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A one-second source pulse shift gave opposite signs in 202 of 739 fitted C. elegans transfer models under a 10% kernel change bound

We tested whether one sign can describe a fitted calcium transfer model for two source inputs with the same height, duration and area. We used 739 selected wild-type C. elegans kernels from a pinned signal propagation atlas. Each had q below 0.05, at least three finite stored response values and a nonzero kernel. We shifted a one-second source calcium pulse by one second and read both model responses at two seconds. The signs differed in 268 kernels. In 202 kernels, both signs remained for every kernel change with total absolute area below 10% of the original absolute kernel area on zero to two seconds. We prove that this change bound is sharp for arbitrary integrable changes. Smooth pulses kept opposite signs in all 202 cases. The same area rule gave 3 cases with half-second pulses and 238 with two-second pulses. Of 198 directions with a direct link in at least one of four native anatomical maps, 43 had the main property. We keep all 302 canonical neuron slots for route checks. A signed-walk argument states a necessary condition at matched neural ports. An exact control also shows that one positive neural route and nonnegative cell filters can give a signed calcium transfer kernel after division by the source calcium filter. Thus these fitted signs do not identify inhibition or prove biological pulse sign reversals. The analysis is exploratory. The export lacks event-level kernel uncertainty and animal identities. High-precision integrals, separate numerical integration, source checks and a complete replay verify the calculations. The package preserves code, derived tables, source provenance, figures and repeat instructions.

connectome · signal propagation · calcium imaging · transfer kernel · pulse timing · response sign · source normalization · positive systems

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References

8
  1. usesdoi:10.1038/s41586-023-06683-4

    We analyze its fitted source-to-target calcium transfer kernels from the pinned WormNeuroAtlas export.

  2. usesdoi:10.17605/OSF.IO/E2SYT

    This is the original data record for the signal propagation study.

  3. usesdoi:10.1098/rstb.1986.0056

    We use two native anatomical exports for direct links and full neuronal route checks.

  4. usesdoi:10.1038/s41586-021-03778-8

    We use native adult maps 7 and 8 for direct links and routes.

  5. In a 30-second window, 315 of 668 selected C. elegans kernels with peaks before one second had most absolute area after one second sci:sha256:1e50fd4224cd00f6660aaf9f078f8be64a368a1b56525e5d355277ba0c49c955

    This earlier study compared kernel peaks with later absolute area. It provides timing context for the pulse test.

  6. At Laplace rates of 0.2 and 1 per second, removing four of 106 C. elegans kernel pairs with strong cancellation cut a reciprocity magnitude bound from 2.60 to 1.39 sci:sha256:d6592a9b70ebda3478fcb41c88b82653f072e54539897371fe9c9f1777827f8b

    This earlier study measured cancellation in signed kernel integrals. We independently recover its 739-direction kernel scope before reciprocal pairing.

  7. At gain 0.5, 33 of 82 signs fixed by uncertainty bounds in a linear C. elegans chemical model opposed measured calcium signs sci:sha256:322a11f656688bfcb3a88107dd7d7f5a669890ab3685bf03723b0a0e853431b6

    This earlier static chemical model tested uncertain edge signs. The present test instead changes input timing while one fitted effective kernel stays fixed.

  8. Anatomical features gave no clear added shape prediction gain in a fixed ridge test of 686 C. elegans transfer kernels sci:sha256:cbf5601ea590f4aa83137cc12fde16e083e067cac724ca2680211ee6cfa8ad4e

    This earlier temporal benchmark tested prediction of normalized response shape. It defines prior work outside the present pulse-sign test.

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