A completely self-indulgent imaginary rework of the EMS system
The EMS is a good system. I like it. I'm glad it exists.
I still think it has stupid parts, and i'd change a few codes if I could.
1. Base colors
The letters are all over the place. Why is red and cream put between the eumelaninistic variant colors? Why is there a big gap in the lettering after j? I know historically why black is n, but i still don't like it. So my suggestion would be:
a - black
b - blue
c - chocolate
d - lilac
e - cinnamon
f - fawn
g - red
h - cream
w - white (white is a freak, it can get it's own letter from the end of the alphabet)
These are the ones usually deemed as base colors. If this ever changes, the new colors can get the letter i, j, k and l.
More simple genes get a color modifier letter after the base color's:
m - caramel
n - sunshine and other bimetal-type golden variants (corin)
o -
p - phoenix (if i'm right with it not changing the nose color)
q - karpati
r - recessive red variants (amber, russet, serdolic; i group them together for now, since they are all restricted to one breed and don't compete; if they become more widespread, they'd probably need an own number) (mc1r)
s - silver/smoke
t - tortoiseshell
Golden doesn't get a letter, because wide band is denoted in the numbering.
2. White spotting
This is the least organised part of the EMS coding. It'd completely overthrow it, and probably rework again when we finally have all the genetics understood.
01 - locket, belly spot ect (very low grade white, no ws allele)
02 - white attributed to DBE. ONLY if there's no other type of white spotting.
03 - glove (wgwg ONLY)
04 - low white (~09 now, and mitted and snowshoe are here too, doesn't get different code until proven different allele)
05 - intermediate white, bicolor
06 - high white, harlequin, van
09 - indeterminable white spotting
3. Wide band
11 - low wide band (golden/silver tabby)
12 - medium wide band (golden/silver shaded/tipped)
13 - high wide band (golden/silver shell/chinchilla)
A black golden ticked tabby would be a 11 25.
4. Tabby pattern
You know, i'm content with this one. I wouldn't touch it, it's good as it is.
5. Color restriction
Same. Mocha could be added as 34, but that'll likely happen anyway.
6. Charcoal
I'd introduce this as an extra letter. It'll probably need some rework when the genetics clear out.
41 - midnight charcoal
42 - twilight charcoal
So. For example a light amber tortoiseshell smoke bicolor would be brst 05, a cinnamon golden tipped tabby would be e 12, a black mink rosetted charcoal would be a 24 32 41.
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i thought too much about sex determination in dragons and now it's one am and i'm manic
color determination must be non-chromosomal, right, otherwise there's no genetic way *at all* to get all the spread of colors in the clutch... but then why is the ratio of F to M so perfectly 50-50... that's sooo easy to explain with XY or ZW or EVEN X0 system
but then why would there be two morphs of female with such ridiculously different hatch rates. i am having SO much trouble finding examples of species with female morphs, it seems like everything that does morphs only has them in the males.
but if they really are just morphs they suck because there isn't even a female-mimic morph and that's like always the second. damn. morph. so they must be distinct sexes, even if they aren't determined chromosomally...
BUT THEN I'M BACK AT THE START. how is it at all useful to evolve five distinct morphs?? what kind of process leads to *five* discrete phenotypes?
eventually i rolled around to the "royal jelly" hypothesis for goldmaking. if a female egg is big enough (or *made* big enough) then getting the right attention will turn her gold. the males just go by size, so small eggs are blue and big ones are bronze.
the only flaw in this plan is that it means greens should grow to any size, not be small. for every gold is a gang of ten monstrous greens as big or bigger than all her bronze suitors. this is not a downside. it solves all of my problems except the one where i want to explain canon...
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Are the druids (especially those that are higher up and closer to haggar) allowed to have children?
And if so then does it have to be with another member of the Druidic Church?
As well as this, if the couple then went on to have a child, then would the child also have druidic capabilities and would they be accepted as part of the Church?
