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A S Feng

Publications and source records attributed to A S Feng.

At least 37 records · Page 2Linked to original sources

Neural ensemble coding of target identity in echolocating bats.

Most insectivorous bats use echolocation to determine the identity of flying insects. Among the many target features that are so extracted, the insect's wingbeat pattern and frequency appear to serve as useful cues for identification. Biosonar pulses impinging on the fluttering wings of an insect are returned as echoes whose amplitudes vary with time, thus providing a characteristic signature of the insect. It has been shown previously that neurons in the inferior colliculus, a midbrain auditory nucleus, of the little brown bat respond to sound stimuli that mimic echoes from fluttering targets. To examine the manner in which target identity is represented in the inferior colliculus, an ensemble coding analysis using a filter-based approach was undertaken. The analysis indicates that a discrete subset of neurons in the inferior colliculus, the onset units, are strongly tuned to wingbeat frequencies of targets that the bat hunts, and that ensemble response reaches a maximum at a distinct phase of the prey capture maneuver: the late approach stage. On the basis of the analysis it is hypothesized that inferior colliculus neurons may play an important role in target detection-identification processing. Although ensemble coding of temporally sequenced information has not been analyzed in the auditory system so far, this study indicates that this method of coding may provide the information necessary to detect and identify targets during prey capture.

Acoustic Stimulation↗

Binaural inhibition is important in shaping the free-field frequency selectivity of single neurons in the inferior colliculus.

1. We have shown previously that under free-field stimulation in the frontal field, frequency selectivity of the majority of inferior colliculus (IC) neurons became sharper when the loudspeaker was shifted to ipsilateral azimuths. These results indicated that binaural inhibition may be responsible for the direction-dependent sharpening of frequency selectivity. To test the above hypothesis directly, we investigated the frequency selectivity of IC neurons under several conditions: monaural stimulation using a semiclosed acoustical stimulation system, binaural stimulation dichotically also using a semiclosed system, free-field stimulation from different azimuths, and free-field stimulation when the ipsilateral ear was occluded monaurally (coated with a thick layer of petroleum jelly, which effectively attenuated acoustic input to this ear). 2. The binaural interaction pattern of 98 IC neurons of northern leopard frogs (Rana pipiens pipiens) were evaluated; of these neurons, there were 34 EE and 64 EO neurons. The majority of IC neurons (92 of 98) showed some degree of binaural inhibition (i.e., showing diminished response when the ipsilateral and contralateral ears were stimulated simultaneously) whether they were designated as EE or EO; these IC neurons thus were classified as EE-I or EO-I. Neurons were classified as exhibiting strong inhibition if the ILD function showed a pronounced response decrement, i.e., a decrease of > or = 50% of the response to monaural stimulation of the contralateral ear. Those neurons that showed smaller response decrements (decrease was > or = 25% but < 50%) were designated as showing weak inhibition. Most of these EE-I and EO-I neurons (n = 68) showed strong binaural inhibition. 3. In agreement with results from our earlier studies, frequency threshold curves (FTCs) of IC neurons were altered by sound azimuth. Independent of binaural interaction pattern, most IC neurons (59 of 98) showed a narrowing of the FTC as sound direction was changed from contralateral 90 deg (c90 degrees) to ipsilateral 90 deg (i90 degrees). IC neurons that exhibited the largest direction-dependent changes in frequency selectivity were typically those that displayed stronger binaural inhibition. Occlusion of the ipsilateral ear, which reduced the strength of binaural inhibition by this ear, abolished direction-dependent frequency selectivity. 4. FTCs of IC neurons that exhibited little to moderate direction-dependent effects on frequency selectivity were associated typically with neurons that displayed weak binaural inhibition. Associated with this weak binaural inhibition, central neural responses under monaural occlusion also displayed only small effects; the FTCs were only slightly broader than those derived in the intact condition, and as before, the experimental manipulation resulted in abolishment of direction-dependent frequency selectivity. 5. In contrast to most IC neurons, which showed direction-dependent narrowing of the FTC, about one-third (34 of 98) of IC neurons studied showed a broadening of the FTC when sound direction was shifted to ipsilateral azimuths. Interestingly, for 90% of these 34 neurons, monaural occlusion resulted in narrowing of the bandwidth at each azimuth instead of broadening of the FTC bandwidth. We have evidence to suggest that this direction-dependent broadening is actually a consequence of a truncation or loss of the tip of the FTC derived at c90 degrees, which results from strong binaural inhibition. 6. To compare the frequency threshold tuning in response to monaural stimulation of each ear with free-field FTCs, we measured FTCs for each of the 34 EE neurons to independent contralateral and ipsilateral stimulation. FTCs derived from ipsilateral monaural stimulation were significantly narrower than those resulting from contralateral monaural stimulation, independent of a neuron's direction-dependent changes in frequency selectivity.

