Identifiability — where it appears
Named by 68 essays across 8 fields — each of them below, with the objects they name alongside it.
Two numbers out of the points
A seed head's divergence angle can be recovered from its spiral counts only to within an interval, because a range of angles gives the same counts. On a stem the counts come with lengths attached, two measurements pin two unknowns, and the lattice comes back to the last digit it was built with.
The noise that arrives through the neighbours
The two kinds of noise this site had were idealisations that bracket the rule's choice. The realistic disturbance is neither: a primordium is placed exactly, and then the organ grows, so by the time the next one forms its neighbours have moved. That is a third kind, and it is invisible in every measurement a plant offers.
The band decides the answer
A fit over a whole tree's junctions returns the exponent the tree was built at, even though most of its junctions are from bands that on their own return 1.6. Least squares is already weighting by leverage. The dangerous sample is not the mixed one — it is the one a person can reach.
What a count is worth
A reported parastichy pair pins the divergence angle to a band 221°/mn wide — so 2 and 3 says almost nothing and 34 and 55 fixes it to a tenth of a degree. Each step up the Fibonacci sequence is worth a factor of φ², and recording the radius a pair was counted at adds only ten per cent.
How many plants would it take
Fourteen specimens separate the geometry's Fibonacci share from a coin weighted to a half. Four separate it from what a grown history gives. One fir cone measured at three rings settles whether its transitions are spaced as a cone's or an ogive's. The sample sizes are small, and that is the uncomfortable part.
What a forgery has to know
A lattice with transported errors reproduces the comb and the pair, so one quantity is left: the two combs' relative strength. Weighted by distance the forgery puts more in the second comb than the first; the rule does the opposite. It matches only if the coupling is turned three to one towards the further neighbour, which no falloff supplies.
Where three and two become one
Two trees, one built to obey Murray's law and one to obey Da Vinci's, are measured through the same fifty junctions with the same instrument. At twelve per cent of error on each radius the two answers overlap, and above twenty and a half the tree built at three measures lower than the tree built at two.
A periodicity is not a lattice
Give a lattice's errors a period of eight and a comb appears at spacing eight, on an arrangement with no rule in it. But the partner it names is 10, then 12, then 11, then nothing — an accident of the disturbance rather than a measurement of the pattern. The forgery is caught by reading a second stem, and by nothing else.
The test a plant could settle
Every other open question in this collection is priced in tens of specimens, and one of them in a hundred and sixty. This one is priced in internodes on a single stem, and the number is fifty-six — because it is a statistic of one sequence rather than a share of a population.
Four fractions with one denominator
The dip in a head's side-count disorder is as wide as 150·q/n², measured over six fractions — every one of them a Fibonacci convergent, which is the emptiest neighbourhood a denominator ever gets. So the law could be about the denominator or about how well the fraction approximates its neighbours. Four fractions of 55 at one head size settle it in one figure.
The ratio was never about the rule
The comb has already been retracted here as evidence that a plant computes its pattern, and one quantity was exempted from the retraction: the ratio of the two combs, which a placement rule and a transported disturbance divide differently. Drive seven disturbances through the same rule and the ratio spans 0.45 to 1.09. The exemption does not hold, and the angle sequence has nothing left.
What a quiet plant is worth
Almost every measurement gets easier as the effect gets larger. This one gets harder — a stem's divergence sequence stops carrying information about its noise at precisely the scatter where the noise becomes obvious. The specimens worth measuring are the ones that look least interesting.
A width read off a staircase
Two fractions of the fourteen measured return a dip width that moves by a factor of two when the head size changes, where the others hold to three per cent. The cause is not their neighbourhood. It is that the disorder statistic changes only when the tessellation changes, so the curve a half-width is read off is a staircase, and a width narrower than the tread cannot be read at all.
How much of a cone to measure
Two rings cannot show a varying exponent — not with difficulty, but in principle, because one gap determines one exponent with nothing left to disagree. Four or five can, if each is found to within a per cent. At three per cent this specimen cannot be told from a power law however many of its rings are recorded.
The symmetry that is not there
A wrecked stem counted 2/6 and a stem grown two organs at a time counted 2/6 are indistinguishable to a spiral counter. Rotate them by half a turn and one lands on itself and the other lands nowhere. A cut does not make a whorled pattern; it makes a pattern that counts like one.
