Where the angle comes from

The shortest hop was a coin flip

The reading that a wrecked stem keeps its shortest hop was refuted at twelve of twenty-nine across the census. Re-scored along a single rung, where the counted pair is held and the step ordering reverses, it is right at sixteen of thirty-one — which is not a refutation but an absence of information.

Worth reading first: The organ that was taken away · Counting the spirals · A head is a set of points.

The first account anybody reaches for is that the rule keeps its shortest hop. It has everything a good guess needs: the rule places each organ at the minimum of a sum of inverse powers of distance, so it is a rule about being far from near things, and the family made of the shortest steps should be the one most strongly held.

It was refuted at twelve of twenty-nine across the census — right less than half the time, which reads as a decisive answer. This essay re-scores it along a single rung and finds sixteen of thirty-one, which reads as no answer at all. Both numbers are correct. The difference between them is the sampling, and the difference is the point.

The two contact steps change places inside the 5/8 rung. Measured at every rise on one rung, where a counter returns 5 and 8 spirals throughout. The settled divergence slides from 136.6406 to 137.8672 degrees. The ratio of the two contact steps falls to 1.0131 at a rise of 0.016 and the ordering changes hands at 0.015: above it the shorter step belongs to the 5-family and below it to the 8-family. Neither quantity is available to a counter, which is shown positions and reports a pair, and both of them move while that pair does not.
Fig. 1 Why a rung is the place to re-score it: the ratio of the second contact step to the shortest crosses one inside the rung, so the ordering the reading is about reverses while nothing a counter measures does.

The ordering reverses inside a rung

Rank the lags of a settled stem by the length of their step across the surface — the distance the placement rule itself uses — and the two contact families come first and second. Which of them is first is not a property of the counted pair.

Across the 5/8 rung, from a rise of 0.018 down to 0.007, the shorter step belongs to the five at the coarse end and to the eight from 0.015 down. At 0.016 the two are within 1.3 per cent of each other.

Which offsets give short hops, at a rise of 0.018. The two lowest points are at 5 and 8, and those are the parastichy numbers. Offset 1 is high because a hop of one node is at least the rise, which is what makes a stem easier to count than a disc.
Fig. 2 The ranking at the coarse end of the rung, where the smaller family carries the shorter step.
Which offsets give short hops, at a rise of 0.008. The two lowest points are at 5 and 8, and those are the parastichy numbers. Offset 1 is high because a hop of one node is at least the rise, which is what makes a stem easier to count than a disc.
Fig. 3 And near the fine end of the same rung, at the same counted pair, with the ordering the other way round.

So a census that takes one rise per rung is not sampling the reading’s own variable. It is sampling a variable the reading depends on, at one arbitrary point per rung, and reporting the result as though it were a property of the rung.

The reversal itself deserves a sentence, because it is not obvious that it should happen at all. The two contact steps are the two shortest distances across the surface between an organ and its neighbours, and their lengths depend on the settled divergence and the rise together. As the rise falls the stem stretches vertically and the divergence slides, and the two effects do not act equally on the two lags: one step is dominated by its azimuthal component and the other by its height. There is therefore a rise at which they must cross, and the only question is whether it falls inside a rung or between two. Here it falls inside — which is what makes the counted pair unable to report it.

Which family survives, along the 5/8 rung. The family a wrecked stem keeps, at every offset that wrecks and every rise on one rung. A counter shown any of these stems returns 5 and 8 spirals, at all twelve rises, so nothing in the pair distinguishes the columns. The cells say otherwise: at an offset of 4 the stem keeps the 5-family at the coarse end of the rung and the other one at the fine end. The offsets that wreck at all grow from 1 to 5 as the rise falls, because the front deepens, and the extra offsets are the ones that keep the larger number. So the rule stated over the offset alone is a rule with the rise left out of it.
Fig. 4 The rung as a grid: every column is a rise a census would have chosen between, and every cell an offset that never repaired.

Sixteen of thirty-one

Re-scored on every wrecked offset at every rise of that rung — thirty-one rows, one counted pair throughout — the survivor is the shorter step at sixteen and the second-shortest at fifteen.