Acoustic Stimulation↗

Classification of the temporal discharge patterns of single auditory neurons in the frog superior olivary nucleus.

Temporal discharge patterns of neurons in the superior olivary nucleus (SON) of the northern leopard frog (Rana pipiens pipiens) were studied by evaluating peri-stimulus time histograms and interspike interval histograms generated from responses to tone bursts at the neuron's characteristic frequency and at 10 dB above neuron's characteristic threshold. Four basic discharge patterns were observed, i.e., primary-like, phasic-burst, phasic, and pauser. Additionally, within each class, different neurons exhibited further subtle differences in temporal discharge patterns and thus subclasses were distinguishable. For most SON neurons, changes in signal level did not affect the discharge pattern. However, there were a few notable exceptions. The firing pattern of 12% of SON neurons changed from one class to another with a change in signal level. Two-thirds of phasic-burst neurons showed increased regularity (i.e., chopping pattern) in their discharges as the signal level was increased. The majority of SON neurons showed monotonic rate-level functions, but one-fourth gave non-monotonic rate-level functions. The presence of a fairly large number of non-monotonic units in the frog SON suggests an additional role of this nucleus in information processing beyond the simple coding of stimulus level. The discharge patterns displayed by SON neurons resembled those seen in the frog cochlear nucleus and in the mammalian superior olivary complex.

Acoustic Stimulation↗

Detection of gaps in sinusoids by frog auditory nerve fibers: importance in AM coding.

Physiological studies were carried out in the frog (Rana pipiens pipiens) eighth nerve to determine: (i) whether the modulation rate or the silent gap was the salient feature that set the upper limit of time-locking to pulsed amplitude-modulated (PAM) stimuli, (ii) the gap detection capacity of individual eighth nerve fibers. Time-locked responses of 79 eighth nerve fibers to PAM stimuli (at the fiber's characteristic frequency) showed that the synchronization coefficient was a low-pass function of the modulation rate. In response to PAM stimuli having different pulse durations, a fiber gave rise to non-overlapping modulation transfer functions. The upper cut-off frequency of time locking was higher when tone-pulses in PAM stimuli had shorter duration. The fact that the cut-off frequency was different for the different PAM series suggested that the AM rate was neither the sole, nor the main, determinant for the decay in time-locking at high AM rates. Gap detection capacity was determined for 69 eighth nerve fibers by assessing fiber's spiking activities to paired tone-pulses during an OFF-window and an ON-window. It was found that the minimum detectable gap of eighth nerve fibers ranged from 0.5 to 10 ms with an average of 1.23-2.16 ms depending on the duration of paired tone pulses. For each fiber, the minimum detectable gap was longer when the duration of tone pulses comprising the twin-pulse stimuli was more than four times longer. When the synchronization coefficient was plotted against the silent gap between tones pulses in the PAM stimuli, the gap response functions of a fiber as derived from multiple PAM series were equivalent to gap response functions deriving from twin-pulse series suggesting that it was the silent gap which primarily determined the upper limit of time-locking to PAM stimuli.

Acoustic Stimulation↗

Single neurons in the frog inferior colliculus exhibit direction-dependent frequency selectivity to isointensity tone bursts.