The window is the neighbour
An integral needs a limit, and this one has two conditions on it that pull opposite ways. It has to scale with the dip, so that two head sizes are comparable, and it has to stay clear of the next rational, which is a fixed distance in degrees. Between them there is no stretch where the answer holds still — and the limit that decides it is the crowding.
What one angle says about the next
A tenth of a degree of placement noise moves a stem's divergence scatter from 0.50° to 0.62°, which nobody would report. It takes the correlation between consecutive angles from 0.54 to below zero. The other two kinds of noise, at scatters where no measurement can separate them, leave it at 0.6.
What the pair costs
The single parastichy number cost sixty internodes. The pair costs two hundred and fifty, and a protractor error of three quarters of a degree takes it to eleven hundred. The arithmetic that predicts the second of those is right about the shape and wrong about the scale by a consistent factor, which is recorded rather than fitted away.
A difference forgets a drift
This collection proposed a second observable and priced it as free: if a plant's errors are inherited between touching organs, the divergence sequence should carry a slow wander as well as a comb. The disturbance with the largest wander of any built here leaves none at all in the sequence, because a divergence is a difference and differencing is what removes a drift.
Fractions with the same neighbours
Every instrument this collection has for the width of a disorder dip has a free parameter set by how close the next rational sits — which makes a hypothesis about the neighbourhood untestable with any of them. The repair is not a better instrument. It is a set of fractions whose neighbourhoods are identical and whose denominators are not, and the arithmetic supplies twenty-four of them.
A correction that keeps the overlap
The duel between a tree built at Murray's exponent and one built at Da Vinci's ended by saying the displacement is the geometry, and that no better estimator removes it. Correcting every replicate by simulation-extrapolation removes 92 per cent of the tree at three's displacement at five per cent of error and 68 per cent at twelve, and the error at which the two means cross leaves the measured range altogether. It pays in spread — the corrected readings are twice as wide at twelve per cent — so the error at which the two trees' intervals overlap does not move. Of the duel's two numbers, the inversion was the estimator's and the overlap is the question's.
What a refusal does not say
The readout can decline for four different reasons — too quiet, too disturbed, too fast, or a window in the wrong place — and a stem that returns nothing does not say which. That is the third time this thread has failed to close the mixture problem, and the first time the failure has a shape.
A count carries no error
Fitting r₀ᵏ = Σrᵢᵏ junction by junction puts a measured radius on both sides of every equation, and at twelve per cent of error a tree built at Murray's three and one built at Da Vinci's two stop being told apart, however the fit is corrected. Fit the same measured radii against the number of tips each branch carries instead — a count, which nobody measures with error — and the two trees read 2.996 and 1.997 at twelve per cent and 3.015 and 2.001 at thirty, never overlapping. The twelve per cent belonged to the junction fit, not to the tree. The count fails in its own way, and the way is stated.
A refusal with a reason
Three note left with the work running have recorded that a refusal has four causes and the sequence separates none of them. With a second window and a protractor, three are separated: silence at 0.38° of scatter is a quiet plant, silence at 56° is a disorderly one, and agreement certifies the rate. The fourth survives, and so does a worse discovery — agreement is not correctness.
The control a survey would need
A comb no longer shows that a plant computes its pattern, so the survey this site has been specifying for a long time has to change. What it loses is its headline; what it gains is a measurement a botanist can actually make — six requirements, four of them already in the specification, and a quantity nobody has ever reported.
Two shapes, one threshold
Read in the same unit, an exponential falloff and a gaussian one disagree about where the lattice ends by half. The quantity they agree on turns out to be one the earlier work measured for an unrelated reason — and it agrees with a bracket left by a sweep of a completely different parameter.
What the growth lines carry
A shell's curve says nothing about how fast the animal grew, and its growth lines say all of it. Under a law that holds the pth power of the radius constant per unit time, the time spent crossing one whorl is proportional to the change in that power across it — so the lines in successive whorls stand in the ratio of the growth factor raised to p, and each whorl holds the count the closed form predicts to within the one line rounding can move. Dividing two counts and taking the logarithm against a growth factor the curve already gives returns p: 17 of 20 readings name their own law, the furthest 0.012 from a whole number. The other three are not wrong, they are uncountable — at 4.5 per turn under a volume clock the inner whorl of the pair holds one line.
Two readings from one stem
Three note left with the work in a row have recorded that the two statistics of a divergence sequence want opposite plants — one quiet, one disturbed. Measured on the same stems they do not. The conflict was in the interpretation of a sign, and the window in which both are readable is wide.