I’m sorry that this was a lot of questions, but i was just curious. 💜
Not only are the druids allowed to have children, they're strongly encouraged to do so!
As Lotor alluded to in chapter 17 when sneaking around the druidic lab—and as I've touched upon in my posts on both quintessence and religion, as well as my galra dictionary—the distinguishing feature of a true druid (as opposed to simply a deacon of the Church) is the ability to manipulate quintessence, and this in turn is dictated by blood: druids are born, not made.
Sa Naacht
[[ s-ar / n-ar-kh-t ]] - Voidsworn; an individual whose life (and arguabley their very soul) belongs to the eternity of Sa Herself, and all the beings that may reside there. Unlike the Li Naacht of any cause, one does not swear themselves as a Sa Naacht, but rather is born into it as a person of Druidic descent, and it is beleived that the Druids’ ability to manipulate raw quintessence energy is a result of their ancestors having provided themselves to the denizens of Sa as vessels on the mortal plane.
So as the druids are the only galra able to manipulate quintessence (and quintessence itself serves as the Empire's primary power-source) this particular skillset is deemed an invaluable imperial resource, which, of course, brings us back to the druids being strongly encouraged to have children,,, and as many as possible at that. Historically, records that predate Brodar indicate that, in a presumed attempt to keep their blood and abilities strong, the druids once limited themselves to reproducing only with their own; although the likelihood of the resultant children inheriting their parent's druidic abilities was extremely high (though still not guaranteed), the transgenerational impact of such a limited genepool lead to an increased likelihood of significant health issues, including:
Reduced fertility
Genetic disorders
Lower birth rate
Higher infant/child mortality
Loss of immune system function
Increased cardiovascular risks
In the modern day, therefore, the Church encourages its druids to sire several children with several different partners (both druidic and otherwise) though it has long-since been the preferred practice for the sa naacht to copulate primarily with those considered to be latent-druidic—here meaning galra who are perhaps the children / grandchildren / great-grandchildren of druids, and do tend to serve as members of the Church despite not being druids themselves—so as to preserve their genetic diversity and produce healthy offspring, even if this means that said offspring are statistically less likely to inherit druidic abilities than they would be were they born of two druidic parents.
[[ Punnett squares depicting all ten potential galra genotypes—druidic & otherwise—via the 55 parental combinations that might produce them. Those squares that are greyed-out are inverted duplicates of those in colour, with the maternal/paternal genotypes switched, a difference that has no bearing at this time. ]]
There exist ten galra genotypes—here meaning the genetic constitution of an individual organism, not to be confused with its phenotype—that are as follows: [GG] [Gg] [gg] [GD] [Gd] [gd] [Dg] [dd] [Dd] [DD].
The nine segments that these punnett squares are divided into indicate parentage: Galra/Galra (top-left), Galra/Latent (top-mid & mid-left), Galra/Druid (top-right & bottom-left), Latent/Latent (middle), Latent/Druid (mid-right & bottom-mid), Druid/Druid (bottom-right).
As illustrated above the ten galra genotypes are each comprised of one maternal allele (x-axis/top) and one paternal allele (y-axis/side); these alleles exist in both the common galra [G/g] and druidic [D/d] forms, manifesting as either dominant (uppercase) or recessive (lowercase). This leaves us with 55 unique parental combinations—each with four potential outcomes, producing one of the aforementioned genotypes—wherein, importantly, dominant alleles always take precedence over recessive alleles, after which [G] takes precedence over [D] due to druidic traits being recessive in their own right: essentially meaning that it is not possible to produce a [DG/dg] child, only ever [GD/gd].
Of the 400 potential children here represented, only 150 (37.5%) are druidic galra (marked in dark purple), with 133 of this number having been born of at least one druidic parent. The remaining 250 non-druidic galra can be further divided into latent-druidic—those 150 (37.5%) children with recessive druidic alleles who therefore have the potential to produce a druidic child despite not being druids themselves—and the 100 (25%) children without.