How many offsets wreck, along the 5/8 rung. The count of offsets that never repair, at each rise on one rung. It runs from 1 at the coarse end to 5 at the fine end, while a counter returns 5 and 8 spirals at every one of them. The front — the run of recent organs at which a removal is felt at all — deepens as the rise falls, so there are simply more places a cut can land and fail to heal. That is the mechanism under the grid: the offsets that appear at the fine end are the ones beyond the smaller contact number, and those are the ones that keep the larger family.
Fig. 5 Where the thirty-one rows come from: the count of offsets that never repair at each rise, growing as the front deepens.

That is a coin flip, and a coin flip is a different result from a refutation. A reading that is right at twelve of twenty-nine has been tested and found wanting. A reading that is right at sixteen of thirty-one has been tested and found to carry no information about the answer — which is worse for it, and better for knowing what to do next.

The distinction is not pedantry. Twelve of twenty-nine invites the obvious follow-up: if the shortest step loses more often than it wins, perhaps the longest wins, and that reading was duly scored and found to hold at seventeen — also not a rule. Sixteen of thirty-one kills both at once. There is no reading of the form “the survivor is the one whose step is longer/shorter” that can do better than chance on rows where the ordering has been decorrelated from everything else, because on those rows the ordering is not carrying the signal. Scoring a statement and its negation on the same rows is the cheapest way to find that out, and it is the shape this collection uses throughout.

Which lag survives, at every lattice and every offset. A row for each of twelve lattices and a column for each offset an organ is removed at, with the lag whose hop survived written in the cell. 30 cells never repair. The lag left standing is one of the two contact families at 29 of them, and at 17 it is the second shortest step on the lattice rather than the shortest, which is what refuses the reading that a rule holds its nearest neighbours. The ringed cells are the five the offset rule gets wrong. Two lattices carry no cells at all because no single removal wrecks them.
Fig. 6 The census the twelve-of-twenty-nine came from, with each lattice contributing one rise.
The hops of a 5/8 lattice, shortest first — golden, rise 0.010Every lattice hop at this rise, ordered by how long its step is across the surface of the stem, with the two that a wrecked stem here leaves standing picked out. The two shortest are the contact families the counter returns, 5 and 8, and they differ in length by a factor of 1.076. The lags left standing after a removal are 5 and 8, sitting at rank 2 and 1 in this order, so the family the rule holds is a short step but not always the shortest one.85133161021181122624629lag, in organs — ordered by the length of its stepstep length, in turns of the stemkept: lag 5, lag 8golden, rise 0.010 · pair 5/8 · offsets that wreck: 4, 5, 6, 7, 8generated from a stated rule, not drawn to look right
Fig. 7 The families being chosen between at one lattice. The slider walks the census, and the marked bars are what was actually left standing.

Why the two numbers differ

The census’s twelve of twenty-nine is not wrong and it is not a smaller sample of the same thing. It is a sample in which the step ordering is correlated with the counted pair, because each pair appears at one rise and that rise fixes the ordering.

There is a second reason the two numbers differ in kind rather than in size, and it matters more than the arithmetic does.

A reading that scores twelve of twenty-nine is not merely unsupported. It is supported in reverse: on a binary choice between two families, being right at twelve rows means the opposite reading — the longer of the two steps survives — is right at seventeen. Seventeen of twenty-nine is not much, but it is on the right side of half, and it is exactly the sort of residue that gets picked up later as a hint worth chasing. A refutation that leaves its own inverse looking mildly promising has not finished the job.

Along the rung it does finish. Sixteen of thirty-one for the shorter step is fifteen of thirty-one for the longer, and neither number is anything. The two are not one right reading and one wrong one; they are a claim and its negation, both indistinguishable from a coin, on a sample built to vary the quantity they disagree about.

That is also the case for re-scoring a reading somebody had already answered, which is usually waste. The case is narrow and stateable. The original score was computed on a sample in which the quantity under test was pinned to the quantity used to select the sample, so the number it produced could not be read as being about that quantity in either direction — not as support and not as refutation. Re-scoring on a sample that breaks the pinning does not overturn the conclusion. It replaces a conclusion that happened to be right with the same conclusion held for a reason, and it shuts the door the first score had left ajar behind it.

