Temporally patterned sound pulse trains affect intensity and frequency sensitivity of inferior collicular neurons of the big brown bat, Eptesicus fuscus (original) (raw)
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Neuroscience Letters, 2008
During hunting, insectivorous bats such as Eptesicus fuscus progressively increase the pulse repetition rate, shorten the pulse duration, and lower the frequency and amplitude of emitted pulses as they search, approach and finally intercept insects or negotiate obstacles. As such, analysis of an echo parameter by the bat is inevitably affected by other co-varying echo parameters. The present study examined the effect of pulse duration on frequency selectivity of neurons in the central nucleus of the inferior colliculus (IC) of the big brown bat. A family of iso-level frequency tuning curves of each IC neuron was first measured with tone bursts of different durations. The bandwidth of iso-level frequency tuning curves within each family was then compared. Our data show that most IC neurons discharge maximally to a particular pulse duration which is defined as the best duration (BDu). The iso-level frequency tuning curves of these duration-selective neurons have the narrowest bandwidth when measured with the BDu pulse than with non-BDu pulses. They also have the narrowest bandwidth when measured with a short than with a long BDu pulse. These data suggest that frequency selectivity of duration-selective IC neurons becomes sharper when short echo duration at the final phase of hunting is encoded by IC neurons that have short BDu.
Hearing Research, 2002
During echolocation, the amplitude and duration of echo pulses of the big brown bat, Eptesicus fuscus, covary throughout the entire course of hunting. The purpose of this study was to examine if variation in sound duration might affect the amplitude selectivity of inferior collicular (IC) neurons of this bat species under free-field stimulation conditions. A family of rate^amplitude functions of each IC neuron was obtained with different sound durations. The effect of sound duration on the neuron's amplitude selectivity was then studied by examining the type, best amplitude, dynamic range and slope of each rate^amplitude function. The rate^amplitude functions of 83 IC neurons determined with different sound durations were either monotonic, saturated or nonmonotonic. Neurons with monotonic rate^amplitude functions had the highest best amplitude, largest dynamic range but smallest slope. Neurons with non-monotonic rate^amplitude functions had the lowest best amplitude, smallest dynamic range but largest slope. The best amplitude, dynamic range and slope of neurons with saturated rate^amplitude functions were intermediate between these two types. Rate^amplitude functions of one group (47, 57%) of IC neurons changed from one type to another with sound duration and one-third of these neurons were tuned to sound duration. As a result, the best amplitude, dynamic range, and slope also varied with sound duration. However, rate^amplitude functions of the other group (36, 43%) of IC neurons were hardly affected by sound duration and two-thirds of these neurons were tuned to sound duration. Biological relevance of these findings in relation to bat echolocation is discussed. ß
Neuroscience, 2008
During hunting, insectivorous bats such as Eptesicus fuscus progressively vary the repetition rate, duration, frequency and amplitude of emitted pulses such that analysis of an echo parameter by bats would be inevitably affected by other co-varying echo parameters. The present study is to determine the variation of echo frequency selectivity of duration-tuned inferior collicular neurons during different phases of hunting using pulse-echo (P-E) pairs as stimuli. All collicular neurons discharge maximally to a tone at a particular frequency which is defined as the best frequency (BF).
The Chinese journal of physiology, 2007
The big brown bats, Eptesicus fuscus, emit ultrasonic signals and analyze the returning echoes in multi-parametric domains to extract target features. The variation of different pulse parameters during hunting predicts that analysis of an echo parameter by bats is inevitably affected by other co-varying echo parameters. In this study, we presented data to show that the bat inferior collicular (IC) neurons have maximal amplitude sensitivity at the best duration (BD). A family of rate-amplitude function (RAF) of each IC neuron is plotted with the BD and non-BD sound pulses. The RAF plotted with BD pulses has sharper slope (SL) and smaller dynamic range (DR) than the RAF plotted with non-BD pulses has. All RAFs can be described as monotonic, saturated or non-monotonic. IC neurons with monotonic RAF are mostly recorded at deeper IC and they have the largest average BD, best amplitude (BA) and DR. Conversely, IC neurons with non-monotonic RAF are mostly recorded at upper IC and they have...
Journal of Comparative Physiology A-neuroethology Sensory Neural and Behavioral Physiology, 1997
Neurons in the inferior colliculus (IC) of the awake big brown bat, Eptesicus fuscus, were examined for joint frequency and latency response properties which could register the timing of the bat's frequency-modulated (FM) biosonar echoes. Best frequencies (BFs) range from 10 kHz to 100 kHz with 50% tuning widths mostly from 1 kHz to 8 kHz. Neurons respond with one discharge per 2-ms tone burst or FM stimulus at a characteristic latency in the range of 3–45 ms, with latency variability (SD) of 50 μs to 4–6 ms or more. BF distribution is related to biosonar signal structure. As observed previously, on a linear frequency scale BFs appear biased to lower frequencies, with 20–40 kHz overrepresented. However, on a hyperbolic frequency (linear period) scale BFs appear more uniformly distributed, with little overrepresentation. The cumulative proportion of BFs in FM1 and FM2 bands reconstructs a scaled version of the spectrogram of FM broadcasts. Correcting FM latencies for absolute BF latencies and BF time-in-sweep reveals a subset of IC cells which respond dynamically to the timing of their BFs in FM sweeps. Behaviorally, Eptesicus perceives echo delay and phase with microsecond or even submicrosecond accuracy and resolution, but even with use of phase-locked FM and tone-burst stimuli the cell-by-cell precision of IC time-frequency registration seems inadequate by itself to account for the temporal acuity exhibited by the bat.
