Theme

The thread: The instrument is the reader — page 15

This is the one subject where the page is displayed on the apparatus under discussion, and the reader's own eye is the measuring device. Several figures here are experiments rather than illustrations.
Near the macula a wrong density moves every experiment together. For an observer at sixty with a lens band at 445 nm and an unmoved macula, two sessions: each of twenty simulated experiments' fitted band amplitude with the macular density held a tenth low, at its truth and a tenth high. A tenth high moves the band by -0.031 on average with a spread of 0.0024 between experiments; a tenth low by 0.030, spread 0.0022; the band's own standard error is 0.023. What the eye does

A wrong density shifts every experiment alike near the macula

Read from the expected matches, a macular density fixed a tenth too high lowers an older observer's lens band at 445 nm by 1.4 of its standard errors and raises a band at 415 nm by 2.4. Real experiments carry noise, and the prediction was that their fits scatter about those biases with the fixed fit's own error, so that a tenth's mistake puts the band beyond twice its error in about a third of experiments at 445 nm and two thirds at 415. Twenty simulated experiments per case, each fitted with the density free and held at 0.9, 1 and 1.1 of its truth, give five of twenty at 445 nm and sixteen at 415 under two sessions — eight and eighteen with a line on the macula's peak. Near the macula the bias is a rigid shift: every experiment moves by the first-order amount to within a tenth of a standard error. Far from it the bias is lopsided — up by 0.058 for a density too high, down by 0.032 for one too low — and a density too low erases the band altogether in one experiment of twenty.

A channel at its own pump reads the long pump better and the short one hardly at all. For the ten locus-built LEDs at each pump: the spread of the camera's colour error, and how far a line in one blue departure — at 440, 450 or 465 nm — with the 500 and 640 nm departures misses it, each LED left out. The 465 nm LEDs fall from ±0.264 with the 450 nm departure to ±0.135 with their own; the 440 nm LEDs from ±0.171 to ±0.149; the prediction was ±0.08. What a camera does

A channel at each pump cannot see the recipe

Thirty white LEDs built onto the Planckian locus defeat a line in a small sensor's three departures, except within one pump: the 452 nm LEDs are read to ±0.047 by the 450 nm channel, the others no better than ±0.15. The proposal was a channel at each pump — 440 and 465 nm beside the 450 — and the prediction that each pump's LEDs would be read from their own channel within ±0.08. The 465 nm LEDs' own channel halves their miss, to ±0.135; the 440 nm LEDs' moves it from ±0.171 to ±0.149. No line in any three of the five departures reads either pump better than ±0.1. Yet the camera's error is simple: a line in what each LED is made of — its red phosphor, its colour temperature and their product — reads every pump within ±0.07, the 440 nm LEDs to ±0.043. The error is easy; the channels cannot see the recipe that sets it. Knowing each LED's pump halves the pooled miss, to ±0.119, and two blue channels can tell only one pump of three from the others.

Two LEDs of one colour, one with a red phosphor. Two white LEDs pumped at 452 nm, both on the Planckian locus at 4,000 K: one with no red phosphor and its converter peaking at 579 nm, one with the full red phosphor and its converter pushed to 529 nm, drawn at equal total power. The red phosphor adds light past 620 nm and the shorter converter takes it away from 570 to 610, so a channel anywhere in the red sees the two changes together. What a camera does

The converter gives the red phosphor away

A camera's error under white LEDs built onto the Planckian locus is simple in what each LED is made of — its red phosphor and its colour temperature — and a small sensor's narrow departures cannot read the red phosphor. The proposal was a channel at 610 nm, where a garnet converter falls and a red phosphor rises, and the prediction that it reads the red-phosphor strength within a tenth of its range. Within a pump it reads nothing: ±0.36 to ±0.43 at 440 and 452 nm against a spread of ±0.36, and no red channel from 600 to 680 nm does better than ±0.22. The reason is the locus. To keep the white's colour, each step of red phosphor pushes the converter's peak shorter, by 29 to 55 nanometres from none to the most, and in every red channel the two changes cancel. What survives is the converter: the 600 nm departure reads its peak to ±5 nm. Read across all thirty LEDs at once, the converter gives the red phosphor away — ±0.12 — and the error read through that estimated recipe comes within ±0.08 at every pump, the 440 nm LEDs at ±0.078, half their own channel's miss.