Galra/Galra parentage
= 100% Galra kits || 0% Latent kits || 0% Druidic kits
Galra/Latent parentage
= 41.7% Galra kits || 50% Latent kits || 8.3% Druidic kits
Galra/Druidic parentage
= 12.5% Galra kits || 62.5% Latent kits || 25% Druidic kits
Latent/Latent parentage
= 25% Galra kits || 44.4% Latent kits || 30.6% Druidic kits
Latent/Druidic parentage
= 6.2% Galra kits || 39.6% Latent kits || 54.2% Druidic kits
Druidic/Druidic parentage
= 1.6% Galra kits || 9.4% Latent kits || 89% Druidic kits
Though the above might give the impression that the majority of the galra populace possess at least one druidic allele, this is not the case. My punnett squares only depict all possible parental combinations, not the statistical likelihood of them occurring as owed to the frequency distribution of genotypes; in truth, the overwhelming majority of galra have no druidic alleles at all (recessive or otherwise) with a whopping 98.65% of them being either [GG/Gg/gg]. The remaining minority of 1.35% comprises all 7 of the outstanding genotypes that contain druidic alleles—only some of which are dominant, and therefore actually druids.
[[ Punnett squares depicting all ten potential galra genotypes—druidic & otherwise—via the 100 parental combinations that might produce them, overlain with two colours: red, to indicate the pregnancy poses increased risk to the mother, and yellow, to indicate the pregnancy poses increased risk of miscarriage. The highlighted 3x3 box (top left corner) indicates those who are without a single druidic allele, as is the case for 98.65% of the galra population. ]]
If the above looks unnecessarily complex and much like it took days to construct,,, that's because it is, and it did. This being said, I am one stubborn bitch, and so I present to you my genotype punnet squares as cross-referenced with whether or not the pregnancy poses a notable risk to the mother (marked in pink for non-druidic foetuses, and red for druidic ones), or comes with an increased risk of miscarriage (marked in yellow for non-druidic foetuses, and mustard-brown for druidic ones). A risk of miscarriage is a direct result of the maternal genotype—as represented above each square—possessing more dominant alleles than the foetus, in which case the womb is likely to reject the pregnancy (and so the probability of miscarrying stands at a rather shockingly high 2:3), while a risk to the mother is caused by the foetal genotype possessing more dominant alleles than its host, in which case it might attempt to consume its mother from the inside, leading to severe hemorrhaging and the death of both parties (with a less frequent, but still alarming mortality rate of 1:3).
But onto the specifics.
For this next part, we're only going to be looking at the parental combinations in which at least one of the parents has a minimum of one [D/d] allele—in other words, everything outside of that highlighted 3x3 box in the top left—as we want to know the contained probability of a child being a druid, if there is a possibility of such (which, of course, there simply isn't for a couple without a single druidic allele between them).
