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v0.8.43

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@gianlucamazza gianlucamazza released this 13 Oct 02:35
· 325 commits to main since this release
v0.8.43
b26a037

Result

  • T4/T5 v1: neither (#84). Photoreceptors fire through the measured eye, but L1–L3 and
    everything downstream stay silent: inhibitory photoreceptor synapses cannot move silent
    spiking lamina neurons, where the fly's are graded with a resting tone. The concrete case
    for graded neurons (#97).

  • Kenyon cell sparseness v3: none (#95, #96). With Hige et al. 2015's odors as DoOR
    vectors the model is either dense (default 36% / 30% of Kenyon cells, 82–99% shared, against
    30–33% measured) or silent (0.2% without the chemical local neuron → PN contacts). The
    sparse regime needs the measured electrical coupling the model lacks (#85).

Pre-registration

  • T4/T5 direction selectivity v1 (#84): moving ON/OFF edges in four directions through
    the measured eye (eye.edge_coverage), 30°/s, acceptance 8.23°; decides polarity and
    preferred direction against Maisak et al. 2013, prior from Lappalainen et al. 2024 stated.
    Locked before its run; flymsg t4t5.

  • Kenyon cell sparseness diagnostic v3 (#95, #96): Hige et al. 2015's odors (3-octanol,
    4-methylcyclohexanol) as DoOR receptor vectors, the same four arms, seeds 80–82, and a
    lower bound (1%) next to the upper ones; the shared share is reported against the 30% and
    33% measured for these odors. Locked before its run.

Odors

  • flymsg odor (#96): DoOR consensus responses (fetched at run time, CC BY-SA 4.0, not
    redistributed) as one response per MaleCNS ORN type, and per-neuron Poisson input
    (odors.kicks). 3-octanol drives 31 ORN types, 4-methylcyclohexanol 22.

Full note: https://github.com/gianlucamazza/flymsg/blob/v0.8.43/CHANGELOG.md