Post-Grokking Collapse at the Representation-Readout Interface in Muon-Trained Transformers

Under the standard split, Muon gets hidden matrices and AdamW embeddings/output head. Muon groks modular addition faster, but its solutions do not hold. All nine configurations on $(a+b) \bmod 113$ grok and later lose generalization. Across five seeds the selected AdamW reference falls below threshold on four, reaching 27.59%. Instability persists across two moduli, two widths, two training fractions, subtraction, and depth. The failure arises at the representation-readout interface, identified only jointly up to an invertible map unselected by the loss. After solving the training set, the gradient falls to order $10^{-6}$ and the optimizers respond differently: step-size elasticity is -0.03 for Muon versus +1.5 for AdamW, and the Muon group moves 8.0 times faster per parameter. From bit-identical states, freezing either group prevents failure. Freezing embeddings/readout removes it in five runs over 451,400 post-grokking steps and five paired seeds: unfrozen arms record 137-321 sub-threshold evaluations, frozen arms none. Removing Muon's normalization and orthogonalization is no substitute: it collapses representation from 326 effective conjugate pairs to 4, shows no recurrent collapse, and fails terminally. Fourier filtering separates circuit failure from masking. Across 43 checkpoints over five seeds and three regimes, the task-aligned family reaches exactly 100% alone. In circuit failure it no longer solves the task; in masking it remains perfect while the full model reaches 45.85%, giving a positive margin on every example, including errors, but being outvoted by a near-equal adversarial remainder. Rescaling it restores 99.9%; grokking is the same condition resolving upward. The task selects the family, swapping $(k,k)$ for $(k,-k)$ under subtraction. Across an abrupt collapse, standard Fourier support is unchanged and the power-distribution cosine remains 0.9899.

A Counterexample to Fourier Alignment in Single-Neuron Modular Addition

We give a negative solution to MAIS-O60. We first construct an example in which an initially active ReLU neuron becomes completely inactive in finite time and thereafter remains frozen at a limit whose Fourier energy is equally distributed among all nonzero real frequency classes. The counterexample holds on an open set of initial conditions and therefore occurs with positive probability under Gaussian initialization. An appendix prepared by GPT-5.6 Sol strengthens the counterexample by showing that the same failure can occur for every Clarke trajectory from an open set of initial conditions, under the convention $\mathrm{ReLU}'(0)=0$, for smooth dead-zone approximations of ReLU, and for fixed-step full-batch gradient descent. Thus, single-frequency alignment is not a general consequence of training a single neuron on modular addition.

Structure-Specific Representational Priors Causally Control the Grokking Delay

Grokking -- generalization long after training-set interpolation -- has been accelerated by structure-agnostic interventions (gradient filtering, weight-norm clamping, geometric penalties). Whether the delay specifically measures the time to form task-structured representations has remained observational. We test it causally by injecting representational priors of varying content into a one-layer transformer learning modular addition, via a supervised-contrastive loss whose positives encode (i) the task's true structure ($(a+b) \bmod p$), (ii) a coherent-but-wrong sibling ($(a-b) \bmod p$), or (iii) a random partition -- all with identical loss form, strength, class sizes, and geometry. Whether generalization occurs follows a clean gradation: true 22/30 runs, sibling (same periodic features, wrong combination) 14/15, random (only memorizable) 0/20 (Fisher $p=1.3\times10^{-7}$). A weight-norm-matched control replaying the norm trajectory onto plain cross-entropy generalizes 0/15, ruling out the norm as mediator. Probes show structure formation precedes and predicts generalization in all runs. Only the true structure also accelerates grokking (up to $2.75\times$), but this is dose-dependent and bimodal. We then confirm the mechanism by prediction: because the acceleration is gated by a weight-norm side-effect, clamping the norm during training yields a reliable, standalone accelerator with a median $8.6\times$ speedup (up to $22\times$ on the fastest seeds, under 1000 epochs), growing monotonically as the norm is held lower; the residual stalls also vanish, though significant only pooled over the two mitigations run at both strengths ($0/40$ vs $6/20$, $p=7.7\times10^{-4}$), not per method. The grokking delay is, causally, the time to form the right representational structure -- decided at the level of features, not labels.