Brain Research, 1993
Single-neuron responses to pulse repetition rate in the inferior colliculus, auditory cortex and pontine nuclei of the FM bat, Eptesicus fuscus were studied under free-field stimulation conditions. The best frequency (BF) and minimum threshold (MT) of each neuron were first determined with a 4 ms pulse broadcast from a specific point (response center) of the bat's frontal auditory space at which the neuron had maximal spatial sensitivity. The neuron's intensity-rate function was then studied with a 4 ms BF pulse delivered at 10 dB increments above its MT in order to determine the best intensity to which the neuron discharged maximally. The neuron's discharge pattern and number of impulses to 32 trials of 300 ms train stimuli, which consisted of different number of 4 ms BF and best intensity pulses (1, 2, 3, 8, 12, 19, 24, 29 pulses/train) and delivered at an interpulse interval of 1000, 250, 170, 100, 40, 25, 15, 12 and 10 ms (i.e. at a pulse repetition rate of 1, 4, 6, 10, 25, 40, 67, 83, 100 pulses/s), were sequentially recorded. All neurons recorded from the inferior colliculus, auditory cortex and pontine nuclei discharged phasically (1-3 impulses) but they responded to the pulse repetition rate in different manners. More than 63% of 38 inferior collicular and 65 pontine neurons studied discharged impulses to each pulse within a train stimulus when the pulse repetition rate was up to 40 pulses/s. Although the number of neurons ~howing such a one-to-one following response decreased with increasing pulse repetition rate, at least 20% of neurons still maintained such a response pattern even at a pulse repetition rate of 100 pulses/s. In contrast, responses of 60% of 36 cortical neurons followed the pulse repetition rate only up to 10 pps beyond which all but one discharged impulses to the first pulse of a train stimulus. We suggest that the different discharge pattern to pulse repetititon rate among individual neurons from these three brain centers is primarily due to their different recovery cycles.
The adaptive value of increasing pulse repetition rate during hunting by echolocating bats
Frontiers in Biology, 2012
During hunting, bats of suborder Microchiropetra emit intense ultrasonic pulses and analyze the weak returning echoes with their highly developed auditory system to extract the information about insects or obstacles. These bats progressively shorten the duration, lower the frequency, decrease the intensity and increase the repetition rate of emitted pulses as they search, approach, and finally intercept insects or negotiate obstacles. This dynamic variation in multiple parameters of emitted pulses predicts that analysis of an echo parameter by the bat would be inevitably affected by other co-varying echo parameters. The progressive increase in the pulse repetition rate throughout the entire course of hunting would presumably enable the bat to extract maximal information from the increasing number of echoes about the rapid changes in the target or obstacle position for successful hunting. However, the increase in pulse repetition rate may make it difficult to produce intense short pulse at high repetition rate at the end of long-held breath. The increase in pulse repetition rate may also make it difficult to produce high frequency pulse due to the inability of the bat laryngeal muscles to reach its full extent of each contraction and relaxation cycle at a high repetition rate. In addition, the increase in pulse repetition rate increases the minimum threshold (i.e. decrease auditory sensitivity) and the response latency of auditory neurons. In spite of these seemingly physiological disadvantages in pulse emission and auditory sensitivity, these bats do progressively increase pulse repetition rate throughout a target approaching sequence. Then, what is the adaptive value of increasing pulse repetition rate during echolocation? What are the underlying mechanisms for obtaining maximal information about the target features during increasing pulse repetition rate? This article reviews the electrophysiological studies of the effect of pulse repetition rate on multipleparametric selectivity of neurons in the central nucleus of the inferior colliculus of the big brown bat, Eptesicus fuscus using single repetitive sound pulses and temporally patterned trains of sound pulses. These studies show that increasing pulse repetition rate improves multiple-parametric selectivity of inferior collicular neurons. Conceivably, this improvement of multiple-parametric selectivity of collicular neurons with increasing pulse repetition rate may serve as the underlying mechanisms for obtaining maximal information about the prey features for successful hunting by bats.
Brain Research, 2002
This study examined the effect of bicuculline application on sharpness of frequency tuning curves (FTCs) of bat inferior collicular neurons plotted under three different pulse repetition rates (PRRs) of 10, 30 and 90 pulses per second. The sharpness of FTCs of collicular neurons, which was expressed in Q (Q , Q , Q ) and bandwidths (90, 75 and 50% of the maximal response at the best frequency), n 10 20 30 improved with increasing PRR. However, this PRR-dependent frequency selectivity of collicular neurons was abolished during bicuculline application. This observation suggests that GABAergic inhibition contributes more effectively to sharpening of FTCs at higher than at lower PRRs.
Time and frequency domain processing in the inferior colliculus of echolocating bats
Hearing Research, 1981
Tone bursts and frequency-modulated (FM) signals were presented to Mexican free-tailed bats and tuning curves, discharge patterns, and discharge latencies of single units in the inferior colliculus were recorded. Cells were broadly tuned to tone bursts, with most Q 10 values ranging from 3 to 20. However, in response to FM stimulation the discharges of neurons were closely synchronized to the time of occurrence of restricted frequency components within the FM sweep. These excitatory frequencies (EFs) were generally unaffected by changes in the starting frequency or intensity of the stimulus. Thus, in response to FM signals, the cells exhibited a much greater frequency selectivity than that observed following tone burst stimulation. Across the population of neurons sampled, EFs covering a wide frequency range were found, and the different EFs were represented in a systematic fashion within the colliculus. The frequencies in an FM biosonar signal or echo will thus be neurally represented both by the time of occurrence of neuronal discharges and by the location of the discharging cells within the nucleus. The potential role of this dual frequency coding in spectral and temporal processing of biosonar signals and echoes is discussed, with emphasis on the neural coding of target range.