matrix that separates most of the embrophemes within a fendument. A number of embrophemes move through the globinscular region, and the effect of daerthropes is communicated through this region. As such, this region is very important.

You may occasionally find that embrophemes within the globinscular region are referred to as grellitrae.

The proportional amount of a particular daerthrope within the globinscular region is referred to as the globinscular density of that daerthrope, and is written as γ(symbol representing daerthrope), e.g. γ(e).

Although it is true to assume that a particular daerthrope would be more prevalent in certain parts of the fendument, it is a feature of the globinscular region that a change to the globinscular density of a given daerthrope is felt globally. For example, when the amount of eolim produced by the Neerg Ristor valve is such that its globinscular density increases to a particular critical value, the effect is felt immediately by an embropheme called Duncan's Band and certain changes are instigated. This is the case even when there may not be any eolim currently in the vicinity of Duncan's Band.

Daerthropes may therefore affect a embropheme in a number of ways:

• by direct external contact with the embropheme
• by daerthropic reaction within the embropheme
• by the embropheme detecting a specific change to the globinscular density of the daerthrope.

Although it is possible for some embrophemes to react to a daerthrope without having physical contact, two daerthropes can only react to each other when they physically meet. Daerthropic reactions do not usually occur within the globinscular region; they tend to take place within a specific embropheme, e.g. xebosynthesis occurs within the corlex rotunda.

As mentioned earlier, daerthropes can be divided into three categories. This depends upon the ability of a given daerthrope to move through the globinscular region. Some daerthropes are unable to enter the region at all — these are called aglobic daerthropes. Some can traverse the region without any problem — these are called autoglobic daerthropes. The third type of daerthrope — phlabaglobic — can also enter the globinscular region, but only carried by a minute embropheme called a phlabum. Phlaba will be discussed in more detail when the pendiphlabatic and dipendiphlabatic neulones are examined.

Globic Types of Daerthrope

A	Autoglobic	Able to traverse the globinscular region unaided by phlabum
B	Phlabaglobic	Needs a phlabum to traverse the globinscular region
C	Aglobic	Unable to traverse the globinscular region even with a phlabum

Like many parts of the fendument, the globinscular region is prone to change under certain circumstances. The most obvious of these changes is an aggravated remorph of the globinscular region — or argrination — which is a cumulative alteration to the physical structure of the matrix. This occurs periodically in that subset of the globinscular region that lies approximately half way along the length of the plaurioa, and more specifically around the corlex region.

Argrination prevents certain embrophemes from occupying that part of the globinscular region. As the argrination increases so does the “no-go” area, and the effect is to effectively repel these embrophemes from that part of the region. This effect is known as Argrinal Repulsion, and it is most noticeable on pendiphlabatic and dipendiphlabatic neulones, embrophemes that otherwise tend to be drawn towards each other. Argrination, and its negation, are caused by changes to Duncan's Band.

Enumerated Similarity States - 5: Quinessivity

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 fifth of five settings under consideration here is:

Quinessivity

This is the fifth identified ESS. When a cruomative force establishes a vasque within a prelentic fendument, daerthropes with that have this ESS enabled have an effect upon sarpoids within the vasque.

The daerthrope(s) with the superior fifth ESS Index Value nullify those sarpoidal ethroceles imposed by subquinessive daerthropes.

Consequently, any metanolic resonance effect instigated by these subquinesisive daerthropes is cancelled within the vasque, irrespective of the location of the source daerthrope.

Nolarin, hidden within the kalim of the Y-body, has already been highlighted as superunessive to all other daerthropes within the periclentious fendument. We can now state that it is also superquinessive to other daerthropes, explaining why embrophemes in the nidroment are not affected via metanolic resonance.

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.

Essential Terminology

The following terms are essential if you wish to gain an understanding of the periclentious fendument.

Embrophemes

An embropheme is the general term for a body within the fendument. Embrophemes can contain other embrophemes, so when it is necessary to identify those that are not within another, we refer to them as high-level embrophemes or grellitrae.
 

Globinscular Region 

This can be thought as the space that separates the high-level embrophemes. It is a diffusional matrix that governs how a number of reactions occur.
 

