Advanced Light And Vision Concepts

This page goes beyond the primer how color vision works.

----------
----------
 

Physics

Fluorescence

"Fluorescence" is the emission of electromagnetic radiation, especially of visible light, stimulated in a substance by the absorption of radiation of another wavelength. The emission persists only as long as the stimulating radiation is continued.

The most common cases of fluorescence convert incoming radiation of a short wavelength (e.g. black light) into longer wavelength visible light. The incoming radiation is absorbed by an atom, kicking an electron up into a higher energy level. When the electron falls back down, it doesn't go all the way down to its base state. The radiation that it emits is less energetic, of a longer wavelength.

In some cases, longer wavelength radiation is converted to shorter wavelength, as in the frequency-doubling crystals used to make green LASER pointers from IR LASER diodes. In this example, one low energy photon kicks an electron up, and a second photon kicks the electron even higher. When the electron returns to the base level, it emits energy corresponding to the sum of the two incoming photons - having a shorter wavelength.

Some fluorescent materials are:

Fluorescence can be stimulated by: We use the phenomenon of fluorescence every day, in the form of fluorescent lights.

Refraction

Light can travel through various transparent materials, media such as air, water, and glass. Light can also move through one medium into another. Consider a shaft of sunlight shining through a glass cup of water. The light is passing through first air, then glass, water, the other side of the glass cup, and back through the air.

Whenever light goes from one medium to another at an angle, the angle changes, making the light beam bend. This is known as "refraction".

When you look from the side at a glass of water with a straw in it, the straw seems to bend. When you stand in a shallow pool and look down at your legs, they seem to bend where they enter the water. This is refraction at work.

This drawing shows a beam of light going straight into a flat piece of glass. The incoming beam is called "incident". The outgoing beam is "transmitted".

Since the incident beam is going straight in, not at an angle, there is no refraction.

Note that most angles are measured with respect to the "normal", an imaginary line perpendicular to the flat surface of the glass.

This beam is hitting the glass at a 45-degree angle, with respect to the normal.

Some of the light bounces off, "reflected". Some of the light goes through, but the angle changes "refracted".

When the refracted beam passes through the other side of the glass, it is refracted again.

This drawing is a little cleaner without the numbers.

The black line indicates where you would expect the beam to be, were it not for refraction.

The amount of the bend can be computed if you know the "index of refraction" ("refractive index") of the two materials. The index of refraction for a given material is defined as the relative speed at which light moves through that material, compared to light speed in a vacuum. The equation is:

N = c/V
where: The refractive index of a vacuum, where light travels as fast as is possible, is defined as 1.0. Because any material will slow down light more than traveling in a vacuum, the refractive indices of all transparent materials are greater than 1.0.

Here are index of refraction values for various materials:
material index of refraction
Air 1.0003
Water 1.33
Glass, Fused Quartz 1.4585
Glycerin 1.47
Linseed Oil 1.48
Microscope Immersion Oil 1.515
Glass, BK 7 1.5168
Glass, Light Barium Crown 1.5411
Glass, Light Flint 1.5725
Glass, Dense Flint 1.620
Glass, Extra Dense Flint 1.6725
Glass, Very Dense Flint 1.728
Zircon 1.92
Co Green 2.00
Diamond 2.42
Ti White 2.5
Lead Sulfide 3.91
The general trend is, the more dense the material, the more it slows down light, and the higher the index of refraction.

So, how does the index of refraction help us predict the angle by which the light will bend? Refraction takes place according to Snell's Law:

N1 x sin(q1) = N2 x sin(q2)
Where: Snell's Law has several important ramifications:

Dispersion

The discussion of refraction was a bit simplified. It turns out that the index of refraction of a material is different, for different wavelengths of light passing through it. As the wavelength increases, the refractive index decreases. So blue light is bent more (shorter wavelength, lower refractive index); red light is bent less (longer wavelength, higher refractive index).

When measuring the refractive index of a transparent substance, one must identify the wavelength used in the measurement. The wavelength most commonly used for this purpose is the yellow "D line spectrum" emitted by a sodium lamp. It actually consists of two strong lines in a closely spaced doublet, with an average wavelength of 5.893 nm.

Since the index of refraction is different for different wavelengths, so is the degree of bending. This phenomenom lets us manufacture a "dispersion prism", that breaks down a ray of sunlight into its component colors. In nature, dispersion is responsible for rainbows.