Both numbers are quoted here for that reason rather than the later one alone. Sixteen of thirty-one on its own tells a reader nothing about whether the sampling was ever a problem, and reporting it without the twelve would repeat the original mistake pointing the other way.

The divergence slides along the 5/8 rung. Measured at every rise on one rung, where a counter returns 5 and 8 spirals throughout. The settled divergence slides from 136.6406 to 137.8672 degrees. The ratio of the two contact steps falls to 1.0131 at a rise of 0.016 and the ordering changes hands at 0.015: above it the shorter step belongs to the 5-family and below it to the 8-family. Neither quantity is available to a counter, which is shown positions and reports a pair, and both of them move while that pair does not.
Fig. 8 The other quantity that slides across the rung, which no counter reports either.

Along a rung the correlation is broken by construction: the pair is held and the ordering moves. What survives the breaking is the information the reading actually carries, and it is none.

It is worth being precise about which correlation is doing the damage, because the census is not badly designed. Each lattice in it appears at one rise, and that rise was chosen to produce the pair. So within the census, “which pair” and “which step is shorter” move together — not because they are physically linked but because one rise was picked per pair. A reading about step lengths scored on that census is therefore partly scored on which pairs happened to be included, and changing the pair list would change its score without anything about the reading or the physics changing at all.

The block is one of the two numbers, and not always the smaller. Every lattice a single organ was removed from, one row each: golden, rise 0.013 carrying 5/8; golden, rise 0.008 carrying 5/8; golden, rise 0.005 carrying 8/13. The two open ticks on each line are that lattice's own parastichy numbers; the filled dots are the blocks the stems that never recovered settled into, one per offset that failed. The claim this table was built to test is that the block is the smaller of the two, which held at the two rises it was first measured at. It does not hold here: 5/8 gives 5 and 8. What survives is weaker and still worth something — every filled dot but 1 sits on one of that row's own ticks, so the orbit carries a count of the lattice it was cut from, and which of the two it carries is decided by the offset rather than by the pattern.
Fig. 9 The same rows in the quantity that first raised the question: the period of the motif a wrecked stem repeats equals the family it kept.

This is a general hazard and it is worth naming in the abstract, because this collection will meet it again. A sample assembled to vary one quantity holds others fixed by construction. Any reading later scored on that sample inherits the constancy, and its score is a statement about the sample’s design as much as about the reading. The only fix is to vary the quantity the reading is about, on purpose, which is what a rung sweep is.

What the finer grid does to the rises already published. The two rises this site has argued from and the one it published as having no answer, each read at both azimuth grids, five stems apiece. A filled mark agrees with the position counter, a half mark contradicts it, an open mark is a refusal. At 0.013 and 0.005 the readings are identical at both grids, so nothing already written depends on the sample count. At 0.008 they are not: 384 azimuths gives 5/8, 5/8 and 1152 gives 8/13, 8/13, against a counter that says 5/8. That rise was chosen in the earlier work because the three shortest lattice offsets there are within a fifth of each other, and a stem with no answer answering differently on a different grid is the object behaving as it was said to.
Fig. 10 The same hazard one level down, in the instrument: what a grid of a stated fineness can and cannot resolve.

What the reading was competing with

The reading that replaced it is the offset — smaller family if the cut lands no further back than the smaller number, larger beyond — and it scores twenty-five of thirty on the same census. Re-scored along this rung it does better than a coin flip and worse than its census figure, for reasons that are about the front rather than about the rule.

Which family survives, along the 5/8 rung. The family a wrecked stem keeps, at every offset that wrecks and every rise on one rung. A counter shown any of these stems returns 5 and 8 spirals, at all twelve rises, so nothing in the pair distinguishes the columns. The cells say otherwise: at an offset of 4 the stem keeps the 5-family at the coarse end of the rung and the other one at the fine end. The offsets that wreck at all grow from 1 to 5 as the rise falls, because the front deepens, and the extra offsets are the ones that keep the larger number. So the rule stated over the offset alone is a rule with the rise left out of it.
Fig. 11 The row where the offset rule’s own answer changes along the rung, which is the part of it the census could not see.
A prediction and its opposite, scored on the same rows. The reading under test said the family whose member was removed is the one that breaks. Scored across every wrecked offset where the removed organ lies on exactly one contact chain — 9 of 30, the other 21 being silent because the organ lies on neither — it is right no times and its opposite is right nine. A chain that loses a member does not stop existing: the organs above the hole are still spaced at that lag and the rule that placed them is still minimising the same sum, while the other chain has lost the organ its members were positioned against.
Fig. 12 And the reading that came after it, which is right at every row it can be asked on and silent at two thirds of them.

