Where the angle comes from

What a count cannot decide

A spiral count is the measurement this whole subject is built on, and it is deliberately blind to everything that varies inside a rung. Four results this collection now holds are results about that blindness rather than about the arrangements.

Worth reading first: Counting the spirals · A head is a set of points.

Count the spirals on a head and two numbers come back. It is the oldest measurement in the subject, it is what a botanist can make in a field without instruments, and this collection makes it on positions rather than on an assumed angle so that it means the same thing on a run as on a plant.

It is also, by construction, blind to almost everything. That sentence is meant literally rather than rhetorically, and the rest of this essay is an inventory of what it is blind to, an inventory of what it is not, and an argument that the two lists are the same fact.

The two spiral families a counter finds between 0.68 and 0.92 of the radius34 spirals one way and 55 the other, found from the point positions alone — the counter is never told the divergence angle.34 and 55 spiralscounted, not assumed
Fig. 1 The measurement itself: chains of near neighbours followed on the positions, and how many run in each direction.

A counted pair is a topological reading. It follows chains of nearest neighbours and reports how many there are, and it returns the same answer for every arrangement in which those chains connect the same way. A whole rung — a range of rises — is by definition the set of geometries about which it says one thing.

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. 2 The ladder that follows: pairs holding constant over ranges of rise, then stepping.

That blindness is the measurement’s virtue. It is why a count is robust to how a plant grew, to how it was photographed, and to where up the stem it is read. It is also why four separate results this collection now holds are results about what the count cannot decide.

The virtue and the limitation are not two properties that happen to coexist; they are the same property described twice. A measurement is robust to a variation exactly when it is blind to it. Asking a counter to distinguish two stems inside a rung is asking it to stop being robust to the thing that makes it useful in the field, and no better counter would fix it — a counter that could tell them apart would be reporting something other than a spiral count.

Four things it does not fix

Which contact step is shorter. Rank the lags by the distance the placement rule actually uses and the two contact families come first and second. Which of them is first reverses inside a single rung without the pair changing.

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. 3 The ratio of the two contact steps across one rung, crossing one at a rise the counted pair cannot report.
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. 4 The ranking those steps come from at one rise, computed from the settled divergence rather than estimated.

How deep the front is. The run of organs at which a removal is felt grows as the rise falls, so the number of places a cut can land and fail to heal grows with it — across one rung, from one offset to five. The larger counted number is often quoted as the front’s depth, and on the rises where both have been measured the two agree; what the pair cannot do is track the depth as it changes across a rung, because the pair is the thing being held while the depth moves.

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 The count of wrecking offsets across one rung, growing five-fold at a fixed pair.

Which family a wrecked stem keeps. At one offset on one lattice the answer changes between the coarse end of a rung and the fine one, which is the result that started this round.

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. 6 The grid it is read off: the pair constant along every row, and one row whose answer is not.

And whether a comparison of two rules has a corner in it. Sweeping the rise moves the contact numbers, and the shape of the comparison changes with them — a corner, then none, then a corner again. That fourth one is different in kind from the first three and is worth separating. The first three are quantities a count holds constant; this one is a comparison between two rules whose outcome turns out to depend on the lattice they are run on. A count cannot decide it not because the count is coarse but because the thing being asked about is not a property of a single arrangement at all.

The deeper rule against the disturbance's memory, at three contact scales. How many of six seeds agree that the deeper rule passed more drift, swept across the correlation length of the disturbance, at three rises. The rule, the amplitude and the run length are identical in every panel; only the rise differs, and with it the contact numbers — 3 and 5, then 5 and 8, then 8 and 13. The shapes are not the same: 3/5 is crossing, 5/8 is no corner, 8/13 is crossing. A corner that sat at a fixed number of organs would look the same in all three, and it does not.
Fig. 7 Three rises carrying three different contact pairs, and three different shapes for the same comparison.

What it does fix, and why that is the strong part

The temptation after four such results is to conclude that counting is a weak measurement. That would be the wrong lesson and the collection’s own strongest result argues against it.

The pair fixes which lags exist. A wrecked stem keeps one hop rigid, and at twenty-nine of thirty offsets that hop is one of the two the counter names. Not one of the twenty-four lags a stem could in principle keep — one of two, and the two are exactly what the count reports.

