Phyllotaxis
the spirals are counted, not admired
Concept

Dislocation — where it appears

The crystallographer's name for a bound five-seven pair, treated as one object with an orientation rather than as two exceptions in a tiling. On a settled head they lie along rings at a fixed spacing — 1.812, 1.810, 1.811 and 1.811 cell spacings on four rings whose radii differ by a factor of 4.2.

Named by 3 essays across one field — each of them below, with the objects they name alongside it.

264 exceptions in a 2400-organ head, and eight circles. A golden, 137.508° head of 2400 organs, tessellated inside 86% of its radius. Every interior cell is drawn, and the 135 five-sided cells and 129 seven-sided ones are marked apart from the 1367 hexagons, and the pale circles are radii computed from the divergence angle through the lattice's third-shortest vector — nothing is fitted. Every defect sits within 0.64 of a cell spacing of one of those eight circles, and between them there is not one exception in hundreds of cells.

The defects lie on rings

The cells in a seed head that are not hexagons are not scattered through it. Every one of 264 sits within a cell of a radius computed from the divergence angle alone, the radii are a factor of φ apart, and between two of them lie 422 consecutive cells without a single exception.

tissue · Topological charge Every five is a cell away from a seven, and the loneliest is 0.927 spacings out. How far a five-sided cell is from the nearest seven-sided one, in cell spacings, on a golden, 137.508° head of 2400 organs. The measured bar runs from the closest five to the loneliest — 0.833 to 0.927, with a median of 0.919. It stops a single cell out, so there is no unpaired tail at all rather than a small one. The nulls are seeded permutations over 200 draws: relabelling which defects are fives puts the average five 1.254 ± 0.064 spacings away, and scattering the whole multiset over the interior cells puts it 1.786 ± 0.092. 100.0% of the fives share a wall with a seven against 68.2% for the strong null, z = 7.3.

Every five is bound to a seven

A five-sided cell beside a seven-sided one is one object in a crystal and two exceptions in a tiling, and the phyllotaxis literature borrows the crystallographic word without measuring the binding. Measured against a seeded permutation null on a 2,400-organ head, every five in the interior shares a wall with a seven, and the loneliest one in the head is 0.927 cell spacings from the nearest.

tissue · Topological charge The defect rings are not where the counts change — they are √φ further out. A logarithmic radius axis for a golden, 137.508° head. The lower marks are the radii at which the counted parastichy pair changes, where the two shortest lattice vectors change places; the upper marks are the radii at which a cell's neighbours change, where the third-shortest does. They interleave, and the ratio of each ring to the transition inside it is 1.2715, 1.2723, 1.2723, 1.2719, 1.2719, 1.2723 against √φ = 1.27202. Consecutive rungs are a factor of φ apart in radius and √φ is their geometric midpoint, so a defect ring sits exactly halfway between two parastichy transitions. Anyone looking for the defect line at the radius where the counts change will not find it there.

The rings are not the transitions

A seed head has two ladders on it — the radii where the counted parastichy pair changes, and the radii where the exceptional cells sit — and the obvious guess is that they are the same ladder. They are not: the second sits a factor of the square root of phi outside the first at every rung of two different divergence ladders, which is exactly halfway between two consecutive transitions.

tissue · Topological charge

Named alongside it

The objects these essays reach for when they reach for this one.

Topological chargeCell spacingDefect ringDisorderGeometric ladderHandoverHonest limitsNull modelPermutation testRim effectAnnulusArtefact

All concepts