Rods — where it appears
Named by 9 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.
Age can size the rod signal, if the lens is known
A rod signal leaking into the colour pathways has no natural size in the model: read as a fraction of each cone's own peak it shrinks as the lens yellows, read as a fixed amount it grows relative to the cones, and the two readings differ by a factor of two over a lifetime. An asymmetric match on observers of different ages can tell them apart, because they predict opposite trends: one says a weight fitted at seventy-five will look sixty per cent larger than at thirty-two, the other says it will not move. A handful of observers per age would show it. But a lens mistaken by ten years looks like forty per cent of the weight, and a tenth of an optical density of macular pigment as much again, so the experiment is only as good as what it knows of each eye's lens and macula.
The matches carry their own lens
A lens mistaken by ten years moves a colour match as far as half the rod signal being measured, and a tenth of an optical density of macular pigment as far again, so an experiment on the rod signal looked as if it needed a densitometer for every observer. It does not. Across a family of surfaces the three move the matches in different patterns, and one session of forty-two settings fits all three together — the lens to within a year and a quarter, better than a densitometer was asked for. The price is the weight's precision, and a second pair of lamps nearly removes it.
A lens of the wrong shape lands in the macula
One session of colour matches can fit an observer's rod signal, lens and macular pigment together — but it fits a lens of the model's shape, one exponential in wavelength scaled by age, and a real lens need not be that shape. Give a sixty-year-old a lens with the right density at 400 nm and its edge ten nanometres off, and the fit puts the error mostly in the macula, moves the rod signal's weight by six tenths of its standard error — six times the predicted tenth — and leaves a misfit the session cannot see. A second lamp pair makes it worse: 3.5 standard errors. Fitting the edge as a fourth number removes the bias, costs the weight three to fourteen per cent, and finds the edge.
A band in the lens reads as age or as macula
A lens whose absorption edge is steeper or shallower than the model's biases a matching session's fit, and fitting the edge's position repairs it. An ageing lens also grows bands: yellow pigments that add a shoulder of absorption just past 400 nanometres. The edge parameter takes none of one. A tenth of an optical density centred at 410 to 430 nm is read as four to six years of extra lens age; centred at 440 to 460, as three to ten hundredths of macular pigment. Either way the rod signal's fitted weight moves, by up to 1.4 of its standard errors in one session and 1.8 in two, and the session's misfit stays within its noise. The lens model has to carry the band, or the experiment has to state what it does not know.
Named alongside it
The objects these essays reach for when they reach for this one.
Measurement uncertaintyCone fundamentalsIndividual variationLens yellowingMesopicObserver variabilityCorresponding coloursIdentifiabilityModelling assumptionStandard errorWhite LEDDegrees of freedom