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. 8 Why: the organs an organ touches are the members of its two contact families, at the two lags the pair names.
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. 9 And the measurement that establishes it, made by lags against a control sharing the stem’s history.

That is a restriction from twenty-four possibilities to two, made by a measurement anybody can take in a field, and none of the four results above touches it. The count decides the menu and not the choice.

The menu result is also the one with a mechanism behind it, which is why it is robust in a way the others are not. A rule minimising a sum of inverse powers of distance is holding its nearest neighbours; the nearest neighbours are what a contact family is; and a count is a way of finding the contact families from positions. So the restriction is not an empirical regularity that a wider census might overturn. It is close to a definition, which is exactly the kind of result a blind measurement can deliver.

Every family but two is the sum of two others. Four heads and the contact families each actually has. An arc arrives at every family that is the sum of two smaller ones; the two with no arc arriving are the generators, and on every head they are the two smallest. whorled, 144°: 2, 3, 5 — golden, 137.508°: 8, 13, 21, 34, 55, 89 — Lucas, 99.502°: 11, 18, 29, 47, 76 — rational, 137.5°: 8, 13, 21, 34, 55, 89 — 137.0°: 8, 13, 21, 29, 50, 71, 92, 113. So once a pair is counted the rest is arithmetic, and a third counted family is a prediction rather than a second measurement.
Fig. 10 The menu itself, family by family, which is what a count is reporting.

Why the two get confused

Because the menu is usually short enough to look like a choice.

On most lattices the two contact numbers are the only plausible answers to anything, so a rule stated over the pair and a rule stated over the geometry agree on nearly every row. They come apart only where the geometry moves and the pair does not — which is inside a rung, and inside a rung is exactly where no census had ever looked.

The agreement is not a coincidence and it is worth understanding rather than noting. The counted numbers are the lags of the two shortest steps, so any quantity that depends on those steps depends on the pair too — through it, but not only through it. Two stems with the same pair have the same two lags and different step lengths, and a rule stated over lags will agree with one stated over lengths until the lengths reorder. Which they do, once per rung, at a rise no count reports.

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 place they come apart, drawn as the sweep a census takes one column of.
A count of m and n pins the divergence to 221°/mn. Each dot is one reported pair, and its height is the total width of the divergence angles that could have produced it at some rise. 2/3 leaves 38.8° open; 34/55 leaves 0.118°. The line is 221°/mn, taken from the three highest pairs and drawn back through the rest.
Fig. 12 And what the count is worth where they agree, which is most places.

There is a second reason and it is linguistic. A rung is called a plateau, and plateau suggests a set of equivalent stems. It is a plateau in one reported number laid over a geometry that slides continuously beneath it, and the finest sweep this collection has run finds no flat stretch anywhere inside one.

The 3/5 rung at a tenth of the ladder's step. Every rise of one rung, sampled ten times as finely as the ladder that found the locked band. All 23 are counted at 3 and 5 spirals and all 23 settle: the largest wander is 0.221 degrees, against the 0.5 degree threshold and against the 0.79 to 1.60 degrees the band on the coarse rung wobbles by. The divergence slides smoothly from 139.0625 to 136.7344 degrees with no rise stuck on a rational and none stuck on anything else. Whatever the band is, it is not something a coarser sampling was hiding here.
Fig. 13 Twenty-three rises inside one rung, with the divergence sliding through all of them.

Three things it can decide that look like it cannot

The list of blindnesses is easy to over-extend, and three near-misses are worth recording so that the boundary is a line rather than a mood.

Whether an arrangement is jugate. A pair whose numbers share a factor is the signature of a pattern arriving several organs at a time, and a count reports the factor directly. What a count cannot do is confirm it — a wrecked stem can be counted at a pair with a shared factor and have no rotational symmetry at all — but the question of whether the factor is there is decided by the pair alone.

Two patterns a counter cannot tell apart — counted 2/6 against 2/6. On the left, the top 120 organs of a spiral stem that never repaired after two organs were removed, settling at 175.01 degrees. On the right, a stem grown by a rule that places two organs at a time on every node. A counter shown the positions returns 2/6 for the first and 2/6 for the second, and a pair whose numbers share a factor is the usual signature of a whorled pattern. Rotate each pattern and the answer separates them at once: the whorled stem maps onto itself at a half turn and the wrecked stem maps onto itself at no fraction of a turn at all. Its shared factor is a fact about where its divergence landed, 4.99 degrees from 1 of 2 turns, and not about how it grew.
Fig. 14 The distinction drawn: a shared factor in the counted pair against the rotational symmetry actually present in the positions.

