Where the angle comes from

The family that lost a member

The offset rule restated in the arrangement predicts that the chain whose organ was taken is the chain that breaks. Scored on the nine offsets where the question can be asked, it is right none of the time and its opposite is right all nine.

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

The best account of which family a wrecked stem keeps is the offset: take the smaller counted number when the removal landed no further back than it, the larger when it landed beyond. Twenty-five of thirty, and the arithmetic form of it explains nothing.

Restated in the arrangement rather than in the sequence it stops being arithmetic. An organ five places back from the tip of a stem counted at 5 and 8 spirals lies on the tip’s own five-chain; an organ eight places back lies on the eight-chain. So the rule reads as a statement about whose neighbour was taken, and it comes with a prediction anybody would make: the chain that lost a member is the chain that breaks.

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. 1 The prediction and its opposite, scored on the same rows. One of them takes every row and it is not the one that was proposed.

It is refuted, and it is refuted backwards. That is a better outcome than a confirmation would have been, and this essay is mostly about why.

A prediction that fails in the direction nobody proposed is worth more than one that succeeds, because success is compatible with the prediction being a restatement of the data it was drawn from. This one was drawn from an intuition about chains, scored on rows the intuition had never seen, and came back inverted at every row — which means the intuition was about the wrong object and now names the right one. The census that raised it could not have found this, because the column it needed was never in the table.

The column the census never carried

The census records, for each stem that never repaired, the lattice, the offset and the surviving family. It does not record which family the removed organ belonged to, and adding it is one line of arithmetic: an organ k places back lies on the tip’s p-chain exactly when p divides k.

Every wrecked offset, and whose neighbour was removed. 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. 2 Every wrecked offset with the column added. Most rows say “neither chain”, which is the first thing the reading has to survive.
A stem unrolled: 180 nodes at 136.78° with a rise of 0.013 circumferences. The counter is shown these coordinates and the circumference, and finds 5 parastichies one way and 8 the other. The faint strips left and right are the same stem: a family leaving one edge re-enters at the other.
Fig. 3 What the column means in the arrangement: five places back and eight places back are the two organs directly below the tip, and everything between them is somewhere else.
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. 4 And the same fact in the packing: the organs an organ touches are the members of its two contact families, at the two lags the pair names.

Of the thirty wrecked offsets in the census, nine remove an organ that lies on exactly one of the two chains. Seven of those are members of the smaller family and two of the larger. Twenty-one remove an organ that lies on neither. None removes an organ on both, which is not an accident: the two counted numbers of a contact pair are coprime, and no offset inside the front is a multiple of both.

The coprimality is worth a sentence because it is what makes the reading testable at all. If the two counted numbers shared a factor there would be offsets belonging to both chains, and every such row would be silent for a different reason — not because the organ was nobody’s neighbour but because it was everybody’s. A pair whose numbers share a factor is exactly what a wrecked stem can be counted at when it lands somewhere the lattice did not come from, so the clean split here is a property of the lattices this census is drawn from rather than of contact pairs in general.

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. 5 The nine rows the question can be asked on, with the family that lost a member beside the family that survived.

Nine of nine, the other way

On all nine, the family that lost a member is the family left standing.

  • A stem counted at 5 and 8 spirals, cut five places back, keeps the five.
  • The same lattice cut eight places back keeps the eight.
  • A Lucas stem counted at 4 and 7 spirals keeps the four when cut four back and the seven when cut seven back.
  • The 7/11 lattice cut seven back keeps the seven; the 8/13 lattice cut eight back keeps the eight.
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. 6 One of the nine read by lags rather than by neighbours, which is the measurement the surviving family is defined by.
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. 7 The census these rows are drawn from, with the offset rule’s own five failures marked.

There is no scatter to argue about and no threshold to tune. The reading was stated before the column was computed, it is a binary prediction on nine independent rows, and it lost all nine.

Nine rows is not many, and it is worth being explicit about what nine buys. If the two outcomes were equally likely on each row, nine of nine in one direction happens by chance about twice in a thousand tries. That is not a p-value anybody should lean on — the rows are not draws from an urn, and two of them share a lattice — but it is enough to say that the result is not the shape a coin makes, and the direction was fixed in advance by a prediction that had already been written down.

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. 8 The same nine in the quantity that first raised the question: the period of the motif a wrecked stem repeats equals the family it kept.

Why backwards is the right way round

The prediction had an intuition behind it — take a link out of a chain and the chain is what breaks — and the intuition is about the wrong object.

A contact family is not a physical thread. It is a set of organs whose angular spacing happens to be a particular lag, and the organs above the hole are still spaced at that lag after the removal, because the rule that placed them is still minimising the same sum of inverse powers. Removing one member does not unpick the others.

What the removal actually costs is the other chain. Every organ near the tip was positioned against a neighbourhood that included the one now missing, and the members of the family the removed organ did not belong to are exactly the ones whose spacing was set with it in view.

