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Takalo, J.

Publications and source records attributed to Takalo, J..

5 recordsLinked to original sources

A model of depth-dependent responses from neural superposition in fly compound eyes

Fly compound eyes pool signals from photoreceptors that sample the same region of visual space through neural superposition in the lamina. The optical axes of photoreceptors projecting to a single lamina cartridge are not perfectly parallel, but instead converge at a point a few millimeters in front of the eye. At short viewing distances (1--10mm) this leads to distance-dependent differences in receptive field overlap. We explored whether it was possible that flies could sense depth in this "personal space" purely from the geometry of neural superposition. To this end, we combined a computational model of fly eye optics with a disparity-tuned lamina model originally developed for stereoscopic prey capture in praying mantises, and simulated the responses of lamina monopolar cells to moving stimuli at different distances. Across variations in stimulus parameters and lamina models, we found that lamina neuron responses indeed contain a distance-dependent component, which can overall be summarised as an enhanced response due to temporally overlapping receptor responses at a critical distance of 3--4mm, the convergence distance of photoreceptor axes. Depending on the lamina model and stimulus size, either response amplitude or onset gradient, or both, exhibited this peak. We further show that changes in eye size systematically shift this preferred distance, such that larger flies had a peak response at a greater distance. Our results demonstrate that lamina cell responses may contain a robust, geometry-derived component that is specific to object distance and invariant to other stimulus properties. This suggests that neural superposition, beyond improving sensitivity, may function analogously to a light-field camera system that is effectively "focused" on a behaviorally relevant distance.

neuroscience↗

Synaptic high-frequency jumping synchronises vision to high-speed behaviour

During high-speed behaviour, animals must synchronise perception and action despite rapid environmental and self-generated motion. How neural systems achieve such precision remains unclear. Here we show how the housefly (Musca domestica) maintains visual accuracy during fast motion. Using intracellular and photomechanical recordings during saccade-like stimulation, we traced information flow from photoreceptors to large monopolar cells (LMCs). Visual neurons achieved record-high information sampling ([~]2,500 bits{middle dot}s-1) and synaptic transmission ([~]4,100 bits{middle dot}s-1), far exceeding previous estimates. We identify a previously unknown mechanism - synaptic high-frequency jumping - in which photoreceptor-LMC synapses dynamically shift transmission toward higher frequencies during saccades, extending visual bandwidth to [~]1,000 Hz, effectively eliminating synaptic delays, and quadrupling classical flicker-fusion limits ([~]230 Hz). Behavioural experiments show flies respond synchronously within [~]13-20 ms, even before photoreceptor responses peak. A biophysically realistic model reveals how photomechanical-stochastic-refractory quantal sampling co-adapts with saccadic behaviour: through self-motion, flies efficiently translate image motion into temporally-precise, predictive high-speed vision.

neuroscience↗

High-speed imaging of light-induced photoreceptor microsaccades in compound eyes

Inside compound eyes, photoreceptors contract to light changes, sharpening retinal images of the moving world in time. Current methods to measure these so-called photoreceptor microsaccades in living insects are spatially limited and technically challenging. Here, we present goniometric high-speed deep pseudopupil (GHS-DPP) microscopy to assess how the rhabdomeric insect photoreceptors and their microsaccades are organised across the compound eyes. This method enables non-invasive rhabdomere orientation mapping, whilst their microsaccades can be locally light-activated, revealing the eyes underlying active sampling motifs. By comparing the microsaccades in wild-type Drosophilas open rhabdom eyes to spam-mutant eyes, reverted to an ancestral fused rhabdom state, and honeybees fused rhabdom eyes, we show how different eye types sample light information. These results show different ways compound eyes initiate the conversion of spatial light patterns in the environment into temporal neural signals and highlight how this active sampling can evolve with insects visual needs.

neuroscience↗

Binocular Mirror-Symmetric Microsaccadic Sampling of Hyperacute 3D-Vision

Neural mechanisms behind stereopsis, which requires simultaneous disparity inputs from two eyes, have remained mysterious. Here we show how ultrafast mirror-symmetric photomechanical contractions in the frontal forward-facing left and right eye photoreceptors give Drosophila super-resolution 3D-vision. By interlinking multiscale in vivo assays with multiscale simulations, we reveal how these photoreceptor microsaccades - by verging, diverging and narrowing the eyes overlapping receptive fields - channel depth information, as phasic binocular image motion disparity signals in time. We further show how peripherally, outside stereopsis, microsaccadic sampling tracks a flying flys optic flow field to better resolve the world in motion. These results change our understanding of how insect compound eyes work and suggest a general dynamic stereo-information sampling strategy for animals, robots and sensors. Significance statementTo move efficiently, animals must continuously work out their x,y,z-positions in respect to real-world objects, and many animals have a pair of eyes to achieve this. How photoreceptors actively sample the eyes optical image disparity is not understood because this fundamental information-limiting step has not been investigated in vivo over the eyes whole sampling matrix. This integrative multiscale study will advance our current understanding of stereopsis from static image disparity comparison to a new morphodynamic active sampling theory. It shows how photomechanical photoreceptor microsaccades enable Drosophila super-resolution 3D-vision and proposes neural computations for accurately predicting these flies depth-perception dynamics, limits, and visual behaviors.

neuroscience↗

Microsaccadic information sampling provides Drosophila hyperacute vision

Small fly eyes should not see fine image details. Because flies exhibit saccadic visual behaviors and their compound eyes have relatively few ommatidia (sampling points), their photoreceptors would be expected to generate blurry and coarse retinal images of the world. Here we demonstrate that Drosophila see the world far better than predicted from the classic theories. By using electrophysiological, optical and behavioral assays, we found that R1-R6 photoreceptors encoding capacity in time is maximized to fast high-contrast bursts, which resemble their light input during saccadic behaviors. Whilst over space, R1-R6s resolve moving objects at saccadic speeds beyond the predicted motion-blur-limit. Our results show how refractory phototransduction and rapid photomechanical photoreceptor contractions jointly sharpen retinal images of moving objects in space-time, enabling hyperacute vision, and explain how such microsaccadic information sampling exceeds the compound eyes optical limits. These discoveries elucidate how acuity depends upon photoreceptor function and eye movements.

neuroscience↗