Which family is the larger. Trivially decided, and it matters because several rules in this collection are stated over “the smaller counted number” and are therefore safe from everything in this essay.

And whether two arrangements are on the same rung. Also decided by the pair, by definition — which is what makes a rung sweep possible at all. The sweeps that found the blindnesses depend on the count being reliable about exactly the thing it is reliable about.

Rises that do not settle, at two resolutions. The count of rises whose divergence never settles, on the rung where the band was found and on the finer rung swept ten times as closely. The coarse rung has six of 19, all of them stuck on three eighths of a turn; the finer rung has none of 23. Sampling is not the explanation: if a band of the same kind sat inside the 3/5 rung it would need to be narrower than a ten-thousandth of rise to have been missed here.
Fig. 15 A sweep that depends on it: two rungs compared, each identified by the pair its rises return.

What a counter is checked against

None of this is an argument for trusting the count less. It is checked here in ways a field measurement cannot be.

It is made on positions rather than on an assumed divergence, so it cannot inherit the answer it is being used to test. It is checked against arrangements written down from formulas where the right pair is known in advance. And it is checked for band dependence, because a count taken at the wrong radius is a different number.

The spiral counts, band by band, in one head. The same flower gives 13/21, 21/34, 34/55, 55/89 at different radii. A caption saying "34 and 55 spirals" is a statement about one annulus.
Fig. 16 The band check: how the reported pair depends on where up the arrangement it is taken.
The spiral counts four different divergence angles produce. Fibonacci counts come from one angle. The Lucas angle — which the same dynamical model reaches on a different branch — gives 47 and 76, and neither number is a Fibonacci number.
Fig. 17 And the angle check, which is what makes a returned pair a property of the arrangement rather than of the reading.

What the checks establish is that the count is right about what it reports. They say nothing about whether what it reports is what a given question needs, and that second thing is what four results have now had to discover separately.

That is a distinction worth carrying beyond this subject. A measurement can be validated exhaustively — against ground truth, against alternative implementations, against its own edge cases — and every one of those checks is a check on fidelity. None of them is a check on sufficiency, which is a relation between the measurement and a question rather than a property of the measurement at all. A collection that validates well and never asks the second question will accumulate correct numbers that do not settle the arguments they are quoted in.

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. 18 The instrument’s resolution, which is a third kind of limit again and is easy to confuse with the other two.

The practical form

Two sentences, and they are the useful residue of the whole round.

If a claim can be evaluated from a counted pair alone, a count is sufficient for it. Which lags are available, whether an arrangement is jugate, which family is larger — all decided by the pair.

If a claim mentions a length, a depth, a divergence or an angle, a count is not sufficient, and the rise has to be reported beside the pair or the claim is underdetermined. This is the rule the sampling essay arrives at from the other direction, and the two together are the round’s method result.

How nearly each angle is a simple fraction of a turn. A dip means a rational approximation and a lattice with visible rows. The golden angle's floor is 0.008; the rational angle reaches exactly zero.
Fig. 19 One of the quantities in the second category: how close a divergence sits to a rational, which no pair reports.
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 0.020 carrying 3/5; golden, rise 0.013 carrying 5/8; golden, rise 0.008 carrying 5/8; golden, rise 0.005 carrying 8/13; Lucas, rise 0.020 carrying 4/7; Lucas, rise 0.013 carrying 4/7. 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: 3/5 gives 5, 5/8 gives 5 and 8, 4/7 gives 4 and 7. 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. 20 And a table in the first, where the pair is doing all the work.

The second sentence needs one refinement, and it is the difference between a rule that works and a rule that looks as though it does.

Reporting the rise beside the pair is not quite enough, because the readings that depend on the rise do not depend on its raw value. They depend on where that rise sits between the ends of its own rung. The two contact steps change places part way along a rung; the front deepens along it; the settled divergence slides across the whole of it. Each is a function of position within a rung, and the same raw rise is a different position on a different rung and on the other branch. A row carrying 0.013 carries a number that cannot be interpreted without knowing which rung it fell in and where that rung ends.

So the sufficient description of a stem, for every claim in the second category, is the pair and the fraction of its rung the rise sits at. The pair says which rung; the fraction says where inside it. Between them they fix the divergence, the step ordering and the depth of the front — which is precisely the list a count alone leaves undetermined.