With the notch in it, the ceiling holds to the deepest column. For the reversed tube on the one-nanometre table, the ceiling over the lamp's true peak in its lowest window against the column's depth: built on the 1.2 nm core with no notch, and with each window's factors taken for its line's notch — from the true depths, from the notch fit's depth read as an optical depth, and from the fitted depth used directly. At a depth of five the four ceilings sit at 0.776, 1.110, 1.295 and 0.972 times the true peak. What light is

A ceiling that knows the notch holds to the deepest column

A lamp's table promises a ceiling for how high any line can rise between its entries, and for a reversed tube — every line notched by a cooler column — that ceiling fails on a one-nanometre table from a column depth of two and a half, because its rule assumes the line it bounds has no notch. The notch fit already reads the yellow line's notch, and the proposal was to build the ceiling for a notched line instead: in each window, the factor for a slit-blurred line carrying that window's notch. The prediction was that it holds to a depth of four. It holds to five, the deepest column the census runs, at every depth and in every one of 440 noisy readings. The fit's depth must be read as an optical depth, −ln(1 − d); taken as the first-order depth it fits as, the ceiling fails from four and a half. Part of the safety is the fit's own error: read that way, a deep notch comes out too deep — 4.25 for a true 2.29 at depth five — and an overstated notch only raises the ceiling.

A coarse table holds to the deepest column on a borrowed notch. For the reversed tube on the two-nanometre table, the ceiling over the lamp's true peak in its lowest window against the column's depth: with no notch, with the true notch, and with the notch borrowed from the one-nanometre fit; beside the one-nanometre table's ceiling on its own fitted notch. Without a notch the coarse ceiling fails from three and a half; with the borrowed notch it stands 8.4 to 42.4 per cent above the true peak at every depth. What light is

A coarse table can borrow a notch, but not a phantom

A one-nanometre table can bound a reversed lamp by building its ceiling for the notch its own fit reads. A two-nanometre table cannot read the notch, and its ceiling, built for an unnotched line, fails from a column depth of three and a half. The proposal was to borrow the notch from the finer table, and the prediction that the coarse ceiling then holds to five with a wider margin. It does: 8 to 42 per cent above the reversed lamp's true peak at every depth, against the fine table's 1 to 29. But borrowed from the fine table's noisy readings, one notch in 440 sinks the coarse ceiling below the true peak — a notch of 0.13 the fit read in noise where there was no column at all. Under a wide slit a shallow notch flattens a line's top, two flanking entries see more of it, and a ceiling that assumes the notch is set lower; the phantom set it too low. Borrowing only notches the depth rule calls — deeper than 0.2 — keeps all 440 safe; borrowing those more than twice their error does not.

One session, two valleys: the macula where it is, or far short. For the observer with a band at 415 nm and an unmoved macula, one session: each of twenty experiments' census fit in band amplitude and macula peak, and, for the 7 the census missed, the better fit, joined to the census's. Every better fit puts the macula seven to nineteen nanometres short: a second valley in which a macula moved far short does part of the band's work. What the eye does

One session has a second valley

Every essay on older observers since the second session has read its fitted lens bands and macula shifts from one census: nine simulated observers, three designs, twenty noisy experiments each, every fit a damped descent from two starts. Two of forty experiments refitted in the last essay found a better fit than the census had. The prediction was that the census misses one fit in twenty, almost all where the band is small, and that the misses change no count it reported by more than a few hundredths. Refitted from three more starts, 66 of its 540 experiments have a better fit — 45 of 180 under one session, 9 and 12 under two and three. Sixty of the 66 better fits move the macula's peak more than two nanometres further short, most shrinking the band, and 31 lie lower by under one unit of χ²: a second valley, nearly level with the first. Two sessions' counts stand to within one or two experiments. One session's do not: with the best fits an unmoved macula is reported moved in eight experiments of twenty, where the census said one.