The effects of sound direction on frequency selectivity of inferior colliculus (IC) neurons were investigated by measuring the neuron's isointensity frequency responses (FRs) to tone bursts emanating from a free-field loudspeaker at several sound levels. The loudspeaker was rotated across the frontal field at 0 degrees elevation through 180 degrees of azimuth (from contralateral 90 degrees or C90 degrees to ipsilateral 90 degrees or I90 degrees). At each frequency, to assess the magnitude of response change with sound direction, the mean spike count obtained at an azimuth was compared to that at C90 degrees. The FR of most IC neurons (75/83 or 90%) was direction dependent. For most of these neurons, bandwidths of FRs were narrower when sounds originated from ipsilateral azimuths. Remarkably, with a change in sound azimuth, some segments of these FRs showed very distinct changes in shape, while other portions of the same FRs remained essentially unchanged. These narrow-band changes associated with restricted portions of the FR, were also exhibited by neurons with direction-dependent frequency-threshold characteristics (Gooler et al., 1993). Additionally, the most frequent direction-dependent change in the FRs occurred in a narrow frequency band around the units' best excitatory frequency.

Acoustic Stimulation↗

Stroboscopic hearing as a mechanism for prey discrimination in frequency-modulated bats?

A hypothesis was proposed that bats employing frequency-modulated (FM) echolocation pulses could utilize dynamic information of a flying insect to discriminate prey on the basis of "stroboscopic hearing." To test this hypothesis, single unit recordings were made from the inferior colliculus (IC) of the little brown bat, Myotis lucifugus. Response characteristics of IC units to trains of modulated and unmodulated sound pulses were analyzed at various pulse repetition rates that corresponded to a bat's pulse emission rates during the different stages of its target directed flight. The results show that amplitude modulation (AM) across a train of sound pulses was faithfully encoded in the units' discharge pattern when the pulse repetition rate was different from the AM frequency. When the AM frequency was integer multiples of the pulse repetition rate, the stimulus amplitude was reduced drastically under these conditions. Consequently, the discharge of an IC unit diminished precipitously, or if there was a phase delay between the pulse onset and the modulating sinusoidal waveform the unit fired to each modulation cycle with more or less the same vigor as if the modulation was absent. These data indicate that the across-pulse amplitude modulation becomes undetectable when the AM frequency is integer multiples of the pulse repetition rate. It is interpreted that FM bats can potentially employ a "stroboscopic hearing" strategy for discriminating insects on the basis of the wing-beat frequency of the prey.

Acoustic Stimulation↗

Processing of amplitude-modulated signals that mimic echoes from fluttering targets in the inferior colliculus of the little brown bat, Myotis lucifugus.

1. Neurophysiological recordings were undertaken to determine how neurons in the central nucleus of the inferior colliculus (ICc) of the little brown bat, Myotis lucifugus, extract amplitude modulations that span across a series of tone pulses (i.e., signals that simulate echoes from fluttering targets). Two types of stimuli were presented to the bats. The first served as a control and consisted of an unmodulated train of tone pulses having different repetition rates (TPu, 5-400 pulses per second). The second was a train of tone pulses that were sinusoidally amplitude modulated (TPm, 5-110 Hz) across sequential pulses. The modulated trains of pulses were presented at five different repetition rates (25, 50, 100, 200, and 400 pulses per second) encompassing the range of biosonar emission rates in these bats at different stages of target-directed flight. 2. One hundred fifty-two single neurons were isolated in the ICc of M. lucifugus; their basic response properties and temporal firing patterns were characterized. The best frequencies (BFs) ranged from 10 to 80 kHz and the minimum thresholds at BF were distributed widely (10-95 dB SPL). The frequency tuning selectivity ranged widely, from very broadly tuned (Q10dB = 1.3) to narrowly tuned (Q10dB = 89). Units with very narrow frequency tuning (Q values > 20) were restricted to BFs of 30-50 kHz. The temporal firing pattern of ICc units could be categorized into primary-like (PL), chopper (C), onset-immediate (OI), and onset-late (OL). 3. In response to TPu ICc units exhibited varying degrees of response selectivities as evidenced by their count-based response functions (using the spike count as a measure) versus repetition rate. The count-based response functions of ICc units exhibited five filtering characteristics including band-pass, low-pass, high-pass, band-suppression, and all-pass characteristics. The temporal firing pattern of a unit showed certain correlations with its count-based response function. For example, the majority of OI and OL units, and about half of the C units, showed tuned band-pass response functions. The remaining C and onset types showed mostly low-pass response functions. In contrast, PL neurons showed mostly high-pass response functions, but one third displayed band-pass response functions. 4. The ability of ICc neurons to time-lock their discharges to the individual pulses in a train was characterized by using the synchronization coefficient (SC) as a measure. The SC was plotted against the repetition rate to construct units' synchronization-based response function.(ABSTRACT TRUNCATED AT 400 WORDS)

Acoustic Stimulation↗

Phase-locked response characteristics of single neurons in the frog "cochlear nucleus" to steady-state and sinusoidal-amplitude-modulated tones.