That is more demanding than it sounds, because the fraction is not observable without sweeping the rung. A rise is a number anybody can write down; the ends of the rung it falls in have to be found by growing stems either side of it until the pair changes. Every row published here carries the first and not the second, which is why the position within a rung can be recovered only for rungs that have been swept, of which there are two.

The consolation is that the requirement is finite. A rung’s ends are a property of the rung rather than of any experiment, so they are found once and then reused by every row that ever falls inside it.

What a plant would have to be measured with

The practical consequence points outward, and it is uncomfortable.

If a claim about ablation depends on the rise, then testing it on a real plant requires the rise to be measured on that plant — and the rise is not a quantity field botany reports. A count is; a divergence sometimes is; the vertical spacing per organ relative to the circumference is not, and it is the quantity that has decided every result in this round.

Both vary; only one of them varies enough to find. Each organ's step exponents, divided by its own mean so the two are comparable. The ogive's run over 15 per cent of their mean across 5 rings. The convex head's run over 1.15 per cent across 5 — inside the band a 3 per cent error on each ring position leaves, so no ruler separates it from a flat disc.
Fig. 21 What the measurable and unmeasurable halves look like on a real specimen: the quantities that survive a stated reading error and the ones that do not.

It is derivable in principle from the same photographs a count comes from, because the contact geometry fixes it: two contact steps of known lags and known lengths determine the rise. That is arithmetic on quantities a careful photograph carries, and it is not currently part of anybody’s protocol — including this collection’s own specification for a survey it cannot do.

What the pair costs, at a rise of 0.005. Five seeded stems at each length, read at four protractor errors. With no reading error the pair needs 250 internodes — against the sixty the single parastichy number costs. At 0.25° per organ it needs 250; At 0.5° per organ it needs 400; At 0.75° per organ it needs 1100. The pattern's own scatter here is 0.70°, so the last of those is a reading error larger than the signal being read.
Fig. 22 The cost side of that: what asking for a pair, rather than for the geometry, buys and gives up.
One packing criterion across the angles, with the others' winners marked. The three criteria pick 137.5°, 138.0° and 135.0°. The golden angle is near the top of all three and the exact winner of none at this size.
Fig. 23 And the several distinct things a packing can be measured by, of which the pair is one.

Where this leaves the subject

The count survives all of it, in a smaller and better-defined role than the one it has usually been given.

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. 24 The measurement again, at a different band, which is the check that the pair belongs to the arrangement.

A plant shows a pair, and a pair is a robust, transferable, checkable fact about it. What a pair does not carry is the rise, and the rise is what decides several of the things this collection has spent a round finding out it decides. Anyone comparing a run to a plant needs both, and until now this site has been recording one of them.

The honest summary is that the subject’s founding measurement is sufficient for the subject’s founding question — what pattern is this — and insufficient for most of the questions that follow it. That is not a criticism of the measurement and it is not news to anybody who has looked closely at one. It is simply a thing worth writing down in a collection whose whole method is to state what each instrument can and cannot settle, and which had gone eleven rounds without stating it about the one instrument every essay uses.

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. 25 And the form the caution takes when that comparison is finally made.

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 stem too fine to settle — both name counting blind, claim testing, contact network, control, honest limits, lattice, measurement, negative result, parastichy, parastichy pair, rise, rung, underdetermination
  • One offset, two answers — both name claim testing, control, honest limits, lattice, measurement, negative result, parastichy pair, rise, rung, underdetermination
  • The family that lost a member — both name claim testing, control, honest limits, lattice, measurement, negative result, parastichy, parastichy pair, rung, underdetermination
  • The organ that was nobody's neighbour — both name claim testing, control, honest limits, lattice, measurement, negative result, parastichy, parastichy pair, rung, underdetermination
  • Two accounts of one number — both name counting blind, claim testing, honest limits, lattice, measurement, negative result, parastichy pair, rise, rung, underdetermination
  • A stem coarse enough to cut — both name counting blind, control, divergence angle, honest limits, lattice, measurement, parastichy pair, rise, rung

Named objects

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

Counting blindClaim testingContact networkControlDivergence angleHonest limitsLatticeMeasurementNegative resultParastichyParastichy pairRiseRungSummary statisticUnderdetermination