Colour Science & Perception
what the eye settles, and what it cannot
Concept

Lens yellowing — where it appears

The crystalline lens absorbing more of the short wavelengths every decade, which is the largest single optical difference between two people. It is why two people with identical cones disagree about blues, and why the short-wave limit of colour vision is a piece of optics rather than a property of the receptors.

Named by 8 essays across 3 fields — each of them below, with the objects they name alongside it.

How far a match comes apart when the observer changes. A broad source and a three-primary source, solved at each primary width so the pair is an exact tristimulus match for the CIE 1931 observer. The pair is then handed to the 1964 observer, and the gap between them is plotted. For the observer they were built for the gap is arithmetic noise at every width. For the other it grows as the primaries narrow, reaching 0.012 at 10 nm — and displays have been getting narrower for twenty years.

Whose eyes

The standard observer is an average over seventeen people, and no reader is it. What that costs was small when displays were broad and grows every time the primaries get narrower.

limits · Limits The share of itself each change leaves behind, and the smallest is inside the eye. The residual as a fraction of the change rather than as a colour difference, which sorts the census differently. At the top is the macular pigment — the filter in front of the central few degrees of one's own retina — leaving 2.4 per cent of itself. It is a fixed transmittance multiplying the light and the white together, which is as close to a pure gain as anything here gets, and it is why nobody notices they have one.

The filters inside the eye

The macular pigment leaves 2.4 per cent of itself after adaptation — the smallest share of anything in this site's census of light changes, and less than half the next smallest. Fifty years of lens yellowing leaves 7.9 per cent, and the difference between the two says what a gain is actually good at.

eye · Cones What reaches the retina, and why the observer's table stops at 360 nanometres. The transmittance of the eye's own optics across the short-wave band, at three ages, with the brightener's absorption shaded underneath. The upper curve is an eye whose lens has been removed — the cornea alone, opaque below about 295 nanometres and transparent above it. The photopigments absorb perfectly well in this band; what stops the light is a piece of optics in front of them, which is why the short-wave limit of colour vision moves with age and can be removed surgically. A twenty-year-old receives 21 times as much of the band a brightener works in as a seventy-year-old does.

The eye stops at the lens

Neither standard observer is tabulated below 360 nanometres, and the reason is not that the photopigments stop absorbing there. It is that the light never arrives — the cornea and the crystalline lens take it — so the short-wave limit of human colour vision is a piece of optics, it moves by a factor of twenty across a lifetime, and it can be surgically removed.

eye · Cones The angle between the lens and the macular pigment, before and after adaptation. On each of 120 surfaces the angle, in the local metric, between what an older lens does to the reading and what a denser macular pigment does, binned in ten-degree steps. Read without adaptation, where both filters yellow the observer's white along with everything else, the two point nearly the same way: a median of 8 degrees. Read after each observer has adapted to its own white, the median is 156, and the two together cost less than the larger alone on 115 of the 120.

Two yellow filters cancel on a slope

An older lens and a denser macular pigment both take blue out of the light, and read before adaptation they move a colour in nearly the same direction, eight degrees apart. Once each eye has adapted to its own white they point a median 156 degrees apart on smooth reflectances and together cost less than the lens alone. On surfaces with a narrow absorption band they still sit 26 degrees apart and add. What decides it is the width of the surface's own features.

difference · Metric The angle between the two filters against how completely the eye has adapted. The angle, in the local metric, between what an older lens does to a reading and what a denser macular pigment does, on 120 smooth reflectances, as the degree of adaptation runs from nought to one. The median angle is 8 degrees unadapted and 156 at complete adaptation, and almost all of the turn happens in the last tenth: it passes a right angle at a degree of 0.928. The marks are the degrees CIECAM16 gives five rooms — an overcast sky 1.00, an office 0.94, a lit living room 0.86, a dim room 0.75, a cinema 0.66 — so only the outdoor one is at the end of the dial.

Two filters cancel only in a bright enough room

An older lens and a denser macular pigment cancel each other once an eye has adapted — and that result belongs to the end of a dial nobody stands at. Read at the degree of adaptation CIECAM16 gives an ordinary room, the two barely cancel; in a living room they add, and in a cinema they cost six times what they cost under the sky. The room has to be about as bright as an office before the cancelling begins at all.

difference · Metric Every pair of departures, before adaptation and after it. The fifteen pairs of the six audited observer departures. Each row runs from the angle between that pair's two deviations with no adaptation to the angle with complete adaptation; an angle past ninety degrees is a pair pointing apart, which is where a pair can cost less together than the larger of the two costs alone. 3 pairs gain that behaviour as the eye adapts, 3 keep it, 5 lose it and 4 never have it. The pair followed here — the lens against the macular pigment — is in the smallest group that is not empty, and every result quoted from it generalises in the wrong direction.

Adaptation turns more pairs off than on

One pair of observer departures was followed across the degree of adaptation and found to cancel only in a bright enough room. The same calculation takes any two, and run over all fifteen pairs it says something the single pair does not: adaptation is a rotation rather than a mechanism for making departures oppose each other. Five pairs lose their cancellation as the eye adapts, three gain it, three keep it and four never have it — and the pair everybody quotes is one of the three it turns on.

difference · Metric Where a surface's band sits decides the room it needs. Each of 168 surfaces at its own crossing — the degree of adaptation at which the part adaptation has yet to remove falls to the size of the part it will leave — against where that surface's absorption band sits. The line joins the median at each band centre and the rooms are marked across. A surface absorbing at 470 nm crosses at 0.883 and one absorbing at 670 nm at 0.972. Both of the filters this is about absorb in the blue, so a surface with a blue band is where the two differ in shape and has a large residual, while a surface with a red band is nearly invisible to both and its whole deviation is the shared yellowing of the observer's white.

The room a surface needs is written in its band

Whether two yellow filters cancel on a surface depends on the room, and each surface has its own crossing — the degree of adaptation at which the shared yellowing falls to the size of what is left underneath. Those crossings run from 0.68 to 0.99, and where a surface's absorption band sits accounts for almost all of the spread while how much light it returns accounts for almost none. The reds need a room brighter than a graphic-arts viewing booth, which is brighter than any room a sample is judged in.

difference · Metric Two ways to ask how much rod signal an older eye has. The rod signal's catch of each lamp divided by the S cones' own catch, against the observer's age, for five lamps — drawn twice. The upper curves take the rod signal at a fixed absolute size, and every one of them roughly doubles from twenty to seventy-five: an older lens cuts the blue before the S cones see it and the rods, peaking further into the green, lose much less. The lower curves take the rod signal at a tenth of each cone's own peak absorptance, which is the model's own definition, and they barely move at all. Nothing about the retina differs between the two; only the normalisation does.

A rod signal has no natural size

An older lens absorbs where the S cones are sensitive, so it should make the uncertain rod-to-S-cone weight cheaper. Measured, the rod signal's catch of a phosphor LED as a share of the S cones' own catch more than doubles from twenty to seventy-five — and the share the model actually uses falls by a fifth. The two differ by the S cone's peak absorptance, which the lens takes 60 per cent of, and which entered the model as a normalisation rather than as a claim.

eye · Cones

Named alongside it

The objects these essays reach for when they reach for this one.

Individual variationMacular pigmentAdaptationObserver metamerismColour differenceDegree of adaptationStandard observerViewing conditionChromatic adaptationCone fundamentalsPhotopigmentReflectance

All concepts