A count that has lost tips
Radii read against the tips each branch carries keep Murray's three apart from Da Vinci's two where junction fits cannot, because a count has no measurement error in it. A count of the tips a tree has is not a count of the tips it grew. Losing them lowers both trees' readings by one factor that belongs to the losses and not to the rule, so the count stops being right long before it stops telling the trees apart: on fifty junctions at twelve per cent of error, to seventy per cent of the tips lost one at a time, and only to about a quarter lost in whole limbs. Counting scars repairs single losses exactly. Nothing countable repairs a shed limb.
A shell that changed its law
An animal that grew as a juvenile under one deposition law and as an adult under another leaves a sequence of whorl ratios rather than one, and the sequence says where the change happened. The ratio across the change is a closed form that is neither law's — 6.72 between a length clock and an area clock at 3.2 per turn, exactly the average of 3.2 and 10.24 — and it is monotone in where inside its whorl the change sits, so it inverts. On a seven-whorl shell of 18,466 lines a change at 3.5 whorls comes back at 3.5001, in a band 0.027 whorls wide that holds the true position. The reading refuses a change in the outer three whorls or the inner three, because a plateau it will trust is two agreeing ratios and two ratios need three untouched whorls.
The comb was never the rule
A control is only as strong as the alternative it builds, and the earlier work built one that varied the rule while holding the disturbance fixed at independence. Five rounds of the angle-sequence thread, with what each claimed and what still stands — and why the next evidence has to come from an intervention rather than from a longer stem.
Which minimum was chosen
The rule takes an argmin, so there are two completely different things noise can do to it: move the answer, or move the question. One of them can change what is chosen and the other cannot, ever — and the difference is exactly zero against one or two placements in a thousand, at amplitudes where every other measurement says the two are identical.
A law that never stopped changing
A shell whose deposition law moved evenly from one end to the other gives a sequence of whorl ratios that is a straight ramp rather than a plateau, a crossing and a plateau, and the two are separated by more than the counts' own rounding on every shell holding three countable ratios. Each ratio on the ramp reads the law at the boundary it straddles — 0.3486, 0.6865, 1.0320, 1.3755, 1.7180 against 0.3333, 0.6667, 1.0000, 1.3333, 1.6667 — so the reading is local where a fit to the curve is global, and a fit handed the same shell returns the geometric mean of its ends with no warning. The reading that locates a single change refuses a drifting shell at every size, naming the number of ratios that agree with neither end.
The boundary belongs to the pattern
Three kinds of noise, in three incommensurable units, destroy a lattice at the same place — about a degree and a half of divergence scatter. The earlier work measured that of two kinds and called it a scale rather than a constant. With a third it looks less like a coincidence and more like a property of what a lattice is.
The order belonged to the method
A residual was left over after the two width laws, and it looked ordered: the most crowded fraction gave the widest dip, in all three families, in the direction a measurement artefact would take. Measured again with an instrument that has no level in it, the order changes with the window, disagrees between families, and in one of them comes out backwards.
The rung was not the instrument
The earlier work said the pair readout has a ceiling one rung above where it works, that this is arithmetic rather than statistics, and that no amount of stem fixes it. The arithmetic is right and gives a band of lag windows that is never empty; what was actually stopping the reading was an eight-node seed and a grid of 384 azimuths.
A window inside a rung
A stem that climbs the ladder has no comb in it at any rate, because the quantity the comb is periodic in changes as it goes. Read a window instead and it comes back, on one condition: the window has to be shorter than a rung — which makes the shoot's rate the thing that decides whether a plant can be asked.
The error budget for a nautilus
Every way a growth factor read off a shell section can be wrong has been priced here, one essay at a time. Added up they come to 332.6 per cent in the worst case and 279.6 in quadrature, against a golden-spiral claim that is 114.2 per cent away — so the budget does not refuse the claim at all. One entry decides it: the dividers, at 278.2 per cent on their own, and the dividers are the historical method and the only route measured that pushes a nautilus towards a golden spiral. Set them aside and the budget falls to 54.4 per cent and the claim is refused twice over. What the same budget cannot settle is anything smaller than half: 3.2 against 3.4 is inside it, and stays inside it until six of the seven sources are controlled.