Three readings, then, in order of what they cost to state and what they buy: the shortest hop, which is free and carries nothing; the offset, which is arithmetic and carries most of the census; and the family that lost a member, which is mechanism-shaped, is right on every row it applies to, and applies to nine.

The offsets where the removed organ belonged to one family. Each row is a stem that never repaired, with the family of the organ that was taken and the family that survived. An organ five places back on a stem counted at 5 and 8 spirals lies on the tip's five-chain, so the question can be asked there; an organ four places back lies on neither chain and it cannot. Of 30 wrecked offsets in the census, 9 remove a member of exactly one family and 21 remove a member of neither. On every one of the 9 the family that lost a member is the family left standing, which is the opposite of what the reading predicted.
Fig. 13 Those nine rows, with the family that lost a member beside the family that survived.

Three controls

The lengths are computed, not estimated. A step’s length is derived from the settled divergence and the rise, not measured off a drawing, so the ordering at 0.016 — where the two differ by 1.3 per cent — is exact arithmetic rather than a close call.

Which offsets give short hops, at a rise of 0.013. The two lowest points are at 5 and 8, and those are the parastichy numbers. Offset 1 is high because a hop of one node is at least the rise, which is what makes a stem easier to count than a disc.
Fig. 14 The ranking at a rise in the middle of the rung, drawn from the same arithmetic.

The result does not rest on the crossing. If the three rises nearest the crossing are dropped, the score moves by less than the difference between sixteen and fifteen. The coin flip is a property of the whole rung, not of the rises where the two steps are nearly tied. That check matters because the obvious objection to a null result is that it was manufactured by including rows where the quantity under test barely varies — rows near a crossing, where “which is shorter” is decided in the third decimal place. Dropping them makes the reading no better, which is the direction the objection needed.

One wrecked stem, lag by lag — golden, rise 0.013, organ 4 back. How much each lattice hop moves from organ to organ in a stem that never repaired after a single removal, over its last 120 organs. The lag-one hop is the divergence itself and it swings by 65 degrees. The lag-5 hop swings by 0.11 degrees and sits 0.09 degrees from where the undisturbed stem put it, so that one family of the original lattice is still standing organ by organ. Its multiples inherit the same steadiness and nothing else comes within a factor of twenty. The block of angles this stem repeats has a period of 5, which is the surviving lag and not a coincidence.
Fig. 15 One row read by lags rather than by neighbours, which is the measurement the surviving family is defined by.

And thirty-one rows is the whole rung, not a selection. Every offset out to two organs past the front is cut at every rise; the rows scored here are every one that failed to repair, and the ones that repaired are reported as such rather than dropped. The thirty-one are also not thirty-one independent experiments, and the essay does not claim they are: rows at neighbouring rises share most of their geometry, so the effective number is smaller than the count. That cuts against reading anything into a sixteen-fifteen split, which is exactly the reading being avoided — the claim is that the split is indistinguishable from chance, and correlated rows make it harder, not easier, to say anything stronger than that.

Take away the organ four places back, and the next one goes into the hole. The last 30 organs of a stem at a rise of 0.013, unrolled. The open circle is the organ removed — four places before the tip. The ring at the top is where the rule puts the next organ with every organ present; the filled mark beside it is where the rule puts it with that one missing. The two are 164.1° apart, against a local spacing of 41°, and the vacancy itself is 172.7° from the undisturbed answer. Nothing else differs between the two runs: same rise, same history, same rule.
Fig. 16 The intervention, unchanged throughout the sweep: one organ removed, with the stem it is removed from varying underneath.
Every open question here needs under 28 specimens. The sample size at which each comparison reaches 80 per cent power at a 5 per cent false-positive rate, from the exact binomial rather than a normal approximation. The census question — do plants show consecutive Fibonacci pairs far more often than the geometry does — needs 4: 14.7% is the share of divergence angles giving a consecutive Fibonacci pair at a fine rise; 90% is what a grown history gives.
Fig. 17 And the form the caution takes when a claim of this size is to be made about real plants rather than runs.

