Field

The pattern itself

A seed head is a set of points, and nearly every claim about one is really a claim about how many spirals run through it. The counting can be done from the points alone, and the answer is not what the captions say.

A head of 200 primordia at a divergence of 137.51°. Nothing is placed by hand: the nth point sits at n·137.51° and radius √n. The closest any two points come is 1.60 of the mean spacing.

A head is a set of points

The nth primordium at n times an angle, and a radius of root n. Two lines of arithmetic produce a sunflower head, which is either remarkable or suspicious depending on how carefully the claim is stated — and stating it carefully is most of the work.

The two spiral families a counter finds between 0.68 and 0.92 of the radius. 34 spirals one way and 55 the other, found from the point positions alone — the counter is never told the divergence angle.

Counting the spirals

Almost every claim about phyllotaxis is a claim about how many spirals run through a pattern, and the count is almost never done. It can be done from the points alone, by a count that is never told what angle built them — and then a count of 34 is evidence rather than a restatement.

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.

The counts change with radius

The same head gives 13 and 21 near the centre, 21 and 34 further out, 34 and 55 beyond that, and 55 and 89 at the rim. The transitions are at computable radii, and a photograph captioned with one pair is a statement about one annulus rather than about a flower.

A round trip on four heads of 400 primordia: the divergence angle recovered from each. The counter is shown the points and nothing else. The worst recovery across the four is 0.035°.

Recovering the angle from the counts

Build a head at a stated divergence angle, forget the angle, and get it back from the spiral counts alone. Four angles, worst error twelve thousandths of a degree — and the only thing that crossed between the two halves was a list of coordinates.

three stems: 1, 2, 3 primordia at a time. 1-jugate at 137.51° counts 2 and 3; 2-jugate at 68.75° counts 2 and 4; 3-jugate at 45.84° counts 3 and 6. Every count shares the factor k, and dividing it out leaves an ordinary lattice: what a k-jugate stem is, exactly, is k copies of an ordinary one wrapped k times round.

Two at a time

Every counter in these essays asks how far it is from element i to element i plus m, and that index is a claim that the elements arrived one at a time. For teasel, for Cephalaria and for a real minority of plants the claim is false — and what those patterns turn out to be is an ordinary lattice, wrapped twice.

Tracing one family: 4 chains. Every node is joined to the node one repeated displacement away, and the chains that result are drawn separately. There are 4 of them, which is the parastichy number of this family. No index of arrival was used anywhere, which is what lets the same count be made on a pattern where 2 primordia appear at once.

Counting without an index

A person counting spirals on a cone puts a finger on one scale, follows a family round, and counts how many distinct chains there are. That needs no order of arrival — and building it turns out to be strictly more general than the counter that reads the order of arrival, and to find a bug in the counting of a bijugate stem that nothing had caught.

The 2-jugate forks converge on 68.7539°. Every fork sits at a rational divergence, with denominator 4(m² + mn + n²) — 10/28, 30/76, 74/196 and so on. The limit is 68.7539°, which is 137.5078 divided by 2, and it is at none of them.

Half the golden angle

The forks of the van Iterson tree converge on 137.5078° and sit at none of them. Divide the whole tree by two and the same thing happens at 68.7539° — which is where teasel is, and where a bijugate sunflower counted 42 and 68 has to be.

A counter that sees no positions

This site has counted spirals two ways, and both were handed coordinates. A third counter is handed a list of angles and nothing else. It returns one number instead of two, it refuses more often, and where it refuses it would have been wrong every time.

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.

Every family but two is a sum

A seed head has six spiral families and everybody reports two. That looks like a convention hiding information and it is the opposite — every family but the two smallest is the sum of two others, so a third count is a prediction rather than a measurement, and a check that catches a wrong pair.

The angles name the branch

Seed the same rule at the Lucas angle and the readout returns 4 and 7, then 7 and 11 — the pairs the position counter finds, and not Fibonacci numbers. So a list of divergence angles carries not only how many spirals there are but which family of ladders the plant is on.

A lattice with an error that repeats every 8 organs. The autocorrelation of 759 divergence angles from a kinematic lattice at a divergence of 137.8261° and a rise of 0.005, with 0.5° of scatter on each azimuth. There is no placement rule anywhere in it: node i is put at exactly i times the divergence and then displaced. The only thing that differs between this figure and the control is the structure of the displacement — here, an error that repeats every 8 organs at period 8, weight 0.7. The largest comb mean is 0.592 against a sampling band of 0.073, and the readout returns 8/10.