Dispersion has its drawbacks, though. Lenses rely on refraction in order to manipulate light. A plain glass lens will disperse light every place that its maker intended to refract light. This results in "chromatic aberration", where the focal length of the lens is different for different wavelengths of light. This is easily noticed around the edges of cheap one-piece "magnifying glasses". In order to correct this problem, multiple element "compound" lenses are used. [Years ago, I wore spectacles with a strong prescription. They worked fine when looking through the center of the glass, where the angle was small. But looking through the sharply curved edges of the glass would produce a rainbow effect.]

Prisms

It is common to think of prisms as the triangular glass objects used in science fairs to break up a ray of sunlight into its component colors. That is but one type of prism.

Prisms can be roughly divided into general categories:

For more information than you ever wanted to know about prisms, please see http://www.olympusmicro.com/primer/lightandcolor/prismsandbeamsplitters.html

Beam Splitters and Image Combiners

A "beam splitter" takes an incoming beam of light, passes some of the light through, and sends the rest elsewhere.

Think of a beam splitter as a partially-silvered mirror.

In practice, beam splitters can be made from mirrors or prisms.

An "image combiner" is just a beam splitter in reverse.

Internal Reflection

The discussion of refraction said that Snell's Law has several important ramifications:

MORE COMING SOON.

Scattering

A sharp beam of light is easily manipulated: bent, reflected, partially reflected. Some materials are good at randomly doing these things and end up scattering light everywhere. Perhaps a better term for this is "diffusion".

This picture shows the small sharp dot of a LASER pointer, shining on a big chunk of quartz rock.

Although the light enters at one spot, the beam is scattered again and again, until the whole rock seems to glow with an internal light.

Coherent Light

Remember all those photons traveling in a beam? When all the photons in a light beam have the same wavelength, the beam is said to be "monochromatic", which means "all the same color".

When all the photons in a monochromatic light beam are synchronized, the beam is said to be "coherent". This is what makes LASER light unique.

 

Polarized Light

Remember that
photon, traveling along like a wave?

This one wiggles up and down (blue axis), while zipping along the green direction.

Another photon in the beam may be wiggling in and out of the page (red axis), while zipping along the green direction.

Envision a bunch of photons, all zipping along the green direction. But each one wiggles in a different direction, along the axis of a different colored arrow.

That's the normal state of affairs in a beam of light.

Think of a polarizing filter as having a slot that only passes light that wiggles in the right direction.

This picture shows a polarizing filter that only allows photons to pass if they are wiggling up and down.

We could twist this filter 90 degrees. It would then only pass photons that wiggle in and out of the page.

This filter is twisted by 90 degrees. It only passes photons that wiggle in and out of the page.

 

Why Is The Sky Blue?

Material in the Earth's atmosphere tends to
scatter light with short wavelengths (i.e. blue). This has several interesting consequences:

Here's what it all means:

 

Biology

 

Photoreceptor Distribution In The Eye

The mechanism of the eye works somewhat like a camera, focusing an image on the light-sensitive surface of the retina. But the retina is not equally sensitive over all its surface. Different areas of the retina have different sensitivity, depending on the particular kinds of photoreceptors there and how many photoreceptors are present.

This is a diagram of the left eye.

The red numbers correspond to light coming in at different angles, with respect to the visual axis. We will refer to these angles in subsequent diagrams.

This graph shows the distribution of cones at various angles from the visual axis.

The central "fovea" area is rich in cones.

If it weren't for the area cut out by the blind spot, the graph would be mostly symmetrical.

This graph shows the distribution of rods at various angles from the visual axis.

The central "fovea" area has fewer rods because of the many cones.

If it weren't for the area cut out by the blind spot, the graph would be mostly symmetrical.

If you were to peel the back of the eyeball like an onion, you would encounter many layers:

In operation, the layers are exactly reversed:

Since the many layers of cells in the retina are "upside-down", the photoreceptors are furthest away from the lens and the signals to the brain are conveyed by nerve fibers along the inner surface of the retina. In order for the nerves to get out of the eye, they must go through the retina. This happens at the "optic disk", resulting in a "blind spot". Blood vessels also enter and leave through the optic disc.

So, the fovea is the sweet-spot of the retina, packed with cones that provide sharp, color vision. The blind spot has no imaging ability at all.