What it does not license

It does not license re-scoring every earlier result along a rung and expecting them all to dissolve. Two of them cannot dissolve this way, and the reason is worth stating.

That the survivor is a contact family at all is a statement about which lags are available, and the available lags are what the counted pair names. Holding the pair and moving the rise cannot disturb it, and the sweep here confirms it: every one of the thirty-one rows keeps one of the two.

A cell's neighbours are its spiral families. Left: part of a 700-point golden, 137.508° head, with every contact between two cells drawn and coloured by the difference between the two nodes' placement indices. Right: the share each difference takes, across all 1459 contacts between interior cells. They are the parastichy numbers — 34, 55, 21, 89, 13, 8 — and the pair a person would count is 34 and 55. The six sides Euler forces are shared out among four of them, 5.64 edges per cell.
Fig. 18 Why that restriction is robust: the organs an organ touches are the members of its two contact families, at the two lags the pair names.
The two spiral families a counter finds between 0.43 and 0.67 of the radius. 21 spirals one way and 34 the other, found from the point positions alone — the counter is never told the divergence angle.
Fig. 19 And where the pair itself comes from — chains of near neighbours, followed on the positions and nothing else.

That a wrecked stem keeps exactly one hop rigid is a statement about the motif it settles into, measured against a control that shares its history, and it is unaffected by which hop that is.

The block a wrecked stem settles into is the count it was cut from. A stem is cut in the middle of its front and followed for 300 organs. It does not come back to its lattice; what it does instead is repeat a fixed sequence of divergences exactly, to the resolution of the azimuth grid. Each row shows that sequence twice over, one bar per organ, drawn to the same scale. At the 5/8 rung the sequence is five angles long and advances -36.1° per block; At the 8/13 rung the sequence is eight angles long and advances 22.5° per block. Every block is the smaller number of the pair that was cut, so the second attractor carries the first one's count — and every precession is one part in twice the block, which makes each of these a two-jugate arrangement with 10 and 16 rows.
Fig. 20 What every one of these rows decides in the end: the length of the motif a wrecked stem repeats.
The same rule, the same rise, two lattices, two fronts. How many organs back a single removal is still felt, on a stem seeded onto the golden lattice and on one seeded onto the Lucas lattice, at seven rises. Everything but the seed is identical at each rise — the rule, the spacing, the heights, the azimuth grid — and the two fronts differ at every one of them. Which branch has the wider front changes hands four times going down the range, so no function of the rise gives the column. The golden branch carries 5/8 at four of these rises, across a factor of two in the rise, and its front is eight at all four.
Fig. 21 And the caution about generalising from one branch, since the two carry fronts of different depth at the same rise.

What is fragile is anything scored over the census as a set of comparable rows. The census was built to answer which pair, and it answers that. Rows drawn from it are not thirty independent tests of a rule about step lengths.

The same caution applies to this essay’s own thirty-one rows, in the other direction. They are one rung of one branch, and the reading could carry information on a rung where the ordering does not reverse — where the shorter step belongs to the same family throughout, and the census’s correlation is a fact rather than an artefact. Whether such a rung exists is a question about the arithmetic of the ladder, and answering it needs the same sweep run on the other branch, where the divergences and the step lengths are different numbers.

