Frequency selectivity of hearing in the green treefrog,Hyla cinerea

Frequency selectivity of hearing was measured in the green treefrog, Hyla cinerea. A psychophysical technique based on reflex modification was used to obtain masked threshold estimates for pure tones (300-5,400 Hz) presented against two levels of broadband masking noise. A pure tone (S-1) presented 200 ms prior to a reflex-eliciting stimulus (S-2) inhibited the motor reflex response to S-2. The magnitude of this reflex modification effect varied systematically with the sound pressure level (SPL) of S-1, and threshold was defined as the SPL of S-1 at which the reflex modification effect disappeared. Masked thresholds were used to calculate critical ratios, an index of the auditory system's frequency selectivity. The frequency selectivity of the treefrog's hearing is greatest and critical ratios are lowest (22-24 dB) at about 900 and 3,000 Hz, the two spectral regions dominant in the male treefrog's species-specific advertisement call. These results suggest that the treefrog's auditory system may be specialized to reject noise at biologically-relevant frequencies. As in other vertebrates, critical ratios remain constant when background noise level is varied; however, the shape of the treefrog's critical ratio function across frequencies differs from the typical vertebrate function that increases with increasing frequency at a slope of about 3 dB/octave. Instead, the treefrog's critical ratio function resembles its pure tone audiogram. Although the shape of the treefrog's critical ratio function is atypical, the critical ratio values themselves are comparable to those of many other vertebrates in the same frequency range. Critical ratio values here measured behaviorally do not match critical ratio values previously measured physiologically in single eighth nerve fibers.(ABSTRACT TRUNCATED AT 250 WORDS)     

Manifestations of dynamic coding of the amplitude-modulated sounds on the level of auditory nerve fibres

Average firing rate of the auditory nerve fiber as function of the level of the tone with the frequency equal to characteristic frequency of the fibers, can be defined as an input-output characteristic. It is known that the steepening of the input-output characteristic of the real auditory nerve fiber is more, and the width is less than the spontaneous activity of the fiber. The latter characterizes fiber's ability to generate spikes, if the stimulus is absent. However it is known, that the real auditory nerve fibers with low spontaneous activity reproduce amplitude modulation of the signals much better, than the fibers with high spontaneous activity. From the results of simulation experiments, it follows that the dynamic properties of the auditory nerve fibers, providing fine tuning or adaptation of a fiber threshold under the stimulus level but not the static input-output characteristics, are the reason of fibers reproduction of stimuli amplitude modulations. However the auditory nerve fibers with high spontaneous activity due to abrupt input-output characteristic are capable to reproduce modulations of sounds whose levels are lower than a threshold of the fiber, if a weak signal adds to a weak broadband noise. This is a phenomenon of stochastic resonance found in the reactions of auditory nerve fibers.     

On the choice of noise for the analysis of the peripheral auditory system

The cross-correlation between output and input of a system containing nonlinearities, when that system is stimulated with Gaussian white noise, is a good estimate of the linear properties of the system. In practice, however, when sequences of pseudonoise are used, great errors may be introduced in the estimate of the linear part depending on the properties of the noise. This consideration assumes special importance in the analysis of the linear properties of the peripheral auditory system, where the rectifying properties of the haircells constitute a second order nonlinearity. To explore this problem, a simple model has been designed, consisting of a second order nonlinearity without memory and sandwiched between two bandpass filters. Different types of pseudonoise are used as input whereupon it is shown that noise based on binary m-sequences, which is commonly used in noise generators, will yield totally incorrect information about this system. Somewhat better results are achieved with other types of noise. By using inverse-repeat sequences the results are greatly improved. Furthermore, certain anomalies obtained in the analysis of responses from single fibers in the auditory nerve are viewed in the light of the present results. The theoretical analysis of these anomalies reveals some information about the organization of the peripheral auditory system. For example, the possibility of the existence of a second bandpass filter in the auditory periphery seems to be excluded.     