In an individual with normal vision, one finds:

[I should find a nice place to mention that some of the information from each eye crosses over to the opposite hemisphere of the brain. It's actually quite orderly: the signals for the outside of each retina goes to the same side of the brain. The signal for the inside part of the retina crosses over.]

 

Is the retina actually a part of the brain?

Some sticklers and many textbooks will claim that the retina is actually a part of the brain. They may present the argument that the retina grows out from the brain during embryonic development. I don't have a degree in anatomy, biology, physiology, psychology, or related field, but I disagree with the experts - based on function.

I would say that a lot of information processing is done in the retina, and a lot of processing is done in the brain proper, and that they are connected by a very high-bandwidth pipeline wherein no significant processing takes place. I consider this distributed processing, not one big processor.

 

How Do Rods and Cones Work?

The eye contains large numbers of "photoreceptors", cells that detect light and send out nerve signals. All four types of photoreceptors (rods and three types of cones) work in a generally similar fashion, by way of a complex series of events.

[There will be numerous references to "cis" and "trans". In organic chemistry, these terms are used to differentiate between "isomers", two versions of a molecule that are built slightly differently. "Cis" means that the hydrogens are on the same side of a carbon-carbon double bond (or ring structure). "Trans" means that the hydrogens are on opposite sides. When dealing with vision, these concepts are used to refer to retinal, which consists of a long chain of carbon atoms, most of which are connected via trans bonds (or bonds that do not have a cis/trans distinction). We will be interested in two isomers, that differ only in the bond between the 11th and 12th carbons in the retinal chain. Depending on the bond between those carbons you get either 11-cis-retinal or all-trans-retinal.]

Each photoreceptor has a light-sensitive "visual pigment", which consists of a light-absorbing chemical called 11-cis-retinal (a derivative of vitamin A), coupled to a protein of the opsin family. Retinal is the same in all cases, but the type of opsin differs for each type of photoreceptor. It is the opsin that "tunes" a photoreceptor to a particular wavelength of light.

photoreceptor visual pigment proteins
rod rhodopsin 11-cis retinal + scotopsin
"blue" cone photopsin III 11-cis retinal + cyanopsin
"green" cone photopsin II 11-cis retinal + iodopsin
"red" cone photopsin I 11-cis retinal + porphyropsin
(There seems to be some confusion about terminology: One source said porphyropsin, iodopsin, and cyanopsin were visual pigments; another said that they were opsins; etc. One source said iodopsin was used in blue photopigment; another said that it was used in green; etc. Some sources call retinal a "chromophore", but retinal is only color-specific when combined with an opsin. Most of this confusion comes from the march of science: as technology advanced, researchers were able to further separate what had been originally thought to be pure materials; better lab techniques and equipment refined, and sometimes corrected the work of earlier pioneers. I think I got these right, but don't take them as gospel. Corrections encouraged.)

Here's a simplified chain of events necessary to turn light into a nerve impulse. [All the references that I have found describe the visual cycle for the rods. They they say that the cones work pretty much the same way. I'll do the same.]

The cones work pretty much the same way. :-)

After the light goes away, the visual pigment must be reconstituted, so that the process can recur:

Then we're ready to begin the process again when exposed to light.

For more detailed information on the biology and chemistry of vision, please see Kimball's Biology Pages.

 

Types Of Opsins

The opsin "tunes" a photoreceptor to a particular wavelength of light. Researchers have been studying the biochemistry of vision for a long time and have discovered numerous different opsins in many species. They'll probably find even more as research continues.

This chart shows numerous opsins, arranged according to the differences in the amino acids in their structure.
[From "Visual pigment: G-protein-coupled receptor for light signals", by Y. Shichida and H. Imai.]

Note that:

 

Light and Dark Adaptation

Consider sitting in a room dimly lit by a candle. Suddenly, somebody turns on the lights The illumination might seem very bright, but you soon adjust to it. When when the lights are turned off again, you see almost nothing, until your eyes adjust to the low illumination of the candle. What's going on?

The sensitivity of your visual system varies, depending on the available illumination. When you multiply all the increases together, the dark-adapted state is well over a million times more sensitive than the light-adapted state.

Chemical Changes

In the discussion of
how rods and cones work, I said that visual pigments are very fast in responding when they are struck by light. After the light goes away, the visual pigments must be regenerated, and that process takes time.