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.

One wrecked stem, lag by lag — golden, rise 0.005, organ 6 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 55 degrees. The lag-4 hop swings by 0.12 degrees and sits 0.01 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 4, which is the surviving lag and not a coincidence.

A period that is not a count

Eighteen wrecked stems settle into a block whose period is one of their own spiral counts, and one settles into a block of four on a lattice counted 8 and 13. The odd one is not noise. It is the case that shows what the rule is actually conserving, and it is the reason this thread is about lattice steps rather than about spirals.

$Everywhere a cut of one to five organs can send a 5/8 stem. Every settled divergence reached by any arrangement of up to five organs removed from a stem at the 5/8 rung, on one axis. There are six of them and no more. three are slips of the lattice the stem was cut from: each keeps the lag-5 family intact and sits a whole number of turns of it from the next, which is the ladder marked below the axis with rungs 72.0 degrees apart. The other three keep no lag at all and sit near a fraction of a turn, marked above: 175.0 degrees near 1 of 2 turns, 190.0 degrees near 1 of 2 turns, 235.0 degrees near 2 of 3 turns. A stem that is cut either slides along the ladder it was on or leaves it for a lattice with files in it.$

A count with a factor in it

Cuts of several organs send a stem to six settled divergences and no more. Three of them are the old lattice with a family left standing. The other three are counted 2/6, 4/6 and 3/6 — and a pair whose numbers share a factor is the classic signature of a pattern that arrives several organs at a time.

$Two patterns a counter cannot tell apart — counted 2/6 against 2/6. On the left, the top 90 organs of a spiral stem that never repaired after two organs were removed, settling at 175.01 degrees. On the right, a stem grown by a rule that places two organs at a time on every node. A counter shown the positions returns 2/6 for the first and 2/6 for the second, and a pair whose numbers share a factor is the usual signature of a whorled pattern. Rotate each pattern and the answer separates them at once: the whorled stem maps onto itself at a half turn and the wrecked stem maps onto itself at no fraction of a turn at all. Its shared factor is a fact about where its divergence landed, 4.99 degrees from 1 of 2 turns, and not about how it grew.$

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.

Two readings of what a stem is, and one of them is wrong. The same runs read twice. On the left is the pair counted from the point positions by machinery that is never shown a divergence angle; on the right is the pair read from the divergence sequence, which is the column the depth thread has been quoting. Every exponent's stems are counted at 5/8 spirals from the points. Read from the angles, the deepest rule's stems come back as something else at every seed, and a pair with a 8 replaced in it is not a near miss but a family whose step is several times as long. The settled divergence moves by 0.118 degrees across all five exponents, so the rules are on one lattice and the disagreement is a defect in one of the two instruments.

The pair read from the angles

Checking that a jostled stem is still the lattice its panel is about turned up a disagreement. Counted from the point positions every rule's stems return five and eight spirals; read from the divergence sequence, the deepest rule's stems come back as five and seven at every seed. The points are right, and this site's founding rule is why.

All 19 destinations, counted at 17 windows from 20 to 800 organs. One row per destination, one cell per counting window, coarsest on the left. A dark cell is a window returning the same pair as the standing 200; a warm cell is a window returning a different one; a pale cell is a window that reaches below the run's own settling organ and was dropped. 5 of the 19 rows differ anywhere, and every difference sits left of the floor its own pair sets — 20 organs for a pair under 14 parastichies and the larger count plus 6 above it. The census read at 25 organs and at 800 is the same census.

The window nobody varied

Every parastichy pair reported for the settling table was counted over the top two hundred organs of a run, and that number had never been moved. Moved seventeen ways across a factor of forty, on all three hundred and eighty-four settled runs, it changes nothing at all.

What a 200-organ window allows against what the offset ceiling allows. Two settings decide what the counter can return, and at this window the offset ceiling is the tighter of them. A window of 200 organs holds a family of at most 194, since the counter scores an offset only where it has 6 hops of it inside the band; the largest offset it looks at is 60, a factor of 3.2 between them. The ticks are the rungs of the two ladders this collection is built on, and the largest counted number anywhere in the settling table is 19 — inside both bounds, which is what makes the table inert.

