Cochleotopic Map Research Articles

The single-cell transcriptomic landscape of the topological differences in mammalian auditory receptors.

Mammalian hair cells (HCs) are arranged spirally along the cochlear axis and correspond to different frequency ranges. Serving as primary sound detectors, HCs spatially segregate component frequencies into a topographical map. HCs display significant diversity in anatomical and physiological characteristics, yet little is known about the organization of the cochleotopic map of HCs or the molecules involved in this process. Using single-cell RNA sequencing, we determined the distinct molecular profiles of inner hair cells and outer hair cells, and we identified numerous position-dependent genes that were expressed as gradients. Newly identified genes such as Ptn, Rxra, and Nfe2l2 were found to be associated with tonotopy. We employed the SCENIC algorithm to predict the transcription factors that potentially shape these tonotopic gradients. Furthermore, we confirmed that Nfe2l2, a tonotopy-related transcription factor, is critical in mice for sensing low-to-medium sound frequencies in vivo. the analysis of cell-cell communication revealed potential receptor-ligand networks linking inner hair cells to spiral ganglion neurons, including pathways such as BDNF-Ntrk and PTN-Scd4, which likely play essential roles in tonotopic maintenance. Overall, these findings suggest that molecular gradients serve as the organizing principle for maintaining the selection of sound frequencies by HCs.

Stimulus-frequency-dependent dominance of sound localization cues across the cochleotopic map of the inferior colliculus.

The horizontal direction of a sound source (i.e., azimuth) is perceptually determined in a frequency-dependent manner: low- and high-frequency sounds are localized via differences in the arrival time and intensity of the sound at the two ears, respectively, called interaural time and level differences (ITDs and ILDs). In the central auditory system, these binaural cues to direction are thought to be separately encoded by neurons tuned to low and high characteristic frequencies (CFs). However, at high sound levels a neuron often responds to frequencies far from its CF, raising the possibility that individual neurons may encode the azimuths of both low- and high-frequency sounds using both binaural cues. We tested this possibility by measuring auditory-driven single-unit responses in the central nucleus of the inferior colliculus (ICC) of unanesthetized female Dutch Belted rabbits with a multitetrode drive. At 70 dB SPL, ICC neurons across the cochleotopic map transmitted information in their firing rates about the direction of both low- and high-frequency noise stimuli. We independently manipulated ITD and ILD cues in virtual acoustic space and found that sensitivity to ITD and ILD, respectively, shaped the directional sensitivity of ICC neurons to low (<1.5 kHz)- and high (>3 kHz)-pass stimuli, regardless of the neuron's CF. We also found evidence that high-CF neurons transmit information about both the fine-structure and envelope ITD of low-frequency sound. Our results indicate that at conversational sound levels the majority of the cochleotopic map is engaged in transmitting directional information, even for sources with narrowband spectra.NEW & NOTEWORTHY A "division of labor" has previously been assumed in which the directions of low- and high-frequency sound sources are thought to be encoded by neurons preferentially sensitive to low and high frequencies, respectively. Contrary to this, we found that auditory midbrain neurons encode the directions of both low- and high-frequency sounds regardless of their preferred frequencies. Neural responses were shaped by different sound localization cues depending on the stimulus spectrum-even within the same neuron.

Neurod1 Is Essential for the Primary Tonotopic Organization and Related Auditory Information Processing in the Midbrain.

Hearing depends on extracting frequency, intensity, and temporal properties from sound to generate an auditory map for acoustical signal processing. How physiology intersects with molecular specification to fine tune the developing properties of the auditory system that enable these aspects remains unclear. We made a novel conditional deletion model that eliminates the transcription factor NEUROD1 exclusively in the ear. These mice (both sexes) develop a truncated frequency range with no neuroanatomically recognizable mapping of spiral ganglion neurons onto distinct locations in the cochlea nor a cochleotopic map presenting topographically discrete projections to the cochlear nuclei. The disorganized primary cochleotopic map alters tuning properties of the inferior colliculus units, which display abnormal frequency, intensity, and temporal sound coding. At the behavioral level, animals show alterations in the acoustic startle response, consistent with altered neuroanatomical and physiological properties. We demonstrate that absence of the primary afferent topology during embryonic development leads to dysfunctional tonotopy of the auditory system. Such effects have never been investigated in other sensory systems because of the lack of comparable single gene mutation models.SIGNIFICANCE STATEMENT All sensory systems form a topographical map of neuronal projections from peripheral sensory organs to the brain. Neuronal projections in the auditory pathway are cochleotopically organized, providing a tonotopic map of sound frequencies. Primary sensory maps typically arise by molecular cues, requiring physiological refinements. Past work has demonstrated physiologic plasticity in many senses without ever molecularly undoing the specific mapping of an entire primary sensory projection. We genetically manipulated primary auditory neurons to generate a scrambled cochleotopic projection. Eliminating tonotopic representation to auditory nuclei demonstrates the inability of physiological processes to restore a tonotopic presentation of sound in the midbrain. Our data provide the first insights into the limits of physiology-mediated brainstem plasticity during the development of the auditory system.

