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Abstract
<p id="P2">Path integration is a widespread navigational strategy in which directional
changes
and distance covered are continuously integrated on an outward journey, enabling a
straight-line return to home. Bees use vision for this task – a celestial-cue based
visual compass, and an optic-flow based visual odometer – but the underlying neural
integration mechanisms are unknown. Using intracellular electrophysiology, we show
that polarized-light based compass-neurons and optic-flow-based speed-encoding neurons
converge in the central complex of the bee brain, and through block-face electron
microscopy we identify potential integrator cells. Based on plausible output targets
for these cells, we propose a complete circuit for path integration and steering in
the central complex, with anatomically-identified neurons suggested for each processing
step. The resulting model-circuit is thus fully constrained biologically and provides
a functional interpretation for many previously unexplained architectural features
of the central complex. Moreover, we show that the receptive fields of the newly discovered
speed neurons can support path integration for the holonomic motion (i.e. a ground
velocity that is not precisely aligned with body orientation) typical of bee-flight,
a feature not captured in any previously proposed model of path integration. In a
broader context, the model-circuit presented provides a general mechanism for producing
steering signals by comparing current and desired headings – suggesting a more basic
function for central-complex connectivity from which path integration may have evolved.
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