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Spike Train Similarity Space (SSIMS) Method Detects Effects of Obstacle Proximity and Experience on Temporal Patterning of Bat Biosonar

Overview
Specialty Psychology
Date 2018 Feb 24
PMID 29472848
Citations 4
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Abstract

Bats emit biosonar pulses in complex temporal patterns that change to accommodate dynamic surroundings. Efforts to quantify these patterns have included analyses of inter-pulse intervals, sonar sound groups, and changes in individual signal parameters such as duration or frequency. Here, the similarity in temporal structure between trains of biosonar pulses is assessed. The spike train similarity space (SSIMS) algorithm, originally designed for neural activity pattern analysis, was applied to determine which features of the environment influence temporal patterning of pulses emitted by flying big brown bats, . In these laboratory experiments, bats flew down a flight corridor through an obstacle array. The corridor varied in width (100, 70, or 40 cm) and shape (straight or curved). Using a relational point-process framework, SSIMS was able to discriminate between echolocation call sequences recorded from flights in each of the corridor widths. SSIMS was also able to tell the difference between pulse trains recorded during flights where corridor shape through the obstacle array matched the previous trials (fixed, or expected) as opposed to those recorded from flights with randomized corridor shape (variable, or unexpected), but only for the flight path shape in which the bats had previous training. The results show that experience influences the temporal patterns with which bats emit their echolocation calls. It is demonstrated that obstacle proximity to the bat affects call patterns more dramatically than flight path shape.

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References
1.
Sandig S, Schnitzler H, Denzinger A . Echolocation behaviour of the big brown bat (Eptesicus fuscus) in an obstacle avoidance task of increasing difficulty. J Exp Biol. 2014; 217(Pt 16):2876-84. DOI: 10.1242/jeb.099614. View

2.
Geberl C, Brinklov S, Wiegrebe L, Surlykke A . Fast sensory-motor reactions in echolocating bats to sudden changes during the final buzz and prey intercept. Proc Natl Acad Sci U S A. 2015; 112(13):4122-7. PMC: 4386384. DOI: 10.1073/pnas.1424457112. View

3.
Moss C, Surlykke A . Auditory scene analysis by echolocation in bats. J Acoust Soc Am. 2001; 110(4):2207-26. DOI: 10.1121/1.1398051. View

4.
Hom K, Linnenschmidt M, Simmons J, Simmons A . Echolocation behavior in big brown bats is not impaired after intense broadband noise exposures. J Exp Biol. 2016; 219(Pt 20):3253-3260. DOI: 10.1242/jeb.143578. View

5.
Warnecke M, Chiu C, Engelberg J, Moss C . Active Listening in a Bat Cocktail Party: Adaptive Echolocation and Flight Behaviors of Big Brown Bats, Eptesicus fuscus, Foraging in a Cluttered Acoustic Environment. Brain Behav Evol. 2015; 86(1):6-16. DOI: 10.1159/000437346. View