Tonotopic action potential tuning of maturing auditory neurons through endogenous ATP.

Following the genetically controlled formation of neuronal circuits, early firing activity guides the development of sensory maps in the auditory, visual and somatosensory system. However, it is not clear whether the activity of central auditory neurons is specifically regulated depending on the position within the sensory map. In the ventral cochlear nucleus, the first central station along the auditory pathway, we describe a mechanism through which paracrine ATP signalling enhances firing in a cell-specific and tonotopically-determined manner. Developmental down-regulation of P2X2/3R currents along the tonotopic axis occurs simultaneously with an increase in AMPA receptor currents, suggesting a high-to-low frequency maturation pattern. Facilitated action potential (AP) generation, measured as higher firing rate, shorter EPSP-AP delay in vivo and shorter AP latency in slice experiments, is consistent with increased synaptic efficacy caused by ATP. The long lasting change in intrinsic neuronal excitability is mediated by the heteromeric P2X2/3 receptors. Synaptic refinement and strengthening are activity-dependent processes that establish orderly arranged cochleotopic maps throughout the central auditory system. The maturation of auditory brainstem circuits is guided by action potentials (APs) arising from the inner hair cells in the developing cochlea. The AP firing of developing central auditory neurons can be modulated by paracrine ATP signalling, as shown for the cochlear nucleus bushy cells and principal neurons in the medial nucleus of the trapezoid body. However, it is not clear whether neuronal activity may be specifically regulated with respect to the nuclear tonotopic position (i.e. sound frequency selectivity). Using slice recordings before hearing onset and in vivo recordings with iontophoretic drug applications after hearing onset, we show that cell-specific purinergic modulation follows a precise tonotopic pattern in the ventral cochlear nucleus of developing gerbils. In high-frequency regions, ATP responsiveness diminished before hearing onset. In low-to-mid frequency regions, ATP modulation persisted after hearing onset in a subset of low-frequency bushy cells (characteristic frequency<10kHz). Down-regulation of P2X2/3R currents along the tonotopic axis occurs simultaneously with an increase in AMPA receptor currents, thus suggesting a high-to-low frequency maturation pattern. Facilitated AP generation, measured as higher firing frequency, shorter EPSP-AP delay in vivo, and shorter AP latency in slice experiments, is consistent with increased synaptic efficacy caused by ATP. Finally, by combining recordings and pharmacology in vivo, in slices, and in human embryonic kidney 293 cells, it was shown that the long lasting change in intrinsic neuronal excitability is mediated by the P2X2/3R.

Cochleotopy of human cochlear nucleus

IntroductionThe human peripheral auditory pathway in infants is a relatively less explored domain in auditory research. In the present study, the cochlea, auditory nerve (AN) and the cochlear nucleus (CN) were examined using immunohistochemistry and light and electron-microscopy. MethodsThe study was performed on specimens retrieved from a 40-day-old infant who could not survive after corrective surgery for congenital cyanotic heart disease. The donation was done in accordance with the protocol approved by the Human Ethics Committee, All India Institute of Medical Sciences (AIIMS), New Delhi, India. ResultsThe AN revealed degeneration of nerve fascicles originating from the spiral ganglion neurons of the middle and basal turns of the cochlea. The proximal and middle segments of the nerve showed varying degrees of degenerating fibers with macrophages whereas the most distal part of the nerve showed dilated endoneurial capillaries without any degeneration. On electron-microscopy, the nerve revealed features of acute myelinopathy. The differential perisomatic synaptophysin immunoreactivity was observed in the CN. The unaffected neurons showed strong microtubule-associated protein 2 (MAP-2) immunoreactivity, while those denervated revealed decreased staining. The VCN showed varying degree of parvalbumin (PV) and calbindin (CB) immunostaining with AN fibers and terminals showing strong immunoreactivity for PV. The AN revealed strong immunoreactivity for CB on the affected side. The spiral ganglion neurons did not reveal any pathological changes. DiscussionThe results provide a cochleotopic map of the human CN that maybe relevant in better understanding of the tonotopic organization and will be helpful during auditory implants in children.

