Neural timing of stimulus events with microsecond precision

Temporal analysis of sound is fundamental to auditory processing throughout the animal kingdom. Echolocating bats are powerful models for investigating the underlying mechanisms of auditory temporal processing, as they show microsecond precision in discriminating the timing of acoustic events. However, the neural basis for microsecond auditory discrimination in bats has eluded researchers for decades. Combining extracellular recordings in the midbrain inferior colliculus (IC) and mathematical modeling, we show that microsecond precision in registering stimulus events emerges from synchronous neural firing, revealed through low-latency variability of stimulus-evoked extracellular field potentials (EFPs, 200–600 Hz). The temporal precision of the EFP increases with the number of neurons firing in synchrony. Moreover, there is a functional relationship between the temporal precision of the EFP and the spectrotemporal features of the echolocation calls. In addition, EFP can measure the time difference of simulated echolocation call–echo pairs with microsecond precision. We propose that synchronous firing of populations of neurons operates in diverse species to support temporal analysis for auditory localization and complex sound processing.
Author summary We routinely rely on a stopwatch to precisely measure the time it takes for an athlete to reach the finish line. Without the assistance of such a timing device, our measurement of elapsed time becomes imprecise. By contrast, some animals, such as echolocating bats, naturally perform timing tasks with remarkable precision. Behavioral research has shown that echolocating bats can estimate the elapsed time between sonar cries and echo returns with a precision in the range of microseconds. However, the neural basis for such microsecond precision has remained a puzzle to scientists. Combining extracellular recordings in the bat’s inferior colliculus (IC)—a midbrain nucleus of the auditory pathway—and mathematical modeling, we show that microsecond precision in registering stimulus events emerges from synchronous neural firing. Our recordings revealed a low-latency variability of stimulus-evoked extracellular field potentials (EFPs), which, according to our mathematical modeling, was determined by the number of firing neurons and their synchrony. Moreover, the acoustic features of echolocation calls, such as signal duration and bandwidth, which the bat dynamically modulates during prey capture, also modulate the precision of EFPs. These findings have broad implications for understanding temporal analysis of acoustic signals in a wide range of auditory behaviors across the animal kingdom.