1. We made extracellular recordings from 164 single neurons in the frog dorsal medullary nucleus (DMN), a homologue of the cochlear nucleus. Phase-locked responses to tones at the unit's characteristic frequency (CF) and to off-CF tones were evaluated. We also stimulated units with tones at CF that were amplitude modulated sinusoidally between 5 and 1,000 Hz and examined responses to these stimuli. 2. Results showed that single neurons in the frog DMN displayed phase-locked discharges to tones at frequencies < or = 800 Hz. Phase-locking was robust at low frequencies (< 400 Hz) and became poorer at higher frequencies; the variation of the synchronization coefficient (SC) with frequency typically showed a low-pass characteristic. 3. The capacity of phase-locking to tones was correlated with the functional classification of a DMN neuron and the firing rate of its CF response. Primarylike neurons exhibited various degrees of phase-locked discharges to tones at off-CF frequencies. The average upper cutoff frequency, i.e., the frequency at which the SC dropped to 0.5 of maximum value, differed for the three classes of primarylike neurons. The average cutoff frequency was respectively 183, 325, and 536 Hz for primarylike neurons that displayed low (PL-1), intermediate (PL-2), and high (PL-3) steady-state firing rates to CF stimulation. The phasic neurons showed poor phase-locking capacities at all tone frequencies. 4. The frequency range of phase-locking to amplitude-modulated stimuli was also different for the different cell types, as evidenced by the units' modulation transfer functions (MTFs). The primarylike neurons exhibited mostly all-pass or low-pass sync-based MTFs. The mean upper cutoff frequencies for primarylike neurons having low-pass MTFs were 155 Hz for PL-1 neurons, 176 Hz for PL-2 neurons, and 218 Hz for PL-3 neurons. Pauser, chopper, phasic, and phasic-burst neurons gave mostly low-pass MTFs having a mean upper cutoff frequency of 219, 235, 242, and 251 Hz, respectively. 5. The phase-locking ability of DMN neurons to tones and to amplitude-modulated stimuli are compared with those of frog's primary afferent fibers and with those of avian and mammalian cochlear nucleus neurons. The significance of results in terms of sound localization and sound pattern recognition is discussed.

Animals↗

Sound direction influences the frequency-tuning characteristics of neurons in the frog inferior colliculus.

1. We investigated the influence of sound direction on the frequency-tuning characteristics of neurons in the frog inferior colliculus, the torus semicircularis. For each neuron, we used tone bursts to determine the frequency-threshold curves (FTCs) for three to seven loudspeaker azimuths. The loudspeaker was mounted on a rotatable arc and could be swung through the frontal field between positions opposite the ear that was contralateral to the recording site (C90 degrees) and the ear that was ipsilateral to the recording site (I90 degrees). 2. Frequency-tuning data from 83 units showed that the characteristic frequency (CF) shift through a 180 degrees change in loudspeaker azimuth was typically small, i.e., 85% of neurons showed maximum absolute changes in CF that were < 0.4 octaves. Paired comparisons of CFs for each neuron when the loudspeaker was located at C90 degrees, and the frontal midline position (0 degree) revealed no significant differences (P > 0.2) between azimuths. The magnitude of CF shift between different sound directions showed no systematic pattern. 3. In contrast to the CF, midbrain neurons showed distinct changes in the minimum threshold (MT) at CF across 180 degrees of azimuth. The maximum absolute change in MT ranged from 0 to 38 dB, with a mean of 10.9 dB. A pair-wise comparison of MTs, for each neuron, derived with the speakers at C90 degrees, 0 degree, and I90 degrees, revealed that the MT typically increased when the loudspeaker was rotated toward I90 degrees (P < 0.0001). 4. The most prominent effect of rotating the loudspeaker from C90 degrees to I90 degrees was a narrowing of the FTC. Sharpness of tuning in simple V-shaped FTCs was most directly shown by changes in the Q factors at 10, 20, and 30 dB above MT as a function of sound direction. A pair-wise comparison for individual neurons showed that all Q factors were significantly larger (sharper tuning) for I90 degrees compared with C90 degrees (P < 0.02). The Q20dB values were also significantly larger for I90 degrees compared with 0 degree (P < 0.05). For the majority of units, the maximum Q10dB and Q20 dB values were displayed when the loudspeaker was positioned at I90 degrees; however, the maximum Q30dB was distributed nearly equally for the three azimuths. These results suggest that a change in sound direction has the most robust effect on tuning properties of the FTCs nearest the MT.(ABSTRACT TRUNCATED AT 400 WORDS)