Extensive Cochleotopic Mapping of Human Auditory Cortical Fields Obtained with Phase-Encoding fMRI

The primary sensory cortices are characterized by a topographical mapping of basic sensory features which is considered to deteriorate in higher-order areas in favor of complex sensory features. Recently, however, retinotopic maps were also discovered in the higher-order visual, parietal and prefrontal cortices. The discovery of these maps enabled the distinction between visual regions, clarified their function and hierarchical processing. Could such extension of topographical mapping to high-order processing regions apply to the auditory modality as well? This question has been studied previously in animal models but only sporadically in humans, whose anatomical and functional organization may differ from that of animals (e.g. unique verbal functions and Heschl's gyrus curvature). Here we applied fMRI spectral analysis to investigate the cochleotopic organization of the human cerebral cortex. We found multiple mirror-symmetric novel cochleotopic maps covering most of the core and high-order human auditory cortex, including regions considered non-cochleotopic, stretching all the way to the superior temporal sulcus. These maps suggest that topographical mapping persists well beyond the auditory core and belt, and that the mirror-symmetry of topographical preferences may be a fundamental principle across sensory modalities.

FMRI spectral analysis reveals multiple cochleotopic maps in human auditory cortex

fMRI spectral analysis reveals multiple cochleotopic maps in human auditory cortex

Spatiotemporal Conversion of Auditory Information for Cochleotopic Mapping

Auditory communication signals such as monkey calls are complex FM vocal sounds and in general induce action potentials in different timing in the primary auditory cortex. Delay line scheme is one of the effective ways for detecting such neuronal timing. However, the scheme is not straightforwardly applicable if the time intervals of signals are beyond the latency time of delay lines. In fact, monkey calls are often expressed in longer time intervals (hundreds of milliseconds to seconds) and are beyond the latency times observed in the brain (less than several hundreds of milliseconds). Here, we propose a cochleotopic map similar to that in vision known as a retinotopic map. We show that information about monkey calls could be mapped on a cochleotopic cortical network as spatiotemporal firing patterns of neurons, which can then be decomposed into simple (linearly sweeping) FM components and integrated into unified percepts by higher cortical networks. We suggest that the spatiotemporal conversion of auditory information may be essential for developing the cochleotopic map, which could serve as the foundation for later processing, or monkey call identification by higher cortical areas.

Feasibility of using silicon-substrate recording electrodes within the auditory nerve

The use of penetrating, silicon-substrate (i.e., “thin-film”) probes within a cross-section of a sensory nerve offers the possibility of assessing the pattern and extent of fiber excitation within the nerve. We used acute cat preparations to assess the feasibility of this technique for recordings within the auditory nerve trunk. Four probe configurations fabricated by the University of Michigan Center for Neural Communication Technology were evaluated using acoustic and electric stimuli. Our main concerns were the nature of the recorded potentials and the degree of spatial selectivity provided by these probes. We also made some basic assessments of electrode-tissue compatibility. The recorded potentials were characterized as field potentials with varying degrees of spatial selectivity. In some cases, responses to pure tones demonstrated good spatial selectivity, with unique responses recorded by different electrode sites. When electrode sites were positioned at different longitudinal positions along the nerve trunk, responses with latencies characteristic of each site were recorded. These results indicate that thin-film electrodes are capable of providing spatially specific response information from sensory nerves. However, in the case of feline auditory nerves, place-specific responses were inconsistently observed, making it difficult to use this technique to obtain detailed cochleotopic maps of neural excitation. More productive results may be possible from other peripheral nerves with less complex spatial arrangements of fibers.

Neural bases of monkey call perception

We propose a three-layered neural network model for the perception of complex FM signals, such as monkey calls. The first layer is a two-dimensional cochleotopic map with a frequency axis and a propagation axis. Stimulation with a monkey call that is characterized by a complex FM signal activates in a temporal manner the peripheral neurons that are arranged along the frequency axis. The activities of the peripheral neurons then propagate to auditory centers along the propagation axis, whereby a spatiotemporal neuronal firing pattern specific to the monkey call emerges. The second layer decomposes the signal into a series of simple FM components that are then integrated by the third layer network. By stimulating the model with various monkey call signals, we show that the monkey call signals are processed in a hierarchal manner, which is quite similar to visual processing in that information about the monkey calls is decomposed into auditory features (simple FMs) by the lower cortical network, and then integrated into a perceptual image by the higher cortical network.

