The original had varying tristimuli, which in my opinion degrades the superimportance of the spatiotemporal articulation.

This demonstration is absolutely crucial to keep at the front of our lens when we hear the rabble discussing nonsense like “gamut mapping”.

There’s a 10000 thread at GitHub on CSS gamut mapping that is going to screw generations of web developers. https://www.w3.org/TR/css-color-4/#css-gamut-mapping

Folks really need to slow down and think more.

Never mistake motion for action.

So what all of these lines of thought succumb to is the brain wormed idea that “colour is stimuli”. We all know this is false, as the Ekroll and Faul demonstration shows with incredible persuasiveness.

So what **can** we learn from Ekroll and Faul? Is there a deeper pattern here?

I believe there is.

First would be to identify a key factor in the Ekroll and Faul demonstration. In my revision, given that the tristimuli are identical, we can get a sense that the local mean energy will be the +

- sole difference between the articulations. That is, we can expect the neurophysiological inhibitory opponent signals to be of similar gradient maxima and minima.

The key point is the polarity of the signal. What do we mean by “polarity”? This is the idea that there appears to be sizable indications that the information inference computations are grounded strongly by the energy “directions”.

Here, the arrows loosely identify the neurophysiological gradients of our biological assemblies.

All of this is rather interesting if we step back and fully appreciate that in terms of the neurophysiological signals, we are quite literally “hard wired” with energy analysis assemblies. The decrement signals could be broadly considered to be “energy down” gradient signals, and the increment signals are “energy up”.

If we compare to the low probability transparency mode upper right quadrant, we can see that the minima of the RGB uniquely “points” in a different direction.