Total number of potentially druidic children
= ((total number of parental combinations) - combinations in which neither parent possesses a single druidic allele) x number of potential children per parental combination
= (( 10 x 10 ) - 9 ) x 4
= 364
To simulate the mortality ratios (pink/red & yellow/brown), I assigned each colour a value correlating to the number of pregnancies likely to be a success out of a maximum 3: lilac/purple squares are worth the full amount, pink/red are worth 2, and yellow/brown a measly 1. The above total of 364 was also multiplied by three to compensate for this change, meaning that the following represents the contained probability of [insert genotype group] kits:
Galra [GG/Gg/gg] kits
= (((#of healthy pregnancies x 3)+ (#of maternal risk pregnancies x 2) + (#of miscarriage risk pregnancies x 1)) ÷ Total ) x 100
= (((32x3) + (16x2) + (16x1)) ÷ 364 x 3 ) x 100
= ((96+32+16) ÷ 1092) x 100
= (144 ÷ 1092) x 100
= 13.2%
Latent-Druidic [GD/Gd/gd] kits
= (((#of healthy pregnancies x 3)+ (#of maternal risk pregnancies x 2) + (#of miscarriage risk pregnancies x 1)) ÷ Total ) x 100
= (((80x3) + (35x2) + (35x1)) ÷ 364 x 3 ) x 100
= ((240+70+35) ÷ 1092) x 100
= (345 ÷ 1092) x 100
= 31.6%
Druidic [Dg/dd/Dd/DD] kits
= (((#of healthy pregnancies x 3)+ (#of maternal risk pregnancies x 2) + (#of miscarriage risk pregnancies x 1)) ÷ Total ) x 100
= (((70x3) + (40x2) + (40x1)) ÷ 364 x 3 ) x 100
= ((210+80+40) ÷ 1092) x 100
= (330 ÷ 1092) x 100
= 30.2%
Non-viable pregnancies = 25%
Of that 75% of pregnancies, wherein the foetus is successfully carried to term and safely delivered, the percentages stand at:
Galra [GG/Gg/gg] kits
= ((32 + 16 + 16) ÷ 364) x 100
= (64 ÷ 364) x 100
= 17.6%
Latent-Druidic [GD/Gd/gd] kits
= ((80 + 35 + 35) ÷ 364) x 100
= (150 ÷ 364) x 100
= 41.2%
Druidic [Dg/dd/Dd/DD] kits
= ((70 + 40 + 40) ÷ 364) x 100
= (150 ÷ 364) x 100
= 41.2%
Which creates a G:L:D ratio of 88:206:206 or, simplified, 44:103:103.
So, if you are (by some miracle) still with me, all that's left to do is take into account the aforementioned frequency distribution of genotypes. This means that the above percentages are, themselves, percentages of that 1.35% of the total population that I mentioned earlier, so by multiplying these two values together we can find the total population percentage for each demographic (Galra/Latent/Druidic).
Galra [GG/Gg/gg]
= (percentage of Galra genotype born of Druidic or Latent-Druidic parentage x 1.35%) + percentage of Galra genotype born of Galra parentage
= (17.6% x 1.35%) + 98.65
= 98.652376%
Latent-Druidic [GD/Gd/gd]
= percentage of Latent-Druidic genotype born of Druidic or Latent-Druidic parentage x 1.35%
= 41.2% x 1.35%
= 0.005562%
Druidic [Dg/dd/Dd/DD]
= percentage of Druidic genotype born of Druidic or Latent-Druidic parentage x 1.35%
= 41.2% x 1.35%
= 0.005562%
So, for argument's sake, in a sample size of 100billion (which is my very conservative estimate for the total galra population) this would look like:
Galra [GG/Gg/gg]
= 100,000,000,000 x 98.2376%
= 98billion, 237million, 600thousand people without a single druidic allele
Latent-Druidic [GD/Gd/gd]
= 100,000,000,000 x 0.005562%
= 5million, 562thousand people with the potential to have a druidic child, but no druidic abilities themselves
Druidic [Dg/dd/Dd/DD]
= 100,000,000,000 x 0.005562%
= 5million, 562thousand people who are, themselves, druids
As a final note, you might be interested to know the mortality rates per genotypal grouping (ie. how likely the pregnancy is to succeed depending on the foetus' genotype) because this does differ ever-so-slightly.
Galra kits [GG/Gg/gg]
= (successful pregnancies ÷ total potential pregnancies) x 100
= (144 ÷ 192) x 100
= 75% success rate
Latent-Druidic kits [GD/Gd/gd]
= (successful pregnancies ÷ total potential pregnancies) x 100
= (345 ÷ 450) x 100
= 77% success rate
Druidic kits [Dg/dd/Dd/DD]
= (successful pregnancies ÷ total potential pregnancies) x 100
= (330 ÷ 450) x 100
= 73% success rate
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