Augmentation of plasticity of the central auditory system by the basal forebrain and/or somatosensory cortex.

Auditory conditioning (associative learning) or focal electric stimulation of the primary auditory cortex (AC) evokes reorganization (plasticity) of the cochleotopic (frequency) map of the inferior colliculus (IC) as well as that of the AC. The reorganization results from shifts in the best frequencies (BFs) and frequency-tuning curves of single neurons. Since the importance of the cholinergic basal forebrain for cortical plasticity and the importance of the somatosensory cortex and the corticofugal auditory system for collicular and cortical plasticity have been demonstrated, Gao and Suga proposed a hypothesis that states that the AC and corticofugal system play an important role in evoking auditory collicular and cortical plasticity and that auditory and somatosensory signals from the cerebral cortex to the basal forebrain play an important role in augmenting collicular and cortical plasticity. To test their hypothesis, we studied whether the amount and the duration of plasticity of both collicular and cortical neurons evoked by electric stimulation of the AC or by acoustic stimulation were increased by electric stimulation of the basal forebrain and/or the somatosensory cortex. In adult big brown bats (Eptesicus fuscus), we made the following major findings. 1) Collicular and cortical plasticity evoked by electric stimulation of the AC is augmented by electric stimulation of the basal forebrain. The amount of augmentation is larger for cortical plasticity than for collicular plasticity. 2) Collicular and cortical plasticity evoked by AC stimulation is augmented by somatosensory cortical stimulation mimicking fear conditioning. The amount of augmentation is larger for cortical plasticity than for collicular plasticity. 3) Collicular and cortical plasticity evoked by both AC and basal forebrain stimulations is further augmented by somatosensory cortical stimulation. 4) A lesion of the basal forebrain tends to reduce collicular and cortical plasticity evoked by AC stimulation. The reduction is small and statistically insignificant for collicular plasticity but significant for cortical plasticity. 5) The lesion of the basal forebrain eliminates the augmentation of collicular and cortical plasticity that otherwise would be evoked by somatosensory cortical stimulation. 6) Collicular and cortical plasticity evoked by repetitive acoustic stimuli is augmented by basal forebrain and/or somatosensory cortical stimulation. However, the lesion of the basal forebrain eliminates the augmentation of collicular and cortical plasticity that otherwise would be evoked by somatosensory cortical stimulation. These findings support the hypothesis proposed by Gao and Suga.

Reorganization of the cochleotopic map in the bat's auditory system by inhibition.

The central auditory system of the mustached bat shows two types of reorganization of cochleotopic (frequency) maps: expanded reorganization resulting from shifts in the best frequencies (BFs) of neurons toward the BF of repetitively stimulated cortical neurons (hereafter centripetal BF shifts) and compressed reorganization resulting from the BF shifts of neurons away from the BF of the stimulated cortical neurons (hereafter centrifugal BF shifts). Facilitation and inhibition evoked by the corticofugal system have been hypothesized to be respectively related to centripetal and centrifugal BF shifts. If this hypothesis is correct, bicuculline (an antagonist of inhibitory GABA-A receptors) applied to cortical neurons would change centrifugal BF shifts into centripetal BF shifts. In the mustached bat, electric stimulation of cortical Doppler-shifted constant-frequency neurons, which are highly specialized for frequency analysis, evokes the centrifugal BF shifts of ipsilateral collicular and cortical Doppler-shifted constant-frequency neurons and contralateral cochlear hair cells. Bicuculline applied to the stimulation site changed the centrifugal BF shifts into centripetal BF shifts. On the other hand, electric stimulation of neurons in the posterior division of the auditory cortex, which are not particularly specialized for frequency analysis, evokes centripetal BF shifts of cortical neurons located near the stimulated cortical neurons. Bicuculline applied to the stimulation site augmented centripetal BF shifts but did not change the direction of the shifts. These observations support the hypothesis and indicate that centripetal and centrifugal BF shifts are both based on a single mechanism consisting of two components: facilitation and inhibition.