Most of the residue is not at the rim. At each coverage of the orange ramp, the residue a single clump on the tile leaves — the least rim the tile can hold — beside thirteen clumps'. The single clump keeps 92 per cent of the thirteen clumps' residue at five per cent and 94 at sixty: the rest of the turn is the tint's bare paper glowing beside ink that does not. What the brain does

The rim was never most of the glow

On brightened paper a halftone tint keeps a hue turn a reader fully adapted to the sheet cannot remove, and five essays have chased the part of it that lives at the ink's thin rim — merging spots, clustering them, growing them — down to a rule: the clump count sets the residue, and only coarser patterns lower it. The proposal was a screen coarse in the pale tints and finer as the tint darkens, and the prediction that six clumps on the tile beat the 150-line screen by more than half a degree below twenty per cent. They beat it by 0.11 to 0.17. Scheduled six, thirteen and twenty-six clumps save a third of a degree at ten per cent and give back a fifth at sixty. The reason is the floor. One clump on the tile — the coarsest pattern it can hold, nearly all its rim gone — still leaves 7.48 degrees of an orange's 8.14 at five per cent and 5.30 of 5.65 at sixty. What screening can move is the rim's tenth; the other nine tenths is bare paper glowing beside ink that does not.

A lighter ink swings the residue through nought. For a five-per-cent tint on brightened office paper, printed instead with the same pigment diluted to a share of its strength over more of the paper — matched in colour on a non-fluorescent sheet — the hue turn a reader fully adapted to the sheet still sees, signed, against the dilution. The orange's -7.2° at full strength passes nought near 0.54 and reaches 10.3° at a quarter. What the brain does

A light ink can cancel the glow at one strength

A pale tint on brightened paper keeps a hue turn a reader fully adapted to the sheet cannot remove, and nine tenths of it survives every screen, because it is the tint's bare paper glowing beside ink that puts the glow out. A light ink — the same pigment diluted, printed over more of the paper — was the proposed lever, and the prediction that a quarter-strength ink lowers a five-per-cent orange's residue by a third. It does not lower it; it reverses it, from −7.2 degrees to +10.2. Somewhere between, the residue passes through nought, and for every one of eight pigments there is a strength that cancels it: 0.41 for the red, 0.54 for the orange, 0.80 for the blue and the cyan at a five-per-cent tint. The cancelling strength moves by under a tenth from five per cent to forty, so one ink per pigment keeps every pale tint within a degree and a quarter to twenty per cent, where full-strength ink leaves up to nine. The lever is real; it has a setting, and the light inks printers carry are diluted past it.

A steep side splits mercury's lines at forty nanometres. Under a clear mercury lamp on a one-nanometre grid, the 25 directions that ask for one of the green and yellow lines reflected and the other absorbed: how many the band pigment loses by more than one per cent, with symmetric bands, with the same bands searched with a fourth number as a control, and with bands whose one side is half the other's. At forty nanometres the symmetric bands lose 15 and the skewed ones 1; the skewed bands lose none at thirty-five or thirty. Where the model breaks

A steep side splits mercury's lines at forty nanometres

Under a clear mercury lamp a pigment built from Gaussian absorption bands no narrower than forty nanometres falls short in fifteen of the twenty-five directions that ask it to reflect the green line and absorb the yellow, or the reverse, because a band's tail reaches the line it should pass. Real dye bands are often lopsided, and the prediction was that a band whose one side is half the other's, the steep side free to face either way, loses at forty nanometres about as many directions as a symmetric band thirty wide — nine — and helps only the directions that pass the green. It loses one. At thirty-five and thirty it loses none. In every one of the twenty-five fits the absorbing band turns its steep side to the line it must pass, and both kinds of direction gain: none of fourteen passing the green is lost, one of eleven passing the yellow. A single band forty nanometres wide with a steep side splits the two lines within 0.37 per cent; a symmetric band must narrow to about twenty-seven to do as well.