The next organ moves for the last 8, and for no others. One row per organ removed, counted back from the tip of a stem at a rise of 0.013 whose counted pair is 5 and 8. Removing any of the last 8 moves the next organ by 4.9° to 164.1°; removing an older one moves it by at most 0.70°, which is under the azimuth grid. The boundary is at 8, and 8 is the larger parastichy number — so the experiment counts the spirals without measuring an angle.
Fig. 9 The immediate effect of a removal, offset by offset: it is large, and it is not the same at every place a cut can land.
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. 10 The intervention itself, held fixed while the offset moves.

So the correct reading is the opposite of the stated one and it is mechanism-shaped in the same way: the chain that keeps its spacing is the chain whose member was taken, because that chain’s remaining members are still mutually consistent while the other chain’s are not.

That has a consequence worth stating even though this census cannot test it. If the surviving chain is the one left mutually consistent, then what survives is not really a family at all — it is whatever subset of the arrangement the removal did not put out of register. The family language is a convenience that fits because the two contact chains are the only subsets a settled lattice has at that scale. On an arrangement with three comparable lags, or one where a removal falls between chains, the same mechanism would predict something the vocabulary of pairs cannot express, and the pair a counter returns would stop being the right way to ask.

On a rung the response is a run of offsets; near a transition it has a hole. One row per rise, from 0.032 at the top to 0.005 at the bottom, and one column per offset: the organ one place back at the left, 14 places back at the right. A cell is filled where removing that organ moves the next organ by more than 2.5°, and empty where it does not. On a rung the filled cells are a run from one to the larger parastichy number — 5, 8, 13 at the pairs shown on the left. Every rise shown here is in the middle of its rung, so every row is a run and nothing past it is felt — what happens between the rungs is a separate matter.
Fig. 11 The range over which a removal is felt, which is what decides how many offsets can be asked about at all.

What it does not cover

Twenty-one offsets of thirty remove an organ on neither chain, and on those the reading has nothing whatever to say.

That is the honest limit and it is a large one. A rule that is perfect on three tenths of a census and silent on the other seven is not the account; it is a clue about what the account will look like. Quoting the nine without the twenty-one would be reporting a subset dressed as a result, which is the failure this collection has already caught itself making with “the shortest hop survives” — right at twelve of twenty-nine and stated as though it were the rule.

Two of those facts fit together, and the fit decides what the reading is actually worth.

On all nine answerable rows the chain reading and the offset rule return the same answer. They have to. An organ five back on a 5/8 stem is on the five-chain, and is also a removal landing no further back than the smaller counted number, so both say five; an organ eight back is on the eight-chain and lands beyond the smaller number, so both say eight. The same holds at 4/7, at 7/11 and at 8/13. The two accounts agree on every row either of them can be checked against.

So the chain reading does not win a single row the offset rule was losing. What it supplies is not accuracy but the boundary — it says why the rule’s cut falls at the smaller counted number rather than anywhere else, which is the one thing the arithmetic form could never say about itself.

It also forces a conclusion about the failures. The offset rule is right at twenty-five of thirty, so five rows defeat it; and since it agrees with the chain reading on all nine rows where the organ taken was somebody’s direct neighbour, and the chain reading takes all nine, every one of those five failures lies inside the silent twenty-one. The rule breaks exactly where the mechanism has nothing to say, and nowhere else.

That is encouraging and damning at once. Encouraging, because two accounts that fail in the same place is what one expects when one of them is the mechanism behind the other. Damning, because it means the nine rows carry no information about the disagreement between them: the census that could separate a mechanism from an arithmetic coincidence is exactly the census of offsets that are nobody’s neighbour, and that census is the one this collection has not run.

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. 12 The families a wrecked stem chooses between at one lattice. The slider walks the census, and the marked bars are what was actually left standing.
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. 13 The lengths those families’ steps have, which is the reading this one replaces rather than joins.

The twenty-one are not a ragged remainder either. They are the offsets strictly between the two counted numbers and below the smaller one, and the offset rule covers them by arithmetic without saying what is physically true of them. Any account that finishes this thread has to say what a removal does when the organ taken was nobody’s direct neighbour.

There is a reading available for those rows and this essay deliberately does not adopt it. An organ four places back on a 5/8 stem is not on either chain through the tip, but it is on the five-chain through the organ one place above the tip, and on the eight-chain through some organ further down. Chains are everywhere; what makes the tip’s own two special is that the tip is where the next organ is about to be placed. Extending the reading to the twenty-one would mean choosing which organ’s chains count, and that choice is exactly the sort of free parameter this collection has been caught by before. It is a hypothesis to test, not a gap to fill in with a definition.

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 0.032, where the pattern is 3/5. 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 5, 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 2.34°. 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. 14 The shape of the table these offsets come from, at a rung where the front is shallow enough to see all of it.

