The Mystery of Tetrachromacy
theneurosphere.com
theneurosphere.com
I always wondered how that's possible.
Also I have problems with big uniform colour areas it there's small amount of green mixed with pink or red and vice-versa. I was making a sunset skybox for a game, and friends were wondering why the sky is slightly green - for me it was pinkish-red-yellow, but I put there some green by mistake.
The closer the spectrum perceived by the M (green) cone is to L (red) cone, the harder is is to differentiate red from green.
[0] https://en.wikipedia.org/wiki/Color_blindness#cite_ref-KallC...
What differs is the amount in which having a fourth type of come allows one to get rid of metameries (https://en.m.wikipedia.org/wiki/Metamerism_(color), a term that the article surprisingly doesn't mention)
If your fourth come type has a response curve that is very similar to one of te 'normal' three, there should still be _some_ effect, but it will be hard to devise an experiment that shows the ability to discriminate additional colors.
But given the impact that not having red or green cones with their fairly similar sensitivity curves has, I suspect having a fourth curve, even if it falls between the two, will have a measurable (in the lab) effect on one's ability to discriminate colors.
The next step, more controversial, would be super-vision of tetrachromacity, perhaps infra-red and ultra-violet sensitivity. Night vision glasses no longer needed for enhanced soldiers.
Utter poppycock.
The cornea and lens in humans are UV opaque, which is a very good thing because UV light is damaging. People without a lens (aphakia) are reported to perceive UV light, but this is otherwise an undesirable condition. As to infrared, some people can already see up to around 750nm or so (NIR) with awful quantum efficiency. Pit vipers and some fish have limited perception of IR, but I'm not aware of any animals that can see IR in the conventional sense… being warm blooded presents a real problem, for one.
Plainly, there are limits to what can be achieved in hyperspectral imaging due to materials, and that's without the constraints of biology thrown in the mix.
That seems... strong, especially if referring to the "Night vision glasses no longer needed for enhanced soldiers" bit.
They eventually formulate a chlorin e6 solution for human use. A few drops are dripped into Licina’s eyes, and they had him look for people hidden among trees as well as symbols on objects in dim light. Licina seemed to perform a lot better than the four other people who did not get eyedrops.
http://gizmodo.com/the-real-science-behind-the-crazy-night-v...
I wouldn't even know where to begin in criticizing their study as disseminated on their website except to say it is completely unscientific. There are no proper controls, for one. I think it's wholly irresponsible of the press to report on this work in this fashion at such a premature stage. I respect the enthusiasm of the citizen science crowd and think it's a neat idea, but stuff like this is going to quickly earn it a very bad reputation.
UV may have the potential to be damaging, but plenty of animals see UV-A safely - for example, bees[2] and mantis shrimp[3] can perceive UV to 300nm. Some birds (whose eyes are much more like ours, of course) can also perceive UV[4][5].
If we wanted some ready-made genes, I vote for borrowing from the European starling, which has receptors that sit in our enormous gap between blue/violet and green as well as UV-A [6].
Near infrared could be very useful, because (in combination with red, green, etc.) it can be used to easily distinguish vegetation, and it scatters less in the atmosphere, so it could allow clear vision at much farther distances. Most materials that are transparent to red/green/blue are also transparent to NIR, so as far as I know, the rest of the eye shouldn't need to be modified.
Most people can apparently see a little bit into the NIR if they wear NIR-bandpass goggles, but it's extremely dim and doesn't have a perceived colour that's distinct from the rest of the visible spectrum, so that's not really what the GP is suggesting. They're suggesting wiring up a true NIR-specific receptor in the eye which would provide a fourth, fifth, or sixth primary colour (in addition to red, green, blue, and optionally the in-between-red-and-green that tetrachromats see as well as a hypothetical UV-A receptor).
I can't find a cite at the moment, but some birds have NIR patterning on their feathers (I have photographed this myself at a zoo), and the last time I looked into it, there was some speculation that tropical birds in particular had some NIR sensitivity (in addition to UV-A) and had evolved spectrally-complex colouration as a result.
Thermal infrared is a much longer wavelength, and I'm not aware of a good material for lenses/eyes that is transparent to both. It's possible to have an uncooled sensor that detects it, but I agree that it's a much larger leap than UV-A or NIR.
[1] http://www.itworld.com/article/2732596/consumer-tech-science...
[2] https://www.agriculture.purdue.edu/agcomm/newscolumns/archiv...
[3] http://www.iflscience.com/plants-and-animals/mantis-shrimp-s...
[4] http://www.livescience.com/26994-how-birds-uv-vision.html
As to the safety of UV-A, I don't think you're correct. A common element of all the comparative species selected is that their life span in the wild is far shorter than our own, and there isn't going to be selection pressure happening before they would accumulate UV damage. UV damage to the eye is kind of like yellowing of plastics, it accumulates over time. As is pointed out in your first linked article, aphakia patients are advised to wear blue-blocking glasses to protect their vision. My first thought as to how bad could it be was retinoblastoma—I am not aware of any studies looking at the incidence rate of Rb in aphakia patients and PubMed doesn't show anything either, but I don't think it's an unreasonable thought.