The losses fall slowly, then all at once. Under a clear mercury lamp, how many of the 25 directions that split its green line from its yellow the band pigment loses by more than one per cent with bands forty nanometres wide, against how lopsided each band is — from symmetric to sides of two thirds and one third — beside the counts the prediction gave. 0.50: 16, 0.55: 13, 0.60: 10, 0.65: 5, 0.67: 1. Where the model breaks

A band must be nearly two to one before its steep side pays

Under a clear mercury lamp, a pigment of absorption bands forty nanometres wide loses fifteen or sixteen of the twenty-five directions that ask it to reflect the green line and absorb the yellow, or the reverse, and the same bands with one side a third of the width and the other two thirds lose one. The prediction for milder skews was that the losses fall in step with a single band's error — to about eight at sides of 0.55 and 0.45, three at 0.6 and 0.4 — so that a three-to-two skew already halves them. It does not. The census loses thirteen at 0.55, ten at 0.6, five at 0.65 and one at two to one: three directions recovered per twentieth of skew at first, twelve at the last. The losses track one band's error against the one-per-cent line the census counts by, and a single band crosses that line only near a skew of 0.62. A dye's modest natural asymmetry buys a few directions; the steep side pays only when it is close to half the other.

Three widths, one count: the steep side decides. Every searched band pigment at thirty, thirty-five and forty nanometres, placed by the half-width of its steep side and by how many of the clear mercury lamp's 25 splitting directions it loses by more than one per cent. The three widths fall on one staircase: 20.0 nm: 16, 18.0 nm: 13, 17.5 nm: 10, 16.0 nm: 9, 15.7 nm: 9, 15.0 nm: 8, 14.9 nm: 8, 14.0 nm: 4, 14.0 nm: 4, 13.3 nm: 1, 13.1 nm: 1, 12.3 nm: 0, 11.7 nm: 0, 10.0 nm: 0. Where the model breaks

A band is only as wide as its steep side

Under a clear mercury lamp, a pigment of absorption bands forty nanometres wide must be skewed nearly two to one before it can split the green line from the yellow, and the prediction for bands five nanometres narrower was that a single band crosses one per cent of error near a skew of 0.57 and the census's losses fall to five or fewer by 0.6. The losses do fall to four by 0.6; the single band crosses one per cent at 0.555. But the forty-nanometre rule that read the losses off that one-per-cent line breaks at once, and what replaces it is simpler: a thirty-five-nanometre band at 0.6 and a forty-nanometre band at 0.65 have the same steep side, fourteen nanometres, and lose the same four directions by the same shortfalls to a hundredth of a point. Three widths and fourteen pigments fall on one staircase in the steep side alone. Searching every loss again from the milder skews' answers finds one direction the census missed, at both widths, and corrects the forty-nanometre counts to nine and four.

Each added channel buys less, and none buys the last light. For a modelled ambient sensor of three to twelve Gaussian channels spread evenly from 445 to 650 nm, its matrix fitted in least squares to the room's forty-seven lights with each light held out of its own fit: how many lights tint the moon picture beyond one ΔEITP unit at a tenth of a candela. 3: 33, 4: 18, 5: 6, 6: 2, 7: 1, 8: 1, 10: 2, 12: 3; channels as wide as their spacing or half as wide again give nearly the same counts. Difference and uniformity

Seven channels end the trade and lose the tube

A three-channel ambient sensor fitted to a room's forty-seven lights trades its error on LEDs against its error on lamps, and a fourth channel moved that trade without closing it. The prediction for more channels was that six, spread from 445 to 650 nm, bring every lamp, mixture and LED under a ΔEITP unit with the lamps within 0.0025 in the CIE 1960 plane, and that nothing short of eight reads the halophosphate tube. Six channels leave the 2,200 K lamp beyond a unit and the lamps at 0.0040; seven bring every lamp, mixture and LED in, with the LEDs and lamps both under 0.001, and the trade is gone — both families improve together. The halophosphate tube is read from six. But the triphosphor tube, held out of its own fit, is read only by three and four broad channels and lost by every finer sensor, its tint growing to thirty-three units at twelve channels. A sensor learns the lights it was fitted on, and a finer one extrapolates further from a light with no relative in the census.