A plateau the instrument should have had

The counting window decides nothing on the settling table, and it has two bounds that decide everything outside it. A window one organ too narrow returns the previous rung of the same ladder, a family past the offset ceiling is reported as a coarser rung at every width there is, and neither failure produces a refusal, noise or a wide error bar.

The window 16 known pairs need, against the 20 organs the counter refuses under. Cylinders built at a stated divergence and rise, counted at every window from 20 organs to 200, so the pair is known before the counter sees it. The smallest window that reads it is 20 organs for every pair up to 14 parastichies and the larger count plus 6 above that — 13 of 16 measured exactly, on both branches, with nothing fitted. A pair of 76 and 123 needs 129 organs where 2 and 3 needs 20; the open marks are pairs the counter's own offset ceiling refuses at every window, read only once that ceiling is raised.

How many organs a pair needs

A count taken over too few organs does not fail. It returns the rung below, which is a perfectly good pair, and nothing anywhere says so. The window that avoids it is not a constant but the counter's own arithmetic, and 384 settled runs sit exactly where that arithmetic puts them.

The five readings of 384 whose two counted families wind the same way. Each row is an additive sequence with the term the counter stepped over drawn open between the two it returned. 4/9 is 1, 4, 5, 9, 14 with 5 skipped, and the pair a crossing requirement would have returned is 4/5 — a sequence the same destination's other runs already sit on. Dropping these readings takes the census at 40 starting angles from 31 arrangements and 15 sequences to 28 and 12, on 5 of 384 runs.

A sequence that was a reading

One of the settling table's additive sequences rested on a single count that skipped a term, and the account of it was that the count had been taken over the wrong patch. It was not. The counter works out whether its two families wind opposite ways and the reading throws the answer away, on five runs in three hundred and eighty-four.

The pairs grown stems of one, two, three and four organs a whorl count as their rise falls, against the folded rise. Four stems grown by the same rule over the same range of folded rise, 0.4 to 0.0012 — the rise between whorls times the jugacy, which puts every jugacy on one lattice axis — each whorl folded to one node and counted in a sliding window. With 1 organ a whorl the counted pairs run 1/2, 2/3, 3/5, 5/8, 8/13, 13/21; with 2 organs a whorl the counted pairs run 2/4, 4/6, 6/10, 10/16, 16/26, 26/42; with 3 organs a whorl the counted pairs run 3/6, 6/9, 9/15, 15/24, 24/39, 39/63; with 4 organs a whorl the counted pairs run 4/8, 8/12, 12/20, 20/32, 32/52, 52/84. Every jugacy passes the same transitions at the same folded rises, with its pairs multiplied by its jugacy.

A grown stem halves its ladder

A bijugate stem at 68.754° was derived to pass the ordinary transitions at half their rises, because a lattice wrapped twice round is the ordinary lattice at twice the rise. No bijugate stem had been grown through them. Grown by the same rule that grows an ordinary shoot, stems of two, three and four organs a whorl walk the ordinary ladder with every pair multiplied by the jugacy, change pair at the ordinary rise divided by the jugacy between whorls — and by its square per organ — lag behind the static ladder by the same hundredth of a rung, and settle within three hundredths of a degree of 137.5078 over the jugacy.

Which rates keep a Lucas seed, on stems of one, two and three organs a whorl, placed by whorls a rung. Every rate each configuration was grown at, drawn at the number of whorls the stem places between one transition and the next: a dark cell keeps the Lucas ladder to the end of the rise, a light cell gives it up. 1 a whorl, 512: kept to 86.6 whorls a rung, lost from 87.6; 1 a whorl, 256: kept to 86.6 whorls a rung, lost from 87.6; 1 a whorl, 1024: kept to 86.6 whorls a rung, lost from 87.6; 2 a whorl, 1024: kept to 87.6 whorls a rung, lost from 88.1; 2 a whorl, 1024, imposed: kept to 87.6 whorls a rung, lost from 88.1; 2 a whorl, 512: kept to 87.6 whorls a rung, lost from 88.5; 2 a whorl, 2048: kept to 87.6 whorls a rung, lost from 88.5; 3 a whorl, 1536: kept to 87.9 whorls a rung, lost from 88.5; 3 a whorl, 1536, imposed: kept to 87.9 whorls a rung, lost from 88.5; 3 a whorl, 768: kept to 86.6 whorls a rung, lost from 88.2. On this axis every edge falls within about two whorls a rung of every other.