Three controls

The column is arithmetic, not judgement. Whether an organ lies on a chain is decided by divisibility, computed from the counted pair the figure itself reports. Nothing about the surviving family enters the classification, so the score is not circular.

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. 15 Where the counted pair comes from in the first place: chains of near neighbours, followed on the positions and nothing else.

The rows are independent. Nine offsets across five lattices on two branches, each a separately grown stem with its own control. They are not nine readings of one run.

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. 16 The two branches carry fronts of different depth at the same rise, which is why a row on one is not a row on the other.
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.

And the reading is not the offset rule in disguise. On these nine rows the two agree, which is why the offset rule scores well: an offset equal to the smaller number is at most the smaller number, and an offset equal to the larger is beyond it. The reading here is narrower and says something the offset rule does not — why those rows come out as they do — and it is falsifiable in a way the offset rule is not, because a single row where the lost chain broke would have ended 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. 18 And the caution the neighbouring result adds: the same offset does not always give the same answer, so a rule scored over offsets alone is scored over a sample that never varied the rise.
Agreement between two windows happens only on a slow enough shoot. Five stems at each of four rates and five disturbances, each read through two overlapping windows of 250 internodes. A filled mark is agreement — both windows reported the same pair; a half mark is a disagreement; a small mark is one window reporting and one refusing; an open mark is silence. Agreement appears 0 times in 25, 1 times in 25, 14 times in 25, 14 times in 25 at 130, 250, 400, 700 nodes per rung, and the two rates it is almost absent from are the two at which a rung is no longer than the window.
Fig. 19 The general shape of a scored comparison: several stated readings, one table, and every score reported rather than the winner alone.

What would settle it

The reading covers nine rows because only nine offsets in this census are multiples of a contact number. That is a property of the census, not of the question, and it can be changed.

A stem at a finer rise has a deeper front and larger counted numbers, so more of its offsets are multiples of one of them: at 8/13 the answerable offsets are 8 and 13, at 13/21 they are 13 and 21. Sweeping the offset at two or three finer rungs would take the reading from nine rows to twenty or thirty without changing what is being asked, which is the cheapest strengthening available.

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. 20 Where those finer rungs are, and how much of the ladder this census has actually visited.
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. 21 And the coarse caution about doing it: whether a stem is wreckable at all is a property of where it sits on the ladder.

The second thing is a genuine test rather than more of the same. If the chain that keeps its spacing is the one whose member was taken, then removing two organs from the same chain should leave that chain standing more surely than removing one from each — and the two-organ census already exists.

Move the second organ far enough back and the experiment is the old one. The displacement of the next organ when two organs are removed — one two places back and one a further gap behind it — against that gap, at a rise of 0.032 where the pattern is 3/5. The dashed line is what removing the single organ two places back does on its own, computed by the earlier one-organ intervention and not by this one. Inside the front the two vacancies interact and the answer swings over 77°; from the gap that puts the second organ 2 places behind the front onwards it settles onto the single cut's 79.0°, within 0.4°. That limit is what makes the second parameter a control rather than a confound.
Fig. 22 The second axis of the two-organ table: where the second removal sits relative to the first, which is what such a test would be read along.
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. 23 What either answer would decide: two wrecked stems settle into motifs of different length, and the length is the family that was kept.

Where this leaves it

The thread has narrowed the question four times: to one of two families, to not-the-shorter, to the offset at twenty-five of thirty, and to a rule that needs the rise attached. This is the first narrowing that says anything about why, and it says it in the only way this collection accepts — by making a prediction, scoring it on rows chosen before the answer was known, and reporting that it came out backwards.

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. 24 The standard the counter itself has to meet before any of this is measurable: what a grid of a stated fineness can and cannot resolve.

A refutation that hands back a cleaner statement than the one it refuted is the best thing a test can do. What it does not hand back is coverage, and the next move is not another argument. It is more rows.

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.

  • The hop that survived — both name ablation, falsifiability, honest limits, lattice, lattice offset, measurement, parastichy pair, the placement rule, rigid hop, rung
  • Two accounts of one number — both name ablation, claim testing, honest limits, lattice, measurement, negative result, parastichy pair, the placement rule, rung, underdetermination
  • What a count cannot decide — both name claim testing, control, honest limits, lattice, measurement, negative result, parastichy, parastichy pair, rung, underdetermination
  • A period that is not a count — both name ablation, falsifiability, honest limits, lattice, lattice offset, measurement, parastichy, parastichy pair, rigid hop
  • A wreck has a short list — both name ablation, falsifiability, honest limits, lattice, measurement, negative result, parastichy pair, the placement rule, rigid hop
  • One turn per survivor — both name ablation, falsifiability, honest limits, lattice, lattice offset, measurement, parastichy pair, the placement rule, rigid hop

Named objects

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

AblationClaim testingControlFalsifiabilityHonest limitsLatticeLattice offsetMeasurementNegative resultParastichyParastichy pairThe placement ruleRigid hopRungUnderdetermination