Given relatives, the tube is read by every fine sensor. The census's triphosphor tube, held out of its own fit, read by sensors of three to twelve channels fitted to the census alone, to the census with three triphosphor siblings at 3,000 to 4,000 K, and with four at 3,000 to 5,000 K. Alone it is beyond a unit from five channels and reaches 33 at twelve; with siblings it is within a unit at every count from five, 0.04 at seven. Difference and uniformity

Relatives, not twins, teach a sensor a tube

An ambient sensor of seven evenly spread channels, fitted to a room's forty-seven lights, reads every lamp, mixture and LED within a ΔEITP unit with each held out of its own fit, and loses the triphosphor tube, which nothing else in the census resembles — thirty-three units out at twelve channels. The prediction was that four triphosphor siblings, the same phosphors mixed for 3,000 to 5,000 K, would bring the tube within a unit at seven and eight channels and stop its rise past eight. They do both: the tube reads at 0.04 with seven channels and 0.06 with twelve, and seven or eight channels then read all fifty-one lights. A twin is not what does it. Three siblings, every one warmer than the tube and the nearest sixty mireds from it, read it within a unit at every count from five. What the siblings cost is paid at the finest sensors: at twelve channels the Planckian lamps' worst error rises fivefold, while from five to eight it moves by under a quarter.

At one half-width, the profile decides everything. The forty-nanometre band pigment with its steep side drawn in four profiles at a half-width of fourteen nanometres, and in two more at the half-widths that give a single band the Gaussian's error: how many of the clear mercury lamp's 25 splitting directions each loses, with its single band's error. At fourteen nanometres: Gaussian⁴ 0, Gaussian 4, sech² 19, Lorentzian 22; matched to the Gaussian's error, the secant at 7.73 nm loses 2 and the power-four Gaussian at 39.1 nm 7. Where the model breaks

At one half-width a flank can lose nothing or nearly everything

Under a clear mercury lamp, a pigment of Gaussian absorption bands splits the green line from the yellow according to its steep side's half-width alone, and a Gaussian flank is fixed by its half-width — so the census could not say whether it measures the half-width or the absorbance left in the flank's foot at the line it should spare. The prediction was that the foot decides: at a half-width of fourteen nanometres, a Lorentzian steep side loses most of the twenty-five splitting directions and a sharper-footed one none. It does. A power-four Gaussian loses none, the Gaussian four, a squared hyperbolic secant nineteen and a Lorentzian twenty-two, in the order of their single bands' errors. But a single band's error is not the whole account: three profiles drawn at the half-widths that give a single band the same error — 7.73, fourteen and 39.1 nanometres — lose two, four and seven directions, and the widest of them loses directions the others keep, because its shoulder starts absorbing nearer the green.

Off the locus, the 600 nm line reads the red as well as on it. For white LEDs built on the Planckian locus and at a Duv of −0.003 and +0.003, the red-phosphor strength read from the 600 nm departure, the mireds and their product by the line learned on the thirty locus LEDs, less the true strength. On the locus, each left out, it misreads by ±0.120; below the locus by ±0.110 and above by ±0.117, reading too little below and too much above. What a camera does

Beside the locus the converter still gives the red away

On the Planckian locus, a white LED's red phosphor pushes its converter to a shorter peak, so an ambient sensor's 600 nm departure, which reads the converter, reads the red phosphor too — within ±0.12 of a spread of ±0.36 — and through it the camera's colour error within ±0.074 ΔE₀₀. Real LEDs are binned a few thousandths off the locus, and the prediction was that a Duv of 0.003 moves the converter about as far as a fifth of the red phosphor does, so that the line learned on the locus misreads off-locus LEDs by a fifth of the range and their error falls back to ±0.12. The converter moves under two nanometres. The line reads the off-locus LEDs' red within ±0.11 and ±0.12, as well as it reads the locus's own held out — with a bias of about a twentieth that follows the Duv's sign. The error reads a third to a half worse, ±0.096 and ±0.107, and most of that is the camera's error itself moving off the locus with nothing in the recipe changed.