Aside from the ionization problem, UV light also has a much higher propensity towards scatter. Floaters are bad enough for some in visible light! Of course, we're talking futuristic gene augmentation, so it's not unreasonable to suggest we'd vacuum the eyes out every now and then, so maybe floaters will not be a problem :) We still have a problem with the much higher dispersion of UV light relative to visible, given the materials we have to work with in the eye; that, plus scatter, means we're probably going to have very fuzzy UV vision. Replace the whole lens system and maybe you get better UV-vis vision, but we still haven't overcome the safety problem. Maybe instead of vacuuming out the eyes, we just swap them out for a new autologous gene-tweaked set every couple years.
NIR would seem to be more realistic than UV (certainly considering safety), but here, the quantum efficiency of the pigments would seem to be a limiting factor. As you point out, we can already actually see a little into NIR (IIRC, in scotopic with something like 10-6 QE at 750nm relative to 555nm). At first glance, the chemical structure of human receptor pigments doesn't look to be super favorable for modification to getting something that would have a good absorption cross-section in NIR. Compare the structure of vitamin A or retinal with a strongly NIR-active chromophore, there's a lot of steps bridging the two and the structure as a whole is hostile towards selective modifications, not to speak of the rings where the modifications need to happen.
As to thermal IR, I think we'd need a metamaterial for something that would work in vis and in LWIR, and that's a handwavey statement on my part. It would definitely be of interest to the military!
Overall, I think it's more plausible to augment our vision by wiring a camera directly into our visual cortex. Biology is too hard.
Creatures with infra-red vision are usually cold blooded. We shine too brightly in infrared from within to be able to see something outside.
But tetrachromacy should rightfully belong to us. It was lost by our pre-mammal ancestors, while reptiles still have base tetrachromacy, and some fish perceive even more colors.
Most animals only perceive two colors and grow two pigments. Makes animal coloring (and animal world) kind of boring for us. Birds use bright colors because they can distinguish them.
Going by wikipedia, humans radiate in the 20-37THz range, which is a long long way away from the 430THz where visible light starts.
There have been some successes curing serious blindness issues but they will be hesitant for a good long while to "cure" things like colorblindness. If things go wrong a blind person is still blind, but a colorblind person has quite a bit to lose.
The usual pattern is that only one X chromosome gets transcribed in any given cell.[1] This keeps the dosage of all those proteins correct. Otherwise there would need to be a separate set of dosage controls for XX and XY people.
The inactivation occurs pretty early in life, and when cells replicate they keep the inactivation. This results in macroscopic regions of the body with consistent inactivation. Usually this isn't noticeable, but in cats coat pigment is on the X chromosome, and heterozygous cats often show "tortoiseshell" or "calico" coloring. The patches of contiguous color there are larger than a retina.
So it seems entirely likely that all the cells in a human woman's retina would use the same X chromosome.
On the other hand, that predicts half of het women would be colorblind, which isn't observed. So maybe not so simple...
I have a second thought about downstream neural hookups and the mechanisms for those, but it'll have to wait for later.
The answer to the question posed by the title is simply that all mutant fourth cone types are not created equal. Most have a spectral response curve similar enough to an existing type not to make a real difference; a few have peak responses more squarely in-between those of the usual trichromat photopigments, allowing more finely graded color perception. (The article takes its time getting round to explaining this, but it's all there.)
Although, on second thought, color vision doesn't seem to work perfectly anyway. I never understood how red+blue can be perceived the same as far violet, it just doesn't make sense if you look at those frequency response curves.
The brain doesn't perceive color just by addition of the stimulation of the cones. Your red and green cones are still (slightly) stimulated when you see blue, and your brain tells you that blue is the color; with violet, the stimulation among the cones have a different proportion, hence violet. Incidentally, this is also why the sky appears blue; the sky is too polluted by other wavelengths to appear violet.
Without it, color printing and color televisions would be way harder to create.
Most metamerism can be trivially explained by different combinations of light stimulating cones in the same way. But it looks like red+blue and violet are different and there is just no reason for them to be perceived the same, except that apparently there is also no reason to distinguish between them.
Wikipedia claims that is because of "a second resonancy of the red-sensitive cone cells." (https://en.m.wikipedia.org/wiki/Violet_light)
None of the red cone sensitivity plots I've seen previously showed secondary peak, but that's because they were always cut somewhere in the blue region.
It does occurs fairly early in the development process (a stage called gastrulation), and the deactivation does persist for all cells that descend from a given cell present. But critically, it's late enough that a retina could conceivably possess cells descending from two different "lineages".
You can actually visibly see the "resolution" of the deactivation by looking at tortoiseshell cats. Each blotch of orange/black represents one cell present at the deactivation stage.