Connectome-constrained neural networks make biological components directly accessible to intervention, but their mechanistic conclusions can still depend on the comparison model, intervention, circuit representation and trained solution. We stress-test these dependencies in flyvis, a \emph{Drosophila} motion-vision model, using its 50-model ensemble, task-matched causal CNN controls and replicated interventions. At the level of model behaviour, three-level reverse-phi reversal in flyvis is strongly period- and velocity-dependent and also appears in task-matched CNNs; neither family reproduces the fly's stationary-sawtooth response. Adversarial direction reversal requires a perturbation bound of 0.21--0.27 times stimulus contrast in flyvis versus 0.13--0.25 in CNNs, but the gap over a parameter-matched CNN largely closes for larger CNNs. At the level of mechanism, matching attribution to the intervention matters: for held-out-mean replacement, first-order edge attribution patching reaches pooled AUROC 0.970 and Spearman 0.872, versus 0.933 and 0.126 when its zero-aligned score is evaluated against the same ground truth. Circuit conclusions also vary with representation and ensemble member. Greedy cell-type sets meet a model-relative T4/T5 tuning criterion in 25 of 50 models, while T4/T5 output silencing reduces the tested optic-flow behaviour to at most two of eight clips in 40. In six models where the cell-type search first succeeds, the corresponding connection sets can be pruned to 13--31 added classes; under an additional two-sided response-amplitude check, only two of those six first-success cell-type sets still meet the tuning threshold. These results support a narrower use of connectome-constrained models: they make mechanistic hypotheses directly testable, but the resulting claims must be scoped to the model family, intervention, representation and trained solution.

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