Only a curve per temperature brings the bin back. The camera's colour error under eighty-nine white LEDs — thirty on the Planckian locus, fifty-nine at a Duv of ±0.003 — read through the red phosphor estimated from the 600 nm line and an error line within each pump, each LED left out, as the Duv enters the lines in turn: not at all, as one term, as a slope in mireds, as a slope for each temperature, and as a slope and a curve for each. Beside them the line learned on the locus alone. With a slope and curve per temperature: ±0.073 on the locus, ±0.056 below, ±0.048 above. What a camera does

Across a bin, the camera's error bends with the temperature

White LEDs a Duv of 0.003 off the Planckian locus have their red phosphor read by an ambient sensor as well as LEDs on it, and their camera colour error read a third to a half worse, because the error itself moves with the Duv. The prediction was that one Duv term in the error's line, learned over all eighty-nine LEDs, brings those beside the locus back to the locus's ±0.074 ΔE₀₀ and costs the locus LEDs nothing. One term buys little: ±0.109 below the locus and ±0.085 above. The error turns across the locus one way at 2,700 K and the other at 4,000 and 6,500 K, and bends most where it is warmest, so the Duv has to enter as a slope and a curve for each temperature — ten numbers a pump, not five — before both sides come back, to ±0.056 and ±0.048. That line then reads the locus LEDs at ±0.073, worse than the ±0.062 a line with no Duv in it manages once it is learned across the bin.

From three nanometres a table needs no notch at all. For the reversed tube read through slits of two to five nanometres, the ceiling built on the line's unnotched core width, over the lamp's true peak in its lowest window, against the column's depth. The two-nanometre ceiling fails from three and a half; the three-, four- and five-nanometre ceilings stay above the true peak at every depth, the least by 4.7 per cent. What light is

A wide table needs no notch to borrow

A two-nanometre table of a reversed tube cannot read the notch a cooler column cuts in its lines, and its ceiling, built for an unnotched line, fails from a column of three and a half; borrowing the notch a one-nanometre table read rescues it at every depth. The prediction for coarser tables was that a shallow notch lifts their flanking-pair factor further — to a fifth at five nanometres — and that the five-nanometre ceiling on a borrowed notch still holds to five. Both hold: the rise is 15, 18 and 20 per cent at three, four and five nanometres, and every borrowed ceiling stays above the true peak. But a table three nanometres wide or wider never needed the notch. Its unnotched ceiling stands at least 4.7 per cent above the true peak at every column depth, because each of its entries carries so little of any line's peak that the ceiling built on them sits high above every line, reversed or not — and borrowing the notch takes up to twenty points of that margin away.

One per cent of Lorentzian nearly triples the losses. The forty-nanometre band pigment with its steep side a pseudo-Voigt fourteen nanometres wide at half depth: how many of the clear mercury lamp's 25 splitting directions it loses by more than one per cent, against the Lorentzian share of that side, beside the Gaussian's four and the counts the prediction gave. Lost with no Lorentzian, 4; 1%: 11, 2%: 14, 5%: 18, 10%: 19, 20%: 20, all: 22. Where the model breaks

A hundredth of Lorentzian undoes a Gaussian flank

Under a clear mercury lamp, a band pigment whose steep side is a Gaussian fourteen nanometres wide at half depth loses four of the twenty-five directions that split the green line from the yellow, and the same side drawn as a Lorentzian loses twenty-two. A real absorption band is usually a Voigt profile, a Gaussian core with a Lorentzian share in its wings, and the prediction was that a twentieth of Lorentzian doubles the Gaussian's losses and a fifth reaches nineteen. The direction is right and the scale is not. A hundredth of Lorentzian takes the pigment from four lost directions to eleven; a fiftieth to fourteen; a twentieth to eighteen; a fifth to twenty. The best-placed band leaves the passed line more than three half-widths from its centre, out in the wing, and there a wing one per cent Lorentzian carries twice the absorbance of the whole Gaussian. The count saturates near twenty while the worst direction's shortfall keeps growing, from 2.8 per cent at a hundredth to 51 with a full Lorentzian.

