Event Abstract

Mapping predictive facilitation in a dragonfly target neuron

  • 1 The University of Adelaide, School of Medical Sciences, Australia

Dragonflies are masters of aerial pursuit, executing prey capture flights with a 97% success rate. In perching Libellulids, such flights are brief (average 184ms, [1]), although target motion is also tracked from the perch prior to take-off. However many dragonflies also engage in longer duration territorial and courtship pursuits of conspecifics, that can last tens of seconds. These chase sequences include changes in velocity and direction, as well as the possibility of target occlusion by matched background texture. Recent work shows that responses of dragonfly small target motion detector (STMD) neurons may be facilitated over prolonged time courses (up to 500ms) of continuous motion [2,3]. We hypothesize that such facilitation may play a role in increasing robustness by predictively increasing the gain of detectors in the direction of future travel.

We tested this in CSTMD1, a dragonfly neuron recently shown to express a form of selective attention for one target in the presence of a distractor [4]. We presented single target stimuli that moved along an initial ‘priming’ path for 500ms before undergoing spatial, temporal or combined discontinuities in their trajectories. We quantified the facilitation state by comparing the neuronal response (spike rate) in a 200ms window following the discontinuity with that for a naive control, tested at the same receptive field location. We found that facilitation is initially spatially localized: only the smallest spatial displacement tested in the direction of target travel (4°) gives significantly stronger responses than control (Fig 1, dashed line). When larger spatial displacements were combined with a delay in reappearance, however, responses were significantly elevated, even for a 20° displacement with a 500ms delay in reappearance. Backward displacements (i.e. across previously traversed location) yield strongly inhibited responses. This suggests that facilitation is mediated by a process of local gain modulation that actively spreads from the last seen location of a stimulus and in the approximate direction of travel. Such predictive modulation of local target salience may be a key mechanism for selective attention during target tracking.

Figure 1

Acknowledgements

We thank the manager of the Botanic Gardens of Adelaide for allowing insect collection. Funding was received from the US Air Force Office of Scientific Research (grants FA2386-10-1-4114 and FA9550-09-1-0116).

References

[1] Olberg, R. M., Worthington, A. H., and Venator, K. R. (2000). Prey pursuit and interception in dragonflies. J. Comp. Physiol. A 186, 155–162.
[2] Nordström, K., Bolzon, D. M., and O’Carroll, D. C. (2011). Spatial facilitation by a high-performance dragonfly target-detecting neuron. Biol. Lett. 7,
588–592.
[3] Dunbier, J.R., Wiederman, S.D., Shoemaker, P.A. and O’Carroll, D.C. (2012). Facilitation of dragonfly target-detecting neurons by slow moving features on continuous paths. Front. Neural Circuits 6:79.
[4] Wiederman, S.D. and O’Carroll D.C. (2013) Selective attention in an insect visual neuron. Curr. Biol. 23, 156-161.

Keywords: salient feature, motion detecion, insect vision, target tracking, feature detection, second order motion

Conference: International Conference on Invertebrate Vision, Fjälkinge, Sweden, 1 Aug - 8 Aug, 2013.

Presentation Type: Poster presentation preferred

Topic: Motion vision

Citation: Dunbier JR, Wiederman SD and O'Carroll DC (2019). Mapping predictive facilitation in a dragonfly target neuron. Front. Physiol. Conference Abstract: International Conference on Invertebrate Vision. doi: 10.3389/conf.fphys.2013.25.00002

Copyright: The abstracts in this collection have not been subject to any Frontiers peer review or checks, and are not endorsed by Frontiers. They are made available through the Frontiers publishing platform as a service to conference organizers and presenters.

The copyright in the individual abstracts is owned by the author of each abstract or his/her employer unless otherwise stated.

Each abstract, as well as the collection of abstracts, are published under a Creative Commons CC-BY 4.0 (attribution) licence (https://creativecommons.org/licenses/by/4.0/) and may thus be reproduced, translated, adapted and be the subject of derivative works provided the authors and Frontiers are attributed.

For Frontiers’ terms and conditions please see https://www.frontiersin.org/legal/terms-and-conditions.

Received: 26 Feb 2013; Published Online: 09 Dec 2019.

* Correspondence: Mr. James R Dunbier, The University of Adelaide, School of Medical Sciences, Adelaide, Australia, james.dunbier@adelaide.edu.au