The band that never heals is what two fixed edges leave over. Each row is one rung. A stem is grown to 400 organs, one organ is removed, and the stem is followed for 300 more. A filled mark is an offset the stem recovers from, with the number of organs it took printed above it; an open ring is an offset it never recovers from. At the 3/5 rung, a front of 5, every offset heals. At the 5/8 rung, a front of 8, the offsets 4, 5 never heal. At the 8/13 rung, a front of 13, the offsets 4, 6, 7, 8, 9 never heal. What is the same at every rung is the two edges: the first three offsets heal, and so do the last few of the front. What is left in the middle is the band, and it widens because the front does.
Fig. 22 The coarsest version of the caution: whether a stem is wreckable at all is a property of where it sits, not of the pair it is counted at.
A second cut moves the next organ, and does not move the boundary. Every pair of organs that can be taken out of a settled stem at a rise of 0.013, where the pattern is 5/8. A row is the offset of the nearer organ removed, counted back from the tip; a column is how many further places back the second one sits. The shade is how far the next organ ends up from where it would have been, from under a degree in the palest cells to a half-turn in the darkest. The run of shaded rows ends at 8, which is the larger parastichy number, and every row below it is blank across the whole width — the largest displacement anywhere past the front is 1.41°. So the nearer of the two organs decides whether the removal is felt at all, and the second one, wherever it is put, cannot make the pattern notice an organ it was not going to notice.
Fig. 23 The table one of those rises produces, with the offset along one axis and the second removal along the other.

Where this leaves it

A refutation that turns into a coin flip is not a weaker result. It is a different one, and it changes what the next measurement should be.

Against a refutation, the move is to find the reading that beats it. Against an absence of information, the move is to stop scoring readings over this census altogether and to sweep the quantity each one is actually about — which for the shortest-hop reading is the step ratio, and for the offset rule is the depth of the front.

Every transition as the rise falls. The pair climbs 1/2 → 2/3 → 3/5 → 5/8 → 8/13. Consecutive transitions are 0.381, 0.382, 0.382 of the previous rise — 1/φ² is 0.3820.
Fig. 24 Where the rest of the ladder is, and how little of it any ablation census has visited.
A window that fits inside a rung. Stems that climb the ladder at four rates, read over a window at the fine end. The condition is a ratio: the window has to be shorter than a rung. 250 internodes at 260 per rung is 0.96 rungs and agrees on 3 of 3; 400 internodes at 260 per rung is 1.54 rungs and agrees on 1 of 3; 250 internodes at 520 per rung is 0.48 rungs and agrees on 2 of 3; 400 internodes at 520 per rung is 0.77 rungs and agrees on 3 of 3. Read over the whole stem instead, every rate returns nothing — 0 of 3, 0 of 3 — because the quantity the comb is periodic in changes as the pattern climbs.
Fig. 25 The general form of reading anything inside one rung, where the pair is fixed and everything else is not.

The reading is not resurrected by any of this. Sixteen of thirty-one is not evidence for it. What the number says is that the census figure of twelve of twenty-nine was never the measurement it looked like, and that a reading can be disposed of for the wrong reason and stay disposed of for the right one.

That is a small thing to be careful about and it is the whole difference between a collection that accumulates results and one that accumulates numbers. The earlier essay reached the right conclusion; its arithmetic simply was not doing the work the prose gave it credit for. Recording that here, against the same reading, with the better sample, costs one sweep and leaves the conclusion where it was — which is the only outcome that would have been worth the sweep either way.

What links here

Computed from the collection, not written here: the essays that point at this one.

Shares its objects with

Essays that name at least two of the same things, and that neither author linked.

  • A survivor has to be a neighbour — both name ablation, falsifiability, honest limits, lattice, lattice offset, measurement, negative result, parastichy pair, the placement rule, rigid hop, rise, rung
  • A stem too fine to settle — both name claim testing, control, honest limits, lattice, measurement, negative result, parastichy pair, the placement rule, rise, rung, underdetermination
  • The hop that survived — both name ablation, falsifiability, honest limits, lattice, lattice offset, measurement, parastichy pair, the placement rule, rigid hop, rise, rung
  • Two accounts of one number — both name ablation, claim testing, honest limits, lattice, measurement, negative result, parastichy pair, the placement rule, rise, rung, underdetermination
  • One turn per survivor — both name ablation, falsifiability, honest limits, lattice, lattice offset, measurement, parastichy pair, the placement rule, rigid hop, rise
  • The panel with no corner — both name claim testing, control, honest limits, lattice, measurement, negative result, parastichy pair, the placement rule, rise, underdetermination

Named objects

A flat tag is an object no other essay names yet.

AblationClaim testingControlFalsifiabilityHonest limitsLatticeLattice offsetMeasurementNegative resultParastichy pairThe placement ruleRigid hopRiseRungUnderdetermination