Dependence of the mouse inferior colliculus neurons activity on position and direction of movement of the spectral contrast

Response variability of the single neurons of the inferior colliculus of mouse (Mus musculus) to series of noise bands and of notch noises with regular 1/12 octave steps of the band/notch center frequency and width of noise band/notch 1/3 octave, was studied. Neurons with strong inhibitory influence in excitatory response area (inhibitory-dominated) show low impulse activity when noise band exceeded excitatory response area. Spectral contrasts crossing the center of excitatory response area (at CF or nearly CF) were found to be the most efficient stimuli for such neurons. Neuron responses to spectral contrasts derived both from noise band and noise notch were identical. Approaching of inhibitory and excitatory inputs is expected to sharpen the auditory neurons frequency tuning to position of spectral contrasts, similar to neuronal processing in visual system. Neuron selectivity to the direction of spectral contrasts movement was determined in neuron response differences when the noise band or notch shifted from excitatory area to inhibitory areas as compared with shift in the opposite direction. Functional role of contrast mechanism for sound localization on the base spectral cues related to external ear transfer characteristics is discussed.     

A dynamical point process model of auditory nerve spiking in response to complex sounds

In this paper, we develop a dynamical point process model for how complex sounds are represented by neural spiking in auditory nerve fibers. Although many models have been proposed, our point process model is the first to capture elements of spontaneous rate, refractory effects, frequency selectivity, phase locking at low frequencies, and short-term adaptation, all within a compact parametric approach. Using a generalized linear model for the point process conditional intensity, driven by extrinsic covariates, previous spiking, and an input-dependent charging/discharging capacitor model, our approach robustly captures the aforementioned features on datasets taken at the auditory nerve of chinchilla in response to speech inputs. We confirm the goodness of fit of our approach using the Time-Rescaling Theorem for point processes.     

Free-field unmasking response characteristics of frog auditory nerve fibers: comparison with the responses of midbrain auditory neurons

Previous studies in the inferior colliculus have shown that spatial separation of signal and noise sources improves signal detection. In this study, we investigated the free-field unmasking response properties of single fibers in the auditory nerve--these were compared to those of inferior colliculus neurons under the same experimental conditions to test the hypothesis that central processing confers advantages for signal detection in the presence of spatially separated noise. For each neuron, we determined the detection threshold for a probe at the unit's best azimuth under three conditions: (1) by itself, (2) when a masker at a constant level was also presented at the unit's best azimuth, and (3) when the masker was positioned at different azimuths. We found that, on average, maskers presented at a unit's best azimuth elevated the probe detection threshold by 4.22 dB in the auditory nerve and 10.97 dB in the inferior colliculus. Angular separation of probe and masker sources systematically reduced the masking effect. The maximum masking release was on average 2.90 dB for auditory nerve fibers and 9.40 dB for inferior colliculus units. These results support the working hypothesis, suggesting that central processing contributes to the stronger free-field unmasking in the inferior colliculus.     

Sensitivity of the neurons in the auditory inferior colliculus of mice to the direction of the shift of broadband spectral notch noise

Series of a notch noise with regular shifts of the notch center frequency: one--from low frequencies to high frequencies and the other--from high frequencies to the low, were synthesized. The notch noise series imitated sound source vertical moving. Single neuron's responses of inferior colliculus of the house mouse (Mus musculus) to the notch-noises altered with notch central frequency varying through excitatory and inhibitory frequency response areas in neurones' receptive fields. The neural responses alteration to the notch noise varying depended on the bandwidth of notch. Disinhibition in inhibitory side band could be higher if the notch overlying the inhibitory areas followed the notch overlying the excitatory areas. The data obtained make it possible to consider the excitatory and inhibitory interaction as a mechanism of neural sensitivity to the notch moving direction. Neurones' response set could provide information about sound source moving over auditory space.     

Auditory processing of complex sounds: an overview.

The past 30 years has seen a remarkable development in our understanding of how the auditory system--particularly the peripheral system--processes complex sounds. Perhaps the most significant has been our understanding of the mechanisms underlying auditory frequency selectivity and their importance for normal and impaired auditory processing. Physiologically vulnerable cochlear filtering can account for many aspects of our normal and impaired psychophysical frequency selectivity with important consequences for the perception of complex sounds. For normal hearing, remarkable mechanisms in the organ of Corti, involving enhancement of mechanical tuning (in mammals probably by feedback of electro-mechanically generated energy from the hair cells), produce exquisite tuning, reflected in the tuning properties of cochlear nerve fibres. Recent comparisons of physiological (cochlear nerve) and psychophysical frequency selectivity in the same species indicate that the ear's overall frequency selectivity can be accounted for by this cochlear filtering, at least in bandwidth terms. Because this cochlear filtering is physiologically vulnerable, it deteriorates in deleterious conditions of the cochlea--hypoxia, disease, drugs, noise overexposure, mechanical disturbance--and is reflected in impaired psychophysical frequency selectivity. This is a fundamental feature of sensorineural hearing loss of cochlear origin, and is of diagnostic value. This cochlear filtering, particularly as reflected in the temporal patterns of cochlear fibres to complex sounds, is remarkably robust over a wide range of stimulus levels. Furthermore, cochlear filtering properties are a prime determinant of the 'place' and 'time' coding of frequency at the cochlear nerve level, both of which appear to be involved in pitch perception. The problem of how the place and time coding of complex sounds is effected over the ear's remarkably wide dynamic range is briefly addressed. In the auditory brainstem, particularly the dorsal cochlear nucleus, are inhibitory mechanisms responsible for enhancing the spectral and temporal contrasts in complex sounds. These mechanisms are now being dissected neuropharmacologically. At the cortical level, mechanisms are evident that are capable of abstracting biologically relevant features of complex sounds. Fundamental studies of how the auditory system encodes and processes complex sounds are vital to promising recent applications in the diagnosis and rehabilitation of the hearing impaired.     