Activants 

An activant is the general term for something that effects a change within the fendument. The primary activant within a fendument is called a daerthrope, and these will be discussed in detail. We will come across a further type called an irethone.

Namli

Whilst embropheme is the general term for a body within a fendument, a namli is a basic embropheme, usually comparatively small in size, occurring in larger numbers. Examples are phlaba, umicrophenes, taebrites and gylons.

Bezet

This is the general term for a physical part of an embropheme. 

Olythin

This is a skin, membrane or other such boundary around an embropheme.

Serbel

This is a channel that connects one area of the fendument to another. It may be a bezet within an embropheme, or a physical connection between two embrophemes.
 

Psericle

 This is an opening, usually in the surface of an embropheme, through which activants may pass in or out.

Elisets and the Prelentic Class

Elisets

This is a term used to describe an aspect of fendumentology that can largely be considered in isolation. This allows us to organise our studies into smaller subject areas, and also assists those who decide to specialise rather than obtain a general overview.

The Prelentic class

All fenduments within the prelentic class have a number of terms in common. As the intention is to study the periclentious fendument, one should be familiar with these terms, of which the following are most common:

• Embrophemes,
• Globinscular Region
• Activants (in particular, Daerthropes),
• Namli,  
• Bezets,
• Olythins
• Serbels and
• Psericles.

From this point, all unqualified references to a fendument will assume we are discussing the periclentious fendument, and consequently these prelentic terms will apply.

The Origins of Fendumentology

The earliest known research regarding the periclentious fendument dates from the early 1980s by undergraduates studying at the University of Hull. The research was instrumental in the formation of the Institute of Fendumentology. An extract of this key work appears below.

“The pendiphlabatic neulones of the globinscular region of the periclentious fendument are somewhat ebaschulent. However, the Snedril-Vasque Theorem pertaining to the egloberal nodes of this region states that any appreciable xebosynthesis during the decanistration period is atypical of an ebaschulent state. In fact, the interaction of the egloberal nodes creates a situation of unstable chysanthropy. Thus it becomes apparent, in this specific case, that the neulones are not only pendiphlabatic but also endocyclonous. This additional property of the neulones acts as a chysanthropic inhibitor, allowing the xebosynthetic process to continue during decanistration.”

To the uninitiated, the quantity of new terminology within the above extract is overwhelming. Any new field has a degree of terminology that the newcomer has to overcome, and this is especially so here, because of the abstract nature of fendumentology. Where possible, terms will be introduced gradually, and analogies will be used where appropriate. One should be prepared for a large learning curve.

Further, whilst the etymology of some terms will be discussed, this will be the exception rather than the rule.

Introduction - What is a Fendument?

A fendument is a closed system. It does not interact with external entities, nor do external entities have an effect upon it. Its purpose is to embody a branch of abstract logic, and the term fendumentology has been coined to represent the investigation of changes that can occur within a fendument.
  
As to the word fendument itself, there are assorted views on the origins of the term, most of which are perfectly acceptable. Some are of the opinion that it is merely a variation of the word fundamental, highlighting its independent nature; i.e. the fact that a fendument is the base level upon which we build all further study. Others note the word stem fend, indicating different aspects of its independence; i.e. it fends for internal entities and fends off external entities. When combined with the word domain we are then referring to an independent environment. Another common interpretation is that the entire word is derived from feigned domain, indicating a simulated environment or sphere of influence; this allows us to interpret the abstract.
 
By its very definition, there are numerous types of fendument, and undoubtedly more may be introduced over time. Most study has been regarding the periclentious fendument, with chronomodular and stasic fenduments also worthy of mention. These are classified as the greater prelentic fenduments. Little work has been done on the melanthic fendument or the numerous lesser prelentic variations.
 
The contents of a fendument are far from static and there are many interactions therein that prompt investigation.
 
The etymology of periclentious indicates peri- i.e. a prefix denoting something that surrounds an object, an example being perimeter. The next part of the word denotes the abbreviation CLENT, denoting controlled logical events: non time-based.
 
Stasic fenduments are heavily subject to spatial constraints and chronomodular fenduments are heavily subject to time constraints. This document is more concerned with pure fendumentology (i.e. the emphasis on logical abstraction) within the prelentic class, so we wish to avoid such constraints. This is our reason for restricting our investigations to the periclentious fendument.