Mesopic — where it appears
Named by 6 essays across one field — each of them below, with the objects they name alongside it.
The eye that has no colour
Rods outnumber cones twenty to one, work alone below a hundredth of a candela, and are absent from the centre of gaze. Between dusk and a lit room both systems run at once, and neither standard curve describes what is happening.
The rods' route is priced by the lamp
A rod signal in a dim room disturbs a colour match, and how much depends on which of the cone pathways it reaches — a weight the physiology leaves uncertain, especially for the blue–yellow pathway. Under daylight the uncertainty is nearly free: a rod signal that skips the S pathway costs 0.90 at the median surface against 1.03 for one that enters all three. Under a phosphor white LED it is worth a factor of 2.75, 0.45 against 1.24. What decides it is one number per lamp: how large the rod signal is compared with each cone class's own catch of the light.
The reference lamp must not move
To measure an uncertain weight, use the condition in which the answer depends on it most. That is right about half of an asymmetric colour match and exactly wrong about the other half: a match measures a difference of two displacements, and a reference field that also moves with the weight cancels the signal the test field carries. Daylight is the least sensitive of five lamps and belongs in every one of the three best pairs — 75 settings against a phosphor LED, 2,804 against the pair of lamps the principle as stated would have chosen.
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.
One field keeps what two rooms divide out
An asymmetric match can measure how strongly the rods feed the blue-yellow pathway, but set with the observer adapted to each lamp in turn it needs seventy-five settings on the best pair of lamps and hours of waiting between them. Putting the two lamps on the two halves of one field was proposed as the quick version, at the cost of a weaker signal. The signal is not weaker. Under one shared adaptation it is three times stronger for daylight against a white LED, and the best pair needs six settings. The adaptation that makes the slow version slow is also what was dividing the rods' contribution out of each half.
A dimmer session hides a lens band in the rods
A band of extra absorption in an older lens is read by a colour-matching session as lens age or as macular pigment, and it pulls the fitted rod weight with it. The rods see the lens and not the macula, so a dimmer session, where they carry a third of the signal instead of a tenth, was predicted to tell the band from the macula. It does the opposite. With the band at 450 nm left out of the fit, the rod weight's shift grows from 1.7 of its standard errors to 2.5, the misfit a session could notice shrinks by a third, and the macula and the band trade more tightly. The rods see the band — and the rod weight, which the fit is free to move, is exactly what absorbs it. What separates the band from the macula is fitting its amplitude as a fourth number, which works in daylight already.
Named alongside it
The objects these essays reach for when they reach for this one.
RodsModelling assumptionCone fundamentalsObserver variabilityWhite LEDCorresponding coloursIndividual variationMeasurement uncertaintyPhotopigmentPsychophysicsSpectral power distributionAdaptation