Acoustic Stimulation↗

Information processing in the auditory brainstem.

The past year has seen significant advances in our understanding of the structural (circuitry and chemistry of synaptic connections) and functional characteristics of the auditory brainstem. Some of the findings that shed light on the mechanisms underlying complex auditory information processing are highlighted.

Animals↗

Temporal coding in the frog auditory midbrain: the influence of duration and rise-fall time on the processing of complex amplitude-modulated stimuli.

1. Single-unit recordings were made in the auditory midbrain, the torus semicircularis (TS) of the northern leopard frog, to independently characterize the processing of different temporal attributes (signal duration, rise-fall time, and rate of amplitude modulation) of natural sounds and to investigate how these temporal variables interact to produce the observed responses to complex amplitude-modulated (AM) signals. Response functions, on the basis of mean spike count, were derived and categorized to describe the unit's temporal response characteristics to each of the variables. 2. To characterize the duration response functions, tone bursts of different durations (stimuli repeated at a constant repetition rate) at the unit's characteristic frequency (CF) and 10 dB above minimum threshold at CF (MT) were presented monaurally to the contralateral ear. The duration response function of a TS neuron was often related to the temporal discharge characteristics of the neuron. Increases in stimulus duration elicited an increase in spike counts (therefore, long-pass response function) from most neurons (74%) in the TS; 91% of these neurons showed tonic discharge patterns. Phasic-burst (PB) cells that were rapidly adapting showed long-pass duration response functions that were highly nonlinear, having peaks and notches embedded within the functions. On the other hand, one-third of phasic neurons tended to be insensitive to stimulus duration, giving similar spike counts in response to stimuli of greatly different durations (i.e., all pass). In the TS, some neurons (9%) only responded to a limited range of durations (i.e., band-duration pass), and still others showed a preference for shorter durations (9%; i.e., short pass); these were exhibited primarily by phasic and PB neurons. 3. To characterize the rise-fall time response functions, tone bursts having different rise-fall times were presented. The rise-fall time response functions of TS neurons had two distinct characteristics. The majority of tonic cells (91%), as well as some PB (38%) and phasic (29%) neurons, gave essentially invariant spike counts for all stimulus rise-fall times (i.e., all pass; 73% of neurons). Despite the relatively stable spike counts of neurons showing all-pass functions, the peristimulus time histograms (PSTHs) deriving from responses to slower rise-fall time stimuli exhibited a longer and somewhat more variable onset latency. About one-fourth (27%) of TS neurons, mostly phasic and PB neurons, showed higher spike counts for signals with rapid rise-fall times.(ABSTRACT TRUNCATED AT 400 WORDS)

Acoustic Stimulation↗

Differential innervation patterns of three divisions of frog auditory midbrain (torus semicircularis).

The connectivity pattern of the laminar, principal, and magnocellular nuclei of the frog torus semicircularis (TS) was investigated. A small amount of horseradish peroxidase was injected focally into individual divisions of the TS and anterograde and retrograde transport patterns were observed. Results of our tracing study showed that these divisions of the TS possessed distinct innervation patterns. The principal nucleus appeared to be the primary input port of the TS receiving extensive inputs from all caudal brainstem auditory nuclei bilaterally, but especially from the contralateral dorsal medullary nucleus and the ipsilateral superior olivary and lateral lemniscus nuclei. Descending projection to this nucleus was limited to that from the posterior thalamic nucleus. In contrast, the laminar nucleus, but even more markedly the magnocellular nucleus, received extensive descending inputs from numerous structures in the dorsal thalamus and less pronounced ascending afferents from caudal brainstem auditory nuclei. Similar to the afferent connection patterns, the efferent projections originating from these three toral divisions differed substantially. The principal nucleus gave restricted ascending projections, limited mainly to the caudal region of the posterior thalamic nucleus, a region important in processing spectral information of complex sounds, and the pretectal gray. Its descending projection was also somewhat restricted, being limited to the superior olivary and lateral lemniscus nuclei. The laminar nucleus and especially the magnocellular nucleus gave robust descending as well as ascending projections; these nuclei serve as the main output paths for the TS and provide the main routes by which auditory input reaches the central thalamic nucleus, a structure previously shown to be involved in temporal information processing.