Auditory cortical plasticity under operation: reorganization of auditory cortex induced by electric cochlear stimulation reveals adaptation to altered sensory input statistics

We introduce a framework based on plastic-adaptational processes for an interpretation of electrical cochlear implant (CI) stimulation. Cochlear prostheses are used to restore sound perception in adults and children with profound deafness. After providing a review of cortical plasticity, we summarize our findings using optical imaging of intrinsic signals to map cat auditory cortex (AI) activated by CI stimulation. In adult AI of neonatally deafened animals, the acoustic deprivation caused a severe distortion of cochleotopic maps. A three-month period of CI-stimulation using the continuous interleaved sampling strategy did not re-install the status typically found in normal adults, but resulted in the emergence of a new topographical organization characterized by large, joint representations of all stimulated electrode sites. We suggest that the effectiveness of CI-stimulation relies primarily on a re-learning of input pattern arising from “artificial” sensory inputs via electrical stimulation, thereby supporting the importance of learning and training for the interpretation and understanding of the effects of CI stimulation. We suggest that the ability for gaining/re-gaining speech understanding mediated by CI-stimulation is accomplished by new strategies of cortical processing due to enhanced cooperativity among large populations of neurons that serve higher processing stages to interpret new patterns arriving from the periphery. These strategies are thought to emerge from adaptational capacities in response to the constraints imposed by the properties of the new input statistics that in turn result from the stimulation strategy employed.

Plasticity of the cochleotopic (frequency) map in specialized and nonspecialized auditory cortices.

Auditory conditioning (associative learning) causes reorganization of the cochleotopic (frequency) maps of the primary auditory cortex (AI) and the inferior colliculus. Focal electric stimulation of the AI also evokes basically the same cortical and collicular reorganization as that caused by conditioning. Therefore, part of the neural mechanism for the plasticity of the central auditory system caused by conditioning can be explored by focal electric stimulation of the AI. The reorganization is due to shifts in best frequencies (BFs) together with shifts in frequency-tuning curves of single neurons. In the AI of the Mongolian gerbil (Meriones unguiculatus) and the posterior division of the AI of the mustached bat (Pteronotus parnellii), focal electric stimulation evokes BF shifts of cortical auditory neurons located within a 0.7-mm distance along the frequency axis. The amount and direction of BF shift differ depending on the relationship in BF between stimulated and recorded neurons, and between the gerbil and mustached bat. Comparison in BF shift between different mammalian species and between different cortical areas of a single species indicates that BF shift toward the BF of electrically stimulated cortical neurons (centripetal BF shift) is common in the AI, whereas BF shift away from the BF of electrically stimulated cortical neurons (centrifugal BF shift) is special. Therefore, we propose a hypothesis that reorganization, and accordingly organization, of cortical auditory areas caused by associative learning can be quite different between specialized and nonspecialized (ordinary) areas of the auditory cortex.

Age-related tonotopic map plasticity in the central auditory pathways.

Inner hair cell lesions to the basal turn of the cochlea effectively result in a partial deafferentation of the auditory system. At the level of the midbrain (central nucleus of inferior colliculus) cochleotopic maps, based on single unit response characteristic frequency, are changed after such deafferentation. When a cochlear lesion is induced in a neonatal animal (chinchilla), the reorganization of the frequency map is more extensive than that resulting from similar deafferentation in the adult subject. Neonatal cochlear lesions result in an over-representation of sound frequencies corresponding to the border of the cochlear lesion, while similar lesions in the adult do not. The results suggest that significant plasticity exists in the auditory midbrain during early post natal development (even in a precocious species, such as chinchilla); however, this plasticity is largely lost in the mature animal. A conceptual model for the frequency map re-wiring is presented.

The corticofugal system for hearing: recent progress.

Peripheral auditory neurons are tuned to single frequencies of sound. In the central auditory system, excitatory (or facilitatory) and inhibitory neural interactions take place at multiple levels and produce neurons with sharp level-tolerant frequency-tuning curves, neurons tuned to parameters other than frequency, cochleotopic (frequency) maps, which are different from the peripheral cochleotopic map, and computational maps. The mechanisms to create the response properties of these neurons have been considered to be solely caused by divergent and convergent projections of neurons in the ascending auditory system. The recent research on the corticofugal (descending) auditory system, however, indicates that the corticofugal system adjusts and improves auditory signal processing by modulating neural responses and maps. The corticofugal function consists of at least the following subfunctions. (i) Egocentric selection for short-term modulation of auditory signal processing according to auditory experience. Egocentric selection, based on focused positive feedback associated with widespread lateral inhibition, is mediated by the cortical neural net working together with the corticofugal system. (ii) Reorganization for long-term modulation of the processing of behaviorally relevant auditory signals. Reorganization is based on egocentric selection working together with nonauditory systems. (iii) Gain control based on overall excitatory, facilitatory, or inhibitory corticofugal modulation. Egocentric selection can be viewed as selective gain control. (iv) Shaping (or even creation) of response properties of neurons. Filter properties of neurons in the frequency, amplitude, time, and spatial domains can be sharpened by the corticofugal system. Sharpening of tuning is one of the functions of egocentric selection.