Encoding of phase spectra by the peripheral auditory system of the bullfrog

In this study we have examined the sensitivity of auditory nerve fibers in the bullfrog (Rana catesbeiana) to changes in the phase spectrum of an equal-amplitude multi-harmonic stimulus which spanned the bullfrog's range of hearing. To assess peripheral auditory phase sensitivity, changes in the response properties of VIIIth nerve fibers were measured when the relative phase angle of a single harmonic component nearest a unit's best excitatory frequency was systematically varied. The results revealed that shifts in the phase spectrum are encoded in at least J different ways by the peripheral auditory system of the bullfrog: 1) by changes in the degree of spike synchronization of fibers from both inner ear organs (the amphibian papilla and the basilar papilla) to the fundamental waveform period; 2) by changes in the shapes of period histograms of fibers from both organs; and 3) by changes in the spike rates of amphibian papilla fibers. The presence of phase sensitivity in the peripheral auditory system of the bullfrog indicates that information regarding the fine-temporal waveshape and the underlying phase spectrum of an acoustic signal is contained within the spike trains of VIIIth nerve fibers. Similar sensitivities to changes in the phase spectra and temporal waveshapes of acoustic signals may also be present in the peripheral auditory system of other vertebrates. Such studies could provide valuable insight into the role that phase spectra and temporal waveshape may play in bioacoustic communication.Abbreviations BEF best excitatory frequency - BEC best excitatory component - CS_{f 1} synchronization to the fundamental period Portions of this study have been summarized in abstract form (Bodnar and Capranica 1991)     

Properties of the derived cochlear action potential during tonal forward masking in guinea pigs]

In awake preimplanted guinea pigs, characteristics of auditory nerve and derived action potentials were investigated using a pure-tone forward masking paradigm. Auditory nerve action potentials are recorded from round window. The derived potential was obtained by subtracting the masked action potential from unmasked response. The results show that the derived potential is more sensitive to changes in auditory nerve action potential during masking than widely used indicator of masking--the decrement in auditory nerve action potential. Derived response reflects the response changes both in amplitude and waveform induced by masker. The differences between the auditory nerve and derived action potentials suggest that the amplitude and time changes in the derived potential give a more detailed information on the characteristics of the auditory nerve fibers responses.     

Temporal summation under masking conditions and speech recognition

Temporal summation was estimated by measuring the detection thresholds for pulses with durations of 1–50 ms in the presence of noise maskers. The purpose of the study was to examine the effects of the spectral profiles and intensities of noise maskers on temporal summation, to investigate the appearance of signs of peripheral processing of pulses with various frequency-time structures in auditory responses, and to test the opportunity to use temporal summation for speech recognition. The central frequencies of pulses and maskers were similar. The maskers had ripple structures of the amplitude spectra of two types. In some maskers, the central frequencies coincided with the spectrum humps, whereas in other maskers, they coincided with spectrum dip (so-called on- and off-maskers). When the auditory system differentiated the masker humps, then the difference between the thresholds of recognition of the stimuli presented together with each of two types of maskers was not equal to zero. The assessment of temporal summation and the difference of the thresholds of pulse recognition under conditions of the presentation of the on- and off-maskers allowed us to make a conclusion on auditory sensitivity and the resolution of the spectral structure of maskers or frequency selectivity during presentation of pulses of various durations in local frequency areas. In order to estimate the effect of the dynamic properties of hearing on sensitivity and frequency selectivity, we changed the intensity of maskers. We measured temporal summation under the conditions of the presentation of on- and off-maskers of various intensities in two frequency ranges (2 and 4 kHz) in four subjects with normal hearing and one person with age-related hearing impairments who complained of a decrease in speech recognition under noise conditions. Pulses shorter than 10 ms were considered as simple models of consonant sounds, whereas tone pulses longer than 10 ms were considered as simple models of vowel sounds. In subjects with normal hearing in the range of moderate masker intensities, we observed an enhancement of temporal summation when the short pulses or consonant sounds were presented and an improvement of the resolution of the broken structure of masker spectra when the short and tone pulses, i.e., consonant and vowel sounds, were presented. We supposed that the enhancement of the summation was related to the refractoriness of the fibers of the auditory nerve. In the range of 4 kHz, the subject with age-related hearing impairments did not recognize the ripple structure of the maskers in the presence of the short pulses or consonant sounds. We supposed that these impairments were caused by abnormal synchronization of the responses of the auditory nerve fibers induced by the pulses, and this resulted in a decrease in speech recognition.     