The ratio of slit to core nearly decides when a notch matters. For the reversed tube with line cores of 1.2, 2.4 and 3.6 nm, read through slits of two to five nanometres: the first column depth at which the ceiling built for an unnotched line falls below the true peak, against the slit over the core, with "never" for tables that hold at every depth. 0.56: 0.5, 0.83: 1, 0.83: 1.5, 1.11: 2.5, 1.25: 2, 1.39: 3, 1.67: 3.5, 1.67: 4, 2.08: 3.5, 2.50: never, 3.33: never, 4.17: never — every ratio of two and a half or more never fails, every ratio up to 2.08 fails, the threshold a little above the predicted two. What light is

A broad line brings the notch back to a wide table

A table of a reversed tube read through a slit three nanometres wide or wider never needs the notch a cooler column cuts in its lines: its ceiling, built for an unnotched line 1.2 nanometres wide, stays above the true peak at every column depth. The reason offered was that a wide entry carries too small a share of a narrow line's peak to be fooled, and the prediction was that broader lines undo it — that at a core of 3.6 nanometres the five-nanometre table fails from a column of about three, and that a table needs the notch wherever its slit is less than about twice the line's core. The five-nanometre table fails from a column of three, exactly. Across twelve tables of three cores and four slits, the column at which the unnotched ceiling first fails rises with the slit-to-core ratio — from a half at 0.56 to three and a half or four near 1.7 — and every table at a ratio of 2.5 or more holds; but a ratio of 2.08 still fails, so the threshold sits a little above two. With the true notch, every table holds.

Bounded, one session stops finding a macula that never moved. For the three bands with the macula unmoved, how many of twenty one-session experiments report it moved beyond twice its standard error: from the census's two starts, from the best of five starts, and from the best of five with the shift held within ±6 nm. The bound brings the false shifts at 415 and 430 nm from 8 and 6 to 1 and 2. What the eye does

A bound on the macula trades false moves for hidden ones

Fitted thoroughly, one session of an older observer's colour matches finds a second valley in a quarter of its experiments — the macula's peak moved ten or more nanometres from the model's, where no real macula sits — and reports a moved macula where there is none in up to eight experiments of twenty. The prediction was that holding the macula's shift within six nanometres either way, the range real pigment mixtures span, restores every observer's one-session counts to within two of the census's and leaves about one fit in four pressed against the bound. The false moves vanish: an unmoved macula is reported moved in one, two and one experiments of twenty for the three bands, against eight, six and two unbounded. Seven of nine observers keep their count of moved maculas within two of the census's. But only one fit in six ends on the bound, and beside the band at 445 nm the bound hides real moves: a macula truly three nanometres short is found in three experiments of twenty, where the census found seven. Two sessions barely notice the bound.

The prior trades the macula's moves for the lens band. For each observer, how many more experiments of twenty find the lens band under the prior than under the census's fits, against how many more find the macula moved. The observers moved short or unmoved gain up to seven bands and lose one to five moves — false ones where the macula never moved, real ones where it did; those moved long gain no band and lose one or two moves, the 445 nm observer losing three bands as well. What the eye does

A soft prior on the macula frees the lens band

One session of an older observer's colour matches, fitted thoroughly, can drift into a valley where the macula's peak sits ten or more nanometres from any real eye's, and a hard bound at ±6 nm removes those false moves at the cost of hiding some real ones — beside a lens band at 445 nm, a macula truly three nanometres short is found in three experiments of twenty where the census found seven. The prediction was that a Gaussian prior four nanometres wide, which lets a fit go further when the matches insist, keeps the false moves away and restores those real ones. It keeps the false moves away — none, one and one for the three bands. It does not restore the real moves: it finds them as seldom as the bound or more seldom, two of twenty beside 445 nm, because it pulls every fitted shift towards nought, to a mean of 1.2 to 1.9 nanometres for moves of three. What it buys instead is the lens band. With the macula held near the standard, the band beside it is found in ten to twelve experiments of twenty, where the census found three to seven.

