Five Japanese macaques and five other Old World monkeys were trained to discriminate among field-recorded Japanese macaque vocalizations. One task required discrimination of a communicatively relevant acoustic feature ("peak"), and a second required discrimination of an orthogonal feature of the same vocalizations ("pitch"). The Japanese animals more proficiently discriminated the peak feature when stimuli were presented to the right ear (primarily left cerebral hemisphere), as opposed to the left ear (primarily right hemisphere). In discriminating the pitch feature, the Japanese animals either showed (i) a left-ear processing advantage or (ii) no ear advantage. The comparison animals, with one exception, showed no ear advantage in processing either feature of the vocalizations. The results suggest that Japanese macaques engage left-hemisphere processors for the analysis of communicatively significant sounds that are analogous to the lateralized mechanisms used by humans listening to speech.
Field studies indicate that Japanese macaque (Macaca fuscata) communication signals vary with the social situation in which they occur [S. Green, "Variation of vocal pattern with social situation in the Japanese monkey (Macaca fuscata): A field study," in Primate Behavior, edited by L. A. Rosenblum (Academic, New York, 1975), Vol. 4]. A significant acoustic property of the contact calls produced by these primates is the temporal position of a frequency peak within the vocalization, that is, an inflection from rising to falling frequency [May et al., "Significant features of Japanese macaque communication sounds: A psychophysical study," Anim. Behav. 36, 1432-1444 (1988)]. The experiments reported here are based on the hypothesis that Japanese macaques derive meaning from this temporally graded feature by parceling the acoustic variation inherent in natural contact calls into two functional categories, and thus exhibit behavior that is analogous to the categorical perception of speech sounds by humans. To test this hypothesis, Japanese macaques were trained to classify natural contact calls by performing operant responses that signified either an early or late frequency peak position. Then, the subjects were tested in a series of experiments that required them to generalize this behavior to synthetic calls representing a continuum of peak positions. Demonstration of the classical perceptual effects noted for human listeners suggests that categorical perception reflects a principle of auditory information processing that influences the perception of sounds in the communication systems not only of humans, but of animals as well.
The study was designed to determine whether the neural lateralization of vocal perception in Japanese macaques depends on the acoustic properties of the calls used or their communicative significance. Four monkeys--two Japanese macaques and two comparison macaques--were trained to discriminate among monaurally presented exemplars of two classes of vocalizations from the Japanese macaque's repertoire. Once the subjects mastered the discrimination, they performed at equivalent accuracy levels for 150 sessions. However, during this time the Japanese monkeys showed a right ear performance advantage, whereas the comparison monkeys showed no ear advantage. In order to assess whether the comparison and Japanese monkeys were attending to the same acoustic cue when performing the discrimination, a generalization test was conducted with 27 novel vocalizations. The individual monkeys' generalization gradients were highly similar and revealed that all subjects were in fact listening to the same feature of the calls. These findings, coupled with the fact that the calls were of biological significance to the Japanese monkeys alone, suggest that the laterality effect is related, in some fashion, to the communicative valence of the signals rather than their purely physical characteristics.
Monkeys were trained to release a telegraph key at the onset of a pure tone. Latency of the response was measured over a 70-db range of sound pressure (re 0.0002 dyn/cm(2)) at six frequencies (250 to 15,000 cps). Latency was found to be an inverse exponential function of intensity at all frequencies. Equal loudness was inferred from the equal latency contours which were constructed from the latency-intensity functions at each frequency. These data indicate peak auditory sensitivity for the monkey near 1000 cps. At the frequencies above and below 1000 cps consistently more sound energy was required for equal latency.
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