Correlation between auditory evoked responses in the thalamus and species-specific call characteristics

This evoked potential study of the bullfrog's auditory thalamic area (an auditory responsive region in the posterior dorsal thalamus) shows that complex processing, distinct from that reported in lower auditory regions, occurs in this center. An acoustic stimulus consisting of two tones, one which stimulates either the low-frequency or the mid-frequency sensitive population of auditory nerve fibers from the amphibian papilla and the other the high-frequency sensitive population of fibers from the basilar papilla, evoked a maximal response. The amplitude of the response to the simultaneous stimulation of the two auditory organs was, in some locations, much larger than the linear sum of the responses to the individual tones presented separately. Bimodal spectral stimuli that had relatively long rise-times (greater than or equal to 100 ms) evoked much larger responses than similar sounds with short rise-times. The optimal rise-times were close to those occurring in the bullfrog's mating call. The response was dependent on the waveform periodicity and harmonic content, with a fundamental frequency of 200 Hz producing a larger response than those with fundamentals of 50, 100 or 300 Hz. Six of the natural calls in the bullfrog's vocal repertoire were tested and the mating call and warning call were found to evoke the best responses. Each of these calls stimulate the two auditory organs simultaneously. The evoked response had a long refractory period which could not be altered by lesioning the efferent telencephalic pathways. The type of spectral and temporal information extracted by the auditory thalamic area suggests that this center is involved in processing complex sounds and likely plays an important role in the bullfrog's detection of some of its vocal signals.     

Spatial and spectral dependence of the auditory periphery in the northern leopard frog

We investigated directionalities of eardrum vibration and auditory nerve response in anesthetized northern leopard frogs (Rana pipiens pipiens). Simultaneous measures of eardrum velocities and firing rates from 282 auditory nerve fibers were obtained in response to free-field sounds from eight directions in the horizontal plane. Sound pressure at the external surface of the ipsilateral eardrum was kept constant for each presentation direction (± 0.5 dB). Significant effects of sound direction on eardrum velocity were shown in 90% of the cases. Maximum or minimum eardrum velocity was observed more often when sounds were presented from the lateral and posterior fields, or from the anterior and contralateral fields, respectively. Firing rates of 38% of the fibers were significantly affected by sound direction and maximum or minimum firing rate was observed more frequently when sounds were delivered from the lateral fields, or from the anterior and contralateral fields, respectively. Directionality patterns of eardrum velocity and nerve firing also vary with sound frequency. Statistically significant correlation between eardrum velocity and nerve fiber firing rate was demonstrated in only 45% of the fibers, suggesting that sound transmission to the inner ear through extratympanic pathways plays a non-trivial role in the genesis of directionality of auditory nerve responses.Abbreviations CF characteristic frequency - SVL snout-vent length - TM tympanic membrane     

Side peak suppression in responses of an across-frequency integration model to stimuli of varying bandwidth as demonstrated analytically and by implementation