Afferent Pathways↗

Processing of behaviorally relevant temporal parameters of acoustic stimuli by single neurons in the superior olivary nucleus of the leopard frog.

Response characteristics of 130 single neurons in the superior olivary nucleus of the northern leopard frog (Rana pipiens pipiens) were examined to determine their selectivity to various behaviorally relevant temporal parameters [rise-fall time, duration, and amplitude modulation (AM) rate] of acoustic signals. Response functions were constructed with respect to each of these variables. Neurons with different temporal firing patterns such as tonic, phasic or phasic-burst firing patterns, participated in time domain analysis in specific manners. Phasic neurons manifested preferences for signals with short rise-fall times, thus possessing low-pass response functions with respect to this stimulus parameter; conversely, tonic and phasic-burst units were non-selective and possessed all-pass response functions. A distinction between temporal firing patterns was also observed for duration coding. Whereas phasic units showed no change in the mean spike count with a change in stimulus duration (i.e., all-pass duration response functions), tonic and phasic-burst units gave higher mean spike counts with an increase in stimulus duration (i.e., primary-like high-pass response functions). Phasic units manifested greater response selectivity for AM rate than did tonic or phasic-burst units, and many phasic units were tuned to a narrow range of modulation rates (i.e., band-pass). The results suggest that SON neurons play an important role in the processing of complex acoustic patterns; they perform extensive computations on AM rate as well as other temporal parameters of complex sounds. Moreover, the response selectivities for rise-fall time, duration, and AM rate could often be shown to contribute to the differential responses to complex synthetic and natural sounds.

Acoustic Stimulation↗

Coding of temporal parameters of complex sounds by frog auditory nerve fibers.

1. Physiological recordings were made from single auditory fibers in the frog eighth nerve to determine quantitatively how the different behaviorally relevant temporal parameters (the signal rise-fall time, duration, and rate of amplitude modulation) of complex sounds are encoded in the auditory periphery. Individual temporal parameters were varied. Response functions (RFs) were constructed with respect to each of these parameters using each unit's best excitatory frequency (BF) as the carrier. 2. In response to a change in signal rise-fall time, auditory nerve fibers showed little change in the mean spike count or firing rate, i.e., all fibers displayed ALL-PASS RFrfts. But the transient components, particularly the early phasic component, of responses varied with rise-fall times; these components were more pronounced in the responses to stimuli with shorter rise-fall times. 3. In response to an increase in signal duration, auditory nerve fibers showed a corresponding increase in firing duration and thus in the mean spike count, giving rise to HIGH-PASS RFdurs. The shape of response curves differed among fibers; the difference appeared to be related to the fiber's temporal adaptation characteristic. When the firing rate was measured, all fibers displayed higher mean firing rates in response to shorter duration stimuli than they did to longer duration stimuli, thus giving rise to LOW-PASS response functions. 4. To determine the response transfer functions to modulation rate, pulsed (PAM) and sinusoidally (SAM) amplitude-modulated signals were used. These signals differed substantially in terms of their envelopes and how they varied with AM rate. Data were analyzed by 1) plotting spike counts against the AM rate to derive modulation transfer functions (MTFspks) and 2) plotting synchronization coefficients (SCs) against the AM rate to generate MTFscs. 5. In response to PAM stimuli, all fibers showed an increase in mean spike count with modulation frequency over the range examined, giving rise to HIGH-PASS MTFspks. 6. For SAM stimuli, the average energy and duty cycle are independent of AM rate. Most (79%) auditory fibers showed little selectivity for AM rate over a range of 5-400 Hz, giving rise to ALL-PASS MTFspks. The remaining auditory fibers displayed LOW-PASS MTFspks, i.e., there was a distinct decline in the mean spike count with increasing AM rate. 7. In response to PAM stimuli, most fibers showed good response synchrony at low AM rates but the SC declined with an increase in the AM rate (i.e., LOW-PASS MTFscs). The cut-off frequency was typically very high, averaging 90 pulses/s.(ABSTRACT TRUNCATED AT 400 WORDS)