The curve holds inside the bin and fails outside it. Four error lines learned on eighty-nine white LEDs at a Duv of nought and ±0.003, each read at those three values with every LED left out and at ±0.0015 and ±0.006 on 119 LEDs none of them was fitted on. The slope and curve per temperature reads ±0.045 and ±0.043 inside the bin and ±0.153 and ±0.161 at twice its edge, where a slope per temperature alone reads ±0.093 and ±0.110. What a camera does

The bin's curve holds between its points and breaks beyond them

A camera's colour error under a white LED was read from an ambient sensor across a manufacturing bin by a line with a slope and a curve in Duv for each colour temperature, fitted at three Duv values — on the locus and 0.003 either side — and reading the LEDs beside the locus within ±0.056 and ±0.048 ΔE₀₀. A curve through three points passes through them whatever happens between them. The prediction was that 119 new LEDs built at ±0.0015 are read within ±0.06, and those at ±0.006 worse than ±0.10. Both halves hold: ±0.045 and ±0.043 inside, ±0.153 and ±0.161 outside. But the error's own mean course stays on its parabola within 0.02 out to ±0.006. The line's bend is not the error's: it is the gap the line leaves between the locus LEDs and the bin's edges, and a gap spent as a curvature quadruples at twice the distance.

With the level placed, the line bends as the error does. At each temperature, the curvature in Duv of the camera error's mean course through nought and ±0.003, beside the curvature each slope-and-curve line implies, averaged over the three pumps. At 2,700 K the course bends by +7,916, the line without a level by +2,803 and the line with one by +8,198; at 4,000 K the course bends by +2,196, the line without a level by +14,591 and the line with one by +2,195; at 6,500 K the course bends by +363, the line without a level by −13,349 and the line with one by +445. What a camera does

A level for each temperature lets the curve be the error's

An error line with a slope and a curve in Duv for each colour temperature read white LEDs inside a manufacturing bin within ±0.045 ΔE₀₀ and LEDs at twice the bin's edge only within ±0.16, though the camera's own error stays on its parabola there. Its curve was borrowed: the line's shared terms could not place each temperature's level, and the square of the Duv absorbed the gap. The prediction was that one more number a pump, the square of the mireds, brings the locus LEDs within ±0.05 and those at ±0.006 within ±0.08. It brings the locus to ±0.025 — three times better than the locus-only line that started this run of essays — and the outer LEDs to ±0.049 and ±0.058. The curvature the line now implies at each temperature is the error's own within a fifth; what it leaves is the warm whites' scatter at the bin's edges.

Each widening of the prior buys moves with bands. Over the six observers whose macula truly moved three nanometres, the real moves one session finds beyond twice their error, against the lens bands found for the four observers whose band the four-nanometre prior freed — under priors four, six and eight nanometres wide, the census's own fits and the hard bound. 4 nm: 14 moves, 44 bands; 6 nm: 22 moves, 34 bands; 8 nm: 25 moves, 25 bands; census 27 and 22; bound 19 and 20. What the eye does

A wider prior gives the moves back by spending the band

One session of an older observer's colour matches, fitted under a Gaussian prior four nanometres wide on the macula's peak shift, finds the lens band beside the macula in ten to twelve experiments of twenty and real three-nanometre moves of the macula as seldom as a hard bound does. The prediction was that a prior six nanometres wide keeps the false moves at two or fewer, finds the real moves within two of the bound's counts and keeps two thirds of the band's gain, and that at eight the far valley reopens at 415 nm. Three parts hold. The fourth fails: six nanometres keeps 55 per cent of the band's gain. Read across the widths the prior traces one trade — 14 real moves and 44 bands at four nanometres, 22 and 34 at six, 25 and 25 at eight, against the unconstrained fit's 27 and 22 — and the hard bound, at 19 and 20, is worse than six nanometres on both.

381 essays on this thread, page 15 of 16 · all threads · all essays