Multiplication-like sound localization models are subjected to phase ambiguities for high-frequency tonal stimuli as multiplication creates several equivalent response peaks in tuning curves. By increasing the bandwidth of the stimulus, phase ambiguities can be reduced, which is often referred to as side peak suppression. In this study we present a Jeffress-based sound localization model, and determine side peak suppression analytically. The results were verified with an implementation of the same model, and compared to physiological data of barn owls. Three types of stimuli were analyzed: pure-tone stimuli, two-tone complexes with varying frequency distances, and noise signals with variable bandwidths. As an additional parameter we also determined the half-width of the main response peak to examine the scaling of tuning curves in azimuth. Results showed that side peak suppression did not only depend on bandwidth, but also on the center frequency and the distance of the side peak to the main response peak. In particular, the analytical model predicted that side peak suppression is a function of relative bandwidth, whereas half-width is inversely proportional to center frequency, with a proportionality factor depending on relative bandwidth. The analytical approach and the implementation yielded equivalent tuning curves (deviation < 1 %). Moreover, the electrophysiological data recorded in barn owls closely matched the predicted tuning curves.     

Fast negative feedback enables mammalian auditory nerve fibers to encode a wide dynamic range of sound intensities

Mammalian auditory nerve fibers (ANF) are remarkable for being able to encode a 40 dB, or hundred fold, range of sound pressure levels into their firing rate. Most of the fibers are very sensitive and raise their quiescent spike rate by a small amount for a faint sound at auditory threshold. Then as the sound intensity is increased, they slowly increase their spike rate, with some fibers going up as high as ～300 Hz. In this way mammals are able to combine sensitivity and wide dynamic range. They are also able to discern sounds embedded within background noise. ANF receive efferent feedback, which suggests that the fibers are readjusted according to the background noise in order to maximize the information content of their auditory spike trains. Inner hair cells activate currents in the unmyelinated distal dendrites of ANF where sound intensity is rate-coded into action potentials. We model this spike generator compartment as an attenuator that employs fast negative feedback. Input current induces rapid and proportional leak currents. This way ANF are able to have a linear frequency to input current (f-I) curve that has a wide dynamic range. The ANF spike generator remains very sensitive to threshold currents, but efferent feedback is able to lower its gain in response to noise.     

The frequency selectivity of information-processing channels in the tactile sensory system

The frequency selectivity of the P, NP I, and NP II channels of the four-channel model of mechanoreception for glabrous skin was measured psychophysically by an adaptation tuning curve procedure. The results substantially extend the frequency range over which the frequency selectivity of these channels is known and further confirm the hypothesis that the input stage of each of these channels consists of specific sensory nerve fibers and associated receptors. Specifically, the frequency characteristics of Pacinian nerve fibers, rapidly adapting (RA) nerve fibers, and slowly adapting Type II (SA II) nerve fibers were found to be the peripheral neurophysiological correlates of the P, NP I, and NP II channels, respectively. The finding that the tuning characteristic for a test stimulus of 250 Hz delivered through a small (0.008 cm2) contactor depended dramatically on the duration of the test stimulus whereas the detection threshold did not, provides new evidence in support of the hypothesis that separate NP II and P channels exist.     

电刺激大马蹄蝠听皮层对下丘神经元听觉敏感性的影响

实验在１２只大马蹄蝠上进行。用常规电生理学方法研究了电刺激听皮层对下丘２１２个神经元的听反应的影响,结果表明,有３２个神经元的听反应被抑制,１９个神经元的听反应褐易化。     

Auditory sensitivity of the diencephalon of the leopard frogRana p. pipiens

Summary Evoked potentials were recorded from the posterocentral nucleus in the dorsal diencephalon of leopard frogs (Rana p. pipiens) in response to acoustic stimulation. This electrophysiological study confirms the anatomical study by Neary (1974) of the existence of an auditory area within this nucleus.The response of the auditory thalamic area showed a selectivity for stimuli that simultaneously excited both the amphibian and the basilar papillae in the inner ear. The magnitude of the evoked potential to the combination of either low (300 Hz) and high (1 700 Hz) or mid (600 Hz) and high (1700 Hz) frequency tones was much greater than the sum of the responses to the component tones individually (Fig. 5). This selective convergence is not seen in the torus semicircularis: in this midbrain center the sum of the responses to the individual tones is approximately equal to the magnitude of the response to the combination tone (Fig. 7).The selectivity of the thalamic center for stimuli with patterned energy distributions is compared to the spectral combinations occurring within several of this species' vocal signals. This comparison indicates that the extraction of spectral patterns involves a hierarchical organization within the anuran's auditory system which probably plays a major role in processing complex sounds.This research was supported by the U.S. Public Health Service (NIH Research Grant NS-09244). We would like to thank Anne Moffat for her assistance in collecting data on the tuning characteristics of the VIIIth nerve units.