At a representative Earth field and room temperature, thermal energy is
millions of times larger than a free electron's magnetic interaction. Compute the
mismatch, then turn the field around a minimal radical-pair model and watch its reaction
yield change without thermal equilibrium. This shows a route by which weak fields can
affect chemistry. It does not prove that birds use this receptor.
Leading hypothesis, no receptor demonstrated in vivo
Layer 1 · the apparent impossibilityMake the signal disappear
Set the magnetic field and temperature. The browser computes the
free-electron Zeeman interaction gμBB, the thermal
scale kBT, their ratio, and the Larmor frequency
from the equations, not a lookup table.
weakerstronger
coolerwarmer
Zeeman interaction
Thermal scale kBT
Thermal / magnetic
Electron Larmor frequency
How far thermal energy leads
If a compass had to align an electron by waiting for thermal equilibrium, this is where
the story would end. The magnetic bias is lost inside a much larger thermal energy scale.
But the ratio is not a universal signal-to-noise ratio, and it is not a proof that every
magnetic response is impossible. It rules out a particular equilibrium intuition.
Layer 2 · the nonequilibrium escapeTurn the field, change the products
A photon can create two radicals whose electron spins begin in a pure
singlet state. Hyperfine coupling to nearby nuclei mixes singlet and triplet character
while the pair exists. Reaction competes with that coherent motion. Nothing here waits
to reach thermal equilibrium.
ρ(0) = |S⟩⟨S| ⊗ ½1nucleus
H = ω B̂·(S1 + S2) + S1·A·I
ΦS = ∫ k exp(−kt) Tr[QSρ(t)] dt
parallelreversed
Bornelectron singlet, nucleus unpolarized
Hyperfine tensorA = [0.4, 0.4, 1.6] MHz
Reaction clockexponential lifetime τ = 1 µs
Integrated singlet yield
Full orientation span
orientation response, recomputed across a half-turncoherent singlet probability before reaction removes the pair
Computing the spin dynamics.
The direction effect comes from the anisotropic hyperfine tensor. It gives the molecule
an internal axis, so rotating the external field changes the Hamiltonian and therefore the
time spent in singlet character before reaction. The field does not have to win an energy
contest with the whole thermal bath. It has to alter a coherent race that ends before
equilibrium.
What the calculation shows
A singlet-born, spin-selective reaction can have a direction-dependent yield at a
representative Earth-strength field even though its Zeeman energy is millions of
times below kBT.
What it does not show
It does not establish which protein, radical pair, retinal cell, or neural pathway a
bird uses. It is a minimal physical counterexample to the thermal objection, not a
model of a robin receptor.
The check
These lines are recomputed in this browser from the same equations used by the separate
dependency-free verifier.
Measured constants and rounded inputs
The Bohr magneton is the 2022 CODATA value. Its quoted uncertainty is tiny on the
scale displayed here. The Boltzmann constant is exact in the SI.
The electron g value is rounded to 2,
and the frequency conversion is rounded to 28 GHz/T. The default
field is representative, not a claim that Earth's field has one value everywhere.
Temperature sets the comparison scale kBT. It is not fed into
the radical-pair dynamics because that toy includes no explicit spin relaxation or
thermally activated kinetic rates.
Free model choices
One spin-half nucleus, the anisotropic hyperfine tensor shown above, a one-microsecond
exponential lifetime, equal first-order removal for all spin states, and an initially
unpolarized nucleus are chosen for legibility. They are not fitted avian receptor values.
The model omits the many nuclei of a real radical pair, electron exchange and dipolar
interactions, spin relaxation, molecular motion, multiple chemical steps, receptor
ordering, amplification, and neural readout.
It evolves the density matrix as an equal mixture of two nuclear basis states. A
fourth-order propagator uses a timestep of 0.0025 µs and
integrates for twelve model lifetimes. The browser and verifier also halve the timestep
at the endpoint orientations and report their agreement.
Open biological questions
Radical-pair magnetoreception is the leading hypothesis, not an established avian
receptor mechanism. No magnetically sensitive receptor has been demonstrated in vivo.
Xu and colleagues measured purified European robin CRY4 in vitro. Their experiments
used fields often far above Earth strength, including millitesla fields. Their
Earth-strength case was addressed by spin-dynamics modelling. This does not show that
CRY4 is the working receptor inside a living bird.
The active radical pair, its lifetime and orientation in tissue, and the route from a
small chemical yield change to a neural compass signal remain unsettled.
Why the thermal comparison is both useful and incomplete
kBT is the right scale for asking whether equilibrium populations
substantially favour one energy level over another. That is why the first instrument is a
real objection, not a straw figure. Radical-pair spin chemistry asks a different question:
can a field alter coherent singlet-triplet motion before a short-lived intermediate reacts?
Nonequilibrium kinetics can preserve a field-dependent product yield without producing a
thermally aligned electron population.
Calling the energy ratio a literal count of noise particles, or a complete biological
signal-to-noise ratio, would be wrong. The page uses it only to show why an equilibrium
compass intuition fails.
B. Y. K. Lam and E. P. Malkemper,
“Magnetosensation: The Unsolved Mystery”,
Physiological Reviews 106 (2026), for the current status of the unresolved receptor and neural circuit.