Two windows on one stem
A pair read off a climbing shoot can only be read through a window, and a window can straddle a transition. Read a second window half a length lower and the outcomes fall into four kinds — and agreement between them never happens on a shoot whose rung is shorter than the window, which turns the most awkward of the four refusal causes into something a reading can certify.
What a scar is worth
Counting the scars a dead shoot leaves does not put a branching count back on the sequence it would have had. A scar records a growing point and a dead growing point takes every branch it would have made, so living points plus scars reach 39.2 per cent of the deathless count after twenty seasons at one death in twenty, and 1.9 per cent at one in five — falling without limit rather than closing. What the scars restore is the other number. Scars per living point settle at q/(x − 1) exactly, so a rate with a scar share beside it recovers the death chance and then the waiting time, where a rate alone is reached by a one-season wait losing a tenth, a two-season wait losing 0.64 per cent and no wait at all losing 27.2 per cent.
The band nobody can be placed in
The boundary between shells whose whorls run into one another and shells whose whorls run free was located here to the last bit a double holds. A specimen is not a point on that line, it is a measurement with an error, and carrying the whole measured error budget onto the boundary turns the line into a band running from 1/(W(1+b)) to 1/(W(1−b)). At the budget with the dividers set aside that band covers 48.2 per cent of the box the morphospace figure here is drawn on, and its share runs from 6.7 to 59.5 per cent across the six boxes in use — the same box-dependence the contact region itself showed. The angle criterion carries the same error better above an expansion of 1 + √2 and worse below it, exactly.
What a sample grid decides
The rule takes its minimum over 384 sampled azimuths, and that number has been a constant since this site's first commit. Tripling it changes nothing at the two rises the collection argues from — five runs of five, identical readings — and changes which answer appears at the one rise published as having no answer. A parameter of the program, measured rather than assumed.
What the axis distance costs
Raup's contact boundary is a relation between two numbers and only one of them has ever been priced here. The second was expected to be the cheaper — a length against another length. It is not: an assumed centre costs it 79.3 per cent where the same centre costs the expansion 6.88, because a ratio of two distances is first order in the centre and a fitted rate is second. But a tilted camera costs it nothing at all, exactly, and averaging the reading round one whorl is free and worth a factor of 4.91. The two numbers fail at opposite ends, and they cross at 1.12 turns of arc.
Matching instead of correcting
Two rounds of work failed on one question because every instrument's free parameter was set by the thing under test. The repair was not a better instrument or a model of the bias: it was choosing what to compare so that the confound could not vary. That move is available in four other places here, and three of them have already used it without anybody naming it.
Three rules, one exponent
A measured branching exponent is quoted as evidence for a sizing rule, and it cannot be. Murray's flow rule conserves three at every length ratio and reads nothing of the lengths at all; equal stress conserves 3/(1 + l) and equal deflection 4/(1 + 2l), where l is log2(1/lambda). So an exponent names a rule only with a length ratio beside it, and even then not everywhere: of ninety-six length ratios between 0.3 and 0.99, thirteen have two rules within five hundredths of each other at a precision of 0.05, in three bands with three different reasons — stress against stiffness where they cross at the planar crown, stiffness against flow where the stiffness curve passes three at 0.8909, and stress against flow only as the branches stop shortening.
A floor no better fit can lift
The band of shells nobody can place was built from one of the two numbers the contact boundary relates, and the other has now been priced. Carried together they widen the band by a third and take 48.2 per cent of the morphospace box to 59.7. The number that matters is further down: with the whorl expansion measured perfectly, 12.6 per cent of the box is still undecidable, and at an expansion controlled to a hundredth 94 per cent of what remains belongs to the second number. And the two errors are not independent — they come out of one guessed centre, which traces a curve across the boundary rather than a rectangle around it.
The lengths that name the rule
A real crown has no single length ratio, and giving every fork a spread of daughter lengths does not blur what a sizing rule conserves: Murray's flow rule still conserves three at every junction, and the two mechanical rules keep their mean exponent, moved only as the square of the spread. What the spread adds is a second number. Each junction's exponent follows its daughters' summed log length with a slope of 0.30 under equal stress and 0.86 under equal bending at the planar crown, where the exponents are both two — and a two per cent error in every radius moves neither slope, while it swamps the scatter that looked like the obvious instrument.