After roughtly 30 minutes in the dark, almost all of the photoreceptors are packed with their visual pigments. Everything is ready for optical stimulation. In this "dark-adapted" state, the visual system is amazingly sensitive. A single photon of light can cause a rod to trigger. You will see a flash of light if as few as seven rods absorb photons at one time.

When the lights come on, all the photoreceptors react, making the the illumination almost painfully bright. In the brightly lit room, visual pigment is used up faster than it is regenerated. The longer you stay in the light, the lower and lower the supply of visual pigment. Over the next few minutes, photoreceptors become insensitive as they run low on visual pigment: your overall light sensitivity decreases. Eventually, the rate of visual pigment use is balanced by the rate at which it is formed. This condition is the "light-adapted" state.

Chemical changes make the dark-adapted state about 25,000 times more sensitive than the light-adapted state.

Central Nervous System Changes

The central nervous system also has mechanisms to adjust light sensitivity...

In bright light, the pupillary constrictor reflex reduces the size of the pupil. This can cut down the amount of incoming light by a factor of 30.

In dim light, the central nervous system can turn up the amplification of signals along the visual pathway, by a factor approaching 3.

 

Acquired Color Vision Deficiencies

Acquired color vision deficiencies are not present at birth. They occur later, due to eye disease, trauma, age, or other factors.

Acquired color vision deficiencies include:

 

Congenital Color Vision Deficiencies (including Color Blindness)

Basics

Congenital color vision deficiencies are present at birth. They are usually inherited from the parent, but may arise from spontaneous mutations which may be subsequently inherited by the children. CVD happens when a flaw in the genetic code causes cones to be manufactured with incorrect color sensitive chemicals.

Overall, congenital CVD comprised of ~8% of males and ~0.5% of females. But there many different types of CVD. Here are the most common:

[These words appear in various forms. A "protanope" is a persion who suffers from "protanopia".]

So, what happens to these cone pigments, so that they are "missing" or "anomalous"?

In the discussion of how rods and cones work, I said that each type of photoreceptor uses a different light-sensitive "visual pigment", which is composed of a light-absorbing chemical called 11-cis-retinal, coupled to a protein of the opsin family. Retinal is the same in all cases, but the type of opsin differs for each type of photoreceptor. It is the opsin that "tunes" a photoreceptor to a particular wavelength of light.

The opsin proteins consist of long chains of nearly 350 amino acids hooked together. An individual's DNA contains instructions for building these proteins: it specifies which amino acids are hooked together, and in what sequence they are to appear. If the DNA instructions specify the wrong amino acid, you may still be able to build a protein, but it won't be exactly what you needed. This altered protein would have different chemical characteristics. It might produce an opsin that is tuned to the wrong color of light, or one that just plain doesn't react to light at all.

Types and Prevalence of CVD

So, how likely is it that the code for an opsin protein will get messed up? The types and prevalence of CVD are:

types of CVD males females person cause
anomalous trichromasy     anomalous trichromat have all three cone photopigments; but one cone photopigment is anomalous
  protanomaly 1% 0.01% protanomal anomalous "red" cone pigment
  deutanomaly 5% 0.4% deuteranomal anomalous "green" cone pigment
  tritanomaly rare rare tritanomal anomalous "blue" cone pigment
dichromasy     dichromat two functioning cone channels; one cone photopigment missing
  protanopia 1% 0.01% protanope missing "red" cone pigment
  deuteranopia 1.5% 0.01% deuteranope missing "green" cone pigment
  tritanopia 0.008% 0.008% tritanope missing "blue" cone pigment
monochromasy     monochromat typically totally color blind; may have one cone pathway in addition to the rod pathway.
  rod monochromasy rare rare rod monochromat
  cone monochromasy rare rare cone monochromat
  atypical monochromasy very rare very rare atypical monochromat
overall ~8% ~0.5%

Why do CVD rates differ by cone pigment color?

