Biomedical subjects

Jonathan B Fritz

Publications and source records attributed to Jonathan B Fritz.

4 recordsLinked to original sources

PubMed2006

Species-specific calls activate homologs of Broca's and Wernicke's areas in the macaque.

The origin of brain mechanisms that support human language-whether these originated de novo in humans or evolved from a neural substrate that existed in a common ancestor-remains a controversial issue. Although the answer is not provided by the fossil record, it is possible to make inferences by studying living species of nonhuman primates. Here we identified neural systems associated with perceiving species-specific vocalizations in rhesus macaques using H(2)(15)O positron emission tomography (PET). These vocalizations evoke distinct patterns of brain activity in homologs of the human perisylvian language areas. Rather than resulting from differences in elementary acoustic properties, this activity seems to reflect higher order auditory processing. Although parallel evolution within independent primate species is feasible, this finding suggests the possibility that the last common ancestor of macaques and humans, which lived 25-30 million years ago, possessed key neural mechanisms that were plausible candidates for exaptation during the evolution of language.

Acoustic Stimulation↗

PubMed2006

Rhesus macaques spontaneously perceive formants in conspecific vocalizations.

We provide a direct demonstration that nonhuman primates spontaneously perceive changes in formant frequencies in their own species-typical vocalizations, without training or reinforcement. Formants are vocal tract resonances leading to distinctive spectral prominences in the vocal signal, and provide the acoustic determinant of many key phonetic distinctions in human languages. We developed algorithms for manipulating formants in rhesus macaque calls. Using the resulting computer-manipulated calls in a habituation/dishabituation paradigm, with blind video scoring, we show that rhesus macaques spontaneously respond to a change in formant frequencies within the normal macaque vocal range. Lack of dishabituation to a "synthetic replica" signal demonstrates that dishabituation was not due to an artificial quality of synthetic calls, but to the formant shift itself. These results indicate that formant perception, a significant component of human voice and speech perception, is a perceptual ability shared with other primates.

Animals↗

PubMed2005

Differential dynamic plasticity of A1 receptive fields during multiple spectral tasks.

Auditory experience leads to myriad changes in processing in the central auditory system. We recently described task-related plasticity characterized by rapid modulation of spectro-temporal receptive fields (STRFs) in ferret primary auditory cortex (A1) during tone detection. We conjectured that each acoustic task may have its own "signature" STRF changes, dependent on the salient cues that the animal must attend to perform the task. To discover whether other acoustic tasks could elicit changes in STRF shape, we recorded from A1 in ferrets also trained on a frequency discrimination task. Overall, we found a distinct pattern of STRF change, characterized by an expected selective enhancement at target tone frequency but also by an equally selective depression at reference tone frequency. When single-tone detection and frequency discrimination tasks were performed sequentially, neurons responded differentially to identical tones, reflecting distinct predictive values of stimuli in the two behavioral contexts. All results were observed in multiunit as well as single-unit recordings. Our findings provide additional evidence for the presence of adaptive neuronal responses in A1 that can swiftly change to reflect both sensory content and the changing behavioral meaning of incoming acoustic stimuli.

Acoustic Stimulation↗

PubMed2004

Dynamics of precise spike timing in primary auditory cortex.

Although single units in primary auditory cortex (A1) exhibit accurate timing in their phasic response to the onset of sound (precision of a few milliseconds), paradoxically, they are unable to sustain synchronized responses to repeated stimuli at rates much beyond 20 Hz. To explore the relationship between these two aspects of cortical response, we designed a broadband stimulus with a slowly modulated spectrotemporal envelope riding on top of a rapidly modulated waveform (or fine structure). Using this stimulus, we quantified the ability of cortical cells to encode independently and simultaneously the stimulus envelope and fine structure. Specifically, by reverse-correlating unit responses with these two stimulus dimensions, we measured the spectrotemporal response fields (STRFs) associated with the processing of the envelope, the fine structure, and the complete stimulus. A1 cells respond well to the slow spectrotemporal envelopes and produce a wide variety of STRFs. In over 70% of cases, A1 units also track the fine-structure modulations precisely, throughout the stimulus, and for frequencies up to several hundred Hertz. Such a dual response, however, is contingent on the cell being driven by both fast and slow modulations, in that the response to the slowly modulated envelope gates the expression of the fine structure. We also demonstrate that either a simplified model of synaptic depression and facilitation, and/or a cortical network of thalamic excitation and cortical inhibition can account for major trends in the observed findings. Finally, we discuss the potential functional significance and perceptual relevance of these coexistent, complementary dynamic response modes.

Acoustic Stimulation↗