A count that can be wrong by one
A reported parastichy pair pins the divergence angle to a band 221°/mn wide only if both counts are right. Allowing either to be off by one adds the bands of every neighbouring pair whose counts share no factor, and those bands sit where their own lattices live: for 2/3 they swallow the whole range, and for 34/55 they are two bands as narrow as the true one at 109° and 113°, twenty-five degrees away. So a high count that may be wrong is not a blurred reading but a short list of sharp candidates, costing log₂ 3 bits. And on the Fibonacci pairs, two in every six — 21/34 and 34/55 among them — cannot be miscounted silently by one count at all, because every such miscount shares a factor.
Seven rises and two seeds
One organ removed from a stem is felt out to the larger of its two spiral counts. Every test of that has confounded the count with the rise, because on one branch the two move together. Grow a second branch beside the first at the same rise and they come apart — and doing it at seven rises turns a matched pair into a design whose last column changes hands four times.
A crown that would rather not buckle
A column held below the load at which it buckles and a cantilever held to a fixed deflection need the same radius at every length, because both hold the bending stiffness against a load times a length squared — so the three halves of elastic similarity is also the buckling law, and a crown whose loads all run along its branches conserves the same exponent under either. Gravity does not run along branches. It divides by the cosine of each branch's tilt, so a buckling junction's exponent is set by the direction its parent points, nothing past level is sized at all, and a crown sized by the larger of the two criteria splits by direction into an upright core and a spreading shell whose boundary junctions conserve more than either rule gives.
The front that reads one short
Eleven cells of a fourteen-cell design put the boundary exactly at the larger spiral count. Three put it one offset earlier, and the tempting move is to lower the threshold until all fourteen agree. Measured instead of tuned, the three turn out to be the three cells nearest below their own rung's boundary — and the last offset of a front is weak because it has only just arrived.
A count that drifts by two
A reported pair of 34 and 55 that may be wrong by one allows three sharp bands; allowed to drift by two it allows thirteen, and by three, twenty-nine — and the information lost is exactly the logarithm of that count, because every band is as narrow as the true one. The nearest wrong band stays twenty-four degrees away until a drift of three brings one to eleven. What does not survive is the protection: 21/34 and 34/55 could not be miscounted silently by one, but every Fibonacci pair can be by two, so a counter who drifts by two as readily as by one reports 34/55 silently wrong 9.5 per cent of the time rather than 0.13.
The flag reads the angle, not the twist
A twisted seed head is caught first by its counts: at half a radian some band stops returning two consecutive Fibonacci numbers, which an untwisted golden head never does. Twist the head in proportion to the square of the radius instead and the organs land exactly where a head grown at the golden angle plus a/(N − 1) puts them — to a billionth of a spacing — so the two read the same pairs in every band, and the flag fires on both. The flag detects a divergence that is not golden, and it has a resolution: 0.015° on 900 organs, 0.01° on 2,400, 0.003° on 9,000. Every twist shape from a half to four is flagged exactly when its change to the divergence in the outer annulus passes that resolution. So a flagged head is not golden, and nothing in its counts says whether it was twisted or grown that way.
Two ways to die, three things to count
Giving a branching plant's waiting buds a death chance of their own leaves its counts a linear recurrence, but breaks the collapse onto the survival: the rate becomes the apex survival times the root of y^(d+1) = y^d + r^d, where r is the bud survival over the apex survival. The one-chance reading then names the wrong waiting time on 171 of 477 plants with waits of two to four seasons, shorter when the buds are the fragile ones and longer when the apices are. The two chances are separable from a rate and a scar share, exactly — but the two counts' loci cross at eight to sixteen degrees, so a one per cent error lets the chances wander by a factor of two. A third count is owed, and it is the scars sorted by kind.
The response with a hole in it
Removing an organ is felt out to the larger parastichy number and no further — that is the intervention's headline, and it holds in the middle of a rung. Swept towards a transition the run of felt offsets stops early and one lone offset past it comes alive, with three quiet organs in between. The lone offset is one place inside the count the stem is about to have.
A bad year does not average out
Let every growing point on a plant share one season's death chance, bad one season in ten and good otherwise, with the average held at 0.1. Averaged over every sequence of seasons the counts are exactly the independent model's. But no plant is an average over sequences: with bad years at 0.5 a plant settles on a rate of 1.3001 against the expected 1.3190, the median plant holds 54 per cent of the expected count by season forty, and the scar share never settles, because it is set by how many seasons ago the last bad year was — 1.35 the season after one, 0.17 twelve seasons on. So the reading of a plant's waiting time from a rate and a scar share gets worse the longer it runs: right for 57 per cent of plants over ten seasons, 22 per cent over eighty.
