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We coupled the Drosophila melanogaster adult connectome with an anatomically faithful eye model to create a connectome-only computational system where only synaptic gains and neuronal thresholds are learned. This model performs multitask vision, including color, shape, and numerical discrimination, exhibiting ratio-dependent scaling for approximate number perception. The biological network demonstrates superior accuracy at matched wiring cost compared to randomized ensembles, suggesting that precise connectivity and eye geometry jointly enable efficient visual computation.
Drosophila's brain performs complex visual tasks with remarkable efficiency, suggesting that its precise wiring, not just raw capacity, is key to computation.
Understanding the extent to which measured synaptic wiring determines computation remains a central challenge. Here, we couple the proofread adult Drosophila melanogaster connectome to an anatomically faithful model of its eye. Visual information is inputted in the eye model, then passed to the connectome, and finally read from a Kenyon-cell-centered linear decoder. This creates a connectome-only model in which the anatomical graph and eye geometry are fixed and only scalar synaptic gains and neuronal thresholds may be learned. The model supports multitask vision, including color discrimination, shape classification, and numerical discrimination that follows a ratio-dependent scaling characteristic of approximate number perception. To test whether precise connectivity is consequential under wiring economy, we compare the biological graph to randomized ensembles that increasingly preserve biological synaptic constraints. At matched wiring cost, the biological network consistently yields higher accuracy, whereas less constrained rewiring surpasses it at the cost of inflated wiring. These findings indicate that the measured connectivity and eye geometry jointly set efficient operating points for visual computation.