A Lucas seed counts whorls

An ordinary stem seeded on the Lucas lattice keeps that ladder when its rise falls fast and gives it up when it falls slowly, with the edge near ninety nodes a rung. A stem that grows two organs a whorl is an ordinary stem folded twice round, so the identity predicts its edge — once it says whether the edge counts placements or whorls. Grown across the edge, stems of one, two and three organs a whorl keep a Lucas seed to 86.6, 87.6 and 87.9 whorls a rung: one number to within a per cent in whorls, and one, two and three times as far out in organs. No grid moves it and imposing exact whorls moves it not at all, even where free trijugate whorls come apart completely as the seed is lost.

How far grown whorls of two to eight members miss exact symmetry, at four lattices. Whorls grown one member at a time at a fixed rise, on a grid of 1,680 azimuths that every jugacy divides, read at folded rises of 0.27, 0.18, 0.09, 0.036. With 2 members the largest miss is 0.00°, 0.00°, 0.00°, 0.00°; with 3 members the largest miss is 0.64°, 1.93°, 0.21°, 0.00°; with 4 members the largest miss is 0.00°, 0.00°, 0.00°, 0.00°; with 5 members the largest miss is 1.29°, 1.29°, 0.21°, 0.21°; with 6 members the largest miss is 0.86°, 0.86°, 0.43°, 0.21°; with 7 members the largest miss is 0.86°, 2.14°, 0.21°, 0.00°; with 8 members the largest miss is 0.00°, 0.00°, 0.00°, 0.00°. Whorls of two, four and eight members are exact at every lattice; three, five, six and seven miss.

A whorl that misses its share

A whorl of k organs is defined by its symmetry, and the rule that grows one places its members one after another, each against the members already there. Nothing tells it to put them a k-th of a turn apart. Grown that way, whorls of two, four and eight members sit exactly on their shares of the turn at every lattice measured, and whorls of three, five, six and seven do not — the pattern a mirror argument predicts, since only a power of two leaves every new member a position that mirrors every member already placed. A trijugate whorl misses by 6.5° at a coarse rise and not at all at a fine one, by an amount the rise sets almost everywhere, and none of it moves a single transition.

How often three counters read a band's own pair, against the width of the band, on an ordinary stem. Bands of 40 to 320 organs slid up an ordinary stem grown at T = 300 over a rise from 0.05 to 0.0005, each read three ways. The counter without an index reads the pair at 65%, 66%, 87%, 88%, 88%, 88%, 89%, 100%, 100%, 92%, 54%, 23%, 8%, 2%, 1%, 0%, 0%, 0%; the counter families required to cross reads the pair at 65%, 66%, 87%, 88%, 88%, 88%, 89%, 100%, 100%, 92%, 54%, 22%, 8%, 2%, 1%, 0%, 0%, 0%; the counter with the index reads the pair at 100%, 100%, 100%, 100%, 100%, 100%, 100%, 100%, 100%, 100%, 100%, 100%, 100%, 100%, 100%, 100%, 100%, 100%. The index-free counter reads nine bands in ten or more only from 80 to 100 organs.

A counter that cannot be slid

The counter that needs no order of arrival follows each family into chains and counts them, and on an ideal lattice it agrees with the counter that does. On a stem whose rise falls it works only inside a band of widths, and outside the band it returns a pair rather than refusing: the rung below when the band is too narrow for the larger count, a pair on no rung when the band spans more than about a third of a rung of rise. The upper edge moves with the rate, so a width that is right on one stem is wrong on another, and on the fastest bijugate stem measured no width works at all.

The band the counter chooses for itself, against how slowly the stem grows. The counter is given positions and no width. It fits the decay of the rise through the spacings of its own band's whorls and takes the band that spans a third of a rung of rise: 49 organs on the stem that falls over 150; 97 organs on the stem that falls over 300; 193 organs on the stem that falls over 600. A stem grown four times as slowly chooses a band 3.94 times as wide, because a third of a rung is a statement about rise and a width is a number of organs. That is exactly why no one width fits the seven stems, and why the previous reading found a stem for which none worked.

A band that follows the rise

The index-free counter reads a growing stem only inside a band of widths, and the upper edge is a third of a rung of rise rather than a number of organs — so a width right on one stem is wrong on another. A counter that fits the decay of the rise through the spacings of its own band's whorls, and takes the band spanning a third of a rung, chooses 49, 97 and 193 organs on stems falling over 150, 300 and 600. Given no width at all it reads within eight points of the best of eighteen fixed widths on six of the seven stems, matching it exactly on one and beating it on two. Refusing any band too narrow to have shown the rung above the pair it counted removes every reading of the rung below, on every stem — and costs between five and fifty-one points of correct reading to do it.