Projections from the medial geniculate body to primary auditory cortex in neonatally deafened cats.

In the present study, anatomical projections from the medial geniculate body (MGB) to primary auditory cortex (AI) were investigated in normal adult cats and in animals that were neonatally deafened with the ototoxic drug amikacin. Cochleotopic/tonotopic maps in AI (based on neural response characteristic frequency) were obtained with microelectrode recording techniques, and single or multiple injections of retrograde tracers (horseradish peroxidase and fluorescent dyes) were introduced into AI. The AI maps of the amikacin-treated cats had an abnormal cochleotopic organization, such that deprived cortical areas exhibited an expanded representation of intact regions of the damaged cochlea. However, retrograde tracer injections into different regions of AI produced a normal pattern of labeling in the ventral division of the medial geniculate body (MGBv). In both experimental and control animals, the main mass of labeled thalamic cells was found in the MGBv. Different isofrequency contours in AI receive input from different portions of the MGBv. Thus, cell arrays labeled by anterior AI injections were situated medially in MGBv, and injections into posterior AI labeled MGBv more laterally. Furthermore, the deafened cats did not develop a more divergent thalamocortical projection compared with normal control animals, indicating that an abnormal spread of the thalamocortical afferents across the frequency domain in AI (anterior-posterior axis) is not responsible for the altered cochleotopic map in these neonatally deafened animals. The relatively normal thalamocortical projection pattern suggests that, after neonatal cochlear lesions, the major reorganization of cochleotopic maps occurs at subthalamic levels.

Neuronal and transneuronal degeneration of auditory axons in the brainstem after cochlear lesions in the chinchilla: cochleotopic and non-cochleotopic patterns

Terminal axonal degeneration in the brain following cochlear lesions was studied with the Nauta-Rasmussen method. Losses of hair cells and myelinated cochlear fibers were assessed. The cochleotopic map projected, from apex to base, on the ventral-to-dorsal axes of the cochlear nuclei. The cochleotopic correspondence was better for loss of cochlear nerve fibers and inner hair cells, than for outer hair cells. Cochlear fibers were traced to all parts of the cochlear nucleus, including the small-cell shell, also to cell-group Y and the flocculus. Terminal axonal degeneration in nuclei of the superior olivary complex, lateral lemniscus, and inferior colliculus was interpreted as transynaptic, since degenerated axons could not be traced to these locations from the cochlear nerve or trapezoid body. Moreover, biotinylated dextran amine injection in the basal turn of scala media of a normal cochlea labeled cochlear nerve fibers projecting to the high-frequency regions of the cochlear nuclei and to the flocculus, but not to more central auditory nuclei. This is the first detailed account of transynaptic degeneration in the ascending auditory pathway resulting from cochlear damage in an adult mammal. These findings are consistent with a dystrophic process depending on hair-cell loss and/or direct damage to cochlear nerve fibers.

Processing of complex sounds in rhesus monkey auditory cortex

Several auditory fields surrounding primary auditory cortex (AI) have been described in the rhesus monkey. Most recently, three areas have been identified in the so-called auditory belt region on the lateral surface of the superior temporal gyrus [Rauschecker et al., Science (1995) (in press)]. Functional identification of these lateral areas (AL, ML, and CL) was based on single unit responses to bandpassed noise (BPN) bursts, which constitute a class of superior stimuli for neurons in this region. Best center frequency (BFc) of the BPN bursts varies systematically along a rostro-caudal axis, revealing three cochleotopic maps. Neurons in the lateral areas also display tuning to a ‘‘best bandwidth’’ of the noise bursts, which varies along a medio-lateral axis, orthogonal to the BFc axis. Digitized vocalizations from the rhesus monkeys’ own repertoire were finally used for presentation during single-unit recording. In many instances, neurons responded even better to the monkey calls than to noise bursts or other synthetic stimuli. It appears that the lateral belt areas of macaque auditory cortex could form an important step in the preprocessing of species-specific communication sounds, somewhat equivalent to superior temporal areas in humans that have been implicated in phonological processing.

Neural basis of amplitude-spectrum representation in auditory cortex of the mustached bat.

Neural basis of amplitude-spectrum representation in auditory cortex of the mustached bat.