CVD rates are higher for some cone pigment colors than others. Why? It is interesting to note that protanomaly and protanopia are equally prevalent within a gender; whereas deutanomaly is much more prevalent than deuteranopia within a gender. And green-cone problems are more likely than red-cone problems overall. If you assume that changes to an opsin are equally likely for red and green opsins, and then look at their effects, one might make several inferences:

A recent study found that the gene that produces the red-cone opsin is unusually likely to undergo variations. [Published in "American Journal of Human Genetics", September 2004. Co-authored by Dr. Brian C. Verrelli. Summary at http://www.reuters.com/newsArticle.jhtml?type=healthNews&storyID=5773899.] They studied 236 samples of DNA from around the world and found 85 variations in the OPN1LW gene. They say this is about three times the number of variations one would see in any other randomly selected gene from the human genome. They conclude that, some time in the evolution that led to humans, it was advantagous to generate numerous variations in the red-cone gene. I'll be interested to see what they find when they look into the other color genes.

Why do CVD rates differ by gender?

Some CVD rates differ by gender and others are the same for both genders. Why?
 

Tetrachromats?

Humans with normal color vision are called trichromats. Their color vision is based on cones with three different visual pigments, each responding to a different part of the spectrum.

Why three? Why not four?

As it happens, three photopigments may be a popular design, but there are others. Let's consider some animals.

Interesting notes:

How do these color receptors develop?

Other species are tetrachromats and better. Why not humans?

I have seen at least two theories of human tetrachromats.

There is an additional question. Even if you find a human eye that contains cones responding to four different wavelengths, is there neurological circuitry capable of conveying and processing the signals?

Let's start in the middle - the optic nerve. There are over 100,000,000 light receptors in the retina. The optic nerve bundle contains approximately 800,000 nerve fibers. The information from many light receptors is boiled down and re-encoded, to be transmitted along fewer nerve fibers. We don't need to speculate that a tetrachromat would need more nerve fibers to carry the new color; it is far more likely that the new color information would be encoded for transmisison along existing pathways.

We're also not suggesting that a tetrachromat has additional cones with the new photopigment. More likely, some of the cones normally dedicated to one pigment would instead be manufactured with the new photopigment. In an individual with normal vision, one finds:

A tetrachromat might instead have:

Processing? I'm actually hopeful in this respect. The human eye/brain visual system has an uncanny ability to extract as much visual information as it can from incoming light, even reprogramming its image processing in order to make sense of the image.

With such interesting examples of adaptation in adult subjects, I would find it fairly easy to believe that the human visual system could extract meaningful information from additional flavors of cones. Especially since tetrachromacy would begin at birth, and the person would have a lifetime for the visual system to adapt.

A recent article suggests that the brain must learn how to process color information. ["Experience in Early Infancy Is Indispensable for Color Perception", by Yoichi Sugita. Published in Current Biology, Volume 14, Number 14, 27 July 2004, pages 1267-1271. Summary at http://www.sciencedaily.com/releases/2004/07/040727085636.htm] This paper says that monkeys raised under monochromatic light performed differently on color-matching tasks. If it is true that mammals must learn to process or interpret color vision information, perhaps tetrachromats would learn to make use of the additional color information available to them.

I stumbled across a paper describing transplating eyes between different species. The description of prior experiments said "Depending on the species,the grafted eye reportedly could endow the recipient with better visual acuity than the animal exhibited preoperatively." The new work concerned the visually evoked, neuro-endocrine skin camouflage reactions of certain salamanders. ("FOREIGN EYE TRANSPLANTS: Do They Work?" by Paul Pietsch and Carl W. Schneider Indiana University, Bloomington, Indiana, USA and Department of Psychology, Indiana University of Pennsylvania, Indiana, Pennsylvania, USA. http://www.indiana.edu/~pietsch/foreign-eyes.html] If substituting a "better" eye from a different species improves vision, there must be some neurological rewiring going on.

Scientists took mice (normally dichromats), and genetically engineered them to be trichromats. The mice were able to efficiently process sensory information from the new photoreceptors in their eyes. ["Genetic Studies Endow Mice With New Color Vision" http://www.sciencedaily.com/releases/2007/03/070322160852.htm]

 

Why Did Humans Develop Color Vision?

TBD

 

Metamers (Metamerism), A.K.A. Monomers

When two colors (either beams of light or perceived colors of objects) look alike to an observer (biology and psychology), but are actually different (physics), they are called "metamers" or "monomers". Maybe I didn't explain it all that well. Let's try some examples...

 

Related Pages

You may be interested in these related pages:

----------

Thank you for visiting. Your comments are welcome.
[back] . . . [paper and pen] . . . [tip jar]

©Copyright 2004 by The Wolfstone Group. All rights reserved. You must read and abide by our terms of service.