Two counts that slip together
A counter who closes the circle a few degrees late counts a sliver of the head twice, in both families at once, so the two counts of a reported pair drift together rather than apart. Coupled that way the count is safer than it was: fourteen Fibonacci pairs in twenty-three admit no silent equal shift of one, against seven that admit no silent single miscount, and 34/55 announces every closing error short of 9.82°. The check is what breaks. Two annuli closed at the same wrong mark pass 17.6 per cent of wrong readings of 34/55 and 76.8 per cent of 13/21's, because a linear relation survives multiplication — and what catches them instead is a protractor good to twelve degrees.
Scars with dates on them
A bad season shared by every growing point wrecks the reading of a branching plant by two totals: over eighty seasons the rate and the scar share name a two-season wait for 22 per cent of plants. Date the scars — by position along a shoot, by growth ring — and each season's death chance is read off its own scars, so the bad years stop being noise and become a known input. Running the branching recurrence through the plant's own seasons names the wait for 94 per cent of plants over twenty seasons whether bad years kill a tenth of the points or seven tenths, and for every plant over eighty. What a plant cannot read from its own scars is the climate: the averaged chance comes only as fast as seasons do.
Two marks chosen by one eye
A counter traces each family of spirals from a starting organ of its own, so a reported pair carries two closing errors, correlated because one eye chose both. Letting them differ costs 34/55 its ten-degree margin — 33/56 and 35/54 share no factor, and marks that err 5.3° in opposite directions reach them — while 21/34 keeps its margin whatever the marks do. And it decides the second annulus. At a spread of 7.2° the relation passes right readings 2.8 times as readily as silent ones when the marks are independent, 1.25 times at a correlation of 0.9, and stops telling them apart at 0.98; where it does work it keeps one reading in forty-six.
A fifth of the hop
The exchanged pair misses one divergence step by up to twelve per cent, and the miss is not scatter: every row keeping a lag of 5 or 7 overshoots and every row keeping a 4 or an 8 falls short. Subtract a fifth of the surviving hop's own angle and the worst row is four per cent.
Two rungs, one angle
Five pairs of rises settle on the same divergence while a counter returns different pairs at them, and four of the five agree to 0.0000° — the same value of a quantity read on a grid of 1,536 azimuths. The rises differ by factors of 1.48 to 5.09.
The last of three quantities
The pair, the divergence and the step ordering move together when the rise is swept, and for a long time no result could be attributed to any of them. Two designs later, two are ruled out as sufficient and the third has never been held still — because holding it is what a rung already does.
The end of a wrecked run
The obvious follow-up to a transition in where one organ goes is whether the stem also finishes somewhere different. On this rung the question has no answer: a wrecked run's final divergence takes four values and changes between rises a thousandth apart, three times inside a nine-rise sweep.
The lag that never survives
A correction to the exchange's size rests on four hop clusters, and a fifth would be the first real test of it. The prediction was written for a golden lattice at a lag of eleven. No golden lattice on this ladder reaches one, and the reason is a fact about the rule rather than about the search.
The level was doing the ordering
Four falloff exponents have been put in order by the rise at which half their runs stop settling, and a half is the only level that order has ever been read at. Read at nine levels the same runs give ten different orderings of the same four numbers, and the one comparison in the whole study that resolves runs the other way.
Four walls closer than they looked
Two of the four falloff exponents had a wall with no upper end at all, and the other two were located to factors of two and a half and nearly four. Nine rises at eighty starting angles close every bracket — and the four walls turn out to sit inside a factor of 1.111 of one another, which is narrower than the narrowest bracket.
A basin has a width
A destination reached from one starting angle is a presence. A destination reached from seven consecutive starting angles spanning forty-five degrees is a basin with an extent, and nine angles could not have measured one — they were too far apart to have two of them land in the same place.
A wall that was never measured
Three samplings of the starting angle give three orderings of the four falloff exponents' walls and a spread that does not shrink, while every error bar behind them halves. The reason is that a wall is a crossing of a nearly flat curve, and nobody had asked how well it is located.
Named alongside it
The objects these essays reach for when they reach for this one.
Honest limitsMeasurementMeasurement errorDivergence angleClaim testingDiscriminationParastichy pairSummary statisticNegative resultAutocorrelationEvidenceEnsemble