Acoustic Stimulation↗

Temporal processing in the dorsal medullary nucleus of the Northern leopard frog (Rana pipiens pipiens).

1. Single-unit responses to different temporal acoustic parameters were characterized in the dorsal medullary nucleus (DMN) of the Northern leopard frog, Rana pipiens pipiens. Our goal was to provide both a quantitative and a qualitative assessment of the neural representation of behaviorally relevant temporal acoustic patterns in the frog's DMN. 2. Acoustic stimuli included tone bursts having different durations, rise times, or rates of amplitude modulation (AM). Several metrics were used to compute temporal response functions for each of these, including mean spike count, average firing rate, and/or peak firing rate. Synchronization coefficients were also used to characterize responses to stimuli presented at different AM rates. 3. On the basis of mean spike count, the temporal response functions of DMN neurons with respect to signal rise time could be characterized as 1) all-pass, in which the mean spike count was largely independent of rise time, or 2) fast-pass, in which the mean spike count decreased with increasing rise time. Fast-pass response functions were of two types, those that decayed rapidly and those that decayed gradually from their peak values. 4. The minimum threshold varied with signal rise time for cells showing fast-pass but not all-pass response functions. Minimum response thresholds for fast-pass neurons were typically higher with slower signal rise time. 5. The filtering characteristics of cells displaying fast-pass rise time response functions were dependent on signal level, becoming all-pass when signal levels exceeded 30-40 dB above the minimum threshold. 6. Approximately 44% of DMN neurons exhibiting fast-pass response functions for signal rise time showed all-pass filtering characteristics when broadband noise rather than best frequency tones were used, thereby signifying an influence of signal spectrum on the pass-band characteristics of these cells. 7. All DMN neurons, regardless of discharge pattern, showed maximal instantaneous firing rates to signals having short (less than 25 ms) rise times. Response functions based on instantaneous firing rate were, therefore, fast-pass in nature. These responses were independent of signal level and spectrum. 8. There was an ordinal relationship between signal duration and the duration of tonic but not phasic unit discharges. This relationship was not intensity dependent. 9. On the basis of mean spike count, the temporal response functions of DMN neurons with respect to signal duration were characterized as 1) all-pass, in which the mean spike count was largely independent of signal duration, or 2) long-pass, in which the mean spike count increased with increasing signal duration.(ABSTRACT TRUNCATED AT 400 WORDS)

Acoustic Stimulation↗

Functional organization of ascending and descending connections of the cochlear nucleus of horseshoe bats.

The ascending projections of the cochlear nucleus (CN) and the sources of descending inputs to the CN were investigated in horseshoe bats (Rhinolophus rouxi) by tracing the anterograde and retrograde transport of horseradish peroxidase (HRP or WGA-HRP) injected into the CN. The tracer was iontophoretically deposited into physiologically characterized regions of the cochlear nucleus (Feng and Vater, '85). We report the course and termination of pathways arising from the anteroventral (AVCN), posteroventral (PVCN), and dorsal (DCN) cochlear nucleus. The projection fields within the auditory brainstem centers (superior olivary complex [SOC]; lateral lemniscus complex [LLC]; and inferior colliculus [IC]) and their tonotopic organization according to the frequency representations at the injection sites are described. While the projection pattern is generally in accordance with other mammals, several species-characteristic features are noted: i) the lateral superior olive (LSO) receives tonotopically organized input from both the AVCN and PVCN; ii) the CN-projections to medial nuclear groups of the SOC located between the LSO and the medial nucleus of the trapezoid body do not support previously suggested homologies; iii) the ventral nucleus of the LLC can be subdivided into two divisions with distinct input patterns from the AVCN and PVCN, respectively.

Animals↗