Read as whorls, the three jugacies fall on one line. The rate at which a stem seeded on the Lucas lattice gives that ladder up, against how long the seed is, for one, two and three organs a whorl. The three lie on top of each other at every seed length: 15 whorls gives 30.80, 30.80, 30.80; 20 whorls gives 42.35, 42.35, 40.42; 30 whorls gives 63.52, 63.52, 63.52; 40 whorls gives 85.66, 87.58, 85.66. Every departure is one or two steps of the grain the edge is bisected to, which is two whorls of rate — 1.925 whorls a rung at every jugacy and every edge drawn.

A seed measured in whorls

A Lucas seed's length counts whorls, and the number published earlier for the rate edge counts nothing at all. Grown from seeds of fifteen to eighty whorls at one, two and three organs a whorl, stems of every jugacy lose the seed at the same rate in whorls a rung for the same seed length in whorls — 30.80 at fifteen, 63.52 at thirty, identically across the three — and at the same seed length in organs they differ by a factor of 3.24. So the seed is measured in whorls, as the edge is. The other half is worse for the earlier reading: the edge is not a constant but 2.24 times the seed less three, straight to within 2.7 whorls a rung over a fivefold range, so the eighty-seven whorls a rung reported everywhere is a property of the forty-whorl seed nobody varied.

The rate at which a Lucas seed is lost, read through four counting windows. Eighteen stems — one, two and three organs a whorl, seeded with 15 to 80 whorls of Lucas lattice — each with the edge found four times, through counting windows of 20, 26, 39, 52 folded nodes, the four dots at each seed drawn side by side. 17 of the 18 stems give the same organ through every window. The exception is three organs a whorl with a 30-whorl seed, where the widest window finds the edge at 207 organs against 201 for the others. A window twice as wide as the one every earlier reading used moves no other edge by an organ, so the window is not what makes the ratio of edge to seed change with the seed.

The window was not carrying it

The ratio of a Lucas seed's rate edge to its length rose from 2.05 at fifteen whorls to 2.20 at eighty, and the suspect was the counting window, which is most of a short seed. Read through windows of 20, 26, 39 and 52 folded nodes, seventeen of the eighteen stems lose the seed at exactly the same organ of rate, so the window carries almost none of it. Part of the rise was the grain of rate the edge was found on, worth up to six hundredths of the ratio. What is left rises by a tenth below thirty whorls and has stopped by sixty, at a level an ordinary stem reaches about one and a half per cent lower than a bijugate or trijugate one — and a trijugate edge is not always a line.

What the round trip returns as the organs are displaced: golden angle, 300 organs. Thirty heads at each size of displacement, from none to two and a half spacings, each run through the round trip and sorted by what came back. The undisplaced head counts 21 and 34. At 0.25 spacings, 97% the undisplaced pair, 3% a neighbouring pair; at 0.5 spacings, 50% the undisplaced pair, 50% a neighbouring pair; at 0.75 spacings, 30% the undisplaced pair, 70% a neighbouring pair; at 1 spacing, 13% the undisplaced pair, 80% a neighbouring pair, 7% a straddling pair; at 1.25 spacings, 7% the undisplaced pair, 57% a neighbouring pair, 7% a straddling pair, 30% refused; at 1.5 spacings, 40% a neighbouring pair, 3% a straddling pair, 57% refused; at 2 spacings, 10% a neighbouring pair, 90% refused; at 2.5 spacings, 3% a neighbouring pair, 97% refused. 10 recovered intervals in all exclude the true angle.

A head displaced before it is counted

The round trip from a head's spiral counts back to its divergence angle was tested on heads whose every organ sat exactly where the rule put it. Displaced by a normal error of up to two and a half spacings, heads of 900 organs keep counting a pair from their own sequence and return intervals holding the true angle to a spacing and a half; heads of 300 organs move to the neighbouring pair by half a spacing and then refuse, nine in ten of them by two spacings. Every moved count brings in the family whose chord was third shortest. Of 898 heads recovered, 19 intervals miss the true angle and 17 of those by about a tenth of a degree — displacement makes the reading coarser and then silent, not confidently wrong.

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